WO2021044633A1 - Endoscope - Google Patents

Endoscope Download PDF

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Publication number
WO2021044633A1
WO2021044633A1 PCT/JP2019/035268 JP2019035268W WO2021044633A1 WO 2021044633 A1 WO2021044633 A1 WO 2021044633A1 JP 2019035268 W JP2019035268 W JP 2019035268W WO 2021044633 A1 WO2021044633 A1 WO 2021044633A1
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WO
WIPO (PCT)
Prior art keywords
nozzle
tip
endoscope
fluid supply
opening
Prior art date
Application number
PCT/JP2019/035268
Other languages
French (fr)
Japanese (ja)
Inventor
雄偉 王
Original Assignee
オリンパス株式会社
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Filing date
Publication date
Application filed by オリンパス株式会社 filed Critical オリンパス株式会社
Priority to PCT/JP2019/035268 priority Critical patent/WO2021044633A1/en
Publication of WO2021044633A1 publication Critical patent/WO2021044633A1/en

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    • 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
    • A61B1/12Instruments 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 with cooling or rinsing arrangements

Definitions

  • the present invention relates to an endoscope provided with a nozzle for injecting a fluid at the tip of an insertion portion.
  • endoscopes are widely used for observing and treating the inside of a living body (inside the body cavity), or for inspection and repair in industrial plant equipment.
  • the endoscope has an insertion section for insertion into a flexible conduit.
  • Such an endoscope is, for example, as disclosed in Japanese Patent Application Laid-Open No. 6-319690, a liquid for cleaning the surface of an observation window, an illumination window, or the like at the tip of an insertion portion, a gas supplied into a body cavity, or the like.
  • An air supply / water supply nozzle that ejects the fluid of the above is provided.
  • a local anesthetic solution such as lidocaine may be sprayed into the trachea and bronchi in order to suppress the cough reflex and vomiting reflex of the patient.
  • the local anesthetic solution is sprayed through the forceps channel, but the drug solution remains in the forceps channel, or a sufficient amount of the drug solution is uniformly sprayed from the tip opening of the forceps channel to the target range. There is a problem that it is difficult.
  • the present invention has been made in view of the above circumstances, and provides an endoscope capable of reducing the diameter of the insertion portion, preventing the drug solution from leaking into the body cavity, and uniformly spraying the drug solution in a target range.
  • the purpose is.
  • the endoscope has an operation unit, a long insertion unit connected to the operation unit and inserted into a subject, and an optical window composed of a light transmitting member of the insertion unit.
  • a nozzle provided with a tip component disposed at the tip portion, a fluid supply tube disposed at the insertion portion, and an opening that communicates with the fluid supply tube and ejects the fluid supplied from the fluid supply tube. And, the nozzle is arranged in the tip component so that the opening faces the outer radial direction of the tip portion not including the optical window.
  • an endoscope capable of reducing the diameter of the insertion portion, preventing the drug solution from leaking into the body cavity, and uniformly spraying the drug solution in the target range.
  • the figure which shows the appearance of the endoscope of one aspect of this invention The same, perspective view which shows the structure of the tip part of the insertion part.
  • the front view showing the structure of the tip of the insertion part.
  • Partial cross-sectional view showing the tip of the insertion part inserted into the trachea and bronchus.
  • the front view showing the structure of the tip of the insertion part having the forceps channel.
  • Front view showing the tip portion of the nozzle of the second modification in a state where the injection port faces the outer diameter direction.
  • Partial sectional view showing the structure of the nozzle provided at the tip of the second modification. The figure which shows the operation part provided with the lever which rotates the nozzle of the 2nd modification.
  • Partial sectional view which shows the structure of the nozzle provided in the tip part of the 3rd modification.
  • Perspective view showing the configuration of the tip portion of the insertion portion of the fourth modified example.
  • Front view showing the configuration of the tip portion of the fourth modification
  • Partial sectional view showing the structure of the tip part provided with the nozzle of the 4th modification.
  • Partial sectional view which shows the structure of the nozzle provided in the tip part of the 5th modification.
  • Top view showing the structure of the nozzle provided at the tip of the fifth modification.
  • Partial cross-sectional view showing a state in which the cleaning liquid is ejected from the first injection port of the nozzle of the fifth modification.
  • Partial sectional view showing a state in which a local anesthetic solution is ejected from the second injection port of the nozzle of the fifth modification.
  • the drawings based on each embodiment are schematic, and the relationship between the thickness and width of each part, the ratio of the thickness of each part, and the like are different from the actual ones. It should be noted that the drawings may include parts having different dimensional relationships and ratios from each other.
  • the endoscope in the following configuration description exemplifies a so-called bronchoscope having a small-diameter insertion portion and used for examination and treatment of trachea, bronchus, etc., but is not limited thereto.
  • This technique can be applied to a so-called flexible endoscope having a flexible insertion portion for insertion into the digestive organs above or below the living body, and a so-called rigid endoscope having a rigid insertion portion used for surgery.
  • the endoscope 1 which is an electronic endoscope of the present embodiment, has a long insertion portion 2 having an outer diameter of about 3 to 4 mm and a base of the insertion portion 2.
  • the insertion portion 2 is a tubular member having flexibility formed by connecting the tip portion 6, the curved portion 7, and the flexible tube portion 8 in this order from the tip side. Of these, an imaging means, a lighting means, and the like are housed and arranged at the tip portion 6.
  • the curved portion 7 is a mechanical portion of the operating member of the operating portion 3 that is configured to be able to be actively curved in two vertical directions (UP-DOWN) of the inserting portion 2 by the rotation operation of the bending lever 13. is there.
  • the curved portion 7 is not limited to a type that actively curves in two vertical directions, and the curved portion 7 is not limited to a type that actively bends in two vertical directions, and the curved portion 7 is not limited to a type that actively bends in two vertical directions. It may be of a type that can be curved in the circumferential direction (UP-DOWN / LEFT-RIGHT).
  • the bending portion 7 may be of a type capable of bending only in one direction in the upward (UP) direction, and further, does not have a mechanism for actively bending by the bending lever 13, and simply passively bends. It may be of the type.
  • the flexible tube portion 8 is a tubular member formed with flexibility so as to be passively flexible.
  • the inside of the flexible tube portion 8 extends from an imaging device (not shown) built in the tip portion 6 and further extends from the operating portion 3 to the inside of the universal cord 4 from an imaging cable and a light source device.
  • a light guide bundle or the like, which will be described later, for guiding the illumination light of the above and emitting it from the tip portion 6 is inserted (these are not shown here).
  • the operation unit 3 is provided on the tip side and covers the base end of the flexible pipe portion 8 and is connected to the flexible pipe portion 8. It has a grip portion 10 that is gripped by hand when the mirror 1 is used.
  • the operation unit 3 includes, as the endoscope operating means, a plurality of various switches 14 for performing each corresponding operation such as a bending lever 13 for performing a bending operation of the bending portion 7, an imaging means, a lighting means, and a liquid feeding tube. Is connected to provide a fluid supply port 15 to which a chemical solution or the like is supplied by a syringe or the like.
  • the universal cord 4 is a light guide bundle that transmits illumination light from a signal cable bundle, a light source device (not shown), etc. from the tip portion 6 of the insertion portion 2 through the inside of the insertion portion 2 to reach the operation unit 3. Is a composite cable inserted.
  • the endoscope connector 5 has an electric connector portion 16 on the side surface to which a signal cable for connecting to a video processor (not shown) of an external device is connected, and also connects to a light source device which is an external device. It is configured to include a light source connector portion 17 having a light source connection plug 18 to which a light guide bundle described later and an electric cable (not shown) are connected.
  • the configuration of the tip portion of the insertion portion 2 of the endoscope 1 of the present embodiment will be described below based on FIGS. 2 and 3. In the following description, the description of the well-known configuration of the insertion portion 2 will be omitted.
  • the tip portion 6 of the insertion portion 2 has a tip frame main body 21 as a tip component made of metal or resin.
  • the tip frame main body 21 is provided with a tip cap 23.
  • Observation light having an optical axis O substantially parallel to the longitudinal axis X of the linear insertion portion 2 is incident on the tip surface 22 of the tip cap 23.
  • it is an optical window of a substantially circular light transmitting member and is built in.
  • An observation optical system 24 arranged at the tip of an imaging device (not shown), an illumination optical system 25 which is an optical window of a substantially circular light transmitting member, and a chemical solution for ejecting a fluid such as a chemical solution or air.
  • the nozzle 31 as a spraying portion is provided so as to be exposed.
  • the observation optical system 24 and the illumination optical system 25 are not limited to one, and may be plural.
  • the outer peripheral portion of the base end of the tip frame main body 21 is covered with the tip portion of the curved rubber 28 which is the outer skin of the curved portion 7.
  • the curved rubber 28 is provided with a pincushion adhesive portion 27 on the outer periphery of the tip portion, and is fixed to the base end outer peripheral portion of the tip frame main body 21.
  • the nozzle 31 is made of a metal such as stainless steel, and is provided so that the injection port 32, which is an opening for ejecting a fluid, faces substantially the opposite side of the observation optical system 24. That is, the injection port 32 faces a direction that does not include the observation optical system 24, and the fluid injected from the injection port 32 is in the outer peripheral (outer diameter) direction of the tip portion 6 that is substantially orthogonal to the longitudinal axis X of the insertion portion 2.
  • the orientation of the nozzle 31 is set as described above.
  • the injection direction of the nozzle 31 from the injection port 32 is substantially orthogonal to the opening surface of the injection port 32, is on the opposite side of the observation optical system 24, and is the center of the observation optical system 24 (the optical axis O passes through). It is set to be in the direction along the line passing through the point) (in the direction of the arrow line R in the figure).
  • a fluid supply tube 33 (see FIG. 4) as a liquid feeding tube is communicated with the nozzle 31.
  • the fluid supply tube 33 is arranged in the insertion portion 2 and the operation portion 3, and the other end thereof is communicated with the fluid supply port 15 (see FIG. 1) provided in the operation portion 3.
  • the insertion portion 2 is inserted into, for example, the trachea and the airway of the bronchus 100.
  • a local anesthetic solution such as lidocaine is administered in order to suppress the cough reflex and vomiting reflex of the patient.
  • the local anesthetic solution When the local anesthetic solution is administered to the trachea and bronchus 100, the local anesthetic solution is injected into the fluid supply tube 33 from the fluid supply port 15 using a syringe or the like to form the airways of the trachea and bronchus 100 from the nozzle 31.
  • a local anesthetic solution is sprayed toward the mucous membrane of the tracheal (bronchial) wall. Then, the local anesthetic solution is sprayed on the mucous membrane of the tracheal (bronchial) wall from the injection port 32 of the nozzle 31 facing the outer diameter direction of the tip portion 6.
  • the endoscope 1 of the present embodiment is different from the conventional configuration in which the local anesthetic solution is sprayed on the mucous membrane of the tracheal (bronchial) wall by using the forceps channel, and the tip portion 6 of the insertion portion 2 is used. It is configured so that it can be sprayed on the mucous membrane of the tracheal (bronchial) wall from the injection port 32 of the nozzle 31 facing the outer radial direction of.
  • a predetermined amount of the drug solution is uniformly applied to the area of the mucous membrane of the target tracheal (bronchial) wall without leaking the local anesthetic solution from the opening of the forceps channel or leaving the drug solution in the treatment tool channel. Can be sprayed on.
  • the dose of the local anesthetic solution can be easily controlled, and the anesthetic effect can be kept constant.
  • the endoscope 1 does not require a forceps channel for spraying the local anesthetic solution, the insertion portion 2 is further reduced in diameter if only the examination is performed without requiring the treatment of the trachea and the bronchus 100. can do. As shown in FIG. 6, the endoscope 1 may have a forceps channel 26.
  • the endoscope 1 may have a predetermined angle ⁇ so that the injection port 32 of the nozzle 31 faces the tip side with respect to the direction orthogonal to the longitudinal axis X of the insertion portion 2. Good.
  • the endoscope 1 can be performed while observing the injection state and the spraying state of the local anesthetic solution from the injection port 32 of the nozzle 31 in a predetermined range of the mucous membrane of the tracheal (branch) wall.
  • the nozzle 31 is rotatable so that the injection port 32 can be changed in the direction facing the outer diameter of the tip portion 6 and the direction facing the observation optical system 24, the illumination optical system 25, and the like. It may be configured as such.
  • the endoscope 1 of this modified example has a configuration in which the nozzle 31 is rotatable so that the injection direction of the fluid from the injection port 32 of the nozzle 31 (R direction along the arrow line in the figure) can be changed.
  • the nozzle 31 here is rotatably arranged so as to be inserted into the hole 29 of the tip frame main body 21 around the longitudinal axis C.
  • a flange 34 is formed in a portion of the nozzle 31 accommodated in the tip frame main body 21, and a sealing member 35 such as an O-ring is provided on the outer peripheral portion of the flange 34.
  • One end of the fluid supply tube 33 is connected to the base end portion of the nozzle 31. Then, the coil tube 37 in which the metal wire that transmits the rotational power to the nozzle 31 and prevents the fluid supply tube 33 from being twisted to the extent that the flexibility of the insertion portion 2 is not impaired is tightly wound around the outer circumference of the fluid supply tube 33. It is provided so as to cover the part.
  • the operation unit 3 is provided with a lever 11 which is an operation member for rotating the nozzle 31.
  • the endoscope 1 of this modified example is configured so that the nozzle 31 can be rotated around the longitudinal axis C, and in addition to spraying the local anesthetic solution on the mucous membrane of the tracheal (branch) wall, from the injection port 32 of the nozzle 31.
  • a cleaning solution such as physiological saline can be sprayed onto the observation optical system 24 and the illumination optical system 25 for cleaning.
  • the nozzle 31 is rotatable, when the local anesthetic solution is sprayed on the mucous membrane of the tracheal (bronchial) wall, the local anesthetic solution is applied to the entire circumference of the tracheal (bronchial) wall without twisting the insertion portion 2. It can be easily sprayed.
  • the nozzle 31 abuts and rotates so that the injection direction of the fluid from the injection port 32 (R direction along the arrow line in the figure) is the observation optical system 24 and the illumination optical system 25.
  • a stopper 37 which is a protrusion whose moving position is defined, may be provided on the tip surface 22.
  • the operation unit 3 may be provided with an index that allows the injection direction of the fluid from the nozzle 31 depending on the operation position of the lever 11 to be confirmed at hand.
  • the nozzle 31 may have a structure that is rotatable and that can be moved forward and backward so as to extend from the tip portion 6 to a predetermined length.
  • the nozzle 31 here has a hard tube portion 36 formed of a metal such as stainless steel having an outer diameter of about 1 mm.
  • the nozzle 31 is set so that the length L2 along the longitudinal axis C of the hard pipe portion 36 is shorter (L1> L2) than the hard length L1 of the tip portion 6.
  • the nozzle 31 here has the same configuration as the second modification except that it has a hard pipe portion 36 having a predetermined length L2.
  • the operation unit 3 is provided with a rotation lever 12 which is an operation member for moving the nozzle 31 forward and backward, and the pedestal 13 provided with the rotation lever 12 is used for the operation unit 3.
  • the nozzle 31 is configured to rotate around the longitudinal axis C by rotating the nozzle 31 around the longitudinal axis Y.
  • the endoscope 1 of this modification is configured so that the nozzle 31 can be moved forward and backward along the longitudinal axis C so as to extend from the tip portion 6. Local anesthetic solution can be sprayed on the mucous membrane of the tracheal (bronchial) wall.
  • the nozzle 31 can move forward and backward, the local anesthetic solution is applied to the mucous membrane of the tracheal (bronchial) wall in the entire circumference of the tracheal (bronchial) wall and in the anterior-posterior direction without pushing and pulling the insertion portion 2. Can be easily sprayed.
  • the tip surface 22 of the tip cap 23 of this modification may have a stepped portion 22a as a recess in the portion where the nozzle 31 is arranged.
  • the step portion 22a is formed up to the outer peripheral portion of the tip cap 23 along the direction in which the injection port 32 of the nozzle 31 faces.
  • the local anesthetic solution sprayed from the injection port 32 of the nozzle 31 does not flow to the observation optical system 24 side, and the field of view is secured. , It is possible to prevent the obstruction of visibility.
  • the nozzle 50 of this modification has a first opening 51 facing the direction of the observation window and a second opening facing the opposite side of the first injection port 51.
  • the second injection port 52 is provided with two openings at both ends.
  • the nozzle 50 has a first flow path 51a communicating with the first injection port 51 and a second flow path 52a communicating with the second injection port 52, and these first flow paths 51a and the second flow path 52a.
  • the flow path 52a is partitioned by the partition wall 54.
  • the nozzle 50 is formed up to an intermediate portion of the tubular portion in which the partition wall 54 is inserted into the tip cap 23, and the first flow path 51a and the second flow path 52a communicate with each other at the base end portion. ..
  • a substantially cylindrical rotating portion 53 as a switching member rotatably held from the partition wall 54 to the base end side is inserted in the tubular portion of the nozzle 50.
  • the rotating portion 53 is integrally formed with the flange 34 provided with the seal member 35, and the fluid supply tube 33 is connected to the proximal end side of the flange 34.
  • An opening is formed in the tip surface of the rotating portion 53 so that when communicating with either the first flow path 51a or the second flow path 52a depending on the rotation position, the rotating portion 53 does not communicate with the other.
  • the flow path 53a of 3 is formed.
  • the third flow path communicates with the fluid supply tube 33.
  • the rotating portion 53 in the tubular portion of the nozzle 50 is rotated, and the opening of the third flow path 53a is opened. It fits into the first flow path 51a or the second flow path 52a, and the third flow path 53a communicates with either the first flow path 51a or the second flow path 52a.
  • the fluid supply tube 33 communicates with either the first flow path 51a or the second flow path 52a according to the rotation position of the rotating portion 53.
  • the cleaning liquid R1 such as physiological saline sent from the fluid supply tube 33 is transferred to the first nozzle 50. Can be cleaned by injecting into the observation optical system 24 and the illumination optical system 25 from the injection port 51 of the above.
  • the local anesthetic solution R2 sent from 33 can be sprayed from the second injection port 52 of the nozzle 50 to the entire circumference of the tracheal (branch) wall.

Abstract

An endoscope 1 comprises: an operation unit 3; a long insertion unit 2 that is connected to the operation unit 3, and that is inserted into a subject of examination; a tip component 21 that has an optical window constituted of a light transmissive member, and that is disposed on a tip 6 of the insertion unit 2; a fluid supply tube 33 that is disposed in the insertion unit 2; and a nozzle 31 that is connected to the fluid supply tube 33, and that discharges, through an opening 32, a fluid supplied from the fluid supply tube 33. The nozzle 31 is disposed on the tip component 21 such that the opening 32 faces the outer diametrical direction of the tip 6 that does not include the optical window.

Description

内視鏡Endoscope
 本発明は、挿入部の先端部に流体を噴射するノズルが設けられた内視鏡に関する。 The present invention relates to an endoscope provided with a nozzle for injecting a fluid at the tip of an insertion portion.
 周知の如く、内視鏡は、生体の体内(体腔内)の観察、処置など、または工業用のプラント設備内の検査、修理などのため広く用いられている。内視鏡は、屈曲する管路に挿入するための挿入部を有している。このような内視鏡は、例えば、特開平6-319690号公報に開示されるように、挿入部の先端部の観察窓、照明窓などの表面を洗浄する液体、体腔内に供給する気体などの流体を噴出する送気送水ノズルが設けられている。 As is well known, endoscopes are widely used for observing and treating the inside of a living body (inside the body cavity), or for inspection and repair in industrial plant equipment. The endoscope has an insertion section for insertion into a flexible conduit. Such an endoscope is, for example, as disclosed in Japanese Patent Application Laid-Open No. 6-319690, a liquid for cleaning the surface of an observation window, an illumination window, or the like at the tip of an insertion portion, a gas supplied into a body cavity, or the like. An air supply / water supply nozzle that ejects the fluid of the above is provided.
 ところで、気管支内視鏡においては、患者の咳反射、嘔吐反射などを抑制するために、リドカインなどの局所麻酔薬液を気管および気管支内に散布する場合がある。従来、局所麻酔薬液の散布は、鉗子チャネルを通じて行っているが、鉗子チャンネル内に薬液が残存したり、鉗子チャンネルの先端開口から目的とする範囲に十分量の薬液を均一に散布したりすることが困難であるという課題がある。 By the way, in bronchial endoscopy, a local anesthetic solution such as lidocaine may be sprayed into the trachea and bronchi in order to suppress the cough reflex and vomiting reflex of the patient. Conventionally, the local anesthetic solution is sprayed through the forceps channel, but the drug solution remains in the forceps channel, or a sufficient amount of the drug solution is uniformly sprayed from the tip opening of the forceps channel to the target range. There is a problem that it is difficult.
 そのため、局所麻酔薬液の投与量は症例によってバラツキが大きく、麻酔効果も一定とならないという問題があった。さらに、気管支内視鏡は、細い気管支内に挿入するため、挿入部をより細径化することが望まれている。 Therefore, there is a problem that the dose of the local anesthetic solution varies greatly depending on the case and the anesthetic effect is not constant. Further, since the bronchial endoscope is inserted into a narrow bronchus, it is desired to make the insertion portion smaller in diameter.
 そこで、本発明は、上記事情に鑑みなされたものであり、挿入部を細径化でき、体腔内への薬液漏れがなく、薬液を目的とする範囲に均一に散布できる内視鏡を提供することを目的とする。 Therefore, the present invention has been made in view of the above circumstances, and provides an endoscope capable of reducing the diameter of the insertion portion, preventing the drug solution from leaking into the body cavity, and uniformly spraying the drug solution in a target range. The purpose is.
 本発明の一態様における内視鏡は、操作部と、前記操作部に接続され、被験体に挿入される長尺の挿入部と、光透過部材からなる光学窓を有し、前記挿入部の先端部に配設される先端構成部と、前記挿入部に配設された流体供給チューブと、前記流体供給チューブに連通し、前記流体供給チューブから供給された流体を噴出する開口を備えたノズルと、を具備し、前記ノズルは、前記開口が前記光学窓を含まない前記先端部の外径方向を臨むように、前記先端構成部に配設されている。 The endoscope according to one aspect of the present invention has an operation unit, a long insertion unit connected to the operation unit and inserted into a subject, and an optical window composed of a light transmitting member of the insertion unit. A nozzle provided with a tip component disposed at the tip portion, a fluid supply tube disposed at the insertion portion, and an opening that communicates with the fluid supply tube and ejects the fluid supplied from the fluid supply tube. And, the nozzle is arranged in the tip component so that the opening faces the outer radial direction of the tip portion not including the optical window.
 本発明によれば、挿入部を細径化でき、体腔内への薬液漏れがなく、薬液を目的とする範囲に均一に散布できる内視鏡を提供することができる。 According to the present invention, it is possible to provide an endoscope capable of reducing the diameter of the insertion portion, preventing the drug solution from leaking into the body cavity, and uniformly spraying the drug solution in the target range.
本発明の一態様の内視鏡の外観を示す図The figure which shows the appearance of the endoscope of one aspect of this invention 同、挿入部の先端部分の構成を示す斜視図The same, perspective view which shows the structure of the tip part of the insertion part. 同、挿入部の先端部の構成を示す正面図The front view showing the structure of the tip of the insertion part. 同、気管、気管支に挿入された挿入部の先端部分を示す部分断面図Partial cross-sectional view showing the tip of the insertion part inserted into the trachea and bronchus. 同、図4のV-V線に沿った気管、気管支に挿入された先端部を示す部分断面図Partial cross-sectional view showing the tip of the trachea and the bronchus along the VV line of FIG. 同、鉗子チャンネルを有する挿入部の先端部の構成を示す正面図The front view showing the structure of the tip of the insertion part having the forceps channel. 第1の変形例の気管、気管支に挿入された挿入部の先端部分を示す部分断面図Partial cross-sectional view showing the tip of the insertion portion inserted into the trachea and bronchus of the first modification. 第2の変形例のノズルの噴射口が外径方向を臨んだ状態の先端部を示す正面図Front view showing the tip portion of the nozzle of the second modification in a state where the injection port faces the outer diameter direction. 第2の変形例のノズルの噴射口が観察光学系を臨んだ状態の先端部を示す正面図Front view showing the tip of the nozzle of the second modification in a state where the injection port faces the observation optical system. 第2の変形例の先端部に設けられるノズルの構成を示す部分断面図Partial sectional view showing the structure of the nozzle provided at the tip of the second modification. 第2の変形例のノズルを回動操作するレバーが設けられた操作部を示す図The figure which shows the operation part provided with the lever which rotates the nozzle of the 2nd modification. 第2の変形例のノズルの噴射口が観察光学系を臨むようにストッパにより回動位置が規制された状態の先端部を示す正面図Front view showing the tip portion in a state where the rotation position is restricted by a stopper so that the injection port of the nozzle of the second modification faces the observation optical system. 第2の変形例のノズルの噴射口が証明光学系を臨むようにストッパにより回動位置が規制された状態の先端部を示す正面図Front view showing the tip portion in a state where the rotation position is regulated by a stopper so that the injection port of the nozzle of the second modification faces the proof optical system. 第3の変形例の挿入部の先端部分の構成を示す斜視図A perspective view showing the configuration of the tip portion of the insertion portion of the third modification. 第3の変形例の挿入部の先端部の構成を示す正面図Front view showing the configuration of the tip of the insertion portion of the third modification. 第3の変形例の先端部に設けられるノズルの構成を示す部分断面図Partial sectional view which shows the structure of the nozzle provided in the tip part of the 3rd modification. 第3の変形例のノズルを回動操作および進退操作するレバーと台座が設けられた操作部を示す図The figure which shows the operation part provided with the lever and the pedestal which rotate and advance / retreat the nozzle of the 3rd modification. 第4の変形例の挿入部の先端部分の構成を示す斜視図Perspective view showing the configuration of the tip portion of the insertion portion of the fourth modified example. 第4の変形例の先端部の構成を示す正面図Front view showing the configuration of the tip portion of the fourth modification 第4の変形例のノズルが設けられた先端部の構成を示す部分断面図Partial sectional view showing the structure of the tip part provided with the nozzle of the 4th modification. 第5の変形例の先端部に設けられるノズルの構成を示す部分断面図Partial sectional view which shows the structure of the nozzle provided in the tip part of the 5th modification. 第5の変形例の先端部に設けられるノズルの構成を示す平面図Top view showing the structure of the nozzle provided at the tip of the fifth modification. 第5の変形例のノズルの第1の噴射口から洗浄液が噴射された状態を示す部分断面図Partial cross-sectional view showing a state in which the cleaning liquid is ejected from the first injection port of the nozzle of the fifth modification. 第5の変形例のノズルの第2の噴射口から局所麻酔薬液が噴射された状態を示す部分断面図Partial sectional view showing a state in which a local anesthetic solution is ejected from the second injection port of the nozzle of the fifth modification.
 以下、本発明である内視鏡の先端ユニットおよび内視鏡の一態様を説明する。なお、以下の説明において、各実施の形態に基づく図面は、模式的なものであり、各部分の厚みと幅との関係、夫々の部分の厚みの比率などは現実のものとは異なることに留意すべきであり、図面の相互間においても互いの寸法の関係や比率が異なる部分が含まれている場合がある。 
 また、以下の構成説明における内視鏡は、細径の挿入部を有し、気管、気管支などの検査、治療に用いられる所謂気管支鏡を例示しているが、これに限定されることなく、生体の上部または下部の消化器官に挿入するため挿入部が可撓性のある所謂軟性鏡、外科用に用いられる挿入部が硬質な所謂硬性鏡にも適用可能な技術である。 
Hereinafter, one aspect of the tip unit of the endoscope and the endoscope according to the present invention will be described. In the following description, the drawings based on each embodiment are schematic, and the relationship between the thickness and width of each part, the ratio of the thickness of each part, and the like are different from the actual ones. It should be noted that the drawings may include parts having different dimensional relationships and ratios from each other.
Further, the endoscope in the following configuration description exemplifies a so-called bronchoscope having a small-diameter insertion portion and used for examination and treatment of trachea, bronchus, etc., but is not limited thereto. This technique can be applied to a so-called flexible endoscope having a flexible insertion portion for insertion into the digestive organs above or below the living body, and a so-called rigid endoscope having a rigid insertion portion used for surgery.
 以下、本発明の一態様の内視鏡について、図面に基づいて説明する。
 図1に示すように、本実施形態の電子内視鏡である内視鏡1は、被検体に挿入される長尺な外径3~4mm程度の挿入部2と、この挿入部2の基端に連設される操作部3と、この操作部3から延設される内視鏡ケーブルであるユニバーサルコード4と、このユニバーサルコード4の先端に配設される内視鏡コネクタ5などによって主に構成されている。
Hereinafter, an endoscope according to one aspect of the present invention will be described with reference to the drawings.
As shown in FIG. 1, the endoscope 1, which is an electronic endoscope of the present embodiment, has a long insertion portion 2 having an outer diameter of about 3 to 4 mm and a base of the insertion portion 2. Mainly composed of an operation unit 3 connected to the end, a universal cord 4 which is an endoscope cable extending from the operation unit 3, and an endoscope connector 5 arranged at the tip of the universal cord 4. It is configured in.
 挿入部2は、先端側から順に、先端部6、湾曲部7および可撓管部8が連設されて形成され可撓性を備えた管状部材である。このうち、先端部6には、撮像手段、照明手段などが収納配置されている。 
 湾曲部7は、操作部3の操作部材のうち湾曲レバー13の回動操作によって、挿入部2の上下2方向(UP-DOWN)へと能動的に湾曲させ得るように構成される機構部位である。
The insertion portion 2 is a tubular member having flexibility formed by connecting the tip portion 6, the curved portion 7, and the flexible tube portion 8 in this order from the tip side. Of these, an imaging means, a lighting means, and the like are housed and arranged at the tip portion 6.
The curved portion 7 is a mechanical portion of the operating member of the operating portion 3 that is configured to be able to be actively curved in two vertical directions (UP-DOWN) of the inserting portion 2 by the rotation operation of the bending lever 13. is there.
 なお、湾曲部7は、上下2方向へ能動的に湾曲するタイプのものに限定されることはなく、上下方向に加えて左右方向をも含めた4方向(上下左右の操作によって軸回りの全周方向、UP-DOWN/LEFT-RIGHT)に湾曲し得るタイプのものであっても良い。 The curved portion 7 is not limited to a type that actively curves in two vertical directions, and the curved portion 7 is not limited to a type that actively bends in two vertical directions, and the curved portion 7 is not limited to a type that actively bends in two vertical directions. It may be of a type that can be curved in the circumferential direction (UP-DOWN / LEFT-RIGHT).
 また、湾曲部7は、上(UP)方向の1方向にのみ湾曲し得るタイプのものでもよく、さらに湾曲レバー13による能動的に湾曲する機構を有しておらず、単に受動的に湾曲するタイプのものであってもよい。 Further, the bending portion 7 may be of a type capable of bending only in one direction in the upward (UP) direction, and further, does not have a mechanism for actively bending by the bending lever 13, and simply passively bends. It may be of the type.
 可撓管部8は、受動的に可撓可能となるように柔軟性を持たせて形成される管状部材である。この可撓管部8の内部には、先端部6に内蔵される撮像装置(不図示)から延出し、さらに操作部3からユニバーサルコード4の内部へと延設される撮像ケーブル、光源装置からの照明光を導光し先端部6から出射させるための後述するライトガイドバンドルなどが挿通している(ここでは、何れも不図示)。 The flexible tube portion 8 is a tubular member formed with flexibility so as to be passively flexible. The inside of the flexible tube portion 8 extends from an imaging device (not shown) built in the tip portion 6 and further extends from the operating portion 3 to the inside of the universal cord 4 from an imaging cable and a light source device. A light guide bundle or the like, which will be described later, for guiding the illumination light of the above and emitting it from the tip portion 6 is inserted (these are not shown here).
 操作部3は、先端側に設けられ可撓管部8の基端を覆って可撓管部8と接続される折れ止め部9と、この折れ止め部9に連設され使用者が内視鏡1を使用する時に手によって把持する把持部10と、を有している。 The operation unit 3 is provided on the tip side and covers the base end of the flexible pipe portion 8 and is connected to the flexible pipe portion 8. It has a grip portion 10 that is gripped by hand when the mirror 1 is used.
 操作部3には、内視鏡操作手段として、例えば湾曲部7の湾曲操作を行う湾曲レバー13、撮像手段、照明手段などの各対応する操作を行うための複数の各種スイッチ14および送液チューブが接続されてシリンジなどにより薬液などが供給される流体供給ポート15が設けられている。 The operation unit 3 includes, as the endoscope operating means, a plurality of various switches 14 for performing each corresponding operation such as a bending lever 13 for performing a bending operation of the bending portion 7, an imaging means, a lighting means, and a liquid feeding tube. Is connected to provide a fluid supply port 15 to which a chemical solution or the like is supplied by a syringe or the like.
 ユニバーサルコード4は、挿入部2の先端部6から、この挿入部2内部を挿通して操作部3に至り、信号ケーブル束、光源装置(不図示)からの照明光を伝送するライトガイドバンドルなどが挿通された複合ケーブルである。 The universal cord 4 is a light guide bundle that transmits illumination light from a signal cable bundle, a light source device (not shown), etc. from the tip portion 6 of the insertion portion 2 through the inside of the insertion portion 2 to reach the operation unit 3. Is a composite cable inserted.
 内視鏡コネクタ5は、外部機器のビデオプロセッサ(不図示)との間を接続する信号ケーブルが接続される電気コネクタ部16を側面部に有すると共に、外部機器である光源装置との間を接続する後述のライトガイドバンドルおよび電気ケーブル(不図示)が接続される光源接続プラグ18を備えた光源コネクタ部17などを有して構成されている。 The endoscope connector 5 has an electric connector portion 16 on the side surface to which a signal cable for connecting to a video processor (not shown) of an external device is connected, and also connects to a light source device which is an external device. It is configured to include a light source connector portion 17 having a light source connection plug 18 to which a light guide bundle described later and an electric cable (not shown) are connected.
 ここで、本実施の形態の内視鏡1の挿入部2の先端部分の構成について、図2および図3に基づき、以下に説明する。なお、以下の説明において、挿入部2の周知の構成に関しては、説明を省略する。 Here, the configuration of the tip portion of the insertion portion 2 of the endoscope 1 of the present embodiment will be described below based on FIGS. 2 and 3. In the following description, the description of the well-known configuration of the insertion portion 2 will be omitted.
 図2および図3に示すように、挿入部2の先端部6は、金属製または樹脂製の先端構成部としての先端枠本体21を有している。この先端枠本体21には先端キャップ23が設けられている。 As shown in FIGS. 2 and 3, the tip portion 6 of the insertion portion 2 has a tip frame main body 21 as a tip component made of metal or resin. The tip frame main body 21 is provided with a tip cap 23.
 先端キャップ23の先端面22には、直線状の挿入部2の長手軸Xと略平行な光軸Oを有する観察光が入射する、ここでは略円形の光透過部材の光学窓であって内蔵される撮像装置(不図示)の先端に配設された観察光学系24と、ここでは略円形の光透過部材の光学窓である照明光学系25と、薬液、エアーなどの流体を噴出する薬液散布部としてのノズル31と、が露出するように設けられている。なお、観察光学系24および照明光学系25は、1つに限定されることなく、複数であってもよい。 Observation light having an optical axis O substantially parallel to the longitudinal axis X of the linear insertion portion 2 is incident on the tip surface 22 of the tip cap 23. Here, it is an optical window of a substantially circular light transmitting member and is built in. An observation optical system 24 arranged at the tip of an imaging device (not shown), an illumination optical system 25 which is an optical window of a substantially circular light transmitting member, and a chemical solution for ejecting a fluid such as a chemical solution or air. The nozzle 31 as a spraying portion is provided so as to be exposed. The observation optical system 24 and the illumination optical system 25 are not limited to one, and may be plural.
 先端枠本体21の基端外周部分には、湾曲部7の外皮となる湾曲ゴム28の先端部分が被覆されている。そして、湾曲ゴム28は、先端部分の外周に糸巻接着部27が設けられて、先端枠本体21の基端外周部に固着されている。 The outer peripheral portion of the base end of the tip frame main body 21 is covered with the tip portion of the curved rubber 28 which is the outer skin of the curved portion 7. The curved rubber 28 is provided with a pincushion adhesive portion 27 on the outer periphery of the tip portion, and is fixed to the base end outer peripheral portion of the tip frame main body 21.
 ノズル31は、ステンレスなどの金属から形成されており、流体を噴出する開口である噴射口32が観察光学系24に対して略反対側を臨むように設けられている。即ち、噴射口32が観察光学系24を含まない方向を臨み、噴射口32から噴射する流体が挿入部2の長手軸Xに対して略直交する先端部6の外周(外径)方向となるようにノズル31の向きが設定されている。 The nozzle 31 is made of a metal such as stainless steel, and is provided so that the injection port 32, which is an opening for ejecting a fluid, faces substantially the opposite side of the observation optical system 24. That is, the injection port 32 faces a direction that does not include the observation optical system 24, and the fluid injected from the injection port 32 is in the outer peripheral (outer diameter) direction of the tip portion 6 that is substantially orthogonal to the longitudinal axis X of the insertion portion 2. The orientation of the nozzle 31 is set as described above.
 さらに、ここではノズル31の噴射口32からの噴射方向は、噴射口32の開口面に略直交し、観察光学系24の反対側であって、観察光学系24の中心(光軸Oが通る点)を通る線に沿った方向(図中矢印線R方向)となるように設定されている。 Further, here, the injection direction of the nozzle 31 from the injection port 32 is substantially orthogonal to the opening surface of the injection port 32, is on the opposite side of the observation optical system 24, and is the center of the observation optical system 24 (the optical axis O passes through). It is set to be in the direction along the line passing through the point) (in the direction of the arrow line R in the figure).
 なお、ノズル31には、送液チューブとしての流体供給チューブ33(図4参照)の一端が連通接続されている。この流体供給チューブ33は、挿入部2および操作部3に配設され、他端が操作部3に設けられた流体供給ポート15(図1参照)と連通接続されている。 One end of a fluid supply tube 33 (see FIG. 4) as a liquid feeding tube is communicated with the nozzle 31. The fluid supply tube 33 is arranged in the insertion portion 2 and the operation portion 3, and the other end thereof is communicated with the fluid supply port 15 (see FIG. 1) provided in the operation portion 3.
 このように構成された内視鏡1は、図4および図5に示すように、挿入部2が、例えば、気管、気管支100の気道内に挿入される。このとき、患者の咳反射、嘔吐反射などを抑制するために、リドカインなどの局所麻酔薬液が投与される。 In the endoscope 1 configured in this way, as shown in FIGS. 4 and 5, the insertion portion 2 is inserted into, for example, the trachea and the airway of the bronchus 100. At this time, a local anesthetic solution such as lidocaine is administered in order to suppress the cough reflex and vomiting reflex of the patient.
 この局所麻酔薬液を気管、気管支100に投与する際、シリンジなどを用いて、流体供給ポート15から流体供給チューブ33内に局所麻酔薬液を注入して、ノズル31から気管、気管支100の気道を形成する気管(支)壁の粘膜に向けて局所麻酔薬液が噴射される。そして、局所麻酔薬液は、先端部6の外径方向に臨んでいるノズル31の噴射口32から気管(支)壁の粘膜に散布される。 When the local anesthetic solution is administered to the trachea and bronchus 100, the local anesthetic solution is injected into the fluid supply tube 33 from the fluid supply port 15 using a syringe or the like to form the airways of the trachea and bronchus 100 from the nozzle 31. A local anesthetic solution is sprayed toward the mucous membrane of the tracheal (bronchial) wall. Then, the local anesthetic solution is sprayed on the mucous membrane of the tracheal (bronchial) wall from the injection port 32 of the nozzle 31 facing the outer diameter direction of the tip portion 6.
 このように、本実施の形態の内視鏡1は、鉗子チャンネルを利用して、局所麻酔薬液を気管(支)壁の粘膜に散布していた従来構成と異なり、挿入部2の先端部6の外径方向を臨むノズル31の噴射口32から気管(支)壁の粘膜に散布できる構成となっている。 As described above, the endoscope 1 of the present embodiment is different from the conventional configuration in which the local anesthetic solution is sprayed on the mucous membrane of the tracheal (bronchial) wall by using the forceps channel, and the tip portion 6 of the insertion portion 2 is used. It is configured so that it can be sprayed on the mucous membrane of the tracheal (bronchial) wall from the injection port 32 of the nozzle 31 facing the outer radial direction of.
 これにより、鉗子チャンネルの開口部から局所麻酔薬液が漏れたり、処置具チャンネル内に薬液が残存したりすることなく、目的とする気管(支)壁の粘膜の範囲に所定の量の薬液を均一に散布することができる。その結果、局所麻酔薬液の投与量の管理を容易に行え、麻酔効果を一定とすることができるようになる。 As a result, a predetermined amount of the drug solution is uniformly applied to the area of the mucous membrane of the target tracheal (bronchial) wall without leaking the local anesthetic solution from the opening of the forceps channel or leaving the drug solution in the treatment tool channel. Can be sprayed on. As a result, the dose of the local anesthetic solution can be easily controlled, and the anesthetic effect can be kept constant.
 また、内視鏡1は、局所麻酔薬液を散布するための鉗子チャンネルを必要としないため、気管、気管支100の処置を必要とせず検査のみ行うものであれば、さらに挿入部2を細径化することができる。なお、内視鏡1は、図6に示すように、鉗子チャンネル26を有するものでもよい。 Further, since the endoscope 1 does not require a forceps channel for spraying the local anesthetic solution, the insertion portion 2 is further reduced in diameter if only the examination is performed without requiring the treatment of the trachea and the bronchus 100. can do. As shown in FIG. 6, the endoscope 1 may have a forceps channel 26.
(第1の変形例)
 内視鏡1は、図7に示すように、挿入部2の長手軸Xに直交する方向に対して、ノズル31の噴射口32が先端側を臨むように所定の角度θを有する構成としてもよい。
(First modification)
As shown in FIG. 7, the endoscope 1 may have a predetermined angle θ so that the injection port 32 of the nozzle 31 faces the tip side with respect to the direction orthogonal to the longitudinal axis X of the insertion portion 2. Good.
 これにより内視鏡1は、気管(支)壁の粘膜の所定の範囲にノズル31の噴射口32からの局所麻酔薬液の噴射状況および散布状況を観察しながら行うことができる。 Thereby, the endoscope 1 can be performed while observing the injection state and the spraying state of the local anesthetic solution from the injection port 32 of the nozzle 31 in a predetermined range of the mucous membrane of the tracheal (branch) wall.
(第2の変形例)
 ノズル31は、図8および図9に示すように、噴射口32が先端部6の外径方向に臨む方向と観察光学系24、照明光学系25などに臨む方向に可変できるように回動自在な構成としてもよい。
(Second modification)
As shown in FIGS. 8 and 9, the nozzle 31 is rotatable so that the injection port 32 can be changed in the direction facing the outer diameter of the tip portion 6 and the direction facing the observation optical system 24, the illumination optical system 25, and the like. It may be configured as such.
 本変形例の内視鏡1は、ノズル31の噴射口32からの流体の噴射方向(図中矢印線R方向)を可変できるように、ノズル31が回動自在な構成となっている。 The endoscope 1 of this modified example has a configuration in which the nozzle 31 is rotatable so that the injection direction of the fluid from the injection port 32 of the nozzle 31 (R direction along the arrow line in the figure) can be changed.
 ここでのノズル31は、図10に示すように、長手軸C回りに先端枠本体21の孔部29内に挿通して回動自在に配設される。そして、ノズル31は、先端枠本体21に収容される部分にフランジ34が形成され、このフランジ34の外周部にOリングなどのシール部材35が設けられている。 As shown in FIG. 10, the nozzle 31 here is rotatably arranged so as to be inserted into the hole 29 of the tip frame main body 21 around the longitudinal axis C. A flange 34 is formed in a portion of the nozzle 31 accommodated in the tip frame main body 21, and a sealing member 35 such as an O-ring is provided on the outer peripheral portion of the flange 34.
 ノズル31の基端部分には、流体供給チューブ33の一端が接続されている。そして、ノズル31へ回動力を伝達すると共に、挿入部2の可撓性を損なわない程度に流体供給チューブ33の捩じれを防止する金属線を密巻きにしたコイルチューブ37が流体供給チューブ33の外周部を覆うように設けられている。 One end of the fluid supply tube 33 is connected to the base end portion of the nozzle 31. Then, the coil tube 37 in which the metal wire that transmits the rotational power to the nozzle 31 and prevents the fluid supply tube 33 from being twisted to the extent that the flexibility of the insertion portion 2 is not impaired is tightly wound around the outer circumference of the fluid supply tube 33. It is provided so as to cover the part.
 なお、図11に示すように、操作部3には、ノズル31を回動操作する操作部材であるレバー11が設けられている。 As shown in FIG. 11, the operation unit 3 is provided with a lever 11 which is an operation member for rotating the nozzle 31.
 本変形例の内視鏡1は、ノズル31を長手軸C回りに回動操作できるように構成し、気管(支)壁の粘膜へ局所麻酔薬液の散布に加え、ノズル31の噴射口32から生理食塩水などの洗浄液を観察光学系24および照明光学系25に噴射して洗浄することができる。 The endoscope 1 of this modified example is configured so that the nozzle 31 can be rotated around the longitudinal axis C, and in addition to spraying the local anesthetic solution on the mucous membrane of the tracheal (branch) wall, from the injection port 32 of the nozzle 31. A cleaning solution such as physiological saline can be sprayed onto the observation optical system 24 and the illumination optical system 25 for cleaning.
 さらに、ノズル31が回動自在であるため、気管(支)壁の粘膜へ局所麻酔薬液の散布時に、挿入部2を捩じり操作しなくとも気管(支)壁全周に局所麻酔薬液を容易に散布することができる。 Further, since the nozzle 31 is rotatable, when the local anesthetic solution is sprayed on the mucous membrane of the tracheal (bronchial) wall, the local anesthetic solution is applied to the entire circumference of the tracheal (bronchial) wall without twisting the insertion portion 2. It can be easily sprayed.
 また、図12および図13に示すように、噴射口32からの流体の噴射方向(図中矢印線R方向)が観察光学系24および照明光学系25となるようにノズル31が当接して回動位置が規定される突起部であるストッパ37を先端面22に設けてもよい。 Further, as shown in FIGS. 12 and 13, the nozzle 31 abuts and rotates so that the injection direction of the fluid from the injection port 32 (R direction along the arrow line in the figure) is the observation optical system 24 and the illumination optical system 25. A stopper 37, which is a protrusion whose moving position is defined, may be provided on the tip surface 22.
 さらに、操作部3は、レバー11の操作位置によるノズル31からの流体の噴射方向が手元で確認できるようにする指標を設けてもよい。 Further, the operation unit 3 may be provided with an index that allows the injection direction of the fluid from the nozzle 31 depending on the operation position of the lever 11 to be confirmed at hand.
(第3の変形例)
 ノズル31は、図14および図15に示すように、回動自在且つ、先端部6から所定の長さに延出可能ように進退自在な構成としてもよい。
(Third variant)
As shown in FIGS. 14 and 15, the nozzle 31 may have a structure that is rotatable and that can be moved forward and backward so as to extend from the tip portion 6 to a predetermined length.
 ここでのノズル31は、外径が1mm程度のステンレスなどの金属から形成された硬質管部36を有している。なお、ノズル31は、先端部6の硬質長L1に対して硬質管部36の長手軸Cに沿った長さL2が短く(L1>L2)設定されている。 The nozzle 31 here has a hard tube portion 36 formed of a metal such as stainless steel having an outer diameter of about 1 mm. The nozzle 31 is set so that the length L2 along the longitudinal axis C of the hard pipe portion 36 is shorter (L1> L2) than the hard length L1 of the tip portion 6.
 即ち、ノズル31が延出していない状態において、硬質管部36が湾曲部7内に到達しないため、湾曲部7の湾曲動作に影響がないようにするためである。 That is, since the hard pipe portion 36 does not reach the inside of the curved portion 7 when the nozzle 31 is not extended, the bending operation of the curved portion 7 is not affected.
 ここでのノズル31は、図16に示すように、所定の長さL2の硬質管部36を有した違いだけで、第2の変形例と同様な構成となっている。 As shown in FIG. 16, the nozzle 31 here has the same configuration as the second modification except that it has a hard pipe portion 36 having a predetermined length L2.
 なお、図17に示すように、操作部3には、ノズル31を進退操作する操作部材である回動レバー12が設けられており、回動レバー12が設けられた台座13を操作部3の長手軸Y回りに回動操作することで、ノズル31を長手軸C回りに回動させる構成となっている。 As shown in FIG. 17, the operation unit 3 is provided with a rotation lever 12 which is an operation member for moving the nozzle 31 forward and backward, and the pedestal 13 provided with the rotation lever 12 is used for the operation unit 3. The nozzle 31 is configured to rotate around the longitudinal axis C by rotating the nozzle 31 around the longitudinal axis Y.
 本変形例の内視鏡1は、第2の変形例の作用効果に加え、ノズル31を長手軸Cに沿って先端部6から延出するように進退操作できるように構成することで、広範囲に気管(支)壁の粘膜へ局所麻酔薬液の散布することができる。 In addition to the effects of the second modification, the endoscope 1 of this modification is configured so that the nozzle 31 can be moved forward and backward along the longitudinal axis C so as to extend from the tip portion 6. Local anesthetic solution can be sprayed on the mucous membrane of the tracheal (bronchial) wall.
 さらに、ノズル31が進退自在であるため、気管(支)壁の粘膜へ局所麻酔薬液の散布時に、挿入部2を押し引き操作しなくとも気管(支)壁全周および前後方向に局所麻酔薬液を容易に散布することができる。 Further, since the nozzle 31 can move forward and backward, the local anesthetic solution is applied to the mucous membrane of the tracheal (bronchial) wall in the entire circumference of the tracheal (bronchial) wall and in the anterior-posterior direction without pushing and pulling the insertion portion 2. Can be easily sprayed.
(第4の変形例)
 本変形例の先端キャップ23の先端面22は、図18から図21に示すように、ノズル31を配置する部分に凹部としての段差部22aを形成してもよい。この段差部22aは、ノズル31の噴射口32が臨む方向に沿って、先端キャップ23の外周部まで形成されている。
(Fourth modification)
As shown in FIGS. 18 to 21, the tip surface 22 of the tip cap 23 of this modification may have a stepped portion 22a as a recess in the portion where the nozzle 31 is arranged. The step portion 22a is formed up to the outer peripheral portion of the tip cap 23 along the direction in which the injection port 32 of the nozzle 31 faces.
 このように先端面22にノズル31が設けられる凹部状の段差部22aを形成する構成により、ノズル31の噴射口32から散布する局所麻酔薬液が観察光学系24側に流れず、視野が確保され、視認性の阻害を防止することができる。 With the configuration of forming the concave step portion 22a in which the nozzle 31 is provided on the tip surface 22 in this way, the local anesthetic solution sprayed from the injection port 32 of the nozzle 31 does not flow to the observation optical system 24 side, and the field of view is secured. , It is possible to prevent the obstruction of visibility.
(第5の変形例)
 本変形例のノズル50は、図21および図22に示すように、観察窓の方向を向く第1開口である第1の噴射口51および第1の噴射口51の反対側を向く第2開口である第2の噴射口52の2つの開口部を両端部分に有している。
(Fifth variant)
As shown in FIGS. 21 and 22, the nozzle 50 of this modification has a first opening 51 facing the direction of the observation window and a second opening facing the opposite side of the first injection port 51. The second injection port 52 is provided with two openings at both ends.
 ノズル50は、第1の噴射口51に連通する第1の流路51aと第2の噴射口52に連通する第2の流路52aを有し、これら第1の流路51aと第2の流路52aが隔壁54により分画されている。なお、ノズル50は、隔壁54が先端キャップ23に挿入されている管状部の中途部位まで形成されており、第1の流路51aと第2の流路52aが基端部分で連通している。 The nozzle 50 has a first flow path 51a communicating with the first injection port 51 and a second flow path 52a communicating with the second injection port 52, and these first flow paths 51a and the second flow path 52a. The flow path 52a is partitioned by the partition wall 54. The nozzle 50 is formed up to an intermediate portion of the tubular portion in which the partition wall 54 is inserted into the tip cap 23, and the first flow path 51a and the second flow path 52a communicate with each other at the base end portion. ..
 ノズル50の管状部には、隔壁54から基端側に回転自在に保持される切り替え部材としての略円柱状の回転部53が挿設されている。なお、回転部53は、シール部材35が設けられたフランジ34と一体形成され、このフランジ34の基端側に流体供給チューブ33が接続されている。 A substantially cylindrical rotating portion 53 as a switching member rotatably held from the partition wall 54 to the base end side is inserted in the tubular portion of the nozzle 50. The rotating portion 53 is integrally formed with the flange 34 provided with the seal member 35, and the fluid supply tube 33 is connected to the proximal end side of the flange 34.
 回転部53には、回転位置に応じて第1の流路51aまたは第2の流路52aのいずれか一方に連通するときは他方には連通しないように、先端面に開口が形成された第3の流路53aが形成されている。なお、第3の流路は、流体供給チューブ33と連通している。 An opening is formed in the tip surface of the rotating portion 53 so that when communicating with either the first flow path 51a or the second flow path 52a depending on the rotation position, the rotating portion 53 does not communicate with the other. The flow path 53a of 3 is formed. The third flow path communicates with the fluid supply tube 33.
 上記のように構成することで、コイルチューブ37に覆われた流体供給チューブ33を回転することにより、ノズル50の管状部内の回転部53が回転し、第3の流路53aの開口部が第1の流路51aまたは第2の流路52aに合わさり、第3の流路53aが第1の流路51aまたは第2の流路52aいずれかに連通する。 With the above configuration, by rotating the fluid supply tube 33 covered with the coil tube 37, the rotating portion 53 in the tubular portion of the nozzle 50 is rotated, and the opening of the third flow path 53a is opened. It fits into the first flow path 51a or the second flow path 52a, and the third flow path 53a communicates with either the first flow path 51a or the second flow path 52a.
 これにより、流体供給チューブ33が回転部53の回転位置に応じて、第1の流路51aまたは第2の流路52aいずれかと連通する。 As a result, the fluid supply tube 33 communicates with either the first flow path 51a or the second flow path 52a according to the rotation position of the rotating portion 53.
 したがって、図23に示すように、第3の流路53aが第1の流路51aに連通したときに、流体供給チューブ33から送液される生理食塩水などの洗浄液R1をノズル50の第1の噴射口51から観察光学系24および照明光学系25に噴射して洗浄することができる。 Therefore, as shown in FIG. 23, when the third flow path 53a communicates with the first flow path 51a, the cleaning liquid R1 such as physiological saline sent from the fluid supply tube 33 is transferred to the first nozzle 50. Can be cleaned by injecting into the observation optical system 24 and the illumination optical system 25 from the injection port 51 of the above.
 一方、図24に示すように、第3の流路53aが第2の流路52aに連通したときに、第3の流路53aが第2の流路52aに連通したときに、流体供給チューブ33から送液される局所麻酔薬液R2をノズル50の第2の噴射口52から気管(支)壁全周に散布することができる。 On the other hand, as shown in FIG. 24, when the third flow path 53a communicates with the second flow path 52a and the third flow path 53a communicates with the second flow path 52a, the fluid supply tube The local anesthetic solution R2 sent from 33 can be sprayed from the second injection port 52 of the nozzle 50 to the entire circumference of the tracheal (branch) wall.
 以上の実施の形態および変形例に記載した発明は、それら実施の形態および変形例に限ることなく、その他、実施段階ではその要旨を逸脱しない範囲で種々の変形を実施し得ることが可能である。さらに、上記実施の形態および変形例には、種々の段階の発明が含まれており、開示される複数の構成要件における適宜な組合せにより種々の発明が抽出され得るものである。 The inventions described in the above embodiments and modifications are not limited to those embodiments and modifications, and various modifications can be carried out at the implementation stage without departing from the gist thereof. .. Further, the above-described embodiments and modifications include inventions at various stages, and various inventions can be extracted by an appropriate combination of a plurality of disclosed constituent requirements.
 例えば、実施の形態および変形例に示される全構成要件から幾つかの構成要件が削除されても、述べられている課題が解決でき、述べられている効果が得られる場合には、この構成要件が削除された構成が発明として抽出され得るものである。 For example, if some of the constituents are removed from all the constituents shown in the embodiments and modifications, but the stated problems can be solved and the stated effects can be obtained, the constituents are found. The configuration in which is deleted can be extracted as an invention.

Claims (9)

  1.  操作部と、
     前記操作部に接続され、被験体に挿入される長尺の挿入部と、
     光透過部材からなる光学窓を有し、前記挿入部の先端部に配設される先端構成部と、
     前記挿入部に配設された流体供給チューブと、
     前記流体供給チューブに連通し、前記流体供給チューブから供給された流体を噴出する開口を備えたノズルと、
     を具備し、
     前記ノズルは、前記開口が前記光学窓を含まない前記先端部の外径方向を臨むように、前記先端構成部に配設されていることを特徴とする内視鏡。
    Operation unit and
    A long insertion part connected to the operation part and inserted into the subject,
    A tip component having an optical window made of a light transmitting member and arranged at the tip of the insertion portion,
    A fluid supply tube arranged in the insertion portion and
    A nozzle having an opening that communicates with the fluid supply tube and ejects the fluid supplied from the fluid supply tube.
    Equipped with
    The endoscope is an endoscope characterized in that the nozzle is arranged in the tip component so that the opening faces the outer diameter direction of the tip portion not including the optical window.
  2.  前記開口が臨む方向は、前記光学窓に対して略反対方向であることを特徴とする請求項1に記載の内視鏡。 The endoscope according to claim 1, wherein the direction in which the opening faces is substantially opposite to the optical window.
  3.  前記ノズルは、前記開口の臨む方向を変更できるように長手軸回りに回動自在に配設され、
     前記ノズルを回動操作する操作部材が前記操作部に設けられることを特徴とする請求項1に記載の内視鏡。
    The nozzle is rotatably arranged around a longitudinal axis so that the direction in which the opening faces can be changed.
    The endoscope according to claim 1, wherein an operating member for rotating the nozzle is provided in the operating portion.
  4.  前記ノズルに当接して、前記開口が前記光学窓に臨む方向を規定するストッパが前記先端部に設けられていることを特徴とする請求項3に記載の内視鏡。 The endoscope according to claim 3, wherein a stopper that comes into contact with the nozzle and defines the direction in which the opening faces the optical window is provided at the tip portion.
  5.  前記ノズルは、前記先端部から延出できるように長手軸方向に進退自在に配設され、
     前記ノズルを進退操作する操作部材が前記操作部に設けられることを特徴とする請求項1に記載の内視鏡。
    The nozzle is arranged so as to be able to advance and retreat in the longitudinal axis direction so as to extend from the tip portion.
    The endoscope according to claim 1, wherein an operating member for moving the nozzle forward and backward is provided in the operating unit.
  6.  前記ノズルは、前記開口の臨む方向を変更できるように長手軸回りに回動自在、且つ前記先端部から延出できるように長手軸方向に進退自在に配設され、
     前記ノズルを回動操作および進退操作する操作部材が前記操作部に設けられることを特徴とする請求項1に記載の内視鏡。
    The nozzle is arranged so as to be rotatable around the longitudinal axis so that the direction in which the opening faces can be changed, and to be movable back and forth in the longitudinal axis direction so as to extend from the tip portion.
    The endoscope according to claim 1, wherein an operation member for rotating and advancing / retreating the nozzle is provided in the operation unit.
  7.  前記先端構成部は、前記開口の臨む方向に沿って凹部が形成され、
     前記ノズルは前記凹部に収容されることを特徴とする請求項2に記載の内視鏡。
    The tip component is formed with a recess along the direction in which the opening faces.
    The endoscope according to claim 2, wherein the nozzle is housed in the recess.
  8.  前記ノズルは、前記先端部の前記外径方向を臨む前記開口とは異なる、前記光学窓を含む方向に臨む第2の開口を有することを特徴とする請求項1に記載の内視鏡。 The endoscope according to claim 1, wherein the nozzle has a second opening facing the direction including the optical window, which is different from the opening facing the outer diameter direction of the tip portion.
  9.  前記ノズルは、前記流体供給チューブに前記開口が連通する状態と、前記流体供給チューブに前記第2の開口が連通する状態とを切り替える切り替え部材が配設されることを特徴とする請求項8に記載の内視鏡。 8. The nozzle is provided with a switching member for switching between a state in which the opening communicates with the fluid supply tube and a state in which the second opening communicates with the fluid supply tube. The endoscope described.
PCT/JP2019/035268 2019-09-06 2019-09-06 Endoscope WO2021044633A1 (en)

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JPS55116333A (en) * 1979-03-01 1980-09-06 Olympus Optical Co Airrfeed and waterrfeed device of endoscope
JPS563035A (en) * 1979-06-25 1981-01-13 Olympus Optical Co Endoscope
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