Intraluminal grafting of a bifurcated artery
Abstract
(57) [Summary] Disclosed is a method of positioning an intracavitary graft into a bifurcation vessel in a patient's body, and a delivery catheter used in this method. The delivery catheter (24) is an elongated catheter preferably having an inflatable balloon (20) adjacent to one end, an intracavitary graft (10) arranged around the balloon, which is two short tubulars. (Branched into an extension (19a, 19b)), and a thin auxiliary catheter (25) containing a guide wire (26), which extends upstream through a first tubular extension (19a). Includes (extending downstream through the other short tubular extension (19b)) of the implant. The method of positioning an intraluminal implant using a delivery catheter is particularly applicable to the proper positioning of a trouser-shaped implant. This is because the trouser-shaped implant bridges an aneurysm that extends from a single vessel, such as the aorta, to one or more bifurcated vessels, such as the iliac artery.
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- 1【特許請求の範囲】 1. 以下を有する送達カテーテル:(a)第1の端部と第2の端部とを有する細長いカテーテル;(b)該細長いカテーテルの周囲に配された本体を有する腔内移植片(ここで、 該本体は、第1の端部に、該細長いカテーテルの第1の端部に隣接して配された 管状部分を有し、第2の端部に、第1および第2の管状の移植片伸長部分への二 分枝を有し、該細長いカテーテルは該第1の管状の移植片伸長部分まで伸長し、 そして該管状部分中に伸長する);および (c)該第1の管状の移植片伸長部分を通って第1の方向に伸長し、第2の異な る方向に該第2の管状の移植片伸長部分中に突出する補助ガイドワイヤー。 2.前記補助ガイドワイヤーが、前記移植片本体内の溝を通って伸長する、請求 項1に記載の送達カテーテル。 3.補助カテーテルが、前記第1の管状の移植片伸長部分を通って前記第1の方 向に、かつ、前記第2の管状の移植片伸長部分中に前記第2の方向に伸長し、該 補助カテーテルが前記補助ガイドワイヤーを含む、請求項1に記載の送達カテー テル。 4.前記細長いカテーテルが、前記第1の端部に隣接する膨張可能なバルーンを 有し、前記腔内移植片が該バルーンの周囲に配される、請求項1に記載の送達カ テーテル。 5.前記第1の端部に近位の前記腔内移植片の一部が、自己膨張可能である、請 求項1に記載の送達カテーテル。 6.前記第1および第2の管状の移植片伸長部分の両方が、さらなる管状腔内移 植片と係合するように適合される、請求項1に記載の送達カテーテル。 7.前記管状の移植片伸長部分の1つが、もう一方の管状の移植片伸長部分より も大きい長さを有する、請求項1に記載の送達カテーテル。 8.前記ガイドワイヤーが比較的に薄く、キンク耐性である、請求項1に記載の 送達カテーテル。 9.前記補助カテーテルが、3Frenchカテーテルである、請求項3に記載の送達 カテーテル。 10.前記補助カテーテルが、前記第1の管状の移植片伸長部分を通って前記第 1の方向に、そして前記第2の管状の移植片伸長部分中に、かつこれを通って前 記第2の方向に伸長する、請求項3に記載の送達カテーテル。 11.前記補助カテーテルが、該補助カテーテルの長さの一部に渡ってバルーン カテーテルに結合する、請求項3に記載の送達カテーテル。 12.前記補助カテーテルの少なくとも一部が、前記腔内移植片の少なくとも一 部に連結する、請求項3に記載の送達カテーテル。 13.前記補助カテーテルが、前記移植片の前記本体内の溝に組み込まれる、請 求項12に記載の送達カテーテル。 14.前記細長いカテーテルが、前記第1の管状の移植片伸長部分まで、かつ前 記移植片本体の前記管状部分を通って伸長する、請求項1に記載の送達カテーテ ル。 15.前記ガイドワイヤーが、前記補助カテーテルの自由端部から突出する、請 求項3に記載の送達カテーテル。 16.前記移植片本体が、該移植本体の第1の端部の近位で、複数の分離した、 間隔をあけて配設された展性ワイヤーで周囲が強化され、該ワイヤーの各々は、 概ね正弦に近い形状を有し、第1のワイヤーは、該第1のワイヤーの交互のクレ ストまたは尖部が該第1の端部の少なくとも一部を越えて突出するように該第1 の端部に隣接して配設される、請求項1に記載の送達カテーテル。 17.前記第1のワイヤーが、次の隣接するワイヤーよりも大きい振幅を有し、 好ましくは次の2つの隣接するワイヤーよりも大きい振幅を有する、請求項16 に記載の送達カテーテル。 18.前記移植片の前記第1の端部に隣接するワイヤーが、該第1の端部と遠位 のワイヤーよりもより近接して間隔をあけて配設される、請求項16に記載の送 達カテーテル。 19.前記ワイヤーが、前記移植片本体に織り込まれる、請求項16に記載の送 達カテーテル。 20.各々のワイヤーの端部が、前記移植片本体の外側で一緒にねじられる、請 求項19に記載の送達カテーテル。 21.前記移植片本体が、ポリエステル、ポリテトラフルオロエチレン、ポリウ レタン、またはその複合体から作られる、請求項16に記載の送達カテーテル。 22.前記管状移植片本体が、該管状移植片本体の長さに沿って、複数の分離し た、間隔をあけて配置されたワイヤーで周囲が支持され、第1のワイヤーは、該 第1のワイヤーの少なくとも一部が前記第1の端部の少なくとも一部を越えて突 出するように該移植片本体の該第1の端部に隣接して配設される、請求項1に記 載の送達カテーテル。 23.各々のワイヤーが、交互の尖部を有する近接した実質的に連続する正弦曲 線の構成を有し、ここで、前記第1のワイヤーの交互の尖部が前記第1の端部の 少なくとも一部を越えて突出する、請求項22に記載の送達カテーテル。 24.前記移植片本体の各々の端部が、該移植片本体の隣接する端部を越えて伸 長する交互のクレストまたは尖部を有するワイヤーを備える、請求項22に記載 の送達カテーテル。 25.前記ワイヤーの各々が、各々のワイヤーの交互の部分が該移植片本体の外 側にあり、各々のワイヤーの残りの部分が該移植片本体の内側にあるように、該 移植片本体に織り込まれる、請求項22に記載の送達カテーテル。 26.前記移植片本体が、複数の穴を有し、ここで、前記ワイヤーの各々が、該 ワイヤーの交互の部分が該移植片本体の外側にあり、各々のワイヤーの残りの部 分が該移植片本体の内側にあるように、該穴を通して貫通される、請求項22に 記載の送達カテーテル。 27.前記ワイヤーが、前記移植片本体に縫合される、請求項22に記載の送達 カテーテル。 28.前記第1のワイヤーが、該第1のワイヤーに隣接するワイヤーよりも大き い振幅を有する、請求項23に記載の送達カテーテル。 29.前記移植片本体の前記第1の端部に隣接する前記ワイヤーが、該移植片本 体の2つの端部の中間のワイヤーよりも、互いにより近接して間隔をあけて配設 される、請求項24に記載の送達カテーテル。 30.前記第1のワイヤーが、前記移植片本体におけるもう一方のワイヤーの大 部分よりも、より大きい振幅とより小さい波長を有する、請求項29に記載の送 達カテーテル。 31.前記ワイヤーの前記波長が、前記移植片本体の長さに沿って実質的に一定 である、請求項23に記載の送達カテーテル。 32.各々のワイヤーが、2つの対向する端部を含み、ここで、各々のワイヤー の両端部は、前記移植片本体の外側で一緒に接合される、請求項22に記載の送 達カテーテル。 33.各々のワイヤーの両端部が、一緒にねじられるか、または圧着される、請 求項32に記載の送達カテーテル。 34.隣接するワイヤーの接合された端部が、前記移植片本体に沿って対向する 方向に突出する、請求項32に記載の送達カテーテル。 35.前記移植片本体の前記第1の端部が、エッジを含み、ここで、該第1の端 部の該エッジは、前記第1のワイヤーの各々の突出する尖部の間で波形にされる 、請求項23に記載の送達カテーテル。 36.前記移植片本体が、該移植片本体の長さに沿って、複数の分離した、間隔 をあけて配置されたワイヤーで周囲が支持され、該ワイヤーの各々が、交互の尖 部を有する近接した実質的に連続する正弦曲線の構成を有する、請求項1に記載 の送達カテーテル。 37.前記移植片本体が、該移植片本体の長さに沿って、複数の分離した、間隔 をあけて配置されたワイヤーで周囲が支持され、該ワイヤーの各々が、該ワイヤ ーの交互の部分が該移植片本体の外側にあり、該ワイヤーの残りの部分が該移植 片本体の内側にあるように、該移植片本体に織り込まれる、請求項1に記載の送 達カテーテル。 38.前記さらなる管状腔内移植片が、その長さに沿って外径が変化する、請求 項6に記載の送達カテーテル。 39.前記外径の変化が、その長さの一部分に沿って前記移植片の内部方向テー パーによって提供される、請求項38に記載の送達カテーテル。 40.前記外径の変化が、その長さの一部分に沿って前記移植片の外部方向テー パーによって提供される、請求項38に記載の送達カテーテル。 41.前記さらなる管状腔内移植片の第1の部分が、第1の外径を有し、第2の 部分が、異なる外径を有する、請求項38に記載の送達カテーテル。 42.患者の体内で分岐血管中に腔内移植片を位置決めする方法であって、該血 管は、単一の分岐前血管(これは、一対の分岐後血管に分岐する)を含み、該方法 は以下を包含する: (a)第1の端部に管状部分を有し、第1および第2の管状の移植片伸長部分に 分岐される第2の端部を有する本体を有する、第1の腔内移植片を分岐後血管の 1つに導入する工程であって、該本体は第1の細長いカテーテルの周囲に配され 、そして該第1の腔内移植片内に、該第1の管状の移植片伸長部分を通って第1 の方向に伸長し、該第2の管状の移植片伸長部分中に第2の異なる方向に突出す る補助ガイドワイヤーが位置決めされる工程;(b)該第1の腔内移植片の該第1の端部と、該第2の管状の移植片伸長部分と を、該分岐前血管内に位置決めし、該移植片の少なくとも該第1の端部が膨張し て該分岐前血管の周囲の壁と係合するようになるまで該移植片を膨張させる工程 ;(c)該補助ガイドワイヤーを該移植片に対して該第2の異なる方向に、該ガイ ドワイヤーが一方の該分岐後血管中に伸長するまで、伸長する工程;(d)上流端部と下流端部とを有する第2の腔内移植片を、もう一方の該分岐後 血管に導入し、その場所に位置決めされた該補助ガイドワイヤーまたは別のガイ ドワイヤーを使用し、その上流端部が該第2の管状の移植片伸長部分の内にある かまたはそれを取り囲み、そしてその下流端部がもう一方の該分岐後血管の内に あるようになるまで該第2の腔内移植片を移動し、該第2の腔内移植片の上流端 部と該第2の管状の移植片伸長部分との流体送達係合を形成させる工程。 43.以下の工程をさらに包含する、請求項42に記載の方法: (e)上流端部と下流端部とを有する第3の腔内移植片を、前記1つの分岐後血 管に導入し、その上流端部が前記第1の管状の移植片伸長部分の内にあるかまた はそれを取り囲み、そしてその下流端部が該1つの分岐後血管の内にあるように なるまで該第3の腔内移植片を移動し、該第3の腔内移植片の上流端部と該第1 の管状の移植片伸長部分との流体送達係合を形成させる工程。 44.1つの前記分岐後血管に前記第1の腔内移植片を導入する方法、および前 記第1の端部と前記第2の管状の移植片伸長部分とを前記分岐前血管内に位置決 めする工程が以下を包含する、請求項42に記載の方法: (a)前記第1の細長いカテーテル(これは、膨張していないバルーンを一方の 端部に隣接して有し、該バルーンの周囲に配される該第1の腔内移植片の該第1 の端部を備える)をより小さい直径のガイドワイヤー上に、かつ、該1つの分岐 後血管と分岐前血管とに予め配設されたより大きい直径のカテーテルシースの内 部にガイドする工程;(b)該カテーテルシースを部分的に引っ込めて、該第1の腔内移植片を離す工 程;(c)該バルーンを膨張させて、それにより、該第1の腔内移植片の該第1の端 部を、それが該分岐前血管の壁に対して係合するようになるまで膨張させる工程 ;および (d)該バルーンを収縮する工程。 45.もう一方の前記分岐後血管に前記第2の腔内移植片を導入し、その上流端 部が前記第2の管状の移植片伸長部分の内にあるようになるまで移動させる工程 が以下を包含する、請求項42に記載の方法: (a)第2の細長いカテーテル(これは、膨張していないバルーンを一方の端部 に隣接して有し、該バルーンの周囲に配される該第2の腔内移植片の該上流端部 を備える)をより小さい直径のガイドワイヤー上に、かつ、該もう一方の分岐後 血管と前記分岐前血管とに予め配設されたより大きい直径のカテーテルシースの 内部にガイドする工程;(b)該カテーテルシースを部分的に引っ込めて、該第2の移植片を離す工程;(c)該バルーンを膨張させて、それにより、該第2の腔内移植片の該上流端部 を、それが該第2の管状の移植片伸長部分に対して係合するようになるまで膨張 させる工程;(d)前記第1の細長いカテーテルを前記1つの分岐後血管から引っ込めながら 、該バルーンの膨張を維持する工程;および (e)該第1の送達カテーテルを該1つの分岐後血管から除くと直ちに、該バル ーンを収縮する工程。 46.前記1つの分岐後血管に前記第3の腔内移植片を導入し、その上流端部が 前記第1の管状の移植片伸長部分の内にあるようになるまで移動させる工程が以 下を包含する、請求項43に記載の方法: (a)第3の細長いカテーテル(これは、膨張していないバルーンを一方の端部 に隣接して有し、該バルーンの周囲に配される該第3の腔内移植片の該上流端部 を備える)をより小さい直径のガイドワイヤー上に、かつ、該一方の分岐後血管 と前記分岐前血管とに予め配設されたより大きい直径のカテーテルシースの内部 にガイドする工程;(b)該カテーテルシースを部分的に引っ込めて、該第3の移植片を離す工程;(c)該バルーンを膨張させて、それにより、該第3の腔内移植片の該上流端部 を、それが該第1の管状の移植片伸長部分に対して係合するようになるまで膨張 させる工程;および (d)該バルーンを収縮する工程。 47.患者の体内で大動脈から少なくとも1つの腸骨動脈中に伸長する動脈瘤を 横切って腔内移植片を位置決めする方法であって、該方法は以下の工程を包含す る: (a)切開または穿刺して、該患者の大腿動脈を露出させる工程;(b)第1のガイドワイヤーを、それが該動脈瘤を横切るように、該露出した大 腿動脈、該対応する腸骨動脈、および該大動脈を通して挿入する工程;(c)第1のカテーテルシースを、それが該動脈瘤を横切るまで、該第1のガイ ドワイヤー上にガイドする工程;(d)該第1のガイドワイヤーを引っ込める工程;(e)第2の比較的剛直なガイドワイヤーを、それが該動脈瘤を横切るまで、該 第1のカテーテルシースを通して挿入する工程;(f)該第1のカテーテルシースを引っ込める工程;(g)第2の比較的大きい直径のカテーテルシースを、それが該動脈瘤を横切る まで、該第2のガイドワイヤー上にガイドする工程;(h)第1の細長いカテーテル(これは、膨張していないバルーンを一方の端部 に隣接して有し、該バルーンの周囲に配される第1の腔内移植片を備える)を該 第2のガイドワイヤー上に、かつ、該第2のより大きい直径のカテーテルシース の内部にガイドする工程(ここで、該第1の腔内移植片は、第1の端部に管状部 分を有し、そして第1および第2の管状の移植片伸長部分に二分枝される第2の 端部を有する)であって、そこで該第1の移植片内に、該第1の管状の移植片伸 長部分を通って第1の方向に、そして該第2の管状の移植片伸長部分中に第2の 異なる方向に伸長する第3のガイドワイヤーを含む第3のカテーテルを位置決め する工程;(i)該第1の細長いカテーテルを、該第1の移植片の該第1の端部が該動脈瘤 の上流であるように位置決めする工程;(j)該第2のより大きい直径のカテーテルシースを部分的に引っ込めて、該第 1の腔内移植片を離す工程;(k)該バルーンを膨張させて、それにより、該第1の腔内移植片の該第1の端 部を、それが該動脈瘤の上で該大動脈の壁に対して係合するようになるまで膨張 させる工程;(l)該バルーンを収縮して、血液により該第1および第2の管状の移植片伸長 部分を膨張させる該第1の移植片が下流に流動することを可能にする工程;(m)該第3のガイドワイヤーを、該第2の方向に、もう一方の該腸骨動脈およ び該大腿動脈中に下流へガイドする工程;(n)切開または穿刺し、そして該第3のガイドワイヤーを該もう一方の大腿動 脈から引き戻す工程;(o)該第3のカテーテルを該1つの大腿動脈を通して引っ込める工程;(p)第4のカテーテルシースを該第3のガイドワイヤー上で、かつ該もう一方 の該大腿動脈および該腸骨動脈を通して、それが該第1の移植片の内部にあり、 そして少なくとも該第2の管状の移植片伸長部分の頂部に到達するまでガイドす る工程;(q)該第3のガイドワイヤーを該1つの大腿動脈を通して引っ込める工程;(r)第4の比較的大きい直径のガイドワイヤーを、該第4のカテーテルシース を通して、該ガイドワイヤーが少なくとも該第2の管状の移植片伸長部分の頂部 に到達するまでガイドする工程;(s)該第4のカテーテルシースを該もう一方の大腿動脈を通して引っ込める工 程;(t)第5の比較的大きい直径のカテーテルシースを、該第4のガイドワイヤー 上に、該第5のカテーテルシースが少なくとも該第2の管状の移植片伸長部分の 頂部に到達するまでガイドする工程;(u)第2の細長いカテーテル(これは、膨張していないバルーンを一方の端部 に隣接して有し、上流端部と下流端部とを有し、該バルーンの周囲に配される第 2の腔内移植片を備える)を該第4のガイドワイヤー上に、かつ、該第5のより 大きい直径のカテーテルシースの内部に、該第2の移植片の上流端部が該第2の 管状の移植片伸長部分の内部にあるようになるまでガイドする工程;(v)該第5のカテーテルシースを部分的に引っ込めて、該第2の腔内移植片を 離す工程;(w)該第2の送達カテーテルにおける該バルーンを膨張させて、それにより、 該第2の腔内移植片の上流端部を、それが該第2の管状の移植片伸長部分に対し て係合するようになるまで膨張させる工程;(x)該第1の細長いカテーテルを該1つの大腿動脈から引っ込めながら、該バ ルーンの膨張を維持する工程;(y)該第1の細長いカテーテルを該1つの大腿動脈から除くと直ちに、該バル ーンを収縮する工程。 (z)該第5のカテーテルシースを、該もう一方の大腿動脈を通して完全に引っ 込める工程;(aa)第3の細長いカテーテル(これは、膨張していないバルーンを一方の端 部に隣接して有し、上流端部と下流端部とを有し、該バルーンの周囲に配される 第3の腔内移植片を備える)を該第2のガイドワイヤー上に、かつ、該第2のカ テーテルシースの内部に、該第3の移植片の上流端部が該第1の管状の移植片伸 長部分の内部にあるようになるまでガイドする工程;(bb)該第2のカテーテルシースを部分的に引っ込めて、該第3の腔内移植片 を離す工程;(cc)該第3の細長いカテーテルにおける該バルーンを膨張させて、それによ り、該第3の腔内移植片の上流端部を、それが該第1の管状の移植片伸長部分に 対して係合するようになるまで膨張させる工程;(dd)該第3の細長いカテーテルにおける該バルーンを収縮する工程;(ee)該第2の細長いカテーテルを該もう一方の大腿動脈を通して、そして該 第3の細長いカテーテルを該1つの大腿動脈を通して引っ込める工程;(ff)該第4のガイドワイヤーと該第5のカテーテルシースとを該もう一方の 大腿動脈を通して引っ込め、該動脈における切開または穿刺を縫合する工程;(gg)該第2のガイドワイヤーと該第2のカテーテルシースとを該1つの大腿 動脈を通して引っ込め、該動脈における切開または穿刺を縫合する工程。 48.別の工程(l)において、前記第1および第2の管状の移植片伸長部分が、 膨張可能なバルーンによってそれぞれ膨張されるか、または自己膨張する、請求 項47に記載の方法。
2 paragraphs, as filed
Description: TECHNICAL FIELD [Detailed description of the invention]
Positioning of intracavitary graft using guide wire And the catheter for it Field of invention The present invention presents a method of positioning an intraluminal implant in a bifurcated artery and the odor of this method. With respect to the catheter used. Background technology Human arteries can easily develop an inflatable sac known as an aneurysm after a disease. As is well known, this aneurysm is prone to rupture. Traditionally, aneurysms are basic surgical Treated by treatment. This treatment is risky to the patient and is often , Impractical due to other pre-existing illness conditions in the patient. Recently, arteries Intracavitary placement of intracavitary grafts that bridge the aneurysm, thereby moving the active ductus arteriosus Many proposals have been made to isolate the aneurysm from the sac. One such trick Is disclosed in Australian Patent Application No. 78835/94. If the aneurysm extends from a single artery to one or more bifurcated arteries, such intracavities Difficulties arise in the placement of the graft. In this case, the so-called "trouser transfer" "Plant" must be used. In such a graft, a single tubular body Is bifurcated into two smaller tubular bodies. The intent is that a single tubular body is single Placed in one artery, and two small tubular bodies each in two bifurcated arteries Be arranged (see, eg, U.S. Pat. No. 5,360,443, Barone) That is. In reality, it is very difficult to place the trouser-shaped graft effectively. It turned out that there was. The present invention is a novel method that facilitates the placement of intracavitary grafts in bifurcated arteries. With respect to catheters so designed. Disclosure of invention In the first aspect, the invention includes a delivery catheter having the following: (a) An elongated catheter with a first end and a second end; (b) An intracavitary graft with a body arranged around an elongated catheter (where, said The body is tubular at the first end, adjacent to the first end of the elongated catheter. Has a portion, at the second end, bifurcates into the first and second tubular graft extension The elongated catheter extends to the extension of the first tubular implant and Extends into the tubular part); and (c) Extend in the first direction through the extension of the first tubular implant and the second different Auxiliary guide wire protruding in the direction into the extension of the second tubular implant. In another aspect, the invention positions an intracavitary implant in a bifurcated vessel within the patient's body. The vessel consists of a single pre-branching vessel, which is one. Including (branching into a pair of post-branching vessels), this method includes: Ru: (a) Have a tubular portion at the first end and on the extension of the first and second tubular grafts Post-branched blood vessel of the first intraluminal graft with a body having a second end that is bifurcated Introducing into one of the first tubular implants, where the first tubular Extends in the first direction through the graft extension of the graft and the second tube in the second different direction. The process in which the guide wire protruding into the elongated portion of the shaped implant is positioned; (b) The first end of the first intraluminal implant and the extension of the second tubular implant. Is positioned within the pre-branch vessel and at least the first end of the implant expands. The step of inflating the implant until it engages with the wall surrounding the pre-branch vessel; (c) The graft with the guidewire until it extends into the other post-branch vessel. The second step of extending in different directions; (d) A second intraluminal graft with an upstream end and a downstream end, after the other branch The guide wire or another guide wire that has been introduced into a blood vessel and positioned at that location. A bite with an ear whose upstream end is within the second tubular graft extension Or surround it, and its downstream end is within the other post-branch vessel. Move the second intraluminal implant until it becomes, and with the upstream end of the second intraluminal implant. The step of forming a fluid delivery engagement with the second tubular implant extension. The catheters and methods according to the invention preferably have an Australian patent application. Utilizing a balloon inflatable implant made in accordance with the disclosure of No. 78835/94, The contents of are incorporated herein by reference. Elongated catheter is inflatable Place the balloon on one end and also with the intracavitary graft placed around the balloon. Can have adjacent to this. Other suitable balloons inflatable or self-inflating Noh stents or implants can be used to carry out the present invention. In a preferred embodiment of the invention, at least partially located in the post-branched blood vessel. Intracavitary grafts to be fitted are provided in various diameters. This is the day in implementation Appropriate grafts are available to fit different diameters of routinely operated post-branch vessels Ensure that it is possible. In some embodiments, the variety of intracavitary graft diameters Is an inward or outward tape of the outer diameter along at least a portion of the shaft length. Achieved by par. Alternatively, the change in diameter is a difference in the diameter at which the implant is constructed. A shorter step-down or step between two substantially cylindrical parts Provided by the pu-up taper. Preferably, the upstream end of the intracavitary implant is That of the tubular graft extension of the intracavitary graft fully positioned within the pre-branch vessel It has a standard diameter to provide a secure connection with each. With reference to the typical application, placement of a trouser-shaped implant in the bifurcated artery, this Ming is disclosed herein below. But the present invention is other such as veins or bile ducts. Can be used for human blood vessels. Intracavitary grafts, the extension of each tubular graft terminates upstream of the bifurcation in the artery It is preferable to have such a length. In this arrangement, a separate tubular graft Is used to connect each tubular extension to its associated distal artery .. In another arrangement, the intraluminal graft is long enough to project into the first distal artery. Includes one tubular extension. In this case, the other tubular extension is the above bifurcation And the second tubular implant connects its extension to the second distal artery To do. Upstream through the first tubular graft extension and the second tubular graft extension The guide wire extending downstream through is preferably very fine and substantially. Kink resistant. In certain embodiments, the auxiliary guide wire is a graft. It can extend through grooves throughout the body. In another embodiment, the auxiliary catheter is the first Upstream through the tubular graft extension and into the second tubular graft extension Can extend downstream, this auxiliary catheter contains a guide wire. 3 French assistance Catheter is particularly preferred. Auxiliary catheter and guide wire are thin Can be loosely placed in the graft before being packaged around a long catheter .. Alternatively, the auxiliary catheter is coupled to the graft body over a portion of its length. It can be. In another alternative, part of the catheter is interwoven with part of the implant. Can be forced or otherwise combined. For further alternatives, auxiliary cutters The tell can be incorporated into a groove in the fabric of the graft wall. These various technologies Auxiliary guide wire and its associated force while inserting the implant into the arterial system Designed to better secure the tatel in the proper position. In a further aspect, the present invention describes both iliac movements from the aorta in the patient's body. It consists of a method of positioning an intracavitary graft across an aneurysm that extends into the pulse. The method includes the following steps: (a) The step of incising or puncturing to expose one of the patient's femoral arteries; (b) The first guide wire is exposed so that it crosses the aneurysm. The step of inserting through the femoral artery, the corresponding iliac artery, and the aorta; (c) The first catheter sheath, the first guy, until it crosses the aneurysm. The process of guiding on the wire; (d) Step of retracting the first guide wire; (e) A second relatively rigid guide wire, said until it crosses the aneurysm. The process of insertion through the first catheter sheath; (f) The step of retracting the first catheter sheath; (g) A second relatively large diameter catheter sheath that crosses the aneurysm Until, the process of guiding on the second guide wire; (h) First delivery catheter, which has a non-inflated balloon at one end (Contains a first intraluminal implant that is adjacent and is placed around the balloon). On the guide wire of 2 and of the second larger diameter catheter sheath Internally guided step (where the first intraluminal implant has a tubular portion at the first end And a second end bifurcated into a first and second tubular graft extension (Having a portion), where the first tubular implant extends within the first implant. A second variant through the portion in the first direction and during the second tubular graft extension. Position a third catheter containing a third guide wire that extends in the same direction Process; (i) The first delivery catheter, the first end of the first implant of the aneurysm The process of positioning to be upstream; (j) The second larger diameter catheter sheath is partially retracted to the second. Step of releasing 1 intracavitary graft; (k) Inflate the balloon, thereby the first end of the first intraluminal implant. Inflate the portion until it engages the wall of the aorta over the aneurysm Process to make; (l) The balloon is contracted and the first and second tubular grafts are elongated by blood. A step that allows the first implant to flow downstream; (m) Place the third guide wire in the second direction to the other iliac artery. And the process of guiding downstream into the femoral artery; (n) Incision or puncture, and the third guide wire to the other femoral movement The process of pulling back from the pulse; (o) The step of retracting the third catheter through the one femoral artery; (p) Place the fourth catheter sheath on the third guide wire and the other Through the femoral artery and the iliac artery of the side, it is inside the first graft , And guide until at least the top of the second tubular graft extension Process to do; (q) The step of retracting the third guide wire through the one femoral artery; (r) A fourth relatively large diameter guide wire, the fourth catheter sheath Through the guide wire is at least the top of the second tubular implant extension The process of guiding until you reach; (s) Retracting the fourth catheter sheath through the other femoral artery About; (t) A fifth relatively large diameter catheter sheath, the fourth guide wire Above, the fifth catheter sheath is at least the extension of the second tubular implant. The process of guiding until you reach the top; (u) Second delivery catheter, which has a non-inflated balloon at one end A second that is adjacent, has an upstream end and a downstream end, and is arranged around the balloon. On the fourth guide wire and the fifth larger Inside the caliber catheter sheath, the upstream end of the second implant is the second tube. The process of guiding until it is inside the elongated part of the graft; (v) Partially retract the fifth catheter sheath to remove the second intraluminal implant. Release process; (w) Inflate the balloon in the second delivery catheter, thereby The upstream end of the second intraluminal implant, which is relative to the extension of the second tubular implant. Inflate until engaged; (x) Withdrawing the first delivery catheter from the one femoral artery, the val The process of maintaining the expansion of the (y) The baru as soon as the first delivery catheter is removed from the one femoral artery. The process of shrinking. (z) Completely pull the fifth catheter sheath through the other femoral artery. Putting process; (aa) Third delivery catheter, which has a non-inflated balloon at one end Adjacent to the balloon, having an upstream end and a downstream end, and arranged around the balloon. 3 Intracavitary implants) on the second guide wire and in the second catheter -Inside the tel sheath, the upstream end of the third graft extends the first tubular graft. The process of guiding until it is inside the part; (bb) The second catheter sheath is partially retracted and the third intraluminal implant The process of releasing; (cc) Inflate the balloon in the third delivery catheter, thereby , The upstream end of the third intraluminal graft, which is paired with the extension of the first tubular graft. And inflate until engaged; (dd) The step of contracting the balloon in the third delivery catheter; (ee) The second delivery catheter is passed through the other femoral artery and the second. Step of retracting the delivery catheter of 3 through the one femoral artery; (ff) The fourth guide wire and the fifth catheter sheath are attached to the one thigh. The step of retracting through an artery and suturing an incision or puncture in that artery; (gg) The second guide wire and the second catheter sheath are attached to the one thigh. The step of retracting through an artery and suturing an incision or puncture in the artery. A brief description of the drawing FIG. 1 has an aortic aneurysm bridged by an intraluminal implant according to the invention. Partially clipped central view of the patient; FIG. 2 is a tubular intraluminal implant used by the method described with reference to FIG. It is a front view of an embodiment of FIG. 3 is a cross-sectional view of the intracavitary graft of FIG. 2 opposite to the longitudinal direction; FIG. 4 is a detailed elevation view of one end of the intracavitary graft of FIG. 2; FIG. 5 is a detailed perspective view of the first end of the intracavitary implant of FIG. 4, the end of the implant. How the alternating crests of wire radiate outward while inserting the implant Indicates whether it is pushed in the direction; 6 and 6a are placed on the delivery catheter used in the practice of the method of the invention. It is a vertical cross-sectional view of two possible embodiments of a bifurcated implant to be made; Figure 6b shows a bulge adjacent to the free end of the catheter and guide wire, respectively. An enlarged view of a stretchable balloon, the balloon is inflated; FIG. 6c is a longitudinal sectional view of the device of FIG. 6b, with the balloon not inflated. I; Figure 6d shows a guide wai with an inflatable umbrella adjacent to its free end. Simplified cross section of Yar; Figures 7a-7i show the steps in which the method according to the invention is practiced; 8a-8f show a simplification of yet another intraluminal implant used in the method according to the invention. It is a side elevation FIG. 9 shows a tube placed on a delivery catheter that can be used to carry out the methods of the invention. FIG. 5 is a vertical cross-sectional view of an embodiment with a shaped implant. Preferred aspects for carrying out the present invention Bifurcated or trouser-shaped graft containing three intracavitary grafts 10, 10a, and 10b Because the piece can bridge and occlude an aortic aneurysm that extends into the left iliac artery Is adapted to be transfemorally inserted into the patient. In Figure 1 As shown, the aorta 11 is connected to the left and right iliac arteries 13 and 12. Aortic aneurysm Placed between the renal arteries 14 and 15 and the iliac arteries 12 and 13, the aneurysm is in the left intestine It extends below the bone artery 13. Each intracavitary implant (as shown in Figures 2-5) is a pleated tube of polyester fabric. Can include 16. Polytetrafluoroethylene, polyurethane, and combinations thereof Other materials, including mixes, may be used. Tube 16 is separated by a plurality of pipes along its length. Reinforced by spaced stainless steel wires 17 (each of these) Each can have a generally closed sinusoidal shape depicted). Wire 17 is preferred Or as thin as possible, and typically 0.3-0.4 mm in diameter. Wire 17 Are malleable and can be bent into any desired shape, i.e. they are any parenchyma Since they do not have elasticity in a certain range, they are more likely to expand due to their own elasticity. Rather, it should be physically inflated into contact with the aorta. wire 17 is each woven into the fabric of tube 16, with alternating crests of each wire 17 of tube 16. On the outside, the rest of the wire 17 is on the inside of the tube 16 (below in the specification). Except for wire 17 at the end as described). The end of each wire 17 is the tube 16 Arranged on the outside of the and twisted together to form the tail 18. The ends together Depicted to be squeezed to form tail 18, but the ends are also folds together Can be done. The tail 18 of the alternating wire 17 is opposite long axis along the outer surface of the tube 16. It is bent so as to extend in the direction. The wire 17a at the end protrudes from each end of the tube 16 and thus theirs. Alternating crests of wire 17a extend longitudinally beyond the end of tube 16. End Wire 17a preferably has an amplitude of about 6 mm and 6 around a 22 mm diameter implant. It has a wavelength such that ~ 8 crests are arranged. The next two adjacent wai The yar 17 is preferably located as close as possible to the wire 17a at the end. And have amplitudes of 4 mm and 5 mm, respectively. These wires are typically It initially has the same wavelength as the terminal wire 17a. Then across the entire graft Wires 17 are spaced 15 mm apart, have an amplitude of 6 mm, and end wires. It has a first wavelength that is substantially the same as Yar 17a. Single because the aneurysm extends from the aorta 11 beyond the bifurcation of the iliac arteries 12 and 13. Tubular grafts move while maintaining blood flowing into each of the iliac arteries 12 and 13. Not enough to bridge the aneurysm. Rather than using a single tubular graft In the method of the invention, three separate tubular implants 10, 10a, and 10b are used. .. A pair of short tubular grafts with bifurcations at the downstream end of the first one of graft 10. Form 10 graft extension portions 19a, 19b. Short tubular graft extension 19a, 19b Can be passively inflated by blood flow, or by inflating a balloon , Or it may be actively inflatable by the self-expansion of the spring. As best illustrated in FIGS. 8 (a)-(f), they extend into the iliac arteries 12 and 13, respectively. Graft portions 10a and 10b adapted to do so have a common diameter upstream Each has an end. The upstream end is adapted to be located inside the aorta 11. It is interlocked at each of the elongated portions 19a.19b of the graft 10. Preferably , This interlock is the friction between the upstream end and the extension 19a, 19b respectively Inflating or splicing the balloon at the upstream end so that there is engagement caused by Achieved by the self-expansion of the In addition to having a straight cylindrical tube, the downstream ends of graft portions 10a and 10b The diameter of 35 is the iliac artery (graft parts 10a and 10b are implanted inside it) It may have a variable diameter to match the diameter of the). Diameter changes can be seen in short step-down sections 31 (see Figure 8c) or steps. By puup part 32 (see Figure 8d) or by graft part 10a or 1 Regions of tapers 33 and 34 extending along the length of 0b (see Figures 8e and 8f) Can be given by. Next, a method of positioning the intracavitary implant will be described with reference to FIGS. 7a-7i. In performing this method, one that is incised or punctured and flows from the corresponding iliac artery. Exposing the femoral artery (eg, ipsilateral) and using Seidinger needle technique, 0.035 Floppy tipped flexible guide wire at the tip of an inch diameter, femoral movement Ilial movement that inserts into the pulse and then enters the aorta 11 so that it crosses the aneurysm Insert it into pulse 12 and pass it through. Then 8French hemostatic sheath to control bleeding Introduce on this wire. Introducing an angiographic catheter to build the patient's blood vessels Take a shadow map to show the location of renal arteries 14, 15 and other relevant anatomical structures of the patient Allows you to Then retract the flexible flexible guide wire at the tip, and then Amplatz Angiographic catheter with a very rigid (AES) guide wire 23 (0.035 inch diameter) Through the aorta 11 (see Figure 7a). Withdraw angiographic catheter After that, leave the rigid guide wire 23 in situ. Then preferably 24 French Introduce the catheter sheath 21 and mantle needle into the aorta 11 over the rigid wire 23 ( See Figure 7a). The balloon catheter 24 is then introduced into the sheath 21. As illustrated in more detail in FIG. 6, the balloon catheter 24 is a delivery catheter. This is the extension of the first and second tubular grafts separated at bifurcation point 40. Through the bifurcated graft 10 with minutes 19a, 19b, as well as the first tubular extension 19a In the first direction, then in the second different direction into the second graft extension 19b Prepackaged with a thin catheter 25 containing an extending guide wire 26. Catheter 24 and thin catheter 25 when placing implant 10 in a blood vessel The role of ensuring accurate positioning of the wheel 25 and guide wire 26 In a common catheter sheath 56 that plays, it can bind together under graft 10. Tubular In addition to being slidable through the graft extension 19a, 19b Le 25 was anchored in place at graft 10 prior to insertion of graft 10 into the blood vessel. obtain. Catheter 26 can be sutured, glued, or woven into the body of implant 10. .. Although the guide wire 26 is shown inside the catheter 25 in FIG. 6, the guide wire 26 is shown inside the catheter 25. Only -26 can be placed in the first and second tubular graft extension 19a, 19b. Can be easily predicted. In another configuration illustrated in Figure 6a, the guide wire 26 is positioned within a tubular channel 22 formed within the body of implant 10. To. After packaging the implant 10 around the balloon 20, the balloon is placed in the aorta 11. Before placing the Tether 24, the groove 22 has the guide wire 26 in the first and second tubular. The role of ensuring that the graft remains in the desired position in the elongated portions 19a, 19b Fulfill. If the balloon catheter 24 is positioned at the desired location inside the aorta 11, Sheath 21 is partially retracted, releasing graft 10 and inflating balloon 20 (See Figure 7b). Inflatation of balloon 20 of catheter 24 is the first transplant Inflate the upstream end of piece 10 and above the aneurysm but downstream of renal arteries 14 and 15. , It causes an engagement with the aortic wall at its upstream end. The first graft 10 is A short tubular graft extension 19a, 19b is located completely inside the aorta 11. Has a length. The balloon 20 is then contracted, but the balloon catheter 24 Is left in place for some time (time being) (see Figure 7c). Ba Due to the contraction of rune 20, blood elongates each of the tubular graft extension parts 19a and 19b. Allows the graft 10 to flow downwards. The thin catheter 25 is preferably 3 French and the guide wire 26 is kin. It is a substance that does not squeeze, so the guide wire 26 is downstream of the catheter 25. Can stretch in the direction (see Figure 7c). The guide wire 26 is small at the tip. Inflatable balloon 55, or other device that obstructs flow as illustrated in Figure 6. You can have a chair. The balloon 55 can be inflated and the guide wire 26 can be stretched As a result, the guide wire 26 is guided by the blood flow to the opposite iliac artery 13. Kake. Is the guide wire 26 preferably a nitinol core with a hydrophilic coating? It consists of. The balloon 50 may also be at the free end of the catheter 25. like that Details of the examples of balloons 50, 55 are illustrated in more detail in FIGS. 6b and 6c. Bar The catheters 25 and 55 are inflated, and the catheter 25 and the guide wire 26 are respectively. Helps to be transported and guided by the bloodstream to the opposite iliac artery 13. Catheter 25 and guide wire 26 provided by FIGS. 6b and 6c The enlarged view of balloons 50 and 55 adjacent to the free end shows two catheters 25, respectively. Represents having cavities 52 and 53. The guide wire 26 passes through the first lumen 52 To. The end of the second lumen 53 is sealed and the small hole 51 is shaped on the outer surface of the catheter 25. It is made. Latex balloon 50 is annular at 50a on the outer surface of catheter 25 Is glued to. When the balloon 50 is inflated, a liquid or gas, it is a hole Injected downward into the second lumen 53 to inflate the balloon 50 through 51 .. Similarly, the guide wire 26 has a lumen 54, which descends and guide wire Air can be infused to inflate the balloon 55 located at the free end of 26. Inflatable balloons are preferred, but other inflatable devices may be recognized. For example, in another embodiment, the catheter 25 and the guide wire 26 Runes 50, 55 can be replaced by inflatable umbrellas. Ann available An example of a Brera type is illustrated in Figure 6d. Arranged at the free end of the guide wire 26 It is Umbrella 70. Umbrella 70 (This is the inflated shape shown in Figure 6d The wire 71 extending through the lumen 72 in the guide wire 26) Inflated by. Joint stay 72 when retracting wire 71 The wire 71 is stung so that it articulates and inflates the umbrella 70. It is attached to -72. Umbrella 70 is on guide wire 26, but catheter 25 It can be easily recognized that a similar configuration can be used for. Further alternative In, the balloon 55 on the guide wire 26 is an epo, as illustrated in FIG. 6e. It can be replaced with small solid beads 80 of a substance such as xy resin or titanium. The beads 80 preferably have a larger profile than the guide wire 26. To. As soon as the catheter 25 is placed in the desired position in the blood vessel in a particular application At the free end of the catheter 25, the balloon 50 engages with the wall of the blood vessel. Then inflate the catheter 25 further until it is fixed in the desired position within the blood vessel. Hope to provide additional fixation while the guide wire 26 passes through the blood vessel Good. Once the guide wire 26 is correctly placed in the contralateral femoral artery, its thigh movement A cut is made in the pulse (which is fastened at the intersection) and an arteriotomy is made. guide Guide wire 26 if wire 26 is completely guided to the opposite femoral artery By retracting the guide wire through an incision or puncture in the artery It is easily collected. Guide wire 26 is completely guided to the opposite femoral artery If not, a snare or similar device passes through the opposite femoral artery. Can be introduced, grab the guide wire 26 and make an incision to retrieve it Pull back to the puncture site. Once the guide wire 26 is recovered, a thin catheter Le 25 is then retracted via the same side, and the other catheter 27 goes up the guide wire 26 through the opposite femoral artery, which is the first graft 10. Go inside and reach at least the top of the second tubular extension 19b (See Figure 7d). The thin guide wire 26 is then pulled Catete through the opposite femoral artery with a squeezed and thinner guide wire 30 It is inserted in Le 27. Catheter 27 is then removed and catheterized. The machine 21a preferably has 24 French, and the mantle needle is a rigid guide wire. Introduced on -30 (see Figure 7e). Prior to extension of the guide wire 26 to the opposite iliac and femoral arteries, the catheter -Tel sheath (which can be similar to catheter sheath 21) is the opposite femoral movement Any that can extend upstream through the veins and iliac arteries and can be present in these arteries The twists and turns can be reduced, thus facilitating the guidance of the guide wire 26 through it. Second balloon catheter 24a (second tubular implant 10a) as illustrated in FIG. (Packaged on this) then passes through the catheter sheath 21a, well that The upper end goes inside the second tubular extension 19b, and at its lower end the intestine It is introduced until it is inside the bone artery. Catheter sheath 24 The rune 20a has the upper end of the implant 10a engaged by friction with the second tubular extension 19b. It is inflated to fit (see Figure 7f). Catheter 24a The swelling of rune 20a is pulled through the ipsilateral artery 12 of the first balloon catheter 24. Support graft 10a while populated. Then the balloon on catheter 24a 20a is contracted, and catheter 24a is positioned with a third implant 10b. Maintained in place to continue to support grafts 10, 10a in artery 11 during Is done. The catheter sheath 21a is then removed (see Figures 7f and 7g). ), And a third balloon catheter (tubular graft 10b packaged on top) (The third balloon catheter and implant 10b are identical to those illustrated in FIG. (Possible) is introduced into the sheath 21 of the guide wire 23. Sheath 21 After partial withdrawal, its upstream end is inside the first tubular graft extension 19a This is advanced until it is then placed. Third balloon category The third implant, 10b, positioned at the cell, is therefore the second at its upstream end. Contact with 1 tubular extension 19a, and at its downstream end the right iliac artery 1 The contact with 2 is pushed forward (see Figure 7h). Here, the rigid guide wires 23 and 30 are retracted, and the opposite incision is made. Or the puncture is sutured. A second angiography test is then performed, and the graft The hemostatic sheath 21 pulls when 10, 10a, and 10b are properly positioned and functioning. It is tucked in and the right thigh incision or puncture is sutured. As a result, Figure 7i As illustrated in, a trouser-shaped implant that bridges the aneurysm functions. This surgery is general anesthesia, epidural anesthesia, or, where appropriate, local anesthesia. Can be carried out using only. A number of changes and / or modifications have been extensively described in the spirit or scope of the invention. What can be done in the present invention as shown in a particular embodiment without departing from , Can be understood by those skilled in the art. Therefore, all of these embodiments are considered exemplary and limited. It should be considered that it should not be regarded as a target.
Every citation, both ways
| Document | Relation | Office | Cited during |
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| US10245166B2 | Cited by | United States of America | Applicant |
| US10772717B2 | Cited by | United States of America | Applicant |
| US10874502B2 | Cited by | United States of America | Applicant |
| JP2008513157A | Cited by | Japan | Examiner |
| US10660775B2 | Cited by | United States of America | Applicant |
| US10874502B2 | Cited by | United States of America | Applicant |
| US9907642B2 | Cited by | United States of America | Applicant |
| US9687374B2 | Cited by | United States of America | Applicant |
| JP2017148525A | Cited by | Japan | Search report |
| US10603196B2 | Cited by | United States of America | Applicant |
| US9700701B2 | Cited by | United States of America | Applicant |
| US11129737B2 | Cited by | United States of America | Applicant |
| US9757262B2 | Cited by | United States of America | Applicant |
| US9700701B2 | Cited by | United States of America | Applicant |
| US11406518B2 | Cited by | United States of America | Applicant |
34 members in 9 offices
Priority claims19
| Document | Office | Kind | Date |
|---|---|---|---|
| PN6512 | Australia | – | |
| PN651295 | Australia | A | |
| PN651295 | Australia | A | |
| PN6513 | Australia | – | |
| PN651395 | Australia | A | |
| PN651395 | Australia | A | |
| PN6514 | Australia | – | |
| PN651495 | Australia | A | |
| PN651495 | Australia | A | |
| 9600714 | Australia | W | |
| 9600714 | Australia | W | |
| 6512 | – | – | – |
| 6513 | – | – | – |
| 6514 | – | – | – |
| AU1995PN06512 | – | – | – |
| AU1995PN06513 | – | – | – |
| AU1995PN06514 | – | – | – |
| PCTAU199600714 | – | – | – |
| WO1996AU00714 | – | – | – |
Members34
| Document | Office | Kind | |
|---|---|---|---|
| CA2236602A1 | Canada | A1 | |
| CA2236905A1 | Canada | A1 | |
| WO9717910A1 | World Intellectual Property Organization (WIPO) | A1 | |
| WO9717911A1 | World Intellectual Property Organization (WIPO) | A1 | |
| WO9718006A1 | World Intellectual Property Organization (WIPO) | A1 | |
| AU7486296A | Australia | A | |
| AU7486396A | Australia | A | |
| AU7486496A | Australia | A | |
| CN1207658A | China | A | |
| CN1207659A | China | A | |
| AU706084B2 | Australia | B2 | |
| EP0955952A1 | European Patent Office (EPO) | A1 | |
| EP0955953A1 | European Patent Office (EPO) | A1 | |
| BR9611371A | Brazil | A | |
| BR9611441A | Brazil | A | |
| JP2000500046A | Japan | A | |
| JP2000500047AThis record | Japan | A | |
| US6045557A | United States of America | A | |
| US6099558A | United States of America | A | |
| AU728276B2 | Australia | B2 | |
| RU2179003C2 | Russian Federation | C2 | |
| RU2179421C2 | Russian Federation | C2 | |
| CA2236905C | Canada | C | |
| JP2004089718A | Japan | A | |
| CA2236602C | Canada | C | |
| JP2004202277A | Japan | A | |
| CN1195459C | China | C | |
| CN1271980C | China | C | |
| JP2006312081A | Japan | A | |
| JP3876246B2 | Japan | B2 | |
| JP2007319694A | Japan | A | |
| JP4036844B2 | Japan | B2 | |
| EP0955952A4 | European Patent Office (EPO) | A4 | |
| EP0955953A4 | European Patent Office (EPO) | A4 |
2 legal events, as the office reported them to INPADOC
Over the term
Point at a mark for the eventEvents
| Event | Code | |
|---|---|---|
| Written withdrawal of applicationJAPANESE INTERMEDIATE CODE: A761A761 | A761 | |
| Re-examination (zenchi) completed and case transferred to appeal boardAppealJAPANESE INTERMEDIATE CODE: A912A912 | A912 |
Numbers
- Publication
- 2000-500047
- Publication, DOCDB
- 2000500047
- Publication, EPODOC
- JP2000500047
- Application
- 9518438
- Application, DOCDB
- 51843897
- Application, EPODOC
- JP19970518438
Titles2
- Japanese
- 【発明の名称】ガイドワイヤーを用いた腔内移植片の位置決めおよびそのためのカテーテル
- English
- INDUSTRIAL APPLICABILITY: Positioning of an intracavitary implant using a guide wire and a catheter for that purpose.
Classification
- CPC, 11
- A61F2/07
- A61F2/848
- A61F2/86
- A61F2/90
- A61F2/954
- A61F2/958
- A61F2002/065
- A61F2002/075
- A61F2002/8483
- A61F2/89
- A61F2002/067
- IPC, 7
- A61B17 00
- A61F2 00
- A61F2 06
- A61F2 86
- A61F2 90
- A61M25 01
- A61M25 09