JP4320207B2 - Endoscopic resection aid - Google Patents

Endoscopic resection aid Download PDF

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Publication number
JP4320207B2
JP4320207B2 JP2003120258A JP2003120258A JP4320207B2 JP 4320207 B2 JP4320207 B2 JP 4320207B2 JP 2003120258 A JP2003120258 A JP 2003120258A JP 2003120258 A JP2003120258 A JP 2003120258A JP 4320207 B2 JP4320207 B2 JP 4320207B2
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Japan
Prior art keywords
clip
hooking
assisting device
endoscopic resection
hooking member
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JP2003120258A
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JP2004321482A (en
Inventor
章 杉山
健一 大原
邦利 池田
忠生 垣添
寿光 小林
卓志 後藤田
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Hoya Corp
National Cancer Center Japan
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Hoya Corp
National Cancer Center Japan
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Description

【0001】
【技術分野】
本発明は、内視鏡観察下で例えば病変部を切除する際に用いる、内視鏡用切除補助装置、及び切除補助装置を用いた内視鏡による処置方法に関する。
【0002】
【従来技術及びその問題点】
従来、通常の手術において人体内部の病変部を切除する場合においては、把持鉗子を用いて病変部を持ち上げることにより病変部と隣接する正常組織との間隔を広げ、その状態で病変部と正常組織との間を切除している。しかし、例えば内視鏡粘膜切除術(EMR)では、体内には内視鏡を一台しか挿入できないため、病変を持ち上げることができず、注射針で病変部の周囲の正常粘膜に生理食塩水を注入して病変部を浮き上がらせ、その状態で高周波ナイフやスネアなどを用いて病変部と正常粘膜の間の切除を行っていた。
【0003】
しかし、このような従来の方法では、病変部を十分な位置まで持ち上げることができなかったため、病変部と正常組織との境界の切除部分を十分確保することができなかった。
また、病変部が扁平な形状である場合は、切除部分を作りだすことができないこともあった。
【0004】
さらに、切除作業中において、すでに切除した病変部が正常組織上に落ち込むことにより内視鏡による視界を妨げることがあり、特に病変部が大きい場合に顕著であった。そのため、切除部分を見ることができず、盲目的に切除するために正常部分を損傷して穿孔などの合併症が発生したり、血管を損傷して大出血をきたし、また出血時も出血部位の確認ができず止血できないことから重篤な合併症を来すことも考えられ、より安全な装置や処置方法が求められていた。
【0005】
そこで本出願人は、これらの問題点を解決すべく、人体内部の病変部を掛着する掛着部材と、該掛着部材と連結される磁性体からなる磁気アンカーと、人体の外部に配置され、磁界を発生して磁気アンカーに動力を与える磁気アンカー誘導装置と、を備え、磁気アンカー誘導装置が発生する磁界によって磁気アンカーに動力を与えて、掛着部材に掛着された病変部を持ち上げることを特徴とする磁気アンカー誘導装置を提案し、特許出願している(特願2002−268239号)。
【0006】
しかし、この磁気アンカー誘導装置を利用した内視鏡では、内視鏡で病変部の観察を行っている最中に、体内の上下左右の方向が分からなくなったり、磁気誘導装置による磁界の方向が分からなくなることがあるため、磁気アンカーにより病変部を所定の方向に移動させるには、熟練を要するという問題があった。
さらに、磁気アンカー誘導装置は高価な装置であるため、より安価に、病変部を確実に切除できる装置や処置方法が望まれていた。
【0007】
【発明の目的】
そこで本発明の目的は、簡単かつ確実、さらに従来より安価に、切除術中に病変部を所定の方向に牽引できるようにした内視鏡用切除補助装置、及び切除補助装置を用いた内視鏡による処置方法を提供することにある。
【0008】
【発明の概要】
本発明の内視鏡用切除補助装置は、対象物内部の対象部位を掛着する第1掛着部材と、この第1掛着部材とは異なる位置で上記対象物内部に掛着される第2掛着部材と、該第1掛着部材と第2掛着部材とを連結し、上記第1掛着部材を上記第2掛着部材側に牽引する牽引連結部材と、を具備することを特徴としている。
【0009】
上記牽引連結部材を、上記第1掛着部材第2掛着部材とに係合される弾性部材とすることが可能である。
【0010】
上記弾性部材は、上記第1掛着部材第2掛着部材とに係合される輪ゴムとするのが実際的である。
【0011】
また、上記弾性部材を、両端部に、上記第1掛着部材第2掛着部材とにそれぞれ係合するフック部を具備する圧縮コイルとすることも可能である。
【0012】
さらに、上記牽引連結部材を、柔軟なひも部と、該ひも部に、その長手方向に並べて固定された少なくとも3つのフック部と、を具備し、上記フック部はそのうちのいずれか2つを選択的に、上記第1掛着部材第2掛着部材とにそれぞれ係合するものとしてもよい。
【0013】
上記第1掛着部材または第2掛着部材の少なくとも一方を、開閉可能で、上記対象部位を挟持可能なクリップとするのが実際的である。
【0014】
上記第1掛着部材と第2掛着部材は同一構造であってもよい。
【0015】
上記牽引連結部材が、上記第1掛着部材及び第2掛着部材に対して着脱自在であってもよい。
【0016】
【0017】
【0018】
【0019】
【0020】
【0021】
【0022】
【発明の実施の形態】
以下、本発明の第1の実施形態を、図1から図9を参照しつつ詳しく説明する。
本実施形態の切除補助装置1は、第1クリップ2、第2クリップ3及び輪ゴム4からなるものである。
【0023】
図1及び図5等に示す第1クリップ第1掛着部材)2は、一端に略円弧状の係合部2aが形成され、他端に先端部2bが形成された第1基片2cと、一端に先端部2dが形成された略直線状の第2基片2eと、第1基片2cと第2基片2eにそれぞれ固着された調整部材2fとを具備している。調整部材2fの詳しい構造に関する説明は省略するが、この調整部材2fは、その幅方向の寸法を調整可能であり、その幅を広げると、第1基片2cと第2基片2eの先端部2b、2dの間隔が広がり、その幅を狭めると、先端部2b、2dの間隔が狭まる。この第1クリップ2は、患者(対象物)体内の病変部(対象部位)Xを掴んで持ち上げるための部材である。
【0024】
同じく図1及び図2等に示す第2クリップ第2掛着部材)3は、第1クリップ2と同じ構成の部材であり、第1クリップ2と同様に、患者A体内の病変部Xを掴むことが出来る。
【0025】
輪ゴム(牽引連結部材)(弾性部材)4は、図1及び図7等に示すように、第1クリップ2と第2クリップ3の係合部2a、3aに係合することにより、両クリップ2、3同士を連結するものである。
図3は、患者Aを載せるためのベッド5を示している。
【0026】
図4は、切除補助装置1を用いた切除術の実施に用いる内視鏡10を示している。
内視鏡10の構造は公知なので詳しい説明は省略するが、体内に挿入される挿入部11の先端面11aには、図5等に示すように、エア及び洗浄水を送るための送気送水ノズル12、切除部及びその周辺を照らすための照明窓13、切除部及びその周辺を観察するために対物レンズを配置した観察窓14、並びに、鉗子チャンネル(図示略)の出口15が設けられている。鉗子チャンネルは挿入部11内に設けられており、その入口16aは鉗子挿入口突起16の端面に形成されている。
【0027】
次に、切除補助装置1を用いた病変部Xの切除要領について説明する。
切除補助装置1を用いた切除術の実施に先立っては、まず、図3に示すように、局所麻酔を施した患者Aをベッド5上に横たわらせる。
次いで、患者Aの体内に図5から図9に示すオーバーチューブ20を、患者Aの口から挿入し、このオーバーチューブ20の先端部を、臓器B内の病変部Xに近接させる。そして、オーバーチューブ20内に内視鏡10の挿入部11を挿入し、その先端部をオーバーチューブ20の先端から突出させ、病変部Xに近接させる。このように、内視鏡10の挿入部11の先端を臓器B内に挿入すると、観察窓14から得られた臓器B内の観察像が、図示を省略したテレビモニタに写し出される。
【0028】
この状態で、鉗子挿入口突起16の入口16aから、先端部に注射針を具備するチューブ状の処置具(図示略)を挿入し、その注射針を挿入部11の出口15から突出させて、注射針を病変部Xの周辺から臓器壁の粘膜下層B1に挿入して生理食塩水を注入し、病変部Xを固有筋層B2から浮き上がらせておく。
【0029】
次に、以下に説明する要領により、第1クリップ2、第2クリップ3及び輪ゴム4を、それぞれ個別に患者Aの臓器B内へ挿入する。
【0030】
まず、患者Aの体外において、弾性材料からなる可撓性チューブ30の先端開口部に、先端部2b、2dが開いた状態の第1クリップ2を嵌合し、その状態のまま、可撓性チューブ30を鉗子挿入口突起16の入口16aから鉗子チャンネル内に挿入し、その先端部を鉗子チャンネルの出口15から突出させる(図5参照)。次いで、可撓性チューブ30を操作して、第1クリップ2を病変部Xに近づけたら、可撓性チューブ30内に事前に挿入してあるプッシングロッド(図示略)を前方に押し出して、第1クリップ2を可撓性チューブ30から脱落させ、病変部X近傍に配置させる(図6参照)。
【0031】
次いで、図示は省略したが、鉗子チャンネルから可撓性チューブ30を一旦引き抜き、体外において、可撓性チューブ30の先端開口部に、先端部3b、3d同士が開いた状態の第2クリップ3を嵌合して、可撓性チューブ30により第2クリップ3を弾性把持し、その状態のまま、可撓性チューブ30を鉗子挿入口突起16の入口16aから鉗子チャンネル内に挿入し、その先端部を鉗子チャンネルの出口15から突出させる。次いで、可撓性チューブ30を操作して、第2クリップ3を病変部Xに近づけたら、プッシングロッドを前方に押し出して、第2クリップ3を可撓性チューブ30から脱落させ、病変部X近傍に配置させる(図6参照)。
【0032】
次いで、鉗子チャンネルから可撓性チューブ30を引き抜き、代わりに、図6に示す把持鉗子40を鉗子チャンネルに挿入し、その先端部を、挿入部11の先端面11aから突出させる。この把持鉗子40は、可撓性チューブ40aの先端に開閉可能な金属製の把持部材41を具備し、かつ、可撓性チューブ40aの基端部に操作部(図示略)を具備するものであり、この操作部を操作すると把持部材41が開閉する。
そして、この把持鉗子41を操作して第1クリップ2の調整部材2fを把持し、その幅を狭めることにより、第1クリップ2の両先端部2b、2dの間で、病変部Xの一方の端部X1を掴む(図6参照)。
さらに、把持鉗子40を操作して、第2クリップ3の調整部材3fを掴み、その幅を狭めることにより、両先端部3b、3dの間で、病変部Xの他方の端部(別の対象部位)X2を掴む(図6参照)。
【0033】
次いで、把持鉗子40を内視鏡10から一旦抜き取り、体外において、把持部材41で輪ゴム4を把持し、その状態で、再度、把持鉗子40を鉗子チャンネルに挿入して、輪ゴム4と挿入部11の先端部を臓器B内に挿入する(図6参照)。
そして、把持鉗子40の操作部を操作することによって、輪ゴム4の一部を、第1クリップ2の係合部2aと調整部材2fの間に通して係合部2aに係合し、さらに、輪ゴム4の他の一部を、第2クリップ3の係合部3aに係合させて、臓器B内において切除補助装置1を完成させる(図7参照)。
【0034】
このように、第1クリップ2と第2クリップ3を病変部Xに掛着させた状態で切除補助装置1を組み立てると、輪ゴム4が初期状態に比べて伸び、輪ゴム4全体に、第1クリップ2と第2クリップ3とを引き寄せ合う張力が生じる。このため、第1クリップ2が第2クリップ3側に引き寄せられ、病変部X1は所望方向に引っ張られた状態となる。
【0035】
このように、病変部Xが所望方向に引っ張られた状態となると、病変部Xと正常組織との境界部に、十分な大きさの切除部分が形成されるので、続いて、把持鉗子40を内視鏡10から取り出し、図7に示すように、高周波メス50などの切開具を鉗子チャネルから臓器B内に挿入し、病変部Xを粘膜とともにその端部X1から切除する。
そして、端部X1を一旦切除すると、病変部Xは、輪ゴム4に生じた張力により、第1クリップ2に掴まれた端部X1部分が、第2クリップ3に掴まれた端部X2側に引き寄せられるので、高周波メス50による切除領域が、端部X1側から端部X2側までスムーズに拡がり(図8参照)、やがて、病変部X全体が完全に切除される(図9参照)。
なお、高周波メス50による切除作業時においては、切除領域が拡がるにつれて、高周波メス50の先端50aの位置の確認はより容易となる。
【0036】
以上のように切除作業を終えると、両クリップ2、3に病変部Xが取り付いた状態になるので、病変部Xが紛失することが防止される。切除した病変部Xを回収するには、連結されたままの第1クリップ2、第2クリップ3、輪ゴム4、及び病変部Xの一部分を把持鉗子40で把持し、そのままの状態で、内視鏡10を体内から抜き去る。そして、その後に、切除した部分の縫合、消毒などの処置を行う。
【0037】
以上のように、本実施形態の切除補助装置1を用いれば、磁気誘導装置のような高価を装置を用いずに、病変部Xを所望方向に十分な距離だけ移動させることができる。そのため、病変部Xと正常組織との境界の切除部分を、容易かつ確実に十分な大きさで確保することができ、また、病変部Xが扁平な形状であっても、十分な大きさの切除部分を作りだすことができ、しかも、高周波メス50等の処置具による切除時に、輪ゴム4の張力により、病変部Xの一方の端部X1が他方の端部X2側に引き寄せられるので、病変部Xを容易に切除することが可能となる。
【0038】
さらに、病変部Xは第1クリップ2により持ち上げられるため、切除部分を十分確保することができ、すでに切除した病変部Xが固有筋層B2上に落ち込むことを防止できる。
また、任意の位置に第1クリップ2と第2クリップ3を配置できるため、切除した病変部Xにより内視鏡の視界が妨げられることがない。
【0039】
次に、本発明の第2の実施形態について、図10及び図11を参照しながら説明する。
なお、第1の実施形態と同じ部材には同じ符号を付すに止めて、その詳細な説明は省略する。
【0040】
本実施形態の切除補助装置60は、第1クリップ61、第2クリップ62、及び圧縮コイルばね63(牽引連結部材)(弾性部材)とからなるものである。
図示する第1クリップ第1掛着部材)61は、患者(対象物)体内の病変部(対象部位)を掴んで持ち上げるための部材である。このクリップ61は、U字状に折り曲げた弾性材料からなるものであり、その弾性により、互いに離れる方向に付勢された一対の開閉片61aを具備しており、両開閉片61aの先端には先端部61bが形成されている。両開閉片61aの相対間隔は可変であり、両開閉片61aには、互いの間隔を調節後に位置固定するラチェット部材61cが備えられている。図11に示すように、このラチェット部材61cは、一対の係合片61c1を具備しており、両係合片61c1の対向面には、互いに係脱可能な係合歯61c2が形成されている。ラチェット部材61cは、対をなす開閉片61aが間隔を縮める方向に弾性変形するときにはその変形を妨げず、かつ両開閉片61aの間隔調整後にその間隔を保持する機能を有する。さらに、両開閉片61aの基端部間には係合孔(係合部)61dが形成されている。
【0041】
同じく図示する第2クリップ第2掛着部材)62は、第1クリップ61と同じ構成のものであり、開閉片62a、先端部62b、ラチェット部材62c、係合孔(係合部)62dを具備しており、両先端部62b間で病変部(対象部位)を掴むものである。
【0042】
圧縮コイルばね63は、ばね部63aの両端部にフック部63b、63cをそれぞれ具備するものである。
【0043】
図示は省略するが、第1クリップ61は、体外において、把持鉗子40の把持部材41により把持され、そのままの状態で把持鉗子40により臓器B内に挿入され、把持部材41を開くことにより、病変部X近傍に載置される。なお、第2クリップ62も同様の要領により、病変部X近傍に載置される。
そして、このように病変部X近傍に第1クリップ61と第2クリップ62を載置した後に、把持鉗子40を操作して第1クリップ61のラチェット部材61cを締めることにより、第1クリップ61の両開閉片61aを閉じて、両先端部61bにより病変部Xの一方の端部X1を掴む(図10参照)。
さらに、同じ要領により、第2クリップ62の両先端部62bにより、病変部Xの他方の端部X2を掴む。
【0044】
圧縮コイルばね63は、体外において、そのフック部63bが把持鉗子40の把持部材41により把持され、そのままの状態で把持鉗子40により臓器B内に挿入される。
そして、把持部材41と圧縮コイルばね63を臓器B内に入れた後に、把持部材41により、圧縮コイルばね63のフック部63bを第1クリップ61の係合孔61dに係合し、その後に、把持部材41により、フック部63cをばね部63aの付勢力に抗しながら第2クリップ62側に引き寄せ、フック部63cを第2クリップ62の係合孔62dに係合させ、臓器B内において切除補助装置60を組み立てる。
【0045】
このように、第1クリップ61と第2クリップ62を病変部Xに掛着させた状態で切除補助装置60を組み立てると、圧縮コイルばね63が初期状態に比べて伸び、ばね部63aに、第1クリップ61と第2クリップ62を互いに引き寄せ合う付勢力が生じる。このため、第1クリップ61が第2クリップ62側に引き寄せられ、病変部X1が所望方向に引っ張られた状態となる。
【0046】
そのため、このような本実施形態によっても、病変部Xと正常組織との境界部に、十分な大きさの切除部分を形成することができ、さらに、高周波メス50などの切開具により、病変部X全体をスムーズに切除することができ(図示略)、第1の実施形態と同様な効果が得られる。
【0047】
最後に、本発明の第3の実施形態について、図12及び図13を参照しながら説明する。
なお、第1及び第2の実施形態と同じ部材には同じ符号を付すに止めて、その詳細な説明は省略する。
【0048】
本実施形態の切除補助装置70は、第2の実施形態と同構成の第1クリップ61と第2クリップ62、及びひも状の柔軟連結具71(牽引連結部材)とからなるものである。
この柔軟連結具71は、柔軟で弾性を有さないひも部71aと、ひも部71aの両端部と中間部とに固着された4個のフック部71b、71c、71d、71eとからなるものである。
【0049】
第1クリップ61と第2クリップ62は、第2の実施形態と同じ要領により、臓器B内に挿入される。そして、把持部材41を利用することにより、両クリップ61、62の先端部61b、62b間で、病変部Xの両端部X1、X2をそれぞれ掴む(図12参照)。
【0050】
柔軟連結具71は、体外において、そのフック部71bが把持鉗子40の把持部材41により把持され、そのままの状態で把持鉗子40により臓器B内に挿入される。
さらに、把持部材41により、一方の端部のフック部71bが第1クリップ61の係合孔61dに係合され、その後さらに、把持部材41により、他方の端部のフック部71eが第2クリップ62の係合孔62dに係合され、臓器B内において切除補助装置70が組み立てられる。
そして、係合孔62dにフック部71eを係合すると、ひも部71aが緊張し、ひも部71aに張力T(図12参照)が生じるので、第1クリップ61が第2クリップ62側に引き寄せられ、病変部X1が所望方向に引っ張られた状態となる。そのため、このような本実施形態によっても、病変部Xと正常組織との境界部に、十分な大きさの切除部分を形成することができ、病変部X全体をスムーズに切除することができる。
【0051】
この後さらに、把持鉗子(図示略)40により、フック部71eを係合孔62dから外し、フック部71dを係合孔62dに係合させると、ひも部71aにさらに大きな張力が生じ、第1クリップ61が第2クリップ62側にさらに引き寄せられるので、高周波メス50による切除力が、病変部X1の一方の端部X1側から他方の端部X2側によりスムーズに拡がる。さらに、図13に示すように、把持鉗子40を使って、係合孔62dにフック部71cを係合させると、ひも部71aにさらに大きな張力が生じ、第1クリップ61が第2クリップ62側にさらに引き寄せられるので、切除領域が端部X2側にさらに拡がり、最終的に病変部Xが完全に切除される(図示略)。
【0052】
このように本実施形態によっても、第1及び第2の実施形態と同様に、病変部Xと正常組織との境界部に、十分な大きさの切除部分を形成することができ、さらに、高周波メス50などの切開具により、病変部X全体をスムーズに切除することができる。
【0053】
さらに、第2クリップ62の係合孔62dに係合させるフック部71c、71d、71eを選択することにより、ひも部71aに生じる張力Tが変化するので、病変部Xと正常組織との境界部に形成しようとする切除部分の大きさを調整することが可能である。
【0054】
以上、本発明について各実施形態を参照しつつ説明したが、本発明は上記実施形態に限定されるものではなく、改良の目的または本発明の思想の範囲内において改良または変更が可能である。例えば、第1クリップ2、61と第2クリップ3、62の代わりに、病変部Xに突き刺すことが可能な釣り針状の針部材(第1掛着部材及び第2掛着部材)(図示略)を2個用意し、これらの針部材同士を、輪ゴム4や圧縮コイルばね63や柔軟連結具71で連結して実施することも可能である。
【0055】
【発明の効果】
以上説明したように、本発明によると、簡単かつ確実、さらに従来より安価に、切除術中に病変部を所定の方向に牽引できるようにした内視鏡用切除補助装置、及び切除補助装置を用いた内視鏡による処置方法を提供できるようになる。
【図面の簡単な説明】
【図1】 本発明の第1の実施形態の切除補助装置の構成を示す図である。
【図2】 クリップの形状を示す図である。
【図3】 ベッドに患者を載せた状態を示す側面図である。
【図4】 病変部の切除を行うときに用いる内視鏡の全体図である。
【図5】 切除補助装置を体内の臓器内へ導入する手順を示す図である。
【図6】 同じく、切除補助装置を体内の臓器内へ導入する手順を示す図である。
【図7】 切除補助装置を用いた病変部の切除工程を示す図である。
【図8】 同じく、切除補助装置を用いた病変部の切除工程を示す図である。
【図9】 切除補助装置を用いた病変部の切除作業により、病変部が完全に切除された状態を示す図である。
【図10】 本発明の第2の実施形態の図7と同様の、病変部の切除工程を示す図である。
【図11】 ラチェット部材の拡大断面図である。
【図12】 本発明の第3の実施形態の図7と同様の、病変部の切除工程を示す図である。
【図13】 同じく、病変部の切除工程を示す図である。
【符号の説明】
1 切除補助装置
第1クリップ第1掛着部材
2a 係合部
2b 先端部
2c 第1基片
2d 先端部
2e 第2基片
2f 調整部材
第2クリップ第2掛着部材
3a 係合部
3b 先端部
3c 第1基片
3d 先端部
3e 第2基片
3f 調整部材
4 輪ゴム(牽引連結部材)(弾性部材)
5 ベッド
10 内視鏡
11 挿入部
11a 先端面
12 送気送水ノズル
13 照明窓
14 観察窓
15 鉗子チャンネルの出口
16 鉗子挿入口突起
16a 入口
20 オーバーチューブ
30 可撓性チューブ
40 把持鉗子
40a 可撓性チューブ
41 把持部材
50 高周波メス
50a 先端部
60 切除補助装置
61 第1クリップ(第1掛着部材)
61a 開閉片
61b 先端部
61c ラチェット部材
61c1 係合片
61c2 係合歯
61d 係合孔(係合部)
62 第2クリップ(第2掛着部材)
62a 開閉片
62b 先端部
62c ラチェット部材
62c1 係合片
62c2 係合歯
62d 係合孔(係合部)
63 圧縮コイルばね(牽引連結部材)(弾性部材)
63a ばね部
63b 63c フック部
70 切除補助装置
71 柔軟連結具(牽引連結部材)
71a ひも部
71b 71c 71d 71e フック部
A 患者(対象物)
A1 頭部
B 臓器
B1 粘膜下層
B2 固有筋層
X 病変部(対象部位)
X1 X2 端部
[0001]
【Technical field】
The present invention relates to an endoscopic resection assisting device and an endoscopic treatment method using the resection assisting device that are used when, for example, a lesion is resected under endoscopic observation.
[0002]
[Prior art and its problems]
Conventionally, when excising a lesion inside a human body in a normal operation, the distance between the lesion and the adjacent normal tissue is widened by lifting the lesion using a grasping forceps, and the lesion and the normal tissue are in that state. It is excised between. However, for example, in endoscopic mucosal resection (EMR), since only one endoscope can be inserted into the body, the lesion cannot be lifted, and physiological saline is applied to the normal mucosa around the lesion with an injection needle. The lesion was lifted by injecting, and in that state, excision between the lesion and the normal mucous membrane was performed using a high-frequency knife or snare.
[0003]
However, in such a conventional method, the lesioned part could not be lifted to a sufficient position, and thus a sufficient excision part at the boundary between the lesioned part and the normal tissue could not be secured.
In addition, when the lesioned part has a flat shape, it may not be possible to create an excised part.
[0004]
Further, during the excision work, the already excised lesioned part may fall on the normal tissue, thereby obstructing the field of view by the endoscope, particularly when the lesioned part is large. For this reason, the excised part cannot be seen, and in order to remove it blindly, the normal part is damaged and complications such as perforation occur, blood vessels are damaged and major bleeding occurs. Since it could not be confirmed and hemostasis could not be achieved, serious complications could occur, and a safer device and treatment method were required.
[0005]
Therefore, in order to solve these problems, the present applicant arranges a hooking member for hooking a lesion inside the human body, a magnetic anchor made of a magnetic body connected to the hooking member, and an outside of the human body. A magnetic anchor guide device that generates a magnetic field and applies power to the magnetic anchor, and supplies the power to the magnetic anchor by the magnetic field generated by the magnetic anchor guide device, thereby causing the lesioned part that is hooked on the hook member to A magnetic anchor guiding device characterized by lifting is proposed and a patent application has been filed (Japanese Patent Application No. 2002-268239).
[0006]
However, in an endoscope using this magnetic anchor guidance device, while observing a lesion with the endoscope, the direction of the body's top, bottom, left and right is not known, or the direction of the magnetic field by the magnetic guidance device is Since it may not be understood, there is a problem that skill is required to move the lesioned part in a predetermined direction by the magnetic anchor.
Furthermore, since the magnetic anchor guidance device is an expensive device, there has been a demand for a device and a treatment method that can reliably excise a lesion at a lower cost.
[0007]
OBJECT OF THE INVENTION
SUMMARY OF THE INVENTION An object of the present invention is to provide an endoscopic resection assisting device capable of pulling a lesioned part in a predetermined direction during resection, and an endoscope using the resection assisting device, which is simple, reliable, and more inexpensive than conventional methods. It is in providing the treatment method by.
[0008]
Summary of the Invention
The endoscopic resection assisting device of the present invention includes a first hooking member that hooks a target portion inside a target object, and a first hooking member that is hooked inside the target object at a position different from the first hooking member . and 2 hooking member, connects the said first hooking member and the second hooking member, and the traction coupling member for pulling the first hooking member in the second hooking member side, by comprising It is a feature.
[0009]
The traction connecting member may be an elastic member that is engaged with the first hooking member and the second hooking member .
[0010]
It is practical that the elastic member is a rubber band that is engaged with the first hooking member and the second hooking member .
[0011]
Further, the elastic member may be a compression coil having hook portions that engage with the first hooking member and the second hooking member at both ends.
[0012]
Further, the traction connecting member comprises a flexible string part and at least three hook parts fixed to the string part in a longitudinal direction, and the hook part selects any two of them. In particular, the first hooking member and the second hooking member may be engaged with each other.
[0013]
It is practical that at least one of the first hooking member and the second hooking member is a clip that can be opened and closed and can clamp the target portion.
[0014]
The first hooking member and the second hooking member may have the same structure.
[0015]
The traction connecting member may be detachable from the first hooking member and the second hooking member.
[0016]
[0017]
[0018]
[0019]
[0020]
[0021]
[0022]
DETAILED DESCRIPTION OF THE INVENTION
Hereinafter, a first embodiment of the present invention will be described in detail with reference to FIGS.
The resection assisting apparatus 1 according to the present embodiment includes a first clip 2, a second clip 3, and a rubber band 4.
[0023]
The first clip ( first hooking member ) 2 shown in FIGS. 1 and 5, etc. has a first base piece 2c in which a substantially arc-shaped engaging portion 2a is formed at one end and a tip portion 2b is formed at the other end. And a substantially linear second base piece 2e having a tip 2d formed at one end, and an adjustment member 2f fixed to the first base piece 2c and the second base piece 2e, respectively. The detailed structure of the adjusting member 2f is omitted, but the adjusting member 2f can be adjusted in the width direction. When the width is increased, the distal ends of the first base piece 2c and the second base piece 2e are adjusted. When the interval between 2b and 2d increases and the width decreases, the interval between the tip portions 2b and 2d decreases. The first clip 2 is a member for grasping and lifting a lesioned part (target part) X in a patient (target) body.
[0024]
Similarly the second clip (second hooking member) 3 shown in FIG. 1 and FIG. 2 or the like is a member of the same configuration as that of the first clip 2, similarly to the first clip 2, the pathological lesion portion X of the patient A body I can grab it.
[0025]
As shown in FIGS. 1 and 7, the rubber band (traction connecting member) (elastic member) 4 is engaged with the engaging portions 2 a and 3 a of the first clip 2 and the second clip 3, thereby both the clips 2. 3 are connected to each other.
FIG. 3 shows a bed 5 on which a patient A is placed.
[0026]
FIG. 4 shows an endoscope 10 used for performing excision using the excision assisting apparatus 1.
Since the structure of the endoscope 10 is well-known, detailed description thereof is omitted. However, as shown in FIG. 5 and the like, air supply / water supply for supplying air and cleaning water to the distal end surface 11a of the insertion portion 11 inserted into the body. There are provided a nozzle 12, an illumination window 13 for illuminating the excision part and the periphery thereof, an observation window 14 in which an objective lens is arranged for observing the excision part and the periphery thereof, and an outlet 15 of a forceps channel (not shown). Yes. The forceps channel is provided in the insertion portion 11, and its inlet 16 a is formed on the end face of the forceps insertion port protrusion 16.
[0027]
Next, the excision procedure of the lesioned part X using the excision assisting apparatus 1 will be described.
Prior to performing excision using the excision assisting apparatus 1, first, as shown in FIG. 3, the patient A that has undergone local anesthesia is laid on the bed 5.
Next, the overtube 20 shown in FIGS. 5 to 9 is inserted into the body of the patient A from the mouth of the patient A, and the tip of the overtube 20 is brought close to the lesion X in the organ B. Then, the insertion portion 11 of the endoscope 10 is inserted into the overtube 20, and the distal end portion thereof protrudes from the distal end of the overtube 20 so as to approach the lesioned portion X. As described above, when the distal end of the insertion portion 11 of the endoscope 10 is inserted into the organ B, an observation image in the organ B obtained from the observation window 14 is displayed on a television monitor (not shown).
[0028]
In this state, a tube-like treatment instrument (not shown) having an injection needle is inserted into the distal end portion from the inlet 16a of the forceps insertion port projection 16, and the injection needle is protruded from the outlet 15 of the insertion portion 11, The injection needle is inserted from the periphery of the lesion X into the submucosa B1 of the organ wall and physiological saline is injected, and the lesion X is lifted from the proper muscle layer B2.
[0029]
Next, the first clip 2, the second clip 3, and the rubber band 4 are individually inserted into the organ B of the patient A according to the procedure described below.
[0030]
First, outside the body of the patient A, the first clip 2 with the distal end portions 2b and 2d opened is fitted into the distal end opening portion of the flexible tube 30 made of an elastic material. The tube 30 is inserted into the forceps channel from the inlet 16a of the forceps insertion port projection 16, and the tip of the tube 30 protrudes from the outlet 15 of the forceps channel (see FIG. 5). Then, by operating the flexible tube 30, the first clip 2 Once close to the lesion X, flexible pushing rod tube 30 to are inserted beforehand (not shown) the extruded forward, the One clip 2 is dropped from the flexible tube 30 and placed near the lesion X (see FIG. 6).
[0031]
Next, although not shown, the flexible tube 30 is once pulled out of the forceps channel, and the second clip 3 in a state where the distal end portions 3b and 3d are opened outside the body at the distal end opening portion of the flexible tube 30. The second clip 3 is elastically gripped by the flexible tube 30, and the flexible tube 30 is inserted into the forceps channel from the inlet 16a of the forceps insertion port projection 16 in the state, and the distal end portion thereof. Project from the outlet 15 of the forceps channel. Next, when the flexible tube 30 is operated to bring the second clip 3 close to the lesioned part X, the pushing rod is pushed forward to drop the second clip 3 from the flexible tube 30 and near the lesioned part X. (See FIG. 6).
[0032]
Next, the flexible tube 30 is pulled out from the forceps channel, and instead, the grasping forceps 40 shown in FIG. 6 is inserted into the forceps channel, and the distal end portion thereof protrudes from the distal end surface 11 a of the insertion portion 11. The gripping forceps 40 includes a metal gripping member 41 that can be opened and closed at the distal end of the flexible tube 40a, and an operation portion (not shown) at the base end of the flexible tube 40a. Yes, when this operation unit is operated, the gripping member 41 opens and closes.
Then, the gripping forceps 41 is operated to grip the adjusting member 2f of the first clip 2, and the width thereof is narrowed, so that one of the lesioned portions X is between the two distal end portions 2b and 2d of the first clip 2. Grasp end X1 (see FIG. 6).
Further, by operating the grasping forceps 40 to grasp the adjusting member 3f of the second clip 3 and narrowing the width thereof, the other end of the lesioned part X (another target) between the two distal ends 3b and 3d. (Part) X2 is gripped (see FIG. 6).
[0033]
Next, the grasping forceps 40 is temporarily extracted from the endoscope 10, and the rubber band 4 is grasped by the grasping member 41 outside the body. In this state, the grasping forceps 40 is inserted into the forceps channel again, and the rubber band 4 and the insertion portion 11 are inserted. Is inserted into the organ B (see FIG. 6).
Then, by operating the operation part of the grasping forceps 40, a part of the rubber band 4 is passed between the engaging part 2a of the first clip 2 and the adjusting member 2f and engaged with the engaging part 2a. The other part of the rubber band 4 is engaged with the engaging portion 3a of the second clip 3 to complete the resection assisting device 1 in the organ B (see FIG. 7).
[0034]
Thus, when the resection assisting apparatus 1 is assembled with the first clip 2 and the second clip 3 hooked to the lesioned part X, the rubber band 4 extends compared to the initial state, and the first clip A tension that draws 2 and the second clip 3 close together is generated. For this reason, the 1st clip 2 is drawn near to the 2nd clip 3 side, and lesioned part X1 will be in the state pulled in the desired direction.
[0035]
Thus, when the lesioned part X is pulled in a desired direction, a sufficiently large excision part is formed at the boundary between the lesioned part X and the normal tissue. As shown in FIG. 7, an incision tool such as a high-frequency knife 50 is inserted into the organ B from the forceps channel and the lesioned part X is excised from the end X1 together with the mucous membrane.
Once the end portion X1 is excised, the lesioned portion X is moved to the end portion X2 side gripped by the second clip 3 from the end portion X1 portion gripped by the first clip 2 due to the tension generated in the rubber band 4. Since it is attracted, the excision area by the high-frequency knife 50 spreads smoothly from the end X1 side to the end X2 side (see FIG. 8), and eventually the entire lesioned part X is completely excised (see FIG. 9).
In the excision work with the high-frequency knife 50, the position of the tip 50a of the high-frequency knife 50 becomes easier to confirm as the excision area expands.
[0036]
When the excision work is completed as described above, the lesioned part X is attached to both the clips 2 and 3, so that the lesioned part X is prevented from being lost. In order to collect the excised lesion part X, the first clip 2, the second clip 3, the rubber band 4, and a part of the lesion part X, which are still connected, are grasped by the grasping forceps 40, and the endoscope Remove the mirror 10 from the body. After that, treatments such as suturing and disinfection of the excised part are performed.
[0037]
As described above, if the resection assisting apparatus 1 of the present embodiment is used, the lesioned part X can be moved in a desired direction by a sufficient distance without using an expensive apparatus such as a magnetic guidance apparatus. Therefore, the excision part of the boundary between the lesioned part X and the normal tissue can be secured easily and reliably with a sufficient size, and even if the lesioned part X has a flat shape, a sufficient size can be obtained. An excision portion can be created, and at the time of excision with a treatment instrument such as the high-frequency knife 50, one end X1 of the lesion X is pulled toward the other end X2 due to the tension of the rubber band 4, so the lesion X can be easily excised.
[0038]
Furthermore, since the lesioned part X is lifted by the first clip 2, a sufficient excised part can be secured, and the already excised lesioned part X can be prevented from falling on the proper muscle layer B2.
Moreover, since the 1st clip 2 and the 2nd clip 3 can be arrange | positioned in arbitrary positions, the visual field of an endoscope is not prevented by the excised lesioned part X. FIG.
[0039]
Next, a second embodiment of the present invention will be described with reference to FIGS.
The same members as those in the first embodiment are designated by the same reference numerals, and detailed description thereof is omitted.
[0040]
The resection assisting device 60 according to this embodiment includes a first clip 61, a second clip 62, and a compression coil spring 63 (traction connecting member) (elastic member).
The illustrated first clip ( first hooking member ) 61 is a member for grasping and lifting a lesion (target site) in a patient (target) body. The clip 61 is made of an elastic material bent into a U-shape, and includes a pair of opening / closing pieces 61a urged away from each other by the elasticity thereof. A tip portion 61b is formed. The relative distance between the two opening / closing pieces 61a is variable, and the both opening / closing pieces 61a are provided with a ratchet member 61c for fixing the position after adjusting the mutual distance. As shown in FIG. 11, the ratchet member 61c includes a pair of engaging pieces 61c1, and engaging teeth 61c2 that can be engaged and disengaged with each other are formed on the opposing surfaces of the engaging pieces 61c1. . The ratchet member 61c has a function of preventing the deformation when the pair of opening / closing pieces 61a is elastically deformed in the direction of reducing the distance and maintaining the distance after adjusting the distance between the opening / closing pieces 61a. Further, an engagement hole (engagement portion) 61d is formed between the base end portions of the both opening and closing pieces 61a.
[0041]
Similarly, a second clip ( second hooking member ) 62 shown in the figure has the same structure as the first clip 61, and includes an opening / closing piece 62a, a tip end portion 62b, a ratchet member 62c, and an engagement hole (engagement portion) 62d. And the lesioned part (target part) is grasped between the two end parts 62b.
[0042]
The compression coil spring 63 includes hook portions 63b and 63c at both ends of the spring portion 63a.
[0043]
Although illustration is omitted, the first clip 61 is grasped outside the body by the grasping member 41 of the grasping forceps 40, inserted into the organ B by the grasping forceps 40 in the state as it is, and the lesion is opened by opening the grasping member 41. Placed near the part X. The second clip 62 is also placed in the vicinity of the lesion X in the same manner.
Then, after thus placed with the first clip 61 second clip 62 in the vicinity of the lesion X, by tightening the ratchet member 61c of the first clip 61 by operating the grasping forceps 40, the first clip 61 Both the open / close pieces 61a are closed, and one end X1 of the lesion X is grasped by the both ends 61b (see FIG. 10).
Further, the other end X2 of the lesion X is grasped by the both ends 62b of the second clip 62 in the same manner.
[0044]
The compression coil spring 63 is inserted into the organ B by the grasping forceps 40 in the state where the hook portion 63b is grasped by the grasping member 41 of the grasping forceps 40 outside the body.
And after putting the grasping member 41 and the compression coil spring 63 into the organ B, the hook member 63b of the compression coil spring 63 is engaged with the engagement hole 61d of the first clip 61 by the grasping member 41, and thereafter The gripping member 41 pulls the hook portion 63c toward the second clip 62 against the urging force of the spring portion 63a, engages the hook portion 63c with the engagement hole 62d of the second clip 62, and resects the organ B. The auxiliary device 60 is assembled.
[0045]
Thus, when assembling the ablation auxiliary device 60 in a state in which the first clip 61 second clip 62 was hooked on the lesion X, the compression coil spring 63 is extended as compared to the initial state, the spring portion 63a, the An urging force that pulls the first clip 61 and the second clip 62 toward each other is generated. For this reason, the first clip 61 is drawn toward the second clip 62, and the lesion X1 is pulled in a desired direction.
[0046]
Therefore, according to this embodiment as well, a sufficiently large excision portion can be formed at the boundary between the lesion X and the normal tissue, and further, the lesion by using an incision tool such as the high-frequency knife 50. The entire X can be cut smoothly (not shown), and the same effect as in the first embodiment can be obtained.
[0047]
Finally, a third embodiment of the present invention will be described with reference to FIGS.
The same members as those in the first and second embodiments are designated by the same reference numerals, and detailed description thereof is omitted.
[0048]
The resection assisting device 70 of the present embodiment includes a first clip 61 and a second clip 62 having the same configuration as that of the second embodiment, and a string-like flexible connector 71 (traction connecting member).
The flexible connector 71 includes a string portion 71a that is flexible and has no elasticity, and four hook portions 71b, 71c, 71d, and 71e fixed to both ends and an intermediate portion of the string portion 71a. is there.
[0049]
The first clip 61 and the second clip 62 are inserted into the organ B in the same manner as in the second embodiment. Then, by using the gripping member 41, both end portions X1 and X2 of the lesioned portion X are gripped between the tip portions 61b and 62b of both the clips 61 and 62 (see FIG. 12).
[0050]
The flexible connector 71 is inserted into the organ B by the grasping forceps 40 in a state where the hook 71b is grasped by the grasping member 41 of the grasping forceps 40 outside the body.
Further, the hook member 71b at one end is engaged with the engagement hole 61d of the first clip 61 by the holding member 41, and then the hook portion 71e at the other end is further connected to the second clip by the holding member 41. The resection assisting device 70 is assembled in the organ B by being engaged with the engagement holes 62 d of 62.
Then, when the hook portion 71e is engaged with the engagement hole 62d, the string portion 71a is tensioned and tension T (see FIG. 12) is generated in the string portion 71a. Therefore, the first clip 61 is drawn toward the second clip 62 side. The lesioned part X1 is pulled in a desired direction. Therefore, according to this embodiment as well, a sufficiently large excision portion can be formed at the boundary between the lesion X and normal tissue, and the entire lesion X can be excised smoothly.
[0051]
Thereafter, when the hook portion 71e is removed from the engagement hole 62d by the grasping forceps (not shown) 40 and the hook portion 71d is engaged with the engagement hole 62d, a greater tension is generated in the string portion 71a . Since the clip 61 is further pulled toward the second clip 62 side, the excision force by the high-frequency knife 50 smoothly spreads from the one end X1 side of the lesion X1 to the other end X2 side. Further, as shown in FIG. 13, when the hook portion 71c is engaged with the engagement hole 62d using the grasping forceps 40, a larger tension is generated in the string portion 71a, and the first clip 61 is moved to the second clip 62 side. Therefore, the excision area further expands toward the end X2, and finally the lesion X is completely excised (not shown).
[0052]
As described above, according to the present embodiment, as in the first and second embodiments, a sufficiently large excision portion can be formed at the boundary portion between the lesion X and the normal tissue. The entire lesioned part X can be smoothly excised with an incision tool such as a scalpel 50.
[0053]
Furthermore, since the tension T generated in the string portion 71a is changed by selecting the hook portions 71c, 71d, 71e to be engaged with the engagement holes 62d of the second clip 62, the boundary portion between the lesioned portion X and the normal tissue It is possible to adjust the size of the excised portion to be formed.
[0054]
The present invention has been described above with reference to each embodiment. However, the present invention is not limited to the above-described embodiment, and can be improved or modified within the scope of the purpose of the improvement or the idea of the present invention. For example, instead of the first clips 2 and 61 and the second clips 3 and 62, fishhook-like needle members ( first hooking member and second hooking member ) (not shown) that can pierce the lesion X It is also possible to prepare two and connect these needle members with the rubber band 4, the compression coil spring 63, and the flexible connector 71.
[0055]
【The invention's effect】
As described above, according to the present invention, an endoscopic resection assisting device and a resection assisting device that are capable of pulling a lesioned part in a predetermined direction during resection, in a simple and reliable manner, and at a lower cost than in the past. It becomes possible to provide a treatment method using an endoscope.
[Brief description of the drawings]
FIG. 1 is a diagram showing a configuration of a resection assisting device according to a first embodiment of the present invention.
FIG. 2 is a diagram showing the shape of a clip.
FIG. 3 is a side view showing a state where a patient is placed on a bed.
FIG. 4 is an overall view of an endoscope used when excising a lesioned part.
FIG. 5 is a diagram showing a procedure for introducing a resection assisting device into an internal organ.
FIG. 6 is also a diagram showing a procedure for introducing a resection assisting device into an internal organ.
FIG. 7 is a diagram showing a lesion excision step using an excision assisting device.
FIG. 8 is a diagram similarly showing a lesion excision step using an excision assisting device.
FIG. 9 is a diagram showing a state in which a lesioned part is completely excised by excision of the lesioned part using the excision assisting device.
FIG. 10 is a diagram showing a lesion excision step similar to FIG. 7 of the second embodiment of the present invention.
FIG. 11 is an enlarged cross-sectional view of a ratchet member.
FIG. 12 is a view showing a lesion excision step similar to FIG. 7 of the third embodiment of the present invention.
FIG. 13 is also a diagram showing a lesion excision step.
[Explanation of symbols]
1 excision assisting device 2 first clip ( first hooking member )
2a engaging portion 2b tip portion 2c first base piece 2d tip portion 2e second base piece 2f adjusting member 3 second clip (second hooking member )
3a Engaging portion 3b Tip portion 3c First base piece 3d Tip portion 3e Second base piece 3f Adjustment member 4 Rubber band (traction connecting member) (elastic member)
5 Bed 10 Endoscope 11 Insertion portion 11a Tip surface 12 Air / water supply nozzle 13 Illumination window 14 Observation window 15 Forceps channel outlet 16 Forceps insertion port projection 16a Inlet 20 Overtube 30 Flexible tube 40 Grip forceps 40a Flexible Tube 41 Gripping member 50 High-frequency knife 50a Tip 60 Resection assisting device 61 First clip (first hooking member)
61a Opening / closing piece 61b Tip 61c Ratchet member 61c1 Engagement piece 61c2 Engagement tooth 61d Engagement hole (engagement part)
62 Second clip (second hooking member)
62a Open / close piece 62b Tip 62c Ratchet member 62c1 Engagement piece 62c2 Engagement tooth 62d Engagement hole (engagement part)
63 Compression coil spring (traction connecting member) (elastic member)
63a Spring part 63b 63c Hook part 70 Cutting assistance device 71 Flexible coupling tool (traction coupling member)
71a String part 71b 71c 71d 71e Hook part A Patient (object)
A1 head B organ B1 submucosa B2 proper muscle layer X lesion (target site)
X1 X2 end

Claims (8)

対象物内部の対象部位を掛着する先端部、及び、該先端部とは異なる位置に形成した係合部を有する第1掛着部材と、
この第1掛着部材とは異なる位置で上記対象物内部に掛着される先端部、及び、該先端部とは異なる位置に形成した係合部を有する第2掛着部材と、
第1掛着部材の上記係合部第2掛着部材の上記係合部とを連結し、上記第1掛着部材を上記第2掛着部材側に牽引する牽引連結部材と、
を具備することを特徴とする内視鏡用切除補助装置。
A first hooking member having a tip part for hooking a target part inside the object , and an engaging part formed at a position different from the tip part ;
A second hooking member having a tip part hooked inside the object at a position different from the first hooking member , and an engaging part formed at a position different from the tip part ;
Traction connecting member connecting the said engaging portion of the engaging portion and the second hooking member of said first hooking member, pulling the first hooking member in the second hooking member side,
An endoscopic resection assisting device comprising:
請求項1記載の内視鏡用切除補助装置において、上記牽引連結部材が、上記第1掛着部材第2掛着部材とに係合される弾性部材である内視鏡用切除補助装置。The endoscopic resection assisting device according to claim 1, wherein the traction connecting member is an elastic member engaged with the first and second engaging members. 請求項2記載の内視鏡用切除補助装置において、上記弾性部材が、上記第1掛着部材第2掛着部材とに係合される輪ゴムである内視鏡用切除補助装置。The endoscopic resection assisting apparatus according to claim 2, wherein the elastic member is a rubber band engaged with the first and second engaging members . 請求項2記載の内視鏡用切除補助装置において、上記弾性部材が、両端部に、上記第1掛着部材第2掛着部材とにそれぞれ係合するフック部を具備する圧縮コイルばねである内視鏡用切除補助装置。The endoscopic resection assisting device according to claim 2, wherein the elastic member is a compression coil spring having hook portions engaged with the first and second hooking members at both ends, respectively. An endoscopic resection assist device. 請求項1記載の内視鏡用切除補助装置において、上記牽引連結部材が、柔軟なひも部と、該ひも部に、その長手方向に並べて固定された少なくとも3つのフック部と、を具備し、上記フック部はそのうちのいずれか2つを選択的に、上記第1掛着部材第2掛着部材とにそれぞれ係合するものである内視鏡用切除補助装置。The endoscopic resection assisting device according to claim 1, wherein the traction connecting member includes a flexible lace portion and at least three hook portions fixed to the lace portion in a longitudinal direction thereof, The endoscopic resection assisting device in which any two of the hook portions are selectively engaged with the first hooking member and the second hooking member , respectively. 請求項1から5のいずれか1項記載の内視鏡用切除補助装置において、上記第1掛着部材または第2掛着部材の少なくとも一方が、開閉可能で、上記対象部位を挟持可能なクリップである内視鏡用切除補助装置。The endoscopic resection assisting device according to any one of claims 1 to 5, wherein at least one of the first hooking member and the second hooking member is openable and closable, and the clip can hold the target portion. Endoscopic resection aid device. 請求項1から6のいずれか1項記載の内視鏡用切除補助装置において、上記第1掛着部材と第2掛着部材が同一構造である内視鏡用切除補助装置。The endoscopic resection assisting device according to any one of claims 1 to 6, wherein the first engaging member and the second engaging member have the same structure. 請求項1から7のいずれか1項記載の内視鏡用切除補助装置において、上記牽引連結部材が、上記第1掛着部材及び第2掛着部材に対して着脱自在である内視鏡用切除補助装置。The endoscopic resection assisting device according to any one of claims 1 to 7, wherein the traction connecting member is detachable with respect to the first and second hooking members. Resection aid.
JP2003120258A 2003-04-24 2003-04-24 Endoscopic resection aid Expired - Lifetime JP4320207B2 (en)

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