JP2004298350A - Clamp plug for endoscope - Google Patents

Clamp plug for endoscope Download PDF

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Publication number
JP2004298350A
JP2004298350A JP2003094158A JP2003094158A JP2004298350A JP 2004298350 A JP2004298350 A JP 2004298350A JP 2003094158 A JP2003094158 A JP 2003094158A JP 2003094158 A JP2003094158 A JP 2003094158A JP 2004298350 A JP2004298350 A JP 2004298350A
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Japan
Prior art keywords
passage
slit
treatment instrument
treatment tool
treatment
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JP2003094158A
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JP4395625B2 (en
Inventor
Joji Watanabe
城治 渡邉
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Fujinon Corp
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Fuji Photo Optical Co Ltd
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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
    • A61B1/012Instruments 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 characterised by internal passages or accessories therefor
    • A61B1/018Instruments 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 characterised by internal passages or accessories therefor for receiving instruments
    • 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
    • A61B1/00137End pieces at either end of the endoscope, e.g. caps, seals or forceps plugs

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Surgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biomedical Technology (AREA)
  • Optics & Photonics (AREA)
  • Pathology (AREA)
  • Radiology & Medical Imaging (AREA)
  • Biophysics (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Endoscopes (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To prevent filth, such as a highly pressurized humor injected from a throttling passage having a smaller pore size than a treatment tool inserting passage provided in an endoscope from flowing out from a clamp plug. <P>SOLUTION: Although the filth, such as the humor etc., flowing from the treatment tool inserting passage 11 to the throttling passage 24, is injected with high pressure from the throttling passage 24 when a suction valve is shut off, the entrance of a slit 33 provided in a treatment tool guiding section 32 on the treatment tool inserting passage 11 side is constituted by deviating the position of the entrance from a position on the extended surface of the throttling passage 24 so that the slit 33 may not receive directly the filth, such as the humor etc., injected from the throttling passage 24. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

【0001】
【発明の属する技術分野】
本発明は、医療用等として用いられる内視鏡に設けられ、鉗子その他の処置具を挿通するための処置具挿通チャンネルにおいて、処置具導入口の口金に着脱可能に装着される鉗子栓に関する。
【0002】
【従来の技術】
体腔内に挿入されて、医療検査等を行う内視鏡は、術者等が手で把持して操作を行う本体操作部に体腔内への挿入部を連設し、さらに本体操作部に光源装置等に着脱可能に接続されるユニバーサルコードを連結して設けることにより大略構成されるものである。挿入部の先端部には体腔内を照明するための照明部と、この照明部から照射される照明下で体腔内の検査を行う観察部とを備えている。
【0003】
例えば、内視鏡による検査の結果、患部等が発見されたときには、所要の処置を行うことができ、また組織細胞のサンプリング等も行えるようにしたものもある。このために、内視鏡には鉗子その他の処置具を挿通するための処置具挿通チャンネルが設けられる。処置具挿通チャンネルは、その先端が照明部及び観察部と共に挿入部の先端部に開口している。一方、処置具挿通チャンネルの基端側は、処置具を挿通するための処置具挿通路と体腔内の汚物などを吸引するための吸引通路とに分岐されている。処置具の処置具挿通チャンネルへの導入は、本体操作部側に設けた処置具挿通路を介して行なわれる。このために、本体操作部または本体操作部と挿入部との連結部に処置具導入口が形成される。
【0004】
体腔内の圧力は大気圧より高いため、また処置具挿通チャンネルを吸引通路と兼用することがある等の点で、処置具導入口を常時開口させておくことはできない。このために、処置具導入口に口金を設けて鉗子栓を装着して、この処置具導入口を密閉する構成とするのが一般的である。そして、処置具を使用する場合、鉗子栓を口金から取り外すのではなく、鉗子栓に開閉弁を設けて、処置具を挿入する際には、この開閉弁を開くようにするのが一般的である。しかも、処置具挿通チャンネルの内部は使用の都度洗浄しなければならないこと等から、鉗子栓は処置具導入口の口金に着脱可能に装着される。
【0005】
従来から知られている鉗子栓としては、処置具導入口の口径より小さい孔径を有する絞り通路と、処置具導入口の口径とほぼ同じかまたはそれより長いスリットとを形成し、このスリットは常時においては密着状態となし、もって処置具導入口を密閉状態に保持するように構成したものは従来から知られている(例えば、特許文献1参照。)。そして、処置具を挿通させる際には、スリットを押し広げるようにするが、細い処置具の場合には、スリットの広がりも小さいので、ある程度の密閉性が確保される。また、太い処置具を挿通させる場合には、スリットは大きく広げられるので、このスリットは密閉機能を発揮し得なくなる。ただし、スリットに加えて絞り通路を備えているので、この絞り通路を押し広げるように挿入されることから、太い処置具を使用する場合にも、処置具導入口は実質的に密閉状態に保持される。その結果、処置具を用いて体腔内で処置等を施している間に、体液等の汚物が逆流して、術者の手等に付着する等といった不都合を防止できるようになる。
【0006】
【特許文献1】
実開平2−136603号公報(第8−10頁、第1図)
【0007】
【発明が解決しようとする課題】
ところで、上述したように、処置具挿通チャンネルは吸引通路としても使用される関係から、本体操作部に設けた吸引バルブを操作して、体内からの吸引を行なった後、吸引バルブを遮断すると、処置具挿通チャンネル内はかなり高い圧力状態となり、鉗子栓内面に圧力が作用する。鉗子栓のスリットは絞り通路の延長線上に設けられているので、絞り通路を取った吸引物質は直接スリットに作用する。このように、スリットに圧力が作用すると、スリットが開口状態になり、吸引物質が鉗子栓から流出し、術者の手などに体液などの汚物が付着するといった不都合や、周囲に撒き散らされるといった不都合が起こる恐れがある。特に、スリットを介して鉗子やチューブなどが繰り返し挿脱されると、スリットの密着力が弱くなり、開口状態になりやすい。このように密着力が弱くなったスリットに、上述したような圧力が作用すると、さらに吸引物質が鉗子栓から流出しやすくなる。
【0008】
そこで、本発明の目的は、絞り通路から流出する吸引物質の圧力をスリットが直接受けないように構成することにより、体液などの汚物が鉗子栓より外部に流出しないようにした内視鏡用鉗子栓を提供することにある。
【0009】
【課題を解決するための手段】
本発明は、以上の目的を達成するために、本発明の内視鏡用鉗子栓は、内視鏡に設けられた処置具挿通路に着脱可能に装着され、前記処置具挿通路より小さい孔径となった絞り通路を設けた栓本体部と、処置具が挿脱可能であり、常時においては密着状態となるスリットを設けた開閉弁部とを有し、前記スリットの少なくとも前記処置具挿通路側への連設部は、前記絞り通路の延長線上の位置からずらした位置に設けられている。
【0010】
【発明の実施の形態】
A.本発明の第1実施形態
以下、図面を参照して、本発明の実施の形態について詳細に説明する。まず、図1に内視鏡の全体構成図を示す。図中において、1は本体操作部、2は挿入部、3はユニバーサルコードである。挿入部2は、本体操作部1への連結側から大半の長さ分は体腔内の挿入経路が曲がっている場合に、その曲がり方向に沿って自在に曲がる軟性部2aとなっており、この軟性部2aには、アングル部2b及び先端硬質部2cが順次連結されている。先端硬質部2cには内視鏡観察手段を構成する照明部と観察部(共に図示せず)とが設けられており、アングル部2bは先端硬質部2cを挿入経路に沿ってガイドしたり、かつ先端硬質部2cに設けた内視鏡観察手段の視野を変えたりするために、所望の方向に向けて湾曲操作できるようになっている。このアングル部2cの湾曲操作は本体操作部1に設けたアングル操作手段4によって遠隔操作で行なわれる。
【0011】
内視鏡は前述した内視鏡観察手段によって、体腔内を観察するだけではなく、内視鏡検査の結果発見された患部に対する処置や組織のサンプリング等も行えるようになっている。このために、本体操作部1には処置具導入部5が設けられ、この処置具導入部5から先端硬質部2cまでの部位には処置具挿通チャンネル6が設けられており、この処置具挿通チャンネル6の先端は照明部及び観察部等と共に先端硬質部2cに開口している。従って、鉗子その他の処置具を処置具導入部5から処置具挿通チャンネル6に挿通させて、先端硬質部2cから所定の長さ導出させることによって、所望の処置を施すことができるようになる。
【0012】
処置具挿通チャンネル6は、また、吸引通路としても利用されるものである。従って、図1に示されているように、処置具挿通チャンネルは本体操作部1内で処置具導入部5に至る処置具挿通路11と、本体操作部1からユニバーサルコード3を経て吸引装置に接続される吸引通路12とに分岐している。さらに、本体操作部1には吸引バルブ7が設けられており、この吸引バルブ7を操作することによって、吸引通路12を連通・遮断できるようになっている。
【0013】
そこで、内視鏡検査が行われる体腔内に体液や汚物が存在していると、吸引バルブを操作することによって、それらを処置具挿通チャンネル6から吸引通路12に排出して、体腔内の観察条件を良好にする。この状態で、体腔内の検査を行い、その結果患部等が存在すると、鉗子その他の処置具を処置具導入部5から処置具挿通チャンネル6内に挿入して、適宜の処置が施されることになる。
【0014】
以上のことから、処置具導入部5は、少なくとも吸引作業を行っている間は密閉状態に保持させる必要があり、しかもそのままで処置具を挿入できるようになっていなければならない。さらに、処置具挿通チャンネル6は体液等で汚損されることから、使用後には、処置具挿通チャンネル6の内部を洗浄しなければならない。従って、処置具導入部5には鉗子栓10が着脱可能に装着されるようになっており、この鉗子栓10は常時には密閉状態に保たれ、かつ処置具が挿通できる構造となっている。
【0015】
次に、図2を用いて本実施形態における鉗子栓10の具体的な構成を示す。図2において、処置具挿通路11の先端部分には口金13が設けられており、この口金13に鉗子栓10が着脱可能に装着される。鉗子栓10は、全体がゴム等の弾性部材で形成されており、栓本体部20と開閉弁部21とを有し、これら栓本体部20と開閉弁部21との間は扁平な帯状の折り返し用連結部22とから構成される。
【0016】
栓本体部20は、外周部が概略円筒状の部材からなり、一端側から円環状に内向きに突出する第1の円環状突条23が形成されており、また中間部には中央に絞り通路24を形成した隔壁25が設けられ、さらに他端部には係止部となる第2の円環状突条26が形成されている。そして、第1の円環状突条23と隔壁25との間には第1の円環状凹部27が、また隔壁25と第2の円環状突条26との間には第2の円環状凹部28が形成されている。また、開閉弁部21は、概略本体板29の端面から突出部30を突出する状態に連設したものからなり、この突出部30には円環状溝31が形成されており、この円環状溝31の両立ち上がり壁によって栓本体部20の係止部となる第2の円環状突条26を挟持する挟持部が構成される。そして、開閉弁部21の本体板29における突出部30の突出方向とは反対側の面には、概略凹半球形状の処置具ガイド部32が形成されており、この処置具ガイド部32の底部にスリット33が形成されている。さらに、スリット33の形成部分には、処置具ガイド部32とは反対側の面に窪み34が形成されている。この窪み34は処置具を挿通させたときに、スリット33が内向きに容易に変形できるようにするためのものであるが、さらに窪み34はスリット33の形成部の厚み調整を行なうためにも利用される。さらにまた、この窪み34は処置具挿通チャンネル6から逆流して体液や汚物などの溜め部として機能する。
【0017】
以上のように構成される鉗子栓10において、図2に示されるように、スリット33の位置は絞り通路24の延長線上からずれた位置に形成されている。すなわち、図3は鉗子栓10の平面図であるが、この図3にも示されているように、処置具の挿脱を行うスリット33は、処置具ガイド部32の絞り通路24の中央位置から間隔dだけずれた位置に形成されている。このとき、dは絞り通路24の半径より大きいことが望ましい。このように絞り通路24の中央位置から間隔dだけずれた位置にスリット33は設けられているが、処置具を絞り通路24内に導くために、隔壁25の上端部にテーパ状の呼び込み部25aが形成されている。
【0018】
このようにスリット33の処置具挿通路11側入口が絞り通路24の延長面からずれた位置に形成した場合において、吸引バルブによる吸引を行った後に遮断した場合の作用について説明する。
【0019】
最初に、体腔内の汚物などの吸引物質の吸引を行った後に、吸引バルブ7を遮断すると、処置具挿通チャンネル6内はかなり高い圧力状態になり、鉗子栓10に圧力が作用する。そのため、処置具挿通チャンネル6内に残存していた吸引物質は、処置具挿通路11の先端方向に向かって流れる力が働くが、吸引物質の通路は処置具挿通路11よりも孔径が小さい絞り通路24から噴出する。このとき、絞り通路24から噴出された吸引物質の流れの方向は開閉弁部21の下面において、最も下方に突出する位置に向けられる。しかしながら、この位置にはスリット33が形成されていないため、絞り通路24から噴出された吸引物質の圧力を直接受けることはなく、圧力が分散される。従って、スリット33に対して強い圧力が作用することはないので、スリットが開口状態になることはなく、大量の吸引物質が鉗子栓から流出し、術者の手などに体液などの汚物が付着するといった不都合や、周囲に撒き散らされるといった不都合が起きることを防止することができる。
【0020】
B.本発明の第2実施形態
次に、本発明の第2実施形態について説明する。本実施形態では、図4に示されているように、スリット33が処置具挿通路11の延長線に対して斜めに設けるように構成したものである。すなわち、スリット33の処置具挿通路11側への連通部は絞り通路24の延長線からずれた位置に形成されているが、スリット33の処置具挿通路11とは反対側の出口は処置具ガイド部32の中心に位置するように設ける。このように設けた場合においても、絞り通路24から噴出された吸引物質の強い圧力をスリット33が直接受けることがないため、スリットが開口状態になることはなく、大量の吸引物質が鉗子栓から流出し、術者の手などに体液などの汚物が付着するといった不都合や、周囲に撒き散らされるといった不都合が起きることを防止することができる。
【0021】
【発明の効果】
以上説明したように、本発明は、絞り通路の延長面上の位置からスリットの処置具挿通路への連通部をずれた位置に形成しているので、絞り通路により絞られて噴出する吸引物質をスリットが直接受けることはないため、吸引物質が鉗子栓から流出し、術者の手などに体液などの汚物が付着するといった不都合や、周囲に撒き散らされるといった不都合が起きることを防止することができる。
【図面の簡単な説明】
【図1】本発明の鉗子栓が装着される内視鏡の一例を示す全体構成図である。
【図2】本発明の第1実施形態における鉗子栓の断面図である。
【図3】本発明の第1実施形態における鉗子栓の平面図である。
【図4】本発明の第2実施形態における鉗子栓の断面図である。
【符号の説明】
1 本体操作部
2 挿入部
5 処置具導入部
6 処置具挿通チャンネル
10 鉗子栓
13 口金
20 栓本体部
21 開閉弁部
24 絞り通路
32 処置具ガイド部
33 スリット
[0001]
TECHNICAL FIELD OF THE INVENTION
The present invention relates to a forceps stopper that is provided in an endoscope used for medical use and the like and that is detachably attached to a mouthpiece of a treatment instrument introduction port in a treatment instrument insertion channel for inserting forceps and other treatment instruments.
[0002]
[Prior art]
An endoscope that is inserted into a body cavity and performs a medical examination or the like has an insertion section into the body cavity connected to a main body operation section that is operated by an operator or the like by hand and furthermore, a light source is connected to the main body operation section. It is generally configured by connecting and providing a universal cord that is detachably connected to a device or the like. The distal end of the insertion unit includes an illumination unit for illuminating the inside of the body cavity, and an observation unit for inspecting the inside of the body cavity under illumination emitted from the illumination unit.
[0003]
For example, when an affected part or the like is found as a result of an inspection using an endoscope, a necessary treatment can be performed, and there is also a configuration in which tissue cells can be sampled. For this purpose, the endoscope is provided with a treatment tool insertion channel for inserting forceps and other treatment tools. The distal end of the treatment instrument insertion channel is open at the distal end of the insertion section together with the illumination section and the observation section. On the other hand, the proximal end side of the treatment instrument insertion channel is branched into a treatment instrument insertion passage for inserting the treatment instrument and a suction passage for sucking dirt and the like in the body cavity. The treatment instrument is introduced into the treatment instrument insertion channel via a treatment instrument insertion passage provided on the main body operation unit side. For this purpose, a treatment instrument introduction port is formed in the main body operation unit or a connecting portion between the main body operation unit and the insertion unit.
[0004]
Since the pressure in the body cavity is higher than the atmospheric pressure, and the treatment tool insertion channel may also be used as a suction passage, the treatment tool introduction port cannot be always opened. For this purpose, it is common to provide a mouthpiece at the treatment instrument introduction port, attach a forceps plug, and seal the treatment instrument introduction port. When using a treatment instrument, it is common practice to provide an open / close valve on the forceps stopper instead of removing the forceps stopper from the base, and to open the valve when inserting the treatment instrument. is there. In addition, since the inside of the treatment instrument insertion channel must be cleaned each time it is used, the forceps stopper is detachably attached to the mouthpiece of the treatment instrument introduction port.
[0005]
Conventionally known forceps stoppers include a throttle passage having a smaller diameter than the diameter of the treatment instrument inlet, and a slit that is substantially the same as or longer than the diameter of the treatment instrument inlet. In the prior art, there has been known a configuration in which the treatment instrument introduction port is configured to be kept in a tightly closed state by making the treatment tool introduction port closed (for example, see Patent Document 1). When the treatment tool is inserted, the slit is pushed and widened. In the case of a thin treatment tool, the spread of the slit is small, so that a certain degree of hermeticity is ensured. Further, when a thick treatment tool is inserted, the slit is greatly widened, so that the slit cannot exhibit a sealing function. However, since the throttle passage is provided in addition to the slit, it is inserted so as to expand the throttle passage, so that even when using a thick treatment instrument, the treatment instrument introduction port is kept substantially sealed. Is done. As a result, while performing treatment or the like in the body cavity using the treatment tool, it is possible to prevent inconveniences such as backflow of dirt such as bodily fluids and adhesion to the operator's hands and the like.
[0006]
[Patent Document 1]
Japanese Utility Model Laid-Open No. 2-136603 (pages 8-10, FIG. 1)
[0007]
[Problems to be solved by the invention]
By the way, as described above, since the treatment tool insertion channel is also used as a suction passage, operating the suction valve provided in the main body operation unit to perform suction from the body, and then shutting off the suction valve, The inside of the treatment tool insertion channel is in a considerably high pressure state, and pressure acts on the inner surface of the forceps stopper. Since the slit of the forceps stopper is provided on an extension of the throttle passage, the suctioned substance that has taken the throttle passage directly acts on the slit. In this way, when pressure acts on the slit, the slit is opened, the suction substance flows out of the forceps plug, and inconvenience such as attachment of dirt such as body fluids to the operator's hand and the like are scattered around. Inconvenience may occur. In particular, when forceps, tubes, and the like are repeatedly inserted and removed through the slit, the adhesive force of the slit is weakened, and the slit is likely to be opened. When the above-described pressure acts on the slit having the weakened adhesion, the suction substance is more likely to flow out of the forceps stopper.
[0008]
SUMMARY OF THE INVENTION An object of the present invention is to provide a forceps for an endoscope that is configured so that a slit does not directly receive the pressure of an aspirated substance flowing out of a throttle passage, thereby preventing dirt such as bodily fluids from flowing out of a forceps plug to the outside. It is to provide a stopper.
[0009]
[Means for Solving the Problems]
In order to achieve the above object, the present invention provides an endoscope forceps plug which is detachably attached to a treatment instrument insertion passage provided in an endoscope, and has a smaller hole diameter than the treatment instrument insertion passage. A stopper main body provided with a throttle passage, and an opening / closing valve portion provided with a slit through which a treatment tool can be inserted and withdrawn at all times, and at least the treatment tool insertion passage of the slit The side connecting portion is provided at a position shifted from a position on an extension of the throttle passage.
[0010]
BEST MODE FOR CARRYING OUT THE INVENTION
A. First Embodiment of the Present Invention Hereinafter, an embodiment of the present invention will be described in detail with reference to the drawings. First, FIG. 1 shows an overall configuration diagram of an endoscope. In the drawing, 1 is a main body operation unit, 2 is an insertion unit, and 3 is a universal cord. The insertion portion 2 is a flexible portion 2a that bends freely along the bending direction when the insertion path in the body cavity is bent for most of the length from the connection side to the main body operation portion 1. An angle part 2b and a hard tip part 2c are sequentially connected to the soft part 2a. The rigid distal end portion 2c is provided with an illuminating portion and an observing portion (both not shown) constituting an endoscope observation means, and the angle portion 2b guides the rigid distal end portion 2c along an insertion path, In addition, in order to change the field of view of the endoscope observation means provided on the distal end hard portion 2c, a bending operation can be performed in a desired direction. The bending operation of the angle section 2c is performed by remote control by an angle operation means 4 provided in the main body operation section 1.
[0011]
The endoscope is not only capable of observing the inside of a body cavity, but also capable of performing a treatment on an affected part found as a result of an endoscopic examination, sampling a tissue, and the like, by the endoscope observation means described above. For this purpose, a treatment instrument introduction section 5 is provided in the main body operation section 1, and a treatment instrument insertion channel 6 is provided in a region from the treatment instrument introduction section 5 to the distal end hard portion 2c. The distal end of the channel 6 is open to the distal end hard portion 2c together with the illuminating unit and the observation unit. Accordingly, a desired treatment can be performed by inserting forceps and other treatment tools from the treatment tool introduction section 5 into the treatment tool insertion channel 6 and leading them out of the predetermined length from the hard distal end portion 2c.
[0012]
The treatment instrument insertion channel 6 is also used as a suction passage. Therefore, as shown in FIG. 1, the treatment instrument insertion channel is connected to the treatment instrument insertion passage 11 that reaches the treatment instrument introduction section 5 in the main body operation section 1, and from the main body operation section 1 to the suction device via the universal cord 3. It branches into a suction passage 12 to be connected. Further, a suction valve 7 is provided in the main body operation unit 1, and by operating the suction valve 7, the suction passage 12 can be communicated / blocked.
[0013]
Therefore, if body fluids and dirt are present in the body cavity where the endoscopic examination is performed, the suction valve is operated to discharge them from the treatment instrument insertion channel 6 to the suction passage 12 to observe the body cavity. Make the conditions good. In this state, the inside of the body cavity is inspected, and as a result, if an affected part or the like is present, forceps or other treatment tools are inserted from the treatment tool introduction unit 5 into the treatment tool insertion channel 6 to perform appropriate treatment. become.
[0014]
From the above, it is necessary that the treatment instrument introduction unit 5 be kept in a sealed state at least during the suction operation, and the treatment instrument must be able to insert the treatment instrument as it is. Furthermore, since the treatment tool insertion channel 6 is contaminated with body fluids and the like, the interior of the treatment tool insertion channel 6 must be cleaned after use. Therefore, the forceps stopper 10 is detachably attached to the treatment instrument introduction part 5, and the forceps stopper 10 is always kept in a sealed state, and has a structure in which the treatment instrument can be inserted.
[0015]
Next, a specific configuration of the forceps plug 10 in the present embodiment will be described with reference to FIG. In FIG. 2, a mouthpiece 13 is provided at a distal end portion of the treatment instrument insertion passage 11, and the forceps plug 10 is detachably attached to the mouthpiece 13. The forceps stopper 10 is entirely formed of an elastic member such as rubber, and has a stopper main body 20 and an opening / closing valve part 21, and a flat band-shaped part is provided between the stopper main body 20 and the opening / closing valve part 21. And a connecting portion 22 for folding back.
[0016]
The stopper main body 20 has a first annular ridge 23 which is formed in a substantially cylindrical shape at an outer peripheral portion and which protrudes inward in an annular shape from one end side. A partition wall 25 having a passage 24 is provided, and a second annular ridge 26 serving as a locking portion is formed at the other end. A first annular recess 27 is provided between the first annular ridge 23 and the partition 25, and a second annular recess is provided between the partition 25 and the second annular ridge 26. 28 are formed. The opening / closing valve portion 21 is substantially continuous with a projecting portion 30 projecting from the end face of the main body plate 29. The projecting portion 30 has an annular groove 31 formed therein. A holding portion for holding the second annular ridge 26 serving as a locking portion of the plug main body portion 20 is constituted by both rising walls 31. A treatment tool guide portion 32 having a substantially concave hemispherical shape is formed on the surface of the main body plate 29 of the opening / closing valve portion 21 opposite to the projecting direction of the projecting portion 30, and a bottom portion of the treatment tool guide portion 32 is formed. Is formed with a slit 33. Further, a depression 34 is formed in a portion of the slit 33 where the treatment instrument guide 32 is located. The depression 34 is for allowing the slit 33 to be easily deformed inward when the treatment instrument is inserted. The depression 34 is also used for adjusting the thickness of the formation portion of the slit 33. Used. Further, the recess 34 flows backward from the treatment instrument insertion channel 6 and functions as a reservoir for bodily fluids and dirt.
[0017]
In the forceps plug 10 configured as described above, as shown in FIG. 2, the position of the slit 33 is formed at a position displaced from the extension of the throttle passage 24. That is, FIG. 3 is a plan view of the forceps plug 10, and as shown in FIG. 3, the slit 33 for inserting and removing the treatment tool is located at the center of the restriction passage 24 of the treatment tool guide 32. Are formed at positions deviated by an interval d from. At this time, d is preferably larger than the radius of the throttle passage 24. As described above, the slit 33 is provided at a position shifted from the center position of the throttle passage 24 by the interval d. However, in order to guide the treatment tool into the throttle passage 24, a tapered inlet 25a is formed at the upper end of the partition wall 25. Is formed.
[0018]
The operation when the suction by the suction valve is performed and then shut off when the entrance of the slit 33 on the treatment tool insertion passage 11 side is shifted from the extension surface of the throttle passage 24 as described above will be described.
[0019]
First, when the suction valve 7 is shut off after suction of a suction substance such as dirt in the body cavity, the inside of the treatment instrument insertion channel 6 is in a considerably high pressure state, and pressure is applied to the forceps plug 10. Therefore, the suction substance remaining in the treatment tool insertion channel 6 exerts a force flowing toward the distal end of the treatment tool insertion passage 11, but the suction substance passage has a smaller aperture than the treatment tool insertion passage 11. It gushes from the passage 24. At this time, the direction of the flow of the suction substance ejected from the throttle passage 24 is directed to the lowermost position on the lower surface of the on-off valve 21. However, since the slit 33 is not formed in this position, the pressure is not directly received by the suction substance ejected from the throttle passage 24, and the pressure is dispersed. Therefore, since a strong pressure does not act on the slit 33, the slit does not open, and a large amount of aspirated substance flows out of the forceps plug, and contaminants such as body fluids adhere to the operator's hand and the like. It is possible to prevent the inconvenience of doing so and the inconvenience of being scattered around.
[0020]
B. Second Embodiment of the Present Invention Next, a second embodiment of the present invention will be described. In the present embodiment, as shown in FIG. 4, the slit 33 is provided obliquely with respect to the extension of the treatment instrument insertion passage 11. That is, the communicating portion of the slit 33 to the treatment instrument insertion passage 11 side is formed at a position shifted from the extension of the throttle passage 24, but the exit of the slit 33 on the opposite side to the treatment instrument insertion passage 11 is connected to the treatment instrument. It is provided so as to be located at the center of the guide portion 32. Even in such a case, since the slit 33 does not directly receive the strong pressure of the suction substance ejected from the throttle passage 24, the slit does not enter an open state, and a large amount of suction substance flows from the forceps stopper. It is possible to prevent inconveniences such as outflow and attachment of dirt such as bodily fluids to the operator's hand and inconvenience such as being scattered around.
[0021]
【The invention's effect】
As described above, according to the present invention, since the communicating portion of the slit to the treatment instrument insertion passage is formed at a position shifted from the position on the extended surface of the throttle passage, the suction substance squeezed and ejected by the throttle passage is formed. To prevent inconveniences such as suction substances flowing out of the forceps plug and sticking of dirt such as bodily fluids to the surgeon's hands, and being scattered around. Can be.
[Brief description of the drawings]
FIG. 1 is an overall configuration diagram showing an example of an endoscope to which a forceps stopper of the present invention is attached.
FIG. 2 is a sectional view of a forceps stopper according to the first embodiment of the present invention.
FIG. 3 is a plan view of the forceps stopper according to the first embodiment of the present invention.
FIG. 4 is a sectional view of a forceps stopper according to a second embodiment of the present invention.
[Explanation of symbols]
DESCRIPTION OF SYMBOLS 1 Main body operation part 2 Insertion part 5 Treatment tool introduction part 6 Treatment tool insertion channel 10 Forceps plug 13 Cap 20 Plug body part 21 Opening / closing valve part 24 Restriction passage 32 Treatment tool guide part 33 Slit

Claims (2)

内視鏡に設けられた処置具挿通路に着脱可能に装着され、前記処置具挿通路の孔径より小さい孔径となった絞り通路を設けた栓本体部と、
処置具が挿脱可能であり、常時においては密着状態となるスリットを設けた開閉弁部と、を有し、
前記スリットの少なくとも前記処置具挿通路側への連通部は、前記絞り通路の延長線上の位置からずらした位置に設けられたことを特徴とする内視鏡用鉗子栓。
A plug body portion detachably attached to a treatment instrument insertion passage provided in the endoscope, and provided with a throttle passage having a hole diameter smaller than the hole diameter of the treatment instrument insertion passage,
A treatment tool is insertable and removable, and has an on-off valve portion provided with a slit that is always in a close contact state,
An endoscope forceps stopper, wherein a communicating portion of the slit at least to the treatment instrument insertion passage side is provided at a position shifted from a position on an extension of the throttle passage.
前記スリットは、前記絞り通路の延長線の方向に対して斜めに設けられていることを特徴とする請求項1記載の内視鏡用鉗子栓。2. The endoscope forceps stopper according to claim 1, wherein the slit is provided obliquely with respect to a direction of an extension of the throttle passage. 3.
JP2003094158A 2003-03-31 2003-03-31 Endoscopy forceps plug Expired - Fee Related JP4395625B2 (en)

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Application Number Priority Date Filing Date Title
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7025721B2 (en) 2004-01-29 2006-04-11 Boston Scientific Scimed, Inc. Endoscope channel cap
KR20210000554U (en) * 2019-08-29 2021-03-10 (주)바이오세상 Cover for forceps hole of endoscpe

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7025721B2 (en) 2004-01-29 2006-04-11 Boston Scientific Scimed, Inc. Endoscope channel cap
US8231525B2 (en) 2004-01-29 2012-07-31 Boston Scientific Scimed, Inc. Endoscope channel cap
KR20210000554U (en) * 2019-08-29 2021-03-10 (주)바이오세상 Cover for forceps hole of endoscpe
KR200493545Y1 (en) 2019-08-29 2021-04-19 (주)바이오세상 Cover for forceps hole of endoscpe

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