JPH08229050A - 電気外科的装置、電気外科的方法、組織の電気外科的処理方法、及び電気外科的インピーダンスフィードバック制御装置 - Google Patents
電気外科的装置、電気外科的方法、組織の電気外科的処理方法、及び電気外科的インピーダンスフィードバック制御装置Info
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Abstract
を判定し、特に組織の凝固終了時点を判定すること。 【解決手段】 治療用電極で処理前、処理中、又は処理
後に、組織の1つ以上の電気的パラメータを測定する照
会電極を含む電気外科的装置であって、被測定パラメー
タは組織の凝固の完了等の組織の特性判定に用いられ、
例えば、被測定組織特性を表す信号に応じた電気外科的
エネルギーの伝達制御信号が与えられ、この制御信号
は、RFエネルギーを完全にシャットオフにするか、ま
たは治療用電極を介して組織に伝達されるエネルギーの
レベル、周波数、その他を調節する。
Description
理に関し、特に、電気外科的装置により処理されている
組織のインピーダンスを測定することにより、組織の電
気外科的処理を制御する電気外科的装置、電気外科的方
法、組織の電気外科的処理方法、及び電気外科的インピ
ーダンスフィードバック制御装置に関するものである。
組織の溶接、切除、及び解剖のために使用される。その
ような器具に高周波(RF)レンジの治療用電気外科的
エネルギーを供給するために電気外科的ジェネレータが
用いられる。通常そのようなジェネレータは電圧及び/
又は電流を調整して選択された範囲のパワーレベルが伝
達され最大パワーレベルを越えないようにする制御を含
む。
主要な制御は、組織がRFエネルギーで処理されるとき
組織に何が起きているかの観察に応答する外科医の経験
によって行われる。しばしば、特に内視鏡検査の処置に
対して、外科医は組織に何が起きているかを容易には見
ることができない。また、RFエネルギーによる組織の
性質の変化は非常に迅速に起きる。この結果、生じるか
もしれないいくつかの問題は組織の焦げ、組織の外科器
具の電極への固着、熱放散、及び組織の過剰な処理又は
処理不足を生じるということである。
ンピーダンスが変わることが認識されている。組織のイ
ンピーダンスが変わるとき組織に伝達されるパワーを制
御する試みがなされてきた。例えば、一定のパワー又は
電圧レベルを維持するために組織のインピーダンスが用
いられてきた。また、組織のインピーダンス、とりわけ
RFパワーが加えられる時の組織のインピーダンスの微
分商は、初期パワーレベルを決定するため及びインピー
ダンスの微分商がプリセットされた値に到達するとRF
パワーを切り替えてオフにするために用いられてきた。
議論にもかかわらず、組織への電気外科的エネルギーの
伝達及び/又はいつ組織の処理が最適のレベルに到達し
たかの決定の制御において、改良が引き続き要求されて
いる。
ンピーダンス変化を測定して組織の特性を判定するこ
と、特に様々な組織のインピーダンス又はある範囲の組
織のインピーダンスに対して凝固の終了点を判定するた
めの装置及び方法を提供するという要求がある。
用電極で処理前、処理中に又は処理後に、組織の1つ以
上の電気的パラメータを測定する照会電極を含む電気外
科的装置を提供する。これらの測定された組織のパラメ
ータは、例えば、組織のタイプ、組織のインピーダンス
特性、組織処理の状態、組織の凝固の完了、その他、様
々な組織の特性の判定に用いられる。この発明の1態様
により、測定された組織の特性を表す信号が提供され
る。1実施例において、測定された組織の特性に応じて
電気外科的エネルギーの伝達を制御する制御信号が与え
られる。この制御信号は、RFエネルギーを完全にシャ
ットオフにするか、または治療用電極を介して組織に伝
達されるエネルギーのレベル、周波数、その他を調節す
る。
いられて組織のインピーダンスを測定する。しかしなが
ら、様々な他の電気的パラメータが測定され又は用いら
れて組織の特性を判定する。
器具の末端効果器の組織に接触する面に連絡(即ち、そ
こに配置され、その上に配置され、そこに重ねられ、そ
こに接着され、その他)している電気的に反対の照会電
極の間に配置された組織のインピーダンスをモニタする
インピーダンスモニタ装置及び/又は方法を提供する。
この器具は更に、末端効果器に関係付けられている、電
気的に反対の治療用電極を備えている。この治療用電極
は、これに接触している組織を処理するために治療用の
電気外科的エネルギーを伝達するようになっている。
ギーが組織に伝達されたとき、連続的又は周期的に組織
のインピーダンスを測定する組織インピーダンスモニタ
が提供される。この発明により、電気外科的エネルギー
で処理する前、処理中、又は処理後に、組織のインピー
ダンスに基づいて、組織の特性が判定される。好ましい
実施例において、モニタされた組織のインピーダンス
は、電気外科的エネルギーが組織に伝達されるとき時間
にわたり予想される組織のインピーダンスの振る舞いの
モデルに基づいて、組織の状態を判定するのに用いられ
る。これを以下に、より詳細に記載する。組織の状態を
表す信号がユーザ又は器具のコントローラに与えられ
る。この装置はまた、処理が完了したとき電気的エネル
ギーを自動的にオフにするスイッチを含んでもよい。
れば、組織のインピーダンスは電気的エネルギーが与え
られると最初に低下し、次いで凝固が起こると再び上昇
し始める。この知られた組織の振る舞いに基づいて、こ
の発明の好ましい実施例においては、組織の処理が完了
する点が選択される。
値、即ちエネルギーが印加されるときのインピーダンス
がその最低値であるとき、が確定される。次いで、所望
の組織の効果をもたらす予測されるインピーダンス値
が、確定された最小インピーダンスの選ばれた関数を計
算することにより決定される。測定されたインピーダン
スが、例えば。凝固、組織の溶接、又はジアテルミーの
レベル、といった所望の結果のためのインピーダンス値
のレベルにまで上昇すると、器具はそのような事情のた
めの応答を表す。この発明は、好ましくは、組織のタイ
プ、面積及び/又は体積によって変化する、予想される
組織のインピーダンスの範囲のための条件が検出される
ように適合されている。
態とは凝固が完了するときである。この点に到達する
と、フィードバック信号が制御ユニット又はユーザに与
えられ、そのときエネルギーの供給はオフに切り替えら
れる。フィードバック信号は、例えば、ユーザへの視
覚、聴覚又は触覚信号でよく、及び/又は制御ユニット
に指令を与えて組織に供給されるエネルギーを自動的に
オフに切り替えてもよい。
に組織を凝固させるための電気外科的装置が提供され
る。この装置は、その間で凝固させるべき組織を係合す
るために互いに対して移動可能な第1及び第2の要素を
含む末端効果器を備えている。第1及び第2の要素の各
々は対向し組織に接触する面を備えている。第1及び第
2の要素の少なくとも1つは、電気的に反対の治療用ポ
ールに関係付けられている第1の治療用電極を含んでい
る。第1の治療用電極は、凝固させるべく係合された組
織と接触するように配置されている。照会電極は第1の
ポールに対応する少なくとも1つの照会電極と、電気的
に反対の第2のポールに対応する少なくとも1つの照会
電極とを備えている。好ましくは、組織が係合させられ
ると、両照会電極が凝固させるべき組織と接触する。照
会電極は好ましくは、所望の情報に依存して戦略的な位
置におけるインピーダンスを測定するように配置されて
いる。例えば、その電極はインターフェースするか対向
し、組織を係合している面の周辺に配置してもよい。パ
ワー制御信号に応答するパワーコントローラはRFエネ
ルギーを第1及び/又は第2の要素の電極に接触してい
る組織に供給する。
照会電極に伝達する電気回路に接続されている。インピ
ーダンス測定回路は照会電極の間の組織のインピーダン
スを測定する。制御信号をジェネレータに供給して治療
用電極への出力を制御するフィードバック回路が、イン
ピーダンス測定回路に接続されている。
への制御信号は、測定されたインピーダンス値に基づい
て、治療用電極への出力を制御する。フィードバック回
路は、最小インピーダンス値を決定しその最小インピー
ダンス値を保持する第1の装置を含んでいる。第2の装
置は第1の装置に接続されたスレショルド決定回路であ
る。スレショルド決定回路は、スレショルドインピーダ
ンス値を保持された最小インピーダンス値の関数として
決定する。
ンスの関数を決定するためのアナログ装置又は、入力さ
れた最小インピーダンス値に基づいてスレショルドイン
ピーダンス値を決定する、例えば、ルックアップテーブ
ルを含むディジタル回路を備えている。
較器は測定されたインピーダンス値をスレショルドイン
ピーダンス値と比較して、パワーコントローラへのパワ
ーコントロール信号を発生し、測定されたインピーダン
ス値がスレショルドインピーダンス値を越えたときに組
織に伝達される治療用RFエネルギー制御する。
ルギーを器具に供給して、第1及び第2の要素の間に配
置された組織を凝固させる少なくとも1つの電気的スイ
ッチを含んでもよい。
たインピーダンス値がスレショルドインピーダンス値を
越えたとき、のような多数の条件下で、組織に供給され
るパワーを選択的にオフに切り替えてもよい。
(即ち、測定されたときの波形でエネルギーを任意のポ
ールから他の任意のポールに位相関係を持ちながら供給
する2つ以上の治療用電極を含む)でよいが、末端効果
器は好ましくは、2つの電気的に反対の治療用ポールに
対応する、2つの電気的に反対の治療用電極を含んでい
る。
会及び治療用電極は対向する組織に接触する面の一方又
は両方の上に配置されている。第1及び第2の電気的に
反対の照会電極の各々は、1つ以上の組織の接触する照
会電極を備え、第1及び第2の治療用電極の各々は1つ
以上の組織の接触する治療用電極を備えている。治療用
電極は電気外科的装置の遠端点に配置されており、第1
及び第2の要素が互いに閉じて組織を係合すると、電気
的に反対の治療用電極は、係合された組織の部分の間
の、同一面上又は対向面上のいずれかに配置される。
されており、第1及び第2の要素が互いに閉じて組織を
係合すると、電気的に反対の照会電極は、係合された組
織の部分の間の、同一面上又は対向面上のいずれかに配
置される。インピーダンスモニタ回路は、低い電圧のR
Fエネルギーが照会電極を通して組織に伝達されると、
照会電極の間の組織のインピーダンスをモニタする。照
会電極を介して伝達されるRFエネルギーの周波数は、
治療用電極を介して伝達されるエネルギーの周波数と異
ならせて、電気的な相互作用を減少させることが好まし
い。
ポールに対応する治療用電極の各々は、インターフェー
ス面に関して、第2のポールに対応する治療用電極の各
々からオフセットされている。換言すれば、治療用電極
は互いにオフセットされており、それによりそれらはイ
ンターフェース面上で正反対には互いに対向しないか、
又は同一面上で互いに分離され絶縁されている。
は、第1のインターフェース面と第2のインターフェー
ス面との間の圧縮ゾーンにおいて組織を圧縮し、その圧
縮ゾーンを通じて治療用電気エネルギーを印加する。よ
り好ましくは、圧縮ゾーンとは、組織を他方のインター
フェース面に対して圧縮するインターフェース面の1つ
の上の圧縮用隆起部により決まる領域である。これに替
えて、又はこれに追加して、両インターフェース面の上
に圧縮用隆起部が存在してもよい。照会電極は、圧縮ゾ
ーン内で、圧縮ゾーンに隣接して離れて、末端効果器上
の遠端点又は近端点に、その他、器具の応用に依存し
て、圧縮ゾーンの横の外側に配置してもよい。
を含む。この切断要素は、凝固位置において又はその近
くで組織を切断するように配置されている。好ましく
は、凝固は、あらゆる機械的又は他の切断の前又は凝固
位置において又はその回りで完了する。照会電極がこう
して配置されるので、インピーダンスセンサは凝固又は
焼灼が切断位置において生じたときを判定できる。次い
で、切断要素が使用されて凝固した組織又は組織の凝固
の2つのゾーンの間を切断する。
は、リニアな切断用の機械的ステープラに類似のリニア
カッターに取り込まれる。この実施例においては、器具
は好ましくは、1つの治療用ポールに結合している2つ
の実質的に平行で伸張した治療用電極棒と、切断手段が
その棒の間を走行するためのスロットとを備えている。
オプションとして、ステープルの1つ以上の列を棒のス
ロットの外側の各側の上に設けて、治療過程での組織の
機械的な安全等を確保するようにしてもよい。
具の2つの要素の間にクランプされ、RFエネルギーの
形の電気エネルギーが圧縮された組織に供給されて、2
つの実質的に平行な棒に沿って組織を凝固又は焼灼す
る。同時に、好ましくはより低い電圧で異なるRF周波
数の電気的エネルギーが照会電極に供給されてその間の
組織のインピーダンスを感知する。この特定の電極形態
を持つ装置のインピーダンスのモデルに基づいて、最小
インピーダンスの適当な関数がインピーダンスフィード
バック回路に取り込まれて適当なスレショルドインピー
ダンスレベルを決定する。警報機構が用いられてインピ
ーダンスがスレショルドインピーダンスレベルの範囲外
又それを越えるとユーザに警告を与える。また、警告信
号は制御回路又はパワーコントローラに伝達されて、R
Fエネルギーをオフに切り替えるか、又は、ジェネレー
タの出力レベル、周波数、波形、その他、治療用電極を
介して伝達されるものを調整する。
外科的処理方法が提供される。好ましくは、この方法
は、電気外科的器具の末端効果器に関係付けられた1つ
以上の組織照会電極を介して、電気外科的に処理される
べき組織にRFエネルギーを印加する段階と、器具の末
端効果器に関係付けられた電気的に反対の照会電極の間
の組織のインピーダンスを測定する段階と、組織の測定
されたインピーダンスを表すインピーダンス信号を発生
する段階と、そしてこのインピーダンス信号に応答して
治療用電極を介して組織に印加されるRFエネルギーを
制御する段階とを備えている。
エネルギーを制御する段階は、最小インピーダンス値を
決定し保持する段階と、最小インピーダンス値の関数に
基づいてスレショルドインピーダンス値を決定する段階
と、測定されたインピーダンス値をスレショルドインピ
ーダンス値と比較する段階と、測定されたインピーダン
ス値がスレショルドインピーダンス値を越えた状態でコ
ントローラを制御し又はそのパワーをオフに切り替える
制御信号を発生する段階とを備えている。
処理の間、組織を電気外科的に処理する方法は、第1及
び第2の組織係合用表面を備える末端効果器を有する電
気外科的器具を用意し、この場合前記第1及び第2の組
織係合用表面の少なくとも1つはその上に、電気外科的
システムの第1のポールに関係付けられた組織に接触す
る治療用電極を含ませ、前記第1及び第2の組織係合用
表面の少なくとも1つはその上に、電気外科的治療シス
テムの第2のポールに関係付けられた組織に接触する治
療用電極を含ませ、前記第1及び第2の組織係合用表面
の少なくとも1つはその上に、インピーダンス感知シス
テムの第1のポールに関係付けられた組織に接触する第
1の照会電極と、インピーダンス感知システムの第2の
ポールに関係付けられた組織に接触する第2の照会電極
とを含ませる段階と、前記第1及び第2の組織係合表面
の間に、処理されるべき組織を係合する段階と、前記第
1及び第2の組織に接触する治療用電極に供給されるR
Fエネルギーを選択的に制御してその間に配置された組
織を凝固させる段階と、処理された組織のインピーダン
スを前記第1及び第2の照会電極で測定する段階と、組
織の処理が完了するときのスレショルドインピーダンス
を設定する段階と、測定されたインピーダンス値を前記
スレショルドインピーダンス値と比較する段階と、そし
て測定されたインピーダンス値が前記スレショルドイン
ピーダンス値に到達するか越えるという条件で、前記第
1及び第2の治療用電極に結合したRFエネルギーを制
御又はオフに切り替える段階とを備えている。
載、添付の図面及び特許請求の範囲から明らかである。
ラ、バイポーラ及びマルチポーラ、及び通常のものと内
視鏡の両方の様々な電気外科的器具に適用可能である
が、以下では内視鏡、バイポーラ、リニアな切断及びス
テープリング器具に関して記載する。
この技術において知られており、例えば、米国特許第
4,608,981号、第4,633,874号、及び参
考のためにここに取り込んだ米国特許出願シリアル番号
第07/917,636号において議論されている。
時間における組織のインピーダンスを決定するために、
照会電極が好ましく使用される。しかしながら、電流又
は電圧の伝達、位相シフト、及び組織の周波数応答のモ
ニタといった他の使用も考えられる。
ピーダンスモニタ装置は、組織がある特別の位置で所望
の度合いにまで処理された時を判定する。この処理は、
過剰な熱の放散、組織の固着、焼け又は焦げが生じる前
で、組織が焼灼した時点で完了することが好ましい。電
気外科的エネルギーで加熱されている時の組織のインピ
ーダンスは、一般に特性組織インピーダンス曲線に従
う。インピーダンス曲線に従って、一般にインピーダン
スは減少して、最小値に達し、次いで凝固と組織の乾燥
が起こると上昇する。特性曲線上のあるインピーダンス
又はある範囲のインピーダンスで、凝固は予測可能に生
じる。
科的装置を用いて電気外科的エネルギーを加えている間
の時間の、組織のインピーダンスの変化を示す特性イン
ピーダンス曲線である。この発明は曲線上で凝固が起き
たスレショルドインピーダンスZTARGETの点146を決
定する。このインピーダンスは曲線上の最低インピーダ
ンスZMINの点145、すなわち、インピーダンスの低
下が停止し、上昇し始める時に基づいている。最低イン
ピーダンスの関数f(ZMINi)は凝固が起きるおよその
点、ZTARGETを予測するために用いられる。
フィードバック装置とともに用いられるこの発明の装置
が示されている。図1から図4において、内腔がその中
を伸びている鞘30と鞘30の遠端点から伸びている末
端効果器15とに結合されたハウジング16を有する内
視鏡のリニアな切断及びステープリング装置10が示さ
れている。末端効果器15は、互いに面と向かう顎部材
32,34からなる第1及び第2要素を備えている。顎
部材32は顎部材34に移動可能に固定されている。ハ
ウジング16は、顎部材32,34を閉じるクランプ用
引き金12と、RFスイッチ戻り止めアーム58(図5
参照)と、RFエネルギーをオンにする電気的スイッチ
59に接続された電気的スイッチ接点67a,67b
(図5)と、切断要素11を組織に進入させる点火用引
き金14と、ステープル17(図17)を適用するため
のくさび13とを有している。図1においては顎部材3
2,34はクランプされていない位置にあり、図2にお
いては電気外科的エネルギーを加える前及び切断とステ
ープリングをする前のクランプされた位置にあり、図3
においては電気外科的エネルギーを加えた後で切断とス
テープリングをする前のクランプされた位置にあり、図
4においては切断とステープリングをした後のクランプ
された位置にある状態が示されている。
金床(以下アンビル称する)18と、顎部材32の長手
方向に沿って伸びているU字形治療用電極39と、U字
形治療用電極39の外側をとりまくU字形絶縁部材31
とを備えている。顎部材32は顎部材34の内面35に
実質的に面している内面33を有している。U字形治療
用電極39は、第1のポールを形成し且つ実質的に内面
33の長手方向に沿ってその上に配置され伸びている2
つの電気的連絡用電極棒27,28を備えている。U字
形治療用電極39はアルミニウム又は外科用のグレード
のステンレススティールといった導体でできている。電
気的連絡用電極棒27,28はU字形治療用電極39の
中央を通って縦方向に伸びているナイフチャネル29に
より分離されている。U字形治療用電極39の各側に一
列のステープルを形成するために、ステープルの端部を
受け入れるアンビル18上に配置されたポケット36
が、電気的連絡用電極棒27,28の長手方向の外側に
沿う内面33に沿って配置されている。
材31は内面33のアンビル部33aに対して外側に伸
びる隆起部56を形成している。U字形治療用電極39
はバイポーラ組織処理又は治療システムの第1ポールと
して働く。アンビル18は導電性材料でできていてバイ
ポーラ組織処理又は治療システムの第2ポールとして働
く。アンビルはU字形治療用電極39と電気的に反対で
ある。アンビル18はU字形絶縁部材31によりU字形
治療用電極39から電気的に分離されている。
カートリッジチャネル22の中に解放可能に挿入された
カートリッジ23を備えている。カートリッジ23はく
さび13のためのトラック25と、カートリッジ23の
中心を通って縦方向に伸びるナイフチャネル26と、2
組の列にそれぞれ配置されたトラック25及びステープ
ル17の中に伸びる一連のドライバ24とを備えてい
る。
に配置され且つカートリッジチャネル22から絶縁材料
により分離されている第1の照会電極51と、ナイフチ
ャネル26によって決められる平面の第1の照会電極5
1と反対側の横のカートリッジチャネル22上に配置さ
れ且つカートリッジチャネル22から絶縁材料により分
離されている第2の照会電極52とを備えている。第1
の照会電極51及び第2の照会電極52は表面35の横
側面周辺に向かって配置されており、それにより、係合
している組織の部分全体を横切る組織のインピーダンス
が測定される。第1の照会電極51及び第2の照会電極
52は又、カートリッジ22により決められる平面から
へこんでおり、それにより顎部材32,34が閉じても
第1の照会電極51及び第2の照会電極52がアンビル
18に接触しないようになっている。
通って伸びている導電性の封止官38を有している(図
1及び図2)。好ましい実施例において、封止官38は
顎封止管及び電気的接点として働く。チャネルリテイナ
37a(図5、図7、図9、図10、図11)が封止官
38の近端点から伸びており、且つ封止官38の残りを
通って遠方に伸びて顎部材34を形成しているチャネル
37に確保されている。
て、組織をその間に係合している顎部材32,34を互
いの方向に閉じさせるクランプ用引き金12を有してい
る。クランプ用引き金12を回転すると、封止官38は
顎部材32のキャミング面32a(図1)にわたって鞘
30を通って同軸的に前進して、顎部材32、34の間
にある組織上で顎部材32、34を閉じさせる。
でドライブロッド41(図5から図11)の同軸的移動
をガイドする。以下に、より詳細に記載するように、ド
ライブロッド41は点火用引き金14の回転により前進
する。ドライブロッド41はその遠端点でブロック43
に結合されている。ブロック43は、切断要素11及び
ステープルドライブ用くさび13に結合されている。ド
ライブロッド41はブロック43によりその切断要素1
1及びステープルドライブ用くさび13を末端効果器1
5内に前進させる。
させると、切断要素11は電気的連絡用電極棒27,2
8の間のナイフチャネル26を通って前進し、顎部材3
2、34に係合されている組織が焼灼されたときにその
組織を切断する。こうして、電気的連絡用電極棒27,
28により形成された凝固ラインに対して、切断ライン
は中間となる。ドライブロッド41は同時にブロック4
3を前進させてくさび13を前進させ、くさび13はド
ライバ24をステープル17の中にドライブしてステー
プル17を組織を通して発射させ且つアンビル18のポ
ケット36の中にドライブする。ステープル17は切断
要素11が組織を切断するとき、切断要素11の各側の
上の単一の縦列内に適用される。
ブ44は、ノブ44に直接的又は間接的に結合している
封止官38、チャネルリテイナ37a、及び末端効果器
15を回転させ、それによりノブ44は顎部材32、3
4の末端効果器15の回転的配置のために使用される。
ノブ44は封止官38の刻み目38aにフィットし且つ
係合するペグ(図示せず)を含んでいる。封止官38は
その近端点でハウジング16にフィットしている。
1、図21、図22)から電気的エネルギーが、以下に
記載するようなコネクタ又は、例えば、米国特許出願シ
リアル番号台08/095,797号に記載の接続手段
を介して、電極39、アンビル18、第1の照会電極5
1、151(図19)又は251(図20)に供給され
る。電気外科的ジェネレータ70、90は、ハウジング
16に配置されたRF電気的スイッチ59によりユーザ
により制御される。
d(図1、図5、図8)が装置のハウジング16内に伸
びており、U字形治療用電極39、アンビル18、第1
の照会電極51、及び第2の照会電極52にそれぞれエ
ネルギーを伝達する。ワイヤ19a、19bは低インピ
ーダンスコンタクト要素20a、20bにそれぞれ接続
されている。線細工ばね47a、47bがそれらの遠端
点で露出している。線細工ばね47a、47bはチャネ
ルリテイナ37aの近端点に配置されている封止官38
及びコンタクトリング49bに向かってそれぞれバイア
スされており、それにより封止官38及びコンタクトリ
ング49bにそれぞれ接触させられている(図14)。
ワイヤ19a、19bはハウジング16内でリボンワイ
ヤ50の形で伸びている(図13)。リボンワイヤ50
はコンタクトフィンガ42c、42dを有するコンタク
トブロック41に接続されている。コンタクトブロック
41はハウジング16に確保されている。ワイヤ19c
はコンタクトフィンガ42cに電気的に接触しており、
ワイヤ19dはコンタクトフィンガ42dに電気的に接
触している。コンタクトフィンガ42c、42dは、チ
ャネルリテイナ37aの近端点に配置されているコンタ
クトリング49c、49dに向けてそれぞれバイアスさ
れており、それによりコンタクトリング49c、49d
にそれぞれ電気的に接触している。
に、ワイヤ19aは線細工ばね47aによってアンビル
18に電気的に接触する。線細工ばね47aはこの時封
止官38に電気的に接触する。封止官38はこの時アン
ビル18に電気的に接触する。
第1の照会電極51の電流を伝達しコンタクトブロック
41の第1のスプリングコンタクトフィンガー42cに
接続されている。第1のスプリングコンタクトフィンガ
ー42cはコンタクトリング49cと電気的に接触する
ようにコンタクトリング49cに対してバイアスされて
いる。コンタクトリング49cは封止管38を介して電
極51まで伸びているワイヤ40cに接触している。
第2の照会電極52に電流を伝達しコンタクトブロック
41の第2のスプリングコンタクトフィンガー42dに
接続されている。第2のスプリングコンタクトフィンガ
ー42dはコンタクトリング49dと電気的に接触する
ようにコンタクトリング49dに対してバイアスされて
いる。コンタクトリング49dは封止管38を介して電
極52まで伸びているワイヤ40dに接触している。
9c、49d及びワイヤフォーム47a、47bと第1
のスプリングコンタクトフィンガー42c、第2のスプ
リングコンタクトフィンガー42dとの間がそれぞれ接
触している間は、封止管38及びリングコンタクト49
b、49c、及び49dはノブ44の回転を可能にす
る。リングコンタクト49b、49c、49dは互いに
電気的に絶縁されており、且つ封止管38からも電気的
に絶縁されている。
aにフィットしているシール45を介して伸びており、
チャネルリテイナ37aは封止管38にフィットしてい
る。
車12aを有しており、歯車12aはヨーク66の歯6
6bに可動的に係合している。ヨーク66はその遠端点
上で封止管38に結合している。クランプ用引き金12
が駆動されると、歯車12aはヨーク66内の歯66b
に係合してヨーク66を遠方に前進させる。封止管38
はキャミング面32aにわたり前進するとき顎32、3
4を閉じる。
の回転よりRFエネルギーがスイッチオンし、治療用及
び照会電極に供給される。RFスイッチ59が回転する
と、RFスイッチ59がその元の位置に手動により回転
して戻されない限り、戻り止め突起59aが戻り止めア
ーム58上の戻り止め突起58aの下にフックする。R
Fエネルギーはまた、下記のように電気的にオフにでき
る。
67bを有する(図7)。スイッチがオンになると可動
接点67aはRFスイッチ59とともに回転して固定接
点67bに接触する。
ク66の近端点上の階段状の出っ張り部66aに隣接す
るヨーク66の近端点に係合している。ヨーク66がク
ランプ用引き金12により前進させられると、出っ張り
部60aはヨーク66の近端点の後ろの下方に回転し、
それにより解放ボタン60を押すまではヨーク66が元
に戻る(リトラクトする)のを防止する。こうして、ユ
ーザが解放ボタン60により顎32、34を解放するま
では顎32、34は閉じている。
上にあるフィンガー59cを含んでいる。解放ボタン6
0の出っ張り部60aはフィンガー59cの間にフィッ
トする。ヨーク66が遠くに前進させられてRFスイッ
チ59のフィンガー59cがヨーク66の近端点の後ろ
で自由に回転するまでは、RFスイッチ59は駆動、即
ち正方向に回転させることはできない。
溝53aに係合する下側フック59bを含んでいる。点
火ラック53は点火引き金14の歯車14aに係合する
歯車53bを含んでいる。点火ラック53はその遠端点
状で歯車54に結合しており、歯車54は駆動ロッド4
1に係合している。
53は遠方に前進させられてピニオン54を回転させ、
ピニオン54は駆動ロッド41を遠方に前進させて切断
要素11を前進させ、ステープル17を末端効果器15
により係合している組織の中にドライブする。
イッチ59の下側フック59bが点火ラック53の溝5
3aからはずれないかぎり、前進することができない。
これはRFスイッチ59が駆動された時にのみ生じる。
2、34が閉じられるまでは、RFエネルギー、ステー
プル又はナイフの駆動の適用を防止する少なくとも1つ
のロックアウト装置を含む。ロックアウト装置は図1か
ら図4に示されるように適切なシーケンスに従うことが
要求される。即ち、顎が閉じた後にRFエネルギーが加
えられ、次いでステープルと切断要素の適用がある。ま
た、RFスイッチは戻り止めされているので、RFスイ
ッチ59が手動で解放されるか、電気外科的ジェネレー
タ70,90への帰還制御信号によりRFエネルギーが
オフに切り替えられるまで、RFエネルギーは連続的に
供給される。
14はインターロックされており、スプリング57は両
引き金12、14に機械的に結合されている。組織がク
ランプされた顎部材32、34の間に係合され、RFエ
ネルギーが加えられると、ハウジング16上に配置され
ている点火引き金14を駆動して係合された組織を通し
て切断要素11を前進させ、組織を切断することができ
る。同時に、点火引き金14が駆動されると、くさび1
3がトラック25を通して前進させられて、ドライバ2
4をステープル17に向けて移動させ,それによりステ
ープル17を組織を通してアンビルポケット36の中に
ドライブする。
効果器を示す。この実施例においては、末端効果器は、
照会電極の配置を除き、図17に付いて記載したものと
同一である。第1の照会電極は、一対の電極151であ
り、ナイフチャネル26の反対側の上のカートリッジチ
ャネル22上に配置され表面35の側部周辺に向かって
いる。第2の照会電極及び第2の治療用電極は同じであ
りアンビル18を備えている。
末端効果器を示す。この実施例においては、照会電極は
一対の電極251であり、アンビル18上に配置されて
おり且つ絶縁部材18aによりアンビル18から電気的
に分離されている。第1の照会電極251はナイフチャ
ネル29の互いに反対側に配置されている。第2の照会
電極は一対の電極252であり、カートリッジチャネル
22の上に配置されており、且つ絶縁部材によりカート
リッジチャネル22から電気的に分離されている。第2
の照会電極252はナイフチャネル29の互いに反対側
に配置されている。第1の照会電極251は装置周辺側
で対応する第2照会電極に直接的に対向しており、それ
によりモニタされるインピーダンスは、組織の凝固が装
置の中央から進む時、典型的に加熱される周辺部におけ
る組織に基づいている。
9及び20に示したが、なかんずく組織のモニタが望ま
れる処理の位置またはステージによって、この発明によ
り照会電極及び治療用電極の多くの位置が可能であるこ
とを理解すべきである。更に、1つ以上の照会電極が1
つ以上の処理電極でジェネレータへの導通パスを分け合
うことができる。
ダンスモニタ装置(インピーダンス測定回路)210の
アナログ装置の実施例の概略的ブロック図が示されてい
る。このインピーダンスモニタ装置は凝固が完了した時
を判定する。
ように位置づけられる。次いで、適切に位置づけられる
と、RFエネルギーが組織に供給される。
療用電極であるU字形治療用電極39及びアンビル18
を介して、装置10の末端効果器15により係合された
組織にRFエネルギーを供給する。好ましくは、約30
0Khzから3Mhzの基本周波数の正弦波の30から
200ボルトRMSで約0.1から4.0アンペアの電
流が、アンビル18とU字形治療用電極39を介して供
給される。第2の電気外科的ジェネレータ90は、その
周波数範囲の上の範囲内の異なる基本周波数で好ましく
は2ボルト以下の電圧と約1mAから100mAの電流
で第1の照会電極51及び第2の照会電極52に電気的
エネルギーを供給する。
2の電気外科的ジェネレータ90はハウジング16に配
置された、ユーザにより操作される電気的スイッチ59
によりオンになる。これに替えて、第2の電気外科的ジ
ェネレータ90は治療用信号から独立にオンに切り替え
ることもできる。
9(図22)はコントローラ79のRF制御入力端子に
信号を与えて、治療用エネルギー信号をオンにする。コ
ントローラ79の出力129はアナログスイッチ130
(図21)に接続されている。出力129がアナログス
イッチ130に「RFオン」信号を与えると、アナログ
スイッチ130を介してアナログ乗算器75に接続され
ている発振器72は知られた周波数の電圧をアナログ乗
算器75に印加する。アナログ乗算器75の出力はドラ
イバ76に接続されており、ドライバ76はRF増幅器
71の入力に接続されている。第1のRF増幅信号は、
電気外科的ジェネレータ70によって、回路80に供給
される。回路80は、装置10により処理されるべき組
織55を含む、装置10の第1の治療用電極であるU字
形治療用電極39と第2の治療用電極であるアンビル1
8とに接続されている。第2の電気外科的ジェネレータ
90は第1の照会電極51及び第2の照会電極52に第
2の電気信号を供給する。発振器91は治療用の発振器
72の出力信号とは異なる周波数の電圧をRF増幅器9
2に印加し、RF増幅器92は第1の照会電極51及び
第2の照会電極52に、より低い電圧信号を与える。
スセンサは、治療用電極であるアンビル18及びU字形
治療用電極39を介して組織に伝達された電流及び電圧
を検出する電圧・電流センサ81を含む。電圧・電流セ
ンサ81は、治療用電極における電気外科的ジェネレー
タ70の出力と直列に低インピーダンス電流変換器82
を含み、治療用電極における電気外科的ジェネレータ7
0の出力と並列に高インピーダンス電圧変換器83を含
んでいる。好ましくは、電流変換器82は、例えば、
1:20の巻き線比と変換器の二次側に並列な50オー
ムの抵抗を有している。好ましくは、電圧変換器83
は、例えば、20:1の巻き線比と変換器の二次側に並
列な1Kオームの抵抗を有している。
84に接続されている。RMSコンバータ84は検出し
た電流をDC信号に変換して、アンビル18とU字形治
療用電極39の間を流れる電流RMSであるITRMSを出
力86に供給する。電圧変換器83の出力はRMSコン
バータ85に接続されている。RMSコンバータ85は
電圧をDC信号に変換して、治療用電極であるアンビル
18とU字形治療用電極39の間の電圧RMSであるV
TRMSを出力87に与える。ここで、照会信号が組織の治
療用信号より極めて低い電圧である場合、VTRMS及びI
TRMSを決定する時に照会信号をフィルタにより除去する
必要がないことに着目すべきである。
ンピーダンスZTが、測定されたIT RMS及びVTRMSから
計算される。出力86及び87におけるITRM及びSV
TRMSはアナログドライバ88に供給される。アナログド
ライバ88はITRMSによってVTRMSをドライブして測定
されたインピーダンスZTを表す出力信号89を出力す
る。
エネルギーの出力を負荷インピーダンスに基づいて制御
する制御装置が提供される。この実施例においては、治
療用電極におけるインピーダンス、すなわち組織のイン
ピーダンスが好ましく用いられる。しかしながら、他の
実施例において、照会電極におけるインピーダンスをジ
ェネレータの出力を制御するために用いてもよい。この
目的のためには、電流、電圧センス回路(図示せず)に
より測定された治療用電極における被測定インピーダン
スを用いても、これに替えて照会電極におけるインピー
ダンスを用いてもよい。治療用電極又は照会電極のいず
れかのインピーダンスは、ジェネレータ、装置、及び/
又はアプリケーションの特定のシステム負荷曲線に基づ
いて、好ましいエネルギーレベル、例えば、電圧、電流
又はパワーレベルを決定するために用いられる。制御装
置は次いで、測定されたインピーダンスに対する実際の
エネルギーレベルを所望のエネルギーレベルと比較し、
その間の差によってジェネレータの出力を調整して、好
ましくはその間の差を最小化する。
ム負荷曲線は、装置の性能を最適化するインピーダンス
の範囲に対する電圧、電流又はパワーを反映しているこ
とが好ましい。
く、例えば、連続でも階段状でも良い。この負荷曲線
は、ジェネレータと共に使用する特定の装置、又はジェ
ネレータの特定の電気外科的アプリケーションに応じて
変化する。例えば、ここに記載したような装置を用いる
1実施例においては、異なるエネルギーが要求される。
即ち、最初は組織のインピーダンスは低い範囲、例えば
およそ20から100オームにある。この低い範囲で
は、組織の凝固を開始するためには十分なパワーを与え
るための電流が要求される。第2のインピーダンスの中
間範囲、例えば100から500オームでは、凝固プロ
セスを維持するために十分なパワーが要求される。凝固
の完了に向けて生じる高インピーダンスの第3の範囲、
例えばおよそ500オーム以上では、スパークと組織の
粘着を防止するために電圧は制限されることが要求され
る。こうして、この実施例におけるシステム負荷曲線
は、ジェネレータの固有の特性と特定のインピーダンス
のための最適パワーが伝達される電圧出力との両方を、
所定の装置及びアプリケーションのための特定のパワー
の要求と共に反映する。
プ制御装置を含んでいる。インピーダンス信号89及び
電圧VTRMS信号87は、ファンクションフィッティング
装置61とエラー増幅器62を備える制御装置を介して
電気外科的ジェネレータ70にフイードバックされる。
この制御装置は電気外科的ジェネレータ70を制御し
て、特定負荷曲線にフィットする負荷インピーダンスに
基づいて所望の範囲内の電圧を発生させる。
ションフィッティング装置61に与えられる。ファンク
ションフィッティング装置61の出力64は入力された
信号線89上のインピーダンスに基づく所望の電圧を表
す。この所望の電圧の機能は、特定の、所定負荷曲線を
生成するために電気外科的ジェネレータ70に要求され
る電圧である。出力64における所望の電圧は実際の電
圧と共にエラー増幅器62に供給される。エラー増幅器
62の出力65は、ダイオード77を介してアナログ乗
算器75に供給されるエラー電圧を表す。
ルギーパラメータを用いて電気外科的ジェネレータ70
の出力を制御してもよい。この場合、目標物のインピー
ダンスに対応する信号がファンクションフィッティング
装置61に入力される。ファンクションフィッティング
装置61は所望の電流、パワー又は他のエネルギーパラ
メータを出力する。このパラメータは次いで測定された
電流、パワー又は他のエネルギーパラメータと比較され
る。
初の四半動作を保証する。アナログ乗算器75は発振器
72の振幅変調器として機能して出力65における大き
いエラー電圧がRF増幅器71からの大きい出力をもた
らすようにする。また、出力65における小さなエラー
電圧はRF増幅器71からの小さいRF出力をもたら
す。こうして、電気外科的ジェネレータ70は、所望の
曲線が得られように電圧に基づく閉じたループのサーボ
システムとして働く。電圧以外の電気的パラメータが用
いられる場合、ファンクションフィッティング装置61
は好ましくはその代替エネルギーパラメータにおける差
を反映した信号を出力する。
極に伝達されたエネルギーに関連するインピーダンス又
は他のエネルギーパラメータを用いてサーボループを介
してジェネレータを制御してもよい。
90は、照会信号を第1の照会電極51及び第2の照会
電極52に供給する。この信号は、治療用信号とは独立
にオンになり且つオンに維持される。照会信号は低電圧
であり組織の処理を行わないので、照会信号はオンに維
持しておいてもよい。第1の照会電極51及び第2の照
会電極52に接続されているインピーダンスセンサは、
第1の照会電極51及び第2の照会電極52を介して組
織に供給される電流及び電圧を感知する電圧及び電流セ
ンサ93を含んでいる。電圧及び電流センサ93は電気
外科的ジェネレータ90と直列の低インピーダンス電流
変換器94と、照会電極への電気外科的ジェネレータ9
0の出力の両端に並列に接続された高インピーダンス電
圧変換器95とを含んでいる。
波数又はその周辺の周波数をフィルタにより除去する一
方で、照会信号の周波数又はその周辺の周波数を通過さ
せるように設けられた帯域通過フィルタ111に接続さ
れている。帯域通過フィルタ111の出力はRMSコン
バータ112に接続されている。RMSコンバータ11
2は感知した電流をDC信号に変換して、2つの照会電
極51、52の間を流れる電流RMSであるIQRMSを表
す出力を与える。電圧変換器95の出力は、治療用信号
の周波数又はその周辺の周波数をフィルタにより除去す
る一方で、照会信号の周波数又はその周辺の周波数を通
過させるように設けられた帯域通過フィルタ113に接
続されている。帯域通過フィルタ113の出力はRMS
コンバータ114に接続されている。RMSコンバータ
114は感知した電圧をDC信号に変換して、照会電極
51、52の間の電圧RMSであるVQRMSを表す出力を
与える。
88と類似のアナログデバイダ117に供給される。ア
ナログデバイダ117はIQRMSによってVQRMSを割り算
して、第1の照会電極51及び第2の照会電極52にお
ける測定されたインピーダンスZaを表す出力信号11
8を出力する。
2を用いて凝固の完了の検出を開始させるために、最小
量の電流が治療用電極であるアンビル18及びU字形治
療用電極39に供給されなくてはならない。RMSコン
バータ84の出力86のITR MS(図21)は比較器11
9に入力され、比較器119の出力は凝固完了回路12
0内のピーク検出器97をイネーブルにする。治療用電
極に供給される最小より大きい電流により凝固完了回路
が以下に記載のように動作を開始する。IQRMS,VQRMS
及び測定されたインピーダンスZaから、インピーダン
ス感知装置は凝固が完了したかどうかを判断する。
る。まず、最小インピーダンスZMINが決定される。次
いで、凝固が完了する目標インピーダンスZTARGETが最
小インピーダンスZMINの関数として計算される。初期
インピーダンス、最小インピーダンスZMIN、目標イン
ピーダンスZTARGET、インピーダンス曲線の勾配、及び
完了までの時間は、与えられたアプリケーション及び/
又は装置によって変化するが、最小インピーダンスZ
MINの関数f(ZMIN)と相互に関係する傾向にある。使
用される装置及び/又は実際の所望の結果に依存して、
最小インピーダンスZMINの実際の関数は変化する。こ
の実施例においては、f(ZMIN)はリニアで、f(Z
MIN)=0.2ZMIN+500である。この関数は制限さ
れている。即ち、ZMINが560オームより大であれ
ば、ZTARGETはZMIN+50オームである。f(ZMIN)
は異なる関数であってもよい。それは連続、非連続、リ
ニア、ノンリニア、区分的近似、及び/又はルックアッ
プテーブルの形式でもよい。f(ZMI N)はまた、異な
る値に制限されてもよい。
たことを以下のようにして判定する。まず測定されたイ
ンピーダンスZaが最小インピーダンスZMINかどうか
を判定する。インピーダンス信号線118上のインピー
ダンスZaはゲインオフセットインバータ96によって
反転され且つオフセットされる。ゲインオフセットイン
バータ96の出力はピーク検出器97に接続されてい
る。ゲインオフセットインバータ96の出力102は測
定されたインピーダンスZaを反転し且つオフセットし
た値、即ち(−Za+k)を表す。ZMINは遭遇する
(−Za+k)の値のうちの最高オフセットによって表
されることになる。
U字形治療用電極39及びアンビル18に供給される
と、ピーク検出器97は比較器119の出力によってイ
ネーブルにされる。これにより、ピーク検出器97は測
定されたインピーダンスZaの最大値、即ちZMIN、を
反転し且つオフセットした値を検出し保持する。ZMIN
が発生すると、ピーク検出器97の出力103は(−Z
MIN+k)を表す。
と、その関数f(ZMIN)が計算されて、処理(凝固)
が完了する時のインピーダンスである目標インピーダン
スZTARG ETが出力される。ピーク検出器97の出力10
3は、f(ZMIN)を計算して目標インピーダンスZ
TARGETを決定するスレショルド決定回路98に接続され
ている。スレショルド決定回路の出力99は測定された
インピーダンスZaがZMINに等しい時のZTARGETを表
す。
われる。ここで、最小インピーダンスZMINが検出され
るまで関数f(ZMIN)は連続的に計算されることに着
目すべきである。この比較は最小インピーダンスZMIN
が決定されるまでは測定されたインピーダンスZaと関
数f(ZMIN)の間で連続的に行われる。しかしなが
ら、組織の処理の間はf(Za)は測定されたインピー
ダンスZaより大きくて早期の凝固完了信号は発生しな
いと予想されるので、これは重大な結論ではない。
ピーダンスZTARGET以下の場合、RFエネルギーは連続
的に供給され凝固完了信号が発生し受け取られるまでは
上記したステップが行われる。測定されたインピーダン
スZaが目標インピーダンスZTARGET以上であれば、凝
固が完了したことを表す信号がコントローラに与えられ
て凝固が完了する。この実施例においても、ピーク検出
器97を介してZMINの決定を調節するために、測定さ
れたインピーダンスZaは反転され且つシフトされてい
ることに着目される。このパラグラフにおいて言及され
ているインピーダンス値とは実際のインピーダンス値で
ある。
るZTARGETは比較器としてのオペアンプ100の非反転
入力101に入力される。ゲインオフセットインバータ
96の出力102はオペアンプ100の反転入力104
に接続されている。オペアンプ100は、オペアンプ1
00の反転入力104に入力される値を示す(−Za+
k)と、(−ZMIN+k)の関数として計算された値を
表す目標インピーダンスZTARGETとを比較する。(−Z
a+k)が目標インピーダンスZTARGET以下であれば、
オペアンプ100の出力105は正である。即ち、測定
されたインピーダンスZaが関数f(ZMIN)より大き
いと、凝固完了信号がオペアンプ100の出力105に
現れる。
存在するかどうかを表し、コントローラ79に与えられ
る。凝固完了条件が存在すると、コントローラによりR
Fエネルギーが自動的にオフになる。
は組織が処理されるべき場所に配置される。次いで、顎
部材32、34が開かれて、組織が顎部材32、34の
互いに向き合っているそれぞれの内側表面33、35間
に配置される。次に、クランプ用引き金12が絞られて
顎部材32、34が閉じ、対向する表面33、35の間
で組織を配置し且つ圧縮する。組織が顎部材32、34
の間に適切に配置されると、ユーザはユーザにより駆動
される電気的スイッチ59を用いて電気外科的ジェネレ
ータ70、90からRFエネルギーを与える。
絡用電極棒27,28及び絶縁部材31は、顎部材34
の内側表面に向けて組織を圧縮する。U字形治療用電極
39、即ち電気的連絡用電極棒27,28と、電気的に
反対の電極、即ちアンビル18との間で、圧縮された組
織を電流が流れる。第1の照会電極51及び第2の照会
電極52の間で、上記電流の周波数とは異なる周波数の
電流が流れる。
されて治療用電極へのRFエネルギーがオフになるま
で、第1の照会電極51及び第2の照会電極52により
インピーダンスが測定される。
14が駆動されて切断要素11をナイフチャネル26を
通して前進させ、電気的連絡用電極棒27,28の間に
係合されている組織の焼灼された部分を切断する。同時
に、点火用引き金14はトラック25を通してくさび1
3を前進させ、且つアンビル18のポケット36の中に
前進させて、ステープル17を発射する。こうして、切
断線は電気的連絡用電極棒27,28により形成された
凝固線に対して中間線となり、ステープル17は、切断
要素11が組織を切断する時の切断要素11の各側の上
の縦方向の単一列の中に適用される。
使用されている腹壁鏡のステープリング内のカートリッ
ジの通常の二重列のステープル及び切断装置とは対照的
に、単一のステープル列を有することによりマルチファ
イヤステープリングが可能になる。よりよい止血を行う
ために、各平行列に二重列のステープルを与えるこのタ
イプのステープラが設計されていた。二重列のステープ
ルを収容するのに必要なスペースの大きさのために、積
み重ねられたステープルを持つ再点火可能なカートリッ
ジは好ましくなっかった。ステープルを積み重ねる追加
のスペースが必要となるからである。マルチファイヤス
テープリングの実施例では、単一の列のステープルが用
いられる。単一の列のステープルを用いると、ステープ
ルの第2の列により予め占められていたスペースにステ
ープルを積み重ねることができ、マルチファイヤを可能
にする。
ラを含んでもよい。円形ステープラの動作はこの技術に
おいて知られており、例えば、米国特許第5,104,
025号に記載されている。記載した実施例の変形によ
り、管内の(イントラルミナルな)ステープラに類似の
組織の溶接、焼灼、及び切断装置を提供できる。この実
施例においては、1993年7月22日出願の、米国特
許出願シリアル番号第08/095,797号に記載さ
れている装置に類似の装置が提供される。電極は絶縁対
で分離された2つの同心円電極の形に形成されている。
この電極は、圧縮用隆起部を形成し且つインターフェー
ス面のいずれかの上にある絶縁体の半径方向内側又は半
径方向外側に配置されている。円形切断装置のステープ
リングの実施例の電極はステープラのカートリッジ又は
アンビルの上に配置されている。
である。 1)前記治療用電極の各々は前記第1及び第2のインタ
ーフェース面の少なくとも1つの上に配置されている、
請求項2記載の電気外科的装置。 2)前記照会電極の各々は前記第1及び第2のインター
フェース面の少なくとも1つの上に配置されている、請
求項2記載の電気外科的装置。 3)前記第1及び第2のインターフェース面の少なくと
も1つは、前記第1及び第2のインターフェース面の間
に組織圧縮ゾーンを形成する隆起部を含み、前記末端効
果器は更に前記インターフェース面と前記隆起部を二分
する平面を備えており、前記照会電極は前記平面に関し
て圧縮用の前記隆起部と反対の横側の上に配置されてい
る、請求項2記載の電気外科的装置。 4)前記治療用電極は、電流が前記第1及び第2の治療
用ポールの間を流れると前記組織圧縮ゾーンにおいて電
気外科的組織処理がなされるように配置されている、実
施態様3に記載の電気外科的装置。 5)前記第1及び第2の治療用電極の1つは前記第1及
び第2の感知用ポールの電位と同じである、請求項2記
載の電気外科的装置。 6)前記末端効果器に結合された切断要素を更に備え、
前記切断要素は前記末端効果器に係合された組織を、切
断線を介してドライブするようになっている、請求項2
記載の電気外科的装置。 7)前記照会電極は前記切断線の対向する側の上に配置
されている、実施態様6に記載の電気外科的装置。 8)前記照会電極はインターフェース面の周囲の上に配
置されてその周囲において係合されている組織のインピ
ーダンスを測定するようになっている、請求項2記載の
電気外科的装置。 9)前記電気的パラメータは前記組織に供給される電流
である、請求項2記載の電気外科的装置。 10)前記電気的パラメータは前記組織に印加される電
圧である、請求項2記載の電気外科的装置。
ピーダンスである、請求項2記載の電気外科的装置。 12)前記電気的パラメータは前記組織に供給される電
圧及び電流であり、それにより前記照会電極の間の組織
のインピーダンスを決定できる、請求項2記載の電気外
科的装置。 13)前記治療用電極の各々は前記第1及び第2のイン
ターフェース面の少なくとも1つの上に配置されてい
る、請求項3記載の電気外科的装置。 14)前記第1及び第2の前記照会電極の各々は前記第
1及び第2のインターフェース面の少なくとも1つの上
に配置されている、請求項3記載の電気外科的装置。 15)前記組織の効果は凝固完了状態である、請求項4
記載の方法。 16)前記電気的パラメータは組織のインピーダンスで
ある、請求項4記載の方法。 17)電気外科的エネルギーを前記治療用電極に供給す
るように配置されたエネルギー源を更に備え、前記エネ
ルギー源は前記制御信号に応答して前記エネルギーを前
記治療用電極に供給するようにした、請求項5記載の電
気外科的装置。 18)前記インピーダンス測定回路は、最小インピーダ
ンス値を決定するための第1の装置と、前記第1の装置
に接続されており、前記目標インピーダンス値を前記最
小インピーダンス値の関数として決定する目標決定装置
と、測定されたインピーダンスを前記目標インピーダン
スと比較して、前記測定されたインピーダンス値が前記
目標インピーダンス値を越えたかどうかを表す信号を発
生する第1の比較装置とを備えた、請求項5記載の電気
外科的装置。 19)前記末端効果器は、組織をその間に係合するため
の互いに相対的に移動可能な第1及び第2の要素を備
え、前記第1の治療用電極は前記第1及び第2の要素の
少なくとも1つの上に配置されている、請求項5記載の
電気外科的装置。 20)前記第2の治療用電極は前記第1及び第2の要素
の少なくとも1つの上に配置されている、実施態様19
に記載の電気外科的装置。
第1及び第2の要素のいずれか1つ又は両方の上に配置
されており、前記インピーダンス測定回路は前記第1及
び第2の照会電極の間で且つ前記第1及び第2の要素の
間に係合されている組織のインピーダンスを測定するよ
うに適合されている、実施態様19に記載の電気外科的
装置。 22)前記1つ以上の第1の治療用電極の各々は、前記
インターフェース面に関して前記1つ以上の第2の治療
用電極からオフセットされている、実施態様21に記載
の電気外科的装置。 23)前記第1及び第2の要素は、電気外科的に処理さ
れるべき組織を係合するための第1及び第2のインター
フェース面を備えており、前記第1の治療用ポールは、
前記第1及び第2のインターフェース面の少なくとも1
つの上に配置された1つ以上の第1の治療用電極を備え
ており、前記第2の治療用ポールは、前記第1及び第2
のインターフェース面の少なくとも1つの上に配置され
た1つ以上の第2の治療用電極を備えている、実施態様
19に記載の電気外科的装置。 24)前記1以上の第1の治療用電極は、前記インター
フェース面に関して前記1つ以上の第2の治療用電極か
らオフセットされている、実施態様23に記載の電気外
科的装置。 25)更に、前記末端効果器に含まれる、組織に接触し
対向する表面を用意し、前記表面の間に処理されるべき
組織を係合している前記表面はその間に処理されるべき
組織を係合するために移動可能であり、前記照会電極及
び前記1つ以上の治療用電極は前記表面のいずれか1つ
または両方に関係付けられている、請求項7記載の方
法。
明によれば、上記したインピーダンスフィードバックシ
ステムは、十分な焼灼が起きた時を示すのに使用され
る。凝固が完了すると、コントローラによりユーザに信
号が与えられるか、あるいはコントローラは自動的にR
Fエネルギーをオフにする。他の信号も同様に装置のユ
ーザに与えることができる。例えば、測定されたインピ
ーダンスに対応する音をユーザに与えてインピーダンス
の変化を聴覚によりモニタすることもできる。以上に記
載されたこの発明及び特定の詳細及び実施の方法は例示
として示した。しかし、記載した基本原理の多数の変
形、修正、拡張が この発明の精神及び範囲を逸脱する
ことなく可能であることは、当業者に容易に理解でき
る。
バイポーラ及びマルティポーラの形態を含む電気外科的
装置の様々なタイプに使用することを意図している。凝
固の完了又は他の組織の特性又は状態を判定するため
に、多数の異なるインピーダンスフィードバックシステ
ムがやはり使用できる。照会電極は、処理を通じて、連
続的に、周期的に、あるいは所定の又はユーザが開始し
た特定の時間に、励起してもよい。インピーダンスフィ
ードバックシステムは実際の装置内と共に、別のユニッ
トとして及び/又はエネルギー源又はジェネレータとし
て、一部又は全体に含ませることができる。
の斜視図である。
された状態で示される、図1の実施例の側面図である。
2の実施例の側面図である。
ルされ且つ切断された後が示される図3と類似の側面図
である。
ある。
る。
で示される、図1の装置の第1の、オープン位置にある
ハンドル部の近傍の側面図である。
を示す左側のハンドル部の内側の側面図である。
トを示す中間部の近端部の側面図である。
である。
るバネを示す斜視図である。
を可能にするバネにおけるわずかなバイアスを示す図1
2のエンドビューを示す図である。
の装置の遠端点の縦断面図である。
である。
である。
面図である。
面図である。
のアナログの実施例の概略ブロック図である。
のアナログの実施例の概略ブロック図である。
電気外科的エネルギーを加えている間のインピーダンス
の変化を示す特性曲線を示す図である。
具) 11 切断要素 15 末端効果器 18 アンビル(治療用電極) 32 顎部材(組織処理部) 34 顎部材(組織処理部) 35 内面(インターフェース面) 39 U字形治療用電極(治療用電極、第1のポール) 51 第1の照会電極(感知用ポール) 52 第2の照会電極(感知用ポール) 56 隆起部 96 ゲインオフセットインバータ 97 ピーク検出器 100 オペアンプ(第1の比較装置) 210 インピーダンスモニタ装置
Claims (9)
- 【請求項1】 処理すべき組織をその間に係合するよう
に適合された第1及び第2の対向するインターフェース
面を備えている末端効果器を含む組織処理部を有する外
科用器具と、 エネルギー源から電気外科的エネルギーを受け取るよう
に適合されており、且つその間で電気的エネルギーを導
通することができ、組織に接触する第1及び第2の治療
用電極を含み、前記第1及び第2の治療用電極の少なく
とも1つは前記第1及び第2のインターフェース面の少
なくとも1つに関係付けられている、第1及び第2の治
療用ポールと、 エネルギー源から電気外科的エネルギーを受け取るよう
に適合されており、且つその間で電気的エネルギーを導
通することができ、組織に接触する第1及び第2の照会
電極を含み、前記第1及び第2の照会電極の少なくとも
1つは前記第1及び第2のインターフェース面の少なく
とも1つに関係付けられている、第1及び第2の照会ポ
ールと、を備えた、外科的処理中に組織を処理する電気
外科的装置。 - 【請求項2】 末端効果器を有し、前記末端効果器は、 その間に組織を係合させることができる第1及び第2の
対向するインターフェース面であって、前記末端効果器
が前記インターフェース面内の電気外科的エネルギーを
受け取ることができるようにしたものと、 その間で電気外科的エネルギーを導通することができ、
電気的に反対の治療用電極を含み、電気的に分離された
第1及び第2の治療用ポールと、そして、 その間で電気外科的エネルギーを導通することができ、
電気的に反対の照会電極を含み、電気的に分離された第
1及び第2の感知用ポールとを備え、 前記治療用電極の少なくとも1つは、前記第1及び第2
のインターフェース面の少なくとも1つの上に配置され
て、それにより前記治療用ポールの間で前記インターフ
ェース面により係合されている組織を通して電気外科的
エネルギーを通過させて、組織を電気外科的に処理する
ことができ、 前記照会電極の少なくとも1つは、前記第1及び第2の
インターフェース面の少なくとも1つの上に配置され
て、それにより前記感知用ポールの間で前記インターフ
ェース面により係合されている組織を通して感知用の電
気外科的エネルギーを通過させて、前記感知用ポールの
間で前記組織の電気的パラメータを測定できるようにし
た、電気外科的装置。 - 【請求項3】 末端効果器を有し、前記末端効果器は、 その間に組織を係合させることができる第1及び第2の
対向するインターフェース面であって、前記末端効果器
が前記インターフェース面内の電気外科的エネルギーを
受け取ることができるようにしたものと、 その間で電気外科的エネルギーを導通することができ、
電気的に反対の治療用電極を含み、電気的に分離された
第1及び第2の治療用ポールと、そして、 その間で電気外科的エネルギーを導通することができ、
電気的に反対の照会電極を含み、電気的に分離された第
1及び第2の感知用ポールとを備え、 前記治療用電極の少なくとも1つは、前記第1及び第2
のインターフェース面の少なくとも1つの上に配置され
て、それにより前記治療用ポールの間で前記インターフ
ェース面により係合されている組織を通して電気外科的
エネルギーを通過させて、組織を電気外科的に処理する
ことができ、 前記照会電極の少なくとも1つは、前記第1及び第2の
インターフェース面の少なくとも1つの上に配置され
て、それにより前記感知用ポールの間で前記インターフ
ェース面により係合されている組織を通して感知用の電
気外科的エネルギーを通過させて、前記感知用ポールの
間に伝達された前記感知用電気外科的エネルギーの電気
的パラメータを測定できるようにした、電気外科的装
置。 - 【請求項4】 末端効果器と、 その間に組織を係合させることができる第1及び第2の
対向するインターフェース面であって、前記末端効果器
が前記インターフェース面内の電気外科的エネルギーを
受け取ることができるようにしたものと、 その間で電気外科的エネルギーを導通することができ、
電気的に反対の治療用電極を含み、電気的に分離された
第1及び第2の治療用ポールと、そして、 その間で電気外科的エネルギーを導通することができ、
電気的に反対の照会電極を含み、電気的に分離された第
1及び第2の感知用ポールとを備え、 前記治療用電極の各々及び前記第1及び第2の照会電極
の各々は、前記第1及び第2のインターフェース面の1
つの上に配置されている末端効果器を有する電気外科的
装置を用意する段階と、 組織を前記インターフェース面の間に係合させる段階
と、 治療用電気外科的エネルギーを前記治療用電極の間の前
記組織に供給する段階と、 組織の効果が生じた時を決定する段階と、 前記組織の効果を表す信号を供給する段階とを備える、
電気外科的方法。 - 【請求項5】 処理すべき組織を係合するように適合さ
れた末端効果器を含む組織処理部を有する外科用器具
と、 エネルギー源から電気外科的エネルギーを受け取るよう
に適合されており、且つその間で電気的エネルギーを導
通することができ、組織に接触する第1及び第2の治療
用電極を含み、前記第1及び第2の治療用電極の少なく
とも1つは前記外科用器具の前記組織処理部に関係付け
られている、第1及び第2の治療用ポールと、 エネルギー源から電気外科的エネルギーを受け取るよう
に適合されており、且つその間で電気的エネルギーを導
通することができ、組織に接触する第1及び第2の照会
電極を含み、前記第1及び第2の照会電極の少なくとも
1つは前記外科用器具の前記組織処理部に関係付けられ
ている、第1及び第2の照会ポールと、 前記治療用電極に供給されるRFエネルギーを制御する
エネルギー制御信号と、 前記照会電極に接続されており、前記末端効果器により
係合されている組織のインピーダンスを測定するインピ
ーダンス測定回路とを備え、 前記インピーダンス測定回路は、前記照会電極の間の前
記組織が処理電極により治療用エネルギーで処理される
とき、前記照会電極の間の組織の最小インピーダンスを
測定し、組織の所望の状態が達成されたときの、前記最
小インピーダンスの関数である目標インピーダンスを決
定し、前記照会電極の間の組織の測定されたインピーダ
ンス値を目標インピーダンス値と比較し、前記測定され
たインピーダンス値が前記目標インピーダンス値を越え
たとき前記制御信号を調整するように適合されている、
外科的処理中に組織を処理する電気外科的装置。 - 【請求項6】 1つ以上の組織処理用電極と電気的に反
対の照会電極とを備えた末端効果器を含む電気外科的器
具を用意する段階と、 電気外科的に処理されるべき組織に、前記1つ以上の組
織処理用電極を通して、感知用電気外科的エネルギーを
供給する段階と、 前記照会電極の間の組織の電気的パラメータを測定する
段階と、 前記照会電極の間の組織の測定された電気的パラメータ
を表す信号を発生する段階と、 前記測定された電気的パラメータから治療用の目標とな
る電気的パラメータを決定する段階と、 続いて測定された電気的パラメータを前記目標値と比較
する段階と、 制御信号を生成して、前記測定された電気的パラメータ
に応答して前記電気外科的器具へのRFエネルギーを制
御し、前記目標値に到達する段階と、 前記1つ以上の治療用電極を通して組織に与えられるエ
ネルギーを、前記制御信号に応じて制御する段階とを備
える、組織の電気外科的処理方法。 - 【請求項7】 1つ以上の組織処理用電極と電気的に反
対の照会電極とを備えた末端効果器を含む電気外科的器
具を用意する段階と、 電気外科的に処理されるべき組織に、前記1つ以上の組
織処理用電極を通して、感知用電気外科的エネルギーを
供給する段階と、 前記照会電極の間の組織のインピーダンスを測定する段
階と、 前記照会電極の間の組織の測定されたインピーダンス値
を表すインピーダンス信号を発生する段階と、 前記インピーダンス信号から代表的最小インピーダンス
を測定する段階と、 最小インピーダンス値の関数としての代表的目標インピ
ーダンス値を決定する段階と、 続いて測定されたインピーダンス信号を前記目標インピ
ーダンス値と比較する段階と、 制御信号を生成して、前記目標インピーダンス値を越え
る前記測定されたインピーダンスに応答して前記電気外
科的器具へのRFエネルギーを制御する段階と、 前記1つ以上の治療用電極を通して組織に与えられるエ
ネルギーを、前記制御信号に応じて制御する段階と、を
備える、組織の電気外科的処理方法。 - 【請求項8】 第1及び第2の組織係合用表面を備える
末端効果器を有する電気外科的器具を用意し、この場合
前記第1及び第2の組織係合用表面の少なくとも1つは
その上に、電気外科的治療システムの第1のポールに関
係付けられた組織に接触する治療用電極を含ませ、前記
第1及び第2の組織係合用表面の少なくとも1つはその
上に、電気外科的治療システムの第2のポールに関係付
けられた組織に接触する治療用電極を含ませ、前記第1
及び第2の組織係合用表面の少なくとも1つはその上
に、インピーダンス感知システムの第1のポールに関係
付けられた組織に接触する第1の照会電極と、インピー
ダンス感知システムの第2のポールに関係付けられた組
織に接触する第2の照会電極とを含ませる段階と、 前記第1及び第2の組織係合表面の間に、処理されるべ
き組織を係合する段階と、 前記第1及び第2の組織に接触する治療用電極に供給さ
れるRFエネルギーを選択的に制御してその間に配置さ
れた組織を処理する段階と、 前記第1及び第2の照会電極の間の処理された組織のイ
ンピーダンスを前記第1及び第2の照会電極で測定する
段階と、 組織の処理が完了するときのスレショルドインピーダン
スを設定する段階と、 測定されたインピーダンス値を前記スレショルドインピ
ーダンス値と比較する段階と、そして、 測定されたインピーダンス値が前記スレショルドインピ
ーダンス値に到達するか越えるという条件で、前記第1
及び第2の治療用電極に結合したRFエネルギーを制御
又はオフに切り替える段階とを備える、電気外科的な組
織の処理方法。 - 【請求項9】 エネルギー源から、外科用器具の組織処
理部に連絡している1つ以上の治療用電極に供給される
電気外科的エネルギーを制御するエネルギー制御信号
と、 前記外科用器具の組織処理部に連絡している組織に接触
する照会電極と、前記外科用器具の組織処理部に連絡し
ている1つ以上の治療用電極に治療用電気外科的エネル
ギーを供給するように配置されたエネルギー源とに、接
続されるようになっているインピーダンス測定回路と、
を備え、 前記インピーダンス測定回路は前記外科用器具の組織処
理部により係合された組織のインピーダンスを測定する
ようになっており、 前記インピーダンス測定回路は、 最小インピーダンス値を決定する第1の装置と、 前記第1の装置に接続され、前記最小インピーダンス値
の関数としての目標インピーダンスを決定する目標決定
装置と、 測定されたインピーダンス値を前記目標インピーダンス
値と比較し、前記測定されたインピーダンス値が前記目
標インピーダンス値を越えたかどうかを示す信号を発生
する第1の比較装置と、 を備えた、電気外科的インピーダンスフィードバック制
御装置。
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36207094A | 1994-12-22 | 1994-12-22 | |
| US362070 | 1994-12-22 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH08229050A true JPH08229050A (ja) | 1996-09-10 |
| JP3857345B2 JP3857345B2 (ja) | 2006-12-13 |
Family
ID=23424572
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP34905695A Expired - Lifetime JP3857345B2 (ja) | 1994-12-22 | 1995-12-21 | 電気外科的装置及び電気外科的インピーダンスフィードバック制御装置 |
Country Status (5)
| Country | Link |
|---|---|
| EP (2) | EP0717967B1 (ja) |
| JP (1) | JP3857345B2 (ja) |
| AU (1) | AU701320B2 (ja) |
| CA (1) | CA2165714C (ja) |
| DE (2) | DE69534437T2 (ja) |
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| KR20230125874A (ko) * | 2022-02-22 | 2023-08-29 | 한양대학교 에리카산학협력단 | 전기 수술 장치, 상기 전기 수술 장치의 임피던스 측정 장치, 조직 응고를 위한 에너지 제어 방법 및 임피던스 측정 방법 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2165714C (en) | 2006-10-24 |
| EP0717967B1 (en) | 2003-05-14 |
| EP1157666B1 (en) | 2005-09-07 |
| CA2165714A1 (en) | 1996-06-23 |
| DE69530747D1 (de) | 2003-06-18 |
| DE69534437D1 (de) | 2005-10-13 |
| EP0717967A3 (en) | 1996-08-14 |
| EP0717967A2 (en) | 1996-06-26 |
| EP1157666A1 (en) | 2001-11-28 |
| JP3857345B2 (ja) | 2006-12-13 |
| DE69530747T2 (de) | 2004-03-25 |
| AU701320B2 (en) | 1999-01-28 |
| DE69534437T2 (de) | 2006-06-22 |
| AU4026495A (en) | 1996-06-27 |
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