JP2003532455A - 吻合、ステープル吻合及び切除器具用の流体搬送機構 - Google Patents
吻合、ステープル吻合及び切除器具用の流体搬送機構Info
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- JP2003532455A JP2003532455A JP2001561233A JP2001561233A JP2003532455A JP 2003532455 A JP2003532455 A JP 2003532455A JP 2001561233 A JP2001561233 A JP 2001561233A JP 2001561233 A JP2001561233 A JP 2001561233A JP 2003532455 A JP2003532455 A JP 2003532455A
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- anastomosis
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Links
- 239000012530 fluid Substances 0.000 title claims description 10
- 230000003872 anastomosis Effects 0.000 title abstract description 55
- 238000002271 resection Methods 0.000 title 1
- 230000007723 transport mechanism Effects 0.000 title 1
- 238000011282 treatment Methods 0.000 claims abstract description 8
- 102000009123 Fibrin Human genes 0.000 abstract description 31
- 108010073385 Fibrin Proteins 0.000 abstract description 31
- BWGVNKXGVNDBDI-UHFFFAOYSA-N Fibrin monomer Chemical compound CNC(=O)CNC(=O)CN BWGVNKXGVNDBDI-UHFFFAOYSA-N 0.000 abstract description 31
- 229950003499 fibrin Drugs 0.000 abstract description 31
- 230000007246 mechanism Effects 0.000 abstract description 21
- 238000012377 drug delivery Methods 0.000 abstract description 14
- 238000002347 injection Methods 0.000 abstract description 2
- 239000007924 injection Substances 0.000 abstract description 2
- 230000002093 peripheral effect Effects 0.000 abstract description 2
- 210000001519 tissue Anatomy 0.000 description 29
- 238000005520 cutting process Methods 0.000 description 22
- 210000002429 large intestine Anatomy 0.000 description 15
- 238000000034 method Methods 0.000 description 10
- 230000035876 healing Effects 0.000 description 9
- 230000006870 function Effects 0.000 description 8
- 210000001035 gastrointestinal tract Anatomy 0.000 description 7
- 239000000126 substance Substances 0.000 description 6
- 238000001356 surgical procedure Methods 0.000 description 6
- 210000001072 colon Anatomy 0.000 description 5
- 239000003814 drug Substances 0.000 description 4
- 229940079593 drug Drugs 0.000 description 4
- 238000003860 storage Methods 0.000 description 3
- 230000002159 abnormal effect Effects 0.000 description 2
- 238000002266 amputation Methods 0.000 description 2
- 210000000436 anus Anatomy 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 238000005304 joining Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 206010002091 Anaesthesia Diseases 0.000 description 1
- 206010017993 Gastrointestinal neoplasms Diseases 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 210000001015 abdomen Anatomy 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000037005 anaesthesia Effects 0.000 description 1
- 230000002457 bidirectional effect Effects 0.000 description 1
- 210000001217 buttock Anatomy 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000012321 colectomy Methods 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 210000002808 connective tissue Anatomy 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000013536 elastomeric material Substances 0.000 description 1
- WABPQHHGFIMREM-AKLPVKDBSA-N lead-210 Chemical compound [210Pb] WABPQHHGFIMREM-AKLPVKDBSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 235000004252 protein component Nutrition 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000037390 scarring Effects 0.000 description 1
- 210000000813 small intestine Anatomy 0.000 description 1
- 230000017423 tissue regeneration Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/11—Surgical instruments, devices or methods, e.g. tourniquets for performing anastomosis; Buttons for anastomosis
- A61B17/1114—Surgical instruments, devices or methods, e.g. tourniquets for performing anastomosis; Buttons for anastomosis of the digestive tract, e.g. bowels or oesophagus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/11—Surgical instruments, devices or methods, e.g. tourniquets for performing anastomosis; Buttons for anastomosis
- A61B17/115—Staplers for performing anastomosis in a single operation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/00491—Surgical glue applicators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/11—Surgical instruments, devices or methods, e.g. tourniquets for performing anastomosis; Buttons for anastomosis
- A61B17/115—Staplers for performing anastomosis in a single operation
- A61B17/1155—Circular staplers comprising a plurality of staples
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Surgery (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Medical Informatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Physiology (AREA)
- Surgical Instruments (AREA)
- Infusion, Injection, And Reservoir Apparatuses (AREA)
- Materials For Medical Uses (AREA)
- Prostheses (AREA)
- Media Introduction/Drainage Providing Device (AREA)
Abstract
Description
一般に関し、とりわけ、上記器具が切除された大腸のステープル吻合部位及び切
断部位にフィブリンをそれによって搬送しうるフィブリン注入機構に関する。
れている。癌の手術の分野、とりわけ、癌性又は他の異常な組織を含む胃腸管の
部分を切除する外科処置の分野には、多数の独自に形成された器具が含まれてい
る。本器具とそれらの機能についての記載と組み合わせて、外科手術における当
業界の状態について記載する。
、癌性の組織の特定の位置に関する。これは、当業界において設けられている器
具は、器具が胃腸管内に挿入する距離に関して制限があるので、非常に重要であ
る。もし癌性の組織が例えば大腸の上であるならば、与えられた標準の器具を使
用することができず、特定の設備が必要となる。これらの設備を用いると、腸管
の中身で周囲の組織を汚染する可能性を一般に増し、また、手術の長さを増し、
これに伴って麻酔が必要となり、機械化された装置によって得られる正確な吻合
及びステープル吻合の利益がなくなってしまう。
最初に開かれて腸管が露出する。外科医は、癌性の組織の両側において大腸の管
を切断するリニアカッタ及びステープル吻合装置を利用し、それにより、腸管の
二つのステープル吻合された端部(肛門に向けられている遠端と、小腸に最も近
い近端)を形成する。これは、一時的に汚染を最小化するためになされる。
腸管が切り抜き要素1、2の間に位置する。外科医は、装置のハンドル4内でト
リガ3を搾ることによって、切り抜き要素1、2を一緒にする。大腸の締め付け
られた端部を通して一連のステープル6を駆動するように第二のトリガ(又は、
同じトリガの第二の動作)が作動され、それにより、端部を閉鎖及び離断する。
能なアンビル部を露出した近端部内に挿入する。この段階は、外科処置の残りの
段階と同様に、外科器具の機能に関連している。とりわけ、図2に関して、外科
医は、器具7を取ることによって始め、ハンドル9の基部にあるダイヤル8を手
動で回転させ、それにより、反対の端部にあるアンビルヘッド10を前進させる
。外科医は、アンビルヘッド10がその最も極端に延伸した位置に前進するまで
、ダイヤル8を回転させ続ける。この手動の回転は、ほぼ30回の360度回転
を必要とする。一旦完全に延伸すると、器具のアンビルヘッドが器具7から取り
外され、連結ポストが近端の部分的な開口部内に挿入され、この開口部を通して
外方向に延びている。この近端の部分的な開口は縫合して閉鎖される。その連結
ステム12がステープル吻合された遠端を貫通するまで、吻合及びステープル吻
合器具7の延伸軸11は肛門を通って下側の大腸内に挿入されて前進させられる
。次いで、外科医は、アンビルの連結端部と軸を共に接合し、再びハンドル内の
ダイヤルを手動で回転し始め、この時、アンビルヘッドを軸の端部13のより近
くにもたらす。
0回手動でダイヤルを回転させた後、ハンドル内のグリップスタイルのトリガ1
4が手動で作動させられる。この作動により、円形のブレード15が軸の先端か
ら半径外方向に前進し、アンビル10の対向面16と接触するようになる。ブレ
ードは、大腸のステープルで閉鎖された近端及び遠端を通して切断し、それによ
り、大腸の新しい一対の近端及び遠端を接続する。切断された組織は、軸の端部
において内部容積部に保持されている。
によって接合される。ステープル17は、軸の先端の周辺部における穴を通して
前進させられる(軸はアンビルの対向面に押圧されかつ軸によって閉鎖されてい
る)。連結された軸及びアンビルは患者から引かれる。
されており、一回の使用の後に実際に捨てられる。これら装置は、多数の可動部
を有する複雑な装置であり、実質的な構造的一体性、それゆえ製造費用を必要と
する。これら装置が一度だけ使用され、いずれの部分も二度と使用することがで
きないという事実により、この装置の使用は高価で資源の無駄となる。
の装置は、克服することが望ましい多数の他の制限を備えている。これらの制限
には、(吻合及びステープル吻合器具のダイヤル及びトリガの機能と、切断及び
ステープル吻合器具の多数のトリガの機能とを含む)多数の異なる機能を外科医
が手動で作動しなければならない要件が含まれている。
る手段を提供できないということである。治癒処置を促進する薬又は他の物質が
、ステープル吻合及び切断処理と同時に又は後に部位へ搬送させられるならば、
組織の治癒又は他の医療任務を迅速に行うことができる。このような物質はフィ
ブリンであり、結合組織の主な蛋白質成分であり、特に、二つの以前の別組織を
接合する時に傷跡を形成する処理などの組織修繕処理の基本的な要素として機能
する。それゆえ、新たにステープル吻合されて切断された組織の部位にこのよう
な物質を注入する能力は、物質を搬送することができない従来技術の装置に対し
て利点がある。
搬送を行うことができる薬搬送機構を提供することである。
とにより資源の無駄を減じる、切断、吻合及びステープル吻合用器具と一体の形
態の薬搬送機構を提供することである。
要求を減じる薬搬送機構を提供することである。
細な記載によって認識することができる。
ープル吻合アタッチメントと一体である薬搬送機構によって与えられる。
3に示されている。ハンドル150は、一つ以上好ましくは二つのフィンガトリ
ガ160を有するピストルグリップスタイル形状を有する。フィンガトリガ16
0は、(以下、より十分に記載される)別個の柔軟な駆動軸170を各々が回転
させる少なくとも一つの好ましくは二つの別個のモータ165に独立に連結され
ている。モータ165は、各々二方向モータであり、ハンドルの頂部の手動駆動
スイッチ172に連結されている。使用者は、このスイッチによって各モータの
回転方向を選択的に変更しすることができる。この二方向の出力は、電流方向に
対応する方向に回転するモータを選択することによって最も簡単に実現すること
ができる。駆動スイッチの作動は、この出力に応じて電流方向を変更する。この
例では、モータに供給する電源175は、バッテリーパック(及び、最も望まし
くは、充電式のバッテリーパック)などの直流電源でなければならない。装置が
交流で使用可能でなければならない場合には、変圧器を備えることができ、より
高性能な中間歯車組立体を設けることができる。この記載と関連して、記載した
本発明の実施例は、直流を提供する充電式バッテリーパックを採用している。
軸操縦185と、オンオフスイッチ(図示せず)とを有するいくつかの他の特徴
をさらに有する。最初に、リモート式状態インジケータは、LCD(又は同様な
読出し装置)を備えうる。使用者は、このインジケータによって、構成要素の位
置(例えば、ステープルを駆動する前に締め付け要素が適切な位置にあるか否か
)を知ることができる。次に、ハンドルは、(以下により十分に記載する軸部に
移植されるガイドワイヤによって)柔軟な軸の運動を指向するために、例えば、
ジョイスティック又はトラックボールなどの、手動で作動可能な操縦手段を有す
る。最後に、ハンドルは、さらなる電源と、電力をアタッチメントに選択的に供
給するためのオンオフスイッチとを有しうる。
つ殺菌可能な(すなわち、オートクレーブに耐えるように十分に凹凸がある)簡
単なエラストマー材料で形成された管状シース195を備えている。種々の長さ
の軸を設けることができる。柔軟な軸とハンドル部は分離可能としうる。もし分
離可能であるならば、軸の近端とハンドルの遠端の間の界面は、駆動構成要素用
の連結手段を備えている。
それぞれが有する一対の比較的に小さな固定管215がエラストマーシース内に
ある。柔軟な駆動軸自体は、ハンドル内のモータから軸の遠端へトルクを伝達す
るが、患者の大腸を通して「曲がりくねる」必要があると外科医がみなす時に、
曲げる、角度を付ける、湾曲するのに十分に柔軟である。しかしながら、本明細
書で説明する吻合及びステープル吻合アタッチメントなどのアタッチメントと駆
動軸の遠端を連結するために、駆動軸の遠端は、連続的にトルクを伝達できる構
造を有しなければならない。例えば、駆動軸の遠端200を六角形とすることが
でき、それにより、アタッチメントの連結界面の六角形凹所内に嵌め込む。適切
なトルクをアタッチメントに与えることを保証するように、適切な歯車機構を軸
の遠端又はアタッチメントの界面部分に設けることができる。
と関連して、シースは、柔軟であるがその遠端近傍においてシースの内面に連結
された少なくとも二つのガイドワイヤ205をさらに有する。ガイドワイヤは、
操縦手段の動作によって別のガイドワイヤに関して軸線方向に移動することがで
き、それに応じてこの動作によりシースを曲げ及び湾曲する。
は電気的な導線210をさらに収納する。この電気的導線は、アタッチメントの
状態について示す(例えば、アンビル部がSBR部に極めて近接しているか否か
について示し、外科医がステープル吻合するのに安全であることを知る)ために
、アタッチメントからハンドルへ信号を伝える。同様に、必要ならば別の態様の
アタッチメントへ電力を供給するために第二の電気的導線を設けることができる
。
アタッチメントと一体に形成されている。このような吻合及びステープル吻合ア
タッチメントは、アンビル部と、ステープル、ブレード及び貯蔵部(SBR部)
とを備え、SBR部は、前述の軸要素の駆動構成要素に連結可能である一対の回
転駆動軸と、回転駆動軸に取り付けられた対応する対の前進及び後退ナットとを
有するが、回転及びそれゆえ駆動軸の回転時の駆動軸に沿った線形的な前進及び
後退が防がれる。
線方向に延びている自由に回転する連結ポストとを有する弾丸状である。この連
結ポストは、回転駆動軸の一つに取り付けられた対応のナットに選択的に連結及
び取外し可能であるように形成されている。
ープル口が、ハウジングの筒状壁の軸線方向外側に面した面上にあり、これらス
テープル口を通して装置のステープルが放出される。ステープル口を通してステ
ープルを駆動するために、一連のステープルドライバがステープル口の下におい
て、筒状壁内に取り付けられている。より正確には、ステープルドライバは、S
BR部の壁に着座する一つの筒状構成要素の外側縁における一連の突出部である
。ステープルは、放出され始める前に穴内に取り付けられており、ステープルド
ライバ及びそれらの突出部の前進運動によって穴を通して前進させられる。
対して着座する。ブレード及びステープルドライバの両方が第二のナットに取り
付けられる。第二のナットは他の回転駆動軸に取り付けられている。回転駆動軸
が回転する時、(回転しないように制限されている)ナットは軸に沿って前進し
、ブレード及びステープルドライバを線形的に前進させる。それゆえ、ブレード
及びステープルドライバは、ハンドルの適切なトリガの作動に応じて、ハウジン
グから軸線方向に外方に選択的に前進可能である。
ち、前述の切断及びステープル吻合動作の直後に、切断及びステープル吻合部位
において、薬やフィブリンなどの治癒物質を搬送する機構に適している。いくつ
かの実施例のうちのいずれかでこの機構を採用しうる。いくつかの実施例のうち
二つを例として以下に記載する。一般に、本発明は、流体を収納する供給室と、
治療部位と供給室の間で連通している流通路と、流通路を通して流体を押すこと
が必要とされる力より大きな力で供給室内で移動する搬送又はプランジャドライ
バとを備えている。
長筒状断面を有する供給室を備え、この供給室は、ステープル吻合口の代わりに
アタッチメントのステープルハウジング内に形成されている。すなわち、ステー
プルハウジングは、ステープル口と共に複数の供給室を有する。これら全ての供
給室は、前述のように同一の部品及び同一の機能を有する。供給室の口部は、内
側に面する突起部又は歯が最も内側の縁周辺部において並べられた流通路を形成
する。供給室はフィブリンで充填された袋を収納する。搬送又はプランジャドラ
イバは供給室内で移動する。搬送又はプランジャドライバは、各ステープルがス
テープルハウジング内のステープル口から突出するのと同様に、供給室の最も内
側の端部から突出している。
バに接続されている)アタッチメントの回転駆動軸が(電子機械ドライバハンド
ル上のトリガを介して)作動させられる時、ステープルドライバは前進し、ステ
ープルハウジング内の対応のステープル口を通してアタッチメントのアンビルに
対して複数のステープルを押し、目標組織を通過してステープル吻合する。同時
に、ステープルドライバは、対応の供給室を通して各搬送又はプランジャドライ
バを押すように前進する。各搬送又はプランジャドライバが供給室を通して前進
する時、ドライバがフィブリンの袋を突起部に対して押圧する。袋が流通路の内
側に面した突起部に対して押圧する時、袋は裂け、フィブリンを流通路を通して
外へ新たにステープル吻合された組織へ解放する。一方、ブレードドライバは、
前方へ移動し、新たにステープル吻合された組織を通してブレードを押し、余剰
分を切断する。アタッチメントが除去され、治癒処理は始まり、切断及びステー
プル吻合部位にフィブリンがあることにより促進される。
に、流通路は障害物がない。しかしながら、フィブリンの袋及び別個の搬送又は
プランジャドライバの代りに、供給室は、鋭い先端を有するカニューレを備えて
いる。カニューレの鋭い先端がステープル吻合面に向けられている(すなわち、
放出室から押し出された時、先端は組織を穿孔し、最終的にアンビルの平坦な切
断面によって止められる)。カニューレの鋭い端部の直に内側において、好適な
実施例の内側に面している突起部と同様に、カニューレの内側の周辺部には内側
に面している突起部が並べられている。フィブリンの袋がカニューレの内側に着
座する。搬送又はプランジャドライバはフィブリンの袋の背後に位置する。この
搬送又はプランジャドライバは、カニューレの壁に取り付けられているが、カニ
ューレの先端がアンビルに到達した後に壁から離れて破断するように設定されて
いる。すなわち、アタッチメントの回転駆動軸が作動させられる時、ステープル
ドライバが前進し、ステープルハウジング内の対応のステープル口を通して、ア
タッチメントのアンビルに抗して複数のステープルを押し、目標組織を通過して
ステープル吻合する。同時に、ステープルドライバは前進して各搬送又はプラン
ジャドライバを押す。搬送又はプランジャドライバは、最初に、カニューレを供
給室から押し出し、組織を通してアンビルに抗して押す。一旦、カニューレの先
端がアンビルに到達すると、搬送又はプランジャドライバは前に押され続ける。
この運動により、搬送又はプランジャドライバを破断させてカニューレの壁から
離し、以後、ドライバをカニューレ自体を通して前進させ続けることができる。
各搬送又はプランジャドライバがカニューレを通して前進する時、ドライバはフ
ィブリンの袋を突起部に対して押圧する。袋がカニューレの内側に面している突
起部に対して押圧する時、袋は裂け、カニューレを通して、新たにステープル吻
合された組織の反対側へフィブリンを解放する。一方、ブレードが前進し、新た
にステープル吻合された組織を通してブレードを押し、余剰分を切断する。アタ
ッチメントが除去され、治癒処理が始まり、切断及びステープル吻合部位にフィ
ブリンがあることにより促進される。
ューレの間の圧縮可能な接続部を備えてもよい。例えば、搬送ドライバをカニュ
ーレに接続するためにばねを使用することができる。これは、最初のカニューレ
のアンビルへの移動中においてカニューレドライバ組立体の剛性を維持すると共
に、袋に対して押圧するように搬送ドライバを前進させ続けることができる。す
なわち、一旦、カニューレの先端がアンビルに到達して停止すると、ばねが圧縮
するので、搬送ドライバは前に押され続け、搬送ドライバを袋に対して押圧させ
ることができる。この装置の残りの操作は前述の通りである。本実施例の別個の
独特な態様は、組立体を再使用することができることである。破壊される搬送ド
ライバとカニューレの間の接続部の代わりに、ばねは装置の操作の後に元の状態
に戻り、組立体を殺菌して別の用途に準備することができる。
に関連して使用することができるということに注意すべきである。例えば、カニ
ューレを採用しない実施例は治療部位の近側に到達することができ、その一方で
、カニューレを採用する実施例は治療部位の遠側に到達することができる。
了する前に)除去される大腸の部分が切除されると、このアタッチメントが使用
される。外科医は、吻合及びステープル吻合アタッチメントを電子機械ドライバ
に連結し、アンビル部を最も完全に前進させることによって始める。アンビルヘ
ッドは、除去され、露出された近端内に挿入される。この近端は、(ステープル
吻合された近端から突出している連結ポストを用いて)ステープル吻合されて閉
鎖される。外科医は、アタッチメントの軸及びSBR部が大腸のステープル吻合
された遠端を貫通するまで大腸の上に前進させる。外科医は、前進及び後退する
対応の駆動軸のナットにアンビルを連結する。次に、ハンドル内のモータの開始
により、アンビルをSBR部に向けて後退させる。アンビル部及びSBR部は、
ブレード及びステープルドライバを駆動するのに十分に近くなり、次に、ハンド
ルの他のトリガを作動することにより、対応の他の回転駆動軸が、ブレード及び
ステープルドライバをアンビル部の平坦な切断支持面に向けて前進させる。ブレ
ードは大腸のステープル吻合された閉鎖された端部を通して切断し、切断された
組織を内側貯蔵部内に残す。切断と同時に、新たに開放された端部が、(アンビ
ルの対向面に当接されて閉鎖される)SBRの周辺縁部内の穴を通して前進させ
られる一連のステープルによって共に接合されている。ステープル吻合と同時に
、ステープルドライバは、供給室内で搬送又はプランジャドライバを前に押す。
ドライバは、内側に面している突起部に対して袋を押し、それにより、袋を破断
し、フィブリンを解放する。次に、フィブリンは、流通路から出て切断及びステ
ープル吻合部位へ押される。アタッチメント及び柔軟な軸が患者から引込められ
る。
ないと装置と関連した用途に使用することができ、むしろ、他の外科装置を含み
かつ関連した用途に使用することができるので、本発明は単独で、又は、ブレー
ド、ステープラー、他の装置、又は、薬又は他の治癒物質を治療部位に搬送する
装置の組み合わせで使用することができるということを注意すべきである。
ているが、当業者は、本発明の機能及び結果を実現しつつ本明細書に記載した本
発明を修正することができるということを最初に理解するべきである。したがっ
て、本発明の広範な範囲内の例示的な特定の構造、態様及び特徴として以下の記
載を理解することができ、本発明の広範な範囲を制限するものとして理解するべ
きでない。同様な参照番号は同様な特徴の同様な要素について指している。
が図4〜9に示されている。とりわけ、図4をここで参照すると、伸長位置にあ
る吻合及びステープル吻合アタッチメントの斜視概観図が示されている。アンビ
ル部20とステープル、ブレード及び貯蔵(SBR)部25が、連結ポスト30
によって接続されており、連結ポスト30は、アンビル部20の平坦支持面35
から延びており、SBR部25の複数の回転駆動軸40の一つに取り付けられた
対応ナットと選択的に連結可能かつ取り外し可能である。
。SBR部25は、筒状であり、中空の内部又は貯蔵部45を有する。ステープ
ル吻合面50は、アンビル部20の切断支持面35に向けて軸線方向外側に面し
、かつ一連のステープル口55(ステープルハウジング58内に形成されている
)を有する。さらに、示しているように、ステープル口55の代わりに、一連の
供給室95が形成されている。ステープル駆動軸80内において、ステープル口
55を通してステープル60を駆動するために対応ステープル口55の背後に一
連のステープルドライバ65が取り付けられている。より正確には、ステープル
ドライバ65は、駆動シリンダ70の外縁部上にある一連の突出部である。駆動
シリンダ70は、SBR部25に着座し、SBR部25の第二の駆動軸(図示せ
ず)に接続されている。ステープル60は、放出される前に、示すステープル口
55の背後に取り付けられており、ステープルドライバ65及びそれらの突出部
の前進運動によってステープル口55を通して前進させられる。ブレード75は
、同様に筒状であり、ステープル駆動軸80に隣接してSBR部に着座している
。示しているように、ブレード75及びステープルドライバ65は駆動シリンダ
70に取り付けられ、駆動シリンダ70はSBR部25の第二の駆動軸(図示せ
ず)に接続されている。
ープル吻合アタッチメントのより接近した断面図が示されている。アタッチメン
トのSBR部25の壁28と、ステープルハウジング58と、ステープル口55
(図5)の代わりの供給室95とが示されている。同様な供給室95が、ステー
プル部55の代わりにステープル面50の周辺部(図4に最もよく示されている
)に沿って形成されている。供給室を筒状とすることができる。又は、供給室は
、図7に示す延長筒状断面、又は、他の形状を有しうる。供給室の口は、内側に
面している突起部又は歯92を有する最も内側の縁周辺部に沿って並べられてい
る流通路90を形成する。搬送又はプランジャドライバ110は供給室95内で
移動している。図5に最もよく示しているように、搬送又はプランジャドライバ
110は、各ステープル60がステープルハウジング58内のステープル口55
から突出する方法と同様に、供給室110の最も内側の端部から突出している。
プル吻合アタッチメントのより接近した断面図が示されている。本実施例の多く
の態様が好適な実施例の態様と同じであり、同じように番号が付けられている。
しかしながら、この別実施例において、流通路90は、内側に面している突起部
又は歯を有さない。その代わり、流通路90は障害物がない。しかしながら、フ
ィブリンの袋及び別個の搬送又はプランジャドライバの代わりに、供給室95は
、鋭い先端を有するカニューレ112を備えている。カニューレ112の鋭い先
端は、ステープル吻合面50に向けられている(すなわち、鋭い先端が供給室9
5から押し出される時、この先端は組織を穿孔し、アンビル(図示せず)の平坦
な切断面によって最終的に止められる)。カニューレ112の鋭い端部の直ぐ内
側において、カニューレ112の内側周辺部には、好適な実施例の内側に面する
突起部と同様に、内側に面する突起部又は歯92が並べられている。フィブリン
の袋100がカニューレ112の内側に着座している。搬送又はプランジャドラ
イバ110が袋100の背後に配置されている。示しているように、この搬送又
はプランジャドライバ110は、カニューレ112の壁に取り付けられているが
、カニューレの先端がアンビルに到達した後に破断して壁から離れるように配置
されている。この破断部114は影で記されている。
な実施例及び別の実施例を互いに関連して使用することができるということを注
意すべきである。
びステープル吻合段階が完了する前)除去すべき大腸の部分が切除されると、ア
タッチメントが使用される。外科医は、吻合及びステープル吻合アタッチメント
を電子機械ドライバに連結し、ハンドル(図示せず)内のモータ(図示せず)の
開始することによってアンビル部20を最も完全に前進させることによって操作
を始める。次いで、アンビル部20は、電子機械ドライバから取り外され、露出
した近端内に挿入される。この近端は、ステープル吻合で閉鎖される(連結ポス
ト30がステープル吻合された近端から突出している)。外科医は、第一の回転
駆動軸40及びアタッチメントのSBR部25を大腸のステープル吻合された遠
端を通過するまで、大腸の上方へ前進させる。次いで、外科医は、連結ポスト3
0を介して、アンビル部20を第一回転駆動軸40に再連結する。次のハンドル
(図示せず)内のモータ(図示せず)を反転させ始めることにより、アンビル部
20をSBR部25に向けて後退させ、ステープルで閉鎖された大腸の基端と大
腸の遠端を一緒にする。アンビル部20及びSBR部25がブレード75及びス
テープルドライバ65を駆動するのに十分に近くなる時、ハンドル(図示せず)
の第二トリガ(図示せず)を次に作動することにより、対応の第二回転駆動軸(
図示せず)はブレード75及びステープルドライバ65をアンビル部25の平坦
な切断支持面35に向けて前進させる。一旦、ブレード75がアンビル部25の
平坦な切断支持面35に到達すると、ブレード75は、ステープル吻合で閉鎖さ
れた大腸の近端と大腸の遠端を通して切断し、ここで切断された組織を貯蔵部4
5内に残す。一方、ステープルドライバ65(切断動作直後に行うステープル吻
合動作の時間を正確に計測するために、ステープルドライバ65は、ブレード7
5の平面のわずか背後に位置決めされており、ブレード75と共に前進する)は
、ステープル60の尻部に到達し、前進し続け、ステープル60をステープル口
55を通して、ステープル吻合面50に向けて、最後に、平坦な切断支持面35
に抗して押し、この動作により、ステープルの突起部を曲げてステープル60を
閉鎖し、それにより、新たに切断された開放した大腸の近端と遠端を共に接合す
る。
供給室95を通して各搬送又はプランジャドライバ110を押す。各搬送又はプ
ランジャドライバ110は、供給室95を通して前進する時、それがフィブリン
の袋100を圧縮する。袋が流通路95の内側に面している突起部又は歯95に
押圧する時、袋は裂け、フィブリンを流通路95を通して新たにステープル吻合
された組織に解放する。一方、ブレードドライバ76(図5)は前方に移動し、
新たにステープル吻合された組織を通してブレード75(図5)を押し、余剰分
を切断する。アタッチメントが除去され、治癒処置が始まり、切断及びステープ
ル吻合部位にフィブリンがあることによって促進される。
、各搬送又はプランジャドライバ110を押すように前進する。搬送又はプラン
ジャドライバ110は、最初にカニューレ112を供給室95から出し、組織を
通して、アンビル部20(図5)の平坦な切断面35に抗して押す。一旦、カニ
ューレ112の先端がアンビル20(図5)に到達すると、搬送又はプランジャ
ドライバ110は前に押され続ける。この運動により、搬送又はプランジャドラ
イバ110をカニューレ112の壁から離れて破断し(剥離部114が破断する
)、以後、ドライバ110は、カニューレ自体を通して前方に移動する時、ドラ
イバ110はフィブリンの袋100を圧縮する。袋100がカニューレ112の
内側に面している突起部92に対して押圧する時、袋100が裂け、カニューレ
112を通して、新たにステープル吻合された組織の反対側へフィブリンを解放
する。一方、ブレードドライバ76(図5)は前方に移動し、新たにステープル
吻合された組織を通してブレード75を押し、余剰分を切断する。アタッチメン
トが除去され、治癒処置が始まり、切断及びステープル吻合部位にフィブリンが
あることによって促進される。
りに、搬送ドライバとカニューレの間の圧縮可能な接続部を採用した実施例も同
様に機能する。例えば、もしばね(図示せず)が破断部の代わりに使用された場
合、一旦、カニューレ112の先端がアンビル(図5)に到達すると、搬送又は
プランジャドライバ110は前に押され続ける。この運動によりばねを圧縮し続
け、搬送又はプランジャドライバ110は、カニューレ112自体を通して前進
し続けることができる。各搬送又はプランジャドライバ110がカニューレを通
して前進し、ドライバ110はフィブリンの袋100を圧縮する。残りの操作は
前述の通りである。
請求の範囲のみによって制限される本発明の広範な精神及び原理から逸脱するこ
となく、変形及び修正が可能であることが当業者に明らかである。
使用される電子機械装置ドライバのハンドル及び柔軟な軸の側断面図である。
斜視図である。
タッチメントの側断面図であり、ステープル口内にあるステープルを示している
。
タッチメントの側断面図であり、供給室内にある袋を示している。
タッチメントの正面断面図であり、供給室内にある袋を示している。
チメントの側断面図であり、カニューレを示している。
チメントの正面断面図であり、カニューレを示している。
Claims (19)
- 【請求項1】 流体を収納する供給室と、 治療部位と前記供給室を連通している流通路と、 前記流通路を通して前記流体を押すのに必要な力よりも大きな力で前記供給室
内で移動する搬送ドライバとを備えた流体搬送装置。 - 【請求項2】 前記供給室内にありかつ前記流体を包囲する袋をさらに備え
、前記供給室及び前記流通路の中の少なくとも一つは、少なくとも一つの鋭い内
側部分を有する請求項1に記載の装置。 - 【請求項3】 前記供給室及び前記流通路の中の少なくとも一つは、内部と
、前記流通路の壁から延びておりかつ前記内部に向けられている少なくとも一つ
の鋭い突起部とを有している請求項2に記載の装置。 - 【請求項4】 前記突起部は、前記搬送ドライバの方向と反対の方向に向け
られている請求項3に記載の装置。 - 【請求項5】 ハウジングをさらに備え、前記ハウジングは、前記供給室を
収納し、かつまっすぐなステープルと適合する口部を有する請求項1に記載の装
置。 - 【請求項6】 前記搬送ドライバは回転駆動軸の延長部であり、前記回転駆
動軸はステープルドライバも駆動する請求項5に記載の装置。 - 【請求項7】 前記搬送ドライバは筒状である請求項5に記載の装置。
- 【請求項8】 カニューレをさらに備え、前記カニューレは、鋭い遠端を有
し、前記カニューレは、前記供給室内で移動する請求項1に記載の装置。 - 【請求項9】 前記カニューレ内にありかつ前記流体を包囲する袋をさらに
備え、前記カニューレは、少なくとも一つの鋭い内側部分を有する請求項8に記
載の装置。 - 【請求項10】 前記カニューレは、内部と、前記流通路の壁から延びてお
りかつ前記内部に向けられている少なくとも一つの鋭い突起部とを有している請
求項9に記載の装置。 - 【請求項11】 前記突起部は、前記搬送ドライバの方向と反対の方向に向
けられている請求項10に記載の装置。 - 【請求項12】 ハウジングをさらに備え、前記ハウジングは、前記供給室
を収納し、かつまっすぐなステープルと適合する口部を有する請求項8に記載の
装置。 - 【請求項13】 前記搬送ドライバは回転駆動軸の延長部であり、前記回転
駆動軸はステープルドライバも駆動する請求項12に記載の装置。 - 【請求項14】 前記搬送ドライバは筒状である請求項12に記載の装置。
- 【請求項15】 前記搬送ドライバは、前記カニューレの近端の延長部であ
る請求項8に記載の装置。 - 【請求項16】 前記搬送ドライバと前記カニューレを接続するコネクタ部
をさらに有する請求項15に記載の装置。 - 【請求項17】 前記コネクタ部は前記搬送ドライバ又は前記カニューレよ
りも構造的に弱い請求項16に記載の装置。 - 【請求項18】 前記コネクタ部は圧縮可能である請求項16に記載の装置
。 - 【請求項19】 前記コネクタ部はばねを有する請求項18に記載の装置。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/510,932 | 2000-02-22 | ||
US09/510,932 US6491201B1 (en) | 2000-02-22 | 2000-02-22 | Fluid delivery mechanism for use with anastomosing, stapling, and resecting instruments |
PCT/US2001/005433 WO2001062162A1 (en) | 2000-02-22 | 2001-02-21 | A fluid delivery mechanism for use with anastomosing, stapling, and resecting instruments |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP2009268155A Division JP5087065B2 (ja) | 2000-02-22 | 2009-11-25 | 吻合、ステープル吻合及び切除器具用の流体搬送機構 |
Publications (2)
Publication Number | Publication Date |
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JP2003532455A true JP2003532455A (ja) | 2003-11-05 |
JP4485730B2 JP4485730B2 (ja) | 2010-06-23 |
Family
ID=24032779
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Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001561233A Expired - Fee Related JP4485730B2 (ja) | 2000-02-22 | 2001-02-21 | 吻合、ステープル吻合及び切除器具用の流体搬送機構 |
JP2009268155A Expired - Fee Related JP5087065B2 (ja) | 2000-02-22 | 2009-11-25 | 吻合、ステープル吻合及び切除器具用の流体搬送機構 |
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JP2009268155A Expired - Fee Related JP5087065B2 (ja) | 2000-02-22 | 2009-11-25 | 吻合、ステープル吻合及び切除器具用の流体搬送機構 |
Country Status (8)
Country | Link |
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US (2) | US6491201B1 (ja) |
EP (1) | EP1257207B1 (ja) |
JP (2) | JP4485730B2 (ja) |
AT (1) | ATE308275T1 (ja) |
AU (1) | AU2001238553A1 (ja) |
DE (1) | DE60114570T2 (ja) |
ES (1) | ES2250361T3 (ja) |
WO (1) | WO2001062162A1 (ja) |
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JP2009202002A (ja) * | 2000-11-28 | 2009-09-10 | Power Medical Interventions Inc | 電気機械的外科医療用装置 |
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Also Published As
Publication number | Publication date |
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EP1257207B1 (en) | 2005-11-02 |
US20030089757A1 (en) | 2003-05-15 |
EP1257207A1 (en) | 2002-11-20 |
US6695199B2 (en) | 2004-02-24 |
JP2010042310A (ja) | 2010-02-25 |
US6491201B1 (en) | 2002-12-10 |
DE60114570D1 (de) | 2005-12-08 |
ATE308275T1 (de) | 2005-11-15 |
WO2001062162A1 (en) | 2001-08-30 |
JP4485730B2 (ja) | 2010-06-23 |
JP5087065B2 (ja) | 2012-11-28 |
ES2250361T3 (es) | 2006-04-16 |
AU2001238553A1 (en) | 2001-09-03 |
DE60114570T2 (de) | 2006-07-06 |
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LAPS | Cancellation because of no payment of annual fees |