WO2019189400A1 - External tube member for endoscope - Google Patents

External tube member for endoscope Download PDF

Info

Publication number
WO2019189400A1
WO2019189400A1 PCT/JP2019/013260 JP2019013260W WO2019189400A1 WO 2019189400 A1 WO2019189400 A1 WO 2019189400A1 JP 2019013260 W JP2019013260 W JP 2019013260W WO 2019189400 A1 WO2019189400 A1 WO 2019189400A1
Authority
WO
WIPO (PCT)
Prior art keywords
endoscope
tube
distal end
needle
mounting
Prior art date
Application number
PCT/JP2019/013260
Other languages
French (fr)
Japanese (ja)
Inventor
駿佑 川瀬
Original Assignee
日本ゼオン株式会社
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 日本ゼオン株式会社 filed Critical 日本ゼオン株式会社
Priority to JP2020509213A priority Critical patent/JP7251543B2/en
Publication of WO2019189400A1 publication Critical patent/WO2019189400A1/en

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor

Definitions

  • the present invention relates to an endoscope external tube member that is used by being attached to the outside of an endoscope as necessary.
  • a suturing device for suturing an incision (including a perforation or a defect) formed in a body tissue such as a digestive tract
  • the thing of patent document 1 is proposed.
  • the suturing device is provided at a sheath portion (arm moving means) disposed along the endoscope shaft, an operation portion provided at a proximal end of the sheath portion, and a distal end of the sheath portion.
  • the stitching portion front arm and rear arm is generally provided.
  • the sheath portion includes a wire for relatively moving the needle of the suture portion and a member on which the suture is supported, and a sheath through which the wire is inserted, and the sheath portion is detachably attached to the endoscope.
  • An external tube member for an endoscope is provided.
  • the external tube member for endoscope is provided integrally with the tube through which the sheath is slidably inserted and the distal end portion of the tube, and the distal end portion of the shaft of the endoscope is press-fitted.
  • the tube is configured to include a single endoscope mounting portion (cylindrical fixing portion) formed in a substantially cylindrical shape for removably fixing the distal end portion of the tube to the endoscope. .
  • the endoscope external tube member has only one endoscope mounting portion and is low in versatility, and therefore, a plurality of types in which the inner diameters of the endoscope mounting portions are different from each other. It is necessary to select and use an endoscope external tube member having an endoscope mounting portion that matches the outer diameter of the endoscope to be used or a suturing device having the tube member. Met.
  • the present invention has been made in view of such a situation, and an object thereof is to provide an external tube member for an endoscope that can improve versatility.
  • an endoscope external tube member includes: An external tube member for an endoscope that is attached to the outside of an endoscope as needed, A tube disposed from the proximal end to the distal end of the endoscope; A plurality of endoscope mounting portions each having a substantially cylindrical shape, each provided at a distal end portion of the tube and having different diameters of lumens into which the endoscope is inserted.
  • the external tube member for an endoscope has a plurality of endoscope mounting portions in which the inner diameter of the portion into which the endoscope is inserted is different from each other, so that it is inserted into the endoscope mounting portion. It is possible to adapt to a plurality of types of endoscopes having different outer diameters at the distal end portion, and improve versatility.
  • the endoscope mounting portion can be individually separated from the tube. By selectively separating and removing the endoscope mounting portion other than the endoscope mounting portion that matches the endoscope to be used, it is possible to prevent the procedure from being hindered.
  • the lumen of the endoscope mounting portion can be tapered so as to expand in the direction in which the endoscope is inserted.
  • FIG. 1A is a front view showing a configuration of an operation unit of the suturing device according to the embodiment of the present invention.
  • FIG. 1B is a front view showing a configuration of a suturing portion of the suturing device according to the embodiment of the present invention.
  • FIG. 2A is a perspective view showing a configuration of an endoscope external tube member having the case tube and the mounting adapter shown in FIG. 1B.
  • 2B is a cross-sectional view taken along the line IIb-IIb in FIG. 2A.
  • FIG. 2C is a cross-sectional view showing a configuration obtained by changing a part of the configuration of FIG. 2B.
  • FIG. 1A is a front view showing a configuration of an operation unit of the suturing device according to the embodiment of the present invention.
  • FIG. 1B is a front view showing a configuration of a suturing portion of the suturing device according to the embodiment of the present invention.
  • FIG. 2A is a perspective view showing a
  • FIG. 3A is a diagram illustrating a procedure of a procedure (suture) performed using the suturing device according to the embodiment of the present invention, and is a diagram illustrating a first step.
  • FIG. 3B is a diagram showing a second step subsequent to FIG. 3A.
  • FIG. 3C is a diagram showing a third step subsequent to FIG. 3B.
  • FIG. 3D is a diagram showing a fourth step that follows FIG. 3C.
  • FIG. 3E is a diagram showing a fifth step subsequent to FIG. 3D.
  • FIG. 3F is a diagram showing a sixth step that follows FIG. 3E.
  • FIG. 3G is a diagram showing a seventh step that follows FIG. 3F.
  • FIG. 3H is a diagram showing an eighth step that follows FIG. 3G.
  • FIG. 3I is a diagram showing a ninth step that follows FIG. 3H.
  • FIG. 3J is a diagram showing a tenth process continued from FIG. 3I.
  • a suturing device including an external tube member for an endoscope to which the present invention is applied will be described in detail with reference to the drawings.
  • the present invention can be applied not only to the endoscope external tube member provided in the suturing apparatus but also to the endoscope external tube member provided in other medical instruments.
  • the present invention is used for introducing various treatment tools (forceps, dilator, high-frequency knife, clip device, ligation device, etc.), or for injecting or aspirating fluid (chemical solution, etc.), for example,
  • a tube arranged along the endoscope such as “impact shooter (trade name)” sold by Top, and a distal end of the endoscope provided at the distal end of the tube It can also be used as a medical instrument having a generally cylindrical tip hood (endoscope mounting portion) to be press-fitted.
  • the suturing device 1 is a device that is inserted into the body while being attached along the outside of an endoscope (soft endoscope) 2, while being visually recognized by a camera (not shown) of the endoscope 2.
  • This is a device for suturing an incision part (including a defect part or a perforation part) formed in an organ or digestive tract by an operation outside the body.
  • the suturing device 1 is provided at a sheath portion 3 disposed along the shaft of the endoscope 2, an operation portion (handle) 4 provided at the proximal end of the sheath portion 3, and a distal end of the sheath portion 3.
  • the sewing part 5 is generally provided.
  • the sheath part 3 is a long member extending along the axial direction, and has two tubes and one wire (or one having flexibility enough to follow the bending of the shaft of the endoscope 2). 3 tubes). That is, the sheath portion 3 is configured to include a front arm moving wire 31, a rear arm moving tube 32, and a case tube (tube) 33.
  • the front arm moving wire 31 is made of a flexible wire, and is slidably inserted into the rear arm moving tube 32.
  • the front arm moving wire 31 moves along the axial direction of the rear arm moving tube 32 and around the axis. It is provided so that it can rotate.
  • a wire rope is used in this embodiment.
  • the wire rope is a rope made of a stranded wire formed by twisting a plurality of wires made of metal (stainless steel) or the like in a spiral shape.
  • the wire 31 may be a single wire. Further, a hollow tube may be used instead of the wire 31.
  • the rear arm moving tube 32 is a hollow tube that is slidably inserted into the case tube 33, and is provided in the case tube 33 so as to move along the axial direction and rotate about the axis.
  • the rear arm moving tube 32 has flexibility and may be a tube made of resin or the like, but in this embodiment, a coil tube having excellent durability is used.
  • As the coil tube a flat wire coil tube formed by spirally winding a long flat plate made of metal (stainless steel) or the like can be used. However, a round wire coil tube or an inner flat coil tube may be used.
  • the wire tube may be used as the rear arm moving tube 32.
  • the wire tube is a tube formed by spirally twisting a plurality of wires made of, for example, metal (stainless steel) or the like.
  • the rear arm moving tube 32 may be a uniform member (for example, a coil tube) from the proximal end to the distal end, but in this embodiment, the distal end of the coil tube is substantially made of a rigid metal.
  • a cylindrical member is fixed by welding to form a distal end portion (tube distal end portion) 32a of the rear arm moving tube 32.
  • the case tube 33 is a hollow tube disposed along the distal end of the endoscope 2 from the proximal end to the distal end, and is formed of a flexible material made of resin or the like.
  • the proximal ends of the front arm moving wire 31 and the rear arm moving tube 32 are connected to the operation unit 4, and the distal ends of the front arm moving wire 31 and the rear arm moving tube 32 are connected to the suture unit 5. Yes.
  • the proximal end of the case tube 33 reaches the vicinity of the operation unit 4, but is not connected to the operation unit 4, and the distal end of the case tube 33 reaches the vicinity of the suture unit 5, It is not connected to the stitched portion 5.
  • the case tube 33 can be formed of a material such as polyethylene or polyvinyl chloride, for example.
  • the mounting adapter 34 is integrally attached to the distal end portion of the case tube 33 as shown in FIGS. 2A and 2B.
  • the case tube 33 and the mounting adapter 34 correspond to the endoscope external tube member according to the present invention.
  • the mounting adapter 34 has a tube mounting portion 34a, an endoscope mounting portion 34b, and an endoscope mounting portion 34c each formed in a substantially cylindrical shape.
  • the mounting adapter 34 is fixed to the distal end portion of the case tube 33 by inserting the distal end portion of the case tube 33 into the tube mounting portion 34a and fixing the mounting adapter 34 by bonding or fusion.
  • the endoscope mounting part 34b and the endoscope mounting part 34c are arranged on both sides with the tube mounting part 34a interposed therebetween.
  • the mounting adapter 34 is integrally formed as a whole by injection molding.
  • at least one of the tube mounting portion 34a, the endoscope mounting portion 34b, and the endoscope mounting portion 34c and the remaining portion may be formed independently of each other, and then integrated with each other by adhesion, fusion, or the like. .
  • the endoscope mounting part 34b and the endoscope mounting part 34c are respectively substantially cylindrical portions into which the distal end portion of the endoscope shaft is press-fitted and fixed.
  • the inner diameter of the endoscope mounting portion 34b and the inner diameter of the endoscope mounting portion 34c are different from each other.
  • the endoscope mounting portion 34b has a relatively large diameter (thick diameter).
  • the endoscope mounting portion 34c is set to have a relatively small diameter (thin diameter) distal end portion so as to be adapted to an endoscope having a distal end portion.
  • a relatively small inner diameter is set to fit the mirror.
  • the endoscope mounting part 34b has a large size (large diameter inner diameter).
  • the character “L” indicating that the attachment portion is for the endoscope) is displayed on the endoscope attachment portion 34c, and the character “S” indicating that the attachment portion is for the small size (small diameter endoscope) is displayed on the endoscope attachment portion 34c.
  • identification characters may be formed by printing or stamping after the mounting adapter 34 is formed, or may be formed integrally so as to be concave or convex at the time of injection molding.
  • characters other than these characters, a symbol, a figure, etc. may be sufficient.
  • the endoscope mounting part 34b and the endoscope mounting part 34c can be separated from the tube mounting part 34a. That is, the joint portion of the endoscope attachment portion 34b and the endoscope attachment portion 34c to the tube attachment portion 34a can be cut using a medical cutter (a surgical knife or the like may be substituted). It has become. You may comprise so that it can cut
  • the endoscope attachment portions 34b and 34c are easy to press-fit when attached to the endoscope, and are preferably difficult to come off after attachment.
  • a material for forming the attachment adapter 34 a polyether block amide copolymer or the like is used.
  • a flexible thermoplastic elastomer or the like can be used.
  • the endoscope attachment portion 34b is selected when a large-diameter endoscope is used, and when the small-diameter endoscope is used.
  • the endoscope attachment part 34c is selected, and the endoscope is inserted into the lumen of the selected endoscope attachment part (here, the endoscope attachment part 34c is selected as a small-diameter endoscope). Press fit the distal end of the mirror.
  • a lubricant such as xylocaine jelly is used in order to reduce friction and enable smooth work or to improve the mounting reliability. Then, after applying to one or both of the distal end portion of the endoscope and the lumen of the selected endoscope mounting portion 34b, press-fitting is performed.
  • the lumens of the endoscope mounting portions 34b and 34c are arranged from the proximal end side (upstream side) to the distal end side (downstream side) with respect to the insertion direction A of the endoscope.
  • the taper is reduced in diameter from the proximal end side (upstream side) to the distal end side (downstream side) along the insertion direction A of the endoscope. It is good also as (taper taper shape). However, with such a taper taper shape, the distal end portion of the endoscope can be easily detached from the endoscope mounting portion 34b or 34c by the action of the taper. It is preferable to do.
  • the longitudinal dimension (axial direction) dimension L1 of the endoscope mounting part 34b can be set in the range of 5 to 15 mm.
  • the dimension L2 in the longitudinal direction (axial direction) of the endoscope mounting portion 34c can be set in the range of 5 to 15 mm. In the present embodiment, these dimensions L1 and L2 are set to the same value. However, they may be different from each other.
  • the inner diameter d1 of the endoscope mounting portion 34b is in the range of 12 to 15 mm
  • the inner diameter d2 of the endoscope mounting portion 34c is in the range of 9 to 12 mm. Can be set.
  • the lumen has a tapered shape (see FIG.
  • the inner diameter on the small diameter side of the endoscope mounting portion 34b is in the same range as d1 described above, and the inner diameter d3 on the large diameter side is d1 + (0.5 Can be set within a range of up to 3.0) mm, the inner diameter of the endoscope mounting portion 34c is in the same range as d2, and the inner diameter d4 of the large diameter side is d2 + (0.5 Can be set in a range of up to 3.0) mm.
  • the outer diameter D1 of the endoscope mounting portion 34b can be set in a range of d1 + (0.5 to 1.5) mm.
  • the outer diameter D2 of the endoscope mounting portion 34c can be set in a range of d2 + (0.5 to 1.5) mm.
  • the suturing device 1 By inserting the distal end portion of the shaft of the endoscope 2 into the endoscope mounting portion 34b or 34c of the mounting adapter 34, the suturing device 1 can be detachably fixed to the endoscope 2. It has become. Note that the case tube 33 may be fixed along the shaft by winding an attachment tape (not shown) at a plurality of locations at appropriate intervals around the shaft of the endoscope.
  • the entire suture unit 5 is moved with respect to the endoscope 2, and the operation unit 4 is moved. Is rotated about its axis with respect to the case tube 33, so that the entire suture portion 5 can be rotated.
  • the suturing portion 5 of the suturing apparatus 1 is configured as shown in FIG. 1B. That is, the suture part 5 includes a front arm 51 to which the suture thread 6 is attached and a rear arm 52 having a needle-like member 52a.
  • the rear arm 52 has a needle-like member 52a, a needle support portion 52b, and a rear guide portion 52c.
  • the rear guide portion 52c is made of a substantially cylindrical member, and one end of a substantially strip-shaped needle support portion 52b is fixed to the upper end side of the rear guide portion 52c.
  • the proximal end portion of the needle-like member 52a is fixed to the other end of the needle support portion 52b so as to be directed forward (distal end side).
  • the needle-like member 52a, the needle support portion 52b, and the rear guide portion 52c are made of, for example, a metal such as stainless steel, and are formed as separate parts, and then fixed integrally with each other by laser welding or the like. Yes.
  • the rear end surface (the end surface on the proximal end side) of the rear guide portion 52c is integrally fixed to the distal end portion 32a of the rear arm moving tube 32 by laser welding or the like.
  • the rear guide portion 52c is inserted inside a front guide portion 53, which will be described later, and is held so as to be slidable along the axial direction and rotatable about the axis.
  • the needle-like member 52a has a straight barrel-shaped ligature attachment portion, a tapered tapered central shaft portion, and a straight barrel-shaped tissue from the proximal end side (needle support portion 52b side) to the distal end side (open end side). It has a penetrating part and a twisting part.
  • a ligation tool 7 for ligating the suture thread 6 is detachably mounted on the ligation tool mounting portion of the needle-like member 52a.
  • the tapping portion is a tapered, generally conical portion whose tip is sharply formed so as to be able to pierce the body tissue, and the outer diameter of the maximum diameter portion of the proximal end is larger than the outer diameter of the tip of the tissue penetrating portion. And is formed so that there is a slight step (barbing) at the connection portion with the tissue penetrating portion.
  • the needle-like member 52a has a base end at the needle support portion 52b so that the tip end thereof (the edge portion) faces the front arm 51 and the center axis thereof is substantially parallel to the center axis of the rear guide portion 52c. Is fixed to the needle support portion 52b. If the rear arm moving tube 32 is rotated around its central axis, the needle-like member 52a is moved to the tip 32a while the central axis of the needle-like member 52a is maintained substantially parallel to the central axis of the tip 32a. It can be rotated (turned) around the central axis.
  • the ligation tool 7 that is detachably attached to the base end portion (ligation tool attachment portion) of the needle-like member 52a has a tightening tube 7a and a main body portion.
  • the main body portion is a connection loop 7b to which a ligation device (not shown) is connected, a ligation loop 7c through which a suture thread 6 to be described later is passed, and an abbreviation for connecting these connection loop 7b and ligation loop 7c.
  • the fastening tube 7a is slidably fitted to the connecting portion.
  • the tightening tube 7a is made of a substantially cylindrical member made of a material having elasticity, and is slid toward the ligation loop 7c so that the ligation loop 7c is drawn into the inner cavity thereof.
  • the ligation loop 7c is used as a locking means for locking a part of the ligation loop 7c so that the ligation loop 7c is not drawn too far into the lumen of the tightening tube 7a and comes out of the tightening tube 7a. 7d.
  • the ligature tool 7 is detachably mounted on the needle-shaped member 52 by inserting (pressing) the proximal end portion (ligation tool mounting portion) of the needle-shaped member 52a into the ligation loop 7c.
  • the coupling loop 7b is gripped by a ligation device (not shown) and moved (pushed down) to the distal end side of the needle-like member 52a.
  • the fastening tube 7a is slid toward the ligating loop 7c so that the ligating loop 7c is pulled into the fastening tube 7a (or the connecting loop 7b with respect to the fastening tube 7a). Pull).
  • a part of the ligation loop 7c and the locking part 7d are press-fitted into the fastening tube 7a together with the suture thread 6, and the end part opposite to the connection part of the ligation loop 7c (the locking part 7d is provided).
  • the drawn portion is pulled to the middle portion in the fastening tube 7a, and the suture thread 6 is ligated.
  • the front arm 51 includes a pair of yarn support portions 51 a and 51 a and a front guide portion 53.
  • the pair of thread support portions 51a and 51a is formed in a substantially V shape (which may be an arc shape, a U shape, a U shape, etc.) and has a bifurcated shape.
  • the suture thread 6 is attached so as to extend between the vicinity of the respective distal end portions. Engagement members 6a and 6b formed in an annular shape are attached to both ends of the suture thread 6, respectively.
  • a through hole (not shown) penetrating over the front surface (distal end side surface) and the rear surface (proximal end side surface) is formed at the tip of each of the yarn support portions 51a and 51a of the front arm 51.
  • An accommodation space (not shown) in which the engagement members 6a and 6b can be engaged is formed on the rear surface side of the through hole.
  • the accommodation space has a diameter slightly larger than that of the through-hole, and the through-hole through which the engaging members 6a and 6b penetrate the front and back are substantially concentric with the through-hole of the yarn support portions 51a and 51a.
  • the diameter is set such that the inner wall can be detachably engaged with the inner wall.
  • the through-holes of the engaging members 6a and 6b can be inserted through the twisted portion of the needle-shaped member 52a. However, when the twisted portion is completely inserted through the through-hole, the engaging members 6a and 6b are moved from the needle-shaped member 52a. It has a structure that does not fall out.
  • the distal end of the front arm moving wire 31 is integrally fixed to the front arm 51 by laser welding or the like via a guide shaft (not shown).
  • the front side guide part 53 is comprised from the substantially cylindrical member.
  • a notch 53 a is formed in the upper part of the front side of the front guide part 53.
  • a penetration guide is formed extending in the vertical direction (direction substantially parallel to the central axis) and penetrating inward and outward.
  • Grooves 53b and 53b are formed. These penetration guide grooves 53b and 53b are portions in which the needle support portion 52b of the rear arm 52 is slidably fitted in either of them to guide the slide in the central axis direction of the rear arm 52. It is.
  • the upper ends (rear ends) of the through guide grooves 53b and 53b reach the bottom side of the notch 53a, and the lower ends (front ends) do not reach the lower portion (front end) of the front guide portion 53.
  • the positions of the lower ends (front ends) of the penetration guide grooves 53b and 53b are such that when the needle support portion 52b of the front arm 51 is fitted and reaches the lower end, the rear end of the needle portion of the needle-like member 52a is sewn.
  • the thread 6 is set at a position where it can be engaged through the engaging member 6a or 6b.
  • the operation unit (handle) 4 of the suturing device 1 is configured as shown in FIG. 1A.
  • the operation unit 4 includes a slider unit 41 and a base unit 42.
  • the slider part 41 is slidably provided on the base part 42, and the slider part 41 moves to the base end (distal end) side and the base end (proximal end) side with respect to the base part 42. It is possible to move to two positions.
  • the slider part 41 is a cylindrical part 41a having a substantially cylindrical shape on the distal end side, and the distal end is fixed to the cylindrical part 41a on the proximal end side.
  • a grip member 41b is provided.
  • the cylindrical portion 41a of the slider portion 41 is formed with a substantially cylindrical wire insertion hole (not shown) that opens at the distal end thereof and extends along the axial center thereof. The portion on the proximal end side is connected and fixed to the cylindrical portion 41 a of the slider portion 41.
  • the base portion 42 is formed of a substantially cylindrical member formed by joining a pair of substantially symmetric half members by a plurality of screws or the like (not shown), and opens at a proximal end thereof. It has a substantially cylindrical slider portion insertion hole (not shown) extending along. By inserting the cylindrical portion 41a of the slider portion 41 into the slider portion insertion hole, the slider portion 41 can be slid along the axis and can rotate about the axis with respect to the base portion. It is attached.
  • the base portion 42 has a substantially cylindrical tube insertion hole (not shown) that opens at the distal end thereof and extends along the axis thereof, and the rear arm moving tube is formed in the tube insertion hole.
  • the proximal end side of the rear arm moving tube 32 is connected and fixed to the base portion 42.
  • an attaching operation for attaching the suturing device 1 to the endoscope 2 is performed. That is, according to the outer diameter of the distal end portion (tip portion) of the shaft of the endoscope 2 used for the procedure, the endoscope mounting portion 34b or 34c having an inner diameter suitable for this is selected.
  • the endoscope mounting portion 34b or 34c having an inner diameter suitable for the endoscope 2 is selected.
  • the endoscope mounting part 34b other than the selected endoscope mounting part 34c is cut and removed by using a cutter or the like or by tearing.
  • a lubricant is applied to the distal end portion of the endoscope 2 and / or the lumen of the endoscope mounting portion 34c, and the distal end portion of the endoscope 2 is applied to the lumen of the endoscope mounting portion 34c.
  • the distal end portion of the case tube 33 of the suturing device 1 is fixed to the distal end portion of the endoscope 2 via the mounting adapter 34 (endoscope mounting portion 34c) by inserting (press-fitting). Thereafter, the case tube 33 is fixed along the shaft by winding a mounting tape (not shown) at a plurality of locations at appropriate intervals around the shaft of the endoscope 2. Thereby, the mounting
  • the ligature tool 7 is attached to the needle-like member 52a of the suturing device 1, the shaft of the endoscope 2 to which the suturing device 1 is attached is inserted into the stomach, and suturing is performed.
  • the suture part 5 of the device 1 is arranged near the incision part to be sutured.
  • the operation unit 4 is operated to bring the rear arm 52 away from the front arm 51 (see FIG. 1B).
  • the first step shown in FIG. 3A is performed.
  • the operating portion 4 is pushed into the distal end side as a whole with respect to the case tube 33 and rotated as necessary, as shown in FIG. Only the front arm 51 that is spaced apart from the rear arm 52 is inserted into the incision SH. Before and after this, the rear arm 52 is rotated with respect to the front arm 51, and one lip of the incision SH is formed by one thread support portion 51a of the front arm 51 and the needle-shaped member 52a.
  • the front arm 51 and the rear arm 52 are arranged so that the portion Sa is sandwiched.
  • the needle-like member 52a pierces one of the mouth edge portions Sa, penetrates the mouth edge portion Sa, Further, the twisting portion of the needle-like member 52a passes through the through hole of the engaging member 6a accommodated (supported) in the accommodation space of the one thread support portion 51a. Thereby, the through hole of the engagement member 6a reaches the tissue penetration part of the needle-like member 52a, and the engagement member 6a is engaged with the needle-like member 52a.
  • the front arm 51a is so held that the other rim portion Sb of the incision SH is sandwiched between the other thread support portion 51a of the front arm 51 and the needle-like member 52a. 51 and the rear arm 52 are arranged.
  • the pair of engaging members 6a and 6b, to which both ends of the suture thread 6 are fixed, are both engaged with the single needle-like member 52a, and the needle-like member 52a (that is, the stomach) is engaged by the suture thread 6.
  • a ring is formed that penetrates the first perforation from the inner side to the outside of the stomach and returns from the outer surface of the stomach to the needle-like member 52a (that is, the stomach) through the second perforation.
  • the operation unit 4 is operated to move the front arm 51 (thread support unit 51a) into the stomach through the incision SH as shown in FIG. 3G.
  • the needle-like member 52a moves away from the incision part SH, and both ends of the suture thread 6 move away from the incision part SH.
  • the portion that penetrates the first perforation and the portion that penetrates the second perforation are drawn, and the end surfaces of the pair of mouth edge portions Sa and Sb of the incision SH are brought into contact with each other and joined.
  • the ligation device 8 includes, for example, a sheath introduced into a lumen via a treatment instrument guide tube of an endoscope, and an operation wire slidably inserted in the sheath, and the distal end of the operation wire At the end, a connecting hook that protrudes from the distal end of the sheath into a substantially V shape by its own elasticity and closes by being pulled into the distal end of the sheath is provided. Can be used.
  • the ligature tool 7 is held in a state where the ligation loop 7c (see FIG. 1B) is inserted into the proximal end portion (ligation tool mounting portion) of the needle-like member 52a. Therefore, the distal end of the ligating device 8 (see FIG. 3H) is disposed in the vicinity of the connecting loop 7b of the ligating device 7, and the connecting loop 7b is grasped by the connecting hook protruding from the ligating device 8 and opened.
  • the ligation tool 7 is connected to the distal end of the sheath of the ligating device 8 by drawing the connecting loop 7 b into the distal end of the sheath of the ligating device 8.
  • the distal end portion of the sheath of the ligation apparatus 8 to which the ligature tool 7 is connected is moved to the incision SH side (downward in FIG. 3H) to Assume that both ends of the suture thread 6 are inserted inside the ligation loop 7c. As a result, the suture thread 6 is squeezed and both ends of the suture thread 6 are bundled.
  • the sheath of the ligation device 8 is moved by sliding the sheath toward the proximal end so as to draw the sheath against the operation wire while keeping the position of the operation wire of the ligation device 8 unchanged.
  • the other end of the connecting hook and the loop member protrudes (exposes) from the distal end, and the connecting hook is opened by its own elasticity to release the grip.
  • the ligation apparatus 8 is separated from the ligature tool 7 that has been determined.
  • the suture thread 6 between the ligature 7 and the suture part 5 is cut with an endoscopic scissors forceps called a loop cutter. Then, the ligature 7 and the stitched portion 5 are separated, and if necessary, the connection loop 7b of the ligature 7 in the ligated state is cut and collected by a loop cutter or the like, and one needle is sutured. A series of procedures is completed.
  • the mounting adapter 34 integrally attached to the distal end portion of the case tube 33 has a plurality of endoscope mounting portions 34b and 34c having different inner diameters of the portions into which the endoscope is press-fitted. have.
  • each of the endoscope mounting portions 34b and 34c of the mounting adapter 34 can be individually separated from the case tube 33 as needed, an endoscope mounting portion (compatible with the endoscope 2 to be used (for example, an endoscope mounting part (for example, 34b) other than 34c) can be selectively separated and removed. If the endoscope mounting portion that is not used is left, there is a possibility that the procedure may be hindered, and this can be prevented.
  • the mounting adapter 34 includes a pair of endoscope mounting portions 34b and 34c.
  • a single or a plurality of other endoscope mounting portions having different inner diameters from these are provided. Further, it may be provided. In this way, versatility can be further improved.

Abstract

Provided is an external tube member for an endoscope which may improve versatility. This external tube member for an endoscope may be externally attached to an endoscope according to need, and has: a tube 33 disposed along the endoscope from the proximal end to the distal end thereof; and multiple substantially cylindrical endoscope attachment parts which are provided at the distal end of the tube 33, each have a lumen through which an endoscope is inserted, and differ in lumen diameter.

Description

内視鏡用外付けチューブ部材External tube member for endoscope
 本発明は、内視鏡の外側に必要に応じて装着されて使用される内視鏡用外付けチューブ部材に関する。 The present invention relates to an endoscope external tube member that is used by being attached to the outside of an endoscope as necessary.
 たとえば、経管腔的内視鏡手術(NOTES:Natural Orifice Translumenal Endoscopic Surgery)において、消化管等の体内組織に形成された切開部(穿孔部や欠損部等を含む)を縫合する縫合装置としては、特許文献1に記載のものが提案されている。この縫合装置は、内視鏡のシャフトに沿って配置されるシース部(アーム移動手段)、該シース部の近位端に設けられた操作部、および該シース部の遠位端に設けられた縫合部(前側アームおよび後側アーム)を概略備えて構成されている。 For example, in a transluminal endoscopic operation (NOTES: Natural Orifice Transluminal Endoscopic Surgary), as a suturing device for suturing an incision (including a perforation or a defect) formed in a body tissue such as a digestive tract The thing of patent document 1 is proposed. The suturing device is provided at a sheath portion (arm moving means) disposed along the endoscope shaft, an operation portion provided at a proximal end of the sheath portion, and a distal end of the sheath portion. The stitching portion (front arm and rear arm) is generally provided.
 シース部は、縫合部の針と縫合糸が支持された部材とを相対移動させるためのワイヤおよび該ワイヤが挿通されたシースを備えるとともに、該シース部を内視鏡に着脱可能に外付けするための内視鏡用外付けチューブ部材を備えている。内視鏡用外付けチューブ部材は、シースがスライド可能に挿通されるチューブと、該チューブの遠位端部に一体的に設けられ、内視鏡のシャフトの遠位端部が圧入されることにより、該チューブの遠位端部を内視鏡に着脱可能に固定するための略円筒状に形成された単一の内視鏡装着部(筒状の固定部)を備えて構成されている。 The sheath portion includes a wire for relatively moving the needle of the suture portion and a member on which the suture is supported, and a sheath through which the wire is inserted, and the sheath portion is detachably attached to the endoscope. An external tube member for an endoscope is provided. The external tube member for endoscope is provided integrally with the tube through which the sheath is slidably inserted and the distal end portion of the tube, and the distal end portion of the shaft of the endoscope is press-fitted. Thus, the tube is configured to include a single endoscope mounting portion (cylindrical fixing portion) formed in a substantially cylindrical shape for removably fixing the distal end portion of the tube to the endoscope. .
 ところで、このような縫合装置が外付けされる内視鏡としては、多種のものが存在し、そのシャフトの遠位端部の外径も多種にわたる。しかしながら、従来は、内視鏡用外付けチューブ部材は、内視鏡装着部を一つしか備えておらず、汎用性が低いため、内視鏡装着部の内径を互いに異ならせた複数の品種を準備しておき、使用する内視鏡の外径に適合する内視鏡装着部を備える内視鏡用外付けチューブ部材または該チューブ部材を備える縫合装置を選択して用いる必要があり、不便であった。 By the way, there are various types of endoscopes to which such a suturing device is externally attached, and the outer diameters of the distal end portions of the shafts are various. However, conventionally, the endoscope external tube member has only one endoscope mounting portion and is low in versatility, and therefore, a plurality of types in which the inner diameters of the endoscope mounting portions are different from each other. It is necessary to select and use an endoscope external tube member having an endoscope mounting portion that matches the outer diameter of the endoscope to be used or a suturing device having the tube member. Met.
特開2017-169941号公報JP 2017-169941 A
 本発明は、このような実状に鑑みてなされ、その目的は、汎用性を向上し得る内視鏡用外付けチューブ部材を提供することである。 The present invention has been made in view of such a situation, and an object thereof is to provide an external tube member for an endoscope that can improve versatility.
 上記目的を達成するために、本発明に係る内視鏡用外付けチューブ部材は、
内視鏡の外側に必要に応じて装着される内視鏡用外付けチューブ部材であって、
内視鏡の近位端から遠位端に沿って配置されるチューブと、
前記チューブの遠位端部にそれぞれ設けられ、内視鏡が挿入される内腔の径が互いに異なる略円筒状の複数の内視鏡装着部と、を有する。
In order to achieve the above object, an endoscope external tube member according to the present invention includes:
An external tube member for an endoscope that is attached to the outside of an endoscope as needed,
A tube disposed from the proximal end to the distal end of the endoscope;
A plurality of endoscope mounting portions each having a substantially cylindrical shape, each provided at a distal end portion of the tube and having different diameters of lumens into which the endoscope is inserted.
 本発明に係る内視鏡用外付けチューブ部材は、内視鏡が挿入される部分の内径が互いに異なる複数の内視鏡装着部を有しているので、該内視鏡装着部に挿入される遠位端部の外径が異なる複数種の内視鏡に適合させることが可能であり、汎用性を向上させることができる。 The external tube member for an endoscope according to the present invention has a plurality of endoscope mounting portions in which the inner diameter of the portion into which the endoscope is inserted is different from each other, so that it is inserted into the endoscope mounting portion. It is possible to adapt to a plurality of types of endoscopes having different outer diameters at the distal end portion, and improve versatility.
 本発明に係る内視鏡用外付けチューブ部材において、前記内視鏡装着部を、前記チューブから個別に切り離し可能とすることが好ましい。使用する内視鏡に適合する内視鏡装着部以外の内視鏡装着部を選択的に切り離して除去することにより、手技の支障となることを防止し得る。 In the endoscope external tube member according to the present invention, it is preferable that the endoscope mounting portion can be individually separated from the tube. By selectively separating and removing the endoscope mounting portion other than the endoscope mounting portion that matches the endoscope to be used, it is possible to prevent the procedure from being hindered.
 本発明に係る内視鏡用外付けチューブ部材において、前記内視鏡装着部の内腔を、内視鏡が挿入される方向に沿って拡径するテーパ状とすることができる。このように構成することにより、内視鏡の遠位端部の挿入時の抵抗を少なくでき、装着作業を容易化し得るとともに、装着の確実性を向上することができる。 In the endoscope external tube member according to the present invention, the lumen of the endoscope mounting portion can be tapered so as to expand in the direction in which the endoscope is inserted. With this configuration, resistance during insertion of the distal end portion of the endoscope can be reduced, the mounting operation can be facilitated, and the mounting reliability can be improved.
図1Aは、本発明の実施形態に係る縫合装置の操作部の構成を示す正面図である。FIG. 1A is a front view showing a configuration of an operation unit of the suturing device according to the embodiment of the present invention. 図1Bは、本発明の実施形態に係る縫合装置の縫合部の構成を示す正面図である。FIG. 1B is a front view showing a configuration of a suturing portion of the suturing device according to the embodiment of the present invention. 図2Aは、図1Bに示したケースチューブおよび装着アダプタを有する内視鏡用外付けチューブ部材の構成を示す斜視図である。FIG. 2A is a perspective view showing a configuration of an endoscope external tube member having the case tube and the mounting adapter shown in FIG. 1B. 図2Bは、図2AのIIb-IIb線に沿った断面図である。2B is a cross-sectional view taken along the line IIb-IIb in FIG. 2A. 図2Cは、図2Bの構成の一部を変更した構成を示す断面図である。FIG. 2C is a cross-sectional view showing a configuration obtained by changing a part of the configuration of FIG. 2B. 図3Aは、本発明の実施形態に係る縫合装置を用いて行われる手技(縫合)の手順を示す図であり、第1工程を示す図である。FIG. 3A is a diagram illustrating a procedure of a procedure (suture) performed using the suturing device according to the embodiment of the present invention, and is a diagram illustrating a first step. 図3Bは、図3Aの続きの第2工程を示す図である。FIG. 3B is a diagram showing a second step subsequent to FIG. 3A. 図3Cは、図3Bの続きの第3工程を示す図である。FIG. 3C is a diagram showing a third step subsequent to FIG. 3B. 図3Dは、図3Cの続きの第4工程を示す図である。FIG. 3D is a diagram showing a fourth step that follows FIG. 3C. 図3Eは、図3Dの続きの第5工程を示す図である。FIG. 3E is a diagram showing a fifth step subsequent to FIG. 3D. 図3Fは、図3Eの続きの第6工程を示す図である。FIG. 3F is a diagram showing a sixth step that follows FIG. 3E. 図3Gは、図3Fの続きの第7工程を示す図である。FIG. 3G is a diagram showing a seventh step that follows FIG. 3F. 図3Hは、図3Gの続きの第8工程を示す図である。FIG. 3H is a diagram showing an eighth step that follows FIG. 3G. 図3Iは、図3Hの続きの第9工程を示す図である。FIG. 3I is a diagram showing a ninth step that follows FIG. 3H. 図3Jは、図3Iの続きの第10工程を示す図である。FIG. 3J is a diagram showing a tenth process continued from FIG. 3I. 図3Kは、図3Jの続きの最終工程を示す図である。FIG. 3K is a diagram showing a final step subsequent to FIG. 3J.
 以下、本発明の実施形態として、本発明が適用された内視鏡用外付けチューブ部材を備える縫合装置について、図面を参照して詳細に説明する。ただし、本発明は、縫合装置に備えられる内視鏡用外付けチューブ部材のみならず、他の医療用器具に備えられる内視鏡用外付けチューブ部材に適用することができる。 Hereinafter, as an embodiment of the present invention, a suturing device including an external tube member for an endoscope to which the present invention is applied will be described in detail with reference to the drawings. However, the present invention can be applied not only to the endoscope external tube member provided in the suturing apparatus but also to the endoscope external tube member provided in other medical instruments.
 また、本発明は、各種の処置具(鉗子、ダイレータ、高周波メス、クリップ装置、結紮装置等)を導入するため、あるいは流体(薬液等)の注入や吸引等のために用いられる、たとえば株式会社トップが販売している「インパクトシューター(商品名)」のような、内視鏡に沿って配置されるチューブと、該チューブの遠位端部に設けられ、内視鏡の遠位端部が圧入される略円筒状の先端フード(内視鏡装着部)を有する医療用器具としても用いることができる。 Further, the present invention is used for introducing various treatment tools (forceps, dilator, high-frequency knife, clip device, ligation device, etc.), or for injecting or aspirating fluid (chemical solution, etc.), for example, A tube arranged along the endoscope, such as “impact shooter (trade name)” sold by Top, and a distal end of the endoscope provided at the distal end of the tube It can also be used as a medical instrument having a generally cylindrical tip hood (endoscope mounting portion) to be press-fitted.
 まず、図1Aおよび図1Bを参照する。縫合装置1は、内視鏡(軟性内視鏡)2の外側に沿って取り付けられた状態で体内に挿入される装置であり、内視鏡2の不図示のカメラによって視認しながら、腹腔内の臓器や消化管に形成された切開部(欠損部や穿孔部を含む)等を体外における操作により縫合するための装置である。 First, refer to FIG. 1A and FIG. 1B. The suturing device 1 is a device that is inserted into the body while being attached along the outside of an endoscope (soft endoscope) 2, while being visually recognized by a camera (not shown) of the endoscope 2. This is a device for suturing an incision part (including a defect part or a perforation part) formed in an organ or digestive tract by an operation outside the body.
 縫合装置1は、内視鏡2のシャフトに沿って配置されるシース部3、シース部3の近位端に設けられた操作部(ハンドル)4、およびシース部3の遠位端に設けられた縫合部5を概略備えて構成されている。 The suturing device 1 is provided at a sheath portion 3 disposed along the shaft of the endoscope 2, an operation portion (handle) 4 provided at the proximal end of the sheath portion 3, and a distal end of the sheath portion 3. The sewing part 5 is generally provided.
(シース部)
 シース部3は、軸方向に沿って延びた長尺な部材であり、内視鏡2のシャフトの屈曲に追従して屈曲できる程度の柔軟性を有する2本のチューブと1本のワイヤ(または3本のチューブ)から構成されている。すなわち、シース部3は、前側アーム移動ワイヤ31、後側アーム移動チューブ32、およびケースチューブ(チューブ)33を概略備えて構成されている。
(Sheath part)
The sheath part 3 is a long member extending along the axial direction, and has two tubes and one wire (or one having flexibility enough to follow the bending of the shaft of the endoscope 2). 3 tubes). That is, the sheath portion 3 is configured to include a front arm moving wire 31, a rear arm moving tube 32, and a case tube (tube) 33.
 前側アーム移動ワイヤ31は、可撓性を有する線材からなり、後側アーム移動チューブ32にスライド可能に挿通されて、該後側アーム移動チューブ32内において、その軸方向に沿って移動かつ軸周りに回転できるように設けられている。前側アーム移動ワイヤ31としては、本実施形態ではワイヤロープを用いている。ワイヤロープは、たとえば金属(ステンレス鋼)等からなる複数本のワイヤを螺旋状に撚ってなる撚り線からなるロープである。ただし、ワイヤ31としては、単線からなるワイヤを用いてもよい。また、ワイヤ31に代えて、中空チューブを用いてもよい。 The front arm moving wire 31 is made of a flexible wire, and is slidably inserted into the rear arm moving tube 32. The front arm moving wire 31 moves along the axial direction of the rear arm moving tube 32 and around the axis. It is provided so that it can rotate. As the front arm moving wire 31, a wire rope is used in this embodiment. The wire rope is a rope made of a stranded wire formed by twisting a plurality of wires made of metal (stainless steel) or the like in a spiral shape. However, the wire 31 may be a single wire. Further, a hollow tube may be used instead of the wire 31.
 後側アーム移動チューブ32は、ケースチューブ33にスライド可能に挿通された中空チューブからなり、ケースチューブ33内において、その軸方向に沿って移動かつ軸周りに回転できるように設けられている。後側アーム移動チューブ32としては、可撓性を有しており、樹脂等からなるチューブを用いてもよいが、本実施形態では、耐久性に優れるコイルチューブを用いている。コイルチューブとしては、金属(ステンレス鋼)等からなる長尺平板を螺旋状に巻回してなる平線コイルチューブを用いることができる。ただし、丸線コイルチューブまたは内面平コイルチューブを用いてもよい。 The rear arm moving tube 32 is a hollow tube that is slidably inserted into the case tube 33, and is provided in the case tube 33 so as to move along the axial direction and rotate about the axis. The rear arm moving tube 32 has flexibility and may be a tube made of resin or the like, but in this embodiment, a coil tube having excellent durability is used. As the coil tube, a flat wire coil tube formed by spirally winding a long flat plate made of metal (stainless steel) or the like can be used. However, a round wire coil tube or an inner flat coil tube may be used.
 なお、後側アーム移動チューブ32としては、ワイヤチューブを用いてもよい。ワイヤチューブは、たとえば金属(ステンレス鋼)等からなる複数本のワイヤを中空となるように螺旋状に撚ってなるチューブである。 Note that a wire tube may be used as the rear arm moving tube 32. The wire tube is a tube formed by spirally twisting a plurality of wires made of, for example, metal (stainless steel) or the like.
 後側アーム移動チューブ32は、その近位端から遠位端まで一様な部材(たとえばコイルチューブ)としてもよいが、本実施形態では、コイルチューブの遠位端に剛性の高い金属からなる略円筒状の部材を溶接固定して、後側アーム移動チューブ32の先端部(チューブ先端部)32aとしている。 The rear arm moving tube 32 may be a uniform member (for example, a coil tube) from the proximal end to the distal end, but in this embodiment, the distal end of the coil tube is substantially made of a rigid metal. A cylindrical member is fixed by welding to form a distal end portion (tube distal end portion) 32a of the rear arm moving tube 32.
 ケースチューブ33は、内視鏡2の近位端から遠位端にわたって、これに沿って配置される中空チューブであり、樹脂等からなる可撓性を有する材料で形成されている。前側アーム移動ワイヤ31および後側アーム移動チューブ32の近位端は操作部4に接続されており、前側アーム移動ワイヤ31および後側アーム移動チューブ32の遠位端は縫合部5に接続されている。ケースチューブ33の近位端は、操作部4の近傍にまで至っているが、操作部4には接続されておらず、ケースチューブ33の遠位端は、縫合部5の近傍まで至っているが、縫合部5には接続されていない。ケースチューブ33は、たとえば、ポリエチレンやポリ塩化ビニル等の素材で形成することができる。 The case tube 33 is a hollow tube disposed along the distal end of the endoscope 2 from the proximal end to the distal end, and is formed of a flexible material made of resin or the like. The proximal ends of the front arm moving wire 31 and the rear arm moving tube 32 are connected to the operation unit 4, and the distal ends of the front arm moving wire 31 and the rear arm moving tube 32 are connected to the suture unit 5. Yes. The proximal end of the case tube 33 reaches the vicinity of the operation unit 4, but is not connected to the operation unit 4, and the distal end of the case tube 33 reaches the vicinity of the suture unit 5, It is not connected to the stitched portion 5. The case tube 33 can be formed of a material such as polyethylene or polyvinyl chloride, for example.
 ケースチューブ33の遠位端部には、図2Aおよび図2Bにも示されているように、装着アダプタ34が一体的に取り付けられている。なお、ケースチューブ33および装着アダプタ34が本発明に係る内視鏡用外付けチューブ部材に相当する。 The mounting adapter 34 is integrally attached to the distal end portion of the case tube 33 as shown in FIGS. 2A and 2B. The case tube 33 and the mounting adapter 34 correspond to the endoscope external tube member according to the present invention.
 装着アダプタ34は、それぞれ略円筒状に形成されたチューブ装着部34a、内視鏡装着部34bおよび内視鏡装着部34cを有している。装着アダプタ34は、チューブ装着部34aにケースチューブ33の遠位端部が挿入されて、互いに接着や融着等により固定されることにより、ケースチューブ33の遠位端部に固定されている。 The mounting adapter 34 has a tube mounting portion 34a, an endoscope mounting portion 34b, and an endoscope mounting portion 34c each formed in a substantially cylindrical shape. The mounting adapter 34 is fixed to the distal end portion of the case tube 33 by inserting the distal end portion of the case tube 33 into the tube mounting portion 34a and fixing the mounting adapter 34 by bonding or fusion.
 内視鏡装着部34bおよび内視鏡装着部34cは、チューブ装着部34aを挟んで両側に配置されている。装着アダプタ34は、本実施形態では、射出成形により、全体として一体的に形成されている。ただし、チューブ装着部34a、内視鏡装着部34bおよび内視鏡装着部34cの少なくとも一つと、その余の部位とを互いに独立して形成した後に、接着や融着等により互いに一体としてもよい。 The endoscope mounting part 34b and the endoscope mounting part 34c are arranged on both sides with the tube mounting part 34a interposed therebetween. In this embodiment, the mounting adapter 34 is integrally formed as a whole by injection molding. However, at least one of the tube mounting portion 34a, the endoscope mounting portion 34b, and the endoscope mounting portion 34c and the remaining portion may be formed independently of each other, and then integrated with each other by adhesion, fusion, or the like. .
 内視鏡装着部34bおよび内視鏡装着部34cは、それぞれ内視鏡のシャフトの遠位端部が圧入・固定される略円筒状の部位である。内視鏡装着部34bの内径と、内視鏡装着部34cの内径とは、互いに異なっており、本実施形態では、内視鏡装着部34bは、比較的に大径(太径)の遠位端部を有する内視鏡に適合するように、比較的に大きい内径に設定されており、内視鏡装着部34cは、比較的に小径(細径)の遠位端部を有する内視鏡に適合するように、比較的に小さい内径に設定されている。 The endoscope mounting part 34b and the endoscope mounting part 34c are respectively substantially cylindrical portions into which the distal end portion of the endoscope shaft is press-fitted and fixed. The inner diameter of the endoscope mounting portion 34b and the inner diameter of the endoscope mounting portion 34c are different from each other. In this embodiment, the endoscope mounting portion 34b has a relatively large diameter (thick diameter). The endoscope mounting portion 34c is set to have a relatively small diameter (thin diameter) distal end portion so as to be adapted to an endoscope having a distal end portion. A relatively small inner diameter is set to fit the mirror.
 内視鏡装着部34bと、内視鏡装着部34cとを識別するため、本実施形態では、図2Aに示されているように、内視鏡装着部34bにはラージサイズ(大径の内視鏡)用の装着部であることを示す文字「L」が、内視鏡装着部34cにはスモールサイズ(小径の内視鏡)用の装着部であることを示す文字「S」が表示されている。このような識別文字を表示することにより、内視鏡の遠位端部を内視鏡装着部34bまたは34cに圧入(挿入)する際の目視による識別を容易に行うことができる。これらの識別文字は、装着アダプタ34を形成した後に印刷や刻印等により形成してもよく、あるいは射出成形時に凹状または凸状となるように一体的に形成するようにしてもよい。なお、これらの識別情報としては、これらの文字以外の文字、または記号や図形等であってもよい。 In order to distinguish between the endoscope mounting part 34b and the endoscope mounting part 34c, in this embodiment, as shown in FIG. 2A, the endoscope mounting part 34b has a large size (large diameter inner diameter). The character “L” indicating that the attachment portion is for the endoscope) is displayed on the endoscope attachment portion 34c, and the character “S” indicating that the attachment portion is for the small size (small diameter endoscope) is displayed on the endoscope attachment portion 34c. Has been. By displaying such identification characters, it is possible to easily perform visual identification when the distal end portion of the endoscope is press-fitted (inserted) into the endoscope mounting portion 34b or 34c. These identification characters may be formed by printing or stamping after the mounting adapter 34 is formed, or may be formed integrally so as to be concave or convex at the time of injection molding. In addition, as these identification information, characters other than these characters, a symbol, a figure, etc. may be sufficient.
 内視鏡装着部34bおよび内視鏡装着部34cは、チューブ装着部34aに対して、切り離し可能となっている。すなわち、内視鏡装着部34bおよび内視鏡装着部34cのチューブ装着部34aに対する接合部を、医療用のカッター(手術用のメス等を代用してもよい)等を用いて切断できるようになっている。当該接合部に溝等を形成して薄肉として脆弱に構成して、カッター等を用いることなく、引きちぎることにより、切断し得るように構成してもよい。このようにすることで、切断に要する手間を大幅に削減することができる。 The endoscope mounting part 34b and the endoscope mounting part 34c can be separated from the tube mounting part 34a. That is, the joint portion of the endoscope attachment portion 34b and the endoscope attachment portion 34c to the tube attachment portion 34a can be cut using a medical cutter (a surgical knife or the like may be substituted). It has become. You may comprise so that it can cut | disconnect by forming a groove | channel etc. in the said junction part, making it thin and weak, and tearing without using a cutter etc. By doing in this way, the effort which a cutting | disconnection requires can be reduced significantly.
 内視鏡装着部34bおよび34cは、内視鏡に装着する際には圧入し易く、装着後は外れ難いことが好ましく、装着アダプタ34を形成する材料としては、ポリエーテルブロックアミド共重合体等の可撓性を有する熱可塑性エラストマー等を用いることができる。 The endoscope attachment portions 34b and 34c are easy to press-fit when attached to the endoscope, and are preferably difficult to come off after attachment. As a material for forming the attachment adapter 34, a polyether block amide copolymer or the like is used. A flexible thermoplastic elastomer or the like can be used.
 装着アダプタ34を内視鏡の遠位端部に装着する際には、大径の内視鏡を用いる場合には内視鏡装着部34bを選択し、小径の内視鏡を用いる場合には内視鏡装着部34cを選択し、選択した内視鏡装着部(ここでは、小径の内視鏡を用いるものとして、内視鏡装着部34cを選択するものとする)の内腔に内視鏡の遠位端部を圧入する。内視鏡装着部34bまたは34cに内視鏡を圧入する際には、摩擦を軽減して円滑な作業を可能とするため、あるいは装着の確実性を向上するため、キシロカインゼリー等の潤滑剤を、内視鏡の遠位端部および選択した内視鏡装着部34bの内腔内の一方または双方に塗布した後に圧入する。 When the attachment adapter 34 is attached to the distal end portion of the endoscope, the endoscope attachment portion 34b is selected when a large-diameter endoscope is used, and when the small-diameter endoscope is used. The endoscope attachment part 34c is selected, and the endoscope is inserted into the lumen of the selected endoscope attachment part (here, the endoscope attachment part 34c is selected as a small-diameter endoscope). Press fit the distal end of the mirror. When the endoscope is press-fitted into the endoscope mounting portion 34b or 34c, a lubricant such as xylocaine jelly is used in order to reduce friction and enable smooth work or to improve the mounting reliability. Then, after applying to one or both of the distal end portion of the endoscope and the lumen of the selected endoscope mounting portion 34b, press-fitting is performed.
 内視鏡装着部34bおよび34cの内腔は、図2Bに示されているように、内視鏡の挿入方向Aに対して近位端側(上流側)から遠位端側(下流側)にわたって一様な内径となっているものとするが、図2Cに示されているように、内視鏡の挿入方向Aに沿って近位端側(上流側)から遠位端側(下流側)に向かって拡径するテーパ状(先太テーパ状)としてもよい。このようにテーパ状とすることにより、内視鏡装着部34bまたは34cの内腔と、内視鏡の遠位端部との圧入の際の摩擦抵抗を低減することができ、圧入の作業性や装着の確実性を向上することができる。 As shown in FIG. 2B, the lumens of the endoscope mounting portions 34b and 34c are arranged from the proximal end side (upstream side) to the distal end side (downstream side) with respect to the insertion direction A of the endoscope. 2C, the proximal end side (upstream side) to the distal end side (downstream side) along the insertion direction A of the endoscope as shown in FIG. 2C. It is good also as a taper shape (taper taper shape) which diameter-expands toward (). By adopting such a taper shape, it is possible to reduce the frictional resistance at the time of press-fitting between the lumen of the endoscope mounting portion 34b or 34c and the distal end portion of the endoscope, and the workability of press-fitting And the certainty of mounting can be improved.
 なお、圧入の際の摩擦抵抗の低減の観点からは、内視鏡の挿入方向Aに沿って近位端側(上流側)から遠位端側(下流側)に向かって縮径するテーパ状(先細テーパ状)としてもよい。しかしながら、このような先細テーパ状とすると、このテーパの作用により、内視鏡装着部34bまたは34cから内視鏡の遠位端部が抜け易くなるため、上述のように、先太テーパ状とすることが好ましい。 From the viewpoint of reducing the frictional resistance at the time of press-fitting, the taper is reduced in diameter from the proximal end side (upstream side) to the distal end side (downstream side) along the insertion direction A of the endoscope. It is good also as (taper taper shape). However, with such a taper taper shape, the distal end portion of the endoscope can be easily detached from the endoscope mounting portion 34b or 34c by the action of the taper. It is preferable to do.
 内視鏡装着部34bの長手方向(軸方向)の寸法L1は、5~15mmの範囲で設定することができる。内視鏡装着部34cの長手方向(軸方向)の寸法L2は、5~15mmの範囲で設定することができる。本実施形態では、これらの寸法L1およびL2は同じ値に設定している。ただし、互いに異なっていてもよい。 The longitudinal dimension (axial direction) dimension L1 of the endoscope mounting part 34b can be set in the range of 5 to 15 mm. The dimension L2 in the longitudinal direction (axial direction) of the endoscope mounting portion 34c can be set in the range of 5 to 15 mm. In the present embodiment, these dimensions L1 and L2 are set to the same value. However, they may be different from each other.
 内腔が直胴状である場合(図2B参照)の内視鏡装着部34bの内径d1は、12~15mmの範囲で、内視鏡装着部34cの内径d2は、9~12mmの範囲で設定することができる。内腔が先太テーパ状である場合(図2C参照)の内視鏡装着部34bの細径側の内径は上記のd1と同様の範囲で、太径側の内径d3はd1+(0.5~3.0)mmの範囲で設定することができ、内視鏡装着部34cの細径側の内径は上記のd2と同様の範囲で、太径側の内径d4は、d2+(0.5~3.0)mmの範囲で設定することができる。 When the lumen is a straight body (see FIG. 2B), the inner diameter d1 of the endoscope mounting portion 34b is in the range of 12 to 15 mm, and the inner diameter d2 of the endoscope mounting portion 34c is in the range of 9 to 12 mm. Can be set. When the lumen has a tapered shape (see FIG. 2C), the inner diameter on the small diameter side of the endoscope mounting portion 34b is in the same range as d1 described above, and the inner diameter d3 on the large diameter side is d1 + (0.5 Can be set within a range of up to 3.0) mm, the inner diameter of the endoscope mounting portion 34c is in the same range as d2, and the inner diameter d4 of the large diameter side is d2 + (0.5 Can be set in a range of up to 3.0) mm.
 内視鏡装着部34bの外径D1は、d1+(0.5~1.5)mmの範囲で設定することができる。内視鏡装着部34cの外径D2は、d2+(0.5~1.5)mmの範囲で設定することができる。 The outer diameter D1 of the endoscope mounting portion 34b can be set in a range of d1 + (0.5 to 1.5) mm. The outer diameter D2 of the endoscope mounting portion 34c can be set in a range of d2 + (0.5 to 1.5) mm.
 装着アダプタ34の内視鏡装着部34bまたは34cに内視鏡2のシャフトの遠位端部が圧入されることにより、縫合装置1を内視鏡2に対して、着脱可能に固定できるようになっている。なお、ケースチューブ33は、内視鏡のシャフトに適宜な間隔をあけて、複数箇所で、不図示の装着テープ等を巻くことにより、該シャフトに沿って固定してもよい。 By inserting the distal end portion of the shaft of the endoscope 2 into the endoscope mounting portion 34b or 34c of the mounting adapter 34, the suturing device 1 can be detachably fixed to the endoscope 2. It has become. Note that the case tube 33 may be fixed along the shaft by winding an attachment tape (not shown) at a plurality of locations at appropriate intervals around the shaft of the endoscope.
 操作部4の全体をケースチューブ33に対して遠位端側または近位端側に移動(スライド)させることにより、内視鏡2に対して、縫合部5の全体を移動させ、操作部4の全体をケースチューブ33に対してその軸周りに回転させることにより、縫合部5の全体を回転させることができる。 By moving (sliding) the entire operation unit 4 to the distal end side or the proximal end side with respect to the case tube 33, the entire suture unit 5 is moved with respect to the endoscope 2, and the operation unit 4 is moved. Is rotated about its axis with respect to the case tube 33, so that the entire suture portion 5 can be rotated.
(縫合部)
 縫合装置1の縫合部5は、図1Bに示されているように構成されている。すなわち、縫合部5は、縫合糸6が装着される前側アーム51と、針状部材52aを有する後側アーム52とを備えて構成されている。
(Suture)
The suturing portion 5 of the suturing apparatus 1 is configured as shown in FIG. 1B. That is, the suture part 5 includes a front arm 51 to which the suture thread 6 is attached and a rear arm 52 having a needle-like member 52a.
 後側アーム52は、針状部材52a、針支持部52b、および後側ガイド部52cを有している。後側ガイド部52cは略円筒状の部材からなり、後側ガイド部52cの上端側に略短冊板状の針支持部52bの一端が固定されている。 The rear arm 52 has a needle-like member 52a, a needle support portion 52b, and a rear guide portion 52c. The rear guide portion 52c is made of a substantially cylindrical member, and one end of a substantially strip-shaped needle support portion 52b is fixed to the upper end side of the rear guide portion 52c.
 針支持部52bの他端には、前方(遠位端側)を指向して、針状部材52aの基端部が固定されている。これらの針状部材52a、針支持部52bおよび後側ガイド部52cは、たとえば、ステンレス鋼等の金属からなり、それぞれ別々の部品として形成された後に、レーザ溶接等により互いに一体的に固定されている。 The proximal end portion of the needle-like member 52a is fixed to the other end of the needle support portion 52b so as to be directed forward (distal end side). The needle-like member 52a, the needle support portion 52b, and the rear guide portion 52c are made of, for example, a metal such as stainless steel, and are formed as separate parts, and then fixed integrally with each other by laser welding or the like. Yes.
 後側アーム52は、後側ガイド部52cの後端面(近位端側の端面)が後側アーム移動チューブ32の先端部32aに、レーザ溶接等により一体的に固定されている。後側ガイド部52cは、後述する前側ガイド部53の内側に挿入され、その軸方向に沿ってスライド可能かつ軸周りに回動可能に保持されるようになっている。 In the rear arm 52, the rear end surface (the end surface on the proximal end side) of the rear guide portion 52c is integrally fixed to the distal end portion 32a of the rear arm moving tube 32 by laser welding or the like. The rear guide portion 52c is inserted inside a front guide portion 53, which will be described later, and is held so as to be slidable along the axial direction and rotatable about the axis.
 針状部材52aは、その基端側(針支持部52b側)から先端側(開放端側)に向かって、直胴状の結紮具装着部、先細テーパ状の中軸部、直胴状の組織貫通部、およびやじり部を有している。針状部材52aの結紮具装着部には、縫合糸6を結紮するための結紮具7が挿抜可能に装着される。やじり部は、その先端が体内組織に突き刺し可能な程度に鋭利に形成された先細の略円錐状の部位であり、その基端の最大径部の外径が組織貫通部の先端の外径よりも大きく、組織貫通部との接続部分に僅かに段差(かえし)ができるように形成されている。 The needle-like member 52a has a straight barrel-shaped ligature attachment portion, a tapered tapered central shaft portion, and a straight barrel-shaped tissue from the proximal end side (needle support portion 52b side) to the distal end side (open end side). It has a penetrating part and a twisting part. A ligation tool 7 for ligating the suture thread 6 is detachably mounted on the ligation tool mounting portion of the needle-like member 52a. The tapping portion is a tapered, generally conical portion whose tip is sharply formed so as to be able to pierce the body tissue, and the outer diameter of the maximum diameter portion of the proximal end is larger than the outer diameter of the tip of the tissue penetrating portion. And is formed so that there is a slight step (barbing) at the connection portion with the tissue penetrating portion.
 針状部材52aは、その先端(やじり部)が前側アーム51に向いた状態かつ、その中心軸が後側ガイド部52cの中心軸と略平行となるように、その基端が針支持部52bに固定されることにより、該針支持部52bに支持されている。後側アーム移動チューブ32をその中心軸周りに回転させれば、針状部材52aの中心軸が先端部32aの中心軸と略平行な状態を維持したまま、針状部材52aを先端部32aの中心軸周りに回動(旋回)させることができる。 The needle-like member 52a has a base end at the needle support portion 52b so that the tip end thereof (the edge portion) faces the front arm 51 and the center axis thereof is substantially parallel to the center axis of the rear guide portion 52c. Is fixed to the needle support portion 52b. If the rear arm moving tube 32 is rotated around its central axis, the needle-like member 52a is moved to the tip 32a while the central axis of the needle-like member 52a is maintained substantially parallel to the central axis of the tip 32a. It can be rotated (turned) around the central axis.
 針状部材52aの基端部(結紮具装着部)に挿抜可能に装着される結紮具7は、締付チューブ7aと、本体部とを有している。本体部は、不図示の結紮装置が連結される連結用ループ7bと、後述する縫合糸6が通される結紮用ループ7cと、これらの連結用ループ7bと結紮用ループ7cとを接続する略円柱状の接続部とを有しており、該接続部には締付チューブ7aがスライド可能に外嵌されている。締付チューブ7aは、弾性を有する素材からなる略円筒状の部材からなり、結紮用ループ7c側にスライドさせることにより、該結紮用ループ7cがその内腔に引き込まれるようになっている。結紮用ループ7cは、締付チューブ7aの内腔に引き込まれ過ぎて、締付チューブ7a内から抜け出さないように、該結紮用ループ7cの一部を係止する係止手段として、係止部7dを有している。 The ligation tool 7 that is detachably attached to the base end portion (ligation tool attachment portion) of the needle-like member 52a has a tightening tube 7a and a main body portion. The main body portion is a connection loop 7b to which a ligation device (not shown) is connected, a ligation loop 7c through which a suture thread 6 to be described later is passed, and an abbreviation for connecting these connection loop 7b and ligation loop 7c. The fastening tube 7a is slidably fitted to the connecting portion. The tightening tube 7a is made of a substantially cylindrical member made of a material having elasticity, and is slid toward the ligation loop 7c so that the ligation loop 7c is drawn into the inner cavity thereof. The ligation loop 7c is used as a locking means for locking a part of the ligation loop 7c so that the ligation loop 7c is not drawn too far into the lumen of the tightening tube 7a and comes out of the tightening tube 7a. 7d.
 結紮具7は、結紮用ループ7cに針状部材52aの基端部(結紮具装着部)が挿入(圧入)されることにより、針状部材52に挿抜可能に装着される。体内組織の縫合が行われた後の縫合糸6を結紮する際には、不図示の結紮装置により連結用ループ7bが把持され、針状部材52aの先端側に移動させる(押し下げる)ことにより、結紮具装着部から抜け出し、さらにやじり部を越えて移動させることにより、結紮用ループ7cに縫合糸6の両端部が束ねて通された状態となる。 The ligature tool 7 is detachably mounted on the needle-shaped member 52 by inserting (pressing) the proximal end portion (ligation tool mounting portion) of the needle-shaped member 52a into the ligation loop 7c. When ligating the suture thread 6 after the body tissue has been sutured, the coupling loop 7b is gripped by a ligation device (not shown) and moved (pushed down) to the distal end side of the needle-like member 52a. By pulling out from the ligation tool mounting portion and moving beyond the tying portion, both ends of the suture thread 6 are bundled and passed through the ligation loop 7c.
 次いで、結紮装置を用いて、結紮用ループ7cが締付チューブ7a内に引き込まれるように、締付チューブ7aを結紮用ループ7c側にスライドさせる(または締付チューブ7aに対して連結用ループ7bを引っ張る)。これにより、結紮用ループ7cおよび係止部7dの一部が縫合糸6とともに締付チューブ7a内に圧入され、結紮用ループ7cの接続部と反対側の端部部分(係止部7dが設けられた部分)が締付チューブ7a内の中間部分まで引き込まれて、縫合糸6が結紮される。 Next, using the ligating apparatus, the fastening tube 7a is slid toward the ligating loop 7c so that the ligating loop 7c is pulled into the fastening tube 7a (or the connecting loop 7b with respect to the fastening tube 7a). Pull). As a result, a part of the ligation loop 7c and the locking part 7d are press-fitted into the fastening tube 7a together with the suture thread 6, and the end part opposite to the connection part of the ligation loop 7c (the locking part 7d is provided). The drawn portion) is pulled to the middle portion in the fastening tube 7a, and the suture thread 6 is ligated.
 前側アーム51は、一対の糸支持部51a,51aおよび前側ガイド部53を概略備えて構成されている。一対の糸支持部51a,51aは、略V状(円弧状、コの字状、U字状等であってもよい)に形成されて二股状になっており、糸支持部51a,51aのそれぞれの先端部近傍間に渡るように、縫合糸6が装着される。縫合糸6の両端には、それぞれ円環状に形成された係合部材6a,6bが取り付けられている。 The front arm 51 includes a pair of yarn support portions 51 a and 51 a and a front guide portion 53. The pair of thread support portions 51a and 51a is formed in a substantially V shape (which may be an arc shape, a U shape, a U shape, etc.) and has a bifurcated shape. The suture thread 6 is attached so as to extend between the vicinity of the respective distal end portions. Engagement members 6a and 6b formed in an annular shape are attached to both ends of the suture thread 6, respectively.
 前側アーム51の糸支持部51a,51aのそれぞれの先端部には、前面(遠位端側の面)および後面(近位端側の面)に渡って貫通する貫通孔(不図示)が形成されており、該貫通孔の後面側に係合部材6a,6bが係合可能な収容空間(不図示)が形成されている。収容空間は、該貫通孔よりも僅かに大きい径であって、係合部材6a,6bがその表裏を貫通する貫通孔が糸支持部51a,51aの貫通孔に対して略同心となるように配置した状態で、その内壁によって係脱可能に係合され得る程度の径に設定されている。 A through hole (not shown) penetrating over the front surface (distal end side surface) and the rear surface (proximal end side surface) is formed at the tip of each of the yarn support portions 51a and 51a of the front arm 51. An accommodation space (not shown) in which the engagement members 6a and 6b can be engaged is formed on the rear surface side of the through hole. The accommodation space has a diameter slightly larger than that of the through-hole, and the through-hole through which the engaging members 6a and 6b penetrate the front and back are substantially concentric with the through-hole of the yarn support portions 51a and 51a. The diameter is set such that the inner wall can be detachably engaged with the inner wall.
 各係合部材6a,6bの貫通孔は、針状部材52aのやじり部を挿通させることはできるが、やじり部が完全に該貫通孔を挿通すると針状部材52aから係合部材6a,6bが抜け落ちない構造となっている。 The through-holes of the engaging members 6a and 6b can be inserted through the twisted portion of the needle-shaped member 52a. However, when the twisted portion is completely inserted through the through-hole, the engaging members 6a and 6b are moved from the needle-shaped member 52a. It has a structure that does not fall out.
 前側アーム51には、不図示のガイドシャフトを介して、前側アーム移動ワイヤ31の遠位端がレーザ溶接等により、一体的に固定されている。 The distal end of the front arm moving wire 31 is integrally fixed to the front arm 51 by laser welding or the like via a guide shaft (not shown).
 前側ガイド部53は、略円筒状の部材から構成されている。前側ガイド部53の正面側の上部には、切欠部53aが形成されている。この切欠部53aの底辺部(前端側の辺部)の両側には、上下方向(中心軸に実質的に平行する方向)に延在するとともに、内外に渡って貫通して形成された貫通ガイド溝53b,53bが形成されている。これらの貫通ガイド溝53b,53bは、そのいずれかに、後側アーム52の針支持部52bがスライド可能に遊嵌されることにより、該後側アーム52の中心軸方向のスライドを案内する部位である。 The front side guide part 53 is comprised from the substantially cylindrical member. A notch 53 a is formed in the upper part of the front side of the front guide part 53. On both sides of the bottom portion (front end side portion) of the notch 53a, a penetration guide is formed extending in the vertical direction (direction substantially parallel to the central axis) and penetrating inward and outward. Grooves 53b and 53b are formed. These penetration guide grooves 53b and 53b are portions in which the needle support portion 52b of the rear arm 52 is slidably fitted in either of them to guide the slide in the central axis direction of the rear arm 52. It is.
 これらの貫通ガイド溝53b,53bの上端(後端)は切欠部53aの底辺部に至っており、下端(前端)は前側ガイド部53の下部(前端)には至っていない。貫通ガイド溝53b,53bの下端(前端)の位置は、前側アーム51の針支持部52bが嵌合されて、当該下端まで至った際に、針状部材52aのやじり部の後端が、縫合糸6の係合部材6aまたは6bを貫通して、係合し得る程度の位置に設定されている。 The upper ends (rear ends) of the through guide grooves 53b and 53b reach the bottom side of the notch 53a, and the lower ends (front ends) do not reach the lower portion (front end) of the front guide portion 53. The positions of the lower ends (front ends) of the penetration guide grooves 53b and 53b are such that when the needle support portion 52b of the front arm 51 is fitted and reaches the lower end, the rear end of the needle portion of the needle-like member 52a is sewn. The thread 6 is set at a position where it can be engaged through the engaging member 6a or 6b.
(操作部)
 縫合装置1の操作部(ハンドル)4は、図1Aに示されているように構成されている。すなわち、操作部4は、スライダ部41およびベース部42を備えて構成されている。スライダ部41がベース部42にスライド可能に設けられており、スライダ部41は、ベース部42に対して、先端(遠位端)側に移動した位置と基端(近位端)側に移動した位置の2つの位置に移動し得るようになっている。
(Operation section)
The operation unit (handle) 4 of the suturing device 1 is configured as shown in FIG. 1A. In other words, the operation unit 4 includes a slider unit 41 and a base unit 42. The slider part 41 is slidably provided on the base part 42, and the slider part 41 moves to the base end (distal end) side and the base end (proximal end) side with respect to the base part 42. It is possible to move to two positions.
 具体的には、スライダ部41は、その遠位端側が略円柱状に形成された円柱部41aとなっており、その近位端側には該円柱部41aにその遠位端が固定されたグリップ部材41bを有している。スライダ部41の円柱部41aには、その遠位端に開口し、その軸芯に沿って延在する略円柱状のワイヤ挿入孔(不図示)が形成されており、前側アーム移動ワイヤ31の近位端側の部分がスライダ部41の円柱部41aに接続固定されている。 Specifically, the slider part 41 is a cylindrical part 41a having a substantially cylindrical shape on the distal end side, and the distal end is fixed to the cylindrical part 41a on the proximal end side. A grip member 41b is provided. The cylindrical portion 41a of the slider portion 41 is formed with a substantially cylindrical wire insertion hole (not shown) that opens at the distal end thereof and extends along the axial center thereof. The portion on the proximal end side is connected and fixed to the cylindrical portion 41 a of the slider portion 41.
 ベース部42は、一対の略対称に形成された半割部材を複数のネジ等(不図示)により接合してなる略円筒状の部材からなり、その近位端に開口し、その軸芯に沿って延在する略円柱状のスライダ部挿入孔(不図示)を有している。このスライダ部挿入孔にスライダ部41の円柱部41aが挿入されることにより、スライダ部41がベース部42に対して、該軸芯に沿ってスライド可能にかつ該軸心周りに回動可能に取り付けられている。 The base portion 42 is formed of a substantially cylindrical member formed by joining a pair of substantially symmetric half members by a plurality of screws or the like (not shown), and opens at a proximal end thereof. It has a substantially cylindrical slider portion insertion hole (not shown) extending along. By inserting the cylindrical portion 41a of the slider portion 41 into the slider portion insertion hole, the slider portion 41 can be slid along the axis and can rotate about the axis with respect to the base portion. It is attached.
 また、ベース部42は、その遠位端に開口し、その軸芯に沿って延在する略円柱状のチューブ挿入孔(不図示)を有しており、チューブ挿入孔に後側アーム移動チューブ32の近位端側が挿入されて、後側アーム移動チューブ32の近位端側の部分がベース部42に接続固定されている。 Further, the base portion 42 has a substantially cylindrical tube insertion hole (not shown) that opens at the distal end thereof and extends along the axis thereof, and the rear arm moving tube is formed in the tube insertion hole. The proximal end side of the rear arm moving tube 32 is connected and fixed to the base portion 42.
(縫合工程)
 以下、上述した縫合装置1を使用した切開部の縫合工程(縫合作業)について、図3A~図3Kを参照して説明する。なお、以下では、胃壁に形成された切開部を縫合する場合を例として説明する。
(Suture process)
Hereinafter, the stitching process (sewing operation) of the incision using the suturing device 1 will be described with reference to FIGS. 3A to 3K. Hereinafter, a case where an incision formed in the stomach wall is sutured will be described as an example.
 縫合工程の実施に先立ち、まず、内視鏡2に縫合装置1を装着する装着作業(装着工程)を実施する。すなわち、手技に使用する内視鏡2のシャフトの遠位端部(先端部)の外径に応じて、これに適合する内径を有する内視鏡装着部34bまたは34cを選択する。ここでは、比較的に小径の内視鏡2を使用するものとして、これに適合する内径を有する内視鏡装着部34cを選択するものとする。次いで、選択した内視鏡装着部34c以外の内視鏡装着部34bを、カッター等を用いて、あるいは引きちぎることにより切断し、除去する。 Prior to performing the suturing step, first, an attaching operation (attaching step) for attaching the suturing device 1 to the endoscope 2 is performed. That is, according to the outer diameter of the distal end portion (tip portion) of the shaft of the endoscope 2 used for the procedure, the endoscope mounting portion 34b or 34c having an inner diameter suitable for this is selected. Here, it is assumed that the endoscope 2 having a relatively small diameter is used, and the endoscope mounting portion 34c having an inner diameter suitable for the endoscope 2 is selected. Next, the endoscope mounting part 34b other than the selected endoscope mounting part 34c is cut and removed by using a cutter or the like or by tearing.
 次いで、内視鏡2の遠位端部および/または内視鏡装着部34cの内腔に潤滑剤を塗布し、内視鏡2の遠位端部を内視鏡装着部34cの内腔に挿入(圧入)して、縫合装置1のケースチューブ33の遠位端部を、装着アダプタ34(内視鏡装着部34c)を介して、内視鏡2の遠位端部に固定する。その後、ケースチューブ33を、内視鏡2のシャフトに適宜な間隔をあけて、複数箇所で、不図示の装着テープを巻くことにより、該シャフトに沿って固定する。これにより、縫合装置1の内視鏡2のシャフトに対する装着が完了する。 Next, a lubricant is applied to the distal end portion of the endoscope 2 and / or the lumen of the endoscope mounting portion 34c, and the distal end portion of the endoscope 2 is applied to the lumen of the endoscope mounting portion 34c. The distal end portion of the case tube 33 of the suturing device 1 is fixed to the distal end portion of the endoscope 2 via the mounting adapter 34 (endoscope mounting portion 34c) by inserting (press-fitting). Thereafter, the case tube 33 is fixed along the shaft by winding a mounting tape (not shown) at a plurality of locations at appropriate intervals around the shaft of the endoscope 2. Thereby, the mounting | wearing with respect to the shaft of the endoscope 2 of the suturing device 1 is completed.
 縫合工程を実施する際には、まず、縫合装置1の針状部材52aに結紮具7を装着しておき、縫合装置1を取り付けた内視鏡2のシャフトを胃内に挿入して、縫合装置1の縫合部5を縫合すべき切開部近傍に配置する。次いで、操作部4を操作して、前側アーム51に対して後側アーム52を離間させた状態とする(図1B参照)。 When performing the suturing step, first, the ligature tool 7 is attached to the needle-like member 52a of the suturing device 1, the shaft of the endoscope 2 to which the suturing device 1 is attached is inserted into the stomach, and suturing is performed. The suture part 5 of the device 1 is arranged near the incision part to be sutured. Next, the operation unit 4 is operated to bring the rear arm 52 away from the front arm 51 (see FIG. 1B).
 この状態で、図3Aに示す第1工程を実施する。図3Aに示す第1工程では、まず、操作部4をケースチューブ33に対して全体的に遠位端側に押し込むとともに、必要に応じて回転させて、同図に示されているように、後側アーム52に対して離間して配置されている前側アーム51のみを切開部SHに挿入する。これと前後して、前側アーム51に対して後側アーム52を回動させて、前側アーム51の一方の糸支持部51aと針状部材52a(やじり部)によって切開部SHの一方の口縁部Saが挟まれた状態となるように、前側アーム51と後側アーム52を配置する。 In this state, the first step shown in FIG. 3A is performed. In the first step shown in FIG. 3A, first, the operating portion 4 is pushed into the distal end side as a whole with respect to the case tube 33 and rotated as necessary, as shown in FIG. Only the front arm 51 that is spaced apart from the rear arm 52 is inserted into the incision SH. Before and after this, the rear arm 52 is rotated with respect to the front arm 51, and one lip of the incision SH is formed by one thread support portion 51a of the front arm 51 and the needle-shaped member 52a. The front arm 51 and the rear arm 52 are arranged so that the portion Sa is sandwiched.
 次いで、後側アーム52に対して前側アーム51を近接させると、図3Bに示されているように、針状部材52aが一方の口縁部Saに突き刺さり、該口縁部Saを貫通し、さらに針状部材52aのやじり部が一方の糸支持部51aの収容空間内に収容(支持)された係合部材6aの貫通孔を貫通して通過する。これにより、係合部材6aの貫通孔は、針状部材52aの組織貫通部に至り、係合部材6aが針状部材52aに係合された状態となる。 Next, when the front arm 51 is brought close to the rear arm 52, as shown in FIG. 3B, the needle-like member 52a pierces one of the mouth edge portions Sa, penetrates the mouth edge portion Sa, Further, the twisting portion of the needle-like member 52a passes through the through hole of the engaging member 6a accommodated (supported) in the accommodation space of the one thread support portion 51a. Thereby, the through hole of the engagement member 6a reaches the tissue penetration part of the needle-like member 52a, and the engagement member 6a is engaged with the needle-like member 52a.
 次いで、操作部4を操作して、縫合部5において、後側アーム52に対して前側アーム51を離間させた状態とすると、図3Cに示されているように、係合部材6aが係合された針状部材52aが一方の口縁部Saに挿通させる際に形成された孔(以下、第1穿孔という)を逆行して胃内に戻る。これにより、縫合糸6の一部(係合部材6a側の一部)が一方の口縁部Saを貫通した状態となる。 Next, when the operation unit 4 is operated so that the front arm 51 is separated from the rear arm 52 in the stitching unit 5, the engagement member 6a is engaged as shown in FIG. 3C. The needle-like member 52a thus made is inserted into one of the mouth edge portions Sa to reverse the hole (hereinafter referred to as the first perforation) and return to the stomach. As a result, a part of the suture thread 6 (a part on the engagement member 6a side) is in a state of penetrating the one edge portion Sa.
 その後、図3Dに示されているように、前側アーム51の他方の糸支持部51aと針状部材52aによって切開部SHの他方の口縁部Sbが挟まれた状態となるように、前側アーム51と後側アーム52を配置する。 Thereafter, as shown in FIG. 3D, the front arm 51a is so held that the other rim portion Sb of the incision SH is sandwiched between the other thread support portion 51a of the front arm 51 and the needle-like member 52a. 51 and the rear arm 52 are arranged.
 この状態から、操作部4を操作して、前側アーム51に対して後側アーム52を近接させると、図3Eに示されているように、針状部材52aが他方の口縁部Sbに突き刺さり、該口縁部Sbを貫通し、さらに針状部材52aのやじり部が他方の糸支持部51aの収容空間内に収容(支持)された係合部材6bの貫通孔を貫通して通過する。これにより、係合部材6bの貫通孔は、針状部材52aの組織貫通部に至り、係合部材6bが針状部材52aに係合された状態となる。 From this state, when the operation unit 4 is operated to bring the rear arm 52 closer to the front arm 51, the needle-like member 52a pierces the other mouth edge Sb as shown in FIG. 3E. The penetrating part of the needle-like member 52a passes through the through hole of the engaging member 6b accommodated (supported) in the accommodation space of the other thread support part 51a. Thereby, the through hole of the engagement member 6b reaches the tissue penetration part of the needle-like member 52a, and the engagement member 6b is engaged with the needle-like member 52a.
 次いで、操作部4を操作して、後側アーム52に対して前側アーム51を離間させた状態とすると、図3Fに示されているように、係合部材6bが係合された針状部材52aが他方の口縁部Sbに挿通させる際に形成された孔(以下、第2穿孔という)を逆行して胃内に戻る。これにより、縫合糸6の一部(係合部材6b側の一部)が他方の口縁部Sbを貫通した状態となる。 Next, when the operation unit 4 is operated so that the front arm 51 is separated from the rear arm 52, as shown in FIG. 3F, the needle-like member with which the engagement member 6b is engaged is obtained. A hole formed when 52a is inserted through the other mouth edge Sb (hereinafter referred to as a second perforation) returns to the stomach. As a result, a part of the suture thread 6 (a part on the engagement member 6b side) enters the other mouth edge Sb.
 これにより、縫合糸6の両端が固定されている一対の係合部材6a,6bがいずれも一本の針状部材52aに係合した状態となり、縫合糸6によって、針状部材52a(つまり胃内)から第1穿孔を貫通して胃外にでて、胃外面から第2穿孔を貫通して針状部材52a(つまり胃内)に戻る輪が形成される。 As a result, the pair of engaging members 6a and 6b, to which both ends of the suture thread 6 are fixed, are both engaged with the single needle-like member 52a, and the needle-like member 52a (that is, the stomach) is engaged by the suture thread 6. A ring is formed that penetrates the first perforation from the inner side to the outside of the stomach and returns from the outer surface of the stomach to the needle-like member 52a (that is, the stomach) through the second perforation.
 次いで、操作部4を操作して、図3Gに示されているように、前側アーム51(糸支持部51a)を、切開部SHを通して胃内に移動させる。前側アーム51(糸支持部51a)が胃内に入ると、針状部材52aが切開部SHから離間し、縫合糸6の両端が切開部SHから離間するように移動するので、縫合糸6において第1穿孔を貫通している部分と第2穿孔を貫通している部分とが引き寄せられ、切開部SHの一対の口縁部Sa,Sbの端面同士が当接して接合される。 Next, the operation unit 4 is operated to move the front arm 51 (thread support unit 51a) into the stomach through the incision SH as shown in FIG. 3G. When the front arm 51 (thread support part 51a) enters the stomach, the needle-like member 52a moves away from the incision part SH, and both ends of the suture thread 6 move away from the incision part SH. The portion that penetrates the first perforation and the portion that penetrates the second perforation are drawn, and the end surfaces of the pair of mouth edge portions Sa and Sb of the incision SH are brought into contact with each other and joined.
 縫合装置1による切開部SHの縫合作業が終了したならば、続いて、縫合糸6の結紮作業を行う。この作業には、図3Hに示されている結紮装置8が用いられる。結紮装置8としては、たとえば、内視鏡の処置具案内管を介して管腔内に導入されるシースおよび該シース内に摺動可能に挿通された操作ワイヤを備え、該操作ワイヤの遠位端に、シースの遠位端から突出することにより自己の弾性により略V字状に開脚し、該シースの遠位端部に引き込まれることにより閉脚するようにした連結フックを設けて構成されたものを用いることができる。 When the suturing operation of the incision SH with the suturing device 1 is completed, the suture 6 is subsequently ligated. For this work, the ligating apparatus 8 shown in FIG. 3H is used. The ligation device 8 includes, for example, a sheath introduced into a lumen via a treatment instrument guide tube of an endoscope, and an operation wire slidably inserted in the sheath, and the distal end of the operation wire At the end, a connecting hook that protrudes from the distal end of the sheath into a substantially V shape by its own elasticity and closes by being pulled into the distal end of the sheath is provided. Can be used.
 図3Gに示されているように、結紮具7は、針状部材52aの基端部(結紮具装着部)に、結紮用ループ7c(図1B参照)が挿入された状態で保持されているので、結紮装置8(図3H参照)の遠位端を結紮具7の連結用ループ7bの近傍に配置し、結紮装置8から突出されて開脚した連結フックで該連結用ループ7bを把持し、該連結用ループ7bを結紮装置8のシースの遠位端部に引き込むことにより、結紮具7を結紮装置8のシースの遠位端に連結する。 As shown in FIG. 3G, the ligature tool 7 is held in a state where the ligation loop 7c (see FIG. 1B) is inserted into the proximal end portion (ligation tool mounting portion) of the needle-like member 52a. Therefore, the distal end of the ligating device 8 (see FIG. 3H) is disposed in the vicinity of the connecting loop 7b of the ligating device 7, and the connecting loop 7b is grasped by the connecting hook protruding from the ligating device 8 and opened. The ligation tool 7 is connected to the distal end of the sheath of the ligating device 8 by drawing the connecting loop 7 b into the distal end of the sheath of the ligating device 8.
 次いで、図3Hに示されているように、結紮具7が連結された結紮装置8のシースの遠位端部を、切開部SH側(図3Hにおいて下方)へ移動させて、結紮具7の結紮用ループ7cの内側に縫合糸6の両端部が挿通された状態とする。これにより縫合糸6が絞り込まれ、縫合糸6の両端部が束ねられた状態となる。 Next, as shown in FIG. 3H, the distal end portion of the sheath of the ligation apparatus 8 to which the ligature tool 7 is connected is moved to the incision SH side (downward in FIG. 3H) to Assume that both ends of the suture thread 6 are inserted inside the ligation loop 7c. As a result, the suture thread 6 is squeezed and both ends of the suture thread 6 are bundled.
 縫合糸6の両端部が束ねられた状態から、結紮装置8の連結フックがシース内にさらに引き込まれるように操作ワイヤをスライドさせると、図3Iに示されているように、締付チューブ7a内に結紮用ループ7cが縫合糸6とともに引き込まれ、締付チューブ7a内に結紮用ループ7cおよび縫合糸6が密着しかつ圧縮された状態で収容される。つまり、結紮用ループ7cと縫合糸6とが締付チューブ7a内に締まり嵌めされた状態で収容されることになるので、縫合糸6および結紮用ループ7cの一端部は、締付チューブ7aから抜け落ちないように固定される。これにより、縫合糸6の結紮が完了する。 When the operation wire is slid from the state where both ends of the suture thread 6 are bundled so that the connecting hook of the ligating device 8 is further pulled into the sheath, as shown in FIG. The ligation loop 7c is drawn together with the suture thread 6, and the ligation loop 7c and the suture thread 6 are accommodated in the tightening tube 7a so as to be in close contact with each other and compressed. That is, since the ligation loop 7c and the suture thread 6 are accommodated in a state of being tightly fitted in the tightening tube 7a, one end of the suture thread 6 and the ligation loop 7c is separated from the tightening tube 7a. It is fixed so that it does not fall out. Thereby, the ligation of the suture thread 6 is completed.
 縫合糸6の結紮が完了したならば、結紮装置8の操作ワイヤの位置が変化しないようにしつつ、該操作ワイヤに対してシースを引き込むように近位端側にスライドすると、結紮装置8のシースの遠位端から連結フックおよびループ部材の他端部が突出(露出)し、連結フックが自己の弾性により開脚して、把持が解除され、図3Jに示されているように、結紮状態とされた結紮具7から結紮装置8が分離される。 When the ligation of the suture thread 6 is completed, the sheath of the ligation device 8 is moved by sliding the sheath toward the proximal end so as to draw the sheath against the operation wire while keeping the position of the operation wire of the ligation device 8 unchanged. The other end of the connecting hook and the loop member protrudes (exposes) from the distal end, and the connecting hook is opened by its own elasticity to release the grip. As shown in FIG. The ligation apparatus 8 is separated from the ligature tool 7 that has been determined.
 最後に、図3Kに示されているように、結紮具7と縫合部5(針状部材52a)との間の縫合糸6をループカッターと称される内視鏡用はさみ鉗子等により切断して、結紮具7と縫合部5とを切り離し、さらに必要に応じて、結紮状態の結紮具7の連結用ループ7bを、ループカッター等により切断し、回収することにより、1針の縫合に係る一連の手技が完了する。 Finally, as shown in FIG. 3K, the suture thread 6 between the ligature 7 and the suture part 5 (needle member 52a) is cut with an endoscopic scissors forceps called a loop cutter. Then, the ligature 7 and the stitched portion 5 are separated, and if necessary, the connection loop 7b of the ligature 7 in the ligated state is cut and collected by a loop cutter or the like, and one needle is sutured. A series of procedures is completed.
 上述した実施形態によると、ケースチューブ33の遠位端部に一体的に取り付けられた装着アダプタ34が、内視鏡が圧入される部分の内径が互いに異なる複数の内視鏡装着部34b,34cを有している。このため、遠位端部の外径の異なる複数種の内視鏡に適合させることが可能であり、従来のように、単一の内視鏡装着部しか備えないものと比較して、汎用性を向上させることができる。したがって、準備しておくべき縫合装置の数を従来よりも少なくすることができ、これを供給するメーカーとしても、これを使用する医療機関としても、経済的負担あるいは収納保管の場所的負担を低減することができる。 According to the above-described embodiment, the mounting adapter 34 integrally attached to the distal end portion of the case tube 33 has a plurality of endoscope mounting portions 34b and 34c having different inner diameters of the portions into which the endoscope is press-fitted. have. For this reason, it is possible to adapt to a plurality of types of endoscopes having different outer diameters at the distal end, and as compared with conventional ones having only a single endoscope mounting part, Can be improved. Therefore, the number of suturing devices to be prepared can be reduced as compared with the conventional one, and both the manufacturer supplying them and the medical institution using them can reduce the economic burden or the storage and storage burden. can do.
 また、装着アダプタ34の各内視鏡装着部34b,34cは、それぞれ必要に応じて、ケースチューブ33から個別に切り離し可能であるため、使用する内視鏡2に適合する内視鏡装着部(たとえば34c)以外の内視鏡装着部(たとえば34b)を選択的に切り離して除去することができる。使用しない内視鏡装着部を残したままであると、手技の支障となる虞があり、これを防止することができる。 In addition, since each of the endoscope mounting portions 34b and 34c of the mounting adapter 34 can be individually separated from the case tube 33 as needed, an endoscope mounting portion (compatible with the endoscope 2 to be used ( For example, an endoscope mounting part (for example, 34b) other than 34c) can be selectively separated and removed. If the endoscope mounting portion that is not used is left, there is a possibility that the procedure may be hindered, and this can be prevented.
 以上説明した実施形態は、本発明の理解を容易にするために記載されたものであって、本発明を限定するために記載されたものではない。従って、上述した実施形態に開示された各要素は、本発明の技術的範囲に属する全ての設計変更や均等物をも含む趣旨である。 The embodiment described above is described for facilitating understanding of the present invention, and is not described for limiting the present invention. Therefore, each element disclosed in the above-described embodiment is intended to include all design changes and equivalents belonging to the technical scope of the present invention.
 たとえば、上述した実施形態では、装着アダプタ34が一対の内視鏡装着部34b,34cを備えているものを例示したが、これらと内径の異なる単一または複数の他の内視鏡装着部をさらに設けてもよい。このようにすることで、さらに汎用性を向上することができる。 For example, in the above-described embodiment, the mounting adapter 34 includes a pair of endoscope mounting portions 34b and 34c. However, a single or a plurality of other endoscope mounting portions having different inner diameters from these are provided. Further, it may be provided. In this way, versatility can be further improved.
1…縫合装置
2…内視鏡
3…シース部
 31…前側アーム移動ワイヤ
 32…後側アーム移動チューブ
 33…ケースチューブ(チューブ)
 34…装着アダプタ
  34a…チューブ装着部
  34b,34c…内視鏡装着部
4…操作部
 41…スライダ部
 42…ベース部
5…縫合部
 51…前側アーム
  51a…糸支持部
 52…後側アーム
  52a…針状部材
  52b…針支持部
  52c…後側ガイド部
 53…前側ガイド部
  53a…切欠部
  53b…貫通ガイド溝
6…縫合糸
 6a,6b…係合部材
7…結紮具
 7a…締付チューブ
 7b…連結用ループ
 7c…結紮用ループ
SH…切開部
Sa,Sb…口縁部
8…結紮装置
DESCRIPTION OF SYMBOLS 1 ... Suture apparatus 2 ... Endoscope 3 ... Sheath part 31 ... Front side arm movement wire 32 ... Rear side arm movement tube 33 ... Case tube (tube)
34 ... Attachment adapter 34a ... Tube attachment part 34b, 34c ... Endoscope attachment part 4 ... Operation part 41 ... Slider part 42 ... Base part 5 ... Suture part 51 ... Front arm 51a ... Yarn support part 52 ... Rear arm 52a ... Needle-like member 52b ... needle support portion 52c ... rear guide portion 53 ... front guide portion 53a ... notch portion 53b ... penetration guide groove 6 ... suture thread 6a, 6b ... engagement member 7 ... ligature 7a ... tightening tube 7b ... Linking loop 7c ... Ligating loop SH ... Incision part Sa, Sb ... Mouth edge 8 ... Ligating device

Claims (3)

  1.  内視鏡の外側に必要に応じて装着される内視鏡用外付けチューブ部材であって、
    内視鏡の近位端から遠位端に沿って配置されるチューブと、
    前記チューブの遠位端部にそれぞれ設けられ、内視鏡が挿入される内腔の径が互いに異なる略円筒状の複数の内視鏡装着部と、を有する内視鏡用外付けチューブ部材。
    An external tube member for an endoscope that is attached to the outside of an endoscope as needed,
    A tube disposed from the proximal end to the distal end of the endoscope;
    An external tube member for an endoscope, comprising a plurality of substantially cylindrical endoscope mounting portions, each provided at a distal end portion of the tube and having different diameters of lumens into which endoscopes are inserted.
  2.  前記内視鏡装着部は、前記チューブから個別に切り離し可能である請求項1に記載の内視鏡用外付けチューブ部材。 The external tube member for an endoscope according to claim 1, wherein the endoscope mounting portion can be individually separated from the tube.
  3.  前記内視鏡装着部の内腔を、内視鏡が挿入される方向に沿って拡径するテーパ状とした請求項1または2に記載の内視鏡用外付けチューブ部材。 The endoscope external tube member according to claim 1 or 2, wherein the lumen of the endoscope mounting portion has a tapered shape whose diameter is increased along a direction in which the endoscope is inserted.
PCT/JP2019/013260 2018-03-30 2019-03-27 External tube member for endoscope WO2019189400A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2020509213A JP7251543B2 (en) 2018-03-30 2019-03-27 External tube member for endoscope

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2018-068909 2018-03-30
JP2018068909 2018-03-30

Publications (1)

Publication Number Publication Date
WO2019189400A1 true WO2019189400A1 (en) 2019-10-03

Family

ID=68059168

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2019/013260 WO2019189400A1 (en) 2018-03-30 2019-03-27 External tube member for endoscope

Country Status (2)

Country Link
JP (1) JP7251543B2 (en)
WO (1) WO2019189400A1 (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6071233A (en) * 1997-10-31 2000-06-06 Olympus Optical Co., Ltd. Endoscope
US20020107530A1 (en) * 2001-02-02 2002-08-08 Sauer Jude S. System for endoscopic suturing
JP2005131107A (en) * 2003-10-30 2005-05-26 Olympus Corp External channel and endoscope apparatus equipped with the same
JP2011067532A (en) * 2009-09-28 2011-04-07 Japan Health Science Foundation Assisting instrument for endoscope, and endoscope
JP2012161454A (en) * 2011-02-07 2012-08-30 Hoya Corp External channel for endoscope

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6071233A (en) * 1997-10-31 2000-06-06 Olympus Optical Co., Ltd. Endoscope
US20020107530A1 (en) * 2001-02-02 2002-08-08 Sauer Jude S. System for endoscopic suturing
JP2005131107A (en) * 2003-10-30 2005-05-26 Olympus Corp External channel and endoscope apparatus equipped with the same
JP2011067532A (en) * 2009-09-28 2011-04-07 Japan Health Science Foundation Assisting instrument for endoscope, and endoscope
JP2012161454A (en) * 2011-02-07 2012-08-30 Hoya Corp External channel for endoscope

Also Published As

Publication number Publication date
JPWO2019189400A1 (en) 2021-04-08
JP7251543B2 (en) 2023-04-04

Similar Documents

Publication Publication Date Title
US7527590B2 (en) Anastomosis system
JP5294181B2 (en) Suture device
EP1769749B1 (en) Surgical suture instrument
JP5248813B2 (en) Endoscopic living body wall fixture
WO2007037335A1 (en) Suturing device
JP2007289673A (en) Treatment tool for endoscope
WO2017111163A1 (en) Endoscopic suture ligation tool
JP2012024607A (en) Suture device
WO2019189400A1 (en) External tube member for endoscope
WO2021193822A1 (en) Mounting member for endoscope
JP2018094325A (en) Suture apparatus
JP7188435B2 (en) Suture device
JP7264149B2 (en) Suture device
JP7056324B2 (en) Medical suture device
CN110099611B (en) Suturing device
JP2017169941A (en) Suture equipment
CN110719756B (en) Suturing device
WO2021145289A1 (en) Surgical suture ligator for endoscopes and ligating device
JP7346877B2 (en) Suture ligation device for endoscope
JP5308734B2 (en) Biological suture tool
JP6670392B2 (en) Surgical instrument and replacement unit for the surgical instrument
JP2018171294A (en) Suture
JP4350472B2 (en) Insertion aid for treatment of full-thickness colorectal resection and its medical instrument system

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: 19778049

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2020509213

Country of ref document: JP

Kind code of ref document: A

122 Ep: pct application non-entry in european phase

Ref document number: 19778049

Country of ref document: EP

Kind code of ref document: A1