JP4349850B2 - Endoscope anchor remote guidance system - Google Patents

Endoscope anchor remote guidance system Download PDF

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Publication number
JP4349850B2
JP4349850B2 JP2003172237A JP2003172237A JP4349850B2 JP 4349850 B2 JP4349850 B2 JP 4349850B2 JP 2003172237 A JP2003172237 A JP 2003172237A JP 2003172237 A JP2003172237 A JP 2003172237A JP 4349850 B2 JP4349850 B2 JP 4349850B2
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JP
Japan
Prior art keywords
anchor
magnetic
endoscope
guidance system
base
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JP2003172237A
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JP2005006754A (en
Inventor
哲也 樽本
健一 大原
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、内視鏡観察下で病変部を切除する際に用いる、内視鏡用アンカー遠隔誘導システムに関する。
【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、例えば内視鏡的粘膜切除術(EMR)では、体内には内視鏡を一台しか挿入できないため、病変部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等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、人体の臓器内部の病変部を把持する把持部材と、磁性体からなる磁気アンカーと、該把持部材と該磁気アンカーとを連結する連結部材と、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、把持部材によって把持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遠隔誘導システムを提案し、特許出願している(特願2002−268239号)。
【0006】
【発明の目的】
本発明の目的は、上記特許出願の発明を改良することにより、対象部位の切除が迅速かつ容易に行うことができるだけでなく、アンカーと把持部材の間の距離を調整可能とすることにより、対象物内部においてアンカーを所定方向に移動させた際に、連結部材が常に緊張するようにした内視鏡用アンカー遠隔誘導システムを提供することにある。
【0007】
【発明の概要】
本発明の内視鏡用アンカー遠隔誘導システムは、対象物内部の対象部位を把持可能な把持部材と、磁性体からなる磁気アンカーと、該把持部材と該磁気アンカーとを接続する変形可能な線状の連結部材と、上記対象物外部に配置され、磁界を発生する磁気アンカー誘導装置と、を具備し、該磁気アンカー誘導装置が発生する磁界からの磁力により、上記磁気アンカーを移動させて、上記把持部材に把持された対象部位を所定方向に移動させる内視鏡用アンカー遠隔誘導システムであって、一端部が上記把持部材に結合された連結部材が、その長手方向に沿って複数の孔部を有し、上記磁気アンカーが、これら孔部のいずれかと選択的に係合する係合部材を具備することを特徴としている。
【0008】
上記磁気アンカー誘導装置は、発生する磁界によって磁力を生じさせて、該磁力によって、上記磁気アンカーを所定方向に移動させる磁気誘導部材と、該磁気誘導部材を特定の一平面内に配置したU字状のフレーム部材に沿って移動させる一平面内移動機構と、上記U字状のフレーム部材を上記一平面と直交する方向に相対移動させる一方向移動機構と、を有するのが実際的である。
【0009】
別の態様によれば、本発明の内視鏡用アンカー遠隔誘導システムは、対象物内部の対象部位を把持可能な把持部材と、非磁性体からなる重力アンカーと、該把持部材と該重力アンカーとを接続する変形可能な線状の連結部材と、を具備し、上記重力アンカーを重力に従って移動させて、上記把持部材に把持された対象部位を所定方向に移動させる内視鏡用アンカー遠隔誘導システムであって、一端部が上記把持部材に結合された連結部材が、その長手方向に沿って複数の孔部を有し、上記磁気アンカーが、これら孔部のいずれかと選択的に係合する係合部材を具備することを特徴としている。
【0010】
いずれの態様でも、上記連結部材が柔軟な連結ひもであり、上記孔部が、該連結ひもを結ぶことにより形成された輪部であるのが実際的である。
【0011】
また、いずれの態様でも、上記連結部材がチェーンをとし、上記孔部を、該チェーンを構成するリングとすることも可能である。
【0012】
いずれの態様でも、上記係合部材が、略C字状をなし、その一方の端部側から上記孔部に係合可能な基部と、該基部の他方の端部に回動可能に枢着され、該基部の両端間に形成された隙間を開閉する開閉片と、を具備するのが実際的である。
【0013】
さらに、いずれの態様でも、上記係合部材が、上記開閉片を、上記基部の隙間を塞ぐ閉方向に常時回転付勢する付勢手段を具備するのが実際的である。
【0014】
いずれの態様でも、さらに、先端が開口し、かつ、上記係合部材の基部が嵌合可能な嵌合溝を有する筒状のシースと、該シース内に該シースの長手方向に相対移動可能に挿入され、かつ、上記係合部材の基部が上記嵌合溝に係合した状態で、該シースに対して相対移動すると、該シースの先端開口より突出している先端部が、上記開閉片を上記隙間を開放する開方向に回転させる棒状の押圧兼掛替部材と、を備える掛替装置を具備するのが実際的である。
【0015】
さらに、上記押圧兼掛替部材が、上記係合部材の基部が上記嵌合溝に係合した状態で、上記先端部により上記開閉片を上記開方向に押圧したまま、上記連結部材に対して上記係合部材を相対移動させることにより、上記基部に係合していた孔部を該基部から抜け出させることが可能であるのが好ましい。
【0016】
さらに、上記押圧兼掛替部材が、上記基部に係合していた孔部が該基部から抜け出し、かつ、上記係合部材の基部が上記嵌合溝に係合している状態で、上記先端部に該基部から抜け出した孔部とは異なる孔部を係合しながら、該先端部により上記開閉片を上記開方向に押圧し、該孔部を上記係合部材の基部に係合させることが可能であるのが好ましい。
【0027】
【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21を参照しながら説明する。本実施形態のアンカー遠隔誘導システムは、磁気アンカー装置10(把持部材11、磁気アンカー12、連結ひも13、牽引分離部材14、筒状締付部材15からなる)と、磁気アンカー装置10の内視鏡20からの分離操作等を行う操作装置30と、磁気アンカー装置10を体外において吸引制御する(磁気アンカー12に磁力を及ぼす)磁気アンカー誘導装置40とからなるものである。
【0028】
まず、図1から図3を参照して、磁気アンカー装置10の構成について説明する。
対称形状をなす把持部材11は、金属板を折曲加工した弾性部材であり、自由状態においてその両側部の先端が接触するCリング状の基部11aと、基部11aの先端から前方に延びつつ拡開する一対の傾斜片11b、11bと、両傾斜片11b、11bの先端から互いに平行に延びる開閉片11c、11cと、両開閉片11c、11cの先端部を折曲して形成した爪部11d、11dとを具備している。さらに、基部11aの後端部には挿入孔11a1が穿設されている。
【0029】
磁気アンカー12は、略円柱状の本体部12aと、該本体部12aに突設された突部12bと、該突部12bに設けられた係合部材12cとからなる。本体部12aと突部12bは、強磁性材料によって成形されており、強磁性材料の具体例としては、純鉄、鉄合金のほか、プラチナマグネット、希土類磁石、テルビウム・ディスプロシウム・鉄合金などの磁石がある。
係合部材12cは、略C字形をなす基部12c1と、基部12c1の一端に回動自在に枢着され、基部12c1の他端に接触することにより、基部12c1の両端間に形成された隙間を塞ぎ、該他端から離間することにより該隙間を開放する開閉片12c2とを具備している。さらに係合部材12cは、開閉片12c2を、該隙間を塞ぐ閉方向に常時付勢する付勢ばね(付勢手段)(図示略)を有しており、そのため、図1から図3等に示すように、常時は開閉片12c2が上記隙間を塞いでいる。
【0030】
把持部材11の基部11aには、柔軟な連結ひも(連結部材)13の基端が、基部11aに対して摺動自在として結ばれている。この連結ひも13には、その中間部分を結ぶことにより、その長手方向に沿って複数の輪部(孔部)13aが形成されている。図1から図3では、連結ひも13の先端に形成された輪部13aに、磁気アンカー12の係合部材12cの基部12c1が挿通しており、このように、連結ひも13によって磁気アンカー12と把持部材11とが連結されている。
【0031】
牽引分離部材14は棒状の部材であり、その先端には、把持部材11の挿入孔11a1を貫通する一対の挿入片14aと、挿入片14aの先端に設けられた、基部11aの内面に係合して、挿入片14aが基部11aから抜け出すのを防止する抜け止め部14bとが設けられている。さらに、牽引分離部材14の基端部には鈎部14cが形成されている。牽引分離部材14は、プラスチックやSUS等の金属材料から成形されており、所定の切断力以上の強い力を受けると切断される程度の強度である。
【0032】
図1から図3等に示す両端が開口する筒状締付部材15は、可撓性のある材料からなるものである。この筒状締付部材15には、筒状締付部材15と同方向を向く一対のスリット15aが形成されている。このスリット15aの前端は開放しており後端は閉塞している。さらに、この筒状締付部材15の内径は、把持部材11の基部11aと傾斜片11bが嵌合可能な寸法となっている。
【0033】
図1に示す状態(把持部材11が筒状締付部材15内に嵌合していない状態)から、筒状締付部材15に対して牽引分離部材14を相対的に後方に引くと、図2に示すように、把持部材11の基部11aが内向きに弾性変形しながら筒状締付部材15の内部に引き込まれる。すると、基部11aの径が小さくなり、両傾斜片11bと両開閉片11cが互いに離れる開状態となる。
図3に示すように、筒状締付部材15に対して牽引分離部材14をさらに相対的に後方に引くと、把持部材11が内向きに弾性変形しながら筒状締付部材15の内部にさらに引き込まれ、その傾斜片11bが筒状締付部材15の先端開口部に接触し、両開閉片11cと両爪部11dが互いに接近する閉状態となる。
【0034】
図4は、アンカー遠隔誘導システムを用いた切除術の実施に用いる内視鏡20を示している。
内視鏡20は周知のように、柔軟で可撓性を有し体内に挿入される挿入部21を有しており、その先端面22には、エア及び洗浄水を送るための送気送水ノズル(図示略)、切除部及びその周辺を照らすための照明窓(図示略)、直後に対物レンズと撮像素子が配置された切除部及びその周辺を観察するための観察窓、並びに、図7等に示された鉗子チャネルCの出口23が設けられている。鉗子チャンネルCは挿入部21内に形成されており、その入口24aは鉗子口24の端面に形成されており、さらに、その出口23は、先端側が拡径するテーパ状となっている。
【0035】
次に、図7を参照しながら、内視鏡20の鉗子チャンネルC内に挿入される操作装置30について説明する。
挿入管31は可撓性を有する筒状の部材であり、内視鏡20の鉗子口24の入口24aから鉗子チャンネルCに挿通可能である。さらに、その内径は、図1の状態の把持部材11及び筒状締付部材15を挿入可能な寸法となっている。挿入管31の内部には、挿入管31に対して相対移動可能な筒状の挿入コイル32が挿通されている。挿入コイル32の先端部には、大径部33aと小径部33bとからなる規制管33の小径部33bが嵌合され、接着剤、はんだ、ロウなどによって、小径部33bが挿入コイル32の先端部に固着されている。
【0036】
大径部33aの外径は挿入管31の内径より小さく、かつ、挿入コイル32の外径とほぼ同一に設定されている。さらに、大径部33aの内径は小径部33bの内径より大きく、筒状締付部材15の外形と略同一に設定されており、大径部33a内面の小径部33b内面との接続部には、規制管33の軸線に対して直交する環状段部33a1が形成されている(図7等参照)。
【0037】
鉗子チャンネルCに挿入された挿入コイル32の内側には、先端にフック部34が設けられた操作ワイヤ35が、挿入コイル32と規制管33に対して相対移動可能に挿入されている。フック部34は、接着剤、はんだ、ロウ等によって、その基端部が操作ワイヤ35の先端部に固着されている。
さらに、挿入管31、挿入コイル32、及び操作ワイヤ35の各基端部は、操作装置30の操作部(図示略)に連結されており、互いに軸方向に相対移動可能となっている。
以上説明した、挿入管31、挿入コイル32、規制管33、フック部34、操作ワイヤ35、及び操作部により操作装置30が構成されている。
【0038】
次に、図5及び図6を用いて、患者Aの体外において磁気アンカー12を吸引制御する磁気アンカー誘導装置40の構成について説明する。
患者Aを載せる床板41aを具備するベッド41の両側部には、一対のXYステージ(一方向移動機構)42、42が配設されている。この一対のXYステージ42は、ベッド41の長手方向に沿って、両者42、42の該長手方向位置が常時同じになるように、直線的に往復移動するものである。さらに、ベッド41の上方には、ベッド41の長手方向と直交する平面内において互いに平行をなす、正面視略逆U字形の二つのレール44、45からなるフレーム/レール(一平面内移動機構)43が配設されており、このフレーム/レール43の両端部は、左右のXYステージ42にそれぞれ固定されている。内側のレール44には、磁気アンカー12を体外において吸引制御する(磁気アンカー12に磁力を及ぼす)磁気誘導部材46が摺動自在に装着されており、磁気誘導部材46は左右のXYステージ42の間を、レール45に沿って移動することができる。磁気誘導部材46は、鉄心にコイルを巻いた構造の電磁石47を基体48上に固定したものであり、その電磁石47は常時、患者A側を向いている(図5参照)。なお、磁気誘導部材46は、永久磁石と電磁石の組み合わせでもよく、また、永久磁石と電磁石を2個以上組み合わせたものでも良い。
【0039】
フレーム/レール43の外側のレール45には、フレーム/レール43全体の重量バランスを保つためのカウンターウエイト49がレール45に摺動自在に装着されている。カウンターウエイト49は、磁気誘導部材46の位置に応じて、その位置が変化する。例えば、磁気誘導部材46が患者Aの正面側に位置するときは、カウンターウエイト49は患者Aの背面側に位置し、磁気誘導部材46が患者Aの背面側にあるときは、カウンターウエイト49は患者Aの正面側に位置して、フレーム/レール43全体の重量バランスをとっている。
そして、以上説明した磁気誘導部材46、XYステージ42、フレーム/レール43により磁気アンカー誘導装置40が構成されている。
【0040】
次に、アンカー遠隔誘導システムを用いた病変部Xの切除要領について説明する。
アンカー遠隔誘導システムを用いた切除術の実施に先立っては、まず、図5及び図6に示すように、局所麻酔を施した患者Aをベッド41の床板41a上に横たわらせる。このとき、XYステージ42を操作して、フレーム/レール43のベッド41の長手方向位置を、患者Aの頭部A1とほぼ同じ位置にしておき、さらに、磁気誘導部材46及びカウンターウエイト49を所定の場所に位置させておく。
次に、XYステージ42を操作してフレーム/レール43を患者Aの正面側に配置させ、さらに、磁気誘導装置46をフレーム/レール43に沿って移動させて、磁気誘導部材46を切除術開始時位置に位置させる(図6参照)。
【0041】
次いで、図示を省略した可撓性を有するオーバーチューブを、患者Aの口から体内に挿入する。続いて、内視鏡20の挿入部21をオーバーチューブ内に挿入し、挿入部21の先端部をオーバーチューブの先端から突出させ、臓器B(対象物)(図8から図10等参照)の病変部(対象部位)Xに近接させる(図示略)。このように、内視鏡20の挿入部21の先端を臓器B内に挿入すると、内視鏡20の挿入部21の先端面22に設けられた観察窓から得られた臓器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。
【0042】
次いで、鉗子口24の入口24a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)を鉗子チャンネルCに挿入して、その注射針を鉗子チャンネルCの出口23から突出させる。そして、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等を注入し、病変部Xを固有筋層B2から浮き上がらせておく(図8から図11、図21、及び図22参照)。
【0043】
続いて、鉗子チャンネルCから該処置具を取り出す。次に、挿入管31、挿入コイル32、規制管33、フック部34、操作ワイヤ35、及び操作部を一体化した操作装置30を、鉗子口24から鉗子チャンネルCに挿入する。
この際、鉗子チャンネルCに操作装置30を挿入すると、操作装置30の操作部及び、挿入管31と挿入コイル32と操作ワイヤ35の基端部が鉗子口24の後方に突出する(図示略)。
また、筒状締付部材15は可撓性を有する材料から成形されており、かつ、挿入コイル32は屈曲自在なので、挿入部21が屈曲していても、これらの部材は鉗子チャンネルC内をスムーズに移動することができる。
【0044】
操作装置30の先端が鉗子チャンネルCの先端部に到達したら、鉗子口24から突出している操作ワイヤ35の基端部を掴んで、操作ワイヤ35を操作してフック部34のみを内視鏡20の先端面22から突出させ、このフック部34に牽引分離部材14の鈎部14cを係合して、操作ワイヤ35を操作部側に引く。すると、図7に示すように、筒状締付部材15の基端部が規制管33の大径部33aに嵌合するとともに、把持部材11と連結ひも13と牽引連結部材14と磁気アンカー12の突部12bが鉗子チャンネルC内に引き込まれ、磁気アンカー12の本体部12aの端面が、挿入部21の先端面22に当接し、磁気アンカー装置10と操作装置30が一体化する。
【0045】
このように、内視鏡20に磁気アンカー装置10と操作装置30をセットしたら、図8に示すように、鉗子口24から後方に突出している挿入管31の基端部を掴み、挿入管31を挿入部21の先端側に移動させて、その先端部を先端面22から突出させ、磁気アンカー12を鉗子チャンネルCから押し出す。
次いで、挿入コイル32を挿入部21の先端側に移動させて、把持部材11を挿入管31の先端から突出させ、把持部材11を病変部Xに近接させる。この状態で操作ワイヤ35を内視鏡20に対して相対的に後方に引くと、把持部材11の基部11aが筒状締付部材15内に引き込まれ、把持部材11は図8に示す開状態となる。
【0046】
さらに操作ワイヤ35を後方に引くと、把持部材11の基部11aが筒状締付部材15内部の後方にさらに引き込まれ、かつ、傾斜片11bが筒状締付部材15の先端開口部に当接するので、把持部材11の開閉片11cが閉じて、両爪部11dにより病変部Xが確実に把持される(図9参照)。
【0047】
この状態で、操作ワイヤ35を上記切断力以上の強い力で後方に引くと、フック部34と係合している牽引分離部材14が、その中間部で切断され、その結果、磁気アンカー装置10が操作ワイヤ35から分離する(図10参照)。
続いて、患者Aの体外に配置されている磁気誘導部材46の発生磁界を強めることによって、磁気アンカー12を磁気誘導部材46側に吸引する。このとき、連結ひも13が緊張すれば、把持部材11によって把持した病変部Xを磁気誘導部材46側に持ち上げることができる。
【0048】
また、図11に示すように、連結ひも13が緊張しない状態で、磁気アンカー12が臓器Bの内壁に接触してしまった場合には、把持部材11によって把持した病変部Xを磁気誘導部材46側に持ち上げることができないので、このような場合には、図12に示す掛替装置50を用いて、連結ひも13の、把持部材11との固着部から係合部材12cとの係合部までの長さを調整する。
【0049】
この掛替装置50は、可撓性を有し両端が開口するシース51と、シース51の内部に相対移動可能に挿通された棒状の押圧兼掛替部材52とからなるものである。シース51の先端面には係合部材12cの基部12c1が嵌合可能な嵌合溝51aが形成されており、押圧兼掛替部材52の先端には、その本体に対して直交する操作片(先端部)52aが形成されている。この操作片52は、常に、シース51の先端から突出しており、さらに、押圧兼掛替部材52の基端部は、シース51の基端から突出している(図示略)。
【0050】
長さ調整を行うには、内視鏡20の鉗子チャンネルCに掛替装置50を挿入して、その先端部を挿入部21の先端面22から突出させ、シース51と押圧兼掛替部材52の基端部を、鉗子口24から突出させる(図示略)。
そして、図13に示すように、シース51の嵌合溝51aに係合部材12cの基部12c1を嵌合し、この状態で、押圧兼掛替部材52の基端部を掴みその基端側に引くと、操作片52aが係合部材12cの開閉片12c2を付勢ばねの付勢力に抗して開方向に押圧し、開閉片12c2を図14に示す開位置に移動させる。
この状態で、基端部を掴みながら押圧兼掛替部材52を操作して、磁気アンカー12を所定の方向に移動させることにより、係合部材12cの基部12c1を連結ひも13の輪部13aから脱出させ、磁気アンカー12と連結ひも13を分離する(図15参照)。
【0051】
続いて、図16に示すように、押圧兼掛替部材52を移動させて、その嵌合溝51aを係合部材12cの基部12c1から脱出させて、その後、図17に示すように、長さ調整部材50を連結ひも13側に移動させて、その操作片52aを、連結ひも13の先端より基端側に位置する輪部13aに係合する。
次いで、磁気誘導部材46の発生磁界を一旦弱めて、磁気アンカー12を病変部X側に接近させる(図示略)。
【0052】
続いて、この状態を維持したまま、図18に示すように、掛替装置50を磁気アンカー12側に接近させ、シース51の嵌合溝51aに係合部材12cの基部12c1を嵌合させる。
この状態で、押圧兼掛替部材52をその基端側に引くと、図19に示すように、その操作片52aが、係合部材12cの開閉片12c2を付勢ばねの付勢力に抗して開方向に押圧するとともに、操作片52aに係合していた輪部13aを基部12c1側に移動させ、基部12c1の一端から基部12c1に係合させる。
【0053】
このように、連結ひも13の、把持部材11との固着部から係合部材12cとの係合部までの長さを短くしたら、磁気誘導部材46の発生磁界を再び強めて、磁気アンカー12を磁気誘導部材46側に吸引する。すると、図20に示すように、磁気アンカー12と把持部材11の間で連結ひも13が緊張して、把持部材11に把持されている病変部Xが図20の上方に十分な距離だけ持ち上げられる。
【0054】
このように、病変部Xを所望方向に所望距離だけ移動させると、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、挿入管31、挿入コイル32、及び操作ワイヤ35を内視鏡20から取り出し、図20に示すように、内視鏡20(図20では図示略)の鉗子チャネルCを利用して高周波メス60などの切開具を臓器B内に挿入し、病変部Xを粘膜とともに一方の端部側から切除する。
そして、病変部Xを一方の端部側から反対の端部側に切除すると、やがて、病変部X全体が完全に切除される(図21参照)。
なお、高周波メス60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60の先端60aの位置の確認は、より容易となる。
【0055】
以上のように切除作業を終えると、正常組織から切り離された病変部Xは把持部材11(磁気アンカー装置10)に把持されたままの状態となるので、病変部Xの紛失が防止される。
切除した病変部Xを回収するには、図21に示すように、内視鏡20の鉗子チャンネルCに、その先端部に開閉可能な一対の把持片71を具備し、さらに、その基端部に操作部(図示略)を具備する把持鉗子70を挿入する。そして、この操作部を操作して、把持片71を開放状態にした状態で牽引分離部材14に近接させ、その後に両把持片71を閉じて、両把持片71により牽引分離部材14を確実に把持する。そして、そのままの状態で内視鏡20を体内から抜き去り、病変部Xを磁気アンカー装置10とともに体外に取り出し、その後に、そして、切除した部分の縫合、消毒などの処置を行う。
【0056】
以上のように、本実施形態のアンカー遠隔誘導システムを用いれば、連結ひも13の、把持部材11との固着部から係合部材12cとの係合部までの長さを調整することにより、臓器Bの大きさに拘わらず、常に連結ひも13を緊張させて、病変部Xを持ち上げることが可能になる。
【0057】
さらに、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る。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るので、このような場合であっても、病変部Xを容易に切除することが可能となる。
【0058】
さらに、病変部Xは把持部材11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、任意の位置に把持部材11を配置できるため、切除した病変部Xにより内視鏡20の視界が妨げられることがない。
【0059】
次に、本発明の第2の実施形態について、図22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。
【0060】
本実施形態のアンカー遠隔誘導システムは、磁気アンカー装置80(把持部材11、磁気アンカー12、チェーン81、牽引分離部材14、筒状締付部材15からなる)と、操作装置30と、磁気アンカー誘導装置40とからなるものである。
【0061】
この実施形態では、連結ひも13の代わりにチェーン(連結部材)81を用いて、把持部材11と磁気アンカー12とを連結している。チェーン81は多数のリング82を連結することにより構成されたものである。図22に示す状態では、その基端に位置するリング82が把持部材11の基部11cに係合し、その先端に位置するリング82が、磁気アンカー12の係合部材12cに係合している。
【0062】
この磁気アンカー装置80は、第1の実施形態と同じ要領により、内視鏡20に装着された状態で臓器B内に挿入された後、その把持部材11が病変部Xを把持する。
そして、磁気誘導部材46から磁界を発生させて磁気アンカー12を移動させても、チェーン81が緊張しない場合は、第1の実施形態と同様に、掛替装置50を用いて、係合部材12cの基部12c1に、先端に位置するリング82より基端側に位置するリング82を係合させる(図示略)。
【0063】
このようにして、チェーン81の基端から、チェーン81の係合部材12cとの係合部までの長さを調整することにより、臓器Bの大きさに拘わらず、磁気誘導部材46から磁界を発生させれば、常にチェーン81を緊張させて、病変部Xを持ち上げることが可能になる。
【0064】
最後に、本発明の第3の実施形態について、図23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。
【0065】
本実施形態のアンカー遠隔誘導システムは、重力アンカー装置90(把持部材11、重力アンカー91、連結ひも13、牽引分離部材14、筒状締付部材15からなる)と、操作装置30とからなるものである。
本実施形態の重力アンカー91は、磁気アンカー12と同形状の本体部91aと突部91bと係合部材12cとを具備しており、本体部91aと突部91bは非磁性材料によって成形されている。非磁性材料の具体例としては、金、銅、アルミニウム、ステンレス(オーステナイト系)、真鍮、セラミック、硝子等がある。
【0066】
この重力アンカー装置90は、第1の実施形態と同じ要領により、内視鏡20に装着された状態で臓器B内に挿入された後、その把持部材11が病変部Xを把持する。
重力アンカー91は重力Pに従って移動するので、患者Aの体勢を変えて、重力アンカー91を重力方向下方に移動させる。そして、連結ひも13が緊張せずに重力アンカー91が臓器Bの内壁に接触する場合には、第1の実施形態と同じ要領により、連結ひも13の、把持部材11との固着部から係合部材12cとの係合部までの長さを調整する。このような調整を行えば、第1の実施形態と同様に、臓器Bの大きさに拘わらず、常に連結ひも13を緊張させて、病変部Xを移動させることが可能になる。
さらに、本実施形態では、第1の実施形態では必要であった高価な装置である磁気アンカー誘導装置40が不要になるので、第1の実施形態に比べて、コスト的に有利である。
【0067】
本発明について上記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2の実施形態の磁気アンカー12を第3の実施形態の重力アンカー91に代え、さらにて、磁気アンカー誘導装置40を省略すれば、チェーン81を利用した重力アンカー装置が得られる。
【0068】
【発明の効果】
以上説明したように、本発明によると、対象部位の切除を迅速かつ容易に行うことができるとともに、アンカーと把持部材の間の距離を調整可能とすることにより、対象物内部においてアンカーを所定方向に移動させた際に、連結部材が常に緊張するようになる。
【図面の簡単な説明】
【図1】本発明の第1の実施形態の磁気アンカー装置の全体図である。
【図2】把持部材が開いた状態の磁気アンカー装置の全体図である。
【図3】把持部材が閉じた状態の磁気アンカー装置の全体図である。
【図4】内視鏡の全体図である。
【図5】病変部の切除が行われる患者を載せたベッドと、磁気アンカー誘導装置を、患者の頭部側から見た図である。
【図6】患者を載せたベッドと、磁気アンカー誘導装置の側面図である。
【図7】鉗子チャンネル内に、磁気アンカー装置と連係した状態で操作装置を挿入した状態を示す、内視鏡先端部の拡大縦断側面図である。
【図8】開いた状態で、内視鏡の先端から突出した把持部材が、病変部を掴む直前の状態を示す拡大縦断側面図である。
【図9】内視鏡の先端から突出した把持部材が閉じて、病変部を掴んだ状態を示す拡大縦断側面図である。
【図10】内視鏡の内部において、磁気アンカー装置と操作装置が分離した状態を示す拡大縦断側面図である。
【図11】把持部材が病変部を把持した後に、磁気アンカー誘導装置を用いて、病変部を持ち上げている状態を示す拡大縦断側面図である。
【図12】掛替装置の先端部の拡大断面図である。
【図13】シースの嵌合溝に磁気アンカーの係合部の基部を嵌合した状態を示す拡大図である。
【図14】押圧兼掛替部材により、開閉片を開方向に移動させている状態を示す拡大図である。
【図15】押圧兼掛替部材により、開閉片を開状態に維持して、連結ひもの輪部を基部から脱出させる状態を示す拡大図である。
【図16】シースの嵌合溝から、磁気アンカーの係合部の基部を離脱させた状態を示す拡大図である。
【図17】押圧兼掛替部材により連結ひもの他の輪部を係合した状態を示す拡大図である。
【図18】押圧兼掛替部材により連結ひもの他の輪部を係合したまま、シースの嵌合溝に磁気アンカーの係合部の基部を嵌合した状態を示す拡大図である。
【図19】押圧兼掛替部材により、開閉片を開方向に回転させ、かつ、連結ひもの他の輪部を、係合部の基部に嵌合させる状態を示す拡大図である。
【図20】連結ひもの長さ調整後に、磁気アンカー誘導装置を用いて、病変部を持ち上げている状態を示す拡大縦断側面図である。
【図21】臓器から切り離された病変部を把持する磁気アンカーを、把持鉗子により把持する状態を示す図である。
【図22】本発明の第2の実施形態の磁気アンカー装置の全体図である。
【図23】本発明の第3の実施形態の重力アンカー装置のチェーンの長さを調整した後に、重力アンカー装置を利用して、病変部を重力方向下方に移動させている状態を示す拡大縦断側面図である。
【符号の説明】
10 磁気アンカー装置
11 把持部材
11a 基部
11a1 挿入孔
11b 傾斜片
11c 開閉片
11d 爪部
12 磁気アンカー
12a 本体部
12b 突部
12c 係合部材
12c1 基部
12c2 開閉片
13 連結ひも(連結部材)
13a 輪部(孔部)
14 牽引分離部材
14a 挿入片
14b 抜け止め部
14c 鈎部
15 筒状締付部材
20 内視鏡
21 挿入部
22 先端面
23 鉗子チャンネルの出口
24 鉗子口
24a 入口
30 操作装置
31 挿入管
32 挿入コイル
33 規制管
33a 大径部
33a1 環状段部
33b 小径部
34 フック部
35 操作ワイヤ
40 磁気アンカー誘導装置
41 ベッド
41a 床板
42 XYステージ(一方向移動機構)
43 フレーム/レール(一平面内移動機構)
44 45 レール
46 磁気誘導部材
47 電磁石
48 基体
49 カウンターウェイト
50 掛替装置
51 シース
51a 嵌合溝
52 押圧兼掛替部材
52a 操作片(先端部)
60 高周波メス
60a 先端部
70 把持鉗子
71 把持片
80 重力アンカー装置
81 チェーン(連結部材)
82 リング(孔部)
90 重力アンカー装置
91 重力アンカー
91a 本体部
91b 突部
A 患者(対象物)
A1 頭部
B 臓器
B1 粘膜下層
B2 固有筋層
C 鉗子チャンネル
P 重力
X 病変部(対象部位)
[0001]
【Technical field】
The present invention relates to an endoscopic anchor remote guidance system used when excising a lesion 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 the normal mucous membrane around the lesion cannot be lifted with an injection needle. Saline was injected to raise the lesion, and in that state, a high-frequency knife or snare was used to perform excision between the lesion and the normal mucosa.
[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 was required.
[0005]
Therefore, in order to solve these problems, the applicant of the present invention has a gripping member for gripping a lesioned part inside a human organ, a magnetic anchor made of a magnetic material, and a connecting member for connecting the gripping member and the magnetic anchor. And a magnetic anchor guiding device that is arranged outside the human body and generates a magnetic field to power the magnetic anchor, and the magnetic anchor is powered by the magnetic field generated by the magnetic anchor guiding device and gripped by the gripping member A magnetic anchor remote guidance system characterized by lifting the lesioned part is proposed and a patent application has been filed (Japanese Patent Application No. 2002-268239).
[0006]
OBJECT OF THE INVENTION
The object of the present invention is to improve the invention of the above-mentioned patent application so that not only can the target site be excised quickly and easily, but also the distance between the anchor and the gripping member can be adjusted. An object of the present invention is to provide an endoscope anchor remote guidance system in which a connecting member is always tensioned when an anchor is moved in a predetermined direction inside an object.
[0007]
Summary of the Invention
An endoscope anchor remote guidance system according to the present invention includes a gripping member capable of gripping a target portion inside a target, a magnetic anchor made of a magnetic material, and a deformable wire connecting the gripping member and the magnetic anchor. And a magnetic anchor guide device that is arranged outside the object and generates a magnetic field, and moves the magnetic anchor by the magnetic force generated by the magnetic field generated by the magnetic anchor guide device, An endoscope anchor remote guidance system for moving a target part gripped by the gripping member in a predetermined direction, wherein a connecting member having one end coupled to the gripping member has a plurality of holes along its longitudinal direction. The magnetic anchor includes an engaging member that selectively engages with any one of these holes.
[0008]
The magnetic anchor guide device generates a magnetic force by a generated magnetic field, and moves the magnetic anchor in a predetermined direction by the magnetic force, and a U-shape in which the magnetic guide member is arranged in a specific plane. It is practical to have an in-plane moving mechanism that moves along the frame member and a unidirectional moving mechanism that relatively moves the U-shaped frame member in a direction perpendicular to the one plane.
[0009]
According to another aspect, an endoscope anchor remote guidance system according to the present invention includes a gripping member capable of gripping a target portion inside a target object, a gravitational anchor made of a nonmagnetic material, the gripping member, and the gravitational anchor. A deformable linear connecting member that connects the two, and remotely moving the gravitational anchor according to gravity to move the target portion gripped by the gripping member in a predetermined direction A connecting member, one end of which is coupled to the gripping member, has a plurality of holes along its longitudinal direction, and the magnetic anchor selectively engages any of these holes. An engaging member is provided.
[0010]
In any aspect, it is practical that the connecting member is a flexible connecting string, and the hole is a ring formed by connecting the connecting strings.
[0011]
In any aspect, the connecting member may be a chain, and the hole may be a ring constituting the chain.
[0012]
In any aspect, the engagement member is substantially C-shaped, and is pivotally attached to the base portion that can be engaged with the hole portion from one end side thereof and to the other end portion of the base portion. And an opening / closing piece that opens and closes a gap formed between both ends of the base.
[0013]
Furthermore, in any aspect, it is practical that the engaging member includes a biasing means that constantly biases the opening / closing piece in the closing direction to close the gap of the base portion.
[0014]
In any aspect, a cylindrical sheath having a fitting groove in which the tip is open and the base of the engaging member can be fitted, and the sheath can be relatively moved in the longitudinal direction of the sheath. When the base portion of the engagement member is inserted and is moved relative to the sheath in a state where the base portion of the engagement member is engaged with the fitting groove, the distal end portion protruding from the distal end opening of the sheath It is practical to have a changing device provided with a rod-like pressing and changing member that rotates in the opening direction to open the gap.
[0015]
Further, the pressing and switching member is pressed against the connecting member while pressing the opening / closing piece in the opening direction by the tip portion in a state where the base portion of the engaging member is engaged with the fitting groove. It is preferable that the hole engaged with the base can be removed from the base by relatively moving the engaging member.
[0016]
Further, in the state in which the hole portion engaged with the base portion is pulled out from the base portion and the base portion of the engagement member is engaged with the fitting groove, The opening / closing piece is pressed in the opening direction by the tip portion and the hole portion is engaged with the base portion of the engaging member while engaging the hole portion different from the hole portion that has come out of the base portion with the portion. Is preferably possible.
[0027]
DETAILED DESCRIPTION OF THE INVENTION
Hereinafter, a first embodiment of the present invention will be described with reference to FIGS. The anchor remote guidance system of the present embodiment includes a magnetic anchor device 10 (consisting of a gripping member 11, a magnetic anchor 12, a connecting string 13, a traction separating member 14, and a cylindrical fastening member 15) and an internal view of the magnetic anchor device 10. The operation device 30 performs a separation operation from the mirror 20 and the like, and the magnetic anchor guide device 40 that controls the magnetic anchor device 10 to be attracted outside the body (applies a magnetic force to the magnetic anchor 12).
[0028]
First, the configuration of the magnetic anchor device 10 will be described with reference to FIGS. 1 to 3.
The gripping member 11 having a symmetric shape is an elastic member obtained by bending a metal plate, and in a free state, a C-ring-shaped base portion 11a with which the tip ends of both sides come into contact with each other, and extending while extending forward from the tip end of the base portion 11a. A pair of inclined pieces 11b, 11b to be opened, opening / closing pieces 11c, 11c extending in parallel with each other from the tips of both inclined pieces 11b, 11b, and a claw portion 11d formed by bending the tip portions of both opening / closing pieces 11c, 11c. 11d. Further, an insertion hole 11a1 is formed in the rear end portion of the base portion 11a.
[0029]
The magnetic anchor 12 includes a substantially cylindrical main body 12a, a protrusion 12b protruding from the main body 12a, and an engaging member 12c provided at the protrusion 12b. The main body 12a and the protrusion 12b are formed of a ferromagnetic material. Specific examples of the ferromagnetic material include pure iron, iron alloy, platinum magnet, rare earth magnet, terbium / dysprosium / iron alloy, etc. There are magnets.
The engaging member 12c is pivotally attached to one end of the base portion 12c1 and a base portion 12c1 having a substantially C shape, and comes into contact with the other end of the base portion 12c1, thereby forming a gap formed between both ends of the base portion 12c1. An opening / closing piece 12c2 that closes and opens the gap by being separated from the other end is provided. Furthermore, the engaging member 12c has a biasing spring (biasing means) (not shown) that constantly biases the opening / closing piece 12c2 in the closing direction to close the gap. As shown, the opening / closing piece 12c2 normally closes the gap.
[0030]
A base end of a flexible connecting string (connecting member) 13 is connected to the base portion 11a of the gripping member 11 so as to be slidable with respect to the base portion 11a. A plurality of ring portions (hole portions) 13 a are formed along the longitudinal direction of the connecting string 13 by connecting the intermediate portions thereof. In FIG. 1 to FIG. 3, the base portion 12 c 1 of the engaging member 12 c of the magnetic anchor 12 is inserted into the ring portion 13 a formed at the distal end of the connecting cord 13, and thus the connecting strap 13 and the magnetic anchor 12 are connected. The holding member 11 is connected.
[0031]
The pulling / separating member 14 is a rod-shaped member, and at the tip thereof is engaged with a pair of insertion pieces 14a penetrating the insertion hole 11a1 of the gripping member 11 and the inner surface of the base portion 11a provided at the tip of the insertion piece 14a. Thus, a retaining portion 14b that prevents the insertion piece 14a from slipping out of the base portion 11a is provided. Furthermore, a flange portion 14 c is formed at the proximal end portion of the traction separation member 14. The pulling / separating member 14 is formed from a metal material such as plastic or SUS, and has such a strength that it can be cut when receiving a strong force exceeding a predetermined cutting force.
[0032]
The cylindrical fastening member 15 having both ends opened as shown in FIGS. 1 to 3 and the like is made of a flexible material. The cylindrical fastening member 15 is formed with a pair of slits 15 a that face in the same direction as the cylindrical fastening member 15. The front end of the slit 15a is open and the rear end is closed. Further, the inner diameter of the cylindrical fastening member 15 is such that the base 11a of the gripping member 11 and the inclined piece 11b can be fitted.
[0033]
From the state shown in FIG. 1 (the state in which the gripping member 11 is not fitted in the cylindrical fastening member 15), when the traction separation member 14 is pulled backward relative to the cylindrical fastening member 15, As shown in FIG. 2, the base 11a of the gripping member 11 is drawn into the cylindrical fastening member 15 while being elastically deformed inward. Then, the diameter of the base portion 11a is reduced, and the both inclined pieces 11b and the both open / close pieces 11c are in an open state in which they are separated from each other.
As shown in FIG. 3, when the traction separating member 14 is pulled further rearward relative to the cylindrical fastening member 15, the gripping member 11 is elastically deformed inward and enters the inside of the cylindrical fastening member 15. Further, the inclined piece 11b comes into contact with the tip opening of the cylindrical fastening member 15, and the open / close pieces 11c and the claws 11d come close to each other.
[0034]
FIG. 4 shows an endoscope 20 used to perform a resection using an anchor remote guidance system.
As is well known, the endoscope 20 has an insertion portion 21 that is soft and flexible and is inserted into the body, and the distal end surface 22 is supplied with air and water for supplying air and cleaning water. A nozzle (not shown), an illumination window (not shown) for illuminating the excision part and its periphery, an observation window for observing the excision part and its periphery where the objective lens and the image sensor are arranged immediately thereafter, and FIG. An outlet 23 of the forceps channel C shown in FIG. The forceps channel C is formed in the insertion portion 21, the inlet 24 a is formed on the end face of the forceps opening 24, and the outlet 23 is tapered so that the diameter of the distal end is increased.
[0035]
Next, the operation device 30 inserted into the forceps channel C of the endoscope 20 will be described with reference to FIG.
The insertion tube 31 is a flexible cylindrical member and can be inserted into the forceps channel C from the entrance 24 a of the forceps port 24 of the endoscope 20. Further, the inner diameter is such that the gripping member 11 and the cylindrical fastening member 15 in the state of FIG. 1 can be inserted. A cylindrical insertion coil 32 that is movable relative to the insertion tube 31 is inserted into the insertion tube 31. A small-diameter portion 33b of a regulation tube 33 composed of a large-diameter portion 33a and a small-diameter portion 33b is fitted to the distal end portion of the insertion coil 32, and the small-diameter portion 33b is distal to the distal end of the insertion coil 32 by an adhesive, solder, brazing, or the like. It is fixed to the part.
[0036]
The outer diameter of the large diameter portion 33 a is smaller than the inner diameter of the insertion tube 31 and is set to be substantially the same as the outer diameter of the insertion coil 32. Furthermore, the inner diameter of the large-diameter portion 33a is larger than the inner diameter of the small-diameter portion 33b and is set to be substantially the same as the outer shape of the cylindrical fastening member 15, and the inner surface of the large-diameter portion 33a is connected to the inner surface of the small-diameter portion 33b. An annular step 33a1 perpendicular to the axis of the restriction tube 33 is formed (see FIG. 7 and the like).
[0037]
Inside the insertion coil 32 inserted into the forceps channel C, an operation wire 35 provided with a hook portion 34 at the tip is inserted so as to be movable relative to the insertion coil 32 and the regulation tube 33. The hook portion 34 has a proximal end portion fixed to the distal end portion of the operation wire 35 by an adhesive, solder, brazing, or the like.
Furthermore, each base end part of the insertion tube 31, the insertion coil 32, and the operation wire 35 is connected with the operation part (not shown) of the operating device 30, and is mutually movable to an axial direction.
The operation device 30 is configured by the insertion tube 31, the insertion coil 32, the restriction tube 33, the hook portion 34, the operation wire 35, and the operation portion described above.
[0038]
Next, the configuration of the magnetic anchor guidance device 40 that controls the magnetic anchor 12 outside the body of the patient A will be described with reference to FIGS. 5 and 6.
A pair of XY stages (one-way moving mechanisms) 42 and 42 are disposed on both sides of the bed 41 having a floor plate 41a on which the patient A is placed. The pair of XY stages 42 reciprocate linearly along the longitudinal direction of the bed 41 so that the longitudinal positions of the both 42 and 42 are always the same. Further, above the bed 41, a frame / rail (two-plane moving mechanism) composed of two rails 44 and 45 that are substantially U-shaped in front view and are parallel to each other in a plane orthogonal to the longitudinal direction of the bed 41. 43, and both ends of the frame / rail 43 are fixed to the left and right XY stages 42, respectively. The inner rail 44 is slidably mounted with a magnetic induction member 46 for attracting and controlling the magnetic anchor 12 outside the body (which exerts a magnetic force on the magnetic anchor 12). The magnetic induction member 46 is attached to the left and right XY stages 42. It is possible to move along the rail 45. The magnetic induction member 46 is obtained by fixing an electromagnet 47 having a structure in which a coil is wound around an iron core on a base 48, and the electromagnet 47 always faces the patient A side (see FIG. 5). The magnetic induction member 46 may be a combination of a permanent magnet and an electromagnet, or a combination of two or more permanent magnets and electromagnets.
[0039]
A counterweight 49 for maintaining the weight balance of the entire frame / rail 43 is slidably mounted on the rail 45 on the rail 45 outside the frame / rail 43. The position of the counterweight 49 changes depending on the position of the magnetic induction member 46. For example, when the magnetic guide member 46 is located on the front side of the patient A, the counterweight 49 is located on the back side of the patient A, and when the magnetic guide member 46 is on the back side of the patient A, the counterweight 49 is Located on the front side of the patient A, the entire frame / rail 43 is balanced in weight.
The magnetic guide member 40, the XY stage 42, and the frame / rail 43 described above constitute the magnetic anchor guide device 40.
[0040]
Next, the excision procedure of the lesion X using the anchor remote guidance system will be described.
Prior to performing excision using the anchor remote guidance system, first, as shown in FIGS. 5 and 6, the patient A subjected to local anesthesia is laid on the floor plate 41 a of the bed 41. At this time, the XY stage 42 is operated so that the longitudinal direction position of the bed 41 of the frame / rail 43 is substantially the same position as the head A1 of the patient A, and the magnetic induction member 46 and the counterweight 49 are set to a predetermined position. Keep it in the place.
Next, the XY stage 42 is operated to place the frame / rail 43 on the front side of the patient A, and the magnetic guiding device 46 is moved along the frame / rail 43 to start excision of the magnetic guiding member 46. Position at the hour position (see FIG. 6).
[0041]
Next, a flexible overtube (not shown) is inserted from the mouth of patient A into the body. Subsequently, the insertion portion 21 of the endoscope 20 is inserted into the overtube, the distal end portion of the insertion portion 21 is protruded from the distal end of the overtube, and the organ B (target) (see FIGS. 8 to 10, etc.) It is made to approach the lesioned part (target site) X (not shown). Thus, when the distal end of the insertion portion 21 of the endoscope 20 is inserted into the organ B, the observation image in the organ B obtained from the observation window provided on the distal end surface 22 of the insertion portion 21 of the endoscope 20. Is displayed on a television monitor (not shown).
[0042]
Next, a tube-like treatment tool (not shown) having an injection needle at the tip is inserted into the forceps channel C from the inlet 24 a of the forceps port 24, and the injection needle protrudes from the outlet 23 of the forceps channel C. Then, an injection needle is inserted from the periphery of the lesion X into the submucosa B1 of the organ wall and physiological saline or the like is injected, and the lesion X is lifted from the proper muscle layer B2 (FIGS. 8 to 11, FIG. 21 and FIG. 22).
[0043]
Subsequently, the treatment tool is taken out from the forceps channel C. Next, the operation device 30 in which the insertion tube 31, the insertion coil 32, the restriction tube 33, the hook portion 34, the operation wire 35, and the operation portion are integrated is inserted into the forceps channel C from the forceps port 24.
At this time, when the operation device 30 is inserted into the forceps channel C, the operation portion of the operation device 30 and the proximal end portions of the insertion tube 31, the insertion coil 32, and the operation wire 35 protrude to the rear of the forceps port 24 (not shown). .
Further, since the cylindrical fastening member 15 is formed from a flexible material and the insertion coil 32 is bendable, these members can be retained in the forceps channel C even when the insertion portion 21 is bent. It can move smoothly.
[0044]
When the distal end of the operation device 30 reaches the distal end portion of the forceps channel C, the proximal end portion of the operation wire 35 protruding from the forceps opening 24 is grasped, and the operation wire 35 is operated so that only the hook portion 34 is endoscope 20. The operation wire 35 is pulled toward the operation portion side by engaging the hook portion 34 with the hook portion 14 c of the pulling separation member 14. Then, as shown in FIG. 7, the proximal end portion of the cylindrical fastening member 15 is fitted to the large diameter portion 33 a of the restriction tube 33, and the gripping member 11, the connecting cord 13, the pulling connecting member 14, and the magnetic anchor 12 are used. The protrusion 12b is pulled into the forceps channel C, the end surface of the main body 12a of the magnetic anchor 12 comes into contact with the distal end surface 22 of the insertion portion 21, and the magnetic anchor device 10 and the operating device 30 are integrated.
[0045]
When the magnetic anchor device 10 and the operating device 30 are set in the endoscope 20 as described above, as shown in FIG. 8, the proximal end portion of the insertion tube 31 protruding rearward from the forceps port 24 is grasped, and the insertion tube 31 is gripped. Is moved to the distal end side of the insertion portion 21, the distal end portion protrudes from the distal end surface 22, and the magnetic anchor 12 is pushed out from the forceps channel C.
Next, the insertion coil 32 is moved to the distal end side of the insertion portion 21, the gripping member 11 is protruded from the distal end of the insertion tube 31, and the gripping member 11 is brought close to the lesioned part X. When the operation wire 35 is pulled backward relative to the endoscope 20 in this state, the base 11a of the gripping member 11 is pulled into the cylindrical fastening member 15, and the gripping member 11 is in the open state shown in FIG. It becomes.
[0046]
When the operation wire 35 is further pulled rearward, the base 11 a of the gripping member 11 is further pulled rearward inside the cylindrical fastening member 15, and the inclined piece 11 b comes into contact with the distal end opening of the cylindrical fastening member 15. Therefore, the opening / closing piece 11c of the grasping member 11 is closed, and the lesioned part X is reliably grasped by the both claws 11d (see FIG. 9).
[0047]
In this state, when the operation wire 35 is pulled backward with a force greater than the above cutting force, the traction separating member 14 engaged with the hook portion 34 is cut at the intermediate portion, and as a result, the magnetic anchor device 10 Is separated from the operation wire 35 (see FIG. 10).
Then, the magnetic anchor 12 is attracted | sucked to the magnetic induction member 46 side by strengthening the magnetic field generated of the magnetic induction member 46 arrange | positioned outside the patient's A body. At this time, if the connecting string 13 is tensed, the lesion X gripped by the gripping member 11 can be lifted to the magnetic induction member 46 side.
[0048]
As shown in FIG. 11, when the magnetic anchor 12 comes into contact with the inner wall of the organ B while the connecting cord 13 is not tensioned, the lesion X gripped by the gripping member 11 is removed from the magnetic induction member 46. In such a case, the connecting device 13 shown in FIG. 12 is used to move the connecting string 13 from the fixing portion with the gripping member 11 to the engaging portion with the engaging member 12c. Adjust the length.
[0049]
The changing device 50 includes a flexible sheath 51 having both ends opened, and a rod-like pressing and changing member 52 inserted into the sheath 51 so as to be relatively movable. A fitting groove 51a into which the base portion 12c1 of the engaging member 12c can be fitted is formed at the distal end surface of the sheath 51, and an operation piece (vertical) with respect to the main body is formed at the distal end of the pressing and switching member 52. A tip 52) is formed. The operation piece 52 always protrudes from the distal end of the sheath 51, and the proximal end portion of the pressing and changing member 52 protrudes from the proximal end of the sheath 51 (not shown).
[0050]
In order to adjust the length, the switching device 50 is inserted into the forceps channel C of the endoscope 20, and the distal end portion thereof protrudes from the distal end surface 22 of the insertion portion 21. Is protruded from the forceps port 24 (not shown).
Then, as shown in FIG. 13, the base portion 12c1 of the engaging member 12c is fitted into the fitting groove 51a of the sheath 51, and in this state, the base end portion of the pressing and changing member 52 is grasped and the base end side thereof is moved to the base end side. When pulled, the operation piece 52a presses the opening / closing piece 12c2 of the engaging member 12c in the opening direction against the urging force of the urging spring, and moves the opening / closing piece 12c2 to the opening position shown in FIG.
In this state, by operating the pressing and switching member 52 while grasping the base end portion and moving the magnetic anchor 12 in a predetermined direction, the base portion 12c1 of the engaging member 12c is moved from the ring portion 13a of the connecting string 13. Escape to separate the magnetic anchor 12 and the connecting cord 13 (see FIG. 15).
[0051]
Subsequently, as shown in FIG. 16, the pressing and changing member 52 is moved to cause the fitting groove 51a to escape from the base portion 12c1 of the engaging member 12c, and thereafter, as shown in FIG. The adjustment member 50 is moved to the connection string 13 side, and the operation piece 52 a is engaged with the ring portion 13 a located on the proximal side from the distal end of the connection string 13.
Next, the magnetic field generated by the magnetic induction member 46 is temporarily weakened to bring the magnetic anchor 12 closer to the lesion X (not shown).
[0052]
Subsequently, while maintaining this state, as shown in FIG. 18, the switching device 50 is brought closer to the magnetic anchor 12 side, and the base portion 12 c 1 of the engaging member 12 c is fitted into the fitting groove 51 a of the sheath 51.
In this state, when the pressing / replacement member 52 is pulled toward the base end side, as shown in FIG. 19, the operation piece 52a opposes the opening / closing piece 12c2 of the engagement member 12c against the urging force of the urging spring. The ring portion 13a engaged with the operation piece 52a is moved to the base portion 12c1 side and engaged with the base portion 12c1 from one end of the base portion 12c1.
[0053]
In this way, when the length of the connecting string 13 from the fixing portion with the gripping member 11 to the engaging portion with the engaging member 12c is shortened, the magnetic field generated by the magnetic induction member 46 is strengthened again, and the magnetic anchor 12 is moved. It attracts | sucks to the magnetic induction member 46 side. Then, as shown in FIG. 20, the connecting string 13 is tensioned between the magnetic anchor 12 and the gripping member 11, and the lesioned part X gripped by the gripping member 11 is lifted by a sufficient distance upward in FIG. .
[0054]
Thus, when the lesioned part X is moved by a desired distance in the desired direction, a sufficiently large excision part is formed at the boundary between the lesioned part X and the normal tissue. Then, the operation wire 35 is taken out from the endoscope 20, and as shown in FIG. 20, an incision tool such as a high-frequency knife 60 is inserted into the organ B using the forceps channel C of the endoscope 20 (not shown in FIG. 20). The lesioned part X is excised together with the mucous membrane from one end side.
When the lesioned part X is excised from one end side to the opposite end side, the entire lesioned part X is eventually completely excised (see FIG. 21).
In the excision work with the high-frequency knife 60, the position of the tip 60a of the high-frequency knife 60 can be confirmed more easily as the excision area increases.
[0055]
When the excision work is completed as described above, the lesioned part X separated from the normal tissue remains in the state of being gripped by the gripping member 11 (magnetic anchor device 10), and thus the lesioned part X is prevented from being lost.
In order to collect the excised lesion part X, as shown in FIG. 21, the forceps channel C of the endoscope 20 is provided with a pair of gripping pieces 71 that can be opened and closed at its distal end, and further, its proximal end A grasping forceps 70 having an operation unit (not shown) is inserted into the. Then, by operating this operation portion, the gripping piece 71 is brought into the open state to be brought close to the traction separation member 14, and then both the gripping pieces 71 are closed so that the traction separation member 14 is reliably secured by the both gripping pieces 71. Hold it. Then, the endoscope 20 is removed from the body as it is, the lesioned part X is taken out of the body together with the magnetic anchor device 10, and thereafter, the excised part is sutured and disinfected.
[0056]
As described above, when the anchor remote guidance system of the present embodiment is used, the length of the connecting string 13 from the fixing portion with the grasping member 11 to the engaging portion with the engaging member 12c is adjusted, thereby organs Regardless of the size of B, it is possible to lift the lesioned part X by always tensioning the connecting string 13.
[0057]
Further, since the lesioned part X can be moved in a desired direction by a sufficient distance, the excised part at the boundary between the lesioned part X and the normal tissue can be easily and reliably secured with a sufficient size. Even if the lesioned part X has a flat shape, a sufficiently large excision part can be created. Even in such a case, the lesioned part X can be easily excised. .
[0058]
Furthermore, since the lesioned part X is lifted by the gripping member 11, a sufficiently excised part can be secured, and the already excised lesioned part X can be prevented from falling on the proper muscle layer B2.
In addition, since the gripping member 11 can be arranged at an arbitrary position, the view of the endoscope 20 is not hindered by the excised lesioned part X.
[0059]
Next, a second embodiment of the present invention will be described with reference to FIG.
The same members as those in the first embodiment are designated by the same reference numerals, and detailed description thereof is omitted.
[0060]
The anchor remote guidance system of this embodiment includes a magnetic anchor device 80 (consisting of a gripping member 11, a magnetic anchor 12, a chain 81, a traction separating member 14, and a cylindrical fastening member 15), an operating device 30, and a magnetic anchor guidance. The apparatus 40 is comprised.
[0061]
In this embodiment, the grip member 11 and the magnetic anchor 12 are connected using a chain (connecting member) 81 instead of the connecting string 13. The chain 81 is configured by connecting a large number of rings 82. In the state shown in FIG. 22, the ring 82 located at the proximal end engages with the base 11 c of the gripping member 11, and the ring 82 located at the distal end engages with the engaging member 12 c of the magnetic anchor 12. .
[0062]
The magnetic anchor device 80 is inserted into the organ B while being attached to the endoscope 20 in the same manner as in the first embodiment, and then the holding member 11 holds the lesion X.
If the chain 81 is not tensioned even when the magnetic anchor 12 is moved by generating a magnetic field from the magnetic induction member 46, the engagement member 12c is used by using the changing device 50 as in the first embodiment. The ring 82 positioned on the base end side is engaged with the base portion 12c1 (not shown).
[0063]
In this way, by adjusting the length from the base end of the chain 81 to the engaging portion of the chain 81 with the engaging member 12c, a magnetic field is applied from the magnetic induction member 46 regardless of the size of the organ B. If generated, the chain 81 can always be tensioned to lift the lesion X.
[0064]
Finally, a third embodiment of the present invention will be described with reference to FIG. The same members as those in the first embodiment are designated by the same reference numerals, and detailed description thereof is omitted.
[0065]
The anchor remote guidance system of this embodiment includes a gravity anchor device 90 (consisting of a gripping member 11, a gravity anchor 91, a connecting string 13, a traction separating member 14, and a cylindrical fastening member 15) and an operation device 30. It is.
The gravity anchor 91 of this embodiment includes a main body 91a, a protrusion 91b, and an engaging member 12c having the same shape as the magnetic anchor 12, and the main body 91a and the protrusion 91b are formed of a nonmagnetic material. Yes. Specific examples of the nonmagnetic material include gold, copper, aluminum, stainless steel (austenite), brass, ceramic, glass, and the like.
[0066]
The gravitational anchor device 90 is inserted into the organ B while being attached to the endoscope 20 in the same manner as in the first embodiment, and then the gripping member 11 grips the lesion X.
Since the gravity anchor 91 moves according to the gravity P, the posture of the patient A is changed and the gravity anchor 91 is moved downward in the gravity direction. Then, when the gravity anchor 91 comes into contact with the inner wall of the organ B without the tension of the coupling string 13 being engaged from the fixing portion of the coupling string 13 with the grasping member 11 in the same manner as in the first embodiment. The length to the engaging part with the member 12c is adjusted. If such adjustment is performed, the lesioned part X can be moved by always tensioning the connecting string 13 regardless of the size of the organ B, as in the first embodiment.
Furthermore, in this embodiment, the magnetic anchor guiding device 40, which is an expensive device necessary in the first embodiment, is not necessary, which is advantageous in terms of cost compared to the first embodiment.
[0067]
Although the present invention has been described with reference to the above embodiment, the present invention is not limited to the above embodiment, and can be improved or changed within the scope of the purpose of the improvement or the idea of the present invention. For example, if the magnetic anchor 12 of the second embodiment is replaced with the gravity anchor 91 of the third embodiment and the magnetic anchor guide device 40 is omitted, a gravity anchor device using the chain 81 can be obtained.
[0068]
【The invention's effect】
As described above, according to the present invention, the target part can be excised quickly and easily, and the distance between the anchor and the gripping member can be adjusted, so that the anchor is placed in a predetermined direction inside the object. When moved to the position, the connecting member is always in tension.
[Brief description of the drawings]
FIG. 1 is an overall view of a magnetic anchor device according to a first embodiment of the present invention.
FIG. 2 is an overall view of the magnetic anchor device with a gripping member open.
FIG. 3 is an overall view of the magnetic anchor device in a state where a gripping member is closed.
FIG. 4 is an overall view of an endoscope.
FIG. 5 is a view of a bed on which a patient whose lesion is to be excised and a magnetic anchor guide device are viewed from the patient's head side.
FIG. 6 is a side view of a bed on which a patient is placed and a magnetic anchor guiding device.
FIG. 7 is an enlarged longitudinal side view of the distal end portion of the endoscope showing a state in which the operating device is inserted into the forceps channel in a state linked to the magnetic anchor device.
FIG. 8 is an enlarged longitudinal sectional side view showing a state immediately before the grasping member protruding from the distal end of the endoscope in the opened state grasps a lesioned portion.
FIG. 9 is an enlarged longitudinal sectional side view showing a state where a gripping member protruding from the distal end of the endoscope is closed and a lesioned part is gripped.
FIG. 10 is an enlarged longitudinal side view showing a state where the magnetic anchor device and the operating device are separated inside the endoscope.
FIG. 11 is an enlarged longitudinal sectional side view showing a state in which a lesioned part is lifted by using a magnetic anchor guiding device after the gripping member grips the lesioned part.
FIG. 12 is an enlarged cross-sectional view of the distal end portion of the switching device.
FIG. 13 is an enlarged view showing a state in which the base portion of the engaging portion of the magnetic anchor is fitted in the fitting groove of the sheath.
FIG. 14 is an enlarged view showing a state where the opening / closing piece is moved in the opening direction by the pressing and changing member.
FIG. 15 is an enlarged view showing a state in which the opening / closing piece is maintained in the open state by the pressing and changing member and the ring portion of the connecting string is escaped from the base portion.
FIG. 16 is an enlarged view showing a state in which the base portion of the engaging portion of the magnetic anchor is detached from the fitting groove of the sheath.
FIG. 17 is an enlarged view showing a state in which another ring portion of the connecting string is engaged by the pressing and changing member.
FIG. 18 is an enlarged view showing a state in which the base portion of the engaging portion of the magnetic anchor is fitted in the fitting groove of the sheath while the other ring portion of the connecting string is engaged by the pressing and changing member.
FIG. 19 is an enlarged view showing a state in which the opening / closing piece is rotated in the opening direction by the pressing and switching member and the other ring portion of the connecting string is fitted to the base portion of the engaging portion.
FIG. 20 is an enlarged vertical side view showing a state in which a lesion is being lifted using a magnetic anchor guiding device after adjusting the length of a connecting string.
FIG. 21 is a view showing a state in which a magnetic anchor that holds a lesioned part separated from an organ is held by holding forceps.
FIG. 22 is an overall view of a magnetic anchor device according to a second embodiment of the present invention.
FIG. 23 is an enlarged vertical cross-sectional view showing a state in which a lesion is moved downward in the gravity direction using the gravity anchor device after adjusting the chain length of the gravity anchor device according to the third embodiment of the present invention. It is a side view.
[Explanation of symbols]
DESCRIPTION OF SYMBOLS 10 Magnetic anchor apparatus 11 Grasp member 11a Base part 11a1 Insertion hole 11b Inclined piece 11c Opening / closing piece 11d Claw part 12 Magnetic anchor 12a Main body part 12b Projection part 12c Engagement member 12c1 Base part 12c2 Opening / closing piece 13 Connection string (connection member)
13a Ring (hole)
14 Pulling / separating member 14a Insertion piece 14b Retaining prevention part 14c Ridge part 15 Cylindrical clamping member 20 Endoscope 21 Insertion part 22 End face 23 Forceps channel outlet 24 Forceps port 24a Inlet 30 Operating device 31 Insertion tube 32 Insertion coil 33 Restriction tube 33a Large diameter portion 33a1 Annular step portion 33b Small diameter portion 34 Hook portion 35 Operation wire 40 Magnetic anchor guide device 41 Bed 41a Floor plate 42 XY stage (unidirectional movement mechanism)
43 Frame / rail (moving mechanism in one plane)
44 45 Rail 46 Magnetic induction member 47 Electromagnet 48 Base 49 Counterweight 50 Replacement device 51 Sheath 51a Fitting groove 52 Pressing and switching member 52a Operation piece (front end)
60 High-frequency knife 60a Tip 70 Grasping forceps 71 Grasping piece 80 Gravity anchor device 81 Chain (connection member)
82 Ring (hole)
90 Gravity Anchor Device 91 Gravity Anchor 91a Main Body 91b Projection A Patient (Subject)
A1 head B organ B1 submucosa B2 proper muscle layer C forceps channel P gravity X lesion (target site)

Claims (10)

対象物内部の対象部位を把持可能な把持部材と、
磁性体からなる磁気アンカーと、
該把持部材と該磁気アンカーとを接続する変形可能な線状の連結部材と、
上記対象物外部に配置され、磁界を発生する磁気アンカー誘導装置と、を具備し、
該磁気アンカー誘導装置が発生する磁界からの磁力により、上記磁気アンカーを移動させて、上記把持部材に把持された対象部位を所定方向に移動させる内視鏡用アンカー遠隔誘導システムであって、
一端部が上記把持部材に結合された連結部材が、その長手方向に沿って複数の孔部を有し、
上記磁気アンカーが、これら孔部のいずれかと選択的に係合する係合部材を具備することを特徴とする内視鏡用アンカー遠隔誘導システム。
A gripping member capable of gripping a target portion inside the target object;
A magnetic anchor made of a magnetic material;
A deformable linear coupling member connecting the gripping member and the magnetic anchor;
A magnetic anchor guiding device that is arranged outside the object and generates a magnetic field,
An endoscopic anchor remote guidance system for moving an object site gripped by the gripping member in a predetermined direction by moving the magnetic anchor by a magnetic force from a magnetic field generated by the magnetic anchor guide device,
A connecting member having one end coupled to the gripping member has a plurality of holes along its longitudinal direction,
The remote anchor guidance system for an endoscope, wherein the magnetic anchor includes an engagement member that selectively engages any one of the holes.
請求項1記載の内視鏡用アンカー遠隔誘導システムにおいて、
上記磁気アンカー誘導装置は、
発生する磁界によって磁力を生じさせて、該磁力によって、上記磁気アンカーを所定方向に移動させる磁気誘導部材と、
該磁気誘導部材を特定の一平面内に配置したU字状のフレーム部材に沿って移動させる一平面内移動機構と、
上記U字状のフレーム部材を上記一平面と直交する方向に相対移動させる一方向移動機構と、
を有する内視鏡用アンカー遠隔誘導システム。
The endoscope anchor remote guidance system according to claim 1,
The magnetic anchor guiding device is
A magnetic induction member that generates a magnetic force by a generated magnetic field and moves the magnetic anchor in a predetermined direction by the magnetic force;
An in-plane movement mechanism for moving the magnetic induction member along a U-shaped frame member arranged in a specific plane;
A one-way moving mechanism for relatively moving the U-shaped frame member in a direction orthogonal to the one plane;
An endoscope remote guidance system for endoscope.
対象物内部の対象部位を把持可能な把持部材と、
非磁性体からなる重力アンカーと、
該把持部材と該重力アンカーとを接続する変形可能な線状の連結部材と、を具備し、
上記重力アンカーを重力に従って移動させて、上記把持部材に把持された対象部位を所定方向に移動させる内視鏡用アンカー遠隔誘導システムであって、
一端部が上記把持部材に結合された連結部材が、その長手方向に沿って複数の孔部を有し、
上記磁気アンカーが、これら孔部のいずれかと選択的に係合する係合部材を具備することを特徴とする内視鏡用アンカー遠隔誘導システム。
A gripping member capable of gripping a target portion inside the target object;
A gravity anchor made of non-magnetic material,
A deformable linear connecting member that connects the gripping member and the gravity anchor;
An endoscope anchor remote guidance system that moves the gravity anchor according to gravity and moves a target portion gripped by the gripping member in a predetermined direction,
A connecting member having one end coupled to the gripping member has a plurality of holes along its longitudinal direction,
The remote anchor guidance system for an endoscope, wherein the magnetic anchor includes an engagement member that selectively engages any one of the holes.
請求項1から3のいずれか1項記載の内視鏡用アンカー遠隔誘導システムにおいて、上記連結部材が柔軟な連結ひもであり、上記孔部が、該連結ひもを結ぶことにより形成された輪部である内視鏡用アンカー遠隔誘導システム。The endoscope anchor remote guidance system according to any one of claims 1 to 3, wherein the connecting member is a flexible connecting string, and the hole portion is formed by connecting the connecting string. Is an endoscope remote guidance system for endoscopes. 請求項1から3のいずれか1項記載の内視鏡用アンカー遠隔誘導システムにおいて、上記連結部材がチェーンであり、上記孔部が、該チェーンを構成するリングである内視鏡用アンカー遠隔誘導システム。The endoscope anchor remote guidance system according to any one of claims 1 to 3, wherein the connecting member is a chain, and the hole portion is a ring constituting the chain. system. 請求項1から5のいずれか1項記載の内視鏡用アンカー遠隔誘導システムにおいて、
上記係合部材が、
略C字状をなし、その一方の端部側から上記孔部に係合可能な基部と、
該基部の他方の端部に回動可能に枢着され、該基部の両端間に形成された隙間を開閉する開閉片と、
を具備する内視鏡用アンカー遠隔誘導システム。
The endoscope anchor remote guidance system according to any one of claims 1 to 5,
The engaging member is
A substantially C-shape, a base that can be engaged with the hole from one end thereof;
An opening / closing piece pivotally attached to the other end of the base and opening / closing a gap formed between both ends of the base;
An anchor remote guidance system for endoscopes comprising:
請求項6記載の内視鏡用アンカー遠隔誘導システムにおいて、
上記係合部材が、上記開閉片を、上記基部の隙間を塞ぐ閉方向に常時回転付勢する付勢手段を具備する内視鏡用アンカー遠隔誘導システム。
The endoscope anchor remote guidance system according to claim 6,
An endoscope anchor remote guidance system, wherein the engagement member includes an urging unit that constantly urges the opening and closing piece in a closing direction to close the gap of the base.
請求項7記載の内視鏡用アンカー遠隔誘導システムにおいて、さらに、
先端が開口し、かつ、上記係合部材の基部が嵌合可能な嵌合溝を有する筒状のシースと、
該シース内に該シースの長手方向に相対移動可能に挿入され、かつ、上記係合部材の基部が上記嵌合溝に係合した状態で、該シースに対して相対移動すると、該シースの先端開口より突出している先端部が、上記開閉片を上記隙間を開放する開方向に回転させる棒状の押圧兼掛替部材と、を備える掛替装置を具備する内視鏡用アンカー遠隔誘導システム。
The endoscope anchor remote guidance system according to claim 7, further comprising:
A cylindrical sheath having a fitting groove that is open at the tip and into which the base of the engaging member can be fitted;
When the sheath is inserted into the sheath so as to be relatively movable in the longitudinal direction of the sheath and the base of the engaging member is engaged with the fitting groove, the distal end of the sheath is moved. A remote anchor anchor guidance system for an endoscope, comprising: a switching device including a rod-shaped pressing and switching member that has a tip protruding from the opening to rotate the opening / closing piece in an opening direction that opens the gap.
請求項8記載の内視鏡用アンカー遠隔誘導システムにおいて、
上記押圧兼掛替部材が、上記係合部材の基部が上記嵌合溝に係合した状態で、上記先端部により上記開閉片を上記開方向に押圧したまま、上記連結部材に対して上記係合部材を相対移動させることにより、上記基部に係合していた孔部を該基部から抜け出させることが可能な内視鏡用アンカー遠隔誘導システム。
The endoscope anchor remote guidance system according to claim 8,
In the state where the base part of the engaging member is engaged with the fitting groove, the pressing and switching member is engaged with the connecting member while pressing the opening / closing piece in the opening direction by the tip part. An anchor remote guidance system for an endoscope which can cause a hole engaged with the base to come out of the base by moving the joint member relative to each other.
請求項9記載の内視鏡用アンカー遠隔誘導システムにおいて、
上記押圧兼掛替部材が、上記基部に係合していた孔部が該基部から抜け出し、かつ、上記係合部材の基部が上記嵌合溝に係合している状態で、上記先端部に該基部から抜け出した孔部とは異なる孔部を係合しながら、該先端部により上記開閉片を上記開方向に押圧し、該孔部を上記係合部材の基部に係合させることが可能な内視鏡用アンカー遠隔誘導システム。
The endoscope anchor remote guidance system according to claim 9,
In the state in which the hole portion engaged with the base portion is pulled out from the base portion and the base portion of the engagement member is engaged with the fitting groove, It is possible to engage the hole with the base of the engaging member by pressing the opening / closing piece in the opening direction with the tip while engaging a hole different from the hole that has come out of the base. Remote anchor anchor guidance system.
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