JP5301933B2 - Medical Advancement and Retraction Control Mechanism - Google Patents

Medical Advancement and Retraction Control Mechanism Download PDF

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JP5301933B2
JP5301933B2 JP2008239507A JP2008239507A JP5301933B2 JP 5301933 B2 JP5301933 B2 JP 5301933B2 JP 2008239507 A JP2008239507 A JP 2008239507A JP 2008239507 A JP2008239507 A JP 2008239507A JP 5301933 B2 JP5301933 B2 JP 5301933B2
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treatment instrument
distal end
endoscope
end surface
treatment tool
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JP2010069003A (en
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浩之 坂口
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Olympus Medical Systems Corp
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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
    • A61B1/00131Accessories for endoscopes
    • A61B1/00133Drive units for endoscopic tools inserted through or with the endoscope

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Abstract

<P>PROBLEM TO BE SOLVED: To provide a medical mechanism for controlling forward/backward movement which can control the forward/backward movement of an endoscope tool within a tool channel to regulate easily the projection, and facilitates the determination of an early position; and a medical method for controlling forward/backward movement. <P>SOLUTION: The medical mechanism for controlling forward/backward movement 50 includes a controller 60 mounted detachably to an insertion hole 40, and an abutment 80 mounted to a bendable tube 210. The end surfaces 65a, 66a of the controller 60 makes the abutment 80 abut against the end surfaces 65a, 66a when the endoscope tool 200 (the bendable tube 210) moves forward/backward within the tool channel 39, thereby regulating the forward/backward shift of the endoscope tool 200. The abutment 80 abuts against the end surface 65a to regulate the projection of a curve 211 projecting from the tool channel 39, while the abutment 80 abuts against the end surface 66a to regulate the backward movement of a tip 212, and determines the early position of the tip 212 within the tool channel 39. <P>COPYRIGHT: (C)2010,JPO&amp;INPIT

Description

本発明は、処置具チャンネル等の体内ガイド部材の先端に対する処置具等の内視鏡用処置具の先端の進退量を規制する医療用進退量規制機構に関する。   The present invention relates to a medical advance / retreat amount regulating mechanism that regulates the advance / retreat amount of the distal end of an endoscopic treatment instrument such as a treatment instrument with respect to the distal end of an in-vivo guide member such as a treatment instrument channel.

一般に内視鏡の挿入部には、体内に挿入される体内挿入部である処置具を挿通させる処置具チャンネルが配置されている。処置具チャンネルを有する内視鏡は、処置具を体内にガイドするためのガイド部材である。   Generally, a treatment instrument channel through which a treatment instrument that is an in-vivo insertion section to be inserted into the body is inserted is disposed in an insertion section of an endoscope. An endoscope having a treatment instrument channel is a guide member for guiding the treatment instrument into the body.

処置具は、例えば鉗子や高周波切除具等であり、多関節を有し、処置具チャンネルを挿通し、体内に向けて突出する。挿入部は、多関節を有しており、操作部によって操作されると、体内に配置されている患部に向かって湾曲する。この状態で、処置具は、患部を処置する。   The treatment tool is, for example, a forceps or a high-frequency resection tool, has a multi-joint, passes through the treatment tool channel, and protrudes toward the body. The insertion part has a multi-joint, and when operated by the operation part, the insertion part curves toward the affected part arranged in the body. In this state, the treatment tool treats the affected area.

例えば特許文献1には、処置具の挿脱動作を中断すべき位置を確実に認識することができる内視鏡用処置具が開示されている。   For example, Patent Literature 1 discloses an endoscope treatment tool that can reliably recognize a position where the insertion / removal operation of the treatment tool should be interrupted.

また例えば特許文献2には、管路内および口金を容易に洗浄し得る内視鏡用洗浄器具が開示されている。   Further, for example, Patent Document 2 discloses an endoscope cleaning instrument that can easily clean the inside of a conduit and a mouthpiece.

また例えば特許文献3には、内視鏡の処置具チャンネルに挿通する際には先端処置片が可撓性シース内に確実に収納された状態を保つことができ、さらに使用時において、撓性シースの先端からの先端処置片の突出長を所定の長さに確実に保持することができる内視鏡用突没型処置具が開示されている。
特開平10−248800号公報 特開平7−194533号公報 特開2005−279126号公報
Further, for example, in Patent Document 3, it is possible to keep the distal treatment piece securely stored in the flexible sheath when inserted into the treatment instrument channel of the endoscope. An endoscopic treatment tool for endoscope that can reliably hold the protruding length of the distal treatment piece from the distal end of the sheath at a predetermined length is disclosed.
JP-A-10-248800 Japanese Patent Laid-Open No. 7-194533 JP-A-2005-279126

術者は、処置具チャンネルから突出する処置具の突出量を、使用中において例えばモニタ等では把握しにくい。また処置具が処置具チャンネル内に収納されると、処置具はモニタには表示されない。そのため術者は、挿入部先端と処置具先端との配置関係を容易に把握できない虞が生じる。言い換えると、処置具チャンネルに対する処置具の進退量が規制されないと、処置具の突出量が規制されず、また処置具チャンネルに挿入された処置具が例えば使用される前に処置具チャンネル内における処置具の初期位置が設定されないこととなる。よって術者の操作に支障をきたす虞が生じる。   It is difficult for the surgeon to grasp the protruding amount of the treatment tool protruding from the treatment tool channel, for example, with a monitor or the like during use. Further, when the treatment instrument is stored in the treatment instrument channel, the treatment instrument is not displayed on the monitor. Therefore, the surgeon may not be able to easily grasp the positional relationship between the insertion portion distal end and the treatment instrument distal end. In other words, if the advancement / retraction amount of the treatment tool with respect to the treatment tool channel is not restricted, the protrusion amount of the treatment tool is not restricted, and the treatment in the treatment tool channel is performed before the treatment tool inserted into the treatment tool channel is used, for example. The initial position of the tool will not be set. Therefore, there is a possibility that the operation of the surgeon may be hindered.

また処置具チャンネル内における処置具の初期位置が設定されないと、例えば挿入部が湾曲した際に、処置具が術者の意図に反して挿入部から突出し、体内が挿入部から突出した処置具によって傷つく虞が生じる。また突出量が規制されず、初期位置が設定されないと、処置具が挿入部から突出した状態で配置される虞も生じる。これにより体内が挿入部から突出している処置具によって傷つく虞が生じる。   If the initial position of the treatment instrument in the treatment instrument channel is not set, for example, when the insertion section is bent, the treatment instrument protrudes from the insertion section against the operator's intention, and the treatment instrument has a body protruding from the insertion section. There is a risk of injury. Further, if the protruding amount is not regulated and the initial position is not set, there is a possibility that the treatment instrument is arranged in a state protruding from the insertion portion. Thereby, there exists a possibility that the inside of a body may be damaged by the treatment tool which protrudes from the insertion part.

そのため処置具チャンネルに対する処置具の進退量を規制することが好適である。つまり処置具チャンネルから突出する処置具の突出量が規制されることが好適である。   Therefore, it is preferable to restrict the advancement / retraction amount of the treatment tool with respect to the treatment tool channel. That is, it is preferable that the protruding amount of the treatment tool protruding from the treatment tool channel is regulated.

また初期位置が設定されず、処置具が処置具チャンネル内に収納され、例えば挿入部が湾曲すると、処置具が術者の意図に反して処置具チャンネルに接触する虞が生じる。これにより処置具が破損してしまう虞が生じる。   Further, when the initial position is not set and the treatment tool is accommodated in the treatment tool channel and the insertion portion is bent, for example, the treatment tool may come into contact with the treatment tool channel against the operator's intention. This may cause the treatment instrument to be damaged.

また処置具が術者の意図に反して挿入部から突出することや処置具チャンネルとの接触を防止するために、処置具チャンネルに挿入された処置具が使用される前に、処置具チャンネル内における処置具の初期位置を、例えば挿入部先端といった所望する位置に設定することが好適である。   In addition, in order to prevent the treatment instrument from protruding from the insertion portion against the operator's intention and contact with the treatment instrument channel, before the treatment instrument inserted into the treatment instrument channel is used, It is preferable to set the initial position of the treatment tool at a desired position such as the distal end of the insertion portion.

そのため本発明は、上記課題を鑑みて、処置具チャンネルに対する内視鏡用処置具の進退量を規制して、突出量を容易に規制でき、初期位置を容易に設定することができる医療用進退量規制機構を提供することを目的とする。   Therefore, in view of the above problems, the present invention regulates the advancement / retraction amount of the endoscope treatment tool with respect to the treatment tool channel, can easily regulate the protrusion amount, and can easily set the initial position. An object is to provide a quantity regulation mechanism.

本発明は目的を達成するために、体内ガイド部材によって体内へとガイドされる内視鏡用処置具が挿通可能な前記体内ガイド部材に配設される処置具チャンネルと連通する挿入口に着脱自在に取り付けられ、前記体内ガイド部材に対する前記内視鏡用処置具の進退移動を規制する医療用進退量規制機構であって、前記内視鏡用処置具が挿通可能な第1の開口部を有し、前記挿入口に接続される先端側端面と、前記内視鏡用処置具が挿通可能な第2の開口部を有する基端側端面と、を含む規制部材と、前記内視鏡用処置具に配設され、前記第2の開口部を挿通し、前記先端側端面と前記基端側端面との間を進退移動することで、前記体内ガイド部材に対する前記内視鏡用処置具の進退移動を規制する当て付き部と、を具備し、前記当て付き部は、前記基端側端面に当て付くことで、前記体内ガイド部材が湾曲状態または非湾曲状態であっても、前記内視鏡用処置具の先端が前記処置具チャンネルの先端から所望の距離だけ基端側に配置され、前記処置具チャンネル内に収納される位置である初期位置を設定することを特徴とする医療用進退量規制機構を提供する。 To achieve the object, the present invention is detachable from an insertion port communicating with a treatment instrument channel disposed in the in-vivo guide member through which an endoscopic treatment instrument guided into the body by an in-vivo guide member can be inserted. Is a medical advance / retreat amount restriction mechanism that restricts the advance / retreat movement of the endoscope treatment tool relative to the in-vivo guide member, and has a first opening through which the endoscope treatment tool can be inserted. A restriction member including a distal end side end surface connected to the insertion port and a proximal end side end surface having a second opening through which the endoscope treatment tool can be inserted; and the endoscope treatment. The endoscope treatment tool advances and retreats with respect to the in-vivo guide member by being inserted into the second opening and moving between the distal end surface and the proximal end surface. comprising the abutting-in portion for restricting the movement, the said abutting with portions By contacting the proximal end surface, the distal end of the endoscopic treatment instrument is proximal by a desired distance from the distal end of the treatment instrument channel even when the in-vivo guide member is in a curved state or a non-curved state. A medical advance / retreat amount regulating mechanism is provided , characterized in that an initial position, which is a position disposed on the side and accommodated in the treatment instrument channel, is set .

また本発明は目的を達成するために、体内ガイド部材によって体内へとガイドされる内視鏡用処置具が挿通可能な前記体内ガイド部材に配設される処置具チャンネルと連通する挿入口に着脱自在に取り付けられ、前記体内ガイド部材に対する前記内視鏡用処置具の進退移動を規制する医療用進退量規制機構であって、前記内視鏡用処置具が挿通可能な第1の開口部を有し、前記挿入口に接続される先端側端面と、前記内視鏡用処置具が挿通可能な第2の開口部を有する基端側端面と、を含む規制部材と、前記内視鏡用処置具に配設され、前記第2の開口部を挿通し、前記先端側端面と前記基端側端面との間を進退移動することで、前記体内ガイド部材に対する前記内視鏡用処置具の進退移動を規制する当て付き部と、を具備し、前記当て付き部が進退移動可能な前記先端側端面から前記基端側端面までの長さは、前記内視鏡用処置具に配設され湾曲可能な湾曲部の基端側から前記内視鏡用処置具の先端までの長さよりも長いことを特徴とする医療用進退量規制機構を提供する。 In order to achieve the object of the present invention , the endoscope treatment tool guided into the body by the in- vivo guide member can be attached to and detached from the insertion port communicating with the treatment instrument channel disposed in the in-vivo guide member. A medical advance / retreat amount regulating mechanism that is freely attached and regulates the advance / retreat movement of the endoscopic treatment tool relative to the in-vivo guide member, wherein the first opening through which the endoscopic treatment tool can be inserted is provided. A restricting member including a distal end side end surface connected to the insertion port and a proximal end end surface having a second opening through which the endoscope treatment instrument can be inserted; and for the endoscope The endoscope treatment tool is disposed on a treatment tool, and is inserted through the second opening and moves forward and backward between the distal end surface and the proximal end surface. A contact portion that regulates forward / backward movement, and the contact The length from the distal end surface to the proximal end surface that can move forward and backward is the length of the endoscope treatment tool from the proximal end of the bending portion that is disposed on the endoscope treatment tool and can be bent. Provided is a medical advance / retreat amount regulating mechanism characterized by being longer than the length to the tip .

本発明によれば、処置具チャンネルに対する内視鏡用処置具の進退量を規制して、突出量を容易に規制でき、初期位置を容易に設定することができる医療用進退量規制機構を提供することができる。   According to the present invention, there is provided a medical advance / retreat amount regulation mechanism that regulates the advance / retreat amount of the endoscope treatment tool relative to the treatment tool channel, can easily regulate the protrusion amount, and can easily set the initial position. can do.

以下、図面を参照して本発明の実施形態について詳細に説明する。
図1乃至図7を参照して一実施形態について説明する。図1は、本実施形態の内視鏡操作システム1の概略構成を示す図である。
図1に示すように内視鏡2には、患者の体内等に挿入される細長い挿入部10と、挿入部10の基端と連結し、挿入部10を操作する操作部30とが設けられている。
Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings.
An embodiment will be described with reference to FIGS. FIG. 1 is a diagram illustrating a schematic configuration of an endoscope operation system 1 according to the present embodiment.
As shown in FIG. 1, the endoscope 2 is provided with an elongated insertion portion 10 that is inserted into a patient's body and the like, and an operation portion 30 that is connected to the proximal end of the insertion portion 10 and operates the insertion portion 10. ing.

本実施形態において、体内とは、例えば消化管や血管などの体腔、腹腔および胸腔とを含む。また本実施形態において内視鏡2は、体内に挿入される内視鏡用処置具を体内へとガイドする体内ガイド部材である。内視鏡用処置具は、例えば後述する内視鏡用処置具200である。   In the present embodiment, the body includes body cavities such as the digestive tract and blood vessels, the abdominal cavity, and the thoracic cavity. In the present embodiment, the endoscope 2 is an in-vivo guide member that guides an endoscopic treatment tool inserted into the body into the body. The endoscope treatment tool is, for example, an endoscope treatment tool 200 described later.

操作部30には、術者が把持する把持部31と、挿入部10の後述する湾曲部12を湾曲させる湾曲操作ノブ32が設けられている。   The operation unit 30 is provided with a gripping unit 31 that the surgeon grips and a bending operation knob 32 that bends the bending unit 12 described later of the insertion unit 10.

把持部31には、ユニバーサルコード33の基端部が連結されている。このユニバーサルコード33の先端部には、図示しない光源装置や、ビデオプロセッサなどに接続されるコネクタ部34が配設されている。   A base end portion of the universal cord 33 is connected to the grip portion 31. A connector portion 34 connected to a light source device (not shown), a video processor, or the like is disposed at the distal end portion of the universal cord 33.

湾曲操作ノブ32には、挿入部10の後述する湾曲部12を左右に湾曲操作させる左右湾曲操作ノブ32aと、湾曲部12を上下に湾曲操作させる上下湾曲操作ノブ32bとが設けられている。左右湾曲操作ノブ32aには、左右湾曲操作ノブ32aによって駆動する左右方向の湾曲操作機構が接続している。また上下湾曲操作ノブ32bには、上下湾曲操作ノブ32bによって駆動する上下方向の湾曲操作機構が接続している。上下方向の湾曲操作機構と左右方向の湾曲操作機構は、湾曲部12全体を湾曲操作する図示しない操作ワイヤの基端と接続している。   The bending operation knob 32 is provided with a left / right bending operation knob 32a for bending a bending portion 12 (to be described later) of the insertion portion 10 to the left and right, and an up / down bending operation knob 32b for bending the bending portion 12 up and down. A left / right bending operation mechanism driven by the left / right bending operation knob 32a is connected to the left / right bending operation knob 32a. Further, an up / down bending operation mechanism driven by the up / down bending operation knob 32b is connected to the up / down bending operation knob 32b. The bending operation mechanism in the vertical direction and the bending operation mechanism in the horizontal direction are connected to the proximal end of an operation wire (not shown) that performs the bending operation on the entire bending portion 12.

操作部30には、吸引ボタン35と、送気・送水ボタン36と、内視鏡撮影用の各種ボタン37と、処置具挿入部38とが設けられている。処置具挿入部38には、後述する内視鏡用処置具200が挿通する挿通部である後述する処置具チャンネル39の挿入口40が設けられている。   The operation unit 30 includes a suction button 35, an air / water supply button 36, various buttons 37 for endoscopic photography, and a treatment instrument insertion unit 38. The treatment instrument insertion portion 38 is provided with an insertion port 40 for a treatment instrument channel 39 (described later), which is an insertion section through which an endoscope treatment instrument 200 (described later) is inserted.

図1に示す挿入部10は、操作部30側から順に可撓管部(蛇管部)11と、湾曲部12と、先端硬性部13とを有している。詳細には、操作部30は、細長い可撓管部11の基端と連結している。可撓管部11の先端は、湾曲部12の基端と連結している。湾曲部12の先端は、先端硬性部13の基端と連結している。   The insertion part 10 shown in FIG. 1 has a flexible tube part (serpentine part) 11, a bending part 12, and a hard end part 13 in order from the operation part 30 side. Specifically, the operation unit 30 is connected to the proximal end of the elongated flexible tube unit 11. The distal end of the flexible tube portion 11 is connected to the proximal end of the bending portion 12. The distal end of the bending portion 12 is connected to the proximal end of the distal end rigid portion 13.

可撓管部11は、弾力性と可撓性とを有し、外力によって曲がる。   The flexible tube portion 11 has elasticity and flexibility, and is bent by an external force.

湾曲部12は、後述する湾曲部211と同様に複数の節輪を有しており、湾曲部211と略同一の構成である。よって湾曲部12は、多関節湾曲機構を有していることとなる。
湾曲部12は、左右湾曲操作ノブ32aが操作されることで、湾曲操作機構を介して図示しない操作ワイヤが押し引きされ、左右方向に湾曲する。また湾曲部12は、上下湾曲操作ノブ32bが操作されることで、湾曲操作機構を介して図示しない操作ワイヤが押し引きされ、上下方向に湾曲する。湾曲部12が湾曲すると、先端硬性部13の位置と向きが変わり、所望する観察対象物(体内の患部や病変部等)が観察視野(または撮像視野)内に捉えられる。
The bending portion 12 has a plurality of node rings like the bending portion 211 described later, and has substantially the same configuration as the bending portion 211. Therefore, the bending part 12 has an articulated bending mechanism.
When the left and right bending operation knob 32a is operated, the bending portion 12 is bent in the left and right direction by pushing an operation wire (not shown) through the bending operation mechanism. Further, when the up / down bending operation knob 32b is operated, the bending portion 12 is bent in the vertical direction by pushing and pulling an operation wire (not shown) through the bending operation mechanism. When the bending portion 12 is bent, the position and orientation of the distal rigid portion 13 are changed, and a desired observation target (an affected area, a lesion area, or the like in the body) is captured in the observation visual field (or imaging visual field).

詳細には、図示しない操作ワイヤは、湾曲部12全体を上下左右の4方向にそれぞれ湾曲操作する。操作ワイヤの先端は、湾曲部12内部に挿通され、先端硬性部13の基端と連結されている。この操作ワイヤの基端は、操作部30の上述した上下方向の湾曲操作機構と左右方向の湾曲操作機構と連結されている。
例えば左右湾曲操作ノブ32aの回動操作にともない、左右方向の湾曲操作機構が移動し、各操作ワイヤがそれぞれ牽引駆動される。これにより、例えば湾曲部12は、図2中に一点鎖線で示すように真っ直ぐに伸びた湾曲角度が0°の通常の直線状態(非湾曲状態)から同図中に実線または二点鎖線で示すように左右方向に任意の湾曲角度に湾曲した湾曲状態に湾曲する。
Specifically, an operation wire (not shown) performs bending operations on the entire bending portion 12 in four directions, up, down, left, and right. The distal end of the operation wire is inserted into the bending portion 12 and connected to the proximal end of the distal end rigid portion 13. The proximal end of the operation wire is connected to the above-described vertical bending operation mechanism and the horizontal bending operation mechanism of the operation unit 30.
For example, with the turning operation of the left / right bending operation knob 32a, the bending operation mechanism in the left / right direction moves, and each operation wire is pulled and driven. Thereby, for example, the bending portion 12 is indicated by a solid line or a two-dot chain line in the drawing from a normal straight line state (non-curved state) in which the bending angle extends straight at 0 ° as shown by a one-dot chain line in FIG. Thus, it is bent in a bending state that is bent at an arbitrary bending angle in the left-right direction.

図1に示すように先端硬性部13の先端面13aには、観察窓14と照明窓15と先端開口部39aとが設けられている。   As shown in FIG. 1, the distal end surface 13a of the distal end rigid portion 13 is provided with an observation window 14, an illumination window 15, and a distal end opening 39a.

観察窓14の内側には、図示しない対物レンズ等の光学系とCCD等の撮像素子を備える撮像部が設けられている。撮像部は、体内の患部等を撮像する。撮像部で得られた撮像信号は、図示しない画像処理装置に送られる。   Inside the observation window 14, an imaging unit including an optical system such as an objective lens (not shown) and an imaging element such as a CCD is provided. The imaging unit images an affected area in the body. The imaging signal obtained by the imaging unit is sent to an image processing device (not shown).

先端開口部39aは、挿入部10内に形成された処置具チャンネル39の先端側と連通している。また処置具チャンネル39の基端側は、挿入口40と連通している。つまり先端開口部39aは、処置具チャンネル39の先端であり、処置具チャンネル39を通じて挿入口40に連通している。処置具チャンネル39は、例えば多関節湾曲機構を有する内視鏡用処置具200が挿入部10を挿通する通路として用いられる。挿入口40と処置具チャンネル39と先端開口部39aには、内視鏡用処置具200が挿通する。内視鏡用処置具200は、挿入口40から挿入され、処置具チャンネル39を挿通し、先端開口部39aから突出する。   The distal end opening 39 a communicates with the distal end side of the treatment instrument channel 39 formed in the insertion portion 10. Further, the proximal end side of the treatment instrument channel 39 communicates with the insertion port 40. That is, the distal end opening 39 a is the distal end of the treatment instrument channel 39 and communicates with the insertion port 40 through the treatment instrument channel 39. The treatment instrument channel 39 is used as a passage through which the endoscope treatment instrument 200 having an articulated bending mechanism is inserted, for example. The endoscope treatment tool 200 is inserted through the insertion port 40, the treatment tool channel 39, and the distal end opening 39a. The endoscope treatment tool 200 is inserted from the insertion port 40, passes through the treatment tool channel 39, and protrudes from the distal end opening 39a.

本実施形態では1つの処置具チャンネル39に対して1つの内視鏡用処置具200が挿通する場合を想定しているが、数は限定する必要はなく、例えば複数の内視鏡用処置具200が処置具チャンネル39に挿入してもよい。また複数の処置具チャンネル39が設けられ、各挿通用チャンネルそれぞれに内視鏡用処置具200が挿通することも可能である。   In the present embodiment, it is assumed that one endoscope treatment tool 200 is inserted into one treatment tool channel 39, but the number is not necessarily limited. For example, a plurality of endoscope treatment tools is provided. 200 may be inserted into the treatment instrument channel 39. Also, a plurality of treatment instrument channels 39 are provided, and the endoscope treatment instrument 200 can be inserted into each insertion channel.

なお可撓管部11や湾曲部12には、図示しない外皮チューブが被覆されている。この外皮チューブは、ゴムなどの弾性材料で可撓管部11や湾曲部12と略同形状(例えば中空形状や円筒形状)に形成されている。この外皮チューブは、熱可塑性エラストマー(スチレン系,オレフィン系,またはウレタン系等)の材質の弾性材料によって射出成形されてもよい。なお、熱可塑性エラストマーの成形は、射出成形に限定されず、注型、押出し、ブロー等の各種成形方法を適用してもよい。   The flexible tube portion 11 and the bending portion 12 are covered with an unshown outer tube. The outer tube is made of an elastic material such as rubber and has substantially the same shape (for example, a hollow shape or a cylindrical shape) as the flexible tube portion 11 and the curved portion 12. The outer tube may be injection-molded with an elastic material made of a thermoplastic elastomer (such as styrene, olefin, or urethane). The molding of the thermoplastic elastomer is not limited to injection molding, and various molding methods such as casting, extrusion, and blow may be applied.

なお先端硬性部13は、可撓管部11や湾曲部12と同様に外皮チューブによって被覆されていても良い。   The distal end rigid portion 13 may be covered with an outer tube similar to the flexible tube portion 11 and the bending portion 12.

また内視鏡2における挿入部10は、湾曲可能なチューブであればよい。   Moreover, the insertion part 10 in the endoscope 2 should just be a bendable tube.

次に本実施形態における内視鏡用処置具200について説明する。
図1に示すように患部を処置する内視鏡用処置具200は、多関節湾曲機構を有している。本実施形態における内視鏡用処置具200は、上述したように体内に挿入される内視鏡用処置具である。
内視鏡用処置具200は、体内に挿入される挿入部202を有している。挿入部202の基端は、内視鏡用処置具200の駆動を制御する駆動制御部203と連結している。駆動制御部203は、挿入部202における湾曲部211を湾曲駆動させる湾曲駆動部である。駆動制御部203には、後述する把持鉗子213を操作する処置具操作部201が設けられている。
Next, the endoscope treatment tool 200 in the present embodiment will be described.
As shown in FIG. 1, an endoscope treatment tool 200 for treating an affected part has a multi-joint bending mechanism. The endoscope treatment tool 200 in this embodiment is an endoscope treatment tool inserted into the body as described above.
The endoscope treatment tool 200 has an insertion portion 202 that is inserted into the body. The proximal end of the insertion unit 202 is connected to a drive control unit 203 that controls the driving of the endoscope treatment tool 200. The drive control unit 203 is a bending drive unit that drives the bending unit 211 in the insertion unit 202 to be bent. The drive control unit 203 is provided with a treatment instrument operation unit 201 that operates a grasping forceps 213 described later.

挿入部202は、図3に示すように可撓管部(軟性部)210と、可撓管部210の先端と連結している湾曲部211と、湾曲部211の先端と連結している先端部212とを有する。図1と図3に示すように挿入部202は、挿入口40と処置具チャンネル39とを通じて先端開口部39aから体内に突出(挿入)される。なお湾曲部211と先端部212とは、内視鏡用処置具200の先端となる。   As shown in FIG. 3, the insertion portion 202 includes a flexible tube portion (soft portion) 210, a bending portion 211 connected to the tip of the flexible tube portion 210, and a tip connected to the tip of the bending portion 211. Part 212. As shown in FIGS. 1 and 3, the insertion portion 202 protrudes (inserts) into the body from the distal end opening 39 a through the insertion port 40 and the treatment instrument channel 39. Note that the bending portion 211 and the distal end portion 212 are the distal end of the endoscope treatment tool 200.

可撓管部210は、弾力性と可撓性を有し、外力によって曲がる。   The flexible tube portion 210 has elasticity and flexibility, and is bent by an external force.

湾曲部211は、多関節湾曲機構を有し、上下左右に所望に湾曲する。詳細には、図3に示すように湾曲部211は、節輪221と節輪222と節輪223と節輪224とを有し、節輪221と節輪222と節輪223と節輪224とが互いに連結することで、構成される。なお連結する節輪の数は、4個に限定する必要はなく、少なくとも2つであればよい。節輪221と節輪222と節輪223と節輪224とは、環状の部材によって形成され、挿入部202の長軸方向へ一列に同軸的に並べて配置される。節輪221と節輪222と節輪223と節輪224とは、隣接する節輪同士で回動自在に連結し、これにより多関節湾曲機構が構成される。なお節輪224は、可撓管部210の先端と連結することとなり、湾曲部211の最も基端側に配設されている節輪である。   The bending portion 211 has an articulated bending mechanism and bends up and down and left and right as desired. Specifically, as shown in FIG. 3, the bending portion 211 includes a node ring 221, a node ring 222, a node ring 223, and a node ring 224, and the node ring 221, the node ring 222, the node ring 223, and the node ring 224. Are connected to each other. Note that the number of node rings to be connected is not limited to four, and may be at least two. The node ring 221, the node ring 222, the node ring 223, and the node ring 224 are formed of an annular member, and are coaxially arranged in a line in the long axis direction of the insertion portion 202. The node ring 221, the node ring 222, the node ring 223, and the node ring 224 are rotatably connected between adjacent node rings, thereby forming an articulated bending mechanism. The node ring 224 is a node ring that is connected to the distal end of the flexible tube portion 210 and is disposed on the most proximal side of the bending portion 211.

節輪221と節輪222は、第1回動軸部225を中心に回動可能に接続し、第1回動軸部225によって回動自在に連結される。節輪221と節輪222は、基端側から見て相対的に左右方向へ回動自在である。
節輪222と節輪223は、第2回動軸部226を中心に回動可能に接続し、第2回動軸部226によって回動自在に連結される。節輪222と節輪223は、基端側から見て相対的に上下方向へ回動自在である。
節輪223と節輪224は、第3回動軸部227を中心に回動可能に接続し、第3回動軸部227によって回動自在に連結される。節輪223と節輪224は、基端側から見て相対的に左右方向へ回動自在である。
The node ring 221 and the node ring 222 are connected so as to be rotatable about the first rotation shaft portion 225, and are connected rotatably by the first rotation shaft portion 225. The node ring 221 and the node ring 222 are relatively rotatable in the left-right direction when viewed from the base end side.
The node ring 222 and the node ring 223 are connected so as to be rotatable about the second rotation shaft portion 226, and are connected rotatably by the second rotation shaft portion 226. The node ring 222 and the node ring 223 are relatively vertically rotatable when viewed from the base end side.
The node ring 223 and the node ring 224 are connected so as to be rotatable about the third rotation shaft portion 227, and are connected rotatably by the third rotation shaft portion 227. The node ring 223 and the node ring 224 are relatively rotatable in the left-right direction as viewed from the base end side.

このように構成された多関節湾曲機構は、柔軟な外皮(図示せず)によって被覆される。これにより湾曲部211が構成される。   The articulated bending mechanism configured as described above is covered with a flexible outer skin (not shown). Thereby, the bending part 211 is comprised.

先端部212には、患部等を処置する処置具本体部である把持鉗子213が設けられている。把持鉗子213は、挿入部202内を挿通する操作ワイヤ234によって図1と図3に示す上下に開閉する把持部材213a,213bを有している。先端部212には、把持鉗子213に限らず、例えば、高周波ナイフまたは高周波凝固子等の処置具が設けられていても良い。   The distal end portion 212 is provided with a grasping forceps 213 that is a treatment instrument main body for treating an affected area. The grasping forceps 213 includes grasping members 213a and 213b that open and close as shown in FIGS. 1 and 3 by an operation wire 234 inserted through the insertion portion 202. The distal end portion 212 is not limited to the grasping forceps 213 but may be provided with a treatment instrument such as a high-frequency knife or a high-frequency coagulator.

なお患部を処置する内視鏡用処置具200は、多関節機構を有さずに、先端に例えば把持鉗子213や高周波ナイフや高周波凝固子等の処置具等のみを有していてもよい。   Note that the endoscopic treatment tool 200 for treating an affected part may have only a treatment tool such as a grasping forceps 213, a high-frequency knife, or a high-frequency coagulator at the tip without having a multi-joint mechanism.

なお上述した節輪221,222,223には、個別的に対応した一対の操作ワイヤ231,232,233が接続している。湾曲部211において、一対の操作ワイヤ231,232,233が適宜選択されて押し引き操作されると、節輪221,222,223は独立して回動する。   Note that a pair of operation wires 231, 232, and 233 that individually correspond to the node rings 221, 222, and 223 described above are connected. In the bending portion 211, when the pair of operation wires 231, 232, 233 is appropriately selected and pushed and pulled, the node rings 221, 222, 223 rotate independently.

これにより多関節機構が形成され、湾曲部211は上下左右の4方向にそれぞれ湾曲できるように構成される。   Thus, a multi-joint mechanism is formed, and the bending portion 211 is configured to be able to bend in four directions, up, down, left, and right.

なお操作ワイヤ231,232,233の先端が節輪221,222,223と接続する手段は、種々の方法を採用することが可能であり、例えばロウ付け固定される。   Various means can be adopted as means for connecting the distal ends of the operation wires 231, 232, 233 to the node rings 221, 222, 223, for example, brazing and fixing.

図3に示すように、駆動制御部203には、湾曲部操作機構及び処置部操作機構が設けられている。   As shown in FIG. 3, the drive control unit 203 is provided with a bending portion operating mechanism and a treatment portion operating mechanism.

湾曲部操作機構は、操作ワイヤ231,232,233をそれぞれ押し引き操作する駆動モータ251,252,253を備える。   The bending portion operating mechanism includes drive motors 251, 252, and 253 that push and pull the operation wires 231, 232, and 233, respectively.

また、処置部操作機構は、操作ワイヤ234を押し引き操作するための駆動モータ254を備える。   The treatment section operation mechanism includes a drive motor 254 for pushing and pulling the operation wire 234.

操作ワイヤ231,232,233は、回動操作対象である節輪221,222,223に対応し、回動操作する。操作ワイヤ234は、把持鉗子213を操作する。   The operation wires 231, 232, and 233 correspond to the node rings 221, 222, and 223 to be rotated and are rotated. The operation wire 234 operates the grasping forceps 213.

駆動モータ251,252,253,254の駆動軸には、それぞれプーリ255が取り付けられている。各駆動軸は、図示しない減速機を介して各プーリ255と連結してもよい。各プーリ255には、操作ワイヤ231,232,233,234が掛けられている。そして、駆動モータ251,252,253,254がそれぞれ個別的に駆動し、プーリ255が回動すると、プーリ255に掛けられた操作ワイヤ231,232,233,234が押し引き操作される。   Pulleys 255 are attached to the drive shafts of the drive motors 251, 252, 253, and 254, respectively. Each drive shaft may be connected to each pulley 255 via a speed reducer (not shown). Operation wires 231, 232, 233, and 234 are hung on each pulley 255. When the drive motors 251, 252, 253, and 254 are individually driven and the pulley 255 rotates, the operation wires 231, 232, 233, and 234 hung on the pulley 255 are pushed and pulled.

湾曲部操作機構及び処置部操作機構は、プーリ255を利用した伝達機構を用いたが、例えばピニオンギアやラックを利用する歯車機構等であってもよい。また湾曲部操作機構及び処置部操作機構は、駆動モータ251,252,253,254の代わりに他の形式の駆動アクチュエータを用いてもよい。   As the bending portion operating mechanism and the treatment portion operating mechanism, a transmission mechanism using a pulley 255 is used. However, for example, a pinion gear or a gear mechanism using a rack may be used. The bending portion operating mechanism and the treatment portion operating mechanism may use other types of drive actuators instead of the drive motors 251, 252, 253, and 254.

図1と図3に示すように、駆動制御部203は、ケーブル257を介して処置具制御部258に接続されている。処置具制御部258には、操作入力装置としての湾曲操作部204がケーブル259を介して接続される。また処置具制御部258には、図3に示すように電力供給用電源コード290が設けられている。   As shown in FIGS. 1 and 3, the drive control unit 203 is connected to the treatment instrument control unit 258 via a cable 257. A bending operation unit 204 as an operation input device is connected to the treatment instrument control unit 258 via a cable 259. The treatment instrument control unit 258 is provided with a power supply power cord 290 as shown in FIG.

湾曲操作部204は、例えば術者によって操作されることで内視鏡用処置具200の位置と姿勢を指示する例えばジョイスティック(操作入力装置)205を有する。このジョイスティック205は、3段重に連接した3つのジョイスティックスイッチ205a,205b,205cを有する。ジョイスティックスイッチ205a,205b,205cは、操作ボックス206に取り付けられている。   The bending operation unit 204 includes, for example, a joystick (operation input device) 205 that instructs the position and posture of the endoscope treatment tool 200 when operated by, for example, an operator. The joystick 205 has three joystick switches 205a, 205b, and 205c that are connected in three layers. The joystick switches 205a, 205b, and 205c are attached to the operation box 206.

なお図3は、1つの内視鏡用処置具200に対する駆動制御部203と処置具制御部258と湾曲操作部204とを図示している。また上述したように、1つの処置具チャンネル39に対して複数の内視鏡用処置具200が挿通される場合、内視鏡用処置具200それぞれに対して駆動制御部203と処置具制御部258と湾曲操作部204が配置されることとなる。   FIG. 3 illustrates the drive control unit 203, the treatment tool control unit 258, and the bending operation unit 204 for one endoscope treatment tool 200. Further, as described above, when a plurality of endoscope treatment tools 200 are inserted into one treatment tool channel 39, the drive control unit 203 and the treatment tool control unit for each of the endoscope treatment tools 200 are provided. 258 and the bending operation unit 204 are arranged.

図1に示すように、処置具制御部258には、ジョイスティック205から出力される指示やジョイスティック205の機能を制御するための条件等を入力する機能制御入力部258aと、駆動モータ251,252,253を駆動制御するモータドライバ(処置具駆動制御部)258bと、駆動制御部203とケーブル257を介して接続し駆動制御部203との間で通信を行うモータユニット通信部258cが設けられている。   As shown in FIG. 1, the treatment instrument control unit 258 has a function control input unit 258 a for inputting an instruction output from the joystick 205, a condition for controlling the function of the joystick 205, and the like, and drive motors 251, 252, A motor driver (treatment instrument drive control unit) 258b that controls the drive of H.253, and a motor unit communication unit 258c that is connected to the drive control unit 203 via the cable 257 and communicates with the drive control unit 203 are provided. .

ジョイスティックスイッチ205a,205b,205cが選択的に操作されると、処置具制御部258は、術者によるジョイスティック205の操作に応じて駆動モータ251,252,253を駆動させる制御信号をモータドライバ258bに送信し、駆動モータ251,252,253を回転させる。つまりジョイスティック205の操作に対応して駆動モータ251,252,253が個別的に駆動する。これにより操作ワイヤ231,232,233は回動するプーリ255によってそれぞれ押し引き操作され、節輪221,222,223は個別的に独立して上下左右方向へ回動し、各関節部は屈曲する。つまり湾曲部211は湾曲する。
このように湾曲操作部204は、駆動制御部203を操作し、湾曲部211を湾曲操作する操作入力装置である。電動式の内視鏡用処置具200は、マニピュレータ(マスタスレーブ)型の電動式の内視鏡用処置具を構成している。なお、内視鏡用処置具200を動かす制御が設定された後に、術者等によりジョイスティック205が操作された場合には、ジョイスティック205の操作指示が優先される。
When the joystick switches 205a, 205b, and 205c are selectively operated, the treatment instrument control unit 258 sends a control signal for driving the drive motors 251, 252, and 253 to the motor driver 258b in accordance with the operation of the joystick 205 by the operator. Then, the drive motors 251, 252, and 253 are rotated. That is, the drive motors 251, 252, and 253 are individually driven in response to the operation of the joystick 205. As a result, the operation wires 231, 232, and 233 are respectively pushed and pulled by the rotating pulley 255, the node rings 221, 222, and 223 are individually independently rotated in the vertical and horizontal directions, and the joint portions are bent. . That is, the bending portion 211 is bent.
As described above, the bending operation unit 204 is an operation input device that operates the drive control unit 203 and performs a bending operation on the bending unit 211. The electric endoscope treatment tool 200 constitutes a manipulator (master slave) type electric endoscope treatment tool. In addition, when the joystick 205 is operated by an operator or the like after the control for moving the endoscope treatment tool 200 is set, the operation instruction for the joystick 205 is given priority.

なお駆動モータ251,252,253には、回転数を計測する図示しないエンコーダが取り付けられている。エンコーダは、回転数に対応した信号を生成し、モータドライバ258bに送信して駆動モータ251,252,253に対するフィードバック制御を行う。   The drive motors 251, 252, and 253 are provided with encoders (not shown) that measure the number of rotations. The encoder generates a signal corresponding to the number of rotations and transmits it to the motor driver 258b to perform feedback control on the drive motors 251, 252, and 253.

次に処置具チャンネル39と先端開口部39aと挿入口40と医療用進退量規制機構50と内視鏡用処置具200とについて説明する。
医療用進退量規制機構50は、内視鏡用処置具200の先端である湾曲部211と先端部212とが処置具チャンネル39の先端である先端開口部39aに対して進退移動する際に、先端開口部39aに対する湾曲部211と先端部212との進退量を規制する。この医療用進退量規制機構50は、図1と図4Aに示すように、挿入口40に着脱自在に取り付けられる規制部材60と、可撓管部210に配設される当て付き部80とを有している。
Next, the treatment instrument channel 39, the distal end opening 39a, the insertion port 40, the medical advance / retreat amount regulating mechanism 50, and the endoscope treatment instrument 200 will be described.
The medical advance / retreat amount regulating mechanism 50 moves forward and backward with respect to the distal end opening 39a, which is the distal end of the treatment instrument channel 39, when the bending portion 211 and the distal end portion 212, which are the distal ends of the endoscope treatment instrument 200, move forward and backward. The advance / retreat amount of the bending portion 211 and the tip portion 212 with respect to the tip opening 39a is restricted. As shown in FIGS. 1 and 4A, the medical advance / retreat amount restriction mechanism 50 includes a restriction member 60 that is detachably attached to the insertion port 40, and a contact portion 80 that is disposed in the flexible tube portion 210. Have.

図4Aと図4Bに示す規制部材60は、例えば円筒形状を有し、弾性材料によって形成されている。この弾性材料とは、例えばエラストマーや、シリコンや、ブチルゴムやイソプロピレンゴムやシリコンゴムといったゴム等である。規制部材60は、規制部材60の先端61aから突出し、規制部材60の周方向に等間隔に配置されている3個の脚部62と、脚部62の先端にそれぞれ設けられている爪部63と、脚部62の内周面に設けられているOリング64とを有している。爪部63とOリング64とは、規制部材60が挿入口40に着脱自在に取り付けられるための取り付け部である。規制部材60が挿入口40に取り付けられる際、脚部62は挿入口40の側面に当接し、爪部63は挿入口40の先端側面に嵌まり込み、Oリング64は挿入口40の基端側面に密着する。   The restricting member 60 shown in FIGS. 4A and 4B has, for example, a cylindrical shape and is made of an elastic material. Examples of the elastic material include elastomers, silicon, rubbers such as butyl rubber, isopropylene rubber, and silicon rubber. The restricting member 60 protrudes from the tip 61 a of the restricting member 60, has three leg portions 62 that are arranged at equal intervals in the circumferential direction of the restricting member 60, and a claw portion 63 that is provided at the tip of the leg portion 62. And an O-ring 64 provided on the inner peripheral surface of the leg portion 62. The claw part 63 and the O-ring 64 are attachment parts for the restriction member 60 to be detachably attached to the insertion port 40. When the restricting member 60 is attached to the insertion port 40, the leg portion 62 comes into contact with the side surface of the insertion port 40, the claw portion 63 is fitted into the distal end side surface of the insertion port 40, and the O-ring 64 is the base end of the insertion port 40. Adhere to the side.

規制部材60は、先端61aにおいて、規制部材60の長手軸方向(内視鏡用処置具200が処置具チャンネル39を進退移動(前進または後退)する方向)に対して規制部材60の側面60aから略垂直に突出している平面である端面65aを有している。言い換えると、端面65aは、側面60aから規制部材60の内周側に向かって突出している面であり、規制部材60の長手軸方向に対して垂直な平面である。また規制部材60は、基端61bにおいて、端面65aと同様の端面66aを有している。端面65aは規制部材60の先端側端面であり、端面66aは規制部材60の基端側端面である。端面65aの先端側には、上述したOリング64が配置されている。端面66aは、例えば上述したような弾性材料によって形成される。   At the distal end 61a, the restricting member 60 extends from the side surface 60a of the restricting member 60 with respect to the longitudinal axis direction of the restricting member 60 (the direction in which the endoscope treatment tool 200 advances or retreats (forwards or retreats) the treatment instrument channel 39). It has an end face 65a which is a plane protruding substantially vertically. In other words, the end surface 65 a is a surface that protrudes from the side surface 60 a toward the inner peripheral side of the regulating member 60, and is a plane that is perpendicular to the longitudinal axis direction of the regulating member 60. The restricting member 60 has an end surface 66a similar to the end surface 65a at the base end 61b. The end surface 65 a is a distal end side end surface of the regulating member 60, and the end surface 66 a is a proximal end side end surface of the regulating member 60. The above-described O-ring 64 is disposed on the distal end side of the end face 65a. The end surface 66a is formed of an elastic material as described above, for example.

また規制部材60は、端面65aに形成されている開口部65bと、端面66aにおいて規制部材60の長手軸方向において開口部65bと同一直線状に形成されている開口部66bとを有している。開口部65bは端面65aの径方向の中央部に形成され、開口部66bは端面66aの径方向の中央部に形成されている。開口部65bの直径D1と開口部66bの直径D2は、可撓管部210等の挿入部202の直径D3よりも大きい。そのため開口部65b,66bには、内視鏡用処置具200(可撓管部210)が自在に挿通する。つまり規制部材60には、内視鏡用処置具200(可撓管部210)が処置具チャンネル39に向かって挿通する。   The restricting member 60 has an opening 65b formed in the end surface 65a and an opening 66b formed in the end surface 66a in the same straight line as the opening 65b in the longitudinal axis direction of the restricting member 60. . The opening 65b is formed in the central portion in the radial direction of the end surface 65a, and the opening 66b is formed in the central portion in the radial direction of the end surface 66a. The diameter D1 of the opening 65b and the diameter D2 of the opening 66b are larger than the diameter D3 of the insertion portion 202 such as the flexible tube portion 210. Therefore, the endoscope treatment tool 200 (flexible tube portion 210) is freely inserted into the openings 65b and 66b. That is, the endoscope treatment tool 200 (flexible tube portion 210) is inserted into the restriction member 60 toward the treatment tool channel 39.

またこのとき端面65a,66aは、内視鏡用処置具200(可撓管部210)が処置具チャンネル39内を進退移動する際に、当て付き部80が端面65a,66aに当て付くことで、内視鏡用処置具200(可撓管部210)の進退移動を規制することとなる。   At this time, the end faces 65a and 66a are caused by the abutting portion 80 coming into contact with the end faces 65a and 66a when the endoscope treatment instrument 200 (flexible tube section 210) moves forward and backward in the treatment instrument channel 39. The advance / retreat movement of the endoscope treatment tool 200 (flexible tube section 210) is restricted.

端面65aと端面66aとの間には、当て付き部80が規制部材60の長手軸方向に沿って進退移動可能な空間部68が形成されている。規制部材60の長手軸方向に対して略直交する方向における空間部68の長さL1は、開口部65bの直径D1と開口部66bの直径D2と挿入部202の直径D3とよりも大きい。長さL1は、空間部68の長さ(直径)であり、規制部材60の内径である。   Between the end surface 65a and the end surface 66a, a space portion 68 is formed in which the abutting portion 80 can move forward and backward along the longitudinal axis direction of the regulating member 60. The length L1 of the space 68 in the direction substantially orthogonal to the longitudinal axis direction of the regulating member 60 is larger than the diameter D1 of the opening 65b, the diameter D2 of the opening 66b, and the diameter D3 of the insertion portion 202. The length L1 is the length (diameter) of the space portion 68 and the inner diameter of the regulating member 60.

当て付き部80は、可撓管部210が規制部材60を挿通し規制部材60に対して進退移動する際に、空間部68に接する端面65aと端面66aとのいずれか一方に当て付き、端面65aに当て付くことで処置具チャンネル39から突出する内視鏡用処置具200の先端である湾曲部211の突出量を規制し、端面66aに当て付くことで内視鏡用処置具200の先端である先端部212の後退量を規制し処置具チャンネル39における先端部212の初期位置を設定する。   The abutting portion 80 abuts against either the end surface 65a or the end surface 66a that contacts the space portion 68 when the flexible tube 210 is inserted through the regulating member 60 and moves forward and backward relative to the regulating member 60. The amount of protrusion of the bending portion 211 that is the tip of the endoscope treatment tool 200 protruding from the treatment tool channel 39 is regulated by being applied to 65a, and the tip of the endoscope treatment tool 200 is applied to the end surface 66a. The retraction amount of the distal end portion 212 is regulated to set the initial position of the distal end portion 212 in the treatment instrument channel 39.

当て付き部80は、図4Cに示すように可撓管部210の外周面の全周に渡り形成されている溝81に嵌め込まれている。当て付き部80は、溝81の深さよりも厚みを有している。   As shown in FIG. 4C, the abutting portion 80 is fitted in a groove 81 formed over the entire circumference of the outer peripheral surface of the flexible tube portion 210. The abutting portion 80 has a thickness that is greater than the depth of the groove 81.

規制部材60が爪部63とOリング64によって挿入口40に取り付けられ、内視鏡用処置具200が規制部材60と挿入口40を介して処置具チャンネル39に挿入される際、図5Aに示すように当て付き部80は端面66aに当て付く。端面66aは弾性材料によって形成されているため、図5Bに示すように端面66aは当て付き部80によって空間部68に向かって弾性変形して当て付き部80によって押し広げられる。これにより当て付き部80は開口部66bを通過し、図4Aと図5Cに示すように空間部68に配置されることとなる。   When the restriction member 60 is attached to the insertion port 40 by the claw portion 63 and the O-ring 64 and the endoscope treatment tool 200 is inserted into the treatment tool channel 39 via the restriction member 60 and the insertion port 40, FIG. As shown, the abutting portion 80 abuts against the end surface 66a. Since the end surface 66a is formed of an elastic material, the end surface 66a is elastically deformed toward the space portion 68 by the abutting portion 80 and is spread by the abutting portion 80 as shown in FIG. 5B. Thereby, the contact part 80 passes the opening part 66b, and will be arrange | positioned in the space part 68, as shown to FIG. 4A and FIG. 5C.

このように当て付き部80が空間部68内に配置されると、当て付き部80は端面65a,66aと開口部65b,66bに対向する。また当て付き部80が空間部68に配置され、内視鏡用処置具200が規制部材60の長手軸方向に沿って進退移動することで、当て付き部80も空間部68を規制部材60の長手軸方向に沿って進退移動する。これにより当て付き部80は、図5Dに示すように端面65aに、または図5Eに示すように端面66aに当て付く(面当接する)。   When the abutting portion 80 is arranged in the space portion 68 in this manner, the abutting portion 80 faces the end surfaces 65a and 66a and the openings 65b and 66b. Further, the abutting portion 80 is disposed in the space portion 68, and the endoscopic treatment instrument 200 moves back and forth along the longitudinal axis direction of the regulating member 60, so that the abutting portion 80 also moves the space portion 68 of the regulating member 60. It moves forward and backward along the longitudinal direction. As a result, the abutting portion 80 abuts against the end surface 65a as shown in FIG. 5D or abuts against the end surface 66a as shown in FIG. 5E (surface contact).

当て付き部80の外径D4は、処置具チャンネル39の直径D5よりも大きい。また当て付き部80の外径D4は、開口部65bの直径D1と開口部66bの直径D2とよりも大きい。   The outer diameter D4 of the abutting portion 80 is larger than the diameter D5 of the treatment instrument channel 39. The outer diameter D4 of the contact portion 80 is larger than the diameter D1 of the opening 65b and the diameter D2 of the opening 66b.

当て付き部80は、上述したように内視鏡用処置具200(可撓管部210)が開口部66bを挿通し、図5Aに示すように当て付き部80が端面66aに当て付いた際に、図5Bに示すように端面66aを弾性変形させて押し広げ、開口部66bを通過できる大きさを有している。言い換えると、端面66aは、当て付き部80が端面66aに当て付いた際に開口部66bを中心に空間部68に向かって弾性変形して押し広げ可能である。また端面66aは、当て付き部80の外径D4よりも直径D2が小さく、端面66aが押し広げられた際に、当て付き部80が通過可能な開口部66bを有していることとなる。   As described above, the abutting portion 80 is obtained when the endoscope treatment instrument 200 (flexible tube portion 210) is inserted through the opening 66b and the abutting portion 80 is abutted against the end surface 66a as shown in FIG. 5A. In addition, as shown in FIG. 5B, the end surface 66a is elastically deformed and expanded so that it can pass through the opening 66b. In other words, the end surface 66a can be expanded by being elastically deformed toward the space 68 around the opening 66b when the abutting portion 80 abuts against the end surface 66a. The end surface 66a has an opening 66b through which the abutting portion 80 can pass when the end surface 66a is expanded when the diameter D2 is smaller than the outer diameter D4 of the abutting portion 80.

また開口部65bの直径D1は、開口部66bの直径D2と当て付き部80の直径D4よりも小さい。そのため端面65aは、当て付き部80が端面65aに当て付いても端面66aとは異なり開口部66bを中心に押し広げられることはない。開口部65bの直径D1は、処置具チャンネル39の直径D5と略同一であることが好適である。   The diameter D1 of the opening 65b is smaller than the diameter D2 of the opening 66b and the diameter D4 of the abutting portion 80. Therefore, unlike the end surface 66a, the end surface 65a is not spread about the opening 66b even when the abutting portion 80 contacts the end surface 65a. The diameter D1 of the opening 65b is preferably substantially the same as the diameter D5 of the treatment instrument channel 39.

開口部65bと端面65aとは、当て付き部80が端面65aよりも先端側(処置具チャンネル39)に前進することを防止する防止部を兼ねている。言い換えると開口部65bと端面65aとは、当て付き部80が端面65aよりも規制部材60の長手軸方向における先端側に前進することを防止し、処置具チャンネル39の先端である先端開口部39aから突出する内視鏡用処置具200の先端である湾曲部211の突出量を規制する規制部でもある。   The opening 65b and the end surface 65a also serve as a prevention unit that prevents the contact portion 80 from moving forward from the end surface 65a to the distal end side (the treatment instrument channel 39). In other words, the opening 65b and the end surface 65a prevent the abutting portion 80 from moving forward in the longitudinal direction of the regulating member 60 relative to the end surface 65a, and the distal end opening 39a that is the distal end of the treatment instrument channel 39. It is also a regulation part which regulates the amount of projection of curved part 211 which is the tip of endoscope treatment tool 200 which projects from.

なお開口部65bの直径D1の大きさは、当て付き部80が開口部66bを通過でき、処置具チャンネル39と空間部68との間を自在に進退移動することを防止できれば、限定されない。   The size of the diameter D1 of the opening 65b is not limited as long as the contact portion 80 can pass through the opening 66b and can be prevented from freely moving back and forth between the treatment instrument channel 39 and the space 68.

当て付き部80は、規制部材60よりも硬質な材料によって形成されることが好適である。また当て付き部80は、例えばポリオレフィン等のプラスチック材料等で形成されていても良い。   The abutting portion 80 is preferably formed of a material harder than the regulating member 60. The abutting portion 80 may be formed of a plastic material such as polyolefin.

上述した処置具チャンネル39から突出する内視鏡用処置具200の先端の突出量について説明する。この突出量とは、内視鏡用処置具200が処置具チャンネル39に挿入された際に、図5Dに示すように当て付き部80が端面65aに当て付くことで、湾曲部12が湾曲状態または非湾曲状態であっても、図6Aに示すように内視鏡用処置具200の先端である湾曲部211において、最も基端側に配設される節輪224が処置具チャンネル39の先端である先端開口部39aから突出する量であり、所望量である。つまり当て付き部80は、端面65aに当て付くことで、先端開口部39aから突出する湾曲部211(節輪224)の突出量を規制し、先端開口部39aから湾曲部211(節輪224)を所望な量だけ突出させる。   The protrusion amount of the distal end of the endoscope treatment tool 200 protruding from the treatment tool channel 39 will be described. This protrusion amount means that when the endoscopic treatment instrument 200 is inserted into the treatment instrument channel 39, the abutting portion 80 abuts against the end surface 65a as shown in FIG. Even in the non-curved state, as shown in FIG. 6A, the node ring 224 disposed on the most proximal side is the distal end of the treatment instrument channel 39 in the bending portion 211 that is the distal end of the endoscope treatment instrument 200. This is an amount protruding from the tip opening 39a, which is a desired amount. That is, the abutting portion 80 abuts against the end surface 65a, thereby restricting the protruding amount of the bending portion 211 (node ring 224) protruding from the tip opening portion 39a and from the tip opening portion 39a to the bending portion 211 (node ring 224). Is projected by a desired amount.

当て付き部80が進退移動可能な端面65aから端面66aまでの長さL2は、図4Aに示すように節輪224から先端部212までの長さL3よりも長い。またこの長さL2は、当て付き部80が進退移動する進退量に一致する。この進退量は、湾曲部211(節輪224)が処置具チャンネル39から突出する位置から、先端部212が処置具チャンネル39に収納され、この状態で内視鏡2を湾曲させても内視鏡用処置具200(例えば先端部212)が例えば処置具チャンネル39の内周面等に接触して破損しない位置までの距離である。   A length L2 from the end surface 65a to the end surface 66a to which the abutting portion 80 can move forward and backward is longer than a length L3 from the node ring 224 to the tip end portion 212 as shown in FIG. 4A. The length L2 is equal to the advance / retreat amount by which the contact portion 80 moves forward / backward. The amount of advancement / retraction is determined even if the distal end 212 is accommodated in the treatment instrument channel 39 from the position where the bending portion 211 (node ring 224) protrudes from the treatment instrument channel 39 and the endoscope 2 is bent in this state. This is the distance to the position where the mirror treatment instrument 200 (for example, the distal end portion 212) does not break due to contact with the inner peripheral surface of the treatment instrument channel 39, for example.

次に上述した内視鏡用処置具200の先端の初期位置について説明する。内視鏡用処置具200の先端の初期位置とは、内視鏡用処置具200が処置具チャンネル39に挿入された際に、図5Eに示すように当て付き部80が端面66aに当て付くことで、湾曲部12が湾曲状態または非湾曲状態であっても、図6Bに示すように内視鏡用処置具200の先端である先端部212が処置具チャンネル39の先端である先端開口部39aから所望の距離だけ基端側に配置され、処置具チャンネル39に収納され、この状態で内視鏡2を湾曲させても内視鏡用処置具200が上述したように破損しない位置である。なおこの位置は、先端部212が先端開口部39aと一致しても良いし、先端部212が先端開口部39aよりも所望な長さだけ基端側に配置されていても良い。   Next, the initial position of the distal end of the above-described endoscope treatment tool 200 will be described. The initial position of the distal end of the endoscope treatment tool 200 means that when the endoscope treatment tool 200 is inserted into the treatment tool channel 39, the contact portion 80 contacts the end surface 66a as shown in FIG. 5E. Thus, even if the bending portion 12 is in a curved state or a non-curved state, the distal end portion 212 that is the distal end of the endoscope treatment instrument 200 is the distal end opening that is the distal end of the treatment instrument channel 39 as shown in FIG. 6B. It is disposed at the base end side by a desired distance from 39a and is accommodated in the treatment instrument channel 39. In this state, even if the endoscope 2 is bent, the endoscope treatment instrument 200 is not damaged as described above. . In this position, the distal end portion 212 may coincide with the distal end opening portion 39a, or the distal end portion 212 may be disposed on the proximal end side by a desired length from the distal end opening portion 39a.

次に本実施形態の動作方法について詳細に説明する。
規制部材60が挿入口40に向かって押し込まれると、脚部62は挿入口40の側面に当接し、爪部63は挿入口40の先端側面に嵌まり込み、Oリング64は挿入口40の基端側面に密着する。これにより図5Aに示すように規制部材60が挿入口40に取り付けられる。このとき処置具チャンネル39は、挿入口40を介して開口部65bと連通することになる。
Next, the operation method of this embodiment will be described in detail.
When the regulating member 60 is pushed toward the insertion port 40, the leg portion 62 comes into contact with the side surface of the insertion port 40, the claw portion 63 fits into the distal end side surface of the insertion port 40, and the O-ring 64 is connected to the insertion port 40. Close contact with the proximal side. As a result, the regulating member 60 is attached to the insertion port 40 as shown in FIG. 5A. At this time, the treatment instrument channel 39 communicates with the opening 65b through the insertion port 40.

挿入部202は、規制部材60と挿入口40を介して処置具チャンネル39に挿入される。このとき挿入部202が処置具チャンネル39を容易に挿通するために、可撓管部11と湾曲部12とは非湾曲状態であることが好適である。ただし、必ずしも非湾曲状態である必要はなく、挿入部202が処置具チャンネル39を容易に挿通できれば良い。   The insertion portion 202 is inserted into the treatment instrument channel 39 via the restriction member 60 and the insertion port 40. At this time, in order for the insertion part 202 to easily pass through the treatment instrument channel 39, it is preferable that the flexible tube part 11 and the bending part 12 are in an uncurved state. However, it is not always necessary to be in a non-curved state, as long as the insertion portion 202 can be easily inserted through the treatment instrument channel 39.

また挿入部202における可撓管部210が処置具チャンネル39に挿入されると、図5Aに示すように当て付き部80は端面66aに当て付く。そのため処置具チャンネル39に対する可撓管部210の挿入が、一時的に停止する。このとき可撓管部210が処置具チャンネル39に挿入される際に用いられた第1の力量、または第1の力量よりも大きい第2の力量によって、可撓管部210が処置具チャンネル39に向かって押し込まれると、図5Bに示すように端面66aが空間部68に向かって弾性変形する。よって当て付き部80は、開口部66bを通過し、図5Cに示すように規制部材60の外部から空間部68に移動する。   When the flexible tube portion 210 in the insertion portion 202 is inserted into the treatment instrument channel 39, the contact portion 80 contacts the end surface 66a as shown in FIG. 5A. Therefore, the insertion of the flexible tube portion 210 into the treatment instrument channel 39 is temporarily stopped. At this time, the flexible tube portion 210 is caused to move to the treatment instrument channel 39 by the first force amount used when the flexible tube portion 210 is inserted into the treatment instrument channel 39 or a second force amount larger than the first force amount. As shown in FIG. 5B, the end surface 66a is elastically deformed toward the space 68. Therefore, the abutting portion 80 passes through the opening 66b and moves from the outside of the regulating member 60 to the space portion 68 as shown in FIG. 5C.

なお当て付き部80が空間部68に移動すると、端面66aは、弾性材料によって形成される端面66aの弾性力によって規制部材60の外部に向かって弾性変形し、図5Cに示すように当て付き部80が開口部66bを通過する前の状態に戻る。   When the abutting portion 80 moves to the space portion 68, the end surface 66a is elastically deformed toward the outside of the regulating member 60 by the elastic force of the end surface 66a formed of an elastic material, and as shown in FIG. 80 returns to the state before passing through the opening 66b.

また可撓管部210は押し込まれると前進し、図5Dに示すように当て付き部80は端面65aと面当接する(当て付く)。このとき内視鏡用処置具200の先端である湾曲部211(節輪224)は、湾曲部12が湾曲状態または非湾曲状態であっても、図6Aに示すように先端開口部39aから所望に突出する。つまり当て付き部80は、図5Dに示すように端面65aと面当接することで、例えば内視鏡用処置具200が使用される際に、先端開口部39aから突出する湾曲部211(節輪224)の突出量を規定することとなる。このとき可撓管部210が第1の力量または第2の力量によって押し込まれても、端面65aと開口部65bは当て付き部80の前進を防止する。よって先端開口部39aから突出する湾曲部211(節輪224)の突出量は、当て付き部80が端面65aと面当接することで、常に同一となる。また湾曲部211(節輪224)は、先端開口部39aから突出する突出量を端面65aと開口部65bによって規制される。   Further, when the flexible tube portion 210 is pushed in, the flexible tube portion 210 moves forward, and as shown in FIG. 5D, the contact portion 80 comes into surface contact (contacts) with the end surface 65a. At this time, the bending portion 211 (node ring 224) which is the distal end of the endoscope treatment tool 200 is desired from the distal end opening 39a as shown in FIG. 6A even when the bending portion 12 is in a curved state or a non-curved state. Protrusively. In other words, the contact portion 80 is in surface contact with the end surface 65a as shown in FIG. 5D, so that, for example, when the endoscope treatment tool 200 is used, the curved portion 211 (node ring) protruding from the distal end opening 39a. 224) is defined. At this time, even if the flexible tube portion 210 is pushed in by the first force amount or the second force amount, the end surface 65a and the opening portion 65b prevent the contact portion 80 from moving forward. Therefore, the protruding amount of the curved portion 211 (node ring 224) protruding from the tip opening 39a is always the same as the contact portion 80 comes into surface contact with the end surface 65a. Further, the bending portion 211 (node ring 224) is regulated by the end face 65a and the opening 65b with respect to the protruding amount protruding from the tip opening 39a.

また可撓管部210は牽引されると後退し、図5Eに示すように当て付き部80は端面66aと面当接する(当て付く)。このとき内視鏡用処置具200の先端である先端部212は、湾曲部12が湾曲状態または非湾曲状態であっても、図6Bに示すように処置具チャンネル39内における初期位置に配置される。この初期位置は、上述したように先端部212が、先端開口部39aから所望の距離だけ基端側に配置され、処置具チャンネル39に収納され、この状態で内視鏡2を湾曲させても内視鏡用処置具200が破損しない位置である。つまり当て付き部80は、図5Eに示すように端面66aと面当接することで、例えば内視鏡用処置具200が使用される前に、処置具チャンネル39内における先端部212の初期位置を設定することとなる。   Further, when the flexible tube portion 210 is pulled, the flexible tube portion 210 moves backward, and as shown in FIG. 5E, the contact portion 80 comes into surface contact (contacts) with the end surface 66a. At this time, the distal end portion 212 which is the distal end of the endoscope treatment instrument 200 is disposed at the initial position in the treatment instrument channel 39 as shown in FIG. 6B even if the bending portion 12 is in a curved state or a non-curved state. The As described above, the initial position is such that the distal end portion 212 is disposed on the proximal end side by a desired distance from the distal end opening 39a and is accommodated in the treatment instrument channel 39, and the endoscope 2 is curved in this state. This is a position where the endoscope treatment tool 200 is not damaged. That is, the contact portion 80 is in surface contact with the end surface 66a as shown in FIG. 5E, so that the initial position of the distal end portion 212 in the treatment instrument channel 39 is determined before the treatment instrument 200 for endoscope is used, for example. It will be set.

また当て付き部80は端面66aと面当接しているため、当て付き部80と端面66aは、内視鏡用処置具200が第1の力量によって牽引されても、内視鏡用処置具200が当て付き部80と端面66aとの面当接している位置よりもさらに後退することを防止している。つまり当て付き部80と端面66aとが互いに面当接することで、可撓管部210は後退することを防止され、先端部212の後退量を規制し、内視鏡用処置具200は挿入口40から引き抜かれることを防止される。   Further, since the abutting portion 80 is in surface contact with the end surface 66a, the abutting portion 80 and the end surface 66a can be used even if the endoscopic treatment tool 200 is pulled by the first force. Is prevented from further retreating than the position where the contact portion 80 and the end surface 66a are in contact with each other. That is, the abutting portion 80 and the end surface 66a are in surface contact with each other, so that the flexible tube portion 210 is prevented from moving backward, the amount of retraction of the distal end portion 212 is restricted, and the endoscope treatment tool 200 is inserted into the insertion port. 40 is prevented from being pulled out.

このあと図5Dに示すように湾曲部211(節輪224)が先端開口部39aから突出すると、内視鏡用処置具200がジョイスティック205によって操作され、内視鏡2が操作部30によって操作され、体内の患部が処置される。   5D, when the bending portion 211 (node ring 224) protrudes from the distal end opening 39a, the endoscope treatment tool 200 is operated by the joystick 205, and the endoscope 2 is operated by the operation unit 30. The affected area in the body is treated.

処置が終了すると、内視鏡用処置具200は、処置具チャンネル39と挿入口40と規制部材60から引き抜かれる。なお内視鏡用処置具200が規制部材60から引き抜かれる際、図5Eに示すように当て付き部80が端面66aに当て付く。その際、上述したように当て付き部80が規制部材60の外部から空間部68に移動することとは逆に、第1の力量、または第2の力量によって、内視鏡用処置具200が引き抜かれることで、図5Bに示すように端面66aが規制部材60の外部に向かって弾性変形する。よって当て付き部80は、開口部66bを通過し、空間部68から規制部材60の外部に移動する。これにより内視鏡用処置具200は、規制部材60から引き抜かれる。   When the treatment is completed, the endoscope treatment tool 200 is pulled out of the treatment tool channel 39, the insertion port 40, and the regulating member 60. When the endoscope treatment tool 200 is pulled out from the restricting member 60, the contact portion 80 contacts the end surface 66a as shown in FIG. 5E. At that time, as described above, the treatment tool 200 for endoscope 200 is moved by the first force amount or the second force amount, contrary to the movement of the contact portion 80 from the outside of the regulating member 60 to the space portion 68. By being pulled out, the end surface 66a is elastically deformed toward the outside of the regulating member 60 as shown in FIG. 5B. Therefore, the abutting portion 80 passes through the opening 66 b and moves from the space portion 68 to the outside of the regulating member 60. As a result, the endoscope treatment tool 200 is pulled out of the regulating member 60.

この後、爪部63が挿入口40から係合解除され、脚部62は挿入口40の側面から離れ、Oリング64が挿入口40から外れる。これにより規制部材60が挿入口40から取り外される。これにより本実施形態の動作が終了する。   Thereafter, the claw portion 63 is disengaged from the insertion port 40, the leg portion 62 is separated from the side surface of the insertion port 40, and the O-ring 64 is detached from the insertion port 40. As a result, the restricting member 60 is removed from the insertion port 40. Thereby, the operation of the present embodiment is completed.

なお規制部材60が挿入口40から取り外されると同時に、内視鏡用処置具200が処置具チャンネル39と挿入口40とから引き抜かれてもよい。   At the same time as the restriction member 60 is removed from the insertion port 40, the endoscope treatment tool 200 may be pulled out of the treatment tool channel 39 and the insertion port 40.

このように本実施形態では、挿入口40に規制部材60を取り付け、当て付き部80を端面65a,66aに当て付けるのみで、処置具チャンネル39に対する挿入部10の進退量を規制して、先端開口部39aから突出する湾曲部211(節輪224)の突出量を容易に規制でき、処置具チャンネル39内における先端部212の初期位置を容易に設定することができる。   As described above, in the present embodiment, the restricting member 60 is attached to the insertion port 40, and the advancing / retreating amount of the insertion portion 10 with respect to the treatment instrument channel 39 is restricted by merely attaching the contact portion 80 to the end surfaces 65a and 66a. The protruding amount of the curved portion 211 (node ring 224) protruding from the opening 39a can be easily regulated, and the initial position of the distal end portion 212 in the treatment instrument channel 39 can be easily set.

また本実施形態は、当て付き部80を端面65aに当て付けることで、湾曲部12が湾曲状態または非湾曲状態であっても、先端部212が処置具チャンネル39から術者の意図に反して必要以上に突出することを防止することができる。   Further, in the present embodiment, the abutting portion 80 is abutted against the end surface 65a, so that the distal end portion 212 is disengaged from the treatment instrument channel 39 against the operator's intention even when the bending portion 12 is in a curved state or a non-curved state. Protruding more than necessary can be prevented.

また本実施形態は、当て付き部80を端面66aに当て付けることで、湾曲部12が湾曲状態または非湾曲状態であっても、先端部212が先端開口部39aから所望の距離だけ基端側に配置され、先端部212が処置具チャンネル39に収納され、内視鏡2を湾曲させても内視鏡用処置具200が破損しないように初期位置を設定している。
これにより本実施形態は、当て付き部80を端面66aに当て付けることで、湾曲部12が湾曲状態または非湾曲状態であっても、先端部212を処置具チャンネル39に確実に収納でき、収納された先端部212が内視鏡2の湾曲によって破損してしまうことを防止することができる。
Further, in the present embodiment, the abutting portion 80 is abutted against the end surface 66a, so that the distal end portion 212 is at the proximal end side by a desired distance from the distal end opening 39a even when the bending portion 12 is in a curved state or a non-curved state. The distal end 212 is accommodated in the treatment instrument channel 39, and the initial position is set so that the endoscope treatment instrument 200 is not damaged even if the endoscope 2 is bent.
Accordingly, in the present embodiment, the abutting portion 80 is applied to the end surface 66a, so that the distal end portion 212 can be reliably stored in the treatment instrument channel 39 even when the bending portion 12 is in a curved state or a non-curved state. It is possible to prevent the distal end 212 thus formed from being damaged by the bending of the endoscope 2.

また本実施形態は、図4Aに示すように端面65aから端面66aまでの長さL2を、節輪224から先端部212までの長さL3より長くすることで、湾曲部211を先端開口部39aから確実に突出させることができ、先端部212を処置具チャンネル39に確実に収納することができる。   Further, in the present embodiment, as shown in FIG. 4A, the length L2 from the end surface 65a to the end surface 66a is made longer than the length L3 from the node ring 224 to the tip portion 212, thereby making the curved portion 211 the tip opening 39a. Thus, the distal end portion 212 can be reliably stored in the treatment instrument channel 39.

また本実施形態は、溝81に当て付き部80を嵌め込ませることで、当て付き部80が端面65a,66aに当て付いても、溝81から抜けることを防止でき、突出量と初期位置のずれを防止することができる。   Further, in this embodiment, by fitting the abutting portion 80 into the groove 81, even if the abutting portion 80 abuts against the end surfaces 65a and 66a, it can be prevented from coming out of the groove 81, and the deviation between the protruding amount and the initial position Can be prevented.

また本実施形態は、挿入口40に規制部材60を取り付けても、処置具チャンネル39と挿入口40と規制部材60から内視鏡用処置具200を引き抜くことができる。よって本実施形態は、内視鏡用処置具200に対する洗浄性や消毒性を確保することができる。   Further, in the present embodiment, even when the restriction member 60 is attached to the insertion port 40, the endoscope treatment tool 200 can be pulled out from the treatment tool channel 39, the insertion port 40, and the restriction member 60. Therefore, the present embodiment can ensure cleanability and disinfection for the endoscope treatment tool 200.

また本実施形態は、挿入口40から規制部材60を取り外すと同時に、内視鏡用処置具200を処置具チャンネル39と挿入口40とから引き抜くことができる。よって本実施形態は、規制部材60を取り外す動作と、内視鏡用処置具200を引き抜く動作とを一度に実施できるために、処置後の手間を省くことができる。   In the present embodiment, the restriction member 60 is removed from the insertion port 40, and at the same time, the endoscope treatment tool 200 can be pulled out from the treatment tool channel 39 and the insertion port 40. Therefore, since this embodiment can implement the operation | movement which removes the control member 60, and the operation | movement which pulls out the treatment tool 200 for endoscopes at once, the effort after a treatment can be saved.

なお本実施形態において、規制部材60は弾性材料によって形成され、当て付き部80は規制部材60よりも硬質な材料によって形成されることが好適としたがこれに限定する必要はない。当て付き部80は例えば弾性材料によって形成され、規制部材60は当て付き部80よりも硬質な材料によって形成されてもよい。   In the present embodiment, it is preferable that the restricting member 60 is formed of an elastic material, and the abutting portion 80 is formed of a material harder than the restricting member 60. However, the present invention is not limited to this. The contact portion 80 may be formed of, for example, an elastic material, and the restriction member 60 may be formed of a material harder than the contact portion 80.

本実施形態において、突出量と初期位置のずれを防止するために、溝81に当て付き部80を嵌め込ませたがこれに限定する必要はない。例えば当て付き部80は、可撓管部210の外周面に直接固着されても良い。また可撓管部210の外周には、当て付き部80と同様の突起が設けられても良い。   In the present embodiment, in order to prevent a deviation between the protruding amount and the initial position, the contact portion 80 is fitted in the groove 81, but it is not necessary to limit to this. For example, the contact portion 80 may be directly fixed to the outer peripheral surface of the flexible tube portion 210. In addition, a protrusion similar to the abutting portion 80 may be provided on the outer periphery of the flexible tube portion 210.

本実施形態において端面66aは、図7に示すように開口部66bの周縁に沿って形成される切り欠き部66cを有していてもよい。なお図7において、爪部63側における可撓管部210の図示を簡略化のため省略している。   In the present embodiment, the end surface 66a may have a notch 66c formed along the periphery of the opening 66b as shown in FIG. In FIG. 7, the illustration of the flexible tube portion 210 on the claw portion 63 side is omitted for the sake of simplicity.

これにより端面66aは当て付き部80によって弾性変形する際に、端面66aは切り欠き部66cによって容易に押し広げられる。よって本実施形態は、開口部66bに対して当て付き部80を容易に通過させることができ、規制部材60に対して当て付き部80を含む内視鏡用処置具200を容易に挿入または抜去することができる。   As a result, when the end surface 66a is elastically deformed by the abutting portion 80, the end surface 66a is easily pushed out by the notch portion 66c. Therefore, in the present embodiment, the abutting portion 80 can be easily passed through the opening 66b, and the endoscope treatment instrument 200 including the abutting portion 80 is easily inserted into or removed from the regulating member 60. can do.

次に本実施形態における第1の変形例について図8A乃至図8Fと図9A乃至図9Cと図10A乃至図10Cとを参照して説明する。
本変形例において、図8Aに示すように当て付き部80と開口部66bとは、内視鏡用処置具200の挿入方向に向かって先細で径が縮径しているテーパ形状を有している。テーパ形状を有している当て付き部80は、テーパ形状を有している開口部66bを挿通可能である。
Next, a first modification of the present embodiment will be described with reference to FIGS. 8A to 8F, FIGS. 9A to 9C, and FIGS. 10A to 10C.
In this modified example, as shown in FIG. 8A, the contact portion 80 and the opening 66b have a tapered shape that is tapered toward the insertion direction of the endoscope treatment tool 200 and whose diameter is reduced. Yes. The abutting portion 80 having a tapered shape can be inserted through the opening 66b having a tapered shape.

図8Bに示すように本変形例における規制部材60は、例えば中空な角柱形状を有している。そのため図8A乃至図8Cに示すように規制部材60は、脚部62と爪部63とを有しておらず、例えばビス42など締結部材によって先端面69に対して着脱自在に取り付け可能な先端取付部材70を有している。   As shown in FIG. 8B, the restricting member 60 in the present modification has, for example, a hollow prismatic shape. Therefore, as shown in FIGS. 8A to 8C, the regulating member 60 does not have the leg portion 62 and the claw portion 63 and can be detachably attached to the distal end surface 69 by a fastening member such as a screw 42. An attachment member 70 is provided.

図8Cに示すように先端取付部材70は、規制部材60の長手軸方向に対して直交する方向から平面視した際に、略コの字形状を有している。先端取付部材70は、先端取付部材70を平面視した際に相対するコの字の辺の一方である第1の脚部(脚部71a)と、先端取付部材70を平面視した際に相対するコの字の辺の他方である第2の脚部(脚部71b)と、脚部71aと脚部71bとの間に形成される溝部71cとを有している。先端取付部材70が先端面69に取り付けられる際に、脚部71aと脚部71bとは、先端面69に当接する。   As shown in FIG. 8C, the tip mounting member 70 has a substantially U-shape when seen in a plan view from a direction orthogonal to the longitudinal axis direction of the regulating member 60. The tip attachment member 70 is relatively opposite to the first leg portion (leg portion 71a) which is one of the U-shaped sides opposed to each other when the tip attachment member 70 is viewed in plan view. A second leg portion (leg portion 71b) which is the other side of the U-shaped side, and a groove portion 71c formed between the leg portion 71a and the leg portion 71b. When the tip attachment member 70 is attached to the tip surface 69, the leg portion 71 a and the leg portion 71 b abut against the tip surface 69.

また先端取付部材70は、ビス42が係合するための4つの係合口72と、内視鏡用処置具200(可撓管部210)が貫通可能な貫通口73とを有している。係合口72と貫通口73とは、規制部材60の長手軸方向において、先端取付部材70を貫通している。貫通口73は先端取付部材70の略中央に配置されており、係合口72は貫通口73の周辺に配置されている。   The tip mounting member 70 has four engagement ports 72 for engaging the screws 42 and a through port 73 through which the endoscope treatment tool 200 (flexible tube portion 210) can pass. The engagement port 72 and the through-hole 73 penetrate the tip mounting member 70 in the longitudinal axis direction of the regulating member 60. The through-hole 73 is disposed in the approximate center of the tip mounting member 70, and the engagement port 72 is disposed around the through-hole 73.

図8Aと図8Bに示すように本変形例における端面65aは、規制部材60の中端61cに配置されている。端面65aの先端側には、Oリング64が配置されている。   As shown in FIGS. 8A and 8B, the end surface 65 a in this modification is disposed at the middle end 61 c of the regulating member 60. An O-ring 64 is disposed on the distal end side of the end surface 65a.

図8Bに示すように規制部材60の先端61aの内側には、空間部68と連通し、空間部68と同様に内視鏡用処置具200(可撓管部210)が挿通可能な空間部68aが形成されている。先端取付部材70が取り付けられる先端面69には、先端面69の略中央に配置され、空間部68aに連通し、内視鏡用処置具200(可撓管部210)が貫通可能な貫通口69aと、貫通口69aの周辺に配置され、先端取付部材70を先端面69に取り付けるビス42が係合するための4つの係合口69bとが配設されている。貫通口69aの直径D6は、挿入口40の外径D7と略同一であり、規制部材60の長手軸方向に対して略直交する方向における空間部68aの長さである。   As shown in FIG. 8B, the space portion 68 is communicated with the space portion 68 on the inner side of the distal end 61 a of the restricting member 60, and the endoscope treatment tool 200 (flexible tube portion 210) can be inserted in the same manner as the space portion 68. 68a is formed. The distal end surface 69 to which the distal end mounting member 70 is attached is disposed at substantially the center of the distal end surface 69, communicates with the space 68a, and allows the endoscope treatment tool 200 (flexible tube portion 210) to pass therethrough. 69a and four engagement ports 69b that are disposed around the through-hole 69a and for engaging the screw 42 that attaches the distal end mounting member 70 to the distal end surface 69 are disposed. The diameter D6 of the through hole 69a is substantially the same as the outer diameter D7 of the insertion port 40, and is the length of the space portion 68a in a direction substantially orthogonal to the longitudinal axis direction of the regulating member 60.

貫通口69aは、貫通口73に対向し、貫通口73と同じ大きさである。係合口69bは、係合口72に対向する。   The through-hole 69 a faces the through-hole 73 and has the same size as the through-hole 73. The engagement port 69 b faces the engagement port 72.

次に本変形例の規制部材60を挿入口40に着脱自在に取り付ける止め金具90について図8D乃至図8Fを参照して説明する。止め金具90は、規制部材60の長手軸方向に対して直交する方向において溝部71cをスライドすることで規制部材60を挿入口40に着脱自在に取り付ける。止め金具90の幅の長さL4は、図8Cに示す溝部71c幅の長さL5よりも短い。なお長さL4は、長さL5と略同一であることが好適である。   Next, a stopper 90 for detachably attaching the regulating member 60 of this modification to the insertion port 40 will be described with reference to FIGS. 8D to 8F. The stopper 90 is detachably attached to the insertion port 40 by sliding the groove 71 c in a direction orthogonal to the longitudinal axis direction of the restriction member 60. The width L4 of the stopper 90 is shorter than the length L5 of the groove 71c shown in FIG. 8C. The length L4 is preferably substantially the same as the length L5.

止め金具90は、挿入口40の外径を貫通可能な貫通口90aと、貫通口90aを貫通した止め金具90が規制部材60の長手軸方向に対して直交する方向にスライドすることで、挿入口40における円筒部41と係合する係合口90bとを有している。   The stopper 90 is inserted by sliding the through hole 90a that can penetrate the outer diameter of the insertion hole 40 and the stopper 90 that penetrates the through hole 90a in a direction perpendicular to the longitudinal axis direction of the regulating member 60. It has an engagement port 90 b that engages with the cylindrical portion 41 in the port 40.

貫通口90aの直径D8は、挿入口40の外径D7よりも大きい。また係合口90bの直径D9は、挿入口40の外径D7よりも小さく、円筒部41の外径D10と略同一である。   The diameter D8 of the through-hole 90a is larger than the outer diameter D7 of the insertion port 40. The diameter D9 of the engagement port 90b is smaller than the outer diameter D7 of the insertion port 40 and is substantially the same as the outer diameter D10 of the cylindrical portion 41.

貫通口90aは、規制部材60を挿入口40から着脱自在に取り付ける際に用いられる。また係合口90bは、貫通口90aと連通し、規制部材60を挿入口40に取り付ける際に用いられる。つまり止め金具90とOリング64とは、規制部材60が挿入口40に着脱自在に取り付けられるための取り付け部である。図8Aと図8Fに示すように止め金具90は、貫通口90aの周辺部90cにおいて、係合口90bから貫通口90aに向かって先細なテーパ形状を有している。   The through-hole 90a is used when the regulating member 60 is detachably attached from the insertion port 40. The engagement port 90 b communicates with the through-hole 90 a and is used when the restricting member 60 is attached to the insertion port 40. That is, the stopper 90 and the O-ring 64 are attachment portions for attaching the regulating member 60 to the insertion port 40 in a detachable manner. As shown in FIGS. 8A and 8F, the fastener 90 has a tapered shape that tapers from the engagement port 90b toward the through port 90a in the peripheral portion 90c of the through port 90a.

次に本変形例における規制部材60の取り付け方法について図9Aと図9Bを参照して説明する。
止め金具90が溝部71cに配置された状態において、脚部71aと脚部71bとが先端面69に当接される。次にビス42が係合口72と係合口69bとに係合されると、図9Aに示すように先端取付部材70は先端面69に取り付けられる。このとき、貫通口90aは貫通口73と貫通口69aに対向している。
Next, a method for attaching the regulating member 60 in this modification will be described with reference to FIGS. 9A and 9B.
In a state where the stopper 90 is disposed in the groove portion 71c, the leg portion 71a and the leg portion 71b are brought into contact with the distal end surface 69. Next, when the screw 42 is engaged with the engagement port 72 and the engagement port 69b, the tip attachment member 70 is attached to the tip surface 69 as shown in FIG. 9A. At this time, the through hole 90a faces the through hole 73 and the through hole 69a.

貫通口73が挿入口40に向かって移動すると、挿入口40は空間部68aに配置されOリング64に当接し、円筒部41は貫通口73に配置される。貫通口69aの直径D6(空間部68aの長さ)と挿入口40の外径D7は、略同一であるため、規制部材60は挿入口40に対して規制部材60の長手軸方向に対して略直交する方向にずれることが防止される。   When the through port 73 moves toward the insertion port 40, the insertion port 40 is disposed in the space portion 68 a and abuts on the O-ring 64, and the cylindrical portion 41 is disposed in the through port 73. Since the diameter D6 of the through hole 69a (the length of the space 68a) and the outer diameter D7 of the insertion port 40 are substantially the same, the restricting member 60 is relative to the insertion port 40 in the longitudinal axis direction of the restricting member 60. It is possible to prevent a shift in a substantially orthogonal direction.

図9Bに示すように止め金具90が規制部材60の長手軸方向に対して直交する方向において溝部71cをスライドすることで、円筒部41は係合口90bと係合する。なお周辺部90cがテーパ形状であるために、止め金具90は滑らかにスライドする。またその際、周辺部90cは挿入口40をOリング64に向かって押圧することとなる。   As shown in FIG. 9B, when the stopper 90 slides in the groove 71c in a direction perpendicular to the longitudinal axis direction of the regulating member 60, the cylindrical portion 41 engages with the engagement port 90b. In addition, since the peripheral part 90c is a taper shape, the fastener 90 slides smoothly. At that time, the peripheral portion 90 c presses the insertion port 40 toward the O-ring 64.

これにより規制部材60は、止め金具90によって挿入口40にがたつくことなく取り付けられる。   Thereby, the restricting member 60 is attached to the insertion port 40 by the stopper 90 without rattling.

なお本変形例において止め金具90は、図9Cに示すようにOリング64の弾性力によって止め金具90がスライドし係合口90bが円筒部41から抜けることを防止する爪部91を有していてもよい。   In this modification, the stopper 90 has a claw portion 91 that prevents the stopper 90 from sliding due to the elastic force of the O-ring 64 and the engagement port 90b from coming off the cylindrical portion 41 as shown in FIG. 9C. Also good.

本変形例において当て付き部80が規制部材60の外部から空間部68に移動する状態を図10A乃至図10Cに示すが、このときの動作方法は、上述した図5A乃至図5Cと略同様であるため、詳細な説明は省略する。また当て付き部80が端面65a,66aに当て付く状態も、上述した図5D乃至図5Eと略同様であるため、詳細な説明は省略する。   FIG. 10A to FIG. 10C show a state in which the abutting portion 80 moves from the outside of the regulating member 60 to the space portion 68 in this modified example, but the operation method at this time is substantially the same as that of FIG. 5A to FIG. 5C described above. Therefore, detailed description is omitted. Further, the state in which the abutting portion 80 abuts against the end faces 65a and 66a is substantially the same as that in FIGS. 5D to 5E described above, and thus detailed description thereof is omitted.

これにより本変形例は、テーパ形状によって当て付き部80を規制部材60の外部から空間部68に容易に挿入させることができ、規制部材60を介して処置具チャンネル39に挿入部202を容易に挿入することができる。なお本変形例において、当て付き部80と開口部66bとの一方のみがテーパ形状を有してもよい。
また本変形例は、止め金具90を規制部材60の長手軸方向に対して直交する方向にスライドさせることで、規制部材60を挿入口40に着脱自在に容易に取り付けることができる。また周辺部90cは挿入口40をOリング64に向かって押圧するため、本変形例は、規制部材60を止め金具90によって挿入口40にがたつくことなく取り付けることができる。
Accordingly, in the present modification, the contact portion 80 can be easily inserted into the space portion 68 from the outside of the restriction member 60 due to the tapered shape, and the insertion portion 202 can be easily inserted into the treatment instrument channel 39 via the restriction member 60. Can be inserted. In this modification, only one of the contact part 80 and the opening 66b may have a tapered shape.
Further, in this modification, the regulating member 60 can be easily attached to the insertion port 40 in a detachable manner by sliding the stopper 90 in a direction orthogonal to the longitudinal axis direction of the regulating member 60. Further, since the peripheral portion 90c presses the insertion port 40 toward the O-ring 64, in this modification, the restricting member 60 can be attached to the insertion port 40 by the stopper 90 without rattling.

次に本実施形態における第2の変形例について図11を参照して説明する。
本変形例において、図11に示すように当て付き部80の周縁部にはおねじであるネジ溝80aが形成され、開口部66bの周縁部にはめねじであるネジ溝66dが形成されている。
また規制部材60は、爪部63とOリング64ではなく、取り付け機構94によって挿入口40に着脱自在に取り付けられる。取り付け機構94は、例えば、脚部62の内周面に形成されるめねじであるネジ溝62aと、挿入口40の周縁部に形成されるおねじであるネジ溝40aとを有している。
Next, a second modification of the present embodiment will be described with reference to FIG.
In the present modification, as shown in FIG. 11, a thread groove 80a that is a male screw is formed on the peripheral edge of the abutting portion 80, and a screw groove 66d that is a female thread is formed on the peripheral edge of the opening 66b.
The restricting member 60 is detachably attached to the insertion port 40 by the attachment mechanism 94 instead of the claw portion 63 and the O-ring 64. The attachment mechanism 94 includes, for example, a screw groove 62 a that is a female screw formed on the inner peripheral surface of the leg portion 62, and a screw groove 40 a that is a male screw formed on the peripheral edge portion of the insertion port 40. .

これにより本変形例は、当て付き部80を開口部66bにねじ込むことで、開口部66bに対して当て付き部80を容易に通過させることができ、規制部材60に対して可撓管部210を容易に挿入または抜去することができる。また本変形例は、ねじ込むことで、開口部66bに対して当て付き部80を容易に通過させることができるため、上述した第2の力量を用いることなく、第1の力量のみで規制部材60に対して内視鏡用処置具200を容易に挿入または抜去することができる。   Thus, in this modification, the abutting portion 80 can be easily passed through the opening 66b by screwing the abutting portion 80 into the opening 66b, and the flexible tube portion 210 can be passed through the restricting member 60. Can be easily inserted or removed. Further, in the present modified example, since the abutting portion 80 can be easily passed through the opening 66b by screwing, the regulating member 60 can be achieved only by the first force amount without using the second force amount described above. On the other hand, the endoscope treatment tool 200 can be easily inserted or removed.

また本変形例は、脚部62を介して規制部材60を挿入口40にねじ込むことで、より強固に挿入口40に対して規制部材60を着脱自在に取り付けることができる。   Further, in this modification, the regulating member 60 can be detachably attached to the insertion port 40 by screwing the regulating member 60 into the insertion port 40 via the leg portion 62.

また当て付き部80と規制部材60とは、ネジ溝62a,66d,80aのために、硬質な金属等によって形成されていてもよい。   The contact portion 80 and the regulating member 60 may be formed of a hard metal or the like for the screw grooves 62a, 66d, and 80a.

次に本実施形態における第3の変形例について図12A乃至図12Dを参照して説明する。
本変形例において、当て付き部80は、図12Aに示すように周方向に例えば2つに分割可能である。当て付き部80は、分割したのち再び係合するための係合部82と、溝81に嵌るための突起部83と、を有している。なお分割する数は、限定されない。
Next, a third modification of the present embodiment will be described with reference to FIGS. 12A to 12D.
In this modification, the contact part 80 can be divided into, for example, two in the circumferential direction as shown in FIG. 12A. The abutting portion 80 has an engaging portion 82 for re-engaging after the division, and a protrusion 83 for fitting into the groove 81. The number to be divided is not limited.

また可撓管部210には、図12Bに示すように複数の溝81が形成されている。本変形例の当て付き部80は、図12B乃至図12Dに示すように可撓管部210の長手軸方向に沿って、移動可能であり、一方の溝81から他方の溝81へと配置変換可能である。
これにより本変形例は、溝81によって、処置具チャンネル39内における先端部212の初期位置を多段に調整可能である。
The flexible tube portion 210 has a plurality of grooves 81 as shown in FIG. 12B. The abutting portion 80 of the present modification is movable along the longitudinal axis direction of the flexible tube portion 210 as shown in FIGS. 12B to 12D, and is changed in arrangement from one groove 81 to the other groove 81. Is possible.
Accordingly, in the present modification, the initial position of the distal end portion 212 in the treatment instrument channel 39 can be adjusted in multiple stages by the groove 81.

次に本実施形態における第4の変形例について図13A乃至図13Dを参照して説明する。
本変形例において当て付き部80は、切り欠き部85を有する略C形状の弾性体である弾性リングであってもよい。当て付き部80は、切り欠き部85を介して可撓管部210に着脱自在に嵌め込まれる。これにより本変形例は、可撓管部210に対して当て付き部80を着脱自在とすることで、当て付き部80を再利用することができる。
Next, a fourth modification of the present embodiment will be described with reference to FIGS. 13A to 13D.
In this modification, the abutting portion 80 may be an elastic ring that is a substantially C-shaped elastic body having a notch 85. The abutting portion 80 is detachably fitted into the flexible tube portion 210 via the notch portion 85. Thus, in the present modification, the abutting portion 80 can be reused by making the abutting portion 80 detachable with respect to the flexible tube portion 210.

なお上述した一実施形態と各変形例において、挿入口40に取り付けられた規制部材60には、図14Aに示すように内視鏡用処置具200を内視鏡2の外部である駆動制御部203から挿入口40を介して処置具チャンネル39までガイドするガイドチューブ(ガイドパイプ)100が着脱自在に取り付けられていてもよい。このときガイドチューブ100は、端面66aに着脱自在に取り付けられればよい。   In the above-described embodiment and each modified example, the restriction member 60 attached to the insertion port 40 includes a drive control unit that is provided with an endoscope treatment tool 200 outside the endoscope 2 as illustrated in FIG. 14A. A guide tube (guide pipe) 100 for guiding from 203 to the treatment instrument channel 39 via the insertion port 40 may be detachably attached. At this time, the guide tube 100 may be detachably attached to the end surface 66a.

次に本実施形態における第5の変形例について図15を参照して説明する。
上述した一実施形態と各変形例において、内視鏡用処置具200(挿入部202)を体内へとガイドする体内ガイド部材となるオーバーチューブ101が用いられても良い。
オーバーチューブ101は、内視鏡用処置具200を挿通可能な処置具チャンネル103と、内視鏡2を挿通可能な内視鏡チャンネル104とを備えている。
Next, a fifth modification of the present embodiment will be described with reference to FIG.
In the above-described embodiment and modifications, the overtube 101 serving as an in-vivo guide member that guides the endoscope treatment tool 200 (insertion unit 202) into the body may be used.
The overtube 101 includes a treatment instrument channel 103 through which the endoscope treatment instrument 200 can be inserted, and an endoscope channel 104 through which the endoscope 2 can be inserted.

処置具チャンネル103には、先端であり内視鏡用処置具200が突出するための突出口である先端開口部103aと、基端である内視鏡用処置具200が処置具チャンネル103に挿入するための挿入口103bとが配設されている。先端開口部103aは、処置具チャンネル103を通じて挿入口103bに連通している。挿入口103bと処置具チャンネル103と先端開口部103aとには、内視鏡用処置具200が挿通する。   In the treatment instrument channel 103, a distal end opening portion 103 a that is a distal end and a projecting opening from which the endoscope treatment instrument 200 projects and an endoscope treatment instrument 200 that is a proximal end are inserted into the treatment instrument channel 103. An insertion port 103b is provided. The distal end opening 103 a communicates with the insertion port 103 b through the treatment instrument channel 103. The endoscope treatment tool 200 is inserted through the insertion port 103b, the treatment tool channel 103, and the distal end opening 103a.

挿入口103bは挿入口40と同様である。そのため挿入口103bには、上述した一実施形態と各変形例と同様に規制部材60が着脱自在に取り付けられる。また処置具チャンネル103は処置具チャンネル39と同様であり、先端開口部103aは先端開口部39aと同様である。
すなわちオーバーチューブ101の構造および作用は、内視鏡2を挿通可能な内視鏡チャンネル104が備えられている点を除き、処置具チャンネル39を備えた内視鏡2の構造および作用と実質的に同一である。
The insertion port 103b is the same as the insertion port 40. Therefore, the restricting member 60 is detachably attached to the insertion port 103b in the same manner as in the above-described embodiment and modifications. The treatment instrument channel 103 is the same as the treatment instrument channel 39, and the distal end opening 103a is similar to the distal opening 39a.
That is, the structure and operation of the overtube 101 are substantially the same as the structure and operation of the endoscope 2 provided with the treatment instrument channel 39 except that the endoscope channel 104 through which the endoscope 2 can be inserted is provided. Are identical.

また内視鏡チャンネル104には、先端であり内視鏡2が突出するための突出口である先端開口部104aと、基端である内視鏡2が内視鏡チャンネル104に挿入するための挿入口104bとが配設されている。先端開口部104aは、内視鏡チャンネル104を通じて挿入口104bに連通している。挿入口104bと内視鏡チャンネル104と先端開口部104aとには、内視鏡2が挿通する。   The endoscope channel 104 has a distal end opening 104 a that is a distal end and a projecting opening from which the endoscope 2 projects, and an endoscope 2 that is a proximal end for insertion into the endoscope channel 104. An insertion port 104b is provided. The distal end opening 104 a communicates with the insertion port 104 b through the endoscope channel 104. The endoscope 2 is inserted through the insertion port 104b, the endoscope channel 104, and the distal end opening 104a.

また図16は、第5の変形例と構成の軌を一にした外付けチャンネル105の斜視図である。外付けチャンネル105は、第5の実施例と同様に、上述した一実施形態と各変形例において内視鏡用処置具200(挿入部202)を体内へとガイドする体内ガイド部材である。外付けチャンネル105は、内視鏡用処置具200(挿入部202)を挿入可能な処置具チャンネル(図示しない)を有しており、内視鏡2に取り付けて使用する。処置具チャンネルの図示しない挿入口に規制部材60が着脱自在に取り付けられる点は、第5の変形例と同様である。   FIG. 16 is a perspective view of the external channel 105 having the same configuration as that of the fifth modification. As in the fifth example, the external channel 105 is an in-vivo guide member that guides the endoscope treatment tool 200 (insertion unit 202) into the body in the above-described embodiment and modifications. The external channel 105 has a treatment instrument channel (not shown) into which the endoscope treatment instrument 200 (insertion section 202) can be inserted, and is used by being attached to the endoscope 2. The point that the restricting member 60 is detachably attached to the insertion port (not shown) of the treatment instrument channel is the same as in the fifth modification.

(付記)
前記の具体的実施形態から、以下のような構成の発明を抽出することができる。
(Appendix)
The invention having the following configuration can be extracted from the specific embodiment.

(1) 体内に挿入される内視鏡用処置具が、前記内視鏡用処置具を前記体内へとガイドする体内ガイド部材に配設される挿入口と前記挿入口に連通する処置具チャンネルとを挿通することで前記体内ガイド部材によって前記体内にガイドされ、ガイドされた前記内視鏡用処置具の先端が前記処置具チャンネルの先端に対して進退移動する際に、前記処置具チャンネルの先端に対する前記内視鏡用処置具の先端の進退量を規制する医療用進退量規制機構であって、
前記挿入口に着脱自在に取り付けられ、前記内視鏡用処置具が前記処置具チャンネルに向かって挿通可能で、前記内視鏡用処置具が前記処置具チャンネル内を進退移動する際に前記内視鏡用処置具の進退移動を規制する先端側端面と基端側端面とを有する規制部材と、
前記内視鏡用処置具に配設され、前記内視鏡用処置具が前記規制部材を挿通し前記規制部材に対して進退移動する際に前記先端側端面と前記基端側端面とのいずれか一方に当て付き、前記先端側端面に当て付くことで前記処置具チャンネルの先端から突出する前記内視鏡用処置具の先端の突出量を規制し、前記基端側端面に当て付くことで前記内視鏡用処置具の先端の後退量を規制し前記処置具チャンネル内における前記内視鏡用処置具の先端の初期位置を設定する当て付き部と、
を具備することを特徴とする医療用進退量規制機構。
(1) An endoscope treatment tool inserted into a body has an insertion port disposed in an in-vivo guide member that guides the endoscope treatment tool into the body, and a treatment tool channel communicating with the insertion port. When the distal end of the guided endoscopic treatment instrument advances and retreats with respect to the distal end of the treatment instrument channel, the guide of the treatment instrument channel is guided. A medical advance / retreat amount regulating mechanism for regulating the advance / retreat amount of the distal end of the endoscope treatment tool with respect to the distal end,
The endoscope treatment tool is detachably attached to the insertion port, the endoscope treatment tool can be inserted toward the treatment tool channel, and the endoscope treatment tool moves forward and backward in the treatment tool channel. A restricting member having a distal end side end surface and a proximal end side end surface for restricting advance / retreat movement of the treatment instrument for endoscope;
Any one of the distal end side end surface and the proximal end side end surface is disposed in the endoscope treatment tool and the endoscope treatment tool is inserted into the restriction member and moves forward and backward with respect to the restriction member. The amount of protrusion of the endoscope treatment instrument protruding from the distal end of the treatment instrument channel is regulated by being applied to either one of them and the end face on the distal end side, and applied to the proximal end face. A contact portion for regulating a retreat amount of the distal end of the endoscope treatment instrument and setting an initial position of the distal end of the endoscope treatment instrument in the treatment instrument channel;
A medical advance / retreat amount regulating mechanism comprising:

(実施形態との対応)
この(1)に記載の医療用進退量規制機構に関する実施形態は、例えば一実施形態と第1乃至第5の変形例が対応する。例えば一実施形態と各変形例において、内視鏡用処置具200が上記内視鏡用処置具に、内視鏡2とオーバーチューブ101とが上記体内ガイド部材にそれぞれ対応する。
(Correspondence with embodiment)
The embodiment relating to the medical advance / retreat amount regulating mechanism described in (1) corresponds to, for example, one embodiment and first to fifth modifications. For example, in one embodiment and each modification, the endoscope treatment tool 200 corresponds to the endoscope treatment tool, and the endoscope 2 and the overtube 101 correspond to the in-vivo guide member.

(作用効果)
この(1)に記載の医療用進退量規制機構によれば、例えば処置具チャンネルに対する内視鏡用処置具の進退量を規制して、処置具チャンネルの先端から突出する内視鏡用処置具の先端の突出量を容易に規制でき、処置具チャンネル内における内視鏡用処置具の先端の初期位置を容易に設定することができる。
(Function and effect)
According to the medical advance / retreat amount regulating mechanism described in (1), for example, an endoscopic treatment tool that regulates the advance / retreat amount of the endoscope treatment tool with respect to the treatment tool channel and projects from the distal end of the treatment tool channel. The projection amount of the distal end of the endoscope can be easily regulated, and the initial position of the distal end of the endoscope treatment instrument in the treatment instrument channel can be easily set.

(2) 前記当て付き部は、前記先端側端面に当て付くことで、前記体内ガイド部材が湾曲状態または非湾曲状態であっても、前記内視鏡用処置具の先端に対する前記処置具チャンネルの先端の前記突出量を規制し、前記内視鏡用処置具の先端から前記処置具チャンネルの先端を所望な量だけ突出させることを特徴とする(1)に記載の医療用進退量規制機構。   (2) The abutting part is abutted against the end surface on the distal end side, so that even if the in-vivo guide member is in a curved state or a non-curved state, The medical advance / retreat amount regulating mechanism according to (1), wherein the projection amount of the distal end is regulated, and the distal end of the treatment instrument channel is projected by a desired amount from the distal end of the endoscope treatment instrument.

(作用効果)
この(2)に記載の医療用進退量規制機構によれば、例えば当て付き部を先端側端面に当て付けることで、体内ガイド部材が湾曲状態または非湾曲状態であっても、内視鏡用処置具の先端が処置具チャンネルから術者の意図に反して必要以上に突出することを防止することができる。
(Function and effect)
According to the medical advance / retreat amount regulating mechanism described in (2), even if the in-vivo guide member is in a curved state or a non-curved state, for example, by applying the abutting portion to the distal end side surface, It can prevent that the front-end | tip of a treatment tool protrudes from a treatment tool channel more than necessary contrary to an operator's intention.

(3) 前記当て付き部は、前記基端側端面に当て付くことで、前記体内ガイド部材が湾曲状態または非湾曲状態であっても、前記内視鏡用処置具の先端が前記処置具チャンネルの先端から所望の距離だけ基端側に配置され、前記処置具チャンネル内に収納される位置である前記初期位置を設定する(1)に記載の医療用進退量規制機構。   (3) The tip of the endoscopic treatment instrument is positioned in the treatment instrument channel even when the in-vivo guide member is in a curved state or a non-curved state by abutting the abutting portion on the proximal end surface. The medical advance / retreat amount regulating mechanism according to (1), wherein the initial position, which is a position that is disposed on the proximal end side by a desired distance from the distal end of the needle and is stored in the treatment instrument channel, is set.

(作用効果)
この(3)に記載の医療用進退量規制機構によれば、例えば当て付き部を基端側端面に当て付けることで、体内ガイド部材が湾曲状態または非湾曲状態であっても、内視鏡用処置具の先端が処置具チャンネルに確実に収納でき、収納された内視鏡用処置具の先端が術者の意図に反して処置具チャンネルの内周面に接触し破損してしまうことを防止することができる。
(Function and effect)
According to the medical advance / retreat amount regulating mechanism described in (3), even when the in-vivo guide member is in a curved state or a non-curved state, for example, by applying the contact portion to the proximal end surface, the endoscope The distal end of the treatment instrument can be securely stored in the treatment instrument channel, and the distal end of the stored endoscope treatment instrument contacts the inner peripheral surface of the treatment instrument channel against the operator's intention and is damaged. Can be prevented.

(4) 前記当て付き部が進退移動可能な前記先端側端面から前記基端側端面までの長さは、前記内視鏡用処置具に配設され湾曲可能な湾曲部から前記内視鏡用処置具の先端までの長さよりも長いことを特徴とする(1)に記載の医療用進退量規制機構。   (4) The length from the distal end surface to the proximal end surface where the abutting portion is movable back and forth is from the curved portion that is disposed on the endoscope treatment tool and can be bent. The medical advance / retreat amount regulating mechanism according to (1), characterized in that it is longer than the length to the distal end of the treatment instrument.

(実施形態との対応)
例えば一実施形態において、端面65aから端面66aまでの長さL2が上記前記先端側端面から前記基端側端面までの長さに、湾曲部211(節輪224)と湾曲部12が上記湾曲部に、節輪224から先端部212までの長さL3が上記湾曲部から前記内視鏡用処置具の先端までの長さに、それぞれ対応する。
(Correspondence with embodiment)
For example, in one embodiment, the length L2 from the end surface 65a to the end surface 66a is the length from the distal end side end surface to the base end side end surface, and the bending portion 211 (node ring 224) and the bending portion 12 are the bending portion. Further, the length L3 from the node ring 224 to the distal end portion 212 corresponds to the length from the curved portion to the distal end of the endoscope treatment tool.

(作用効果)
この(4)に記載の医療用進退量規制機構によれば、例えば湾曲部を処置具チャンネルの先端から確実に突出させることができ、内視鏡用処置具の先端を処置具チャンネル内に確実に収納することができる。
(Function and effect)
According to the medical advance / retreat amount regulating mechanism described in (4), for example, the bending portion can be reliably protruded from the distal end of the treatment instrument channel, and the distal end of the endoscope treatment instrument can be reliably inserted into the treatment instrument channel. Can be stored.

(5) 体内に挿入される内視鏡用処置具が、前記内視鏡用処置具を前記体内へとガイドする体内ガイド部材に配設される挿入口と前記挿入口に連通する処置具チャンネルとを挿通することで前記体内ガイド部材によって前記体内にガイドされ、ガイドされた前記内視鏡用処置具の先端が前記チャンネルの先端に対して進退移動する際に、前記処置具チャンネルの先端に対する前記内視鏡用処置具の先端の進退量を規制する医療用進退量規制方法であって、
前記内視鏡用処置具が前記処置具チャンネルに向かって挿通可能で、前記内視鏡用処置具が前記処置具チャンネル内を進退移動する際に前記内視鏡用処置具の進退移動を規制する先端側端面と基端側端面とを有する規制部材を前記挿入口に着脱自在に取り付ける第1の工程と、
前記内視鏡用処置具を前記規制部材と前記挿入口を介して前記処置具チャンネルに挿通させる第2の工程と、
前記内視鏡用処置具に配設され、前記内視鏡用処置具が前記規制部材を挿通し前記規制部材に対して進退移動する際に前記先端側端面と前記基端側端面とのいずれか一方に当て付く当て付き部を前記先端側端面に当て付けて前記処置具チャンネルの先端から突出する前記内視鏡用処置具の先端の突出量を規制する第3の工程と、
前記当て付き部を前記基端側端面に当て付けて前記内視鏡用処置具の先端の後退量を規制し前記処置具チャンネル内における前記内視鏡用処置具の先端の初期位置を設定する第4の工程と、
を具備することを特徴とする医療用進退量規制方法。
(5) An endoscope treatment tool inserted into the body has an insertion port disposed in an in-vivo guide member for guiding the endoscope treatment tool into the body, and a treatment tool channel communicating with the insertion port. Is inserted into the body by the in-vivo guide member, and the guided distal end of the endoscope treatment tool moves forward and backward relative to the distal end of the channel. A medical advance / retreat amount regulating method for regulating the advance / retreat amount of the distal end of the endoscope treatment tool,
The endoscope treatment tool can be inserted toward the treatment tool channel, and the endoscope treatment tool is restricted from moving forward and backward when the endoscope treatment tool moves back and forth in the treatment tool channel. A first step of detachably attaching a regulating member having a distal end side end surface and a proximal end side end surface to the insertion port;
A second step of inserting the endoscope treatment instrument into the treatment instrument channel via the restriction member and the insertion port;
Any one of the distal end side end surface and the proximal end side end surface is disposed in the endoscope treatment tool and the endoscope treatment tool is inserted into the restriction member and moves forward and backward with respect to the restriction member. A third step of restricting the protruding amount of the distal end of the treatment instrument for an endoscope projecting from the distal end of the treatment instrument channel by applying an abutting portion to be applied to either one of the distal end side surfaces;
The abutting portion is applied to the proximal end surface to regulate the retreat amount of the distal end of the endoscope treatment instrument, and the initial position of the distal end of the endoscope treatment instrument in the treatment instrument channel is set. A fourth step;
A medical advance / retreat amount regulating method characterized by comprising:

(実施形態との対応)
この(5)に記載の医療用進退量規制方法に関する実施形態は、例えば一実施形態と第1乃至第5の変形例が対応する。(5)に記載の医療用進退量規制方法における各構成部材は、上述した(1)に記載の医療用進退量規制機構の構成部材と略同様である。
また例えば一実施形態と各変形例において、図5Aに示す状態が上記第1の工程に、図5Aと図5Bと図5Cに示す状態が上記第2の工程に、図5Dに示す状態が上記第3の工程に、図5Eに示す状態が上記第4の工程に、それぞれ対応する。
(Correspondence with embodiment)
In the embodiment relating to the medical advance / retreat amount regulating method described in (5), for example, one embodiment corresponds to the first to fifth modifications. Each component in the medical advance / retreat amount regulating method described in (5) is substantially the same as the component of the medical advance / retreat amount regulating mechanism described in (1).
For example, in one embodiment and each modification, the state shown in FIG. 5A is the first step, the states shown in FIGS. 5A, 5B, and 5C are the second step, and the state shown in FIG. The state shown in FIG. 5E corresponds to the third step and corresponds to the fourth step.

このように本発明は、上記実施形態と変形例そのままに限定されるものではなく、実施段階ではその要旨を逸脱しない範囲で構成要素を変形して具体化できる。また、上記実施形態に開示されている複数の構成要素の適宜な組み合せにより種々の発明を形成できる。   As described above, the present invention is not limited to the above-described embodiments and modifications as they are, and can be embodied by modifying the components without departing from the scope of the invention in the implementation stage. Further, various inventions can be formed by appropriately combining a plurality of constituent elements disclosed in the embodiment.

図1は、本発明の一実施形態に係る内視鏡システムを概略的に示す図である。FIG. 1 is a diagram schematically showing an endoscope system according to an embodiment of the present invention. 図2は、湾曲部の湾曲状態を示す図である。FIG. 2 is a diagram illustrating a bending state of the bending portion. 図3は、内視鏡用処置具を概略的に示す斜視図である。FIG. 3 is a perspective view schematically showing the endoscope treatment tool. 図4Aは、規制部材が挿入口に取り付けられ、内視鏡用処置具が規制部材と挿入口と処置具チャンネルとを挿通し、当て付き部が空間に配置されている状態を示す断面図である。FIG. 4A is a cross-sectional view showing a state in which the restriction member is attached to the insertion port, the endoscope treatment tool is inserted through the restriction member, the insertion port, and the treatment tool channel, and the contact portion is disposed in the space. is there. 図4Bは、規制部材の斜視図である。FIG. 4B is a perspective view of the regulating member. 図4Cは、可撓管部の側面図である。FIG. 4C is a side view of the flexible tube portion. 図5Aは、当て付き部が規制部材の外部から空間に移動する状態を示す図である。FIG. 5A is a diagram illustrating a state in which the contact portion moves from the outside of the regulating member to the space. 図5Bは、当て付き部が規制部材の外部から空間に移動する状態を示す図である。FIG. 5B is a diagram illustrating a state in which the contact portion moves from the outside of the regulating member to the space. 図5Cは、当て付き部が空間部に配置されている状態を示す図である。FIG. 5C is a diagram illustrating a state in which the contact portion is disposed in the space portion. 図5Dは、当て付き部が先端側端面に面当接している状態を示す図である。FIG. 5D is a diagram illustrating a state in which the abutting portion is in surface contact with the end surface on the front end side. 図5Eは、当て付き部が基端側端面に面当接している状態を示す図である。FIG. 5E is a diagram illustrating a state in which the abutting portion is in surface contact with the proximal end surface. 図6Aは、処置具チャンネルから突出する内視鏡用処置具の先端の突出量について説明している図である。FIG. 6A is a diagram for explaining the protruding amount of the distal end of the endoscope treatment tool protruding from the treatment tool channel. 図6Bは、内視鏡用処置具の先端の初期位置について説明している図である。FIG. 6B is a diagram illustrating an initial position of the distal end of the endoscope treatment tool. 図7は、開口部の周縁に沿って形成される切り欠き部を有する規制部材の斜視図である。FIG. 7 is a perspective view of a regulating member having a notch formed along the periphery of the opening. 図8Aは、第1の変形例における規制部材が挿入口に取り付けられ、内視鏡用処置具が規制部材と挿入口と処置具チャンネルとを挿通し、当て付き部が空間に配置されている状態を示す断面図である。In FIG. 8A, the restriction member in the first modification is attached to the insertion port, the endoscope treatment tool is inserted through the restriction member, the insertion port, and the treatment tool channel, and the contact portion is disposed in the space. It is sectional drawing which shows a state. 図8Bは、第1の変形例における規制部材の断面図である。FIG. 8B is a cross-sectional view of the regulating member in the first modification. 図8Cは、第1の変形例における規制部材の斜視図である。FIG. 8C is a perspective view of a regulating member in the first modified example. 図8Dは、止め金具の斜視図である。FIG. 8D is a perspective view of a fastener. 図8Eは、止め金具の正面図である。FIG. 8E is a front view of the fastener. 図8Fは、止め金具の断面図である。FIG. 8F is a cross-sectional view of the fastener. 図9Aは、第1の変形例において、規制部材が挿入口に取り付けられる状態を示す図である。FIG. 9A is a diagram illustrating a state in which the restriction member is attached to the insertion port in the first modification. 図9Bは、第1の変形例において、規制部材が挿入口に取り付けられる状態を示す図である。FIG. 9B is a diagram illustrating a state in which the restriction member is attached to the insertion port in the first modification. 図9Cは、第1の変形例において、爪部を有する規制部材を示す図である。FIG. 9C is a diagram illustrating a regulating member having a claw portion in the first modification. 図10Aは、第1の変形例において、当て付き部が規制部材の外部から空間に移動する状態を示す図である。FIG. 10A is a diagram illustrating a state in which the contact portion moves from the outside of the regulating member to the space in the first modification. 図10Bは、第1の変形例において、当て付き部が規制部材の外部から空間に移動する状態を示す図である。FIG. 10B is a diagram illustrating a state in which the contact portion moves from the outside of the regulating member to the space in the first modification. 図10Cは、第1の変形例において、当て付き部が空間部に配置されている状態を示す図である。FIG. 10C is a diagram illustrating a state in which the contact portion is disposed in the space portion in the first modification. 図11は、第2の変形例における規制部材が挿入口に取り付けられ、内視鏡用処置具が規制部材と挿入口と処置具チャンネルとを挿通し、当て付き部が空間に配置されている状態を示す断面図である。In FIG. 11, the restriction member in the second modification is attached to the insertion port, the endoscope treatment tool passes through the restriction member, the insertion port, and the treatment tool channel, and the contact portion is disposed in the space. It is sectional drawing which shows a state. 図12Aは、第3の変形例における当て付き部の断面図である。FIG. 12A is a cross-sectional view of a contact portion in a third modification. 図12Bは、第3の変形例において、複数の溝を有する可撓管部と、一方の溝に嵌め込まれた当て付き部との状態を示す図である。FIG. 12B is a diagram illustrating a state of the flexible tube portion having a plurality of grooves and the abutting portion fitted in one groove in the third modification. 図12Cは、第3の変形例において、一方の溝から他方の溝に移動する当て付き部と、可撓管部との状態を示す図である。FIG. 12C is a diagram illustrating a state of the abutting portion moving from one groove to the other groove and the flexible tube portion in the third modification. 図12Dは、第3の変形例において、可撓管部と、他方の溝に嵌め込まれた当て付き部との状態を示す図である。FIG. 12D is a diagram showing a state of the flexible tube portion and the abutting portion fitted in the other groove in the third modified example. 図13Aは、第4の変形例における当て付き部と、当て付き部が嵌め込まれた可撓管部との断面図である。FIG. 13A is a cross-sectional view of an abutting portion and a flexible tube portion into which the abutting portion is fitted in a fourth modification. 図13Bは、第4の変形例における当て付き部と、当て付き部が嵌め込まれた可撓管部との斜視図である。FIG. 13B is a perspective view of the abutting portion and the flexible tube portion into which the abutting portion is fitted in the fourth modified example. 図13Cは、可撓管部から当て付き部を取り外す状態を示す図である。FIG. 13C is a diagram illustrating a state in which the contact portion is removed from the flexible tube portion. 図13Dは、第4の変形例における当て付き部と、当て付き部が取り外された可撓管部とを示す図である。FIG. 13D is a diagram illustrating a contact portion and a flexible tube portion from which the contact portion has been removed in a fourth modified example. 図14は、挿入口に取り付けられた第2の変形例における規制部材にガイドチューブを取り付けた状態を示す断面図である。FIG. 14 is a cross-sectional view showing a state in which the guide tube is attached to the restriction member in the second modified example attached to the insertion port. 図15は、第5の変形例におけるオーバーチューブの斜視図である。FIG. 15 is a perspective view of an overtube in a fifth modification. 図16は、第5の変形例と構成の軌を一にした外付けチャンネルの斜視図である。FIG. 16 is a perspective view of an external channel having the same configuration as that of the fifth modification.

符号の説明Explanation of symbols

2…内視鏡、10…挿入部、11…可撓管部、12…湾曲部、13…先端硬性部、13a…先端面、39…処置具チャンネル、39a…先端開口部、40…挿入口、50…医療用進退量規制機構、60…規制部材、62…脚部、63…爪部、64…Oリング、65a…端面、65b…開口部、66a…端面、66b…開口部、68…空間部、80…当て付き部、100…ガイドチューブ、101…オーバーチューブ、103…処置具チャンネル、103a…先端開口部、103b…挿入口、104…内視鏡チャンネル、105…外付けチャンネル、200…内視鏡用処置具、202…挿入部、210…可撓管部、211…湾曲部、212…先端部、213…把持鉗子、221,222,223,224…節輪。   DESCRIPTION OF SYMBOLS 2 ... Endoscope, 10 ... Insertion part, 11 ... Flexible tube part, 12 ... Bending part, 13 ... Hard tip part, 13a ... Tip surface, 39 ... Treatment instrument channel, 39a ... Tip opening part, 40 ... Insertion opening , 50 ... Medical advance / retreat amount regulating mechanism, 60 ... regulating member, 62 ... leg, 63 ... claw, 64 ... O-ring, 65a ... end face, 65b ... opening, 66a ... end face, 66b ... opening, 68 ... Space part, 80 ... Abutting part, 100 ... Guide tube, 101 ... Over tube, 103 ... Treatment instrument channel, 103a ... Tip opening, 103b ... Insertion port, 104 ... Endoscope channel, 105 ... External channel, 200 DESCRIPTION OF SYMBOLS Endoscopic treatment tool, 202 ... Insertion part, 210 ... Flexible tube part, 211 ... Bending part, 212 ... Tip part, 213 ... Grasping forceps, 221, 222, 223, 224 ... Node ring.

Claims (6)

体内ガイド部材によって体内へとガイドされる内視鏡用処置具が挿通可能な前記体内ガイド部材に配設される処置具チャンネルと連通する挿入口に着脱自在に取り付けられ、前記体内ガイド部材に対する前記内視鏡用処置具の進退移動を規制する医療用進退量規制機構であって、
前記内視鏡用処置具が挿通可能な第1の開口部を有し、前記挿入口に接続される先端側端面と、前記内視鏡用処置具が挿通可能な第2の開口部を有する基端側端面と、を含む規制部材と、
前記内視鏡用処置具に配設され、前記第2の開口部を挿通し、前記先端側端面と前記基端側端面との間を進退移動することで、前記体内ガイド部材に対する前記内視鏡用処置具の進退移動を規制する当て付き部と、
を具備し、
前記当て付き部は、前記基端側端面に当て付くことで、前記体内ガイド部材が湾曲状態または非湾曲状態であっても、前記内視鏡用処置具の先端が前記処置具チャンネルの先端から所望の距離だけ基端側に配置され、前記処置具チャンネル内に収納される位置である初期位置を設定することを特徴とする医療用進退量規制機構。
An endoscope treatment instrument guided into the body by an in-vivo guide member is detachably attached to an insertion port communicating with a treatment instrument channel disposed in the in-vivo guide member through which the endoscope treatment instrument can be inserted. A medical advance / retreat amount regulation mechanism for regulating the advance / retreat movement of the endoscope treatment tool,
The endoscope treatment instrument has a first opening through which the endoscope treatment instrument can be inserted, and has a distal end side end face connected to the insertion port , and a second opening through which the endoscope treatment instrument can be inserted. A restricting member including a proximal end surface;
The endoscope is disposed on the endoscope treatment tool, passes through the second opening, and moves forward and backward between the distal end side end surface and the proximal end side end surface, whereby the endoscopic guide member with respect to the in-vivo guide member is moved. The abutting part that regulates the forward and backward movement of the mirror treatment tool,
Equipped with,
The abutting portion is abutted against the proximal end surface, so that the distal end of the endoscopic treatment instrument is separated from the distal end of the treatment instrument channel even when the in-vivo guide member is in a curved state or a non-curved state. A medical advance / retreat amount regulating mechanism , wherein an initial position, which is a position that is disposed on a proximal end side by a desired distance and is stored in the treatment instrument channel, is set .
前記当て付き部は、前記先端側端面に当て付くことで、前記体内ガイド部材が湾曲状態または非湾曲状態であっても、前記内視鏡用処置具の先端の前記処置具チャンネルの先端に対する前記突出量を規制し、前記内視鏡用処置具の先端を前記処置具チャンネルの先端から所望な量だけ突出させることを特徴とする請求項1に記載の医療用進退量規制機構。   The abutting portion is abutted against the distal end side end surface, so that the distal end of the endoscope treatment instrument with respect to the distal end of the treatment instrument channel even when the in-vivo guide member is in a curved state or a non-curved state. 2. The medical advance / retreat amount regulating mechanism according to claim 1, wherein a projection amount is regulated, and a distal end of the endoscope treatment instrument is projected from a distal end of the treatment instrument channel by a desired amount. 前記当て付き部が進退移動可能な前記先端側端面から前記基端側端面までの長さは、前記内視鏡用処置具に配設され湾曲可能な湾曲部の基端側から前記内視鏡用処置具の先端までの長さよりも長いことを特徴とする請求項1に記載の医療用進退量規制機構。   The length from the distal end side end surface to which the abutting portion is movable back and forth to the proximal end side surface is set on the endoscope from the proximal end side of the bending portion that is disposed on the endoscope treatment tool and can be bent. The medical advance / retreat amount regulating mechanism according to claim 1, wherein the medical advancement / retraction amount regulating mechanism is longer than a length of the treatment instrument. 体内ガイド部材によって体内へとガイドされる内視鏡用処置具が挿通可能な前記体内ガイド部材に配設される処置具チャンネルと連通する挿入口に着脱自在に取り付けられ、前記体内ガイド部材に対する前記内視鏡用処置具の進退移動を規制する医療用進退量規制機構であって、  An endoscope treatment instrument guided into the body by an in-vivo guide member is detachably attached to an insertion port communicating with a treatment instrument channel disposed in the in-vivo guide member through which the endoscope treatment instrument can be inserted. A medical advance / retreat amount regulation mechanism for regulating the advance / retreat movement of the endoscope treatment tool,
前記内視鏡用処置具が挿通可能な第1の開口部を有し、前記挿入口に接続される先端側端面と、前記内視鏡用処置具が挿通可能な第2の開口部を有する基端側端面と、を含む規制部材と、  The endoscope treatment instrument has a first opening through which the endoscope treatment instrument can be inserted, and has a distal end side end face connected to the insertion port, and a second opening through which the endoscope treatment instrument can be inserted. A restricting member including a proximal end surface;
前記内視鏡用処置具に配設され、前記第2の開口部を挿通し、前記先端側端面と前記基端側端面との間を進退移動することで、前記体内ガイド部材に対する前記内視鏡用処置具の進退移動を規制する当て付き部と、  The endoscope is disposed on the endoscope treatment tool, passes through the second opening, and moves forward and backward between the distal end side end surface and the proximal end side end surface, whereby the endoscopic guide member with respect to the in-vivo guide member is moved. The abutting part that regulates the forward and backward movement of the mirror treatment tool,
を具備し、  Comprising
前記当て付き部が進退移動可能な前記先端側端面から前記基端側端面までの長さは、前記内視鏡用処置具に配設され湾曲可能な湾曲部の基端側から前記内視鏡用処置具の先端までの長さよりも長いことを特徴とする医療用進退量規制機構。  The length from the distal end side end surface to which the abutting portion is movable back and forth to the proximal end side surface is set on the endoscope from the proximal end side of the bending portion that is disposed on the endoscope treatment tool and can be bent. A medical advance / retreat amount regulating mechanism characterized by being longer than the length to the distal end of the medical treatment instrument.
前記当て付き部は、前記先端側端面に当て付くことで、前記体内ガイド部材が湾曲状態または非湾曲状態であっても、前記内視鏡用処置具の先端の前記処置具チャンネルの先端に対する前記突出量を規制し、前記内視鏡用処置具の先端を前記処置具チャンネルの先端から所望な量だけ突出させることを特徴とする請求項4に記載の医療用進退量規制機構。  The abutting portion is abutted against the distal end side end surface, so that the distal end of the endoscope treatment instrument with respect to the distal end of the treatment instrument channel even when the in-vivo guide member is in a curved state or a non-curved state. 5. The medical advance / retreat amount regulating mechanism according to claim 4, wherein a projection amount is regulated, and a distal end of the endoscope treatment instrument is projected by a desired amount from a distal end of the treatment instrument channel. 前記当て付き部は、前記基端側端面に当て付くことで、前記体内ガイド部材が湾曲状態または非湾曲状態であっても、前記内視鏡用処置具の先端が前記処置具チャンネルの先端から所望の距離だけ基端側に配置され、前記処置具チャンネル内に収納される位置である初期位置を設定することを特徴とする請求項4に記載の医療用進退量規制機構。  The abutting portion is abutted against the proximal end surface, so that the distal end of the endoscopic treatment instrument is separated from the distal end of the treatment instrument channel even when the in-vivo guide member is in a curved state or a non-curved state. The medical advance / retreat amount regulating mechanism according to claim 4, wherein an initial position, which is a position that is disposed at a proximal end side by a desired distance and is stored in the treatment instrument channel, is set.
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