WO2015053313A1 - Mouthpiece for endoscopic examination and de-aeration prevention valve device - Google Patents

Mouthpiece for endoscopic examination and de-aeration prevention valve device Download PDF

Info

Publication number
WO2015053313A1
WO2015053313A1 PCT/JP2014/076947 JP2014076947W WO2015053313A1 WO 2015053313 A1 WO2015053313 A1 WO 2015053313A1 JP 2014076947 W JP2014076947 W JP 2014076947W WO 2015053313 A1 WO2015053313 A1 WO 2015053313A1
Authority
WO
WIPO (PCT)
Prior art keywords
mouthpiece
endoscope
valve device
prevention valve
endoscopy
Prior art date
Application number
PCT/JP2014/076947
Other languages
French (fr)
Japanese (ja)
Inventor
泰 大森
秀明 松波
池田 昌夫
新悦 原田
秀昭 浅井
愛 志賀
芳樹 豊田
Original Assignee
住友ベークライト株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 住友ベークライト株式会社 filed Critical 住友ベークライト株式会社
Publication of WO2015053313A1 publication Critical patent/WO2015053313A1/en

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/04Tracheal tubes
    • A61M16/0488Mouthpieces; Means for guiding, securing or introducing the tubes
    • A61M16/049Mouthpieces
    • A61M16/0493Mouthpieces with means for protecting the tube from damage caused by the patient's teeth, e.g. bite block
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M16/00Devices for influencing the respiratory system of patients by gas treatment, e.g. mouth-to-mouth respiration; Tracheal tubes
    • A61M16/04Tracheal tubes
    • A61M16/0488Mouthpieces; Means for guiding, securing or introducing the tubes
    • A61M16/049Mouthpieces
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/34Trocars; Puncturing needles
    • A61B17/3462Trocars; Puncturing needles with means for changing the diameter or the orientation of the entrance port of the cannula, e.g. for use with different-sized instruments, reduction ports, adapter seals

Definitions

  • the present invention relates to an endoscopy mouthpiece that can be used for oral endoscopy and an anti-aeration valve device used for an endoscope mouthpiece.
  • This application is filed on October 10, 2013, Japanese Patent Application No. 2013-212462, filed on October 10, 2013, Japanese Patent Application No. 2013-212484, filed on Japan, April 25, 2014 Claims priority based on Japanese Patent Application No. 2014-91182 filed in Japan, the contents of which are incorporated herein by reference.
  • the diameter of the endoscope insertion hole in the conventional mouthpiece is designed to be larger than the diameter of the endoscope. Therefore, when a conventional mouthpiece is used when examining the middle and lower pharynx, breath is leaked from between an endoscope insertion hole provided in the mouthpiece and an endoscope inserted through the endoscope insertion hole.
  • the present invention has been made in view of the above-described problems.
  • a gas such as breath from leaking out of the body from the mouth during the test, in response to a new problem that it is desirable to be able to breathe with the mouthpiece attached.
  • a mouthpiece for endoscopy is provided.
  • this invention provides the deaeration prevention valve apparatus used for the mouthpiece for endoscopes made
  • the mouthpiece for endoscopy of the present invention includes a mouthpiece body having an insertion hole through which an endoscope can be inserted and removed, and between the endoscope inserted through the insertion hole and the mouthpiece body. And a deaeration prevention valve device that hermetically seals.
  • the first deaeration prevention valve device of the present invention is detachably attached to the proximal end portion of the mouthpiece inserted into the oral cavity having a lumen through which the endoscope is inserted and removed.
  • an annular endoscope insertion portion that is circumferentially attached to the endoscope, and a flexible expansion / contraction means provided around the endoscope insertion portion.
  • the second deaeration prevention valve device of the present invention is detachably attached to the base end portion of the mouthpiece inserted into the oral cavity having a lumen through which the endoscope is inserted and removed.
  • a deaeration prevention valve device used for an endoscope mouthpiece a frame portion mounted on an inner peripheral surface of the base end portion of the mouthpiece, and provided on the frame portion, A locking portion that is detachably locked to the inner peripheral surface, and a valve body portion provided inside the frame portion, wherein the valve body portion is provided at a substantially central portion of the valve body portion.
  • An annular endoscope insertion portion provided around the endoscope and a flexible extension / contraction means provided around the endoscope insertion portion.
  • the mouthpiece for endoscopy of the present invention has an insertion hole through which an endoscope can be inserted and removed.
  • the insertion hole is provided with a deaeration prevention valve device that hermetically seals between the insertion hole and the endoscope. Therefore, the mouthpiece for endoscopy of the present invention can prevent gas leakage from the insertion hole through which the endoscope is inserted.
  • the deaeration prevention valve device of the present invention by using the mouthpiece for an endoscope, the visual field of the hypopharynx can be secured by filling the oral pharynx with air in the Valsalva method, and further It is possible to reduce mirror breakage and endoscope operability degradation.
  • the deaeration prevention valve device of the present invention can be attached to and detached from the endoscope mouthpiece, airtightness securing by the deaeration prevention valve device can be selected and performed when necessary. Therefore, a specific endoscope mouthpiece can be applied not only to the Valsalva method but also to various examinations and treatments.
  • FIG. 2 is an XX cross-sectional view of the mouthpiece for endoscopy shown in FIG. It is a reverse view of the mouthpiece for endoscopy shown in FIG. It is a disassembled perspective view of the mouthpiece for endoscopy shown in FIG. It is a front view of the mouthpiece body in the first embodiment of the present invention. It is a side view of the mouthpiece body in a first embodiment of the present invention. It is a perspective view which shows an example of the mouthpiece for endoscopy concerning 2nd embodiment of this invention.
  • FIG. 9 is a YY sectional view of the mouthpiece for endoscopy shown in FIG. 8. It is a disassembled perspective view of the mouthpiece for endoscopy concerning a third embodiment of the present invention.
  • FIG. 12 is a ZZ sectional view of the mouthpiece for endoscopy shown in FIG. 11. It is the perspective view which looked at the state which attached the coating
  • the upper view is a perspective view in which the deaeration prevention valve device according to the fifth embodiment of the present invention is mounted on an endoscope mouthpiece, and the lower view is a perspective view before the mounting.
  • proximal end indicates a specific region or specific location of the mouthpiece of the present invention or each member constituting the mouthpiece in a use state when the patient holds the mouthpiece of the present invention in his / her mouth.
  • distal end indicates the end on the patient side (inner oral cavity)
  • proximal end indicates the end on the opposite side (outer oral cavity) from the patient side.
  • the distal end portion refers to a predetermined length region including the distal end
  • the proximal end portion refers to a predetermined length region including the proximal end.
  • endoscopy is used where appropriate.
  • the above terms are used not only for endoscopic examination in a narrow sense such as observing the state of the affected area using an endoscope, but also for performing operations such as treating the affected area using an endoscope and collecting tissues of the affected area.
  • the endoscopic examination in a broad sense is also included as appropriate.
  • the person who holds the mouthpiece and undergoes endoscopy may be referred to as a patient.
  • a person who handles an endoscope using a mouthpiece may be called an operator.
  • FIG. 1 is a perspective view showing an example of a mouthpiece 100 according to the first embodiment of the present invention.
  • FIG. 2 is a front view of the mouthpiece 100 shown in FIG.
  • FIG. 3 is a cross-sectional view of the mouthpiece 100 shown in FIG.
  • FIG. 4 is a rear view of the mouthpiece 100 shown in FIG.
  • FIG. 5 is an exploded perspective view of the mouthpiece 100 shown in FIG.
  • FIG. 6 is a front view of the mouthpiece body 11 in the first embodiment of the present invention.
  • FIG. 7 is a side view of the mouthpiece body 11 in the first embodiment of the present invention. Both the front view of the mouthpiece 100 and the front view of the mouthpiece body 11 are views observed from the long axis direction of the tooth receiving portion 26 (FIGS. 3 and 4).
  • the mouthpiece 100 includes a mouthpiece body 11 having an insertion hole 12 through which an endoscope (not shown) can be inserted and removed freely, and between the endoscope inserted through the insertion hole 12 and the mouthpiece body 11. And an anti-aeration valve device 18 for hermetically sealing.
  • the endoscope includes an oral endoscope or a nasal endoscope, and is a medical instrument that is inserted into a body cavity and used to examine or treat an affected area.
  • the mouthpiece 100 is positioned in front of the pharynx with the distal end of the mouthpiece 100 in a state where the patient is in the mouth. That is, the mouthpiece 100 does not extend beyond the pharynx at the distal end of the overtube as in the so-called overtube.
  • the insertion hole 12 is a lumen of both end openings provided in the mouthpiece body 11. In the present embodiment, the insertion hole 12 is reduced to such an extent that the flow of gas between the endoscope and the mouthpiece body 11 does not hinder the inspection in the region of the opening or any place between the openings. Or substantially shieldable.
  • the deaeration prevention valve device 18 in the present embodiment is detachable from the mouthpiece body 11 as will be described later.
  • the mouthpiece 100 in the present embodiment includes an aspect including a deaeration prevention valve device 18 that is fixedly installed on the mouthpiece body 11 and cannot be repeatedly attached and detached.
  • the mouthpiece body 11 has an insertion hole 12 penetrating the inside.
  • the insertion hole 12 opens at the proximal end and the distal end of the mouthpiece body 11.
  • the insertion hole 12 in the present embodiment has a constricted shape having a reduced diameter portion 110 and an enlarged diameter portion 111 from the proximal end to the distal end of the mouthpiece body 11.
  • the boundary between the reduced diameter portion 110 and the enlarged diameter portion 111 is a boundary portion 112.
  • the reduced diameter portion 110 refers to a region in which the inner diameter of the insertion hole 12 that is the lumen of the mouthpiece body 11 decreases continuously or stepwise.
  • the enlarged diameter portion 111 is a region in which the inner diameter of the insertion hole 12 that is the lumen of the mouthpiece body 11 increases continuously or stepwise.
  • the stepwise change in the diameter of the reduced diameter portion 110 or the enlarged diameter portion 111 may be a change in only one step, or may be a change in two or more steps.
  • the reduced diameter portion 110 is a proximal end portion of the mouthpiece body 11 and is provided closer to the proximal end.
  • the operation of the endoscope inserted through the insertion hole 12 is generally a parallel operation of moving the entire endoscope in a direction substantially parallel to the insertion direction, arbitrarily twisting the endoscope in the insertion direction, This is performed by a rotation operation for guiding the endoscope tip to a target position and a combination thereof.
  • the parallel operation area is limited by the boundary portion 112, and the rotation operation area is sufficiently secured. Is possible. That is, when the endoscope inserted through the insertion hole 12 is operated in parallel or rotated, the movement of the endoscope by the operation causes distortion in the expansion / contraction part 16 (extension / contraction means).
  • the stretchable part 16 can absorb the strain.
  • the stretchable portion 16 cannot absorb the strain, and as a result, the endoscope insertion portion 17 is deformed, and a gap is generated between the endoscope insertion portion 17 and the endoscope.
  • the reduced diameter portion 110 in the present embodiment has a circular funnel shape (see FIG. 3). For this reason, it is possible to smoothly guide the start of insertion of the endoscope through the insertion hole 12.
  • the insertion hole 12 in the present embodiment has a diameter that increases in the vicinity of the boundary portion 112 and has a straight cylindrical shape on the distal end side.
  • the long cylindrical region is an ellipse whose outer shape and inner shape of a cross section cut perpendicularly to the insertion direction are substantially similar.
  • a vertical section with respect to the insertion direction on the distal end side from the boundary portion 112 forms an ellipse including a short axis and a long axis that are larger than the inner diameter of the reduced diameter portion 110.
  • the mouthpiece body 11 has a cylindrical tooth receiving portion 26 at the distal end.
  • the outer diameter of the tooth receiving portion 26 has a major axis 36 and a minor axis 38 (see FIG. 4). That is, the cross-sectional shape when the tooth receiving portion 26 is cut in the direction perpendicular to the longitudinal direction is not a perfect circle but is long in one direction.
  • the cross-sectional shape of the tooth receiving portion 26 is an ellipse (including an ellipse).
  • the tooth receiving part 26 having such a cross-sectional shape can easily bring the lip and the tooth receiving part 26 into close contact with each other in a state where the patient holds the mouthpiece 100 as compared with a case where the cross-sectional shape is a perfect circle.
  • the tooth receiving part 26 having an oval cross section can be given to the patient so that the major axis direction is substantially parallel to the direction connecting the mouth angle and the mouth angle of the patient, and the mouth can be closed. In such a case, the mouth corner and the ellipse fit, and it is difficult for the breath to leak from the mouth corner.
  • the inner diameter of the tooth receiving portion 26 also has a major axis and a minor axis.
  • the tooth receiving portion 26 is formed in an oval shape by a substantially uniform wall. Since the inner diameter shape of the tooth receiving portion 26 is formed in an ellipse, the operation range of the endoscope is large particularly in the long axis direction.
  • the tooth receiving portion 26 has a convex portion 30 protruding outward in the radial direction at the distal end portion of the tooth receiving portion 26. When the patient grips the mouthpiece 100 by directly applying teeth to the tooth receiving portion 26, the convex portion 30 functions as a stop portion of the patient's teeth and prevents the mouthpiece 100 from falling from the mouth. Is possible.
  • the mouthpiece 100 has a flange 42 extending outward from the outer peripheral surface 40 (FIG. 3) between the distal end portion and the proximal end portion of the mouthpiece body 11.
  • the outer peripheral surface 40 is a surface constituting the outer side surface of the mouthpiece body 11.
  • the collar portion 42 extends longer in the extending direction of the short shaft 38 than in the extending direction of the long shaft 36 of the tooth receiving portion 26.
  • the collar portion 42 in the present embodiment is curved in a convex shape in a direction from the distal end to the proximal end of the mouthpiece body 11.
  • the details of the curved shape are not particularly limited, but, for example, when the collar portion 42 is observed with the long axis 36 set in the left-right direction, the collar portion 42 has a convex shape from the distal end portion toward the proximal end portion. (See FIG. 7).
  • the collar part 42 is a cylindrical surface which is a shape that forms a part of the outer surface of the cylindrical body.
  • the central axis of the cylindrical body having the cylindrical surface is the same direction as the axial direction of the short axis 38. That is, the collar part 42 has a shape along the outer peripheral surface of the virtual cylindrical body.
  • the deaeration prevention valve device 18 As shown in FIG. 3, the deaeration prevention valve device 18 is provided around the insertion hole 12. Further, the deaeration prevention valve device 18 is attached to an endoscope (not shown) inserted through the insertion hole 12. That the deaeration prevention valve device 18 is provided around the insertion hole 12 means that the deaeration prevention valve device 18 is attached to the entire circumference of the insertion hole 12 at at least one end or in the middle of the insertion hole 12. Means. Specifically, in this embodiment, the expansion / contraction part 16 provided in the deaeration prevention valve device 18 is provided around the insertion hole 12 and is attached to the endoscope inserted through the insertion hole 12.
  • the deaeration prevention valve device 18 is provided with a fixing ring 59 which is a fixing member for crimping the deaeration prevention valve device 18 to the open end surface on the proximal end side of the mouthpiece body 11 ( FIG. 3).
  • the fixing ring 59 constitutes an expansion / contraction section fixing member for fixing the expansion / contraction section 16 to the frame section 14 (FIG. 3).
  • the fixing ring 59 is a substantially ring-shaped member, and is provided in an intermediate region between the lower end portion 23 and the upper end portion 25 inside the frame portion 14.
  • the insertion hole 12 is a hole provided in the mouthpiece 100 and into which the endoscope is inserted.
  • the deaeration prevention valve device 18 can be provided in one or more places in either the intermediate region of the insertion hole 12 or the opening region in the proximal end or the distal end of the insertion hole 12.
  • the deaeration prevention valve device 18 is directly or indirectly provided in the insertion hole 12.
  • the deaeration prevention valve device 18 in the present embodiment has a flexible expansion / contraction part 16 (extension / contraction means) provided around the insertion hole 12 (FIG. 1).
  • the expansion / contraction part 16 has an endoscope insertion part 17 that is provided at a substantially central part of the expansion / contraction part 16 and is attached to an endoscope (not shown).
  • the expansion / contraction part 16 is comprised with the flexible member which can contact
  • the flexible expansion / contraction part 16 is comprised from the member which is film
  • the film-shaped or disk-shaped stretchable part 16 includes both an aspect in which the in-plane is a substantially smooth surface and an aspect in which an uneven portion is provided in the plane.
  • the uneven portion includes a bellows portion 120.
  • the stretchable portion 16 may be a flat plate member made of a flat portion or a bellows member having the bellows portion 120, but is preferably a bellows member from the viewpoint of airtightness.
  • the bellows member includes both an aspect in which the bellows part 120 is provided in the in-plane direction in substantially the entire stretchable part 16 and an aspect in which the flat part and the bellows part 120 are combined.
  • the endoscope insertion part 17 into which the endoscope is inserted by the extension / contraction of the extension / contraction part 16 can move following the endoscope by operation of the endoscope.
  • the endoscope insertion portion 17 is movable in the radial direction, the forward / backward direction of the endoscope, and the rotation direction (the neck swinging direction or the twisting direction of the endoscope). For this reason, when the endoscope inserted in the endoscope insertion portion 17 is operated, the airtightness between the deaeration prevention valve device 18 and the endoscope is maintained without impairing the operability of the endoscope. Is possible. As shown in FIG.
  • a closing plug portion 60 that abuts the engagement receiving portion 54 of the mouthpiece body 11 and hermetically seals the opening on the proximal end side of the mouthpiece body 11 is provided on the outer edge of the expansion / contraction portion 16. Is provided. Details of the engagement receiving portion 54 will be described later.
  • the closing plug portion 60 may be formed integrally with the stretchable portion 16, or may be formed by joining another member to the outer edge of the stretchable portion 16.
  • the closing plug portion 60 can be formed of, for example, an elastic resin member.
  • the closing plug portion 60 is similar to the stretchable portion 16 and can be formed of the same or different resin material.
  • the endoscope insertion portion 17 according to the present embodiment is annular.
  • the endoscope insertion portion 17 in the present invention is not limited to this.
  • the endoscope insertion portion 17 may be a cut portion that is formed in the plane of the stretchable portion 16 and can penetrate the endoscope in the insertion direction of the insertion hole 12.
  • the diameter of the endoscope insertion portion 17 formed in an annular shape can be smaller than the diameter of the endoscope scheduled to be used. As a result, the peripheral attachment to the endoscope is ensured, and the airtight effect can be improved.
  • the expansion / contraction part 16 has a bellows part 120, a valley part 116, a valley part 114, a valley part 116, and a bellows part 120 which are provided concentrically with the annular endoscope insertion part 17.
  • the bellows portion 120 By having the bellows portion 120, the operability of the endoscope inserted into the endoscope insertion portion 17 can be further improved, and as a result, sufficient airtightness is maintained.
  • the inner edge of the bellows portion 120 is a valley portion 116 that overlaps most with the endoscope insertion portion 17.
  • the part other than the bellows part 120 is referred to as a non-bellows part.
  • the non-bellows part is a part other than the bellows part 120 in the stretchable part 16, and the stretchability in the in-plane direction of the non-bellows part is smaller than the stretchability in the in-plane direction of the bellows part 120.
  • the non-accordion portion includes a flat portion.
  • a flat part means the part which does not have an unevenness
  • the stretchable portion 16 is formed of a flexible member, and the bellows portion 120 is provided.
  • the stretchable portion 16 can be formed of a member having no flexibility or low flexibility, and the bellows portion 120 can be provided.
  • the deaeration prevention valve device 18 in the present embodiment has a frame portion 14 that is detachably attached to the mouthpiece body 11. With this configuration, the deaeration prevention valve device 18 can be attached to and detached from the mouthpiece body 11. For this reason, for example, after endoscopic examination of the middle and lower pharynx is performed in an airtight state, the deaeration prevention valve device 18 can be removed, and another endoscopic examination such as the esophagus and stomach can be subsequently performed. That is, when an examination of the esophagus and stomach is performed following the examination of the middle and lower pharynx where airtightness is important, it is not necessary to ensure airtightness so that the patient can fully breathe.
  • the presence or absence of ensuring airtightness is controllable suitably by attachment or detachment of the deaeration prevention valve apparatus 18 with respect to the mouthpiece main body 11.
  • FIG. More specifically, in general, in the examination of the esophagus and stomach, it is not necessary to ensure airtightness unlike the examination of the middle and lower pharynx by the Valsalva method described above. It is envisaged that the patient will be able to breathe well. However, if the field of view necessary for gastric observation cannot be obtained even if air is supplied through an endoscope, the air leakage from the mouth can be minimized by installing the deaeration prevention valve device 18 again. , Securing a field of view.
  • the deaeration prevention valve device 18 can be attached to and detached from the mouthpiece main body 11, so that the deaeration prevention valve device 18 is arbitrarily attached according to the endoscopy situation or the patient's situation.
  • the non-wearing can be selected.
  • the frame portion 14 can take various shapes according to the attachment position of the mouthpiece body 11.
  • the frame portion 14 in the present embodiment has a substantially cylindrical shape.
  • An elastic part 16 is provided on the inner surface of the frame part 14.
  • the frame part 14 and the expansion / contraction part 16 are formed by separate members, and the member constituting the frame part 14 is harder than the member constituting the expansion / contraction part 16.
  • the expansion / contraction part 16 may be directly fixed to the frame part 14 in addition to the aspect fixed to the frame part 14 by the fixing ring 59. Or the aspect fixed to the arbitrary arbitrary members provided in the frame part 14 and provided in the frame part 14 may be sufficient.
  • the frame part 14 can be attached to and detached from the mouthpiece body 11 by using a relatively hard material.
  • the material of the frame portion 14 include hard vinyl chloride resin, polyurethane resin, hard polyurethane resin, polyethylene resin, polyamide resin, polypropylene resin, polyacetal resin, fluorinated polyethylene resin, and acrylonitrile-butadiene-styrene.
  • Polymer (ABS) resin or the like can be used.
  • the stretchable part 16 is preferably made of a material having flexibility as compared with the frame part 14.
  • the material of the stretchable portion 16 is preferably a stretchable material such as natural rubber, synthetic rubber, polyurethane elastomer, styrene-butadiene-styrene terpolymer, silicone rubber, and the like. It is also preferable to use the above-mentioned material containing oil in order to improve the friction with the stretchable part 16.
  • the attachment / detachment of the deaeration prevention valve device 18 with respect to the mouthpiece body 11 is realized as follows. That is, the frame portion 14 includes a locking portion 24 that detachably locks the frame portion 14 to the proximal end of the mouthpiece body 11 (see FIGS. 1 to 3).
  • the locking portion 24 in the present embodiment is provided on the circumference of the outer edge of the frame portion 14.
  • the locking portion 24 extends along the outer edge of the frame portion 14 beyond the upper and lower ends of the outer edge.
  • the lower end 23 extending beyond the lower end of the frame portion 14 of the locking portion 24 is provided with an engaging protrusion 22 (locking means) protruding toward the inside of the frame portion 14 (FIG. 2). And FIG. 3).
  • the engagement protrusion 22 is a proximal end portion of the mouthpiece body 11 and engages with the outer surface.
  • the mouthpiece body 11 is provided with an annular engagement receiving portion 54 that is continuous from the proximal end of the reduced diameter portion 110 and extends radially outward (FIGS. 6 and 7).
  • the deaeration prevention valve device 18 is attached to the mouthpiece 100 by the engagement protrusion 22 engaging with the engagement receiver 54.
  • the up-down direction here makes the proximal end side of the mouthpiece 100 upward, and makes the distal end side downward.
  • a knob portion 20 (finger hook portion) is provided on an upper end portion 25 that extends beyond the upper end of the frame portion 14 of the locking portion 24.
  • the knob portion 20 is provided on the outer side surface at the upper end of the locking portion 24.
  • finger sliding is prevented and operability is good.
  • the upper end portion 25 of the locking portion 24 By pushing the upper end portion 25 of the locking portion 24 inward in the radial direction, the lower end portion 23 opens outward in the radial direction. Thereby, the engagement protrusion 22 can be engaged with or released from the engagement receiving portion 54.
  • the mouthpiece body 11 can secure the strength of the mouthpiece 100 and can sufficiently secure the inner diameter of the insertion hole 12 that is the lumen of the mouthpiece body 11.
  • the mouthpiece body 11 is made of hard vinyl chloride resin, hard polyurethane resin, polyethylene resin, polyamide resin, polypropylene resin, polyacetal resin, fluorinated polyethylene resin, acrylonitrile-butadiene-styrene copolymer (ABS) resin, or the like. These resin materials can be used.
  • the mouthpiece main body 11 can be formed of a kind of resin material, and the type of material constituting each arbitrary location can be changed.
  • the mouthpiece body 11 may be formed of the same material as that of the frame portion 14 described above from the viewpoint of using a relatively hard material. At this time, the mouthpiece main body 11 and the frame portion 14 may be formed of the same kind of material or different kinds of materials having the same hardness.
  • the number of the locking portions 24 is not particularly limited, and may be arbitrarily determined as long as the deaeration prevention valve device 18 can be attached to and detached from the mouthpiece body 11.
  • the mouthpiece 100 according to the present embodiment is provided with locking portions 24 at two locations that are substantially opposed to each other with the frame portion 14 therebetween.
  • a finger can be applied to the outer surface of the two locking portions 24 that are substantially opposed to each other, or three or more locking portions 24 provided at arbitrary positions, and pressed inward. Thereby, the lower end part 23 of the latching
  • the locking portion 24 in the present embodiment is located on the outer surface of the mouthpiece body 11. Therefore, when the deaeration prevention valve device 18 is attached to the mouthpiece body 11, the range of motion of the endoscope in the lumen of the mouthpiece body 11 is not narrowed, and the operability of the endoscope is not impaired.
  • the mechanism for attaching / detaching the deaeration prevention valve device 18 to / from the mouthpiece body 11 is not limited to this.
  • the locking portion 24 may be provided on the circumference of the inner edge of the frame portion 14, and may be engaged with or fitted to any location on the inner side surface of the proximal end portion of the mouthpiece body 11 to perform the above attachment / detachment.
  • the attachment / detachment of the deaeration prevention valve device 18 in the present invention is not limited to the locking means.
  • a friction element such as silicone rubber having a predetermined friction coefficient provided on the frame portion 14 and a biasing member such as a spring that biases the friction element toward the outer peripheral surface or inner peripheral surface of the mouthpiece body 11 are provided. You may combine.
  • the mouthpiece body 11 has the cylindrical tooth receiving portion 26 at the distal end portion.
  • the mouthpiece body 11 may further include a covering portion 28 that covers the outer periphery of the tooth receiving portion 26.
  • the hardness of the covering portion 28 is lower than the hardness of the tooth receiving portion 26. Therefore, when the patient picks up the tooth receiving portion 26 from above the covering portion 28, it is possible to give the patient a favorable experience and maintain the strength of the tooth receiving portion 26.
  • a flexible resin member such as silicone rubber
  • the teeth slightly bite into the covering portion 28. The shift of the biting position is suppressed. Therefore, the mouthpiece is prevented from dropping from the mouth during the endoscopy.
  • the covering portion 28 By using a relatively soft material for the covering portion 28, when the patient hits the teeth from the outer peripheral surface, the covering portion 28 is given a good feeling of comfort, and the teeth are difficult to slip on the surface of the covering portion 28.
  • a highly elastic material such as silicone rubber, polyurethane elastomer, natural rubber, synthetic rubber, styrene-butadiene-styrene terpolymer is preferable.
  • the term “hardness” means the hardness measured by a known means suitable for each component.
  • the hardness of an arbitrary configuration of the present invention formed of a resin member can be measured according to durometer hardness JIS K 6253.
  • the covering portion 28 in this embodiment is detachable from the mouthpiece body 11. As a result, a patient with a small mouth can remove the covering portion 28 to directly grip the tooth receiving portion 26 in order to reduce the diameter of the gripping portion. Further, by preparing two or more kinds of covering portions 28 having different thicknesses, it is possible to further finely adjust the diameter of the portion that the patient can hold according to the size of the patient's mouth. However, the present invention does not exclude the covering portion 28 that cannot be repeatedly attached to and detached from the mouthpiece body 11 (that is, fixed to the tooth receiving portion 26).
  • the covering portion 28 in the present embodiment covers at least a region that is the tooth receiving portion 26 and is in contact with the teeth of the patient holding the mouthpiece body 11.
  • the covering portion 28 may have an O-ring shape that covers the entire outer periphery of the tooth receiving portion 26.
  • the covering portion 28 can be formed of an elastic member that can be easily deformed from a predetermined shape and can be restored to the predetermined shape. If the covering portion 28 is formed of such an elastic member, for example, it can have a cylindrical shape with a substantially circular cross section, and can be in close contact with the tooth receiving portion 26 that is a cylindrical portion with an elliptical cross section. It is.
  • the shape of the covering portion 28 is not limited to the O-ring shape.
  • the covering portion 28 may have a C-shaped cross section when cut perpendicularly to the longitudinal direction.
  • the covering portion 28 has a second convex portion 50 protruding outward in the radial direction at the distal end portion of the covering portion 28 on the outer peripheral surface side.
  • the second convex portion 50 functions as a tooth stopping portion when the patient hits the covering portion 28 with the tooth receiving portion 26 covered with the covering portion 28, and the mouthpiece 100 falls from the mouth. Can be prevented.
  • the tooth receiving portion 26 and the covering portion 28 in the present embodiment are in a relationship of engaging with each other, and are configured so that the covering portion 28 is not detached when the covering portion 28 covers the tooth receiving portion 26. . That is, as shown in FIG. 3, the tooth receiving portion 26 has a convex portion 30 protruding outward in the radial direction at the distal end portion of the tooth receiving portion 26.
  • the covering portion 28 has a small diameter portion 34 and a large diameter portion 32 on the inner peripheral surface side.
  • the covering portion 28 has a step portion 37 that is formed by steps of the small-diameter portion 34 and the large-diameter portion 32 on the inner peripheral surface side, and whose diameter changes discontinuously.
  • the projecting portion 30 and the stepped portion 37 engage with each other, thereby preventing the covering portion 28 from shifting from the proximal end of the mouthpiece body 11 toward the distal end.
  • step-difference part 37 are contact
  • the covering portion 28 is provided with a small diameter portion 34 on the proximal end side and a large diameter portion 32 on the distal end side.
  • region of the large diameter part 32 becomes a recessed part with respect to the area
  • the end surface 51 of the distal end of the covering portion 28 and the end surface 52 of the distal end of the tooth receiving portion 26 are substantially in the same plane. .
  • the mouthpiece 100 includes the cylindrical tooth receiving portion 26 provided at the distal end portion of the mouthpiece main body 11 and the covering portion 28 that covers the outer periphery of the tooth receiving portion 26.
  • the mouthpiece 100 has a flange 42 extending outward from an outer peripheral surface provided between the distal end portion and the proximal end portion of the mouthpiece body 11.
  • the mouthpiece 100 according to the present embodiment includes the shortest distance A from the proximal end portion of the back surface 210 of the collar portion 42 to the distal end of the mouthpiece body 11 and the length of the covering portion 28 in the longitudinal direction (covering portion 28. The length along the direction connecting the distal end and the proximal end of the mouthpiece body 11) is substantially the same.
  • the back surface 210 of the collar part 42 means the surface of the back side of the collar part 42 when the mouthpiece 100 is seen from the proximal end side. According to such a configuration, substantially the entire portion of the tooth receiving portion 26 where the patient applies teeth is covered with the covering portion 28. Therefore, the patient can experience the elasticity of the covering portion 28 in the same manner regardless of where the tooth is applied to the tooth receiving portion 26.
  • the proximal end of the mouthpiece body 11 is set to the upper side and the distal end is set to the lower side
  • the proximal end portion of the collar portion 42 of the present embodiment is provided at a height position substantially equal to the boundary portion 112 described above. ing.
  • the telescopic part 16 has an annular bellows part 120 that is concentric with the annular endoscope insertion part 17 and is provided with a trough part 116 and a peak part 114 in the radial direction.
  • the bellows part 120 is arranged coaxially with an inner circle 112 ⁇ / b> A surrounded by a boundary part 112 that is a boundary between the reduced diameter part 110 and the enlarged diameter part 111.
  • the diameter of the outer edge 120A of the bellows portion 120 is larger than the diameter of the inner circle 112A.
  • the outer edge 120 ⁇ / b> A of the bellows part 120 refers to a peak part 114 or a valley part 116 that is located farthest from the center among the peak parts 114 or the valley parts 116 constituting the bellows part 120.
  • the outer edge 120 ⁇ / b> A of the bellows portion 120 is a circle connecting the vertices of the outer peak portions 114 of the peak portions 114 provided concentrically and double.
  • the bellows portion 120 in the present invention can absorb strain generated in the telescopic portion 16 due to the movement of the endoscope in the radial direction.
  • the bellows portion 120 is a peak portion or a concave valley portion that is convex in a direction different from the extending direction of the stretchable portion 16.
  • the apex of the peak or valley includes both an acute angle and an obtuse angle.
  • the bellows part 120 can be constituted by, for example, at least one peak part 114 or at least one valley part 116 provided in the stretchable part 16.
  • the bellows part 120 may be composed of two or more adjacent peak parts 114 and valley parts 116.
  • the bellows part 120 may have a flat part (not shown) between the peak part 114 and the valley part 116.
  • the flat portion is included in a plane in a direction substantially perpendicular to the insertion direction of the insertion hole 12.
  • the present invention has a non-accordion portion around the endoscope insertion portion 17 and further has a bellows portion around the non-accordion portion, and a non-accordion portion around the endoscope insertion portion 17.
  • Any of the embodiments in which the bellows portion 120 is disposed in contact with the endoscope insertion portion 17 is also included.
  • the present invention includes a mode in which the endoscope insertion portion 17 has a flat portion that is a non-accordion portion and the bellows portion 120 is provided around the flat portion.
  • the mouthpiece 100 according to this embodiment does not have a non-accordion portion around the endoscope insertion portion 17, and the bellows portion 120 is disposed in contact with the endoscope insertion portion 17.
  • the bellows portion 120 can satisfactorily absorb the strain generated in the stretchable portion 16 due to the movement of the endoscope inside the inner circle 112A. Further, the endoscope insertion portion 17 that is in close contact with the peripheral surface of the endoscope satisfactorily follows the movement of the endoscope when the endoscope is operated. Therefore, the state where the endoscope and the endoscope insertion portion 17 are in close contact with each other is well maintained, and the gap between the endoscope and the mouthpiece body 11 is sealed with high airtightness.
  • the diameter of the inner edge 120B of the bellows portion 120 is smaller than the diameter of the inner circle 112A, it is possible to provide excellent operability and airtightness when operating the endoscope (particularly parallel operation). The effect is remarkable.
  • the diameter of the inner edge 120B of the bellows part 120 is smaller than the diameter of the inner circle 112A, and the above-described non-bellows part is not provided between the endoscope insertion part 17 and the inner edge 120B, or the non-bellows It is preferable that it is an aspect which has a part but few.
  • the bellows part 120 can be deformed before the endoscope insertion part 17, and the airtightness between the endoscope insertion part 17 and the endoscope can be maintained high.
  • the mouthpiece body 11 and the deaeration prevention valve device 18 described above may constitute a mouthpiece kit for endoscopy in a state where they are separated from each other.
  • the mouthpiece body 11, the anti-aeration valve device 18, and the covering portion 28 may constitute an endoscopic examination mouthpiece kit in a state of being separated from each other.
  • the above-mentioned mouthpiece kit for endoscopy is combined in use to constitute the mouthpiece of the present invention.
  • FIG. 8 is a perspective view showing an example of a mouthpiece 200 according to the second embodiment of the present invention.
  • FIG. 9 is an exploded perspective view of the mouthpiece 200 shown in FIG.
  • FIG. 10 is a YY sectional view of the mouthpiece 200 shown in FIG.
  • the mouthpiece 200 has a mouthpiece body 61 having an insertion hole 12 through which an endoscope (not shown) can be inserted and removed freely, and the endoscope inserted through the insertion hole 12 and the mouthpiece body 61 are airtight. And a deaeration preventing valve device 418 for sealing.
  • the deaeration prevention valve device 418 includes a frame part 414, an expansion / contraction part 16 (extension / contraction means), and an endoscope insertion part 17.
  • the frame part 414 includes a locking part that detachably locks the frame part 414 to the proximal end of the mouthpiece body 61.
  • the locking portion is a fitting convex portion 422 (locking means) convex in the radial direction on the outer surface of the distal end portion of the frame portion 414.
  • two fitting protrusions 422 are provided at opposing positions, but the present invention is not limited to this, and the number of fitting protrusions 422 may be one, or three or more.
  • the mouthpiece 200 has the same configuration as the mouthpiece 100 except that the configuration of the locking portion is different from that of the mouthpiece 100. Therefore, regarding the mouthpiece 200, description of other configurations other than the locking portion is omitted.
  • An engagement receiving portion 420 is provided on the proximal end side of the mouthpiece main body 61 with respect to the collar portion 42.
  • the engagement receiving part 420 has a fitting part that can be engaged with the fitting convex part 422.
  • the up-down direction mentioned regarding description of a fitting part is a paper surface up-down direction in FIG.
  • the engagement receiving part 420 is a cylinder part 421 that stands up from the surface on the proximal end part side of the flange part 42, and has a fitting recess 425 as a fitting part on the side surface of the cylinder part 421.
  • a fitting retaining portion 426 is provided.
  • the fitting recess 425 is a groove-like recess formed from the upper end to the lower end on the inner wall surface of the cylindrical portion 421.
  • the width dimension of the fitting recess 425 is equal to or greater than the width dimension of the fitting protrusion 422.
  • the fitting retaining portion 426 is a concave portion that is continuous with the fitting concave portion 425 and extends in a direction different from the extending direction of the grooves constituting the fitting concave portion 425.
  • the fitting retaining portion 426 is continuous with the lower end of the fitting recess 425 and extends in a direction substantially perpendicular to the extending direction of the fitting recess 425.
  • the description of the locking part in the mouthpiece 100 and the mouthpiece 200 described above shows an example of the locking part of the present invention, and does not limit the present invention.
  • FIG. 11 is an exploded perspective view of the mouthpiece 300 according to the third embodiment of the present invention.
  • 12 is a ZZ cross-sectional view of the mouthpiece 300 shown in FIG.
  • the mouthpiece 300 is the same as the mouthpiece 100 for the deaeration prevention valve device 18 and the mouthpiece body 11, and the covering portion 29 is different from the covering portion 28 provided on the mouthpiece 100.
  • the covering portion 29 in this embodiment has a cylindrical shape having an outer diameter having a major axis 310 and a minor axis 320.
  • the second protrusion 50 includes a first extension 312 extending on the major axis 310 with a first length 311 and a second extension extending on a minor axis with a second length 321. Part 322.
  • the covering portion 29 is configured such that the first length 311 is larger than the second length 321.
  • the covering part 29 has a long outer shape in at least one of the cross sections.
  • the shape of the cross section includes an ellipse and an ellipse.
  • the second convex portion 50 is preferably provided at the distal end portion of the covering portion 29, and more preferably provided at the distal end as in this embodiment. preferable.
  • the first extending portion 312 and the second extending portion 322 are continuous in the outer peripheral direction. From the top view, the first extension 312 includes an extension of the major axis 310, and the second extension 322 includes an extension of the minor axis 320.
  • the present invention is not limited to this, and although not illustrated, the first extending portion 312 and the second extending portion 322 may be provided discontinuously in the circumferential direction of the tooth receiving portion 26.
  • the second extension 322 can contact the back of the patient's teeth and prevents the mouthpiece 300 from falling out of the oral cavity.
  • the extension portion extending outward from the second protrusion 50 may be substantially only the first extension portion 312 and the second extension portion 322 may be omitted.
  • abuts to a cheek back it is possible to prevent that the mouthpiece 300 falls out from the inside of the oral cavity.
  • the first length 311 is a dimension in the extending direction of the second convex portion 50 measured along the extension line of the long axis 310 from the outer peripheral surface of the tooth receiving portion 26.
  • the second length 321 is a dimension in the extending direction of the second convex portion 50 measured along the extension line of the short axis 320 from the outer peripheral surface of the tooth receiving portion 26.
  • the ratio between the first length 311 and the second length 321 is not particularly limited.
  • the first length 311 is preferably set to be twice or more the second length 321.
  • the length of the first extension portion 312 (first length 311) is provided long enough to exert the effect of preventing breath leakage, and the second extension arranged on the back of the lips.
  • the length of the existing portion 322 (second length 321) can be appropriately shortened.
  • the 2nd convex part 50 provided with the 1st extension part 312 and the 2nd extension part 322 has good insertion property in an oral cavity, and the balance in an intraoral area is aimed at, and the discomfort to a patient is felt. Can be reduced.
  • the first length 311 is in the range of 5 mm to 10 mm and the second length 321 is in the range of 2 mm to 5 mm.
  • the outer diameter of the covering portion 29 can be, for example, a major axis in the major axis 310 direction in the range of 30 mm to 40 mm and a minor axis in the minor axis 320 direction in the range of 25 mm to 35 mm.
  • the long axis direction of the collar portion 42 and the extending direction of the first extending portion 312 are orthogonal to each other. Therefore, when the patient holds the mouthpiece 300, the buttocks 42 abut against the patient's lips to prevent the mouthpiece 300 from entering the oral cavity, and the first extension 312 abuts the cheek back. This prevents the mouthpiece 300 from falling out of the oral cavity.
  • the second projecting portion 50 is provided with a second extending portion 322 orthogonal to the first extending portion 312. The mouthpiece 300 is well prevented from falling out of the oral cavity by the second extending portion 322 abutting on the upper and lower teeth and the first extending portion 312 contacting the cheek back.
  • the first extending portion 312 in the present embodiment is formed thin toward the outer edge.
  • the proximal side surface of the first extending portion 312 is inclined so as to taper toward the outer edge of the second convex portion 50.
  • the inclination may be provided on the distal side surface of the first extension portion 312.
  • the proximal side surface of the first extending portion 312 that can hit the cheek back is inclined toward the outer edge, so that the way of hitting the cheek back can be made softer.
  • FIG. 13 shows a modification of the present embodiment.
  • FIG. 13 is a perspective view of the mouthpiece body 11 as viewed from the back side with the covering portion 29A used in a modification of the third embodiment of the present invention.
  • the covering portion 29 ⁇ / b> A is communicated with the insertion hole 12 provided in the mouthpiece main body 11 on the distal side surface of the first extending portion 312, and is thinned leaving the outer periphery 313.
  • the thinned region is thinner than the surrounding region, and as a result, the flexibility of the first extension portion 312 is enhanced. From such a viewpoint, although not shown in the drawings, the above-described thinning may be performed on the proximal side surface of the first extension portion 312.
  • the term “thinning” refers to providing a portion having a smaller thickness than the surroundings in the thickness direction, and the concave portion 314 is formed by thinning the distal side surface of the first extending portion 312.
  • the recess 314 communicates with the insertion hole 12 and terminates on the inner surface of the outer periphery 313.
  • the height of the outer periphery of the thinned region (concave portion 314) is higher than the distal opening of the insertion hole 12, and the thinned region is It communicates with the opening.
  • the chamfering includes both so-called C chamfering and R chamfering.
  • the inner diameter of the tooth receiving portion 26 has a major axis and a minor axis in the same direction as the outer diameter of the covering portion 29.
  • the inner shape of the cross section of the covering portion 29 is, for example, an ellipse or an ellipse, and is configured in a shape substantially equal to the outer shape of the tooth receiving portion 26. Therefore, the mounting direction of the covering portion 29 with respect to the tooth receiving portion 26 can be easily understood.
  • each of the major axis and the minor axis at the inner diameter of the covering portion 29 is formed slightly larger than the major axis and the minor axis at the outer diameter of the tooth receiving portion 26.
  • the covering portion 29 includes a convex contact portion 316 that is continuous in a circumferential direction in contact with the outer peripheral surface of the tooth receiving portion 26 on the inner peripheral surface.
  • a convex contact portion 316 that is continuous in a circumferential direction in contact with the outer peripheral surface of the tooth receiving portion 26 on the inner peripheral surface.
  • the contact portion 316 in the present embodiment is a single band-shaped body that protrudes inward in the radial direction and that circulates in the circumferential direction in which the protruding tip is hemispherical.
  • the contact portion 316 is not limited to this, and two or more contact portions 316 that circulate in the circumferential direction may be provided, and the protruding tip has a shape other than a hemisphere (for example, a planar shape). There may be.
  • FIG. 12 shows a state where the abutting portion 316 having a hemispherical protruding tip abuts on the outer peripheral surface of the tooth receiving portion 26 and the tip is flat. Further, the abutting portion 316 shown in the drawing circulates in the circumferential direction in a plane orthogonal to the central axis of the covering portion 29, but is not limited thereto.
  • the airtightness between the tooth receiving portion 26 and the contact portion 316 can be 3 kPa or more.
  • the mouthpiece 300 that exhibits such airtightness is suitable for performing tests and treatments that increase the pressure in the oral cavity, such as the Valsalva method.
  • the airtightness between the tooth receiving portion 26 and the contact portion 316 is 3 kPa, which means that the outer peripheral surface of the tooth receiving portion 26 and the tip of the contact portion 316 are brought into close contact with each other and closer to the distal side of the contact portion 316. It means that gas does not leak between the tooth receiving portion 26 and the abutting portion 316 when a pressure difference of 3 kPa is applied to the rear side.
  • the endoscope is inserted in close contact with the endoscope insertion portion 17, sealed so as to cover the distal side of the mouthpiece 300 from the middle in the axial direction of the tooth receiving portion 26, and gas is inserted into the insertion hole 12. Air is supplied and the internal pressure is set to 3 kPa. At this time, it is possible to confirm that the airtightness between the tooth receiving portion 26 and the contact portion 316 is 3 kPa by preventing gas from leaking between the tooth receiving portion 26 and the contact portion 316. .
  • the present invention omits the contact portion 316 and directly contacts the outer peripheral surface of the tooth receiving portion 26 and the inner peripheral surface of the covering portion 29.
  • the major axis and the minor axis of the inner diameter of the covering portion 29 are substantially the same as the major axis and the minor axis of the outer diameter of the tooth receiving portion 26, and the outer peripheral surface of the tooth receiving portion 26 and the covering portion 29. It is preferable that there is no gap communicating with the inner peripheral surface in the axial direction.
  • a first positioning portion 323 and a second positioning portion 324 may be provided on the mouthpiece body 11 in order to easily attach the covering portion 29 ⁇ / b> A at an intended position. That is, as shown in FIG. 13, the tooth receiving portion 26 (see FIG. 11) has a convex portion 30 protruding radially outward at the distal end portion of the tooth receiving portion 26, and the covering portion 29 ⁇ / b> A has an outer peripheral surface. On the side, it has the 2nd convex part 50 which protrudes in the radial direction outer side in the distal end part of 29 A of coating
  • a first positioning portion 323 provided on the distal end surface of the convex portion 30 and a second positioning portion 324 provided on the distal end surface of the second convex portion 50 and facing the first positioning portion 323 are provided. .
  • the covering portion 29A By attaching the covering portion 29A to the mouthpiece body 11 so that the first positioning portion 323 and the second positioning portion 324 are opposed to each other, the positioning of the covering portion 29A with respect to the mouthpiece body 11 is easy and reliable.
  • At least one set of the first positioning part 323 and the second positioning part 324 is provided.
  • a first positioning portion 323 and a second positioning portion 324 facing the first positioning portion 323 are provided at each of two locations where the convex portion 30 and the second convex portion 50 are closest to each other.
  • the first positioning portion 323 and the second positioning portion 324 are appropriately implemented in various aspects of the mouthpiece of the present invention having the convex portion provided in the tooth receiving portion and the second convex portion provided in the covering portion. can do.
  • the mouthpiece for endoscopy according to the fourth embodiment is different from the mouthpiece for endoscopy 100 according to the first embodiment in the points described below, and in other respects the endoscopy Since it can be configured in the same manner as the mouthpiece 100 for a product, description thereof will be omitted as appropriate.
  • a perspective view of the mouthpiece body 11 and the covering portion 35 used in the fourth embodiment is shown in FIG.
  • the mouthpiece for endoscopy in the fourth embodiment has a covering portion 35 that covers the outer periphery of the tooth receiving portion 26.
  • the proximal end surface 351 of the covering portion 35 and the distal side surface 352 of the collar portion 42 are configured to have shapes corresponding to each other.
  • the distal side surface 352 of the collar portion 42 (the back surface of the collar portion 42) and the proximal end surface 351 of the covering portion 35 are fitted to each other. It has a concavo-convex portion 353 provided non-circularly.
  • the proximal end surface 351 is convex
  • the distal side surface 352 corresponding to the proximal end surface 351 is concave, and these are fitted to each other to form an uneven portion 353.
  • the proximal end surface 351 (not shown) may be concave, and the distal side surface 352 corresponding to this may be convex.
  • the uneven portion 353 is provided at least at one place, preferably at two or more places.
  • a similar concavo-convex portion 353 is provided so as to face approximately 180 ° (not shown). Since the uneven portion 353 is non-circular, the covering portion 35 is difficult to rotate in the circumferential direction when the proximal end surface 351 and the distal side surface 352 having shapes corresponding to each other are fitted in the correct direction. Therefore, the covering portion 35 can be properly aligned with the tooth receiving portion 26.
  • FIG. 15 is a perspective view in which the deaeration prevention valve device according to the fifth embodiment of the present invention is mounted on an endoscope mouthpiece.
  • the lower view of FIG. 15 is a perspective view before the deaeration prevention valve device and the endoscope mouthpiece according to the fifth embodiment of the present invention are mounted.
  • FIG. 16 is a cross-sectional view in which the deaeration prevention valve device according to the fifth embodiment of the present invention is attached to an endoscope mouthpiece.
  • FIG. 17 is a front view of a deaeration prevention valve device according to a fifth embodiment of the present invention.
  • FIG. 18 is a plan view of a deaeration prevention valve device according to the fifth embodiment of the present invention.
  • 19 is a cross-sectional view taken along the line BB in FIG.
  • FIG. 20 is a rear view of the deaeration prevention valve device according to the fifth embodiment of the present invention.
  • the deaeration prevention valve device 501 of the present embodiment has an insertion hole 562 through which an endoscope (not shown) can be inserted and removed freely, and a proximal end of a mouthpiece 504 (mouthpiece body) that is inserted into the oral cavity.
  • the unit 543 is detachably attached.
  • a frame portion 503 attached to the base end portion 543 of the mouthpiece 504, a locking portion 502 provided on the frame portion 503 and removably locked to the base end portion 543, and provided inside the frame portion 503.
  • the valve body portion 505 of the present embodiment is provided at an approximately central portion of the valve body portion 505 and is provided around the endoscope insertion portion 506 and an annular endoscope insertion portion 506 that is attached to the endoscope.
  • the deaeration prevention valve device 501 of the present embodiment will be described in more detail.
  • the deaeration prevention valve device 501 of this embodiment is attached to a mouthpiece 504 to be inserted into the oral cavity, and more specifically, an external body 544 of the mouthpiece 504. It is attached to a base end portion 543 provided on the base end side.
  • locking part 502 of the deaeration prevention valve apparatus 501 latches to the base end part 543 of the mouthpiece 504 so that engagement / disengagement is possible by the latching means 521 which protruded toward the inner side of the flame
  • the mouthpiece 504 includes a body exterior 544, a buttocks 545, and an oral cavity interior 546, and an outer surface of the oral cavity interior 546 is detachably covered with a cover 549 made of an elastic material.
  • the buttocks 545 are in contact with the lip surface and serve to prevent excessive insertion of the mouthpiece. With the buttocks 545 as a boundary, the proximal end side is the body exterior 544 and the distal end side is the mouth interior 546. Yes.
  • the oral cavity interior 546 has a lumen 542 that is inserted into the oral cavity and through which the endoscope can be inserted and removed via the mouthpiece 504, and includes a first opening 547 on the endoscope insertion side and a second mouth inner outlet.
  • the external body 544 only needs to have a lumen 542 into which the endoscope can be inserted and removed, and the base end portion 543 of the external body 544 can take various shapes, but from the viewpoint of the insertion property of the endoscope, it is typical. It has a circular funnel shape. That is, as shown in FIG. 16, the external body 544 of the mouthpiece 504 to which the deaeration prevention valve device 501 of this embodiment is attached has a tapered diameter-enlarged portion 541 whose diameter gradually increases toward the base end side. Accordingly, a base end portion 543 is provided on the base end side. In this embodiment, the base end portion 543 of the mouthpiece 504 is a proximal end side region having a predetermined length, and the base end portion 543 includes a tapered diameter-enlarged portion 541.
  • the mouthpiece 504 to which the deaeration prevention valve device 501 is attached is not limited to the above.
  • the enlarged diameter portion 541 whose diameter gradually increases toward the proximal end side, it may be a simple cylindrical portion.
  • the frame portion 503 of the deaeration prevention valve device 501 is a frame body attached to the base end portion 543.
  • the frame portion 503 can take various shapes according to the shape of the proximal end portion 543 of the mouthpiece 504, but in the present embodiment, has a substantially cylindrical shape.
  • the frame portion 503 is integrally formed with an inward flange-shaped fixing portion 531 with a predetermined width.
  • the valve body portion 505 is a flexible member that is airtightly attached to the endoscope, and is provided on the inner surface of the frame portion 503. More specifically, the valve body portion 505 is manufactured in a substantially disk shape as a separate member from the frame portion 503, and is mounted inside the cylindrical frame portion 503 and fixed to the fixing portion 531.
  • An annular endoscope insertion portion 506 having a substantially circular insertion hole 562 is provided at a substantially central portion of the valve body portion 505.
  • the endoscope insertion part 506 is elastically deformable, and the endoscope is inserted into the insertion hole 562 so as to be freely inserted and removed, and the endoscope insertion part 506 is tightly sealed around the endoscope. .
  • An expansion / contraction means 508 (expansion / contraction part) is formed on the outer peripheral edge of the endoscope insertion part 506.
  • the expansion / contraction means 508 can move the endoscope insertion portion 506 in the radial direction (left-right direction in FIG. 17), the forward / backward direction (up-down direction in FIG. 17), and the rotation direction (twist direction or swing direction of the endoscope). It is a flexible member.
  • the expansion / contraction means 508 may have a flat plate shape or a bellows shape, but preferably includes a bellows shape from the viewpoint of further improving the movement of the endoscope insertion portion 506 in the above direction.
  • the valve body portion 505 is deformed following the endoscope. For this reason, when an operator moves the endoscope inserted through the lumen 542 of the mouthpiece 504, the operability of the endoscope is not impaired.
  • a closing plug portion 554 (see FIGS. 17 and 20) that fits with the opening on the proximal end side of the lumen 542 of the mouthpiece 504 and hermetically seals the opening on the outer peripheral edge of the valve body 505. ) Is formed integrally with the expansion / contraction means 508.
  • the deaeration prevention valve device 501 of this embodiment is detachably attached to the proximal end portion 543 of the mouthpiece 504 by operating the locking portion 502.
  • the locking portion 502 is provided on the circumference of the outer edge of the frame portion 503.
  • the deaeration prevention valve device 501 of the present embodiment engages a locking means (locking claw; locking protrusion) 521 protruding toward the inside of the frame portion 503 with respect to the base end portion 543 of the mouthpiece 504. (See FIG. 16).
  • the locking means 521 of the present embodiment is formed at the tip of the locking portion 502 that protrudes in the axial direction and distally from the cylindrical frame portion 503.
  • the present invention is not limited to this, and although not shown in the figure, the locking means 521 may be formed on the inner peripheral surface of the cylindrical frame portion 503, for example, on the outer peripheral surface from the axial direction.
  • a locking portion 502 may be formed so as not to protrude.
  • the deaeration prevention valve device 501 of the present embodiment is detachably attached to the base end portion 543 of the mouthpiece 504 using a locking portion 502 that is detachably locked to the base end portion 543 of the mouthpiece 504. Installed. That is, the deaeration prevention valve device 501 of this embodiment is attached to the outside of the mouthpiece 504. For this reason, even if the deaeration prevention valve device 501 is attached to the mouthpiece 504, the movable range of the endoscope in the lumen 542 of the mouthpiece 504 is not narrowed, and the operability of the endoscope is not impaired. .
  • the proximal end of the lumen 542 is airtightly held by the valve body portion 505 that is worn around the endoscope. For this reason, even if the endoscope inserted through the lumen 542 is moved back and forth, left and right, etc., it is possible to reduce leakage of pressurized air supplied into the body cavity to the proximal end side of the mouthpiece 504. Can do. Therefore, the larynx can be raised by the Valsalva method and the visual field of the hypopharynx can be secured.
  • the deaeration prevention valve device 501 can be detached from the mouthpiece 504. After the observation of the middle and lower pharynx, when the esophagus and stomach are subsequently examined, the deaeration prevention valve device 501 is removed from the mouthpiece 504 while the endoscope is inserted into the lumen 542. Can do. Thus, following the examination of the middle and lower pharynx by the Valsalva method, which requires airtightness, the esophagus and stomach can be examined without replacing the mouthpiece.
  • the deaeration prevention valve device 501 In general, in the examination of the esophagus and stomach, it is not necessary to ensure airtightness unlike the examination of the middle and lower pharynx by the Valsalva method described above, so it is assumed that the deaeration prevention valve device 501 is removed. . However, if the field of view necessary for gastric observation cannot be obtained even if air is fed through an endoscope, the air leakage from the mouth can be minimized by installing the deaeration prevention valve device 501 again. , Securing a field of view. Thus, the deaeration prevention valve device 501 can be attached to and detached from the mouthpiece 504, so that the deaeration prevention valve device 501 can be arbitrarily attached according to the status of the endoscopy or the condition of the subject. Non-wearing can be selected.
  • the locking portion 502 has a finger hook portion 522 (knob portion) formed integrally with the locking means 521.
  • the finger hook portion 522 is a portion that the operator opens and closes in a closed state in which the locking means 521 can be locked to the enlarged diameter portion 541 or an open state in which the locking means 521 can be detached from the enlarged diameter portion 541.
  • the locking part 502 has a locking means 521 at the lower part (distal side) and a finger hooking part 522 at the upper part (closer to the proximal side).
  • the frame portion 503 is joined at a joint portion 523 that is in the middle of the portion 522.
  • the joint portion 523 is movably joined to the frame portion 503.
  • a prevention valve device 501 is attached to the mouthpiece 504.
  • the distance between the locking means 521 and the locking means 521 facing each other increases, and the distance is larger than the outer diameter of the proximal end portion 543 of the mouthpiece 504 Is also in a largely open state (open state) (not shown). Accordingly, the locking means 521 can pass through the proximal end portion 543 of the mouthpiece 504, and the deaeration prevention valve device 501 can be detached from the mouthpiece 504.
  • the number of the locking portions 502 is not particularly limited, and may be one or two or more.
  • the locking portions 502 are provided at two or more locations around the frame portion 503 so as to be separated from each other.
  • the locking portion 502 of this embodiment is formed at two locations facing each other with respect to the central axis of the cylindrical frame portion 503.
  • three locking portions 502 may be formed at an angular interval of 120 degrees with respect to the central axis of the frame portion 503, or four locking portions at an angular interval of 90 degrees with respect to the central axis. 502 may be formed.
  • the locking portion 502 may be provided only at one place on the circumference of the frame portion 503. That is, the deaeration prevention valve device 501 is fixed to the base end portion 543 of the mouthpiece 504 with one locking portion 502 and the frame portion 503, and the deaeration prevention valve device 501 is fixed to the mouthpiece by opening the locking portion 502. It may be possible to detach from 504.
  • the deaeration prevention valve device 501 of this embodiment can be detached from the mouthpiece 504 with the other hand.
  • the number of the locking portions 502 is preferably three or less.
  • the locking portion 502 can be opened by simply picking it with a finger, it is preferable to provide the locking portions 502 at two opposite locations on the circumference of the frame portion 503.
  • the locking portion 502 may be integrally formed with the frame portion 503, or may be formed as a separate member from the frame portion 503 and may be movably joined and fixed to the frame portion 503.
  • these materials are the same as the material of the frame portion 14 described in the first embodiment, and therefore specific listing is omitted here.
  • polyethylene resin, polyamide resin, or polypropylene resin is used from the viewpoint of the durability of the hinge of the joint portion 523 that is a fixing portion between the locking portion 502 and the frame portion 503. preferable.
  • the material of the locking portion 502 is not particularly limited, but it is necessary to withstand the strength of applying an external force to the finger hook portion 522 and tilting the locking portion 502 as a whole. A relatively hard material is desirable.
  • the material of the locking portion 502 is the same as that of the frame portion 14 described in the first embodiment.
  • the material of the frame portion 503 is not particularly limited. However, the material does not deform due to the external force applied to the locking portion 502, and the valve body portion 505 is sufficiently formed. It is preferable to have strength that can be fixed. Further, by using a relatively hard material for the frame portion 503, the inner diameter of the lumen 542 is sufficiently secured, and the operability of the endoscope is improved.
  • the material of the frame part 503 is the same as that of the frame part 14 described in the first embodiment.
  • the deaeration prevention valve device 501 of the present embodiment has a fixing portion 531 for fixing the valve body portion 505 in an inward flange shape on one opening end surface of the cylinder of the frame portion 503.
  • the valve body portion 505 may be bonded and fixed to the fixing portion 531, or the valve body portion 505 may be sandwiched between the fixing portion 531 and another member.
  • the deaeration prevention valve device 501 of this embodiment includes a substantially ring-shaped fixing member (fixing ring 507) that fixes the valve body portion 505 to the frame portion 503. ing.
  • the fixing ring 507 has a ring shape having an outer shape that can be accommodated inside the cylindrical frame portion 503, and the fixing ring 507 and the fixing portion 531 press and hold the outer peripheral edge of the valve body portion 505.
  • the claw 532 is a stopper that prevents the fixing ring 507 from falling off the frame portion 503.
  • the fixing ring 507 can be prevented from falling off by bringing the distal side surface of the fixing ring 507 into contact with the proximal side surface of the claw 532.
  • the material of the fixing ring 507 is not particularly limited, but the endoscope is provided by firmly fixing the valve body 505 to the frame portion 503 while thinning the entire deaeration prevention valve device 501 to improve the operability of the endoscope. It is preferable to have sufficient strength to withstand the frictional force between the valve body portion 505 and the valve body portion 505.
  • the material of the fixing ring 507 the same material as that of the locking portion 502 or the frame portion 503 can be used.
  • the deaeration prevention valve device 501 of this embodiment includes a reinforcing member 509 between the outer peripheral edge portion of the endoscope insertion portion 506 and the inner peripheral edge portion of the expansion / contraction means 508.
  • the reinforcing member 509 is a member for increasing the elasticity of the endoscope insertion portion 506 as compared with the expansion / contraction means 508 and improving the adhesiveness with the endoscope.
  • the reinforcing member 509 of the present embodiment is integrally formed of a material common to the annular endoscope insertion portion 506. For example, as shown in FIG. 19, the reinforcing member 509 has a cross-sectional diameter of the reinforcing member 509 that is an O-ring larger than the thickness dimension of the expansion / contraction means 508.
  • the reinforcing member 509 of the present embodiment is formed in an O-ring shape.
  • the endoscope insertion portion 506 is evenly worn around the endoscope, so even if the endoscope is moved forward, backward, up, down, left and right, and rotated, the endoscope outer surface and the endoscope are inserted. Formation of a gap between the portion 506 is prevented.
  • the expansion / contraction means 508 has a bellows portion that expands and contracts in the circumferential plane direction of the insertion hole 562 of the endoscope insertion portion 506, as shown in FIG.
  • the bellows part can be constituted by an inclined part 583 that inclines in opposite directions to each other via the folded part 582.
  • the bellows portion contracts or extends, There is no hindrance to the free movement of the endoscope. Further, since the bellows portion is more flexible than the endoscope insertion portion 506, the endoscope insertion portion 506 is displaced with respect to the frame portion 503 while being in close contact with the outer surface of the endoscope. Thereby, the clearance gap between the endoscope insertion part 506 and an endoscope can be minimized, and the airtightness of an endoscope and the deaeration prevention valve apparatus 501 can be maintained.
  • FIG. 21 is a cross-sectional view of a deaeration prevention valve device 501 according to a first modification of the present invention.
  • the expansion / contraction means 508 can make the peak portion and the valley portion (folded portion 582) of the bellows portion thinner than other flat portions (inclined portion 583). By doing so, the contraction or extension of the bellows part becomes softer, and friction with the endoscope can be reduced during insertion / extraction of the endoscope and operation of the endoscope, so that the operability of the endoscope is further improved. .
  • an operation of rotating the shaft around the endoscope insertion portion 506 is also performed.
  • the endoscope insertion portion 506 rotates together with the endoscope due to the high elastic force of the thick inclined portion 583 in the bellows portion with respect to the axial rotation movement around the endoscope insertion portion 506. And curbing around this.
  • the endoscope insertion part 506 can follow suitably with respect to the back-and-forth, right-and-left movement of an endoscope with the low elastic force which the thin folding
  • the inner diameter of the endoscope insertion portion 506 is equal to or smaller than the outer diameter of the endoscope inserted through the endoscope insertion portion 506. More specifically, the inner diameter of the endoscope insertion portion 506 is preferably smaller than the outer diameter of the endoscope inserted therethrough in the range of 0 mm or more and 5 mm or less, and smaller in the range of 2 mm or more and 4 mm or less. More preferably.
  • valve body part 505 Since the material of the valve body part 505 is the same as the material of the expansion / contraction part 16 in the first embodiment, the example listing is omitted here.
  • FIG. 22 is a cross-sectional view of a deaeration prevention valve device 501 according to a second modification of the present invention.
  • the endoscope insertion portion 506 has a straight tube portion 565 extending in the thickness direction of the valve body portion 505.
  • the deaeration prevention valve device 501 of the present modification is the above embodiment (see FIG. 19) in that the endoscope insertion portion 506 is in close contact with the outer peripheral surface of the endoscope over a predetermined extension length. Is different.
  • the O-ring-shaped reinforcing member 509 is formed on the outer peripheral side of the straight tube portion 565, and the inner peripheral surface of the straight tube portion 565 has a cylindrical surface shape.
  • the adhesion between the endoscope insertion portion 506 and the endoscope is improved, and the endoscope around the endoscope insertion portion 506 is attached to the lumen 542.
  • the O-ring-shaped reinforcing member 509 does not roll and rotate with respect to the endoscope. This prevents a gap from being generated between the endoscope insertion portion 506 and the endoscope when the operator operates the endoscope.
  • FIG. 23A is a perspective view of the sixth embodiment before the deaeration prevention valve device 600 and the endoscope mouthpiece 640 are attached
  • FIG. 23B is the attachment of the deaeration prevention valve device 600 to the endoscope mouthpiece 640
  • 23C is a cross-sectional view of the deaeration preventing valve device 600
  • FIG. 23D is a cross-sectional view of the endoscope mouthpiece 640.
  • the deaeration prevention valve device 600 has a locking portion (locking means; locking claw) 620 having a protruding convex shape.
  • the locking part 620 is provided on the outer peripheral surface of the deaeration prevention valve device 600, for example, and protrudes outward in the radial direction.
  • the mouthpiece 640 has a groove 631 on the lumen side of the proximal end 630, a hole 632 continuous with the groove 631 in the circumferential direction, and a protrusion on the proximal end of the hole 632. 633.
  • the deaeration prevention valve device 600 is installed in the base end portion 630 of the mouthpiece 640.
  • the distal end side of the protruding locking portion 620 of the deaeration prevention valve device 600 is inserted from the proximal end side of the groove portion 631 of the base end portion 630 in the mouthpiece 640.
  • the locking portion 620 is positioned in the insertion direction by contacting the collar portion 650 and then rotated in the circumferential direction, so that the locking portion 620 fits into the hole portion 423, and the vertical direction (distal side and proximal side) Direction). Furthermore, the locking portion 620 is fixed in the circumferential direction because of the protrusion 633. Therefore, in the sixth embodiment, the deaeration prevention valve device 600 can be attached to and detached from the mouthpiece 640 by grasping an arbitrary portion of the outer surface of the deaeration prevention valve device 600 with a finger or the like.
  • the deaeration prevention device of the present invention described above can be used as appropriate as the deaeration prevention device provided in the endoscope mouthpiece of the present invention.
  • the endoscope mouthpiece of the present invention includes an endoscope mouthpiece comprising the endoscope mouthpiece and the deaeration prevention valve device of the present invention.
  • Each configuration of the deaeration prevention valve device in the endoscopic examination mouthpiece of the present invention described above and each configuration of the deaeration prevention valve device in the present invention may be appropriately transferred to each other.
  • the mouthpiece for endoscopy of the present invention described above and the mouthpiece for endoscope provided with the deaeration prevention valve device of the present invention are airtight between the deaeration prevention valve device and the mouthpiece body.
  • the property can be 3 kPa or more.
  • Such a mouthpiece that exhibits airtightness is suitably used for performing tests and treatments for increasing the pressure in the oral cavity, such as the Valsalva method.
  • the airtightness between the deaeration prevention valve device and the mouthpiece body is 3 kPa.
  • the inside and outside of the joint surface between the mouthpiece body and the deaeration prevention valve device when the deaeration prevention valve device is attached to the mouthpiece body. Means that no gas leaks between the mouthpiece body and the deaeration preventive valve device when a pressure of 3 kPa is applied between them.
  • a mouthpiece 504 to which a deaeration prevention valve device 501 shown in FIG. 16 is attached.
  • the endoscope is inserted in close contact with the endoscope insertion portion 506 and sealed to cover the distal side of the mouthpiece 504 to which the deaeration prevention valve device 501 is attached from the middle in the axial direction of the cover 549.
  • a gas is supplied into the interior of the chamber and the internal pressure is set to 3 kPa.
  • the airtightness between the mouthpiece 504 and the deaeration prevention valve device 501 is 3 kPa because gas does not leak from the joint surface between the mouthpiece 504 and the deaeration prevention valve device 501. be able to.
  • the desirable airtightness described above is, for example, deaerated in a state where the valve body portion 505 (see FIG. 17) and the base end portion 543 that are sandwiched by pressing the outer peripheral edge with the fixing ring 507 and the fixing portion 531 are in contact with each other. This can be realized by attaching the prevention valve device 501 to the mouthpiece 504.
  • the mouthpiece for endoscopy of the present invention enables proper breathing in endoscopic examination of the middle and lower pharynx using the Valsalva method, and it is possible to observe the affected area in detail by raising the larynx
  • the mouthpiece for endoscopy of the present invention is not limited to the middle hypopharyngeal examination using the Valsalva method described above, and can be used for various oral endoscopy.
  • the mouthpiece for endoscopy according to the present invention does not exclude that it is used for purposes other than endoscopy, for example, in the case of treatment using an endoscope. Can be widely used as a piece.
  • the deaeration prevention valve device of the present invention is attached to the endoscope mouthpiece to prevent leakage from the oral cavity during operation of the endoscope and to be detached from the endoscope mouthpiece.
  • the mouthpiece can be applied to an endoscope operation in which securing airtightness is not important.
  • the above embodiment includes the following technical idea.
  • a mouthpiece body having an insertion hole through which an endoscope can be inserted and removed freely;
  • a deaeration preventive valve device that hermetically seals between the endoscope and the mouthpiece body inserted through the insertion hole;
  • a mouthpiece for endoscopy having an endoscope.
  • the deaeration prevention valve device has a flexible expansion and contraction portion provided around the insertion hole, The endoscopic examination mouthpiece according to (1) or (2), wherein the extendable portion includes an endoscope insertion portion that is provided at a substantially central portion of the extendable portion and is attached to the endoscope.
  • a cylindrical tooth receiving portion provided at a distal end portion of the mouthpiece body; A covering portion covering the outer periphery of the tooth receiving portion, The mouthpiece for endoscopy according to any one of (1) to (5), wherein the hardness of the covering portion is lower than the hardness of the tooth receiving portion. (7) The mouthpiece for endoscopy according to (6), wherein the covering portion is detachable from the mouthpiece body.
  • the covering portion has, on the inner peripheral surface side, a small diameter portion and a large diameter portion, and a step portion that is formed by a step of the small diameter portion and the large diameter portion and the diameter changes discontinuously
  • the covering portion has, on the outer peripheral surface side, a second convex portion protruding outward in the radial direction at the distal end portion of the covering portion,
  • the first positioning portion provided on the distal end surface of the convex portion and the second positioning portion provided on the distal end surface of the second convex portion and facing the first positioning portion.
  • the covering portion has a cylindrical shape with an outer diameter having a major axis and a minor axis
  • the second convex portion has a first extending portion extending at a first length on the major axis and a second extending portion extending at a second length on the minor axis.
  • Said 1st length is a mouthpiece for endoscopy as described in said (9) or (10) larger than said 2nd length.
  • the distal side surface of the first extending portion communicates with the insertion hole provided in the mouthpiece body, and is hollowed out leaving the outer periphery, any of (11) to (13) The mouthpiece for endoscopy according to claim 1.
  • a cylindrical tooth receiving portion provided at a distal end portion of the mouthpiece body, The mouthpiece for endoscopy according to any one of (1) to (9), wherein an outer diameter of the tooth receiving portion has a major axis and a minor axis.
  • a cylindrical tooth receiving portion provided at a distal end portion of the mouthpiece body; A covering portion covering the outer periphery of the tooth receiving portion; Between the distal end portion and the proximal end portion of the mouthpiece body, has a flange extending outward from the outer peripheral surface, Any one of the above (1) to (21), wherein the shortest distance from the base end portion of the back surface of the collar portion to the distal end of the mouthpiece body is substantially equal to the length of the covering portion in the longitudinal direction.
  • the mouthpiece for endoscopy according to Item.
  • the deaeration prevention valve device includes a flexible expansion / contraction portion that is provided around the insertion hole, and the expansion / contraction portion is provided at a substantially central portion of the expansion / contraction portion, and surrounds the endoscope.
  • the telescopic part is concentric with the annular endoscope insertion part, and has an annular bellows part in which a peak part and a valley part are provided in a radial direction,
  • the bellows portion is arranged coaxially with an inner circle surrounded by a boundary portion that is a boundary between the reduced diameter portion and the enlarged diameter portion, and the outer edge diameter of the bellows portion is larger than the diameter of the inner circle.
  • the mouthpiece for endoscopy according to any one of (1) to (25), which is large. (27) The mouthpiece for endoscopy according to (26), wherein an inner edge diameter of the bellows portion is smaller than a diameter of the inner circle.
  • a prevention valve device A frame portion attached to an outer peripheral surface of the base end portion of the mouthpiece; A locking portion provided in the frame portion and releasably locked to the outer peripheral surface of the base end portion; A valve body provided inside the frame part; Have The valve body is An annular endoscope insertion portion that is provided at a substantially central portion of the valve body portion and is attached to the endoscope; Flexible telescopic means provided around the endoscope insertion portion; The deaeration prevention valve device characterized by having. (30) The removal portion according to (29), wherein the engagement portion is detachably engaged with the outer peripheral surface of the base end portion by engagement means protruding toward the inside of the frame portion. Qi prevention valve device.
  • Aeration used for an endoscope mouthpiece that is detachably attached to a proximal end portion of a mouthpiece that is inserted into an oral cavity having a lumen through which an endoscope can be inserted and removed.
  • a prevention valve device A frame portion attached to an inner peripheral surface of the base end portion of the mouthpiece; A locking portion provided on the frame portion and releasably locked to the inner peripheral surface of the base end portion; A valve body provided inside the frame part; Have The valve body is An annular endoscope insertion portion that is provided at a substantially central portion of the valve body portion and is attached to the endoscope; Flexible telescopic means provided around the endoscope insertion portion;
  • the deaeration prevention valve device characterized by having.
  • Deaeration prevention valve device (33) The deaeration prevention valve device according to any one of (29) to (32), wherein the locking portions are provided at two or more locations apart from each other around the frame portion.
  • the locking portion is formed integrally with the locking means, and is in a closed state in which the locking means can be locked with respect to the base end portion or in an open state in which the locking means can be detached from the base end portion.
  • Second positioning part 351 Proximal end face 352 ... Distal side face 353 ... Concave and convex part 414 ... Frame part 418 ... Deaeration prevention valve device 420 ... Engagement receiving part 421 ... Tube part 422 ... Fitting convex part 423 ... Hole part 425 ... Fitting concave part 426 ... Fitting retention 501 ... Deaeration prevention valve device 502 ... Locking part 503 ... Frame part 504 ... Ma Spiece 505 ... Valve body part 506 ... Endoscope insertion part 507 ... Fixing ring 508 ... Telescopic means 509 ... Reinforcing member 513 ... Telescopic part 521 ...

Landscapes

  • Health & Medical Sciences (AREA)
  • Pulmonology (AREA)
  • Biomedical Technology (AREA)
  • Emergency Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Otolaryngology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Endoscopes (AREA)

Abstract

Provided is a mouthpiece for endoscopic examinations, comprising: a mouthpiece main body having an insertion hole through which an endoscope is freely inserted and removed; and a de-aeration prevention valve device that provides an airtight seal between the endoscope inserted into the insertion hole and the mouthpiece main body.

Description

内視鏡検査用マウスピースおよび脱気防止弁装置Mouthpiece for endoscopy and anti-aeration valve device
 本発明は、経口内視鏡検査をする際に用いることのできる内視鏡検査用マウスピースおよび内視鏡用マウスピースに用いられる脱気防止弁装置に関する。
 本願は、2013年10月10日に、日本に出願された特願2013-212462号、2013年10月10日に、日本に出願された特願2013-212484号、2014年4月25日に、日本に出願された特願2014-91182号に基づき優先権を主張し、その内容をここに援用する。
The present invention relates to an endoscopy mouthpiece that can be used for oral endoscopy and an anti-aeration valve device used for an endoscope mouthpiece.
This application is filed on October 10, 2013, Japanese Patent Application No. 2013-212462, filed on October 10, 2013, Japanese Patent Application No. 2013-212484, filed on Japan, April 25, 2014 Claims priority based on Japanese Patent Application No. 2014-91182 filed in Japan, the contents of which are incorporated herein by reference.
 従来、内視鏡を複数回出し入れすることが予定される内視鏡を用いた治療等には、体腔の保護や、患部より採取した組織と体腔とが接触することを防止するために、オーバーチューブなどと称される長尺管を予め体腔に挿入することが一般的である。上記長尺管は、咽頭あるいは食道といった径の小さい体腔を経て、内視鏡の挿通路を確保する。 Conventionally, in the treatment using an endoscope that is scheduled to be inserted and removed multiple times, in order to protect the body cavity and prevent the tissue collected from the affected part from coming into contact with the body cavity, It is common to insert a long tube called a tube or the like into a body cavity in advance. The long tube secures an insertion path of the endoscope through a small body cavity such as the pharynx or the esophagus.
 これに対し、通常の内視鏡検査においては、内視鏡の挿通や抜去が可能なマウスピースを患者の口に装着した状態で行うのが一般的であり、多数の内視鏡用マウスピースが知られている。(例えば特許文献1)。 On the other hand, in normal endoscopy, it is common to carry out a mouthpiece that can be inserted and removed from the mouth of the patient, and a large number of endoscope mouthpieces. It has been known. (For example, patent document 1).
 ところで、近年、内視鏡技術の発展により、多くの表在癌が発見可能となった。これに伴い食道癌の治療が普及し発展していく中で、食道癌と中下咽頭部癌の密接な関係も年々明らかになっている。そして、食道癌治療のフォローアップとして中下咽頭癌の検査を実施し、中下咽頭癌を早期発見することの重要性が提唱されている。
 ただし、中下咽頭部には、形状が複雑であって観察の難しい部位が存在する。これに対し、患者に息堪えをさせるValsalva(バルサルバ)法を用い、喉頭を拳上させて口腔咽頭に空気を充満させた状態で視野展開を図り内視鏡観察する手法が着目されている。
By the way, in recent years, many superficial cancers have become discoverable due to the development of endoscopic technology. As the treatment of esophageal cancer spreads and develops along with this, the close relationship between esophageal cancer and cancer of the middle and lower pharynx has become clear year by year. The importance of early detection of mesopharyngeal cancer by conducting tests for mesopharyngeal cancer as a follow-up to esophageal cancer treatment has been proposed.
However, there are parts of the middle and lower pharynx that are difficult to observe because of their complex shapes. On the other hand, attention has been paid to a technique for performing endoscopic observation by using the Valsalva method that makes the patient breathe, with the larynx raised and the oral pharynx filled with air.
特開2012-231833号公報JP 2012-231833 A
 しかし、一般的に、従来の内視鏡用マウスピースは、使用時に息漏れを防止し口腔内の気密性を上げるという観点で改善されたものがなく、バルサルバ法を適切に実行することが困難であった。例えば、具体的な例としては、内視鏡の径に対し、従来のマウスピースにおける内視鏡挿通孔の径は大きく設計されている。したがって中下咽頭を検査する際に、従来のマウスピースを用いると、当該マウスピースに設けられる内視鏡挿通孔と、これに挿通される内視鏡との間から息が漏れてしまう。 However, in general, conventional endoscope mouthpieces are not improved in terms of preventing breathing and improving air tightness in the oral cavity during use, and it is difficult to properly perform the Valsalva method. Met. For example, as a specific example, the diameter of the endoscope insertion hole in the conventional mouthpiece is designed to be larger than the diameter of the endoscope. Therefore, when a conventional mouthpiece is used when examining the middle and lower pharynx, breath is leaked from between an endoscope insertion hole provided in the mouthpiece and an endoscope inserted through the endoscope insertion hole.
 また、息堪えを確実に行うために、マウスピースを用いずに直接内視鏡を口から中下咽頭に挿入し、バルサルバ法にて内視鏡観察を行うことも試みられている。しかし、かかる試みでは、患者が口を閉じることにより息堪えはしやすいものの、患者が内視鏡を噛んでしまい、内視鏡の損傷が発生しやすいという問題が生じる。また上記試みでは、内視鏡を患者が強く咥えてしまい、内視鏡の操作性が低減するという問題も生じうる。
 上述のとおり、従来のマウスピースを使用する検査では、一般的には、体内より空気などの気体が漏れ出ることを防止するという要望自体がなかった。
 ところが、バルサルバ法のごとき新手法を実施するにおいて、息堪えをして喉頭を拳上することが求められた場合に、従来のマウスピースでは充分な息堪えができなかった。マウスピースを咥えた状態で、喉頭を拳上することができず、中下咽頭部の充分な観察ができないという問題があった。
In addition, in order to reliably hold the breath, it has been attempted to insert an endoscope directly into the middle and lower pharynx without using a mouthpiece and perform endoscopic observation by the Valsalva method. However, in such attempts, although the patient can easily take a breath by closing his / her mouth, there arises a problem that the patient bites the endoscope and the endoscope is easily damaged. In the above attempt, there is a problem that the patient strongly holds the endoscope and the operability of the endoscope is reduced.
As described above, in a test using a conventional mouthpiece, there is generally no desire to prevent a gas such as air from leaking from the body.
However, when a new technique such as the Valsalva method is required to breathe and raise the larynx, the conventional mouthpiece cannot be fully breathed. There was a problem that the larynx could not be raised with the mouthpiece held in place, and the middle and lower pharynx could not be observed sufficiently.
 本発明は上述のような課題に鑑みてなされたものである。即ち、マウスピースを使用する検査において、マウスピースを装着した状態で望ましく息堪えを可能とするという新規な課題に対し、検査中に息などの気体が口から体外に漏れることを防止可能な内視鏡検査用マウスピースを提供するものである。また本発明は、上記課題に鑑みてなされた、内視鏡用マウスピース用に用いられる脱気防止弁装置を提供する。 The present invention has been made in view of the above-described problems. In other words, in a test using a mouthpiece, it is possible to prevent a gas such as breath from leaking out of the body from the mouth during the test, in response to a new problem that it is desirable to be able to breathe with the mouthpiece attached. A mouthpiece for endoscopy is provided. Moreover, this invention provides the deaeration prevention valve apparatus used for the mouthpiece for endoscopes made | formed in view of the said subject.
 本発明の内視鏡検査用マウスピースは、内視鏡を挿入抜去自在に挿通する挿通孔を有するマウスピース本体と、上記挿通孔に挿通された上記内視鏡と上記マウスピース本体との間を気密に封止する脱気防止弁装置と、を有する。 The mouthpiece for endoscopy of the present invention includes a mouthpiece body having an insertion hole through which an endoscope can be inserted and removed, and between the endoscope inserted through the insertion hole and the mouthpiece body. And a deaeration prevention valve device that hermetically seals.
 また本発明の第一の脱気防止弁装置は、内視鏡を挿入抜去自在に挿通する内腔を有する口腔内に挿入されるマウスピースの基端部に対して着脱自在に装着される、内視鏡用マウスピースに用いられる脱気防止弁装置であって、上記マウスピースの上記基端部の外周面に装着されるフレーム部と、上記フレーム部に設けられて上記基端部の上記外周面に係脱可能に係止する係止部と、上記フレーム部の内側に設けられた弁体部と、を有し、上記弁体部は、上記弁体部の略中央部に設けられて上記内視鏡に周着する環状の内視鏡挿入部と、 上記内視鏡挿入部に周設された可撓性の伸縮手段と、を有していることを特徴とする。 Further, the first deaeration prevention valve device of the present invention is detachably attached to the proximal end portion of the mouthpiece inserted into the oral cavity having a lumen through which the endoscope is inserted and removed. A deaeration prevention valve device used for an endoscope mouthpiece, the frame portion mounted on the outer peripheral surface of the base end portion of the mouthpiece, and the frame portion provided on the base end portion and the base end portion And a valve body portion provided inside the frame portion, the valve body portion being provided at a substantially central portion of the valve body portion. And an annular endoscope insertion portion that is circumferentially attached to the endoscope, and a flexible expansion / contraction means provided around the endoscope insertion portion.
 また本発明の第二の脱気防止弁装置は、内視鏡を挿入抜去自在に挿通する内腔を有する口腔内に挿入されるマウスピースの基端部に対して着脱自在に装着される、内視鏡用マウスピースに用いられる脱気防止弁装置であって、上記マウスピースの上記基端部の内周面に装着されるフレーム部と、上記フレーム部に設けられて上記基端部の上記内周面に係脱可能に係止する係止部と、上記フレーム部の内側に設けられた弁体部と、を有し、上記弁体部は、上記弁体部の略中央部に設けられて上記内視鏡に周着する環状の内視鏡挿入部と、 上記内視鏡挿入部に周設された可撓性の伸縮手段と、を有していることを特徴とする。 The second deaeration prevention valve device of the present invention is detachably attached to the base end portion of the mouthpiece inserted into the oral cavity having a lumen through which the endoscope is inserted and removed. A deaeration prevention valve device used for an endoscope mouthpiece, a frame portion mounted on an inner peripheral surface of the base end portion of the mouthpiece, and provided on the frame portion, A locking portion that is detachably locked to the inner peripheral surface, and a valve body portion provided inside the frame portion, wherein the valve body portion is provided at a substantially central portion of the valve body portion. An annular endoscope insertion portion provided around the endoscope and a flexible extension / contraction means provided around the endoscope insertion portion.
 本発明の内視鏡検査用マウスピースは、内視鏡を挿入抜去自在に挿通する挿通孔を有する。上記挿通孔には、当該挿通孔と内視鏡との間を気密に封止する脱気防止弁装置が設けられている。したがって、本発明の内視鏡検査用マウスピースは、内視鏡を挿通する挿入孔からの気体漏れを防止することができる。
 また本発明の脱気防止弁装置によれば、内視鏡用マウスピースに用いることにより、バルサルバ法において口腔咽頭に空気を充満させることによって下咽頭の視野を確保することができ、さらに内視鏡の破損および内視鏡の操作性低下を低減することができる。また、本発明の脱気防止弁装置は、内視鏡用マウスピースに対し着脱可能であるため、脱気防止弁装置による気密性確保は、必要時に選択して行なえることができる。そのため特定の内視鏡用マウスピースを、バルサルバ法だけでなく、種々の検査、治療等に適用させ得る。
The mouthpiece for endoscopy of the present invention has an insertion hole through which an endoscope can be inserted and removed. The insertion hole is provided with a deaeration prevention valve device that hermetically seals between the insertion hole and the endoscope. Therefore, the mouthpiece for endoscopy of the present invention can prevent gas leakage from the insertion hole through which the endoscope is inserted.
Further, according to the deaeration prevention valve device of the present invention, by using the mouthpiece for an endoscope, the visual field of the hypopharynx can be secured by filling the oral pharynx with air in the Valsalva method, and further It is possible to reduce mirror breakage and endoscope operability degradation. In addition, since the deaeration prevention valve device of the present invention can be attached to and detached from the endoscope mouthpiece, airtightness securing by the deaeration prevention valve device can be selected and performed when necessary. Therefore, a specific endoscope mouthpiece can be applied not only to the Valsalva method but also to various examinations and treatments.
本発明の第一実施形態にかかる内視鏡検査用マウスピースの一例を示す斜視図である。It is a perspective view which shows an example of the mouthpiece for endoscopy concerning 1st embodiment of this invention. 図1に示す内視鏡検査用マウスピースの正面図である。It is a front view of the mouthpiece for endoscopy shown in FIG. 図1に示す内視鏡検査用マウスピースのX-X断面図である。FIG. 2 is an XX cross-sectional view of the mouthpiece for endoscopy shown in FIG. 図1に示す内視鏡検査用マウスピースの裏面図である。It is a reverse view of the mouthpiece for endoscopy shown in FIG. 図1に示す内視鏡検査用マウスピースの分解斜視図である。It is a disassembled perspective view of the mouthpiece for endoscopy shown in FIG. 本発明の第一実施形態におけるマウスピース本体の正面図である。It is a front view of the mouthpiece body in the first embodiment of the present invention. 本発明の第一実施形態におけるマウスピース本体の側面図である。It is a side view of the mouthpiece body in a first embodiment of the present invention. 本発明の第二実施形態にかかる内視鏡検査用マウスピースの一例を示す斜視図である。It is a perspective view which shows an example of the mouthpiece for endoscopy concerning 2nd embodiment of this invention. 図8に示す内視鏡検査用マウスピースの分解斜視図である。It is a disassembled perspective view of the mouthpiece for endoscopy shown in FIG. 図8に示す内視鏡検査用マウスピースのY-Y断面図である。FIG. 9 is a YY sectional view of the mouthpiece for endoscopy shown in FIG. 8. 本発明の第三実施形態にかかる内視鏡検査用マウスピースの分解斜視図である。It is a disassembled perspective view of the mouthpiece for endoscopy concerning a third embodiment of the present invention. 図11に示す内視鏡検査用マウスピースのZ-Z断面図である。FIG. 12 is a ZZ sectional view of the mouthpiece for endoscopy shown in FIG. 11. マウスピース本体に本発明の第三実施例の変形例に用いられる被覆部を取り付けた状態を背面側から見た斜視図である。It is the perspective view which looked at the state which attached the coating | coated part used for the modification of the 3rd Example of this invention to the mouthpiece main body from the back side. 本発明の第四実施形態に用いられるマウスピース本体および被覆部の斜視図である。It is a perspective view of the mouthpiece main body and cover part used for 4th embodiment of this invention. 上図は本発明の第五実施形態に係る脱気防止弁装置を内視鏡用マウスピースに装着した斜視図であり、下図はその装着前の斜視図である。The upper view is a perspective view in which the deaeration prevention valve device according to the fifth embodiment of the present invention is mounted on an endoscope mouthpiece, and the lower view is a perspective view before the mounting. 本発明の第五実施形態に係る脱気防止弁装置を内視鏡用マウスピースに装着した断面図である。It is sectional drawing which mounted | wore the endoscope mouthpiece with the deaeration prevention valve apparatus which concerns on 5th embodiment of this invention. 本発明の第五実施形態に係る脱気防止弁装置の正面図である。It is a front view of the deaeration prevention valve apparatus which concerns on 5th embodiment of this invention. 本発明の第五実施形態に係る脱気防止弁装置の平面図である。It is a top view of the deaeration prevention valve apparatus which concerns on 5th embodiment of this invention. 図18のB-B断面図である。It is BB sectional drawing of FIG. 本発明の第五実施形態に係る脱気防止弁装置の背面図である。It is a rear view of the deaeration prevention valve apparatus which concerns on 5th embodiment of this invention. 本発明の第一変形例に係る脱気防止弁装置の断面図である。It is sectional drawing of the deaeration prevention valve apparatus which concerns on the 1st modification of this invention. 本発明の第二変形例に係る脱気防止弁装置の断面図である。It is sectional drawing of the deaeration prevention valve apparatus which concerns on the 2nd modification of this invention. 本発明の第六実施形態に係る脱気防止弁装と内視鏡用マウスピースとの装着前の斜視図である。It is a perspective view before mounting | wearing with the deaeration prevention valve equipment which concerns on 6th embodiment of this invention, and the mouthpiece for endoscopes. 本発明の第六実施形態に係る脱気防止弁装置を内視鏡用マウスピースに装着した断面図である。It is sectional drawing which mounted | wore the mouthpiece for endoscopes with the deaeration prevention valve apparatus which concerns on 6th embodiment of this invention. 本発明の第六実施形態に係る脱気防止弁装置の断面図である。It is sectional drawing of the deaeration prevention valve apparatus which concerns on 6th embodiment of this invention. 本発明の第六実施形態に係る内視鏡用マウスピースの断面図である。It is sectional drawing of the mouthpiece for endoscopes which concerns on 6th embodiment of this invention.
 以下、本発明の実施形態について説明する。当該説明において用いるすべての図面において、同様の構成要素には同一の符号を付し、重複する説明は適宜に省略する。
 なお、本明細書において説明する全ての実施形態では図示するように前後左右上下の方向を規定して説明する場合がある。しかし、これは構成要素の相対関係を簡単に説明するために便宜的に規定するものであり、本発明を実施する製品の製造時や使用時の方向を限定するものではない。
 本発明の内視鏡検査用マウスピースおよび脱気防止弁装置の各種の構成要素は、個々に独立した存在である必要はなく、複数の構成要素が一個の部材として形成されていること、一つの構成要素が複数の部材で形成されていること、ある構成要素が他の構成要素の一部であること、ある構成要素の一部と他の構成要素の一部とが重複していること、等を許容する。
Hereinafter, embodiments of the present invention will be described. In all the drawings used in the description, the same components are denoted by the same reference numerals, and redundant descriptions are appropriately omitted.
In all of the embodiments described in the present specification, there may be cases where the front, rear, left, right, and top directions are defined and illustrated as illustrated. However, this is provided for convenience in order to simply explain the relative relationship of the components, and does not limit the direction during the manufacture or use of the product implementing the present invention.
The various constituent elements of the mouthpiece for endoscopy and the deaeration prevention valve device of the present invention do not have to be independent of each other, and a plurality of constituent elements are formed as one member. One component is made up of multiple members, one component is a part of another component, and one component is a part of another component , Etc.
 本発明を説明する際、適宜、近位端部、遠位端部、近位端、遠位端という用語を使用する。これらの用語は、患者が本発明のマウスピースを口にくわえたときの使用状態において、本発明のマウスピースあるいは当該マウスピースを構成する各部材の特定の領域または特定の箇所を示す。具体的には、遠位端とは患者側の端部(口腔内側)、近位端は患者側とは反対側(口腔外側)の端部を示す。また遠位端部とは、遠位端を含む所定の長さ領域をいい、近位端部とは、近位端を含む所定の長さ領域をいう。
 本発明を説明する際に、適宜、内視鏡検査という用語を使用する。上記用語は、内視鏡を用いて患部の状態を観察するなどの狭義の内視鏡検査だけではなく、内視鏡を用いて患部を処置し、患部の組織を採取するなどの操作を行う場合の広義の内視鏡検査も適宜、含む。
 本明細書において、マウスピースを咥えて内視鏡検査を受ける者を患者という場合がある。またマウスピースを用いて内視鏡を取り扱う者を操作者という場合がある。
In describing the present invention, the terms proximal end, distal end, proximal end, and distal end are used where appropriate. These terms indicate a specific region or specific location of the mouthpiece of the present invention or each member constituting the mouthpiece in a use state when the patient holds the mouthpiece of the present invention in his / her mouth. Specifically, the distal end indicates the end on the patient side (inner oral cavity), and the proximal end indicates the end on the opposite side (outer oral cavity) from the patient side. The distal end portion refers to a predetermined length region including the distal end, and the proximal end portion refers to a predetermined length region including the proximal end.
In describing the present invention, the term endoscopy is used where appropriate. The above terms are used not only for endoscopic examination in a narrow sense such as observing the state of the affected area using an endoscope, but also for performing operations such as treating the affected area using an endoscope and collecting tissues of the affected area. In this case, the endoscopic examination in a broad sense is also included as appropriate.
In this specification, the person who holds the mouthpiece and undergoes endoscopy may be referred to as a patient. A person who handles an endoscope using a mouthpiece may be called an operator.
<第一実施形態>
 以下、本発明の実施形態について内視鏡検査用マウスピース(以下、単に「マウスピース」という場合がある)の第一実施形態にかかるマウスピース100について、図1から図7を用いて、詳細に説明する。図1は、本発明の第一実施形態にかかるマウスピース100の一例を示す斜視図である。図2は、図1に示すマウスピース100の正面図である。図3は、図1に示すマウスピース100のX-X断面図である。図4は、図1に示すマウスピース100の裏面図である。図5は、図1に示すマウスピース100の分解斜視図であり、脱気防止弁装置18、マウスピース本体11および被覆部28に分解した状態を示す。図6は、本発明の第一実施形態におけるマウスピース本体11の正面図である。図7は、本発明の第一実施形態におけるマウスピース本体11の側面図である。
 尚、マウスピース100の正面図およびマウスピース本体11の正面図は、いずれも、歯受部26(図3、図4)の長軸の軸線方向から観察した図である。
<First embodiment>
Hereinafter, the mouthpiece 100 according to the first embodiment of the mouthpiece for endoscopy (hereinafter sometimes simply referred to as “mouthpiece”) according to the embodiment of the present invention will be described in detail with reference to FIGS. 1 to 7. Explained. FIG. 1 is a perspective view showing an example of a mouthpiece 100 according to the first embodiment of the present invention. FIG. 2 is a front view of the mouthpiece 100 shown in FIG. FIG. 3 is a cross-sectional view of the mouthpiece 100 shown in FIG. FIG. 4 is a rear view of the mouthpiece 100 shown in FIG. FIG. 5 is an exploded perspective view of the mouthpiece 100 shown in FIG. 1, showing a state in which the mouthpiece 100, the mouthpiece body 11, and the covering portion 28 are disassembled. FIG. 6 is a front view of the mouthpiece body 11 in the first embodiment of the present invention. FIG. 7 is a side view of the mouthpiece body 11 in the first embodiment of the present invention.
Both the front view of the mouthpiece 100 and the front view of the mouthpiece body 11 are views observed from the long axis direction of the tooth receiving portion 26 (FIGS. 3 and 4).
 マウスピース100は、内視鏡(図示せず)を挿入抜去自在に挿通する挿通孔12を有するマウスピース本体11と、挿通孔12に挿通された内視鏡とマウスピース本体11との間を気密に封止する脱気防止弁装置18と、を有する。
 上記内視鏡は、経口内視鏡または経鼻内視鏡を含み、体腔に挿入して患部を検査し、または処置するために用いられる医療用器具である。
 本実施形態において、マウスピース100は、患者が口に咥えた状態で、遠位端が咽頭部より手前に位置する。即ち、マウスピース100は、所謂、オーバーチューブのように、当該オーバーチューブの遠位端が咽頭部に至ることはなく、また咽頭部を超えて伸長していない。
The mouthpiece 100 includes a mouthpiece body 11 having an insertion hole 12 through which an endoscope (not shown) can be inserted and removed freely, and between the endoscope inserted through the insertion hole 12 and the mouthpiece body 11. And an anti-aeration valve device 18 for hermetically sealing.
The endoscope includes an oral endoscope or a nasal endoscope, and is a medical instrument that is inserted into a body cavity and used to examine or treat an affected area.
In the present embodiment, the mouthpiece 100 is positioned in front of the pharynx with the distal end of the mouthpiece 100 in a state where the patient is in the mouth. That is, the mouthpiece 100 does not extend beyond the pharynx at the distal end of the overtube as in the so-called overtube.
 かかる構成により、マウスピース100は、挿通孔12に内視鏡を挿通して検査を行う際に、挿通孔12に挿通された内視鏡とマウスピース本体11との間から息などの気体が口により漏れることを防止あるいは低減することができる。したがって、例えば息堪えをして喉頭を拳上した状態で、下咽頭部の状態を内視鏡にて詳細に観察することが可能となる。
 本実施形態において、挿通孔12は、マウスピース本体11に設けられた両端開口の内腔である。本実施形態において、挿通孔12は、上記開口の領域あるいは開口間の任意の箇所において、内視鏡とマウスピース本体11との間における気体の流通が、検査の支障にならない程度に、低減されるかまたは実質的に遮蔽可能である。
With this configuration, when the mouthpiece 100 is inspected by inserting the endoscope through the insertion hole 12, gas such as breath flows from between the endoscope inserted through the insertion hole 12 and the mouthpiece body 11. Leakage through the mouth can be prevented or reduced. Therefore, it is possible to observe the state of the hypopharynx in detail with an endoscope, for example, in a state where the patient is breathing and the larynx is raised.
In the present embodiment, the insertion hole 12 is a lumen of both end openings provided in the mouthpiece body 11. In the present embodiment, the insertion hole 12 is reduced to such an extent that the flow of gas between the endoscope and the mouthpiece body 11 does not hinder the inspection in the region of the opening or any place between the openings. Or substantially shieldable.
 本実施形態における脱気防止弁装置18は、後述するとおり、マウスピース本体11に対し、着脱可能である。ただし、本実施形態におけるマウスピース100は、マウスピース本体11に固定されて設置され、繰り返しの着脱ができない脱気防止弁装置18を備える態様を含む。 The deaeration prevention valve device 18 in the present embodiment is detachable from the mouthpiece body 11 as will be described later. However, the mouthpiece 100 in the present embodiment includes an aspect including a deaeration prevention valve device 18 that is fixedly installed on the mouthpiece body 11 and cannot be repeatedly attached and detached.
 以下に、マウスピース100の各構成を詳細に説明する。
 マウスピース本体11は、内部を貫通する挿通孔12を有する。挿通孔12は、マウスピース本体11の近位端および遠位端において開口している。
 本実施形態における挿通孔12は、図3に示されるようにマウスピース本体11の近位端から遠位端へ向けて縮径部110と拡径部111とを有するくびれ形状をなしている。
 縮径部110と拡径部111との境界は、境界部112である。
 縮径部110とは、マウスピース本体11の内腔である挿通孔12の内径が連続的または段階的に小さくなる領域をいう。拡径部111は、マウスピース本体11の内腔である挿通孔12の内径が連続的または段階的に大きくなる領域をいう。縮径部110または拡径部111の径の段階的な変化は、一段のみの変化であってもよいし、二段以上の変化であってもよい。
 本実施形態において、縮径部110は、マウスピース本体11の近位端部であって、近位端寄りに設けられている。
Below, each structure of the mouthpiece 100 is demonstrated in detail.
The mouthpiece body 11 has an insertion hole 12 penetrating the inside. The insertion hole 12 opens at the proximal end and the distal end of the mouthpiece body 11.
As shown in FIG. 3, the insertion hole 12 in the present embodiment has a constricted shape having a reduced diameter portion 110 and an enlarged diameter portion 111 from the proximal end to the distal end of the mouthpiece body 11.
The boundary between the reduced diameter portion 110 and the enlarged diameter portion 111 is a boundary portion 112.
The reduced diameter portion 110 refers to a region in which the inner diameter of the insertion hole 12 that is the lumen of the mouthpiece body 11 decreases continuously or stepwise. The enlarged diameter portion 111 is a region in which the inner diameter of the insertion hole 12 that is the lumen of the mouthpiece body 11 increases continuously or stepwise. The stepwise change in the diameter of the reduced diameter portion 110 or the enlarged diameter portion 111 may be a change in only one step, or may be a change in two or more steps.
In the present embodiment, the reduced diameter portion 110 is a proximal end portion of the mouthpiece body 11 and is provided closer to the proximal end.
 挿通孔12に挿通された内視鏡の操作は、一般的には、挿通方向に対し略平行方向に内視鏡の全体を動かす平行操作、挿通方向に対し内視鏡を任意に捻じり、内視鏡先端を目的の位置に誘導する回転操作、およびこれらの組み合わせで行われる。
 このような内視鏡の操作において、縮径部110と拡径部111とを備える本実施形態によれば、平行操作の領域を境界部112で制限するとともに、回転操作の領域を充分に確保することが可能である。即ち、挿通孔12に挿通する内視鏡を平行操作または回転操作するとき、操作による内視鏡の移動が伸縮部16(伸縮手段)にひずみを発生させる。このとき、伸縮部16は上記ひずみを吸収可能である。しかし上記ひずみが大きすぎると、伸縮部16は、ひずみを吸収しきれず、この結果、内視鏡挿入部17が変形し、内視鏡挿入部17と内視鏡との間に隙間が発生する虞がある。そこで内視鏡の操作範囲(特に平行操作の範囲)を境界部112によって制限することにより、上記虞の発生を防止し、高い気密性によって内視鏡挿入部17と内視鏡との間を封止可能とすることができる。伸縮部16の詳細については後述する。
 かかる構成は、内視鏡の挿入地点(即ち、患者の口)から比較的近い患部である咽頭あるいは食道を観察する場合に、詳細な観察の観点から望ましい。
The operation of the endoscope inserted through the insertion hole 12 is generally a parallel operation of moving the entire endoscope in a direction substantially parallel to the insertion direction, arbitrarily twisting the endoscope in the insertion direction, This is performed by a rotation operation for guiding the endoscope tip to a target position and a combination thereof.
In the operation of such an endoscope, according to the present embodiment including the reduced diameter portion 110 and the enlarged diameter portion 111, the parallel operation area is limited by the boundary portion 112, and the rotation operation area is sufficiently secured. Is possible. That is, when the endoscope inserted through the insertion hole 12 is operated in parallel or rotated, the movement of the endoscope by the operation causes distortion in the expansion / contraction part 16 (extension / contraction means). At this time, the stretchable part 16 can absorb the strain. However, if the strain is too large, the stretchable portion 16 cannot absorb the strain, and as a result, the endoscope insertion portion 17 is deformed, and a gap is generated between the endoscope insertion portion 17 and the endoscope. There is a fear. Therefore, by restricting the operation range of the endoscope (particularly the range of parallel operation) by the boundary portion 112, the occurrence of the above-mentioned fear is prevented, and the space between the endoscope insertion portion 17 and the endoscope is prevented by high airtightness. It can be made sealable. Details of the stretchable part 16 will be described later.
Such a configuration is desirable from the viewpoint of detailed observation when observing the pharynx or esophagus, which is an affected area relatively close to the insertion point of the endoscope (that is, the patient's mouth).
 本実施形態における縮径部110は、円形の漏斗状をなしている(図3参照)。このため、挿通孔12における内視鏡の挿通の開始をスムーズにガイド可能である。
 本実施形態における挿通孔12は、境界部112の付近で拡径するとともに、さらに遠位端部側では直筒形状となっている。上記長筒形状の領域は、挿通方向に対して垂直に切断した断面の外形および内形が略相似の長円をなす。
 境界部112より遠位端側の挿通方向に対する垂直断面は、縮径部110の内径よりも大きい短軸と長軸を含む長円をなす。
The reduced diameter portion 110 in the present embodiment has a circular funnel shape (see FIG. 3). For this reason, it is possible to smoothly guide the start of insertion of the endoscope through the insertion hole 12.
The insertion hole 12 in the present embodiment has a diameter that increases in the vicinity of the boundary portion 112 and has a straight cylindrical shape on the distal end side. The long cylindrical region is an ellipse whose outer shape and inner shape of a cross section cut perpendicularly to the insertion direction are substantially similar.
A vertical section with respect to the insertion direction on the distal end side from the boundary portion 112 forms an ellipse including a short axis and a long axis that are larger than the inner diameter of the reduced diameter portion 110.
 マウスピース本体11は、遠位端部に筒状の歯受部26を有する。歯受部26の外径は、長軸36および短軸38を有する(図4参照)。
 即ち、歯受部26を長尺方向に対し垂直方向に切断したときの断面形状が、真円ではなく、一方方向に長い。たとえば、歯受部26の上記断面形状は、長円(楕円を含む)をなす。
 かかる断面形状を有する歯受部26は、断面形状が真円である場合に比べて、患者がマウスピース100を咥えた状態で、唇と歯受部26とを密着させ易い。そのため、唇と歯受部26との間からの息漏れを良好に防止可能である。たとえば、上記断面が長円である歯受部26を、長軸方向を患者の口角と口角とを結ぶ方向と概略平行として患者に咥えさせ口を閉じさせることができる。かかる場合、当該口角と長円とがフィットして、口角部分から息が漏れにくい。
The mouthpiece body 11 has a cylindrical tooth receiving portion 26 at the distal end. The outer diameter of the tooth receiving portion 26 has a major axis 36 and a minor axis 38 (see FIG. 4).
That is, the cross-sectional shape when the tooth receiving portion 26 is cut in the direction perpendicular to the longitudinal direction is not a perfect circle but is long in one direction. For example, the cross-sectional shape of the tooth receiving portion 26 is an ellipse (including an ellipse).
The tooth receiving part 26 having such a cross-sectional shape can easily bring the lip and the tooth receiving part 26 into close contact with each other in a state where the patient holds the mouthpiece 100 as compared with a case where the cross-sectional shape is a perfect circle. For this reason, it is possible to satisfactorily prevent breath leakage from between the lips and the tooth receiving portion 26. For example, the tooth receiving part 26 having an oval cross section can be given to the patient so that the major axis direction is substantially parallel to the direction connecting the mouth angle and the mouth angle of the patient, and the mouth can be closed. In such a case, the mouth corner and the ellipse fit, and it is difficult for the breath to leak from the mouth corner.
 本実施形態におけるマウスピース本体11は、歯受部26の内径も、長軸と短軸とを有している。歯受部26は、図6および図7に示すように略均一な肉厚の壁により長円に構成されている。歯受部26の内径形状が長円に形成されているため、特に長軸方向において、内視鏡の操作範囲が大きい。
 歯受部26は、歯受部26の遠位端部において径方向の外側に突出する凸部30を有する。患者が、歯受部26に直接に歯を当ててマウスピース100を咥える場合、凸部30は、患者の歯の停止部として機能し、マウスピース100が口から落下することを防止することが可能である。
In the mouthpiece body 11 in this embodiment, the inner diameter of the tooth receiving portion 26 also has a major axis and a minor axis. As shown in FIGS. 6 and 7, the tooth receiving portion 26 is formed in an oval shape by a substantially uniform wall. Since the inner diameter shape of the tooth receiving portion 26 is formed in an ellipse, the operation range of the endoscope is large particularly in the long axis direction.
The tooth receiving portion 26 has a convex portion 30 protruding outward in the radial direction at the distal end portion of the tooth receiving portion 26. When the patient grips the mouthpiece 100 by directly applying teeth to the tooth receiving portion 26, the convex portion 30 functions as a stop portion of the patient's teeth and prevents the mouthpiece 100 from falling from the mouth. Is possible.
 マウスピース100は、マウスピース本体11の遠位端部と近位端部との間において、外周面40(図3)から外方向に延在する鍔部42を有する。外周面40とは、マウスピース本体11の外側側面を構成する面である。
 鍔部42は、図4から理解されるとおり、歯受部26の長軸36の伸長方向よりも短軸38の伸長方向に長く延在している。
 たとえば、患者が、長軸36の伸長方向と、口角と口角とを結んだ線と、が略平行となるようマウスピース100を咥えたとき、鍔部42が上唇と下唇とに当接する。これによって、患者がマウスピース100を咥えた状態が安定するとともに、口からの息漏れがし難い。
The mouthpiece 100 has a flange 42 extending outward from the outer peripheral surface 40 (FIG. 3) between the distal end portion and the proximal end portion of the mouthpiece body 11. The outer peripheral surface 40 is a surface constituting the outer side surface of the mouthpiece body 11.
As can be understood from FIG. 4, the collar portion 42 extends longer in the extending direction of the short shaft 38 than in the extending direction of the long shaft 36 of the tooth receiving portion 26.
For example, when the patient grips the mouthpiece 100 so that the extension direction of the long axis 36 and the line connecting the mouth angle and the mouth angle are substantially parallel, the buttocks 42 abut on the upper lip and the lower lip. As a result, the state in which the patient holds the mouthpiece 100 is stabilized, and it is difficult for the patient to leak from the mouth.
 図1に示すように、本実施形態における鍔部42は、マウスピース本体11の遠位端から近位端に向かう方向に凸状に湾曲している。湾曲形状の詳細は、特に限定されないが、例えば、長軸36を左右方向にして、鍔部42を観察したとき、鍔部42が遠位端部から近位端部に向けて凸形状をなしている(図7参照)。
 鍔部42を上述のとおり湾曲させることにより、鍔部42の遠位端側の面が、歯受部26を咥えた患者の唇に沿いやすい。これにより、マウスピース100の装着性と気密性が向上しうる。
 本実施形態において鍔部42は、円筒体の外面の一部をなす形状である円筒面となっている。上記円筒面を有する当該円筒体の中心軸は、短軸38の軸線方向と同一方向である。
 即ち、鍔部42は、仮想の円筒体の外周面に沿う形状となっている。たとえば、当該円筒体の中心軸方向が上唇と下唇との方向となるようにマウスピース本体11を咥えたとき、左右の口角を結ぶ方向は当該円筒体の円周方向となる。これにより、マウスピース本体11を咥えた状態で、鍔部42が患者の口に良好に密着可能であり、マウスピース本体11の装着性が良い。
As shown in FIG. 1, the collar portion 42 in the present embodiment is curved in a convex shape in a direction from the distal end to the proximal end of the mouthpiece body 11. The details of the curved shape are not particularly limited, but, for example, when the collar portion 42 is observed with the long axis 36 set in the left-right direction, the collar portion 42 has a convex shape from the distal end portion toward the proximal end portion. (See FIG. 7).
By curving the buttocks 42 as described above, the surface on the distal end side of the buttocks 42 tends to be along the lips of the patient holding the tooth receiving portion 26. Thereby, the mounting property and airtightness of the mouthpiece 100 can be improved.
In this embodiment, the collar part 42 is a cylindrical surface which is a shape that forms a part of the outer surface of the cylindrical body. The central axis of the cylindrical body having the cylindrical surface is the same direction as the axial direction of the short axis 38.
That is, the collar part 42 has a shape along the outer peripheral surface of the virtual cylindrical body. For example, when the mouthpiece body 11 is held so that the central axis direction of the cylinder is the direction of the upper lip and the lower lip, the direction connecting the left and right mouth corners is the circumferential direction of the cylinder. Thereby, in the state which held the mouthpiece main body 11, the collar part 42 can contact | adhere well to a patient's mouth, and the mounting property of the mouthpiece main body 11 is good.
 次に脱気防止弁装置18について説明する。
 図3に示されるとおり、脱気防止弁装置18は、挿通孔12に周設されている。また脱気防止弁装置18は、挿通孔12に挿通される内視鏡(図示せず)に周着する。
 脱気防止弁装置18が挿通孔12に周設されているとは、挿通孔12の少なくとも一方の端部または中間において挿通孔12の全周に脱気防止弁装置18が取り付けられていることを意味する。本実施形態では、具体的には、脱気防止弁装置18に設けられた伸縮部16が、挿通孔12に周設され、挿通孔12に挿通される内視鏡に周着する。
 かかる構成によれば、挿通孔12に挿通される内視鏡が脱気防止弁装置18を通過するとき、当該内視鏡は、挿通孔12の内壁面に当接することなく、脱気防止弁装置18に気密に周着する。このため、内視鏡と挿通孔12との間に隙間部が発生し難く、口からの空気漏れを防止することができる。
 本実施形態において、脱気防止弁装置18は、脱気防止弁装置18をマウスピース本体11の近位端側の開口端面に圧着させるための固定部材である固定リング59が設けられている(図3)。
 本実施形態において、固定リング59は、伸縮部16をフレーム部14に固定するための伸縮部用固定部材をなしている(図3)。
 固定リング59は、略リング状の部材であって、フレーム部14の内側において、下端部23と上端部25との中間領域に設けられている。
Next, the deaeration prevention valve device 18 will be described.
As shown in FIG. 3, the deaeration prevention valve device 18 is provided around the insertion hole 12. Further, the deaeration prevention valve device 18 is attached to an endoscope (not shown) inserted through the insertion hole 12.
That the deaeration prevention valve device 18 is provided around the insertion hole 12 means that the deaeration prevention valve device 18 is attached to the entire circumference of the insertion hole 12 at at least one end or in the middle of the insertion hole 12. Means. Specifically, in this embodiment, the expansion / contraction part 16 provided in the deaeration prevention valve device 18 is provided around the insertion hole 12 and is attached to the endoscope inserted through the insertion hole 12.
According to this configuration, when the endoscope inserted through the insertion hole 12 passes through the deaeration prevention valve device 18, the endoscope does not contact the inner wall surface of the insertion hole 12, and the deaeration prevention valve Around the device 18 is airtight. For this reason, it is difficult to generate a gap between the endoscope and the insertion hole 12, and air leakage from the mouth can be prevented.
In the present embodiment, the deaeration prevention valve device 18 is provided with a fixing ring 59 which is a fixing member for crimping the deaeration prevention valve device 18 to the open end surface on the proximal end side of the mouthpiece body 11 ( FIG. 3).
In the present embodiment, the fixing ring 59 constitutes an expansion / contraction section fixing member for fixing the expansion / contraction section 16 to the frame section 14 (FIG. 3).
The fixing ring 59 is a substantially ring-shaped member, and is provided in an intermediate region between the lower end portion 23 and the upper end portion 25 inside the frame portion 14.
 本実施形態における挿通孔12とは、マウスピース100の内部に設けられる孔であって、内視鏡が挿入される孔である。脱気防止弁装置18は、挿通孔12の中間領域、または挿通孔12の近位端あるいは遠位端における開口領域のいずれかに1か所または2か所以上、設けることができる。脱気防止弁装置18は、挿通孔12に直接または間接に周設される。 In the present embodiment, the insertion hole 12 is a hole provided in the mouthpiece 100 and into which the endoscope is inserted. The deaeration prevention valve device 18 can be provided in one or more places in either the intermediate region of the insertion hole 12 or the opening region in the proximal end or the distal end of the insertion hole 12. The deaeration prevention valve device 18 is directly or indirectly provided in the insertion hole 12.
 本実施形態における脱気防止弁装置18は、挿通孔12に周設された可撓性の伸縮部16(伸縮手段)を有する(図1)。伸縮部16は、伸縮部16の略中央部に設けられ図示省略する内視鏡に周着する内視鏡挿入部17を有する。
 伸縮部16は、内視鏡に気密に密着可能な可撓性の部材で構成されている。
 可撓性の伸縮部16は、たとえば膜形状あるいは円板形状であって面内方向において伸縮可能な部材より構成される。上記膜形状または上記円板形状の伸縮部16とは、面内が概略平滑な面である態様、および面内に凹凸部が設けられた態様をいずれも包含する。上記凹凸部には、蛇腹部120を含む。
 より具体的には、伸縮部16は、平坦部からなる平板部材、蛇腹部120を有する蛇腹部材であってもよいが、気密性の観点から、蛇腹部材であることが好ましい。上記蛇腹部材は、伸縮部16の略全体において面内方向に蛇腹部120が設けられた態様、および平坦部と蛇腹部120の組み合わせよりなる態様のいずれも包含する。
 伸縮部16の伸縮により、内視鏡が挿入された内視鏡挿入部17は、当該内視鏡の操作により内視鏡に追随して移動可能である。内視鏡挿入部17は、径方向、内視鏡の進退方向、および回転方向(内視鏡の首ふり方向あるいは捻じれ方向)に移動可能である。
 このため、内視鏡挿入部17に挿入された内視鏡が操作されたとき、内視鏡の操作性を損なわずに脱気防止弁装置18と内視鏡との気密性を維持することが可能である。
 図3に示すとおり、伸縮部16の外縁には、マウスピース本体11の係合受部54に当接してマウスピース本体11の近位端側の開口を気密に封止する閉止栓部60が設けられている。係合受部54の詳細は後述する。閉止栓部60は、伸縮部16と一体的に形成されてもよいし、伸縮部16の外縁に別部材を接合することにより形成されてもよい。閉止栓部60は、たとえば、弾力性のある樹脂部材で形成することができる。具体的には、たとえば閉止栓部60は、伸縮部16と同様であって同質または異質の樹脂材料で形成することができる。
The deaeration prevention valve device 18 in the present embodiment has a flexible expansion / contraction part 16 (extension / contraction means) provided around the insertion hole 12 (FIG. 1). The expansion / contraction part 16 has an endoscope insertion part 17 that is provided at a substantially central part of the expansion / contraction part 16 and is attached to an endoscope (not shown).
The expansion / contraction part 16 is comprised with the flexible member which can contact | adhere airtightly to an endoscope.
The flexible expansion / contraction part 16 is comprised from the member which is film | membrane shape or disk shape, for example, and can be expanded-contracted in an in-plane direction. The film-shaped or disk-shaped stretchable part 16 includes both an aspect in which the in-plane is a substantially smooth surface and an aspect in which an uneven portion is provided in the plane. The uneven portion includes a bellows portion 120.
More specifically, the stretchable portion 16 may be a flat plate member made of a flat portion or a bellows member having the bellows portion 120, but is preferably a bellows member from the viewpoint of airtightness. The bellows member includes both an aspect in which the bellows part 120 is provided in the in-plane direction in substantially the entire stretchable part 16 and an aspect in which the flat part and the bellows part 120 are combined.
The endoscope insertion part 17 into which the endoscope is inserted by the extension / contraction of the extension / contraction part 16 can move following the endoscope by operation of the endoscope. The endoscope insertion portion 17 is movable in the radial direction, the forward / backward direction of the endoscope, and the rotation direction (the neck swinging direction or the twisting direction of the endoscope).
For this reason, when the endoscope inserted in the endoscope insertion portion 17 is operated, the airtightness between the deaeration prevention valve device 18 and the endoscope is maintained without impairing the operability of the endoscope. Is possible.
As shown in FIG. 3, a closing plug portion 60 that abuts the engagement receiving portion 54 of the mouthpiece body 11 and hermetically seals the opening on the proximal end side of the mouthpiece body 11 is provided on the outer edge of the expansion / contraction portion 16. Is provided. Details of the engagement receiving portion 54 will be described later. The closing plug portion 60 may be formed integrally with the stretchable portion 16, or may be formed by joining another member to the outer edge of the stretchable portion 16. The closing plug portion 60 can be formed of, for example, an elastic resin member. Specifically, for example, the closing plug portion 60 is similar to the stretchable portion 16 and can be formed of the same or different resin material.
 本実施形態にかかる内視鏡挿入部17は、環状である。ただし、本発明における内視鏡挿入部17は、これに限定されない。たとえば、内視鏡挿入部17は、伸縮部16の面内に形成された、挿通孔12の挿通方向に内視鏡を貫通可能な切り込み部であってもよい。 The endoscope insertion portion 17 according to the present embodiment is annular. However, the endoscope insertion portion 17 in the present invention is not limited to this. For example, the endoscope insertion portion 17 may be a cut portion that is formed in the plane of the stretchable portion 16 and can penetrate the endoscope in the insertion direction of the insertion hole 12.
 環状に形成された内視鏡挿入部17の径は、使用が予定される内視鏡の径よりも小さい径とすることができる。これによって、内視鏡に対する周着が確実となり、上記気密性の効果を良好とすることができる。 The diameter of the endoscope insertion portion 17 formed in an annular shape can be smaller than the diameter of the endoscope scheduled to be used. As a result, the peripheral attachment to the endoscope is ensured, and the airtight effect can be improved.
 伸縮部16は、環状の内視鏡挿入部17と同心円状において、谷部116、山部114、谷部116、および山部114が連続して設けられてなる蛇腹部120を有する。蛇腹部120を有することにより、内視鏡挿入部17に挿入された内視鏡の操作性をさらに向上させることができ、結果として充分な気密性も維持される。
 本実施形態において蛇腹部120の内縁は、最も内視鏡挿入部17に重複する谷部116である。本発明の伸縮部16において、蛇腹部120以外の部分を非蛇腹部という。非蛇腹部は、伸縮部16において、蛇腹部120以外の部分であり、非蛇腹部の面内方向における伸縮性は、蛇腹部120の面内方向の伸縮性より小さい。非蛇腹部には平坦部を含む。平坦部とは、伸縮部16を目視で観察したときに、面内において実質的に凹凸がない部分を意味する。
 本実施形態は、伸縮部16を可撓性のある部材で形成し、かつ、蛇腹部120を設けている。本実施態様の変形例としては、伸縮部16を可撓性のない、あるいは可撓性の小さい部材で形成し、かつ、蛇腹部120を設けることもできる。
The expansion / contraction part 16 has a bellows part 120, a valley part 116, a valley part 114, a valley part 116, and a bellows part 120 which are provided concentrically with the annular endoscope insertion part 17. By having the bellows portion 120, the operability of the endoscope inserted into the endoscope insertion portion 17 can be further improved, and as a result, sufficient airtightness is maintained.
In the present embodiment, the inner edge of the bellows portion 120 is a valley portion 116 that overlaps most with the endoscope insertion portion 17. In the stretchable part 16 of the present invention, the part other than the bellows part 120 is referred to as a non-bellows part. The non-bellows part is a part other than the bellows part 120 in the stretchable part 16, and the stretchability in the in-plane direction of the non-bellows part is smaller than the stretchability in the in-plane direction of the bellows part 120. The non-accordion portion includes a flat portion. A flat part means the part which does not have an unevenness | corrugation substantially in the surface, when the expansion-contraction part 16 is observed visually.
In this embodiment, the stretchable portion 16 is formed of a flexible member, and the bellows portion 120 is provided. As a modification of the present embodiment, the stretchable portion 16 can be formed of a member having no flexibility or low flexibility, and the bellows portion 120 can be provided.
 本実施形態における脱気防止弁装置18は、マウスピース本体11に着脱可能に装着されるフレーム部14を有している。
 かかる構成により、脱気防止弁装置18がマウスピース本体11に着脱可能となっている。このため、例えば中下咽頭部の内視鏡検査を気密状態で行った後、脱気防止弁装置18を取り外し、続けて食道や胃などの他の内視鏡検査を行うことができる。
 即ち、気密性が重要な中下咽頭部の検査に引き続いて、食道・胃の検査を実施しようとした場合、患者の呼吸が十分に行えるように、気密性確保は不必要である。これに対し、上記構成によれば、マウスピース本体11に対する脱気防止弁装置18の着脱により気密性の確保の有無を適宜コントロール可能である。
 より具体的には、一般的に、食道や胃の検査では、上述のバルサルバ法による中下咽頭部の検査のように、気密性確保が必要とはされないため、脱気防止弁装置18は外し、患者が十分に呼吸できるようにすることが想定される。しかし、内視鏡で送気をしても胃の観察に必要な視野が得られない場合には、脱気防止弁装置18をあらためて装着すれば、口からの空気漏れを最低限に抑えて、視野確保ができる。このように、脱気防止弁装置18がマウスピース本体11に対して、着脱可能であることで、内視鏡検査の状況や患者の状況に応じて、脱気防止弁装置18は任意に装着、非装着を選択することができる。
The deaeration prevention valve device 18 in the present embodiment has a frame portion 14 that is detachably attached to the mouthpiece body 11.
With this configuration, the deaeration prevention valve device 18 can be attached to and detached from the mouthpiece body 11. For this reason, for example, after endoscopic examination of the middle and lower pharynx is performed in an airtight state, the deaeration prevention valve device 18 can be removed, and another endoscopic examination such as the esophagus and stomach can be subsequently performed.
That is, when an examination of the esophagus and stomach is performed following the examination of the middle and lower pharynx where airtightness is important, it is not necessary to ensure airtightness so that the patient can fully breathe. On the other hand, according to the said structure, the presence or absence of ensuring airtightness is controllable suitably by attachment or detachment of the deaeration prevention valve apparatus 18 with respect to the mouthpiece main body 11. FIG.
More specifically, in general, in the examination of the esophagus and stomach, it is not necessary to ensure airtightness unlike the examination of the middle and lower pharynx by the Valsalva method described above. It is envisaged that the patient will be able to breathe well. However, if the field of view necessary for gastric observation cannot be obtained even if air is supplied through an endoscope, the air leakage from the mouth can be minimized by installing the deaeration prevention valve device 18 again. , Securing a field of view. Thus, the deaeration prevention valve device 18 can be attached to and detached from the mouthpiece main body 11, so that the deaeration prevention valve device 18 is arbitrarily attached according to the endoscopy situation or the patient's situation. The non-wearing can be selected.
 フレーム部14は、マウスピース本体11の取り付け位置に応じて種々の形状をとることができる。本実施形態におけるフレーム部14は、略円筒状をなしている。
 フレーム部14の内面に伸縮部16が設けられている。フレーム部14と伸縮部16とは別部材により形成されており、伸縮部16を構成する部材よりもフレーム部14を構成する部材は硬質である。伸縮部16は、固定リング59によりフレーム部14に固定される態様のほか、フレーム部14に直接に固定される態様であってもよい。あるいはフレーム部14に設けられた異なる任意の部材に固定されて、フレーム部14に設けられる態様であってもよい。
The frame portion 14 can take various shapes according to the attachment position of the mouthpiece body 11. The frame portion 14 in the present embodiment has a substantially cylindrical shape.
An elastic part 16 is provided on the inner surface of the frame part 14. The frame part 14 and the expansion / contraction part 16 are formed by separate members, and the member constituting the frame part 14 is harder than the member constituting the expansion / contraction part 16. The expansion / contraction part 16 may be directly fixed to the frame part 14 in addition to the aspect fixed to the frame part 14 by the fixing ring 59. Or the aspect fixed to the arbitrary arbitrary members provided in the frame part 14 and provided in the frame part 14 may be sufficient.
 フレーム部14は、比較的硬質の材質を用いることにより、マウスピース本体11に対する着脱操作が良好となる。具体的には、フレーム部14の材料としては、例えば硬質塩化ビニル樹脂、ポリウレタン樹脂、硬質ポリウレタン樹脂、ポリエチレン樹脂、ポリアミド樹脂、ポリプロピレン樹脂、ポリアセタール樹脂、フッ素化ポリエチレン樹脂、アクリルニトリルーブタジエンースチレン共重合体(ABS)樹脂などが利用できる。 The frame part 14 can be attached to and detached from the mouthpiece body 11 by using a relatively hard material. Specifically, examples of the material of the frame portion 14 include hard vinyl chloride resin, polyurethane resin, hard polyurethane resin, polyethylene resin, polyamide resin, polypropylene resin, polyacetal resin, fluorinated polyethylene resin, and acrylonitrile-butadiene-styrene. Polymer (ABS) resin or the like can be used.
 伸縮部16は、フレーム部14と比較して柔軟性を有する材料で構成されることが好ましい。具体的には、伸縮部16の材料としては、例えば天然ゴム、合成ゴム、ポリウレタンエラストマー、スチレン-ブタジエン-スチレン3元共重合体、シリコーンゴム等の伸縮性のある材料が望ましく、内視鏡と伸縮部16との摩擦の向上のためにオイルを含有させた上記の材質を用いることも好ましい。 The stretchable part 16 is preferably made of a material having flexibility as compared with the frame part 14. Specifically, the material of the stretchable portion 16 is preferably a stretchable material such as natural rubber, synthetic rubber, polyurethane elastomer, styrene-butadiene-styrene terpolymer, silicone rubber, and the like. It is also preferable to use the above-mentioned material containing oil in order to improve the friction with the stretchable part 16.
 本実施形態において、マウスピース本体11に対する脱気防止弁装置18の着脱は、以下のとおり実現される。
 即ち、フレーム部14は、フレーム部14をマウスピース本体11の近位端に係脱可能に係止する係止部24を備えている(図1から図3参照)。
 本実施形態における係止部24は、フレーム部14の外縁の円周上に設けられている。係止部24は、フレーム部14の外縁に沿って、当該外縁の上端および下端を超えて延在する。係止部24のフレーム部14の下端を超えて延在する下端部23には、フレーム部14の内側に向かって突き出した係合突起部22(係止手段)が設けられている(図2および図3)。係合突起部22は、マウスピース本体11の近位端部であって外側面に係合する。マウスピース本体11は、縮径部110の近位端から連続し径方向の外側に向かって延在する環状の係合受部54が設けられている(図6および図7)。係合突起部22が、係合受部54に係合することによって、脱気防止弁装置18がマウスピース100に装着される。
 なお、ここでいう上下方向は、マウスピース100の近位端側を上方向、遠位端側を下方向としている。
 係止部24のフレーム部14の上端を超えて延在する上端部25には、つまみ部20(指掛け部)が設けられている。つまみ部20は、係止部24の上端であって外側側面に設けられており、係止部24の上端に指を当てて着脱の操作をする際に指滑りが防止され操作性がよい。係止部24の上端部25を径方向の内向きに押すことによって下端部23が径方向の外向きに開く。これによって、係合突起部22を係合受部54に対して係合させ、または係合を解除させることができる。
In this embodiment, the attachment / detachment of the deaeration prevention valve device 18 with respect to the mouthpiece body 11 is realized as follows.
That is, the frame portion 14 includes a locking portion 24 that detachably locks the frame portion 14 to the proximal end of the mouthpiece body 11 (see FIGS. 1 to 3).
The locking portion 24 in the present embodiment is provided on the circumference of the outer edge of the frame portion 14. The locking portion 24 extends along the outer edge of the frame portion 14 beyond the upper and lower ends of the outer edge. The lower end 23 extending beyond the lower end of the frame portion 14 of the locking portion 24 is provided with an engaging protrusion 22 (locking means) protruding toward the inside of the frame portion 14 (FIG. 2). And FIG. 3). The engagement protrusion 22 is a proximal end portion of the mouthpiece body 11 and engages with the outer surface. The mouthpiece body 11 is provided with an annular engagement receiving portion 54 that is continuous from the proximal end of the reduced diameter portion 110 and extends radially outward (FIGS. 6 and 7). The deaeration prevention valve device 18 is attached to the mouthpiece 100 by the engagement protrusion 22 engaging with the engagement receiver 54.
In addition, the up-down direction here makes the proximal end side of the mouthpiece 100 upward, and makes the distal end side downward.
A knob portion 20 (finger hook portion) is provided on an upper end portion 25 that extends beyond the upper end of the frame portion 14 of the locking portion 24. The knob portion 20 is provided on the outer side surface at the upper end of the locking portion 24. When the finger is applied to the upper end of the locking portion 24 for attaching and detaching, finger sliding is prevented and operability is good. By pushing the upper end portion 25 of the locking portion 24 inward in the radial direction, the lower end portion 23 opens outward in the radial direction. Thereby, the engagement protrusion 22 can be engaged with or released from the engagement receiving portion 54.
 マウスピース本体11は、比較的硬質の材料を用いることにより、マウスピース100の強度を確保するとともに、マウスピース本体11の内腔である挿通孔12の内径を充分に確保可能である。具体的には、マウスピース本体11は、硬質塩化ビニル樹脂、硬質ポリウレタン樹脂、ポリエチレン樹脂、ポリアミド樹脂、ポリプロピレン樹脂、ポリアセタール樹脂、フッ素化ポリエチレン樹脂、アクリロニトリル-ブタジエン-スチレン共重合体(ABS)樹脂などの樹脂材料を用いることができる。マウスピース本体11は、一種の樹脂材料で形成することもできるし、任意の箇所ごとに構成する材料の種類を変更することもできる。
 またマウスピース本体11は、比較的硬質の材料を用いるという観点からは、上述するフレーム部14と同様の材料で形成してもよい。このとき、マウスピース本体11とフレーム部14とは、互いに、同種の材料で形成してもよいし異種の材料であって同等な硬度の材料で形成してもよい。
By using a relatively hard material, the mouthpiece body 11 can secure the strength of the mouthpiece 100 and can sufficiently secure the inner diameter of the insertion hole 12 that is the lumen of the mouthpiece body 11. Specifically, the mouthpiece body 11 is made of hard vinyl chloride resin, hard polyurethane resin, polyethylene resin, polyamide resin, polypropylene resin, polyacetal resin, fluorinated polyethylene resin, acrylonitrile-butadiene-styrene copolymer (ABS) resin, or the like. These resin materials can be used. The mouthpiece main body 11 can be formed of a kind of resin material, and the type of material constituting each arbitrary location can be changed.
The mouthpiece body 11 may be formed of the same material as that of the frame portion 14 described above from the viewpoint of using a relatively hard material. At this time, the mouthpiece main body 11 and the frame portion 14 may be formed of the same kind of material or different kinds of materials having the same hardness.
 係止部24の数は、特に限定されず、マウスピース本体11に対する脱気防止弁装置18の着脱を可能とする範囲において、任意に決定してよい。本実施形態にかかるマウスピース100は、フレーム部14を介して略対向する2か所に係止部24が設けられている。略対向する2か所の係止部24、あるいは任意の位置に3か所以上設けられた係止部24の上端であって外側面に指を当て、内側に押圧することができる。これにより、係止部24の下端部23を外方向に移動させることができる。
 本実施形態における係止部24は、マウスピース本体11の外側面に位置する。そのため、脱気防止弁装置18をマウスピース本体11に装着したとき、マウスピース本体11の内腔における内視鏡の可動域を狭めることがなく、内視鏡の操作性を損なうことがない。
The number of the locking portions 24 is not particularly limited, and may be arbitrarily determined as long as the deaeration prevention valve device 18 can be attached to and detached from the mouthpiece body 11. The mouthpiece 100 according to the present embodiment is provided with locking portions 24 at two locations that are substantially opposed to each other with the frame portion 14 therebetween. A finger can be applied to the outer surface of the two locking portions 24 that are substantially opposed to each other, or three or more locking portions 24 provided at arbitrary positions, and pressed inward. Thereby, the lower end part 23 of the latching | locking part 24 can be moved to an outward direction.
The locking portion 24 in the present embodiment is located on the outer surface of the mouthpiece body 11. Therefore, when the deaeration prevention valve device 18 is attached to the mouthpiece body 11, the range of motion of the endoscope in the lumen of the mouthpiece body 11 is not narrowed, and the operability of the endoscope is not impaired.
 ただし、本発明において脱気防止弁装置18をマウスピース本体11に対し着脱させる機構はこれに限定されるものではない。たとえば係止部24が、フレーム部14の内縁の円周上に設けられ、マウスピース本体11の近位端部の内側面の任意の箇所に係合あるいは嵌合させ、上記着脱を行ってもよい。
 また、本発明における脱気防止弁装置18の着脱は、係止手段に限定されるものではない。たとえば、フレーム部14に設けられた所定の摩擦係数を有するシリコーンゴムなどの摩擦要素と、この摩擦要素をマウスピース本体11の外周面または内周面に付勢するバネなどの付勢部材とを組み合わせてもよい。
However, in the present invention, the mechanism for attaching / detaching the deaeration prevention valve device 18 to / from the mouthpiece body 11 is not limited to this. For example, the locking portion 24 may be provided on the circumference of the inner edge of the frame portion 14, and may be engaged with or fitted to any location on the inner side surface of the proximal end portion of the mouthpiece body 11 to perform the above attachment / detachment. Good.
Further, the attachment / detachment of the deaeration prevention valve device 18 in the present invention is not limited to the locking means. For example, a friction element such as silicone rubber having a predetermined friction coefficient provided on the frame portion 14 and a biasing member such as a spring that biases the friction element toward the outer peripheral surface or inner peripheral surface of the mouthpiece body 11 are provided. You may combine.
 次に、歯受部26の周囲に設けられる被覆部28について説明する。
 上述のとおりマウスピース本体11は、遠位端部に筒状の歯受部26を有する。
マウスピース本体11は、歯受部26の外周を被覆する被覆部28をさらに備えてもよい。被覆部28の硬度は、歯受部26の硬度よりも低い。そのため、患者が、被覆部28の上から歯受部26を咥えたとき、患者に対し好ましい体感を与えるとともに、歯受部26の強度を維持することが可能である。
 また、被覆部28をシリコーンゴムなどの柔軟な樹脂部材で構成することにより、被覆部28の表面に歯をあてて、歯受部26を咥えたとき、当該歯がわずかに被覆部28に食い込み、噛み位置のずれが抑制される。したがって内視鏡検査の際に、マウスピースが口から落下することが防止される。
Next, the covering portion 28 provided around the tooth receiving portion 26 will be described.
As described above, the mouthpiece body 11 has the cylindrical tooth receiving portion 26 at the distal end portion.
The mouthpiece body 11 may further include a covering portion 28 that covers the outer periphery of the tooth receiving portion 26. The hardness of the covering portion 28 is lower than the hardness of the tooth receiving portion 26. Therefore, when the patient picks up the tooth receiving portion 26 from above the covering portion 28, it is possible to give the patient a favorable experience and maintain the strength of the tooth receiving portion 26.
Further, by forming the covering portion 28 with a flexible resin member such as silicone rubber, when the teeth are applied to the surface of the covering portion 28 and the tooth receiving portion 26 is gripped, the teeth slightly bite into the covering portion 28. The shift of the biting position is suppressed. Therefore, the mouthpiece is prevented from dropping from the mouth during the endoscopy.
 被覆部28は比較的軟質の材料を用いることにより、外周面から患者が歯をあてたときに、良好な咥え心地を与え、また歯が被覆部28の表面で滑りにくい。具体的には、シリコーンゴム、ポリウレタンエラストマー、天然ゴム、合成ゴム、スチレン-ブタジエン-スチレン3元共重合体等の弾力性の高い材料が好ましい。 By using a relatively soft material for the covering portion 28, when the patient hits the teeth from the outer peripheral surface, the covering portion 28 is given a good feeling of comfort, and the teeth are difficult to slip on the surface of the covering portion 28. Specifically, a highly elastic material such as silicone rubber, polyurethane elastomer, natural rubber, synthetic rubber, styrene-butadiene-styrene terpolymer is preferable.
 なお、本発明の説明において硬度という場合には、各構成部材に適した公知の手段で測定された硬度を意味する。たとえば、樹脂部材で構成された本発明の任意の構成の硬度は、デュロメーター硬度 JIS K 6253に準拠して測定することができる。 In the description of the present invention, the term “hardness” means the hardness measured by a known means suitable for each component. For example, the hardness of an arbitrary configuration of the present invention formed of a resin member can be measured according to durometer hardness JIS K 6253.
 本実施形態における被覆部28は、マウスピース本体11に対して脱着可能である。これにより、口の小さな患者には、咥える部分の径を小さくするために被覆部28を取り外して歯受部26を直接に咥えさせることができる。また、肉厚の異なる2種以上の被覆部28を準備することで、患者の口の大きさに合わせて患者の咥える部分の径をさらに細かく調整することも可能である。
 ただし、本発明は、マウスピース本体11に繰り返しの着脱ができない(つまり歯受部26に対して固定されている)被覆部28を除外するものではない。
The covering portion 28 in this embodiment is detachable from the mouthpiece body 11. As a result, a patient with a small mouth can remove the covering portion 28 to directly grip the tooth receiving portion 26 in order to reduce the diameter of the gripping portion. Further, by preparing two or more kinds of covering portions 28 having different thicknesses, it is possible to further finely adjust the diameter of the portion that the patient can hold according to the size of the patient's mouth.
However, the present invention does not exclude the covering portion 28 that cannot be repeatedly attached to and detached from the mouthpiece body 11 (that is, fixed to the tooth receiving portion 26).
 本実施形態における被覆部28は、歯受部26であってマウスピース本体11を咥える患者の歯が当たる領域を少なくとも被覆する。たとえば、被覆部28は、図5に示すとおり、歯受部26の外側の概略全周を覆うOリング形状であってもよい。
 被覆部28は、所定の形状から容易に変形し、かつ所定の形状に復元可能な弾性部材で構成することができる。かかる弾性部材で構成される被覆部28であれば、たとえば断面略真円の円筒形状をなすとともに、断面が長円の円筒部である歯受部26に対し、密着して被覆することが可能である。
 ただし、被覆部28の形状はOリング形状に限定されず、例えば、長尺方向に対し垂直に切断したときの断面形状がC字形状である被覆部28であってもよい。
The covering portion 28 in the present embodiment covers at least a region that is the tooth receiving portion 26 and is in contact with the teeth of the patient holding the mouthpiece body 11. For example, as shown in FIG. 5, the covering portion 28 may have an O-ring shape that covers the entire outer periphery of the tooth receiving portion 26.
The covering portion 28 can be formed of an elastic member that can be easily deformed from a predetermined shape and can be restored to the predetermined shape. If the covering portion 28 is formed of such an elastic member, for example, it can have a cylindrical shape with a substantially circular cross section, and can be in close contact with the tooth receiving portion 26 that is a cylindrical portion with an elliptical cross section. It is.
However, the shape of the covering portion 28 is not limited to the O-ring shape. For example, the covering portion 28 may have a C-shaped cross section when cut perpendicularly to the longitudinal direction.
 被覆部28は、外周面側において、被覆部28の遠位端部において径方向の外側に突出する第二凸部50を有している。第二凸部50は、歯受部26が被覆部28に被覆された状態で、被覆部28に患者が歯を当てたときの歯の停止部として機能し、マウスピース100が口から落下することを防止可能である。 The covering portion 28 has a second convex portion 50 protruding outward in the radial direction at the distal end portion of the covering portion 28 on the outer peripheral surface side. The second convex portion 50 functions as a tooth stopping portion when the patient hits the covering portion 28 with the tooth receiving portion 26 covered with the covering portion 28, and the mouthpiece 100 falls from the mouth. Can be prevented.
 本実施形態における歯受部26と被覆部28とは、互いに係合する関係にあり、これによって被覆部28が歯受部26を被覆したときに、被覆部28が離脱しないよう構成されている。
 即ち、図3に示されるように、歯受部26は、歯受部26の遠位端部において径方向の外側に突出する凸部30を有している。被覆部28は、内周面側において、小径部34および大径部32を有している。加えて、被覆部28は、内周面側において、小径部34および大径部32の段差により形成され径が不連続に変化する段差部37を有している。
 凸部30と段差部37とは係合し、これによって被覆部28が、マウスピース本体11の近位端から遠位端方向へずれることが防止される。本実施形態では、凸部30と段差部37とは当接しており、係合した状態で両者の位置ずれが防止されている。
The tooth receiving portion 26 and the covering portion 28 in the present embodiment are in a relationship of engaging with each other, and are configured so that the covering portion 28 is not detached when the covering portion 28 covers the tooth receiving portion 26. .
That is, as shown in FIG. 3, the tooth receiving portion 26 has a convex portion 30 protruding outward in the radial direction at the distal end portion of the tooth receiving portion 26. The covering portion 28 has a small diameter portion 34 and a large diameter portion 32 on the inner peripheral surface side. In addition, the covering portion 28 has a step portion 37 that is formed by steps of the small-diameter portion 34 and the large-diameter portion 32 on the inner peripheral surface side, and whose diameter changes discontinuously.
The projecting portion 30 and the stepped portion 37 engage with each other, thereby preventing the covering portion 28 from shifting from the proximal end of the mouthpiece body 11 toward the distal end. In this embodiment, the convex part 30 and the level | step-difference part 37 are contact | abutting, and both position shift is prevented in the engaged state.
 被覆部28は近位端側に小径部34が設けられ、遠位端側に大径部32が設けられている。大径部32の領域が小径部34の領域に対し凹部となっており、歯受部26の凸部30が、当該に凹部に嵌合している。
 また図3に示されるとおり、被覆部28の遠位端の端面51と、歯受部26の遠位端(即ち、凸部30の遠位端)の端面52とが略同一平面上にある。
The covering portion 28 is provided with a small diameter portion 34 on the proximal end side and a large diameter portion 32 on the distal end side. The area | region of the large diameter part 32 becomes a recessed part with respect to the area | region of the small diameter part 34, and the convex part 30 of the tooth receiving part 26 is fitted to the concave part.
As shown in FIG. 3, the end surface 51 of the distal end of the covering portion 28 and the end surface 52 of the distal end of the tooth receiving portion 26 (that is, the distal end of the convex portion 30) are substantially in the same plane. .
 上述のとおり、マウスピース100は、マウスピース本体11の遠位端部に設けられた筒状の歯受部26と、歯受部26の外周を被覆する被覆部28と、を有する。加えてマウスピース100は、マウスピース本体11の遠位端部と近位端部との間に設けられた外周面から外方向に延在する鍔部42を有している。
 本実施形態にかかるマウスピース100は、鍔部42の裏面210の基端部からマウスピース本体11の遠位端までの最短距離Aと、被覆部28の長尺方向の長さ(被覆部28の、マウスピース本体11の遠位端と近位端とを結ぶ方向に沿った長さ)とが略同等である。尚、鍔部42の裏面210とは、マウスピース100を近位端側からみたときの鍔部42の裏側の面のことを意味する。
 かかる構成によれば、歯受部26において実質的に患者が歯を当てる部分の概略全体が、被覆部28で覆われる。そのため、患者は、歯受部26のいずれの箇所に歯を当てても同様に被覆部28の弾力性を体感することができる。
 マウスピース本体11の近位端を上側、遠位端を下側としたときに、本実施形態の鍔部42の基端部は、上述する境界部112と略同等の高さ位置に設けられている。
As described above, the mouthpiece 100 includes the cylindrical tooth receiving portion 26 provided at the distal end portion of the mouthpiece main body 11 and the covering portion 28 that covers the outer periphery of the tooth receiving portion 26. In addition, the mouthpiece 100 has a flange 42 extending outward from an outer peripheral surface provided between the distal end portion and the proximal end portion of the mouthpiece body 11.
The mouthpiece 100 according to the present embodiment includes the shortest distance A from the proximal end portion of the back surface 210 of the collar portion 42 to the distal end of the mouthpiece body 11 and the length of the covering portion 28 in the longitudinal direction (covering portion 28. The length along the direction connecting the distal end and the proximal end of the mouthpiece body 11) is substantially the same. In addition, the back surface 210 of the collar part 42 means the surface of the back side of the collar part 42 when the mouthpiece 100 is seen from the proximal end side.
According to such a configuration, substantially the entire portion of the tooth receiving portion 26 where the patient applies teeth is covered with the covering portion 28. Therefore, the patient can experience the elasticity of the covering portion 28 in the same manner regardless of where the tooth is applied to the tooth receiving portion 26.
When the proximal end of the mouthpiece body 11 is set to the upper side and the distal end is set to the lower side, the proximal end portion of the collar portion 42 of the present embodiment is provided at a height position substantially equal to the boundary portion 112 described above. ing.
 図3に示されるとおり、伸縮部16は、環状の内視鏡挿入部17と同心であって、径方向に谷部116、山部114とが設けられてなる環状の蛇腹部120を有している。
 図4から理解されるとおり、蛇腹部120は、縮径部110と拡径部111との境界である境界部112で囲まれる内円112Aと同軸で配置されている。蛇腹部120の外縁120Aの径は、内円112Aの径よりも大きい。
 蛇腹部120の外縁120Aとは、蛇腹部120を構成する山部114または谷部116のうち、中心より最も離れた位置にある山部114または谷部116を指す。本実施形態では、蛇腹部120の外縁120Aは、同心に二重に設けられた山部114のうちの外側の山部114の頂点を結んだ円である。
 本発明における蛇腹部120は、径方向における内視鏡の移動により、伸縮部16に発生するひずみを吸収可能である。蛇腹部120は、伸縮部16の延在方向とは異なる方向に凸の山部または凹の谷部である。山または谷の頂点は、鋭角である場合と鈍角である場合のいずれも含む。
 蛇腹部120は、例えば、伸縮部16に設けられた、少なくとも一つの山部114、または少なくとも一つの谷部116により構成可能である。あるいは、蛇腹部120は、2以上の隣り合う山部114と谷部116とから構成されてもよい。あるいは、蛇腹部120は、山部114と谷部116との間に、図示省略する平坦部を有していてもよい。上記平坦部は、挿通孔12の挿通方向に対し略垂直な方向における面内に含まれる。
As shown in FIG. 3, the telescopic part 16 has an annular bellows part 120 that is concentric with the annular endoscope insertion part 17 and is provided with a trough part 116 and a peak part 114 in the radial direction. ing.
As understood from FIG. 4, the bellows part 120 is arranged coaxially with an inner circle 112 </ b> A surrounded by a boundary part 112 that is a boundary between the reduced diameter part 110 and the enlarged diameter part 111. The diameter of the outer edge 120A of the bellows portion 120 is larger than the diameter of the inner circle 112A.
The outer edge 120 </ b> A of the bellows part 120 refers to a peak part 114 or a valley part 116 that is located farthest from the center among the peak parts 114 or the valley parts 116 constituting the bellows part 120. In the present embodiment, the outer edge 120 </ b> A of the bellows portion 120 is a circle connecting the vertices of the outer peak portions 114 of the peak portions 114 provided concentrically and double.
The bellows portion 120 in the present invention can absorb strain generated in the telescopic portion 16 due to the movement of the endoscope in the radial direction. The bellows portion 120 is a peak portion or a concave valley portion that is convex in a direction different from the extending direction of the stretchable portion 16. The apex of the peak or valley includes both an acute angle and an obtuse angle.
The bellows part 120 can be constituted by, for example, at least one peak part 114 or at least one valley part 116 provided in the stretchable part 16. Alternatively, the bellows part 120 may be composed of two or more adjacent peak parts 114 and valley parts 116. Alternatively, the bellows part 120 may have a flat part (not shown) between the peak part 114 and the valley part 116. The flat portion is included in a plane in a direction substantially perpendicular to the insertion direction of the insertion hole 12.
 本発明は、内視鏡挿入部17の周囲に非蛇腹部を有し、さらに当該非蛇腹部の周囲に蛇腹部を有する態様、および内視鏡挿入部17の周囲に非蛇腹部を有さず内視鏡挿入部17に接して蛇腹部120が配置される態様のいずれも包含する。例えば、図示省略するが、本発明は内視鏡挿入部17の周囲に非蛇腹部である平坦部を有し、当該平坦部の周囲に蛇腹部120を有する態様を包含する。
 本実施形態におけるマウスピース100は、内視鏡挿入部17の周囲に非蛇腹部を有さず内視鏡挿入部17に接して蛇腹部120が配置されている。
The present invention has a non-accordion portion around the endoscope insertion portion 17 and further has a bellows portion around the non-accordion portion, and a non-accordion portion around the endoscope insertion portion 17. Any of the embodiments in which the bellows portion 120 is disposed in contact with the endoscope insertion portion 17 is also included. For example, although not shown in the drawings, the present invention includes a mode in which the endoscope insertion portion 17 has a flat portion that is a non-accordion portion and the bellows portion 120 is provided around the flat portion.
The mouthpiece 100 according to this embodiment does not have a non-accordion portion around the endoscope insertion portion 17, and the bellows portion 120 is disposed in contact with the endoscope insertion portion 17.
 蛇腹部120の外縁120Aの径が、内円112Aの径よりも大きいことにより、内視鏡の操作(特には平行操作)の際、優れた操作性および気密性を提供可能である。具体的には、かかる構成により、内円112Aの内部において内視鏡の移動により、伸縮部16において発生するひずみを良好に蛇腹部120に吸収させることができる。また、内視鏡の周面に対し密着する内視鏡挿入部17が、内視鏡の操作時に当該内視鏡の移動に良好に追従する。そのため、内視鏡と内視鏡挿入部17とが密着した状態を良好に維持され、高い気密性により内視鏡とマウスピース本体11との間が封止される。 Since the diameter of the outer edge 120A of the bellows portion 120 is larger than the diameter of the inner circle 112A, it is possible to provide excellent operability and airtightness when operating the endoscope (particularly parallel operation). Specifically, with this configuration, the bellows portion 120 can satisfactorily absorb the strain generated in the stretchable portion 16 due to the movement of the endoscope inside the inner circle 112A. Further, the endoscope insertion portion 17 that is in close contact with the peripheral surface of the endoscope satisfactorily follows the movement of the endoscope when the endoscope is operated. Therefore, the state where the endoscope and the endoscope insertion portion 17 are in close contact with each other is well maintained, and the gap between the endoscope and the mouthpiece body 11 is sealed with high airtightness.
 特に、蛇腹部120の内縁120Bの径が、内円112Aの径よりも小さいとき、内視鏡の操作(特には平行操作)の際に、優れた操作性および気密性を提供可能であるという効果が顕著である。
 特に、蛇腹部120の内縁120Bの径が、内円112Aの径よりも小さく、かつ、内視鏡挿入部17と内縁120Bとの間に、上述する非蛇腹部を有しない態様、あるいは非蛇腹部を有するがわずかである態様であることが好ましい。
 かかる構成では、内視鏡挿入部17に挿通する内視鏡を操作したとき、内視鏡の移動による上記ひずみが速やかに蛇腹部120において吸収される。そのため、内視鏡挿入部17よりも先に蛇腹部120を変形させることができ、内視鏡挿入部17と内視鏡との気密性を高く維持することができる。
In particular, when the diameter of the inner edge 120B of the bellows portion 120 is smaller than the diameter of the inner circle 112A, it is possible to provide excellent operability and airtightness when operating the endoscope (particularly parallel operation). The effect is remarkable.
In particular, the diameter of the inner edge 120B of the bellows part 120 is smaller than the diameter of the inner circle 112A, and the above-described non-bellows part is not provided between the endoscope insertion part 17 and the inner edge 120B, or the non-bellows It is preferable that it is an aspect which has a part but few.
In such a configuration, when the endoscope inserted through the endoscope insertion portion 17 is operated, the strain due to the movement of the endoscope is quickly absorbed by the bellows portion 120. Therefore, the bellows part 120 can be deformed before the endoscope insertion part 17, and the airtightness between the endoscope insertion part 17 and the endoscope can be maintained high.
 上述するマウスピース本体11および脱気防止弁装置18は、互いに分離した状態で、内視鏡検査用マウスピースキットを構成してもよい。
 あるいは、マウスピース本体11、脱気防止弁装置18および被覆部28は、互いに分離した状態で、内視鏡検査用マウスピースキットを構成してもよい。
 上記内視鏡検査用マウスピースキットは、使用時において組み合わされて本発明のマウスピースを構成する。
The mouthpiece body 11 and the deaeration prevention valve device 18 described above may constitute a mouthpiece kit for endoscopy in a state where they are separated from each other.
Alternatively, the mouthpiece body 11, the anti-aeration valve device 18, and the covering portion 28 may constitute an endoscopic examination mouthpiece kit in a state of being separated from each other.
The above-mentioned mouthpiece kit for endoscopy is combined in use to constitute the mouthpiece of the present invention.
 <第二実施形態>
 次に、本発明の第二実施形態について図8から図10を用いて説明する。図8は、本発明の第二実施形態にかかるマウスピース200の一例を示す斜視図である。図9は、図8に示すマウスピース200の分解斜視図である。図10は、図8に示すマウスピース200のY-Y断面図である。
<Second embodiment>
Next, a second embodiment of the present invention will be described with reference to FIGS. FIG. 8 is a perspective view showing an example of a mouthpiece 200 according to the second embodiment of the present invention. FIG. 9 is an exploded perspective view of the mouthpiece 200 shown in FIG. FIG. 10 is a YY sectional view of the mouthpiece 200 shown in FIG.
 マウスピース200は、図示省略する内視鏡を挿入抜去自在に挿通する挿通孔12を有するマウスピース本体61と、挿通孔12に挿通された内視鏡とマウスピース本体61との間を気密に封止する脱気防止弁装置418と、を有する。
 脱気防止弁装置418は、フレーム部414と、伸縮部16(伸縮手段)および内視鏡挿入部17を有している。
The mouthpiece 200 has a mouthpiece body 61 having an insertion hole 12 through which an endoscope (not shown) can be inserted and removed freely, and the endoscope inserted through the insertion hole 12 and the mouthpiece body 61 are airtight. And a deaeration preventing valve device 418 for sealing.
The deaeration prevention valve device 418 includes a frame part 414, an expansion / contraction part 16 (extension / contraction means), and an endoscope insertion part 17.
 フレーム部414は、フレーム部414をマウスピース本体61の近位端に係脱可能に係止する係止部を備える。上記係止部は、具体的には、フレーム部414の遠位端部の外側面において径方向に凸の嵌合凸部422(係止手段)である。本実施形態において嵌合凸部422は、対向する位置に2か所設けられているが、これに限定されず、嵌合凸部422は1つ、または3つ以上であってもよい。
 マウスピース200は、上記係止部の構成がマウスピース100と異なること以外は、マウスピース100と同様の構成が採用される。そのため、マウスピース200に関し、係止部以外のその他の構成は、説明を省略する。
The frame part 414 includes a locking part that detachably locks the frame part 414 to the proximal end of the mouthpiece body 61. Specifically, the locking portion is a fitting convex portion 422 (locking means) convex in the radial direction on the outer surface of the distal end portion of the frame portion 414. In the present embodiment, two fitting protrusions 422 are provided at opposing positions, but the present invention is not limited to this, and the number of fitting protrusions 422 may be one, or three or more.
The mouthpiece 200 has the same configuration as the mouthpiece 100 except that the configuration of the locking portion is different from that of the mouthpiece 100. Therefore, regarding the mouthpiece 200, description of other configurations other than the locking portion is omitted.
 マウスピース本体61の鍔部42よりも近位端部側には係合受部420が設けられている。係合受部420は、嵌合凸部422と係合可能な嵌合部を有する。尚、嵌合部の説明に関し言及する上下方向は、図9における紙面上下方向である。
 具体的には、係合受部420は、鍔部42の近位端部側の面から起立する筒部421であって、筒部421の側面に、上記嵌合部として嵌合凹部425と嵌合留部426を備えている。
 嵌合凹部425は、筒部421の内壁面において、上端から下端に向けて形成された溝状の凹部である。嵌合凹部425の幅寸法は、嵌合凸部422の幅寸法以上である。嵌合凹部425の上端から、嵌合凸部422を嵌合させて、嵌合凹部425の下端方向に嵌合凸部422をガイドすることにより、マウスピース本体61と脱気防止弁装置418とを係合させることができる。
 当該係合により、フレーム部414の外側面が筒部421の内側面に対向し、係合受部420にフレーム部414が内装された状態となる。
An engagement receiving portion 420 is provided on the proximal end side of the mouthpiece main body 61 with respect to the collar portion 42. The engagement receiving part 420 has a fitting part that can be engaged with the fitting convex part 422. In addition, the up-down direction mentioned regarding description of a fitting part is a paper surface up-down direction in FIG.
Specifically, the engagement receiving part 420 is a cylinder part 421 that stands up from the surface on the proximal end part side of the flange part 42, and has a fitting recess 425 as a fitting part on the side surface of the cylinder part 421. A fitting retaining portion 426 is provided.
The fitting recess 425 is a groove-like recess formed from the upper end to the lower end on the inner wall surface of the cylindrical portion 421. The width dimension of the fitting recess 425 is equal to or greater than the width dimension of the fitting protrusion 422. By fitting the fitting convex portion 422 from the upper end of the fitting concave portion 425 and guiding the fitting convex portion 422 in the lower end direction of the fitting concave portion 425, the mouthpiece body 61 and the deaeration prevention valve device 418 Can be engaged.
As a result of the engagement, the outer surface of the frame portion 414 faces the inner surface of the cylindrical portion 421, and the frame portion 414 is built in the engagement receiving portion 420.
 嵌合留部426は、嵌合凹部425に連続し、嵌合凹部425を構成する溝の伸長方向とは異なる方向に伸長する凹部である。
 嵌合留部426は、嵌合凹部425の下端と連続しており、嵌合凹部425の伸長方向とは略垂直な方向に伸長する。嵌合凹部425の下端まで嵌合凸部422が嵌合した状態で、フレーム部414とマウスピース本体61とを紙面左右方向に捻ることにより、嵌合凸部422を嵌合留部426に嵌合させることができる。これによって、嵌合凸部422が、上方に抜けづらくなり、脱気防止弁装置418とマウスピース本体61とが係脱可能に安定的に固定される。
The fitting retaining portion 426 is a concave portion that is continuous with the fitting concave portion 425 and extends in a direction different from the extending direction of the grooves constituting the fitting concave portion 425.
The fitting retaining portion 426 is continuous with the lower end of the fitting recess 425 and extends in a direction substantially perpendicular to the extending direction of the fitting recess 425. In a state where the fitting convex portion 422 is fitted to the lower end of the fitting concave portion 425, the fitting convex portion 422 is fitted to the fitting retaining portion 426 by twisting the frame portion 414 and the mouthpiece body 61 in the left-right direction on the paper surface. Can be combined. As a result, the fitting convex portion 422 is difficult to come out upward, and the deaeration prevention valve device 418 and the mouthpiece body 61 are stably fixed so as to be detachable.
 上述するマウスピース100およびマウスピース200における係止部の説明は、本発明の係止部の例を示すものであって、本発明を何ら限定するものではない。 The description of the locking part in the mouthpiece 100 and the mouthpiece 200 described above shows an example of the locking part of the present invention, and does not limit the present invention.
<第三実施形態>
 次に本発明の第三実施形態について図11および図12を用いて説明する。
 本実施形態に係る内視鏡検査用マウスピース300(以下、単にマウスピース300ともいう)は、以下に説明する点で、上記の第一実施形態にかかる内視鏡検査用マウスピース100と相違し、その他の点では内視鏡検査用マウスピース100と同様に構成することができるため、適宜説明を省略する。
 図11は、本発明の第三実施形態にかかるマウスピース300の分解斜視図である。図12は、図11に示すマウスピース300のZ-Z断面図である。
<Third embodiment>
Next, a third embodiment of the present invention will be described with reference to FIGS.
The mouthpiece 300 for endoscopy according to the present embodiment (hereinafter also simply referred to as mouthpiece 300) is different from the mouthpiece 100 for endoscopy according to the first embodiment in the points described below. In other respects, the configuration can be the same as that of the mouthpiece 100 for endoscopy, and the description thereof will be omitted as appropriate.
FIG. 11 is an exploded perspective view of the mouthpiece 300 according to the third embodiment of the present invention. 12 is a ZZ cross-sectional view of the mouthpiece 300 shown in FIG.
 マウスピース300は、脱気防止弁装置18およびマウスピース本体11はマウスピース100と同様のものが用いられ、被覆部29がマウスピース100に設けられた被覆部28と異なっている。
 本実施形態における被覆部29は、外径が長軸310と短軸320とを有する円筒形である。
 本実施形態における第二凸部50は、長軸310上に第一長さ311で延在する第一延在部312と、短軸上に第二長さ321で延在する第二延在部322と、を有している。
 被覆部29は、第一長さ311が、第二長さ321よりも大きくなるよう構成されている。
The mouthpiece 300 is the same as the mouthpiece 100 for the deaeration prevention valve device 18 and the mouthpiece body 11, and the covering portion 29 is different from the covering portion 28 provided on the mouthpiece 100.
The covering portion 29 in this embodiment has a cylindrical shape having an outer diameter having a major axis 310 and a minor axis 320.
In the present embodiment, the second protrusion 50 includes a first extension 312 extending on the major axis 310 with a first length 311 and a second extension extending on a minor axis with a second length 321. Part 322.
The covering portion 29 is configured such that the first length 311 is larger than the second length 321.
 被覆部29は、横断面における外形が、少なくとも一方に長い形状をなす。上記横断面の形状は、楕円および長円を含む。長軸310を口角方向に合わせ、第二凸部50よりも近位側をまで口腔内に含んだ状態で、マウスピース300を咥えることにより、第一延在部312が頬と歯との間に位置し、口角からの息漏れが防止される。
 また第二延在部322は、第一延在部312よりも短いため、唇と歯との間に収まり易い。
The covering part 29 has a long outer shape in at least one of the cross sections. The shape of the cross section includes an ellipse and an ellipse. By aligning the long axis 310 in the mouth angle direction and holding the mouthpiece 300 in a state where the proximal side of the second convex portion 50 is included in the oral cavity, the first extension portion 312 is placed between the cheek and teeth. Located between them, breath leakage from the corner of the mouth is prevented.
Moreover, since the 2nd extension part 322 is shorter than the 1st extension part 312, it is easy to fit between lips and teeth.
 患者がマウスピース300を咥えやすいという観点からは、第二凸部50は、被覆部29の遠位端部に設けられることが好ましく、本実施形態のごとく遠位端に設けられることがより好ましい。 From the viewpoint that the patient can easily hold the mouthpiece 300, the second convex portion 50 is preferably provided at the distal end portion of the covering portion 29, and more preferably provided at the distal end as in this embodiment. preferable.
 本実施形態における被覆部29においては、図11に示すとおり第一延在部312と第二延在部322とが、外周方向において連続している。上面視上、第一延在部312は長軸310の延長線を含み、第二延在部322は、短軸320の延長線を含んでいる。ただしこれに限定されず、図示省略するが、歯受部26の周方向において、第一延在部312と第二延在部322とが不連続に設けられていてもよい。第二延在部322は患者の歯の裏に当接可能であり、マウスピース300が口腔内から脱落することを防止する。ただし本実施形態は、第二凸部50から外方向に延在する延在部を、実質的に第一延在部312だけとし、第二延在部322を省略してもよい。第二凸部50において、第一延在部312が、頬裏に当接することによって、マウスピース300が口腔内から脱落することを防止することが可能である。 In the covering portion 29 in the present embodiment, as shown in FIG. 11, the first extending portion 312 and the second extending portion 322 are continuous in the outer peripheral direction. From the top view, the first extension 312 includes an extension of the major axis 310, and the second extension 322 includes an extension of the minor axis 320. However, the present invention is not limited to this, and although not illustrated, the first extending portion 312 and the second extending portion 322 may be provided discontinuously in the circumferential direction of the tooth receiving portion 26. The second extension 322 can contact the back of the patient's teeth and prevents the mouthpiece 300 from falling out of the oral cavity. However, in the present embodiment, the extension portion extending outward from the second protrusion 50 may be substantially only the first extension portion 312 and the second extension portion 322 may be omitted. In the 2nd convex part 50, when the 1st extension part 312 contact | abuts to a cheek back, it is possible to prevent that the mouthpiece 300 falls out from the inside of the oral cavity.
 第一長さ311は、歯受部26の外周面から長軸310の延長線に沿って計測された第二凸部50の延在方向における寸法である。第二長さ321は、歯受部26の外周面から短軸320の延長線に沿って計測された第二凸部50の延在方向における寸法である。 The first length 311 is a dimension in the extending direction of the second convex portion 50 measured along the extension line of the long axis 310 from the outer peripheral surface of the tooth receiving portion 26. The second length 321 is a dimension in the extending direction of the second convex portion 50 measured along the extension line of the short axis 320 from the outer peripheral surface of the tooth receiving portion 26.
 第一長さ311と第二長さ321との比率は特に限定されないが、たとえば、第一長さ311は、第二長さ321の2倍以上とすることが好ましい。
 かかる比率によれば、第一延在部312の長さ(第一長さ311)を、息漏れ防止効果が発揮される程度に充分に長く設けるとともに、唇の裏に配置される第二延在部322の長さ(第二長さ321)を、適度に短くすることが可能である。これにより、第一延在部312および第二延在部322を備える第二凸部50は、口腔内への挿入性が良好で、かつ、口腔内におけるバランスが図られ、患者への違和感を低減させ得る。
 より具体的には、たとえば成人に使用されるマウスピース300において、第一長さ311を5mm以上10mm以下の範囲とし、第二長さ321を2mm以上5mm以下の範囲とすることが好適である。
 またこのとき被覆部29の外径は、たとえば、長軸310方向における長径を30mm以上40mm以下の範囲、短軸320方向における短径を25mm以上35mm以下の範囲とすることができる。
 被覆部29の上記短径に対する上記長径の比率よりも、第二長さ321に対する第一長さ311の比率の方を大きくすることにより、患者がマウスピース300を咥えやすく、かつ、息漏れを防止する効果が高い。
The ratio between the first length 311 and the second length 321 is not particularly limited. For example, the first length 311 is preferably set to be twice or more the second length 321.
According to such a ratio, the length of the first extension portion 312 (first length 311) is provided long enough to exert the effect of preventing breath leakage, and the second extension arranged on the back of the lips. The length of the existing portion 322 (second length 321) can be appropriately shortened. Thereby, the 2nd convex part 50 provided with the 1st extension part 312 and the 2nd extension part 322 has good insertion property in an oral cavity, and the balance in an intraoral area is aimed at, and the discomfort to a patient is felt. Can be reduced.
More specifically, for example, in the mouthpiece 300 used for adults, it is preferable that the first length 311 is in the range of 5 mm to 10 mm and the second length 321 is in the range of 2 mm to 5 mm. .
At this time, the outer diameter of the covering portion 29 can be, for example, a major axis in the major axis 310 direction in the range of 30 mm to 40 mm and a minor axis in the minor axis 320 direction in the range of 25 mm to 35 mm.
By making the ratio of the first length 311 to the second length 321 larger than the ratio of the major axis to the minor axis of the covering portion 29, the patient can easily hold the mouthpiece 300 and breathe out. The effect of preventing is high.
 マウスピース300は、鍔部42の長軸方向と、第一延在部312の延在方向とが直交している。そのため、患者がマウスピース300を咥えた状態で、鍔部42が患者の唇と当接することで口腔内にマウスピース300が入り込むことが防止され、第一延在部312が頬裏に当接することでマウスピース300が口腔外に脱落することが防止される。
 また図11に示すとおり、第二凸部50には、第一延在部312と直交する第二延在部322が設けられている。第二延在部322が上下の歯裏に当接するとともに、第一延在部312が頬裏に当接することによって、マウスピース300が口腔外に脱落することが良好に防止されている。
In the mouthpiece 300, the long axis direction of the collar portion 42 and the extending direction of the first extending portion 312 are orthogonal to each other. Therefore, when the patient holds the mouthpiece 300, the buttocks 42 abut against the patient's lips to prevent the mouthpiece 300 from entering the oral cavity, and the first extension 312 abuts the cheek back. This prevents the mouthpiece 300 from falling out of the oral cavity.
As shown in FIG. 11, the second projecting portion 50 is provided with a second extending portion 322 orthogonal to the first extending portion 312. The mouthpiece 300 is well prevented from falling out of the oral cavity by the second extending portion 322 abutting on the upper and lower teeth and the first extending portion 312 contacting the cheek back.
 図11および図12に示すとおり、本実施形態における第一延在部312は、外縁に向かって肉薄に形成されている。
 換言すると、第一延在部312の近位側面には、第二凸部50の外縁に向かって先細りに傾斜している。
 このように、第一延在部312が肉薄に形成されることによって、第一延在部312に柔軟性が付与され、マウスピース300を咥えたときの口腔内における違和感を減少させることができる。
 かかる趣旨からは、上記傾斜は、第一延在部312の遠位側面に設けられてもよい。ただし、頬裏に当たり得る第一延在部312の近位側面を外縁に向かって傾斜させることにより、頬裏への当たり方をより柔らかくし得るため好ましい。
As shown in FIGS. 11 and 12, the first extending portion 312 in the present embodiment is formed thin toward the outer edge.
In other words, the proximal side surface of the first extending portion 312 is inclined so as to taper toward the outer edge of the second convex portion 50.
Thus, by forming the first extension portion 312 to be thin, flexibility is imparted to the first extension portion 312, and it is possible to reduce a sense of discomfort in the oral cavity when the mouthpiece 300 is held. .
From this point of view, the inclination may be provided on the distal side surface of the first extension portion 312. However, it is preferable that the proximal side surface of the first extending portion 312 that can hit the cheek back is inclined toward the outer edge, so that the way of hitting the cheek back can be made softer.
 第一延在部312に柔軟性を付与するという観点から、図13に本実施形態の変形例を示す。図13は、マウスピース本体11に本発明の第三実施例の変形例に用いられる被覆部29Aを取り付けた状態を背面側から見た斜視図である。 From the viewpoint of imparting flexibility to the first extension portion 312, FIG. 13 shows a modification of the present embodiment. FIG. 13 is a perspective view of the mouthpiece body 11 as viewed from the back side with the covering portion 29A used in a modification of the third embodiment of the present invention.
 図13に示すとおり、被覆部29Aは、第一延在部312の遠位側面において、マウスピース本体11に設けられた挿通孔12に連通させ、かつ外周313を残して肉抜きされている。肉抜きされた領域は、周囲の領域よりも肉薄になっており、結果として第一延在部312の柔軟性を高めている。係る観点からは、図示省略するが、第一延在部312の近位側面において上記肉抜きがなされていてもよい。 As shown in FIG. 13, the covering portion 29 </ b> A is communicated with the insertion hole 12 provided in the mouthpiece main body 11 on the distal side surface of the first extending portion 312, and is thinned leaving the outer periphery 313. The thinned region is thinner than the surrounding region, and as a result, the flexibility of the first extension portion 312 is enhanced. From such a viewpoint, although not shown in the drawings, the above-described thinning may be performed on the proximal side surface of the first extension portion 312.
 ここで肉抜きとは、厚さ方向に周囲より厚みの小さい部分を設けることをいい、第一延在部312の遠位側面が肉抜きされることによって凹部314が形成されている。凹部314は、挿通孔12に連通するとともに、外周313の内側面において終端している。
 遠位側を上方向としたとき、肉抜きされた領域(凹部314)の外周の高さは、挿通孔12の遠位側の開口よりも高い位置にあり、当該肉抜きされた領域は、当該開口に連通している。
Here, the term “thinning” refers to providing a portion having a smaller thickness than the surroundings in the thickness direction, and the concave portion 314 is formed by thinning the distal side surface of the first extending portion 312. The recess 314 communicates with the insertion hole 12 and terminates on the inner surface of the outer periphery 313.
When the distal side is the upward direction, the height of the outer periphery of the thinned region (concave portion 314) is higher than the distal opening of the insertion hole 12, and the thinned region is It communicates with the opening.
 頬裏に対する第一延在部312の当たりを柔軟にし、口腔内において感じる違和感を低減させるという観点からは、図11および図12に示すとおり、第一延在部312の近位側面の外縁315を面取りすることが好ましい。
 上記面取りには、所謂、C面取りおよびR面取りのいずれも含む。
From the viewpoint of softening the contact of the first extension part 312 against the back of the cheek and reducing the uncomfortable feeling in the oral cavity, as shown in FIGS. 11 and 12, the outer edge 315 of the proximal side surface of the first extension part 312. It is preferable to chamfer.
The chamfering includes both so-called C chamfering and R chamfering.
 次に、被覆部29と歯受部26との関係について説明する。
 図11に示すとおり、歯受部26の内径は、被覆部29の外径と同方向に長軸と短軸とを有している。被覆部29の断面内形は、たとえば長円または楕円であり、歯受部26の外形形状と略等しい形状に構成されている。そのため、歯受部26に対する被覆部29の装着方向が、容易に理解可能である。
 本実施形態において、被覆部29の内径における長軸および短軸のそれぞれは、歯受部26の外径における長軸および短軸よりも僅かに大きく形成されている。
Next, the relationship between the covering portion 29 and the tooth receiving portion 26 will be described.
As shown in FIG. 11, the inner diameter of the tooth receiving portion 26 has a major axis and a minor axis in the same direction as the outer diameter of the covering portion 29. The inner shape of the cross section of the covering portion 29 is, for example, an ellipse or an ellipse, and is configured in a shape substantially equal to the outer shape of the tooth receiving portion 26. Therefore, the mounting direction of the covering portion 29 with respect to the tooth receiving portion 26 can be easily understood.
In the present embodiment, each of the major axis and the minor axis at the inner diameter of the covering portion 29 is formed slightly larger than the major axis and the minor axis at the outer diameter of the tooth receiving portion 26.
 本実施形態における被覆部29は、内周面に、歯受部26の外周面に当接する周方向に周回状に連続した凸状の当接部316を備える。
 当接部316が設けられたことにより、歯受部26の外周面と、被覆部29の内周面との間が当接部316において封止されるため、マウスピース300の気密性が高まる。
 また、当接部316を設けずに歯受部26の外周面と被覆部29の内周面とを直接に接触させた場合に比べ、本実施形態は、両者の接触面積を著しく小さくすることができる。そのため、歯受部26に対し被覆部29を取り付けた際、取り付け位置がずれたときには、被覆部29を周方向に回転させて、取り付け位置の調整を行いやすい。
The covering portion 29 according to the present embodiment includes a convex contact portion 316 that is continuous in a circumferential direction in contact with the outer peripheral surface of the tooth receiving portion 26 on the inner peripheral surface.
By providing the contact portion 316, the space between the outer peripheral surface of the tooth receiving portion 26 and the inner peripheral surface of the covering portion 29 is sealed by the contact portion 316, so that the airtightness of the mouthpiece 300 is increased. .
Moreover, compared with the case where the outer peripheral surface of the tooth receiving portion 26 and the inner peripheral surface of the covering portion 29 are brought into direct contact without providing the contact portion 316, this embodiment significantly reduces the contact area between the two. Can do. For this reason, when the covering portion 29 is attached to the tooth receiving portion 26, when the attachment position is shifted, the covering portion 29 is rotated in the circumferential direction, and the attachment position can be easily adjusted.
 本実施形態における当接部316は、径方向の内側に突出し、その突出先端が半球状である周方向に周回する一本の帯状体である。ただし当接部316はこれに限定されず、周方向に周回する二本以上の当接部316が設けられていてもよいし、また突出先端が半球状以外の形状(たとえば平面状)などであってもよい。図12では、突出先端が半球状である当接部316が歯受部26の外周面と当接し、先端が平坦状になっている状態を示している。
 また図示する当接部316は、被覆部29の中心軸に直行する平面内で周方向に周回しているが、これに限定されない。
The contact portion 316 in the present embodiment is a single band-shaped body that protrudes inward in the radial direction and that circulates in the circumferential direction in which the protruding tip is hemispherical. However, the contact portion 316 is not limited to this, and two or more contact portions 316 that circulate in the circumferential direction may be provided, and the protruding tip has a shape other than a hemisphere (for example, a planar shape). There may be. FIG. 12 shows a state where the abutting portion 316 having a hemispherical protruding tip abuts on the outer peripheral surface of the tooth receiving portion 26 and the tip is flat.
Further, the abutting portion 316 shown in the drawing circulates in the circumferential direction in a plane orthogonal to the central axis of the covering portion 29, but is not limited thereto.
 上述する当接部316を備えるマウスピース300は、歯受部26と、当接部316との間の気密性が3kPa以上とすることができる。
 かかる気密性を発揮するマウスピース300は、バルサルバ法などの口腔内の気圧を高める検査や治療を実施するに好適である。
In the mouthpiece 300 including the contact portion 316 described above, the airtightness between the tooth receiving portion 26 and the contact portion 316 can be 3 kPa or more.
The mouthpiece 300 that exhibits such airtightness is suitable for performing tests and treatments that increase the pressure in the oral cavity, such as the Valsalva method.
 歯受部26と、当接部316との間の気密性が3kPaとは、歯受部26の外周面と当接部316の先端とを密着させ、当接部316の遠位側と近位側との間に3kPaの気圧差を付加したときに、歯受部26と、当接部316との間を気体が漏れないことをいう。
 一例として、内視鏡挿入部17に内視鏡を密着させて挿入し歯受部26の軸方向の中間からマウスピース300の遠位側を覆うよう密封して挿通孔12の内部に気体を給気し内部圧力を3kPaとする。このとき、歯受部26と、当接部316との間から気体が漏れないことにより歯受部26と、当接部316との間の気密性が3kPaであることを確認することができる。
The airtightness between the tooth receiving portion 26 and the contact portion 316 is 3 kPa, which means that the outer peripheral surface of the tooth receiving portion 26 and the tip of the contact portion 316 are brought into close contact with each other and closer to the distal side of the contact portion 316. It means that gas does not leak between the tooth receiving portion 26 and the abutting portion 316 when a pressure difference of 3 kPa is applied to the rear side.
As an example, the endoscope is inserted in close contact with the endoscope insertion portion 17, sealed so as to cover the distal side of the mouthpiece 300 from the middle in the axial direction of the tooth receiving portion 26, and gas is inserted into the insertion hole 12. Air is supplied and the internal pressure is set to 3 kPa. At this time, it is possible to confirm that the airtightness between the tooth receiving portion 26 and the contact portion 316 is 3 kPa by preventing gas from leaking between the tooth receiving portion 26 and the contact portion 316. .
 以上、当接部316を有する本実施形態について説明したが、本発明は、当接部316を省略し、歯受部26の外周面と被覆部29の内周面とを直接に当接させる態様を包含する。この場合には、被覆部29の内径における長軸および短軸それぞれと、歯受部26の外径における長軸および短軸とを略同一とし、歯受部26の外周面と被覆部29の内周面との間において軸方向に連通する隙間がないよう構成することが好ましい。 Although the present embodiment having the contact portion 316 has been described above, the present invention omits the contact portion 316 and directly contacts the outer peripheral surface of the tooth receiving portion 26 and the inner peripheral surface of the covering portion 29. Includes embodiments. In this case, the major axis and the minor axis of the inner diameter of the covering portion 29 are substantially the same as the major axis and the minor axis of the outer diameter of the tooth receiving portion 26, and the outer peripheral surface of the tooth receiving portion 26 and the covering portion 29. It is preferable that there is no gap communicating with the inner peripheral surface in the axial direction.
 本実施形態は、図13に示すとおり、マウスピース本体11に対し、意図した位置に被覆部29Aを容易に装着するために、第一位置決め部323および第二位置決め部324を設けてもよい。
 即ち、図13に示すとおり、歯受部26(図11参照)は、歯受部26の遠位端部において径方向の外側に突出する凸部30を有するとともに、被覆部29Aは、外周面側において、被覆部29Aの遠位端部において径方向の外側に突出する第二凸部50を有している。凸部30の遠位端面に設けられた第一位置決め部323と、第二凸部50の遠位端面に設けられ第一位置決め部323に対向する第二位置決め部324と、が設けられている。第一位置決め部323と第二位置決め部324とを対向させるよう、マウスピース本体11に対し、被覆部29Aを装着することによりマウスピース本体11に対する被覆部29Aの位置決めが容易かつ確実である。
 第一位置決め部323と第二位置決め部324は少なくとも一組設けられる。図13では、凸部30と第二凸部50とが互いに最接近する2か所のそれぞれにおいて、第一位置決め部323と、これに対向する第二位置決め部324とが設けられている。
 第一位置決め部323および第二位置決め部324は、歯受部に設けられる上記凸部と、被覆部に設けられる上記第二凸部とを有する本発明のマウスピースの種々の態様において、適宜実施することができる。
In the present embodiment, as shown in FIG. 13, a first positioning portion 323 and a second positioning portion 324 may be provided on the mouthpiece body 11 in order to easily attach the covering portion 29 </ b> A at an intended position.
That is, as shown in FIG. 13, the tooth receiving portion 26 (see FIG. 11) has a convex portion 30 protruding radially outward at the distal end portion of the tooth receiving portion 26, and the covering portion 29 </ b> A has an outer peripheral surface. On the side, it has the 2nd convex part 50 which protrudes in the radial direction outer side in the distal end part of 29 A of coating | coated parts. A first positioning portion 323 provided on the distal end surface of the convex portion 30 and a second positioning portion 324 provided on the distal end surface of the second convex portion 50 and facing the first positioning portion 323 are provided. . By attaching the covering portion 29A to the mouthpiece body 11 so that the first positioning portion 323 and the second positioning portion 324 are opposed to each other, the positioning of the covering portion 29A with respect to the mouthpiece body 11 is easy and reliable.
At least one set of the first positioning part 323 and the second positioning part 324 is provided. In FIG. 13, a first positioning portion 323 and a second positioning portion 324 facing the first positioning portion 323 are provided at each of two locations where the convex portion 30 and the second convex portion 50 are closest to each other.
The first positioning portion 323 and the second positioning portion 324 are appropriately implemented in various aspects of the mouthpiece of the present invention having the convex portion provided in the tooth receiving portion and the second convex portion provided in the covering portion. can do.
<第四実施形態>
 第四実施形態に係る内視鏡検査用マウスピースは、以下に説明する点で、上記の第一実施形態にかかる内視鏡検査用マウスピース100と相違し、その他の点では内視鏡検査用マウスピース100と同様に構成することができるため、適宜説明を省略する。
 第一実施形態からの変更点を説明するために、第四実施形態に用いられるマウスピース本体11および被覆部35の斜視図を図14に示す。
<Fourth embodiment>
The mouthpiece for endoscopy according to the fourth embodiment is different from the mouthpiece for endoscopy 100 according to the first embodiment in the points described below, and in other respects the endoscopy Since it can be configured in the same manner as the mouthpiece 100 for a product, description thereof will be omitted as appropriate.
In order to explain the changes from the first embodiment, a perspective view of the mouthpiece body 11 and the covering portion 35 used in the fourth embodiment is shown in FIG.
 第四実施形態における内視鏡検査用マウスピースは、歯受部26の外周を被覆する被覆部35を有している。被覆部35の近位端面351と、鍔部42の遠位側面352とが、互いに対応する形状となるよう構成されている。 The mouthpiece for endoscopy in the fourth embodiment has a covering portion 35 that covers the outer periphery of the tooth receiving portion 26. The proximal end surface 351 of the covering portion 35 and the distal side surface 352 of the collar portion 42 are configured to have shapes corresponding to each other.
 より具体的には、第四実施形態における内視鏡検査用マウスピースは、鍔部42の遠位側面352(鍔部42の裏面)と被覆部35の近位端面351とが互いに嵌合し非周回に設けられた凹凸部353を有している。
 図14には、近位端面351が凸状であり、これに対応する形状である遠位側面352が凹状の形状であり、これらが互いに嵌合して凹凸部353が形成されている。もちろん、図示省略する近位端面351が凹状であり、これに対応する形状である遠位側面352が凸状の形状であってもよい。
More specifically, in the mouthpiece for endoscopy in the fourth embodiment, the distal side surface 352 of the collar portion 42 (the back surface of the collar portion 42) and the proximal end surface 351 of the covering portion 35 are fitted to each other. It has a concavo-convex portion 353 provided non-circularly.
In FIG. 14, the proximal end surface 351 is convex, and the distal side surface 352 corresponding to the proximal end surface 351 is concave, and these are fitted to each other to form an uneven portion 353. Of course, the proximal end surface 351 (not shown) may be concave, and the distal side surface 352 corresponding to this may be convex.
 凹凸部353は、少なくとも1カ所、好ましくは2か所以上、設けられる。本実施形態では、略180°対向して、同様の凹凸部353が設けられている(図示省略)。
 凹凸部353が非周回であることにより、互いに対応する形状の近位端面351と遠位側面352とが正しい方向で嵌合した場合には、被覆部35は、周方向に回転し難い。そのため、歯受部26に対し被覆部35を適切に位置合わせすることができる。
The uneven portion 353 is provided at least at one place, preferably at two or more places. In the present embodiment, a similar concavo-convex portion 353 is provided so as to face approximately 180 ° (not shown).
Since the uneven portion 353 is non-circular, the covering portion 35 is difficult to rotate in the circumferential direction when the proximal end surface 351 and the distal side surface 352 having shapes corresponding to each other are fitted in the correct direction. Therefore, the covering portion 35 can be properly aligned with the tooth receiving portion 26.
<第五実施形態>
 以下、内視鏡用マウスピースに用いられる本発明の脱気防止弁装置を添付図面に示す好適実施例に基づいて詳細に説明する。
<Fifth embodiment>
Hereinafter, the deaeration prevention valve device of the present invention used for an endoscope mouthpiece will be described in detail based on preferred embodiments shown in the accompanying drawings.
 以下、本発明の脱気防止弁装置の実施形態について、図面を参照して説明する。 Hereinafter, embodiments of the deaeration prevention valve device of the present invention will be described with reference to the drawings.
 図15の上図は、本発明の第五実施形態に係る脱気防止弁装置を内視鏡用マウスピースに装着した斜視図である。図15の下図は、本発明の第五実施形態に係る脱気防止弁装置と内視鏡用マウスピースの装着前の斜視図である。図16は、本発明の第五実施形態に係る脱気防止弁装置を内視鏡用マウスピースに装着した断面図である。図17は、本発明の第五実施形態に係る脱気防止弁装置の正面図である。図18は、本発明の第五実施形態に係る脱気防止弁装置の平面図である。図19は、図18のB-B断面図である。図20は、本発明の第五実施形態に係る脱気防止弁装置の背面図である。 15 is a perspective view in which the deaeration prevention valve device according to the fifth embodiment of the present invention is mounted on an endoscope mouthpiece. The lower view of FIG. 15 is a perspective view before the deaeration prevention valve device and the endoscope mouthpiece according to the fifth embodiment of the present invention are mounted. FIG. 16 is a cross-sectional view in which the deaeration prevention valve device according to the fifth embodiment of the present invention is attached to an endoscope mouthpiece. FIG. 17 is a front view of a deaeration prevention valve device according to a fifth embodiment of the present invention. FIG. 18 is a plan view of a deaeration prevention valve device according to the fifth embodiment of the present invention. 19 is a cross-sectional view taken along the line BB in FIG. FIG. 20 is a rear view of the deaeration prevention valve device according to the fifth embodiment of the present invention.
 本実施形態の脱気防止弁装置501は、内視鏡(図示せず)を挿入抜去自在に挿通する挿通孔562を有し口腔内に挿入されるマウスピース504(マウスピース本体)の基端部543に対して着脱自在に装着される。
 マウスピース504の基端部543に装着されるフレーム部503と、フレーム部503に設けられて基端部543に係脱可能に係止する係止部502と、フレーム部503の内側に設けられた弁体部505と、を有している。
 そして、本実施形態の弁体部505は、弁体部505の略中央部に設けられて内視鏡に周着する環状の内視鏡挿入部506と、内視鏡挿入部506に周設された可撓性の伸縮手段508と、を有している。
The deaeration prevention valve device 501 of the present embodiment has an insertion hole 562 through which an endoscope (not shown) can be inserted and removed freely, and a proximal end of a mouthpiece 504 (mouthpiece body) that is inserted into the oral cavity. The unit 543 is detachably attached.
A frame portion 503 attached to the base end portion 543 of the mouthpiece 504, a locking portion 502 provided on the frame portion 503 and removably locked to the base end portion 543, and provided inside the frame portion 503. And a valve body portion 505.
The valve body portion 505 of the present embodiment is provided at an approximately central portion of the valve body portion 505 and is provided around the endoscope insertion portion 506 and an annular endoscope insertion portion 506 that is attached to the endoscope. Flexible expansion / contraction means 508.
 以下、本実施形態の脱気防止弁装置501について、より詳細に説明する。
 図15、図16に示すように、本実施形態の脱気防止弁装置501は、口腔内に挿入されるマウスピース504に装着されるもので、より詳しくは、マウスピース504の体外部544の基端側に設けられた基端部543に装着されている。
 そして、脱気防止弁装置501の係止部502は、フレーム部503の内側に向かって突き出した係止手段521によってマウスピース504の基端部543に係脱可能に係止する。
Hereinafter, the deaeration prevention valve device 501 of the present embodiment will be described in more detail.
As shown in FIGS. 15 and 16, the deaeration prevention valve device 501 of this embodiment is attached to a mouthpiece 504 to be inserted into the oral cavity, and more specifically, an external body 544 of the mouthpiece 504. It is attached to a base end portion 543 provided on the base end side.
And the latching | locking part 502 of the deaeration prevention valve apparatus 501 latches to the base end part 543 of the mouthpiece 504 so that engagement / disengagement is possible by the latching means 521 which protruded toward the inner side of the flame | frame part 503.
 マウスピース504は、体外部544、鍔部545と口腔内部546からなり、口腔内部546の外表面には弾性材料からなるカバー549が着脱自在に被覆されている。
 鍔部545は口唇表面に当接して、マウスピースの過挿入を防止する役割を果たし、鍔部545を境に、近位端側を体外部544、遠位端側を口腔内部546となっている。
 口腔内部546は、口腔内に挿入され、マウスピース504を介して内視鏡が挿入抜去可能な内腔542を有し、内視鏡挿入側の第一開口部547と口腔内側出口の第二開口部548を有している。
 体外部544は、内視鏡が挿入抜去可能な内腔542を有すれば良く、体外部544の基端部543の形状は種々を採りうるが、内視鏡の挿通性の観点から、典型的には円形の漏斗状をなしている。
 すなわち、図16に示すように、本実施形態の脱気防止弁装置501が装着されるマウスピース504の体外部544は、径が基端側に徐々に拡大するテーパー状の拡径部541を介して、基端側に基端部543が設けられている。
 なお、本実施形態においてマウスピース504の基端部543は所定の長さをもつ近位端側の領域であり、基端部543はテーパー状の拡径部541を含んでいる。
The mouthpiece 504 includes a body exterior 544, a buttocks 545, and an oral cavity interior 546, and an outer surface of the oral cavity interior 546 is detachably covered with a cover 549 made of an elastic material.
The buttocks 545 are in contact with the lip surface and serve to prevent excessive insertion of the mouthpiece. With the buttocks 545 as a boundary, the proximal end side is the body exterior 544 and the distal end side is the mouth interior 546. Yes.
The oral cavity interior 546 has a lumen 542 that is inserted into the oral cavity and through which the endoscope can be inserted and removed via the mouthpiece 504, and includes a first opening 547 on the endoscope insertion side and a second mouth inner outlet. An opening 548 is provided.
The external body 544 only needs to have a lumen 542 into which the endoscope can be inserted and removed, and the base end portion 543 of the external body 544 can take various shapes, but from the viewpoint of the insertion property of the endoscope, it is typical. It has a circular funnel shape.
That is, as shown in FIG. 16, the external body 544 of the mouthpiece 504 to which the deaeration prevention valve device 501 of this embodiment is attached has a tapered diameter-enlarged portion 541 whose diameter gradually increases toward the base end side. Accordingly, a base end portion 543 is provided on the base end side.
In this embodiment, the base end portion 543 of the mouthpiece 504 is a proximal end side region having a predetermined length, and the base end portion 543 includes a tapered diameter-enlarged portion 541.
 ただし、脱気防止弁装置501が装着されるマウスピース504は上記に限られるものではない。たとえば、径が基端側に徐々に拡大する拡径部541でなくとも、単なる円筒部であっても良い。 However, the mouthpiece 504 to which the deaeration prevention valve device 501 is attached is not limited to the above. For example, instead of the enlarged diameter portion 541 whose diameter gradually increases toward the proximal end side, it may be a simple cylindrical portion.
 図15から図17に示すように、脱気防止弁装置501のフレーム部503は、基端部543に装着される枠体である。
 フレーム部503は、マウスピース504の基端部543の形状に応じて種々の形状をとることができるが、本実施形態では略円筒状をなしている。また、フレーム部503には、内向きフランジ状の固定部531が所定幅で一体に形成されている。
As shown in FIGS. 15 to 17, the frame portion 503 of the deaeration prevention valve device 501 is a frame body attached to the base end portion 543.
The frame portion 503 can take various shapes according to the shape of the proximal end portion 543 of the mouthpiece 504, but in the present embodiment, has a substantially cylindrical shape. The frame portion 503 is integrally formed with an inward flange-shaped fixing portion 531 with a predetermined width.
 弁体部505は、内視鏡に気密に密着する可撓性の部材であり、フレーム部503の内面に設けられている。より具体的には、弁体部505はフレーム部503と別部材として略円板形状に作製され、円筒状のフレーム部503の内部に装着されて固定部531に固定される。 The valve body portion 505 is a flexible member that is airtightly attached to the endoscope, and is provided on the inner surface of the frame portion 503. More specifically, the valve body portion 505 is manufactured in a substantially disk shape as a separate member from the frame portion 503, and is mounted inside the cylindrical frame portion 503 and fixed to the fixing portion 531.
 弁体部505の略中央部には、略円形の挿通孔562を有する環状の内視鏡挿入部506が設けられている。内視鏡挿入部506は弾性的に伸縮変形可能であり、内視鏡が挿入抜去自在に挿通孔562に挿通されるとともに、内視鏡挿入部506は内視鏡の周囲に気密に密着する。 An annular endoscope insertion portion 506 having a substantially circular insertion hole 562 is provided at a substantially central portion of the valve body portion 505. The endoscope insertion part 506 is elastically deformable, and the endoscope is inserted into the insertion hole 562 so as to be freely inserted and removed, and the endoscope insertion part 506 is tightly sealed around the endoscope. .
 内視鏡挿入部506の外周縁部には伸縮手段508(伸縮部)が形成されている。伸縮手段508は、内視鏡挿入部506を径方向(図17における左右方向)、進退方向(同図における上下方向)および回転方向(内視鏡の捩れ方向または首振り方向)に移動可能とする柔軟な部材である。伸縮手段508の形状は、平板状であっても、蛇腹状であってもよいが、内視鏡挿入部506の上記方向への移動をより向上させる観点から、蛇腹状を含むことが好ましい。本実施形態の脱気防止弁装置501によれば、伸縮手段508を備えることにより、弁体部505が内視鏡に追随して変形する。このため、マウスピース504の内腔542に挿通された内視鏡を術者が動かす際に、内視鏡の操作性が損なわれることがない。
 弁体部505の外周縁部には、マウスピース504の内腔542の近位端側の開口と嵌合して当該開口を気密に封止する閉止栓部554(図17、図20を参照)が伸縮手段508と一体に形成されている。
An expansion / contraction means 508 (expansion / contraction part) is formed on the outer peripheral edge of the endoscope insertion part 506. The expansion / contraction means 508 can move the endoscope insertion portion 506 in the radial direction (left-right direction in FIG. 17), the forward / backward direction (up-down direction in FIG. 17), and the rotation direction (twist direction or swing direction of the endoscope). It is a flexible member. The expansion / contraction means 508 may have a flat plate shape or a bellows shape, but preferably includes a bellows shape from the viewpoint of further improving the movement of the endoscope insertion portion 506 in the above direction. According to the deaeration prevention valve device 501 of the present embodiment, by providing the expansion / contraction means 508, the valve body portion 505 is deformed following the endoscope. For this reason, when an operator moves the endoscope inserted through the lumen 542 of the mouthpiece 504, the operability of the endoscope is not impaired.
A closing plug portion 554 (see FIGS. 17 and 20) that fits with the opening on the proximal end side of the lumen 542 of the mouthpiece 504 and hermetically seals the opening on the outer peripheral edge of the valve body 505. ) Is formed integrally with the expansion / contraction means 508.
 本実施形態の脱気防止弁装置501は、係止部502の操作によってマウスピース504の基端部543に対して着脱可能に装着される。
 係止部502は、フレーム部503の外縁の円周上に設けられている。
The deaeration prevention valve device 501 of this embodiment is detachably attached to the proximal end portion 543 of the mouthpiece 504 by operating the locking portion 502.
The locking portion 502 is provided on the circumference of the outer edge of the frame portion 503.
 本実施形態の脱気防止弁装置501は、マウスピース504の基端部543に対して、フレーム部503の内側に向かって突き出した係止手段(係止爪;係止突起部)521を掛合させることにより装着される(図16参照)。
 本実施形態の係止手段521は、円筒状のフレーム部503より軸方向であって遠位側に突出した係止部502の先端部に形成されている。
 ただし、本発明はこれに限られるものではなく、図示省略するが、係止手段521は、たとえば円筒状のフレーム部503の内周面上に形成されてもよく、外周面上に軸方向より突出しないように係止部502が形成されていてもよい。
The deaeration prevention valve device 501 of the present embodiment engages a locking means (locking claw; locking protrusion) 521 protruding toward the inside of the frame portion 503 with respect to the base end portion 543 of the mouthpiece 504. (See FIG. 16).
The locking means 521 of the present embodiment is formed at the tip of the locking portion 502 that protrudes in the axial direction and distally from the cylindrical frame portion 503.
However, the present invention is not limited to this, and although not shown in the figure, the locking means 521 may be formed on the inner peripheral surface of the cylindrical frame portion 503, for example, on the outer peripheral surface from the axial direction. A locking portion 502 may be formed so as not to protrude.
 本実施形態の脱気防止弁装置501は、マウスピース504の基端部543に係脱可能に係止する係止部502を用いて、マウスピース504の基端部543に対して着脱自在に装着される。すなわち、本実施形態の脱気防止弁装置501はマウスピース504の外部に装着される。このため、脱気防止弁装置501をマウスピース504に装着したとしても、マウスピース504の内腔542における内視鏡の可動域を狭めることがなく、内視鏡の操作性を損なうことがない。 The deaeration prevention valve device 501 of the present embodiment is detachably attached to the base end portion 543 of the mouthpiece 504 using a locking portion 502 that is detachably locked to the base end portion 543 of the mouthpiece 504. Installed. That is, the deaeration prevention valve device 501 of this embodiment is attached to the outside of the mouthpiece 504. For this reason, even if the deaeration prevention valve device 501 is attached to the mouthpiece 504, the movable range of the endoscope in the lumen 542 of the mouthpiece 504 is not narrowed, and the operability of the endoscope is not impaired. .
 また、脱気防止弁装置501をマウスピース504に装着した状態では、内視鏡に周着した弁体部505によって内腔542の近位端が気密に保持される。このため、内腔542に挿通された内視鏡を前後左右などに動かしたとしても、体腔内に送気された加圧空気がマウスピース504の近位端側に漏れ出すことを低減することができる。よって、バルサルバ法によって喉頭を挙上し、下咽頭の視野の確保をすることができる。 Further, in a state where the deaeration prevention valve device 501 is attached to the mouthpiece 504, the proximal end of the lumen 542 is airtightly held by the valve body portion 505 that is worn around the endoscope. For this reason, even if the endoscope inserted through the lumen 542 is moved back and forth, left and right, etc., it is possible to reduce leakage of pressurized air supplied into the body cavity to the proximal end side of the mouthpiece 504. Can do. Therefore, the larynx can be raised by the Valsalva method and the visual field of the hypopharynx can be secured.
 さらに、脱気防止弁装置501はマウスピース504から脱離可能である。中下咽頭部の観察終了後に、引き続き行われる食道や胃の検査時においては、内視鏡を内腔542に挿通した状態のまま、脱気防止弁装置501をマウスピース504から外しておくことができる。これにより、気密性確保が必要となるバルサルバ法による中下咽頭部の検査に引き続き、マウスピースの交換作業なしに食道や胃の検査を実施することができる。 Furthermore, the deaeration prevention valve device 501 can be detached from the mouthpiece 504. After the observation of the middle and lower pharynx, when the esophagus and stomach are subsequently examined, the deaeration prevention valve device 501 is removed from the mouthpiece 504 while the endoscope is inserted into the lumen 542. Can do. Thus, following the examination of the middle and lower pharynx by the Valsalva method, which requires airtightness, the esophagus and stomach can be examined without replacing the mouthpiece.
 また、一般的に、食道や胃の検査では、上述のバルサルバ法による中下咽頭の検査のように、気密性確保が必要とはされないため、脱気防止弁装置501は外すことが想定される。しかし、内視鏡で送気をしても胃の観察に必要な視野が得られない場合には、脱気防止弁装置501をあらためて装着すれば、口からの空気漏れを最低限に抑えて、視野確保ができる。このように、脱気防止弁装置501がマウスピース504に対して、着脱可能であることで、内視鏡検査の状況や被験者の状況に応じて、脱気防止弁装置501は任意に装着、非装着を選択することができる。 In general, in the examination of the esophagus and stomach, it is not necessary to ensure airtightness unlike the examination of the middle and lower pharynx by the Valsalva method described above, so it is assumed that the deaeration prevention valve device 501 is removed. . However, if the field of view necessary for gastric observation cannot be obtained even if air is fed through an endoscope, the air leakage from the mouth can be minimized by installing the deaeration prevention valve device 501 again. , Securing a field of view. Thus, the deaeration prevention valve device 501 can be attached to and detached from the mouthpiece 504, so that the deaeration prevention valve device 501 can be arbitrarily attached according to the status of the endoscopy or the condition of the subject. Non-wearing can be selected.
 係止部502は、係止手段521と一体に形成された指掛け部522(つまみ部)を有している。指掛け部522は、係止手段521を拡径部541に対して係止可能な閉状態、または拡径部541から脱離可能な開状態に術者が開閉操作する部位である。 The locking portion 502 has a finger hook portion 522 (knob portion) formed integrally with the locking means 521. The finger hook portion 522 is a portion that the operator opens and closes in a closed state in which the locking means 521 can be locked to the enlarged diameter portion 541 or an open state in which the locking means 521 can be detached from the enlarged diameter portion 541.
 図17に示すように、係止部502は下部(遠位側寄り)に係止手段521を有し、上部(近位側寄り)には指掛け部522を有し、係止手段521と指掛け部522との中間にあたる接合部523にてフレーム部503と接合されている。図16に示すとおり接合部523は、フレーム部503に対して可動に接合されている。指掛け部522に外力を加えない状態(閉状態)では、マウスピース504を介して向かい合う係止手段521と係止手段21とがマウスピース504の基端部543の外面に嵌着し、脱気防止弁装置501がマウスピース504に装着される。指掛け部522を指でフレーム部503の中心軸方向に倒し込むことで、向かい合う係止手段521と係止手段521と距離が広がり、当該距離が、マウスピース504の基端部543の外径よりも大きく開いた状態(開状態)となる(図示省略)。これにより、係止手段521がマウスピース504の基端部543を通過可能となり、脱気防止弁装置501をマウスピース504から取り外すことができる。 As shown in FIG. 17, the locking part 502 has a locking means 521 at the lower part (distal side) and a finger hooking part 522 at the upper part (closer to the proximal side). The frame portion 503 is joined at a joint portion 523 that is in the middle of the portion 522. As shown in FIG. 16, the joint portion 523 is movably joined to the frame portion 503. In a state where no external force is applied to the finger hook portion 522 (closed state), the locking means 521 and the locking means 21 that face each other via the mouthpiece 504 are fitted to the outer surface of the base end portion 543 of the mouthpiece 504 to deaerate. A prevention valve device 501 is attached to the mouthpiece 504. By tilting the finger hook portion 522 in the direction of the central axis of the frame portion 503 with a finger, the distance between the locking means 521 and the locking means 521 facing each other increases, and the distance is larger than the outer diameter of the proximal end portion 543 of the mouthpiece 504 Is also in a largely open state (open state) (not shown). Accordingly, the locking means 521 can pass through the proximal end portion 543 of the mouthpiece 504, and the deaeration prevention valve device 501 can be detached from the mouthpiece 504.
 係止部502の個数は特に限定されず、一箇所でも、二箇所以上でもよい。
 本実施形態の脱気防止弁装置501においては、図15に示すように、係止部502は、フレーム部503の周囲に互いに離間して二箇所以上に設けられている。
The number of the locking portions 502 is not particularly limited, and may be one or two or more.
In the deaeration prevention valve device 501 of the present embodiment, as shown in FIG. 15, the locking portions 502 are provided at two or more locations around the frame portion 503 so as to be separated from each other.
 より具体的には、本実施形態の係止部502は、円筒状のフレーム部503の中心軸に対して、互いに向かい合う二箇所に形成されている。
 このほか、フレーム部503の中心軸に対して互いに120度の角度間隔で3つの係止部502を形成してもよく、または中心軸に対して互いに90度の角度間隔で4つの係止部502を形成してもよい。さらに、係止部502はフレーム部503の周上の一箇所のみに設けられてもよい。すなわち、一つの係止部502とフレーム部503とでマウスピース504の基端部543に脱気防止弁装置501を固定し、当該係止部502の開放により脱気防止弁装置501をマウスピース504から脱離可能としてもよい。
More specifically, the locking portion 502 of this embodiment is formed at two locations facing each other with respect to the central axis of the cylindrical frame portion 503.
In addition, three locking portions 502 may be formed at an angular interval of 120 degrees with respect to the central axis of the frame portion 503, or four locking portions at an angular interval of 90 degrees with respect to the central axis. 502 may be formed. Further, the locking portion 502 may be provided only at one place on the circumference of the frame portion 503. That is, the deaeration prevention valve device 501 is fixed to the base end portion 543 of the mouthpiece 504 with one locking portion 502 and the frame portion 503, and the deaeration prevention valve device 501 is fixed to the mouthpiece by opening the locking portion 502. It may be possible to detach from 504.
 なお、術者が片方の手で内視鏡を操作している場合は、もう片方の手で、本実施形態の脱気防止弁装置501をマウスピース504から取り外せることが好ましい、片手での取り外し易さを考慮すると係止部502は三箇所以下が好ましい。さらに、術者が指で摘むだけで係止部502を開状態にすることができるという観点から、係止部502はフレーム部503の周上で対向する二箇所に設けることが好ましい。 When the operator operates the endoscope with one hand, it is preferable that the deaeration prevention valve device 501 of this embodiment can be detached from the mouthpiece 504 with the other hand. In consideration of easiness, the number of the locking portions 502 is preferably three or less. Furthermore, from the viewpoint that the locking portion 502 can be opened by simply picking it with a finger, it is preferable to provide the locking portions 502 at two opposite locations on the circumference of the frame portion 503.
 以下、本実施形態の脱気防止弁装置501をさらに詳細に説明する。係止部502は、フレーム部503と一体成形されていてもよく、またはフレーム部503と別部材として成形され、フレーム部503に対して可動に接合固定されてもよい。係止部502とフレーム部503とを一体成形する場合、これらの材質としては、第一実施形態において説明したフレーム部14の材料と同様であるため、ここでは具体的列挙を省略する。特に係止部502とフレーム部503とを一体成形する場合は、係止部502とフレーム部503との固定部にあたる接合部523のヒンジの耐久性の点からポリエチレン樹脂、ポリアミド樹脂またはポリプロピレン樹脂が好ましい。 Hereinafter, the deaeration prevention valve device 501 of the present embodiment will be described in more detail. The locking portion 502 may be integrally formed with the frame portion 503, or may be formed as a separate member from the frame portion 503 and may be movably joined and fixed to the frame portion 503. When the locking portion 502 and the frame portion 503 are integrally formed, these materials are the same as the material of the frame portion 14 described in the first embodiment, and therefore specific listing is omitted here. In particular, when the locking portion 502 and the frame portion 503 are integrally formed, polyethylene resin, polyamide resin, or polypropylene resin is used from the viewpoint of the durability of the hinge of the joint portion 523 that is a fixing portion between the locking portion 502 and the frame portion 503. preferable.
 係止部502とフレーム部503とを個別に成形する場合、係止部502の材質は特に限定されないが、指掛け部522に外力を加え係止部502全体を傾ける強度に耐える必要があるため、比較的硬質の材質が望ましい。係止部502の材料は、第一実施形態において説明したフレーム部14と同様である。 When the locking portion 502 and the frame portion 503 are molded separately, the material of the locking portion 502 is not particularly limited, but it is necessary to withstand the strength of applying an external force to the finger hook portion 522 and tilting the locking portion 502 as a whole. A relatively hard material is desirable. The material of the locking portion 502 is the same as that of the frame portion 14 described in the first embodiment.
 また係止部502とフレーム部503とが個別成形される場合、フレーム部503の材質は特に限定されないが、係止部502に与えられる外力に耐え変形を生じず、弁体部505を十分に固定できる強度を有することが好ましい。また、フレーム部503として比較的硬質の材質を用いることにより、内腔542の内径を十分に確保して内視鏡の操作性が良好となる。フレーム部503の材料は、第一実施形態において説明したフレーム部14と同様である。 Further, when the locking portion 502 and the frame portion 503 are individually molded, the material of the frame portion 503 is not particularly limited. However, the material does not deform due to the external force applied to the locking portion 502, and the valve body portion 505 is sufficiently formed. It is preferable to have strength that can be fixed. Further, by using a relatively hard material for the frame portion 503, the inner diameter of the lumen 542 is sufficiently secured, and the operability of the endoscope is improved. The material of the frame part 503 is the same as that of the frame part 14 described in the first embodiment.
 図17から図19に示すように、本実施形態の脱気防止弁装置501は、フレーム部503の円筒の一方の開口端面に、弁体部505を固定する固定部531を内向きフランジ状に有している。弁体部505は固定部531に対して接着固定してもよく、または固定部531と他の部材とで弁体部505を挟持してもよい。 As shown in FIGS. 17 to 19, the deaeration prevention valve device 501 of the present embodiment has a fixing portion 531 for fixing the valve body portion 505 in an inward flange shape on one opening end surface of the cylinder of the frame portion 503. Have. The valve body portion 505 may be bonded and fixed to the fixing portion 531, or the valve body portion 505 may be sandwiched between the fixing portion 531 and another member.
 図17、図19、および図20に示すとおり、本実施形態の脱気防止弁装置501は、弁体部505をフレーム部503に固定する略リング状の固定部材(固定リング507)を有している。
 固定リング507は、円筒状のフレーム部503の内部に収容可能な外形を有するリング状をなし、固定リング507と固定部531とで弁体部505の外周縁を圧接して挟持する。
 フレーム部503の円筒の内側には、図20に示すように爪532が突出して形成されている。爪532は、固定リング507がフレーム部503から抜け落ちることを防止するストッパーである。たとえば、固定リング507の遠位側面と爪532の近位側面とを当接させることにより固定リング507の抜け落ちを防止することができる。
As shown in FIGS. 17, 19, and 20, the deaeration prevention valve device 501 of this embodiment includes a substantially ring-shaped fixing member (fixing ring 507) that fixes the valve body portion 505 to the frame portion 503. ing.
The fixing ring 507 has a ring shape having an outer shape that can be accommodated inside the cylindrical frame portion 503, and the fixing ring 507 and the fixing portion 531 press and hold the outer peripheral edge of the valve body portion 505.
On the inner side of the cylinder of the frame portion 503, as shown in FIG. The claw 532 is a stopper that prevents the fixing ring 507 from falling off the frame portion 503. For example, the fixing ring 507 can be prevented from falling off by bringing the distal side surface of the fixing ring 507 into contact with the proximal side surface of the claw 532.
 固定リング507の材質は特に限定はしないが、脱気防止弁装置501全体を薄型化して内視鏡の操作性を高めつつ、弁体部505をフレーム部503に強固に固定して内視鏡と弁体部505との摩擦力に十分耐える強度を有することが好ましい。具体的には、固定リング507の材料として、係止部502またはフレーム部503の材料と同様のものを用いることができる。 The material of the fixing ring 507 is not particularly limited, but the endoscope is provided by firmly fixing the valve body 505 to the frame portion 503 while thinning the entire deaeration prevention valve device 501 to improve the operability of the endoscope. It is preferable to have sufficient strength to withstand the frictional force between the valve body portion 505 and the valve body portion 505. Specifically, as the material of the fixing ring 507, the same material as that of the locking portion 502 or the frame portion 503 can be used.
 本実施形態の脱気防止弁装置501は、内視鏡挿入部506の外周縁部と、伸縮手段508の内周縁部との間に、補強部材509を有している。
 補強部材509は、内視鏡挿入部506の弾性率を伸縮手段508よりも高め、内視鏡との密着性を向上するための部材である。
 本実施形態の補強部材509は環状の内視鏡挿入部506と共通の材料にて一体成形されている。たとえば補強部材509は、図19に示すとおり、Oリングである補強部材509の断面直径が伸縮手段508の厚み寸法よりも大きい。かかるOリングである補強部材509を用いることにより伸縮手段508の内周縁部の強度を補強し、かつ内視鏡と脱気防止弁装置501との密着性を良好にし得る。
The deaeration prevention valve device 501 of this embodiment includes a reinforcing member 509 between the outer peripheral edge portion of the endoscope insertion portion 506 and the inner peripheral edge portion of the expansion / contraction means 508.
The reinforcing member 509 is a member for increasing the elasticity of the endoscope insertion portion 506 as compared with the expansion / contraction means 508 and improving the adhesiveness with the endoscope.
The reinforcing member 509 of the present embodiment is integrally formed of a material common to the annular endoscope insertion portion 506. For example, as shown in FIG. 19, the reinforcing member 509 has a cross-sectional diameter of the reinforcing member 509 that is an O-ring larger than the thickness dimension of the expansion / contraction means 508. By using the reinforcing member 509 which is such an O-ring, the strength of the inner peripheral edge of the expansion / contraction means 508 can be reinforced and the adhesion between the endoscope and the deaeration prevention valve device 501 can be improved.
 本実施形態の補強部材509は、Oリング状に形成されている。これにより、内視鏡挿入部506は内視鏡の周囲に均一に周着されるため、内視鏡を前進後退、上下左右および回転させても、内視鏡の外表面と内視鏡挿入部506と間に隙間が形成されることが防止される。 The reinforcing member 509 of the present embodiment is formed in an O-ring shape. As a result, the endoscope insertion portion 506 is evenly worn around the endoscope, so even if the endoscope is moved forward, backward, up, down, left and right, and rotated, the endoscope outer surface and the endoscope are inserted. Formation of a gap between the portion 506 is prevented.
 伸縮手段508は、図19に示すとおり、内視鏡挿入部506の挿通孔562の円周平面方向に拡縮径する蛇腹部を有している。例えば、当該蛇腹部は、折り返し部582を介して互いに逆方向に傾斜する傾斜部583とから構成することができる。蛇腹部を伸縮手段508に付設することで、特に内視鏡の挿入抜去時に内視鏡挿入部506にかかる応力を緩和することができ、内視鏡をスムーズに挿入抜去できる。また、挿通孔562に挿入された内視鏡が内視鏡挿入部506を中心にして前進後退、上下左右および回転のあらゆる方向に操作されても、蛇腹部が収縮または伸展することで、内視鏡の自由な動きを妨げることが無い。さらに、蛇腹部が内視鏡挿入部506よりも可撓性が高いことにより、内視鏡挿入部506は内視鏡の外表面に密着した状態でフレーム部503に対して変位する。これにより、内視鏡挿入部506と内視鏡との隙間を最小にすることができ、内視鏡と脱気防止弁装置501との気密性を維持することができる。 The expansion / contraction means 508 has a bellows portion that expands and contracts in the circumferential plane direction of the insertion hole 562 of the endoscope insertion portion 506, as shown in FIG. For example, the bellows part can be constituted by an inclined part 583 that inclines in opposite directions to each other via the folded part 582. By attaching the bellows portion to the expansion / contraction means 508, stress applied to the endoscope insertion portion 506 can be relieved particularly when the endoscope is inserted and removed, and the endoscope can be smoothly inserted and removed. Even if the endoscope inserted into the insertion hole 562 is operated in all directions of forward / backward, up / down / left / right and rotation around the endoscope insertion portion 506, the bellows portion contracts or extends, There is no hindrance to the free movement of the endoscope. Further, since the bellows portion is more flexible than the endoscope insertion portion 506, the endoscope insertion portion 506 is displaced with respect to the frame portion 503 while being in close contact with the outer surface of the endoscope. Thereby, the clearance gap between the endoscope insertion part 506 and an endoscope can be minimized, and the airtightness of an endoscope and the deaeration prevention valve apparatus 501 can be maintained.
(第一変形例)
 次に本発明の第五実施形態の第一変形例について図21を用いて説明する。
 以下では、第一変形例について、第五実施形態との相違点を中心に説明し、第五実施形態と同様の事項についてはその説明を適宜省略する。
(First modification)
Next, a first modification of the fifth embodiment of the present invention will be described with reference to FIG.
Below, a 1st modification is demonstrated centering around difference with 5th embodiment, The description is abbreviate | omitted suitably about the matter similar to 5th embodiment.
 図21は、本発明の第一変形例に係る脱気防止弁装置501の断面図である。 FIG. 21 is a cross-sectional view of a deaeration prevention valve device 501 according to a first modification of the present invention.
 図21に示すように、伸縮手段508は、蛇腹部の山部および谷部(折り返し部582)を、他の平坦部(傾斜部583)に比べて肉薄にすることができる。このようにすることで、蛇腹部の収縮または伸展がよりソフトになり内視鏡の挿入抜去及び内視鏡操作時に内視鏡との摩擦を低減できるため内視鏡の操作性が更に向上する。 As shown in FIG. 21, the expansion / contraction means 508 can make the peak portion and the valley portion (folded portion 582) of the bellows portion thinner than other flat portions (inclined portion 583). By doing so, the contraction or extension of the bellows part becomes softer, and friction with the endoscope can be reduced during insertion / extraction of the endoscope and operation of the endoscope, so that the operability of the endoscope is further improved. .
 内視鏡は、内視鏡挿入部506を中心として、前進後退及び上下左右の動きに加え、内視鏡挿入部506を中心とした軸回転の操作も実施される。このとき、内視鏡挿入部506を中心とした軸回転の動きに対しては、蛇腹部における肉厚の傾斜部583が有する高い弾性力により、内視鏡挿入部506が内視鏡と共に回転してこれに巻き付いてしまうことを抑制する。そして、蛇腹部における肉薄の折り返し部582が有する低い弾性力により、内視鏡の前後左右の動きに対して内視鏡挿入部506が好適に追随することができる。 In the endoscope, in addition to the forward / backward movement and the up / down / left / right movement around the endoscope insertion portion 506, an operation of rotating the shaft around the endoscope insertion portion 506 is also performed. At this time, the endoscope insertion portion 506 rotates together with the endoscope due to the high elastic force of the thick inclined portion 583 in the bellows portion with respect to the axial rotation movement around the endoscope insertion portion 506. And curbing around this. And the endoscope insertion part 506 can follow suitably with respect to the back-and-forth, right-and-left movement of an endoscope with the low elastic force which the thin folding | turning part 582 in a bellows part has.
 内視鏡挿入部506の内径は、これに挿通される内視鏡の外径以下である。
 より具体的には、内視鏡挿入部506の内径は、これに挿通される内視鏡の外径より0mm以上、5mm以下の範囲で小さいことが好ましく、2mm以上、4mm以下の範囲で小さいことが更に好ましい。上記範囲で内視鏡挿入部506の内径を内視鏡の外径より小さくすることで、内視鏡の挿入時および抜去時の抵抗の抑制と、内視鏡に対する内視鏡挿入部506の密着性を両立することができる。これによって、内視鏡と内視鏡挿入部506との間に適度な摩擦力が得られるため、内視鏡を動かした場合の内腔542からの空気漏れを防止しつつ、内視鏡の操作時に脱気防止弁装置501が内視鏡と共にマウスピース504から抜けてしまうことを防止できる。
The inner diameter of the endoscope insertion portion 506 is equal to or smaller than the outer diameter of the endoscope inserted through the endoscope insertion portion 506.
More specifically, the inner diameter of the endoscope insertion portion 506 is preferably smaller than the outer diameter of the endoscope inserted therethrough in the range of 0 mm or more and 5 mm or less, and smaller in the range of 2 mm or more and 4 mm or less. More preferably. By making the inner diameter of the endoscope insertion portion 506 smaller than the outer diameter of the endoscope within the above range, resistance during insertion and removal of the endoscope can be suppressed, and the insertion of the endoscope insertion portion 506 with respect to the endoscope can be reduced. It is possible to achieve both adhesion. As a result, an appropriate frictional force is obtained between the endoscope and the endoscope insertion portion 506, so that air leakage from the lumen 542 when the endoscope is moved is prevented, and the endoscope It is possible to prevent the deaeration prevention valve device 501 from being detached from the mouthpiece 504 together with the endoscope during operation.
 弁体部505の材質は、第一実施形態における伸縮部16の材料と同様であるため、ここでは例示列挙を省略する。 Since the material of the valve body part 505 is the same as the material of the expansion / contraction part 16 in the first embodiment, the example listing is omitted here.
(第二変形例)
 次に第五実施形態の他の変形例である第二変形例について図22を用いて説明する。
 以下では、第二変形例について第五実施形態との相違点を中心に説明し、第五実施形態と同様の事項についてはその説明を適宜省略する。
(Second modification)
Next, a second modification which is another modification of the fifth embodiment will be described with reference to FIG.
Below, it demonstrates centering around difference with 5th embodiment about a 2nd modification, and the description is abbreviate | omitted suitably about the matter similar to 5th embodiment.
 図22は、本発明の第二変形例に係る脱気防止弁装置501の断面図である。 FIG. 22 is a cross-sectional view of a deaeration prevention valve device 501 according to a second modification of the present invention.
 図22に示すように、本変形例の脱気防止弁装置501は、内視鏡挿入部506が、弁体部505の厚み方向に延在する直管部565を有している。
 本変形例の脱気防止弁装置501は、内視鏡の外周面に対して内視鏡挿入部506が所定の延在長さに亘って密着する点で上記実施形態(図19を参照)と相違している。
 Oリング状の補強部材509は直管部565の外周側に形成され、直管部565の内周面は円筒面状をなしている。
As shown in FIG. 22, in the deaeration prevention valve device 501 of this modification, the endoscope insertion portion 506 has a straight tube portion 565 extending in the thickness direction of the valve body portion 505.
The deaeration prevention valve device 501 of the present modification is the above embodiment (see FIG. 19) in that the endoscope insertion portion 506 is in close contact with the outer peripheral surface of the endoscope over a predetermined extension length. Is different.
The O-ring-shaped reinforcing member 509 is formed on the outer peripheral side of the straight tube portion 565, and the inner peripheral surface of the straight tube portion 565 has a cylindrical surface shape.
 本変形例に係る脱気防止弁装置501によれば、内視鏡挿入部506と内視鏡との密着性が向上し、内視鏡挿入部506を周着した内視鏡を内腔542に対して進退させた場合に、Oリング状の補強部材509が内視鏡に対して転がり回転することがない。これにより、術者による内視鏡の操作時に内視鏡挿入部506と内視鏡との間に隙間が生じることが防止されている。 According to the deaeration prevention valve device 501 according to the present modification, the adhesion between the endoscope insertion portion 506 and the endoscope is improved, and the endoscope around the endoscope insertion portion 506 is attached to the lumen 542. In this case, the O-ring-shaped reinforcing member 509 does not roll and rotate with respect to the endoscope. This prevents a gap from being generated between the endoscope insertion portion 506 and the endoscope when the operator operates the endoscope.
<第六実施形態>
 次に本発明の第六実施形態について図23A~Dを用いて説明する。
 以下では、第六実施形態について説明するが、第五実施形態との相違点を中心に説明し、同様の事項についてはその説明を省略する。
<Sixth embodiment>
Next, a sixth embodiment of the present invention will be described with reference to FIGS. 23A to 23D.
In the following, the sixth embodiment will be described. However, differences from the fifth embodiment will be mainly described, and description of similar matters will be omitted.
 図23Aは第六実施形態における脱気防止弁装置600と内視鏡用マウスピース640との装着前の斜視図、図23Bは脱気防止弁装置600を内視鏡用マウスピース640に装着した断面図、図23Cは脱気防止弁装置600の断面図、図23Dは内視鏡用マウスピース640の断面図である。 FIG. 23A is a perspective view of the sixth embodiment before the deaeration prevention valve device 600 and the endoscope mouthpiece 640 are attached, and FIG. 23B is the attachment of the deaeration prevention valve device 600 to the endoscope mouthpiece 640. 23C is a cross-sectional view of the deaeration preventing valve device 600, and FIG. 23D is a cross-sectional view of the endoscope mouthpiece 640.
 図23A~Dに示すように、脱気防止弁装置600には、突起状の凸部形状である係止部(係止手段;係止爪)620を有する。係止部620は、たとえば、脱気防止弁装置600の外周面上に設けられ、径方向の外側に突出する。一方、マウスピース640の基端部630の内腔側には溝部631を有し、溝部631の周方向側に連続して穴部632を有し、穴部632の近位端側に突起部633を有している。
 第六の実施形態においては、脱気防止弁装置600がマウスピース640の基端部630に内装される。
 詳しくは、マウスピース640における基端部630の溝部631の近位端側から、脱気防止弁装置600の突起状の係止部620の遠位端側が挿入される。係止部620は、鍔部650に当接して挿入方向において位置決めされた後に、周方向に回転することで、係止部620が穴部423に嵌り、上下方向(遠位側と近位側との方向)に固定される。さらに、突起部633があることで、係止部620は、周方向に固定される。
 よって、第六実施形態においては、脱気防止弁装置600の外表面の任意の箇所を指などで把持して、マウスピース640に脱気防止弁装置600を着脱することができる。
As shown in FIGS. 23A to 23D, the deaeration prevention valve device 600 has a locking portion (locking means; locking claw) 620 having a protruding convex shape. The locking part 620 is provided on the outer peripheral surface of the deaeration prevention valve device 600, for example, and protrudes outward in the radial direction. On the other hand, the mouthpiece 640 has a groove 631 on the lumen side of the proximal end 630, a hole 632 continuous with the groove 631 in the circumferential direction, and a protrusion on the proximal end of the hole 632. 633.
In the sixth embodiment, the deaeration prevention valve device 600 is installed in the base end portion 630 of the mouthpiece 640.
Specifically, the distal end side of the protruding locking portion 620 of the deaeration prevention valve device 600 is inserted from the proximal end side of the groove portion 631 of the base end portion 630 in the mouthpiece 640. The locking portion 620 is positioned in the insertion direction by contacting the collar portion 650 and then rotated in the circumferential direction, so that the locking portion 620 fits into the hole portion 423, and the vertical direction (distal side and proximal side) Direction). Furthermore, the locking portion 620 is fixed in the circumferential direction because of the protrusion 633.
Therefore, in the sixth embodiment, the deaeration prevention valve device 600 can be attached to and detached from the mouthpiece 640 by grasping an arbitrary portion of the outer surface of the deaeration prevention valve device 600 with a finger or the like.
 以上に説明する本発明の脱気用防止装置は、本発明の内視鏡用マウスピースに設けられる脱気用防止装置として適宜、使用することができる。
 また本発明の内視鏡用マウスピースは、内視鏡用マウスピースと本発明の脱気防止弁装置からなる内視鏡用マウスピースを包含する。
 以上に説明する本発明の内視鏡検査用マウスピースにおける脱気防止弁装置の各構成および、本発明における脱気防止弁装置の各構成は、互いに適宜転用してもよい。
The deaeration prevention device of the present invention described above can be used as appropriate as the deaeration prevention device provided in the endoscope mouthpiece of the present invention.
The endoscope mouthpiece of the present invention includes an endoscope mouthpiece comprising the endoscope mouthpiece and the deaeration prevention valve device of the present invention.
Each configuration of the deaeration prevention valve device in the endoscopic examination mouthpiece of the present invention described above and each configuration of the deaeration prevention valve device in the present invention may be appropriately transferred to each other.
 以上に説明する本発明の内視鏡検査用マウスピース、および本発明の脱気防止弁装置を設置した内視鏡用マウスピースは、脱気防止弁装置と、マウスピース本体との間の気密性が3kPa以上とすることが可能である。かかる気密性を発揮するマウスピースは、バルサルバ法などの口腔内の気圧を高める検査や治療を実施するにおいて好適に使用される。
 脱気防止弁装置とマウスピース本体との間の気密性が3kPaとは、マウスピース本体に脱気防止弁装置を装着し、マウスピース本体と脱気防止弁装置との接合面の内側と外側との間に3kPaの気圧を付加したときに、マウスピース本体と、脱気防止弁装置との間を気体が漏れないことをいう。
The mouthpiece for endoscopy of the present invention described above and the mouthpiece for endoscope provided with the deaeration prevention valve device of the present invention are airtight between the deaeration prevention valve device and the mouthpiece body. The property can be 3 kPa or more. Such a mouthpiece that exhibits airtightness is suitably used for performing tests and treatments for increasing the pressure in the oral cavity, such as the Valsalva method.
The airtightness between the deaeration prevention valve device and the mouthpiece body is 3 kPa. The inside and outside of the joint surface between the mouthpiece body and the deaeration prevention valve device when the deaeration prevention valve device is attached to the mouthpiece body. Means that no gas leaks between the mouthpiece body and the deaeration preventive valve device when a pressure of 3 kPa is applied between them.
 一例として、図16に示す脱気防止弁装置501が取り付けられたマウスピース504を用いて説明する。内視鏡挿入部506に内視鏡を密着させて挿入しカバー549の軸方向の中間から脱気防止弁装置501の取り付けられたマウスピース504の遠位側を覆うよう密封して内腔542の内部に気体を給気し内部圧力を3kPaとする。このとき、マウスピース504と、脱気防止弁装置501との接合面から気体が漏れないことによりマウスピース504と、脱気防止弁装置501との間の気密性が3kPaであることを確認することができる。
 上述する望ましい気密性は、たとえば、固定リング507および固定部531とで外周縁を圧接して挟持された弁体部505(図17参照)と基端部543とが当接した状態で脱気防止弁装置501がマウスピース504に取り付けられることにより実現可能である。
As an example, description will be made using a mouthpiece 504 to which a deaeration prevention valve device 501 shown in FIG. 16 is attached. The endoscope is inserted in close contact with the endoscope insertion portion 506 and sealed to cover the distal side of the mouthpiece 504 to which the deaeration prevention valve device 501 is attached from the middle in the axial direction of the cover 549. A gas is supplied into the interior of the chamber and the internal pressure is set to 3 kPa. At this time, it is confirmed that the airtightness between the mouthpiece 504 and the deaeration prevention valve device 501 is 3 kPa because gas does not leak from the joint surface between the mouthpiece 504 and the deaeration prevention valve device 501. be able to.
The desirable airtightness described above is, for example, deaerated in a state where the valve body portion 505 (see FIG. 17) and the base end portion 543 that are sandwiched by pressing the outer peripheral edge with the fixing ring 507 and the fixing portion 531 are in contact with each other. This can be realized by attaching the prevention valve device 501 to the mouthpiece 504.
 本発明の内視鏡検査用マウスピースは、バルサルバ法を利用した中下咽頭の内視鏡検査において、適切な息堪えを可能とし、喉頭を拳上して患部を詳細に観察することを可能とする。
 本発明の内視鏡検査用マウスピースは、上述するバルサルバ法を用いた中下咽頭検査に限定されず、種々の経口内視鏡検査に利用可能である。
 もちろん本発明の内視鏡検査用マウスピースは、内視鏡検査以外の目的で、例えば内視鏡を用いた治療の際に使用されることを除外するものではなく、内視鏡用のマウスピースとして広く使用することができる。
 また本発明の脱気防止弁装置は、内視鏡用マウスピースに着設することにより内視鏡の操作時に口腔内からの息漏れを防止するとともに、内視鏡用マウスピースから脱離することにより当該マウスピースを気密性確保が重視されない内視鏡操作に適用可能である。
The mouthpiece for endoscopy of the present invention enables proper breathing in endoscopic examination of the middle and lower pharynx using the Valsalva method, and it is possible to observe the affected area in detail by raising the larynx And
The mouthpiece for endoscopy of the present invention is not limited to the middle hypopharyngeal examination using the Valsalva method described above, and can be used for various oral endoscopy.
Of course, the mouthpiece for endoscopy according to the present invention does not exclude that it is used for purposes other than endoscopy, for example, in the case of treatment using an endoscope. Can be widely used as a piece.
The deaeration prevention valve device of the present invention is attached to the endoscope mouthpiece to prevent leakage from the oral cavity during operation of the endoscope and to be detached from the endoscope mouthpiece. Thus, the mouthpiece can be applied to an endoscope operation in which securing airtightness is not important.
 上記実施形態は、以下の技術思想を包含するものである。
(1)内視鏡を挿入抜去自在に挿通する挿通孔を有するマウスピース本体と、
前記挿通孔に挿通された前記内視鏡と前記マウスピース本体との間を気密に封止する脱気防止弁装置と、
 を有する内視鏡検査用マウスピース。
(2)前記脱気防止弁装置は、前記挿通孔に周設されているとともに、前記挿通孔に挿通される前記内視鏡に周着する上記(1)に記載の内視鏡検査用マウスピース。
(3)前記脱気防止弁装置は、前記挿通孔に周設された可撓性の伸縮部を有し、
 前記伸縮部が、当該伸縮部の略中央部に設けられ前記内視鏡に周着する内視鏡挿入部を有する上記(1)または(2)に記載の内視鏡検査用マウスピース。
(4)前記脱気防止弁装置は、前記マウスピース本体に着脱可能に装着されるフレーム部を有する上記(1)から(3)のいずれか一項に記載の内視鏡検査用マウスピース。
(5)前記フレーム部が、当該フレーム部を前記マウスピース本体の近位端に係脱可能に係止する係止部を備える上記(4)に記載の内視鏡検査用マウスピース。
(6)前記マウスピース本体の遠位端部に設けられた筒状の歯受部と、
 前記歯受部の外周を被覆する被覆部と、を有し、
 前記被覆部の硬度が、前記歯受部の硬度よりも低い上記(1)から(5)のいずれか一項に記載の内視鏡検査用マウスピース。
(7)前記被覆部が、前記マウスピース本体に対して脱着可能である上記(6)に記載の内視鏡検査用マウスピース。
(8)前記歯受部が、当該歯受部の遠位端部において径方向の外側に突出する凸部を有するとともに、
 前記被覆部が、内周面側において、小径部および大径部と前記小径部および前記大径部の段差により形成され径が不連続に変化する段差部とを有しており、
 前記凸部と前記段差部とが係合する上記(6)または(7)に記載の内視鏡検査用マウスピース。
(9)前記被覆部は、外周面側において、当該被覆部の遠位端部において径方向の外側に突出する第二凸部を有する上記(6)から(8)のいずれか一項に記載の内視鏡検査用マウスピース。
(10)前記歯受部が、当該歯受部の遠位端部において径方向の外側に突出する凸部を有するとともに、
 前記被覆部は、外周面側において、当該被覆部の遠位端部において径方向の外側に突出する第二凸部を有し、
 前記凸部の遠位端面に設けられた第一位置決め部と、前記第二凸部の遠位端面に設けられ前記第一位置決め部に対向する第二位置決め部と、を有する上記(6)に記載の内視鏡検査用マウスピース。
(11)前記被覆部が、外径が長軸と短軸とを有する円筒形であって、
 前記第二凸部は、前記長軸上に第一長さで延在する第一延在部と、前記短軸上に第二長さで延在する第二延在部と、を有し、
 前記第一長さは、前記第二長さよりも大きい上記(9)または(10)に記載の内視鏡検査用マウスピース。
(12)前記第一長さは、前記第二長さの2倍以上である上記(11)に記載の内視鏡検査用マウスピース。
(13)前記第一延在部は、外縁に向かって肉薄に形成されている上記(11)または(12)に記載の内視鏡検査用マウスピース。
(14)前記第一延在部の遠位側面は、前記マウスピース本体に設けられた前記挿通孔に連通させ、かつ外周を残して肉抜きされている上記(11)から(13)のいずれか一項に記載の内視鏡検査用マウスピース。
(15)前記第一延在部の近位側面の外縁が面取りされている上記(11)から(14)のいずれか一項に記載の内視鏡検査用マウスピース。
(16)前記マウスピース本体の遠位端部に設けられた筒状の歯受部を有し、
 前記歯受部の外径が、長軸および短軸を有する上記(1)から(9)のいずれか一項に記載の内視鏡検査用マウスピース。
(17)前記被覆部の内周面に、前記歯受部の外周面に当接する周方向に周回状に連続した凸状の当接部を備える上記(6)から(14)のいずれか一項に記載の内視鏡検査用マウスピース。
(18)前記歯受部と、前記当接部との間の気密性が3kPa以上である上記(17)に記載の内視鏡検査用マウスピース。
(19)前記マウスピース本体の遠位端部と近位端部との間には、外周面から外方向に延在する鍔部を有し、
 前記鍔部は、前記歯受部の前記長軸の伸長方向よりも前記短軸の伸長方向に長く延在している上記(16)に記載の内視鏡検査用マウスピース。
(20)前記鍔部の長軸方向と、前記第一延在部の延在方向とが直交している上記(19)に記載の内視鏡検査用マウスピース。
(21)前記鍔部は、前記マウスピース本体の遠位端から近位端に向けて凸状に湾曲している上記(19)または(20)に記載の内視鏡検査用マウスピース。
(22)前記マウスピース本体の遠位端部に設けられた筒状の歯受部と、
 前記歯受部の外周を被覆する被覆部と、
 前記マウスピース本体の遠位端部と近位端部との間には、外周面から外方向に延在する鍔部と、を有し、
 前記鍔部の裏面の基端部から前記マウスピース本体の遠位端までの最短距離と、前記被覆部の長尺方向の長さと、が略同等である上記(1)から(21)のいずれか一項に記載の内視鏡検査用マウスピース。
(23)前記歯受部の外周を被覆する被覆部を有し、
 前記被覆部の近位端面と、前記鍔部の遠位側面とが、互いに対応する形状である上記(19)から(22)のいずれか一項に記載の内視鏡検査用マウスピース。
(24)前記鍔部の遠位側面と前記被覆部の近位端面とが互いに嵌合し非周回に設けられた凹凸部を有する上記(23)に記載の内視鏡検査用マウスピース。
(25)前記挿通孔が、前記マウスピース本体の近位端から遠位端に向けて、縮径部と拡径部とを有するくびれ形状である上記(1)から(24)のいずれか一項に記載の内視鏡検査用マウスピース。
(26)前記脱気防止弁装置は、前記挿通孔に周設された可撓性の伸縮部を有するとともに、前記伸縮部が、当該伸縮部の略中央部に設けられ前記内視鏡に周着する内視鏡挿入部を有し、
 前記伸縮部は、環状の前記内視鏡挿入部と同心であって、径方向に山部と谷部とが設けられてなる環状の蛇腹部を有し、
 前記蛇腹部が、前記縮径部と前記拡径部との境界である境界部で囲まれる内円と同軸で配置され、かつ、前記蛇腹部の外縁の径は、前記内円の径よりも大きい上記(1)から(25)のいずれか一項に記載の内視鏡検査用マウスピース。
(27)前記蛇腹部の内縁の径が、前記内円の径よりも小さい上記(26)に記載の内視鏡検査用マウスピース。
(28)前記脱気防止弁装置と、前記マウスピース本体との間の気密性が3kPa以上である上記(1)から(27)のいずれか一項に記載の内視鏡検査用マウスピース。
(29)内視鏡を挿入抜去自在に挿通する内腔を有する口腔内に挿入されるマウスピースの基端部に対して着脱自在に装着される、内視鏡用マウスピースに用いられる脱気防止弁装置であって、
 前記マウスピースの前記基端部の外周面に装着されるフレーム部と、
 前記フレーム部に設けられて前記基端部の前記外周面に係脱可能に係止する係止部と、
 前記フレーム部の内側に設けられた弁体部と、
を有し、
 前記弁体部は、
 前記弁体部の略中央部に設けられて前記内視鏡に周着する環状の内視鏡挿入部と、
 前記内視鏡挿入部に周設された可撓性の伸縮手段と、
 を有していることを特徴とする脱気防止弁装置。
(30)前記係止部は、前記フレーム部の内側に向かって突き出した係止手段によって前記基端部の前記外周面に係脱可能に係止するものである上記(29)に記載の脱気防止弁装置。
(31)内視鏡を挿入抜去自在に挿通する内腔を有する口腔内に挿入されるマウスピースの基端部に対して着脱自在に装着される、内視鏡用マウスピースに用いられる脱気防止弁装置であって、
 前記マウスピースの前記基端部の内周面に装着されるフレーム部と、
 前記フレーム部に設けられて前記基端部の前記内周面に係脱可能に係止する係止部と、
 前記フレーム部の内側に設けられた弁体部と、
を有し、
 前記弁体部は、
 前記弁体部の略中央部に設けられて前記内視鏡に周着する環状の内視鏡挿入部と、
 前記内視鏡挿入部に周設された可撓性の伸縮手段と、
 を有していることを特徴とする脱気防止弁装置。
(32)前記係止部は、前記フレーム部の外側に向かって突き出した係止手段によって前記基端部の前記内周面に係脱可能に係止するものである上記(31)に記載の脱気防止弁装置。
(33)前記係止部は、前記フレーム部の周囲に互いに離間して二箇所以上に設けられている上記(29)から(32)のいずれか一項に記載の脱気防止弁装置。
(34)前記係止部は、前記係止手段と一体に形成されて、前記係止手段を前記基端部に対して係止可能な閉状態または前記基端部から脱離可能な開状態に開閉操作する指掛け部をさらに有する上記(29)または(30)に記載の脱気防止弁装置。
(35)前記内視鏡挿入部は、前記弁体部の厚み方向に延在する直管部を有していることを特徴とする上記(29)から(34)のいずれか一項に記載の脱気防止弁装置。
(36)前記弁体部を前記フレーム部に固定する略リング状の固定部材を有している上記(29)から(35)のいずれか一項に記載の脱気防止弁装置。
(37)前記伸縮手段は、蛇腹部を含むものである上記(29)から(36)のいずれか一項に記載の脱気防止弁装置。
(38)前記蛇腹部は、平坦な傾斜部および隣接する傾斜部同士の間の折り返し部で構成され、前記折り返し部が前記傾斜部に比べて肉薄である上記(37)に記載の脱気防止弁装置。
(39)前記内視鏡挿入部の外周縁部と、前記伸縮手段の内周縁部との間に補強部材を有している上記(29)から(38)のいずれか一項に記載の脱気防止弁装置。
(40)前記補強部材がOリング状に形成されている上記(39)に記載の脱気防止弁装置。
(41)前記内視鏡挿入部の内径は、これに挿通される前記内視鏡の外径以下である上記(29)から(40)のいずれか一項に記載の脱気防止弁装置。
The above embodiment includes the following technical idea.
(1) a mouthpiece body having an insertion hole through which an endoscope can be inserted and removed freely;
A deaeration preventive valve device that hermetically seals between the endoscope and the mouthpiece body inserted through the insertion hole;
A mouthpiece for endoscopy having an endoscope.
(2) The mouse for endoscopy according to (1), wherein the deaeration prevention valve device is provided around the insertion hole and is worn around the endoscope inserted through the insertion hole. piece.
(3) The deaeration prevention valve device has a flexible expansion and contraction portion provided around the insertion hole,
The endoscopic examination mouthpiece according to (1) or (2), wherein the extendable portion includes an endoscope insertion portion that is provided at a substantially central portion of the extendable portion and is attached to the endoscope.
(4) The mouthpiece for endoscopy according to any one of (1) to (3), wherein the deaeration prevention valve device has a frame portion that is detachably attached to the mouthpiece body.
(5) The mouthpiece for endoscopy according to (4), wherein the frame portion includes a locking portion that detachably locks the frame portion to the proximal end of the mouthpiece body.
(6) a cylindrical tooth receiving portion provided at a distal end portion of the mouthpiece body;
A covering portion covering the outer periphery of the tooth receiving portion,
The mouthpiece for endoscopy according to any one of (1) to (5), wherein the hardness of the covering portion is lower than the hardness of the tooth receiving portion.
(7) The mouthpiece for endoscopy according to (6), wherein the covering portion is detachable from the mouthpiece body.
(8) While the tooth receiving portion has a convex portion protruding radially outward at the distal end portion of the tooth receiving portion,
The covering portion has, on the inner peripheral surface side, a small diameter portion and a large diameter portion, and a step portion that is formed by a step of the small diameter portion and the large diameter portion and the diameter changes discontinuously
The mouthpiece for endoscopy according to (6) or (7), wherein the convex portion and the stepped portion are engaged.
(9) The covering portion according to any one of (6) to (8), wherein the covering portion has a second convex portion protruding outward in a radial direction at a distal end portion of the covering portion on the outer peripheral surface side. Mouthpiece for endoscopy.
(10) While the tooth receiving portion has a convex portion protruding outward in the radial direction at the distal end portion of the tooth receiving portion,
The covering portion has, on the outer peripheral surface side, a second convex portion protruding outward in the radial direction at the distal end portion of the covering portion,
In the above (6), the first positioning portion provided on the distal end surface of the convex portion and the second positioning portion provided on the distal end surface of the second convex portion and facing the first positioning portion. The mouthpiece for endoscopy as described.
(11) The covering portion has a cylindrical shape with an outer diameter having a major axis and a minor axis,
The second convex portion has a first extending portion extending at a first length on the major axis and a second extending portion extending at a second length on the minor axis. ,
Said 1st length is a mouthpiece for endoscopy as described in said (9) or (10) larger than said 2nd length.
(12) The mouthpiece for endoscopy according to (11), wherein the first length is twice or more the second length.
(13) The mouthpiece for endoscopy according to (11) or (12), wherein the first extending portion is formed thin toward the outer edge.
(14) The distal side surface of the first extending portion communicates with the insertion hole provided in the mouthpiece body, and is hollowed out leaving the outer periphery, any of (11) to (13) The mouthpiece for endoscopy according to claim 1.
(15) The mouthpiece for endoscopy according to any one of (11) to (14), wherein an outer edge of the proximal side surface of the first extension portion is chamfered.
(16) A cylindrical tooth receiving portion provided at a distal end portion of the mouthpiece body,
The mouthpiece for endoscopy according to any one of (1) to (9), wherein an outer diameter of the tooth receiving portion has a major axis and a minor axis.
(17) Any one of the above (6) to (14), wherein the inner peripheral surface of the covering portion is provided with a convex contact portion that is continuous in a circumferential direction in contact with the outer peripheral surface of the tooth receiving portion. The mouthpiece for endoscopy according to Item.
(18) The mouthpiece for endoscopy as described in (17) above, wherein the airtightness between the tooth receiving portion and the contact portion is 3 kPa or more.
(19) Between the distal end portion and the proximal end portion of the mouthpiece main body, there is a flange portion extending outward from the outer peripheral surface,
The mouthpiece for endoscopy according to (16), wherein the collar portion extends longer in the extending direction of the short axis than in the extending direction of the long axis of the tooth receiving portion.
(20) The mouthpiece for endoscopy according to (19), wherein the major axis direction of the buttocks and the extending direction of the first extending portion are orthogonal to each other.
(21) The mouthpiece for endoscopy according to (19) or (20), wherein the buttocks are curved in a convex shape from the distal end to the proximal end of the mouthpiece body.
(22) a cylindrical tooth receiving portion provided at a distal end portion of the mouthpiece body;
A covering portion covering the outer periphery of the tooth receiving portion;
Between the distal end portion and the proximal end portion of the mouthpiece body, has a flange extending outward from the outer peripheral surface,
Any one of the above (1) to (21), wherein the shortest distance from the base end portion of the back surface of the collar portion to the distal end of the mouthpiece body is substantially equal to the length of the covering portion in the longitudinal direction. The mouthpiece for endoscopy according to claim 1.
(23) having a covering portion covering the outer periphery of the tooth receiving portion;
The mouthpiece for endoscopy according to any one of (19) to (22), wherein a proximal end surface of the covering portion and a distal side surface of the flange portion have shapes corresponding to each other.
(24) The mouthpiece for endoscopy according to (23), wherein the distal side surface of the buttocks and the proximal end surface of the covering portion are fitted to each other and have a concavo-convex portion provided non-circularly.
(25) Any one of (1) to (24) above, wherein the insertion hole has a constricted shape having a reduced diameter portion and an enlarged diameter portion from the proximal end to the distal end of the mouthpiece body. The mouthpiece for endoscopy according to Item.
(26) The deaeration prevention valve device includes a flexible expansion / contraction portion that is provided around the insertion hole, and the expansion / contraction portion is provided at a substantially central portion of the expansion / contraction portion, and surrounds the endoscope. Having an endoscope insertion part to wear,
The telescopic part is concentric with the annular endoscope insertion part, and has an annular bellows part in which a peak part and a valley part are provided in a radial direction,
The bellows portion is arranged coaxially with an inner circle surrounded by a boundary portion that is a boundary between the reduced diameter portion and the enlarged diameter portion, and the outer edge diameter of the bellows portion is larger than the diameter of the inner circle. The mouthpiece for endoscopy according to any one of (1) to (25), which is large.
(27) The mouthpiece for endoscopy according to (26), wherein an inner edge diameter of the bellows portion is smaller than a diameter of the inner circle.
(28) The mouthpiece for endoscopy according to any one of (1) to (27), wherein an airtightness between the deaeration prevention valve device and the mouthpiece body is 3 kPa or more.
(29) Deaeration used for an endoscope mouthpiece that is detachably attached to a proximal end portion of a mouthpiece that is inserted into an oral cavity having a lumen through which an endoscope can be inserted and removed. A prevention valve device,
A frame portion attached to an outer peripheral surface of the base end portion of the mouthpiece;
A locking portion provided in the frame portion and releasably locked to the outer peripheral surface of the base end portion;
A valve body provided inside the frame part;
Have
The valve body is
An annular endoscope insertion portion that is provided at a substantially central portion of the valve body portion and is attached to the endoscope;
Flexible telescopic means provided around the endoscope insertion portion;
The deaeration prevention valve device characterized by having.
(30) The removal portion according to (29), wherein the engagement portion is detachably engaged with the outer peripheral surface of the base end portion by engagement means protruding toward the inside of the frame portion. Qi prevention valve device.
(31) Deaeration used for an endoscope mouthpiece that is detachably attached to a proximal end portion of a mouthpiece that is inserted into an oral cavity having a lumen through which an endoscope can be inserted and removed. A prevention valve device,
A frame portion attached to an inner peripheral surface of the base end portion of the mouthpiece;
A locking portion provided on the frame portion and releasably locked to the inner peripheral surface of the base end portion;
A valve body provided inside the frame part;
Have
The valve body is
An annular endoscope insertion portion that is provided at a substantially central portion of the valve body portion and is attached to the endoscope;
Flexible telescopic means provided around the endoscope insertion portion;
The deaeration prevention valve device characterized by having.
(32) The locking portion according to (31), wherein the locking portion is detachably locked to the inner peripheral surface of the base end portion by locking means protruding toward the outside of the frame portion. Deaeration prevention valve device.
(33) The deaeration prevention valve device according to any one of (29) to (32), wherein the locking portions are provided at two or more locations apart from each other around the frame portion.
(34) The locking portion is formed integrally with the locking means, and is in a closed state in which the locking means can be locked with respect to the base end portion or in an open state in which the locking means can be detached from the base end portion. The deaeration-preventing valve device according to (29) or (30), further including a finger-hanging portion that opens and closes.
(35) The endoscope insertion portion according to any one of (29) to (34), wherein the endoscope insertion portion includes a straight pipe portion extending in a thickness direction of the valve body portion. Anti-aeration valve device.
(36) The deaeration-preventing valve device according to any one of (29) to (35), further including a substantially ring-shaped fixing member that fixes the valve body portion to the frame portion.
(37) The deaeration prevention valve device according to any one of (29) to (36), wherein the expansion / contraction means includes a bellows portion.
(38) The degassing prevention according to (37), wherein the bellows part includes a flat inclined part and a folded part between adjacent inclined parts, and the folded part is thinner than the inclined part. Valve device.
(39) The removal according to any one of (29) to (38), wherein a reinforcing member is provided between an outer peripheral edge portion of the endoscope insertion portion and an inner peripheral edge portion of the expansion / contraction means. Qi prevention valve device.
(40) The deaeration prevention valve device according to (39), wherein the reinforcing member is formed in an O-ring shape.
(41) The deaeration prevention valve device according to any one of (29) to (40), wherein an inner diameter of the endoscope insertion portion is equal to or smaller than an outer diameter of the endoscope inserted through the endoscope insertion portion.
11・・・マウスピース本体
12・・・挿通孔
14・・・フレーム部
16・・・伸縮部
17・・・内視鏡挿入部
18・・・脱気防止弁装置
20・・・つまみ部
21・・・係止手段
22・・・係合突起部
23・・・下端部
24・・・係止部
25・・・上端部
26・・・歯受部
28、29、29A・・・被覆部
30・・・凸部
32・・・大径部
34・・・小径部
35・・・被覆部
36・・・長軸
37・・・段差部
38・・・短軸
40・・・外周面
42・・・鍔部
50・・・第二凸部
51、52・・・端面
54・・・係合受部
59・・・固定リング
60・・・閉止栓部
61・・・マウスピース本体
100・・・内視鏡検査用マウスピース
110・・・縮径部
111・・・拡径部
112・・・境界部
112A・・・内円
114・・・山部
116・・・谷部
120・・・蛇腹部
120A・・・外縁
120B・・・内縁
200・・・マウスピース
210・・・裏面
300・・・内視鏡検査用マウスピース
310・・・長軸
311・・・第一長さ
312・・・第一延在部
313・・・外周
314・・・凹部
315・・・外縁
316・・・当接部
320・・・短軸
321・・・第二長さ
322・・・第二延在部
323・・・第一位置決め部
324・・・第二位置決め部
351・・・近位端面
352・・・遠位側面
353・・・凹凸部
414・・・フレーム部
418・・・脱気防止弁装置
420・・・係合受部
421・・・筒部
422・・・嵌合凸部
423・・・穴部
425・・・嵌合凹部
426・・・嵌合留部
501・・・脱気防止弁装置
502・・・係止部
503・・・フレーム部
504・・・マウスピース
505・・・弁体部
506・・・内視鏡挿入部
507・・・固定リング
508・・・伸縮手段
509・・・補強部材
513・・・伸縮部
521・・・係止手段
522・・・指掛け部
523・・・接合部
531・・・固定部
532・・・爪
541・・・拡径部
542・・・内腔
543・・・基端部
544・・・体外部
545・・・鍔部
546・・・口腔内部
547・・・第一開口部
548・・・第二開口部
549・・・カバー
554・・・閉止栓部
562・・・挿通孔
565・・・直管部
582・・・折り返し部
583・・・傾斜部
600・・・脱気防止弁装置
620・・・係止部
630・・・基端部
631・・・溝部
632・・・穴部
633・・・突起部
640・・・マウスピース
650・・・鍔部
A・・・最短距離
 
DESCRIPTION OF SYMBOLS 11 ... Mouthpiece main body 12 ... Insertion hole 14 ... Frame part 16 ... Telescopic part 17 ... Endoscope insertion part 18 ... Deaeration prevention valve apparatus 20 ... Knob part 21 ... Locking means 22 ... Engaging projection 23 ... Lower end 24 ... Locking part 25 ... Upper end 26 ... Tooth receiving part 28, 29, 29A ... Covering part 30 ... convex part 32 ... large diameter part 34 ... small diameter part 35 ... covering part 36 ... major axis 37 ... stepped part 38 ... minor axis 40 ... outer peripheral surface 42 ··· flange 50 ··· second convex portions 51 and 52 ··· end surface 54 ··· engagement receiving portion 59 ··· fixing ring 60 · closure plug portion 61 ··· mouthpiece body 100 ··· ..Endoscopic mouthpiece 110... Diameter reduction part 111... 120 ... Bellows 120A ... Outer edge 120B ... Inner edge 200 ... Mouthpiece 210 ... Back 300 ... Endoscopic examination mouthpiece 310 ... Long axis 311 ... No. One length 312 ... first extension part 313 ... outer periphery 314 ... recess 315 ... outer edge 316 ... contact part 320 ... minor axis 321 ... second length 322 .... Second extension part 323 ... First positioning part 324 ... Second positioning part 351 ... Proximal end face 352 ... Distal side face 353 ... Concave and convex part 414 ... Frame part 418 ... Deaeration prevention valve device 420 ... Engagement receiving part 421 ... Tube part 422 ... Fitting convex part 423 ... Hole part 425 ... Fitting concave part 426 ... Fitting retention 501 ... Deaeration prevention valve device 502 ... Locking part 503 ... Frame part 504 ... Ma Spiece 505 ... Valve body part 506 ... Endoscope insertion part 507 ... Fixing ring 508 ... Telescopic means 509 ... Reinforcing member 513 ... Telescopic part 521 ... Locking means 522 ··· Fingering portion 523 ··· Joint portion 531 ··· Fixing portion 532 ··· Nail 541 · · · Diameter-enlarged portion 542 ··· Lumen 543 · · · Base end portion 544 · · · Body external portion 545鍔 part 546 ... oral cavity 547 ... first opening part 548 ... second opening part 549 ... cover 554 ... closing plug part 562 ... insertion hole 565 ... straight pipe part 582 ... turn-up part 583 ... inclined part 600 ... deaeration prevention valve device 620 ... locking part 630 ... base end part 631 ... groove part 632 ... hole part 633 ... Projection 640 ... mouthpiece 650 ... collar A ... shortest distance

Claims (38)

  1.  内視鏡を挿入抜去自在に挿通する挿通孔を有するマウスピース本体と、
    前記挿通孔に挿通された前記内視鏡と前記マウスピース本体との間を気密に封止する脱気防止弁装置と、
     を有する内視鏡検査用マウスピース。
    A mouthpiece body having an insertion hole through which an endoscope can be inserted and removed freely;
    A deaeration preventive valve device that hermetically seals between the endoscope and the mouthpiece body inserted through the insertion hole;
    A mouthpiece for endoscopy having an endoscope.
  2.  前記脱気防止弁装置は、前記挿通孔に周設されているとともに、前記挿通孔に挿通される前記内視鏡に周着する請求項1に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to claim 1, wherein the deaeration prevention valve device is provided around the insertion hole and is worn around the endoscope inserted through the insertion hole.
  3.  前記脱気防止弁装置は、前記挿通孔に周設された可撓性の伸縮部を有し、
     前記伸縮部が、当該伸縮部の略中央部に設けられ前記内視鏡に周着する内視鏡挿入部を有する請求項1または2に記載の内視鏡検査用マウスピース。
    The deaeration prevention valve device has a flexible expansion and contraction portion provided around the insertion hole,
    The mouthpiece for endoscopy according to claim 1 or 2, wherein the expansion / contraction part has an endoscope insertion part that is provided at a substantially central part of the expansion / contraction part and is worn around the endoscope.
  4.  前記脱気防止弁装置は、前記マウスピース本体に着脱可能に装着されるフレーム部を有する請求項1から3のいずれか一項に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to any one of claims 1 to 3, wherein the deaeration prevention valve device has a frame portion that is detachably attached to the mouthpiece body.
  5.  前記フレーム部が、当該フレーム部を前記マウスピース本体の近位端に係脱可能に係止する係止部を備える請求項4に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to claim 4, wherein the frame portion includes a locking portion that detachably locks the frame portion to a proximal end of the mouthpiece body.
  6.  前記マウスピース本体の遠位端部に設けられた筒状の歯受部と、
     前記歯受部の外周を被覆する被覆部と、を有し、
     前記被覆部の硬度が、前記歯受部の硬度よりも低い請求項1から5のいずれか一項に記載の内視鏡検査用マウスピース。
    A cylindrical tooth receiving portion provided at the distal end of the mouthpiece body;
    A covering portion covering the outer periphery of the tooth receiving portion,
    The mouthpiece for endoscopy as described in any one of Claims 1-5 whose hardness of the said coating | coated part is lower than the hardness of the said tooth receiving part.
  7.  前記被覆部が、前記マウスピース本体に対して脱着可能である請求項6に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to claim 6, wherein the covering portion is detachable from the mouthpiece body.
  8.  前記歯受部が、当該歯受部の遠位端部において径方向の外側に突出する凸部を有するとともに、
     前記被覆部が、内周面側において、小径部および大径部と前記小径部および前記大径部の段差により形成され径が不連続に変化する段差部とを有しており、
     前記凸部と前記段差部とが係合する請求項6または7に記載の内視鏡検査用マウスピース。
    The tooth receiving portion has a convex portion protruding outward in the radial direction at the distal end portion of the tooth receiving portion, and
    The covering portion has, on the inner peripheral surface side, a small-diameter portion and a large-diameter portion, and a step portion that is formed by a step of the small-diameter portion and the large-diameter portion and whose diameter changes discontinuously,
    The mouthpiece for endoscopy according to claim 6 or 7, wherein the convex portion and the stepped portion are engaged with each other.
  9.  前記被覆部は、外周面側において、当該被覆部の遠位端部において径方向の外側に突出する第二凸部を有する請求項6から8のいずれか一項に記載の内視鏡検査用マウスピース。 The endoscopic examination according to any one of claims 6 to 8, wherein the covering portion has a second convex portion projecting radially outward at a distal end portion of the covering portion on the outer peripheral surface side. Mouthpiece.
  10.  前記歯受部が、当該歯受部の遠位端部において径方向の外側に突出する凸部を有するとともに、
     前記被覆部は、外周面側において、当該被覆部の遠位端部において径方向の外側に突出する第二凸部を有し、
     前記凸部の遠位端面に設けられた第一位置決め部と、前記第二凸部の遠位端面に設けられ前記第一位置決め部に対向する第二位置決め部と、を有する請求項6に記載の内視鏡検査用マウスピース。
    The tooth receiving portion has a convex portion protruding outward in the radial direction at the distal end portion of the tooth receiving portion, and
    The covering portion has, on the outer peripheral surface side, a second convex portion protruding outward in the radial direction at the distal end portion of the covering portion,
    The first positioning portion provided on the distal end surface of the convex portion and the second positioning portion provided on the distal end surface of the second convex portion and facing the first positioning portion. Mouthpiece for endoscopy.
  11.  前記被覆部が、外径が長軸と短軸とを有する円筒形であって、
     前記第二凸部は、前記長軸上に第一長さで延在する第一延在部と、前記短軸上に第二長さで延在する第二延在部と、を有し、
     前記第一長さは、前記第二長さよりも大きい請求項9または10に記載の内視鏡検査用マウスピース。
    The covering portion has a cylindrical shape with an outer diameter having a major axis and a minor axis,
    The second convex portion has a first extending portion extending at a first length on the major axis and a second extending portion extending at a second length on the minor axis. ,
    The mouthpiece for endoscopy according to claim 9 or 10, wherein the first length is larger than the second length.
  12.  前記第一長さは、前記第二長さの2倍以上である請求項11に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to claim 11, wherein the first length is at least twice as long as the second length.
  13.  前記第一延在部は、外縁に向かって肉薄に形成されている請求項11または12に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to claim 11 or 12, wherein the first extending portion is formed thin toward the outer edge.
  14.  前記第一延在部の近位側面の外縁が面取りされている請求項11から13のいずれか一項に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to any one of claims 11 to 13, wherein an outer edge of a proximal side surface of the first extension portion is chamfered.
  15.  前記マウスピース本体の遠位端部に設けられた筒状の歯受部を有し、
     前記歯受部の外径が、長軸および短軸を有する請求項1から9のいずれか一項に記載の内視鏡検査用マウスピース。
    It has a cylindrical tooth receiving portion provided at the distal end of the mouthpiece body,
    The mouthpiece for endoscopy according to any one of claims 1 to 9, wherein an outer diameter of the tooth receiving portion has a major axis and a minor axis.
  16.  前記被覆部の内周面に、前記歯受部の外周面に当接する周方向に周回状に連続した凸状の当接部を備える請求項6から14のいずれか一項に記載の内視鏡検査用マウスピース。 The internal view according to any one of claims 6 to 14, further comprising a convex contact portion that is continuous in a circumferential direction in contact with an outer peripheral surface of the tooth receiving portion on an inner peripheral surface of the covering portion. Speculum mouthpiece.
  17.  前記歯受部と、前記当接部との間の気密性が3kPa以上である請求項16に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to claim 16, wherein airtightness between the tooth receiving part and the contact part is 3 kPa or more.
  18.  前記マウスピース本体の遠位端部と近位端部との間には、外周面から外方向に延在する鍔部を有し、
     前記鍔部は、前記歯受部の前記長軸の伸長方向よりも前記短軸の伸長方向に長く延在している請求項15に記載の内視鏡検査用マウスピース。
    Between the distal end portion and the proximal end portion of the mouthpiece body, it has a flange extending outward from the outer peripheral surface,
    The mouthpiece for endoscopy according to claim 15, wherein the collar portion extends longer in the extending direction of the short axis than in the extending direction of the long axis of the tooth receiving portion.
  19.  前記鍔部の長軸方向と、前記第一延在部の延在方向とが直交している請求項18に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to claim 18, wherein the major axis direction of the buttocks and the extending direction of the first extending part are orthogonal to each other.
  20.  前記鍔部は、前記マウスピース本体の遠位端から近位端に向けて凸状に湾曲している請求項18または19に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to claim 18 or 19, wherein the buttocks are curved in a convex shape from the distal end to the proximal end of the mouthpiece body.
  21.  前記マウスピース本体の遠位端部に設けられた筒状の歯受部と、
     前記歯受部の外周を被覆する被覆部と、
     前記マウスピース本体の遠位端部と近位端部との間に、外周面から外方向に延在する鍔部と、を有し、
     前記被覆部の、前記マウスピース本体の遠位端と近位端とを結ぶ方向に沿った長さと、前記鍔部の裏面の基端部から前記マウスピース本体の遠位端までの最短距離と、が同等である請求項1から20のいずれか一項に記載の内視鏡検査用マウスピース。
    A cylindrical tooth receiving portion provided at the distal end of the mouthpiece body;
    A covering portion covering the outer periphery of the tooth receiving portion;
    Between the distal end portion and the proximal end portion of the mouthpiece body, has a flange extending outward from the outer peripheral surface,
    The length of the covering portion along the direction connecting the distal end and the proximal end of the mouthpiece body, and the shortest distance from the base end portion of the back surface of the flange to the distal end of the mouthpiece body The mouthpiece for endoscopy as described in any one of Claims 1-20 which are equivalent.
  22.  前記歯受部の外周を被覆する被覆部を有し、
     前記被覆部の近位端面と、前記鍔部の遠位側面とが、互いに対応する形状である請求項18から21のいずれか一項に記載の内視鏡検査用マウスピース。
    Having a covering portion covering the outer periphery of the tooth receiving portion;
    The mouthpiece for endoscopy according to any one of claims 18 to 21, wherein a proximal end surface of the covering portion and a distal side surface of the flange portion have shapes corresponding to each other.
  23.  前記鍔部の遠位側面と前記被覆部の近位端面とが互いに嵌合し非周回に設けられた凹凸部を有する請求項22に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to claim 22, wherein the distal side surface of the buttocks and the proximal end surface of the covering portion are fitted to each other and have an uneven portion provided non-circularly.
  24.  前記挿通孔が、前記マウスピース本体の近位端から遠位端に向けて、縮径部と拡径部とを有するくびれ形状である請求項1から23のいずれか一項に記載の内視鏡検査用マウスピース。 The internal view according to any one of claims 1 to 23, wherein the insertion hole has a constricted shape having a reduced diameter portion and an enlarged diameter portion from a proximal end to a distal end of the mouthpiece body. Speculum mouthpiece.
  25.  前記脱気防止弁装置は、前記挿通孔に周設された可撓性の伸縮部を有するとともに、前記伸縮部が、当該伸縮部の略中央部に設けられ前記内視鏡に周着する内視鏡挿入部を有し、
     前記伸縮部は、環状の前記内視鏡挿入部と同心であって、径方向に山部と谷部とが設けられてなる環状の蛇腹部を有し、
     前記蛇腹部が、前記縮径部と前記拡径部との境界である境界部で囲まれる内円と同軸で配置され、かつ、前記蛇腹部の外縁の径は、前記内円の径よりも大きい請求項1から24のいずれか一項に記載の内視鏡検査用マウスピース。
    The deaeration prevention valve device includes a flexible expansion / contraction portion that is provided around the insertion hole, and the expansion / contraction portion is provided in a substantially central portion of the expansion / contraction portion and is attached to the endoscope. Having an endoscope insertion part,
    The telescopic part is concentric with the annular endoscope insertion part, and has an annular bellows part in which a peak part and a valley part are provided in a radial direction,
    The bellows portion is arranged coaxially with an inner circle surrounded by a boundary portion that is a boundary between the reduced diameter portion and the enlarged diameter portion, and the outer edge diameter of the bellows portion is larger than the diameter of the inner circle. The mouthpiece for endoscopy according to any one of claims 1 to 24, which is large.
  26.  前記蛇腹部の内縁の径が、前記内円の径よりも小さい請求項25に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to claim 25, wherein a diameter of an inner edge of the bellows portion is smaller than a diameter of the inner circle.
  27.  前記脱気防止弁装置と、前記マウスピース本体との間の気密性が3kPa以上である請求項1から26のいずれか一項に記載の内視鏡検査用マウスピース。 The mouthpiece for endoscopy according to any one of claims 1 to 26, wherein an airtightness between the deaeration prevention valve device and the mouthpiece body is 3 kPa or more.
  28.  内視鏡を挿入抜去自在に挿通する内腔を有する口腔内に挿入されるマウスピースの基端部に対して着脱自在に装着される、内視鏡用マウスピースに用いられる脱気防止弁装置であって、
     前記マウスピースの前記基端部の外周面又は内周面に装着されるフレーム部と、
     前記フレーム部に設けられて前記基端部の前記外周面又は内周面に係脱可能に係止する係止部と、
     前記フレーム部の内側に設けられた弁体部と、
    を有し、
     前記弁体部は、
     前記弁体部の略中央部に設けられて前記内視鏡に周着する環状の内視鏡挿入部と、
     前記内視鏡挿入部に周設された可撓性の伸縮手段と、
     を有していることを特徴とする脱気防止弁装置。
    A deaeration prevention valve device used for an endoscope mouthpiece, which is detachably attached to a proximal end portion of a mouthpiece inserted into an oral cavity having a lumen through which an endoscope can be inserted and removed. Because
    A frame portion attached to an outer peripheral surface or an inner peripheral surface of the base end portion of the mouthpiece;
    A locking portion provided on the frame portion and detachably locked to the outer peripheral surface or inner peripheral surface of the base end portion;
    A valve body provided inside the frame part;
    Have
    The valve body is
    An annular endoscope insertion portion that is provided at a substantially central portion of the valve body portion and is attached to the endoscope;
    Flexible telescopic means provided around the endoscope insertion portion;
    The deaeration prevention valve device characterized by having.
  29.  前記係止部は、前記フレーム部の内側又は外側に向かって突き出した係止手段によって、前記基端部の前記外周面又は内周面に係脱可能に係止するものである請求項28に記載の脱気防止弁装置。 29. The locking portion according to claim 28, wherein the locking portion is detachably locked to the outer peripheral surface or the inner peripheral surface of the base end portion by a locking means protruding toward the inner side or the outer side of the frame portion. The deaeration prevention valve device as described.
  30.  前記係止部は、前記フレーム部の周囲に互いに離間して二箇所以上に設けられている請求項28又は29に記載の脱気防止弁装置。 30. The deaeration prevention valve device according to claim 28 or 29, wherein the locking portions are provided at two or more locations apart from each other around the frame portion.
  31.  前記係止部は、前記基端部の前記外周面に係止し、
     前記係止部は、前記係止手段と一体に形成されて、前記係止手段を前記基端部に対して係止可能な閉状態または前記基端部から脱離可能な開状態に開閉操作する指掛け部をさらに有する請求項28~30のいずれか一項に記載の脱気防止弁装置。
    The locking portion is locked to the outer peripheral surface of the base end portion,
    The locking portion is formed integrally with the locking means, and is opened and closed in a closed state in which the locking means can be locked with respect to the base end portion or in an open state in which the locking means can be detached from the base end portion. The deaeration prevention valve device according to any one of claims 28 to 30, further comprising a finger hooking portion.
  32.  前記内視鏡挿入部は、前記弁体部の厚み方向に延在する直管部を有していることを特徴とする請求項28から31のいずれか一項に記載の脱気防止弁装置。 The deaeration prevention valve device according to any one of claims 28 to 31, wherein the endoscope insertion portion has a straight pipe portion extending in a thickness direction of the valve body portion. .
  33.  前記弁体部を前記フレーム部に固定する略リング状の固定部材を有している請求項28から32のいずれか一項に記載の脱気防止弁装置。 The deaeration prevention valve device according to any one of claims 28 to 32, further comprising a substantially ring-shaped fixing member that fixes the valve body portion to the frame portion.
  34.  前記伸縮手段は、蛇腹部を含むものである請求項28から33のいずれか一項に記載の脱気防止弁装置。 The deaeration prevention valve device according to any one of claims 28 to 33, wherein the expansion / contraction means includes a bellows portion.
  35.  前記蛇腹部は、平坦な傾斜部および隣接する傾斜部同士の間の折り返し部で構成され、前記折り返し部が前記傾斜部に比べて肉薄である請求項34に記載の脱気防止弁装置。 35. The deaeration prevention valve device according to claim 34, wherein the bellows part includes a flat inclined part and a folded part between adjacent inclined parts, and the folded part is thinner than the inclined part.
  36.  前記内視鏡挿入部の外周縁部と、前記伸縮手段の内周縁部との間に補強部材を有している請求項28から35のいずれか一項に記載の脱気防止弁装置。 36. The deaeration prevention valve device according to any one of claims 28 to 35, further comprising a reinforcing member between an outer peripheral edge portion of the endoscope insertion portion and an inner peripheral edge portion of the expansion / contraction means.
  37.  前記補強部材がOリング状に形成されている請求項36に記載の脱気防止弁装置。 The deaeration prevention valve device according to claim 36, wherein the reinforcing member is formed in an O-ring shape.
  38.  前記内視鏡挿入部の内径は、これに挿通される前記内視鏡の外径以下である請求項28から37のいずれか一項に記載の脱気防止弁装置。 38. The deaeration prevention valve device according to any one of claims 28 to 37, wherein an inner diameter of the endoscope insertion portion is equal to or smaller than an outer diameter of the endoscope inserted through the endoscope insertion portion.
PCT/JP2014/076947 2013-10-10 2014-10-08 Mouthpiece for endoscopic examination and de-aeration prevention valve device WO2015053313A1 (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
JP2013212484 2013-10-10
JP2013-212462 2013-10-10
JP2013212462 2013-10-10
JP2013-212484 2013-10-10
JP2014091182 2014-04-25
JP2014-091182 2014-04-25

Publications (1)

Publication Number Publication Date
WO2015053313A1 true WO2015053313A1 (en) 2015-04-16

Family

ID=52813128

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2014/076947 WO2015053313A1 (en) 2013-10-10 2014-10-08 Mouthpiece for endoscopic examination and de-aeration prevention valve device

Country Status (2)

Country Link
JP (1) JP6428127B2 (en)
WO (1) WO2015053313A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108882833A (en) * 2016-06-14 2018-11-23 日本光电工业株式会社 Sting block and gas sensor external member
CN114557733A (en) * 2022-02-28 2022-05-31 常州市久虹医疗器械有限公司 Biopsy valve for endoscope

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3714764A4 (en) 2017-12-28 2021-06-30 Allis Inc. Oral photographing apparatus, medical apparatus, and program
KR102461698B1 (en) * 2021-02-26 2022-11-01 김기명 the oral cavity cleaner for gastrofiberscope
KR102513633B1 (en) * 2021-02-26 2023-03-24 성도윤 the oral cavity cleaner for gastrofiberscope
KR102330589B1 (en) * 2021-04-01 2021-11-23 김기명 the oral cavity cleaner with elastic plate for gastrofiberscope

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0975303A (en) * 1995-09-12 1997-03-25 Fuji Photo Optical Co Ltd Mouthpiece or medical treatment
JP2000237125A (en) * 1999-02-22 2000-09-05 Fuji Photo Optical Co Ltd Mouthpiece for endoscope
JP2008220794A (en) * 2007-03-15 2008-09-25 Top:Kk Overtube for endoscope
JP2008289520A (en) * 2007-05-22 2008-12-04 Top:Kk Mouthpiece for endoscope

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5810561Y2 (en) * 1978-09-14 1983-02-26 オリンパス光学工業株式会社 Mouthpiece for endoscope
JPS5915606Y2 (en) * 1979-04-07 1984-05-09 富士写真光機株式会社 Mouthpiece for oral endoscopy
JPH0751221A (en) * 1993-08-18 1995-02-28 Sumitomo Bakelite Co Ltd Guide tube
JP2002065589A (en) * 2000-08-30 2002-03-05 Olympus Optical Co Ltd Endoscope device
CN101980654B (en) * 2008-03-24 2013-08-07 住友电木株式会社 De-aeration prevention valve unit for an overtube
JP5221194B2 (en) * 2008-04-17 2013-06-26 高史 豊永 Endoscope deaeration prevention valve
JP5678439B2 (en) * 2010-03-09 2015-03-04 住友ベークライト株式会社 Attachment for preventing deaeration, overtube and overtube set equipped with the attachment
JP5751515B2 (en) * 2011-08-19 2015-07-22 国立大学法人 香川大学 Endoscope insertion aids

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0975303A (en) * 1995-09-12 1997-03-25 Fuji Photo Optical Co Ltd Mouthpiece or medical treatment
JP2000237125A (en) * 1999-02-22 2000-09-05 Fuji Photo Optical Co Ltd Mouthpiece for endoscope
JP2008220794A (en) * 2007-03-15 2008-09-25 Top:Kk Overtube for endoscope
JP2008289520A (en) * 2007-05-22 2008-12-04 Top:Kk Mouthpiece for endoscope

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
RIEKO NAKAMURA: "Inkoto Hyozai Gan Screening Kensa no Kufu -Aratana Koto Tenkaiho", GASTROENTEROLOGICAL ENDOSCOPY, vol. 54, no. 2, 2012, pages 2829 *
TAI OMORI: "Inkoto no Naishikyo Kansatsu -Kohen", 13 February 2013 (2013-02-13), Retrieved from the Internet <URL:https://mdplus.medy-id.jp/?m=d&cid=003sy&n=>> *
TAKESHI TAKAHASHI: "Keiko Naishikyo Kensa ni Okeru Aratana Into Tenkaiho (Mouthpiece-ho to Kuchi Subome-ho", GASTROENTEROLOGICAL ENDOSCOPY, vol. 54, no. SUPPLE, 2012, pages 1062 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108882833A (en) * 2016-06-14 2018-11-23 日本光电工业株式会社 Sting block and gas sensor external member
CN108882833B (en) * 2016-06-14 2021-08-13 日本光电工业株式会社 Bite block and gas sensor kit
US11766533B2 (en) 2016-06-14 2023-09-26 Nihon Kohden Corporation Bite block and gas sensor kit
CN114557733A (en) * 2022-02-28 2022-05-31 常州市久虹医疗器械有限公司 Biopsy valve for endoscope

Also Published As

Publication number Publication date
JP2015213733A (en) 2015-12-03
JP6428127B2 (en) 2018-11-28

Similar Documents

Publication Publication Date Title
JP6428127B2 (en) Mouthpiece for endoscopy
US6589167B1 (en) Valve and valved trocar jacket tube
JP6785355B2 (en) Airway adapter and suction catheter system
JP2957134B2 (en) Valve and valved trocar mantle
CN101396309B (en) Surgical portal with gel and fabric seal assembly
EP2020901B1 (en) Endoscopic sleeve seal
US9131831B2 (en) Integrated locking device with passive sealing
JP5490733B2 (en) Instrument seal
US7749161B2 (en) Hand assisted laparoscopic device
EP3313489B1 (en) Positive pressure mask and related adapters and applicances
JP5120449B2 (en) Degassing prevention valve unit for overtube
TW201726201A (en) Artificial airway device
JP5383312B2 (en) Duckbill valve
EP2323540B1 (en) Integrated locking device with fluid control
US20080249371A1 (en) Hand assisted laparoscopic seal assembly with detachable attachment ring
CA2632369A1 (en) Access apparatus with shallow zero closure valve
JP6337438B2 (en) Endoscope mouthpiece
JP6225627B2 (en) Endoscope mouthpiece
JP5678439B2 (en) Attachment for preventing deaeration, overtube and overtube set equipped with the attachment
JP3957151B2 (en) Endoscopy forceps plug
CN210541853U (en) Endoscope clamp channel sealing element
US20230082888A1 (en) Endoscope mouthpiece, drape adapter, and endoscope mouthpiece disposal method
CN113940616A (en) Device with lip pharynx protection and biological aerosol prevention for endoscope diagnosis and treatment
TWM338639U (en) Closed structure of catheter needle for preventing air from escaping
JP2009183432A (en) Biopsy port of endoscope

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 14851466

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 14851466

Country of ref document: EP

Kind code of ref document: A1