JPH1033666A - Bypass tube - Google Patents

Bypass tube

Info

Publication number
JPH1033666A
JPH1033666A JP8190610A JP19061096A JPH1033666A JP H1033666 A JPH1033666 A JP H1033666A JP 8190610 A JP8190610 A JP 8190610A JP 19061096 A JP19061096 A JP 19061096A JP H1033666 A JPH1033666 A JP H1033666A
Authority
JP
Japan
Prior art keywords
tube
bypass tube
catheter
insertion member
bypass
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP8190610A
Other languages
Japanese (ja)
Inventor
Sunao Watanabe
直 渡辺
Nobumasa Tsutsui
宣政 筒井
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BUAAYU KK
Original Assignee
BUAAYU KK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by BUAAYU KK filed Critical BUAAYU KK
Priority to JP8190610A priority Critical patent/JPH1033666A/en
Publication of JPH1033666A publication Critical patent/JPH1033666A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide a bypass tube which his used with a catheter, by which a required blood flow is secured to prevent a lesion caused by ischemia. SOLUTION: A bypass tube 1 comprises two tubes 14, each one end of which is connected to both sides of a valve member 10 through a connector 12, and an insert member 16 connected to the other end of each tube 14 through a connector 12. The bypass tube 1 is used jointly with an IABP balloon catheter, for example, and in the case of inserting the catheter from one femoral artery, the tube is installed in such a manner as to communicate the femoral artery on the periphery side from the insert position with the other femoral artery. Thus, even if a catheter insert position is obstructed in the catheter insert position, ischemia of the legs can be prevented by blood flowing-in from the other femoral artery.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、血流障害部分より
も下流側血管への血流を確保するために使われるバイパ
スチューブに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a bypass tube used to secure blood flow to a blood vessel downstream of a blood flow obstruction.

【0002】[0002]

【従来の技術】近年、医療技術の進歩に伴い、以前であ
れば外科手術を要したような症例であっても、カテーテ
ルを経皮的に大腿動脈等から挿入して、血管内を通して
心臓付近までもって行き、各種検査、治療等を行うこと
により、患者への負担が少ない治療を実施できるように
なっている。
2. Description of the Related Art In recent years, with the advance of medical technology, even in cases where surgery was required before, a catheter is percutaneously inserted from a femoral artery or the like, and the vicinity of the heart is passed through a blood vessel. By carrying out various tests, treatments, and the like, treatments with little burden on patients can be performed.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、カテー
テルを使った治療にも更に改善すべき点は残されてお
り、そのひとつにカテーテル使用時の下肢虚血があっ
た。これはカテーテル等を下肢の大腿動脈から血管内に
挿入した際に、カテーテル自体あるいは経皮的に挿入す
るために利用する筒(シース)などが障害物となって血
流障害が発生し、その障害物よりも末梢の血管に血液が
流れにくくなるために起きる問題で、この様な下肢虚血
が起こると、最悪の場合には、人体組織の一部に壊死を
招く恐れがあった。
However, there are still points to be improved in treatment using a catheter, one of which is lower limb ischemia when using a catheter. This is because when a catheter or the like is inserted into the blood vessel from the femoral artery of the lower limb, the catheter itself or a tube (sheath) used for percutaneous insertion becomes an obstacle, causing blood flow obstruction. In the worst case, if the ischemia of the lower limb occurs, there is a risk of causing necrosis in a part of human body tissue.

【0004】そのため、従来はカテーテルやシースの外
径寸法をできる限り細くすることで、血流を確保するよ
うに努力していたが、カテーテルの細径化にも限界があ
り、比較的血管径の細い患者に対してはカテーテルを使
った治療を実施できない場合があった。また、カテーテ
ル径が太くなるようでは、カテーテルの機能面又は強度
面などの改良ができないといった問題もあった。
For this reason, in the past, efforts have been made to ensure blood flow by making the outer diameter of the catheter or sheath as small as possible. However, there is a limit in reducing the diameter of the catheter, and the blood vessel diameter is relatively small. In some cases, treatment using a catheter cannot be performed for patients with small sickness. Further, when the diameter of the catheter is increased, there is a problem that the functional aspect or the strength aspect of the catheter cannot be improved.

【0005】本発明は、上記問題を解決するためになさ
れたものであり、その目的は、カテーテル使用時等に併
用され、必要な血流を確保して虚血に伴う障害を防止可
能なバイパスチューブを提供することにある。
SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned problems, and an object of the present invention is to provide a bypass which can be used together with a catheter to secure a necessary blood flow and prevent a failure caused by ischemia. To provide a tube.

【0006】[0006]

【課題を解決するための手段、および発明の効果】上述
の目的を達成するため、本発明のバイパスチューブは、
請求項1記載の通り、長尺で柔軟なチューブと、該チュ
ーブの両端に設けられ、先端側は血管内へ挿入可能な形
状とされ、先端から前記チューブ内へ貫通する貫通穴が
形成された挿入部材とを備えたことを特徴とする。
Means for Solving the Problems and Effects of the Invention In order to achieve the above-mentioned object, a bypass tube of the present invention comprises:
As described in claim 1, a long and flexible tube, provided at both ends of the tube, the distal end is shaped to be insertable into a blood vessel, and a through-hole penetrating from the distal end into the tube is formed. And an insertion member.

【0007】本発明のバイパスチューブによれば、チュ
ーブの両端にある挿入部材の先端を血管内へ挿入する
と、血液が一端の挿入部材の貫通穴を介してチューブ内
へ流入し、その血液がチューブに誘導され、他端の挿入
部材の貫通穴を介して流出するので、十分な血流が確保
されている部位から虚血気味の部位へ血液を供給するこ
とができる。したがって、一方の足(例えば右足)の大
腿動脈からカテーテル等を血管内に挿入した場合には、
一端の挿入部材をもう一方の足(例えば左足)の大腿動
脈に挿入すると共に、他端の挿入部材をカテーテル挿入
部位よりも血流方向下流側で大腿動脈に挿入すること
で、もう一方の足からの血液をカテーテル挿入部位より
末梢の血管に流入させることができ、たとえカテーテル
挿入部位において血流が妨げられていたとしても下肢虚
血を招くことがない。
According to the bypass tube of the present invention, when the distal ends of the insertion members at both ends of the tube are inserted into the blood vessel, blood flows into the tube through the through-hole of the insertion member at one end, and the blood flows through the tube. , And flows out through the through hole of the insertion member at the other end, so that blood can be supplied from a site where a sufficient blood flow is secured to a site that is likely to be ischemic. Therefore, when a catheter or the like is inserted into a blood vessel from the femoral artery of one foot (for example, the right foot),
By inserting the insertion member at one end into the femoral artery of the other foot (for example, the left foot) and inserting the insertion member at the other end into the femoral artery downstream of the catheter insertion site in the blood flow direction, the other foot is inserted. Can flow into peripheral blood vessels from the catheter insertion site, and even if blood flow is blocked at the catheter insertion site, lower limb ischemia does not occur.

【0008】この様なバイパスチューブを使えば、カテ
ーテル等を使った治療における安全性をより高くするこ
とができ、更に、例えば血管が細くて従来はカテーテル
の使用が困難であったような患者に対してでも、カテー
テルを使った治療ができるようになる。また、バイパス
チューブで血流を確保できれば、従来よりも外径が太い
カテーテルでも使用可能になるので、例えば従来は外径
寸法との兼ね合いで断念せざるを得なかった様なカテー
テルの強度面や機能面での改良も可能となる。
By using such a bypass tube, safety in treatment using a catheter or the like can be further enhanced, and further, for example, for patients whose blood vessels are thin and the use of a catheter has been difficult in the past. In contrast, treatment using a catheter can be performed. In addition, if blood flow can be secured by the bypass tube, it is possible to use a catheter having a larger outer diameter than before, so for example, the strength aspect of the catheter which had to be abandoned in the past in consideration of the outer diameter dimension and Functional improvements are also possible.

【0009】なお、上記チューブ及び挿入部材は、医療
器具用として一般に使用されている樹脂材料等によって
形成すればよい。より具体的には、例えばチューブにつ
いては、折れ曲がって血流を妨げるようなことのないも
のなら何でもよいが、取り扱いやすさなどを考えると、
塩化ビニル、シリコン、ウレタン、ナイロン、テフロ
ン、ポリプロピレン、ポリエチレン等で作製するとよ
い。また、挿入部材については、挿入性、成形性が良好
であるものほど望ましく、それにはポリプロピレン、ポ
リエチレン、テフロン、ナイロン、ウレタンなどで作製
されているとよい。
The tube and the insertion member may be formed of a resin material generally used for medical instruments. More specifically, for example, as for the tube, anything may be used as long as it does not bend and hinder blood flow.
It may be made of vinyl chloride, silicon, urethane, nylon, Teflon, polypropylene, polyethylene, or the like. Further, as for the insertion member, it is preferable that the insertion member and the moldability are good, and it is preferable that the insertion member is made of polypropylene, polyethylene, Teflon, nylon, urethane or the like.

【0010】また、請求項2記載の如く、血液と接触す
る部分の一部又は全部が、抗血栓性材料によってコーテ
ィングされていると、血栓の生成が抑制されるので、よ
り長時間にわたっての使用が可能となるという利点があ
る。抗血栓性材料については、公知の材料を常法に従っ
てコーティングしてあればよく、特に限定されるべきも
のではないが、具体例をいくつか挙げるとすれば、例え
ば、含フッ素セグメント化ポリウレタン、含フッ素アク
リルスチレンウレタンシリコン共重合体、含シリコンポ
リウレタン(商品名:カルディオサン)、2−ヒドロキ
シエチルメタクリレート−スチレンブロック共重合体、
メタクリル酸エステル(例えばメタクリロイルオキシエ
チルホスホリルコリン)とn−ブチルメタクリレートの
共重合体、ポリアミノ酸ブロックとポリブタジエンブロ
ックからなるブロック共重合体、水溶性高分子物質又は
その誘導体を適当なバインダーで固定することにより表
面が潤滑性を示すもの、ヘパリン、ウロキナーゼ等の抗
血栓性あるいは抗血液凝固性剤、またはプロスタサイク
リン等の抗血小板凝集剤を適当な方法で基材上に固定し
たものなどを考え得る。
[0010] Further, when a part or all of a part which comes into contact with blood is coated with an antithrombotic material, the formation of a thrombus is suppressed, so that it can be used for a longer time. There is an advantage that it becomes possible. The antithrombotic material may be coated with a known material according to a conventional method, and is not particularly limited. Examples of the antithrombotic material include a fluorine-containing segmented polyurethane and a specific example. Fluorinated acrylic styrene urethane silicon copolymer, silicon-containing polyurethane (trade name: Cardiosan), 2-hydroxyethyl methacrylate-styrene block copolymer,
By fixing a copolymer of methacrylic acid ester (for example, methacryloyloxyethyl phosphorylcholine) and n-butyl methacrylate, a block copolymer consisting of a polyamino acid block and a polybutadiene block, a water-soluble polymer substance or a derivative thereof with an appropriate binder One having a lubricating surface, one having an antithrombotic or anticoagulant such as heparin or urokinase, or one having an antiplatelet aggregating agent such as prostacyclin fixed on a substrate by an appropriate method can be considered.

【0011】ところで、本発明のバイパスチューブにお
いて、請求項3記載の如く、前記チューブの両端間の所
定位置に設けられ、該チューブの内腔に連通する連通穴
を有し、当該連通穴を開放又は閉塞可能なバルブ部材を
備えていると、上記バイパスチューブを介して血液を流
す場合に、バルブ部材を介して上記チューブ及び挿入部
材内の空気を吸引して除去することができるので便利で
ある。また、バルブ部材を介してヘパリンあるいはその
他の必要な薬液等を投入して、血栓の生成を抑制するた
めの処置等を施すことができる。更に、トランスデュー
サ等を接続してバイパスチューブ内での血圧を測定する
ことが可能となるので、患者の血圧変化、特に、バイパ
スチューブが正常に機能していることを監視することが
できるようになる。
According to a third aspect of the present invention, there is provided a bypass tube provided at a predetermined position between both ends of the tube and having a communication hole communicating with an inner cavity of the tube, and opening the communication hole. Alternatively, when a valve member that can be closed is provided, when blood flows through the bypass tube, air in the tube and the insertion member can be suctioned and removed through the valve member, which is convenient. . In addition, heparin or other necessary drug solution or the like may be supplied through a valve member to perform a treatment or the like for suppressing thrombus formation. Furthermore, since it becomes possible to measure the blood pressure in the bypass tube by connecting a transducer or the like, it is possible to monitor a change in the blood pressure of the patient, particularly, whether the bypass tube is functioning normally. .

【0012】なお、バイパスチューブ内の空気を除去す
るだけであれば、一方の挿入部材だけを血管内に挿入
し、その状態でチューブ内に血液を導入しつつ空気を吸
引除去し、その後で他方の挿入部材を血管内に挿入する
といった方法をとることもでき、この場合は、請求項3
記載の如きバルブ部材がなくてもよい。
If only air in the bypass tube is to be removed, only one of the insertion members is inserted into the blood vessel, and in this state, air is sucked and removed while introducing blood into the tube, and then the other is inserted. It is also possible to adopt a method of inserting the insertion member into the blood vessel.
The valve member as described may not be provided.

【0013】また、本発明のバイパスチューブにおい
て、請求項4記載の如く、前記チューブと前記挿入部材
とが、コネクタを介して着脱自在に連結されていると、
まず、挿入部材を血管内に挿入しておき、その後でコネ
クタを介してチューブを連結すればよいので、人体への
穿刺を行う際にチューブがまとわりついたりせず、挿入
部材の取り扱いが容易になる。
In the bypass tube according to the present invention, the tube and the insertion member are detachably connected to each other via a connector.
First, the insertion member is inserted into the blood vessel, and then the tube may be connected via the connector, so that the tube does not cling to the body when puncturing the human body, and the handling of the insertion member is facilitated. .

【0014】コネクタは、チューブと挿入部材とを連結
可能な構造であれば、チューブ側又は挿入部材側のいず
れか一方又は両方と一体に形成されているものでも、チ
ューブ及び挿入部材とは別体で両者の間に介在するもの
でもよい。また特に、挿入部材を着脱可能に構成した場
合は、請求項5記載の如く、前記挿入部材の貫通穴内に
挿入した状態に配置され、該挿入部材を血管内に挿入し
た後には、該挿入部材の後端側から抜去可能な穿刺針を
備えていれば、穿刺針と一体になった挿入部材を血管内
へ挿入することができるので、事前に別の穿刺針等を使
って穴を開けておかなくてもよくなり、手間がかからな
い。また、血管への挿入時には、穿刺針によって挿入部
材の貫通穴が潰れないように保持される。
As long as the connector can be connected to the tube and the insertion member, even if the connector is formed integrally with one or both of the tube and the insertion member, the connector is separate from the tube and the insertion member. May be interposed between them. In particular, when the insertion member is configured to be detachable, the insertion member is disposed in a state of being inserted into a through hole of the insertion member as described in claim 5, and after the insertion member is inserted into a blood vessel, the insertion member is inserted. If you have a puncture needle that can be removed from the back end side, the insertion member integrated with the puncture needle can be inserted into the blood vessel, so make a hole in advance using another puncture needle etc. You don't have to worry about it. Further, at the time of insertion into a blood vessel, the puncture needle is held so that the through hole of the insertion member is not crushed.

【0015】[0015]

【発明の実施の形態】次に、本発明の実施形態を図面に
基づいて説明する。なお、以下に説明するバイパスチュ
ーブは、本発明の実施形態の一例に過ぎず、本発明の構
成手段を以下に例示する具体的な装置等に限定するもの
ではない。
Next, embodiments of the present invention will be described with reference to the drawings. The bypass tube described below is merely an example of the embodiment of the present invention, and the constituent means of the present invention is not limited to a specific device or the like exemplified below.

【0016】バイパスチューブ1は、図1に示す通り、
バルブ部材10を中心に対称な構造になっており、バル
ブ部材10の両側にコネクタ12を介して一方の端部が
接続された2本のチューブ14と、各チューブ14のも
う一方の端部にコネクタ12を介して接続された挿入部
材16とで構成されている。
The bypass tube 1 is, as shown in FIG.
It has a symmetrical structure around the valve member 10, two tubes 14 having one end connected to both sides of the valve member 10 via a connector 12, and the other end of each tube 14. And an insertion member 16 connected via a connector 12.

【0017】これらの内、バルブ部材10は、ポリプロ
ピレン樹脂製で、二股に分岐して3つの開口をなす連通
路を有し、その内、2つの開口には上記コネクタ12を
介して2本のチューブ14が接続され、残りの1つの開
口には、この開口を手動操作によって開放又は閉塞する
コック20が設けられている。
Of these, the valve member 10 is made of polypropylene resin and has a communicating path which branches into two branches to form three openings. Of these, two openings are connected to the two openings through the connector 12. The tube 14 is connected, and the other opening is provided with a cock 20 for opening or closing the opening by manual operation.

【0018】コネクタ12は、ポリプロピレン樹脂製
で、バルブ部材10、チューブ14、又は挿入部材16
に圧入可能な外径寸法とされたパイプ状のもので、その
外周には取り扱いを容易にするため、鍔22が一体に成
形されている。チューブ14は、塩化ビニル樹脂製で、
内径3mm、長さ300mm程度の柔軟なもので、チュ
ーブ14の内壁面には、抗血栓性材料(本例では、含フ
ッ素アクリルスチレンウレタンシリコン共重合体)によ
るコーティングが施されている。
The connector 12 is made of polypropylene resin and has a valve member 10, a tube 14, or an insertion member 16.
The outer periphery of the pipe is integrally formed with a flange 22 for easy handling. The tube 14 is made of vinyl chloride resin,
The inner wall surface of the tube 14 is coated with an antithrombotic material (a fluorine-containing acrylic styrene urethane silicon copolymer in this example).

【0019】挿入部材16は、ポリプロピレン樹脂製
で、中心に貫通穴を有し、図示の如く先端側ほど細くな
る形状にされている。なお、この挿入部材16は、使用
前の状態においては、図2(a)に示す様に、穿刺針2
4を貫通穴内に挿入した状態で提供されるが、この穿刺
針24は、図2(b)に示す様に、挿入部材16の後端
側から抜去することができ、この状態にしてから、図1
に示した様に、挿入部材16とチューブ14がコネクタ
12を介して接続される。
The insertion member 16 is made of a polypropylene resin, has a through hole at the center, and has a shape that becomes thinner toward the distal end as shown in the figure. The insertion member 16 is in a state before use, as shown in FIG.
4 is provided with the puncture needle 24 inserted into the through hole. As shown in FIG. 2B, the puncture needle 24 can be removed from the rear end side of the insertion member 16. FIG.
As shown in (1), the insertion member 16 and the tube 14 are connected via the connector 12.

【0020】なお、コネクタ12と他の各部品との連結
箇所は、バイパスチューブ1の使用時にはずれては困る
ので、できる限りはずれにくい構造とすることが望まし
く、それには、上記の如く強い力で圧入する構造の他、
例えばコネクタ12と他の各部品とがネジ溝で螺合する
など、確実にロックできる構造なっているとよい。特
に、バルブ部材10とコネクタ12との間等は、その構
造上、他の連結箇所以上にはずれやすい恐れがあるの
で、圧入以上に確実なロック構造を採用するとよい。
The connecting portion between the connector 12 and each of the other components should not be displaced when the bypass tube 1 is used. Therefore, it is desirable that the connecting portion be structured so as not to be displaced as much as possible. Other than press-fitting structure,
For example, it is preferable that the connector 12 and the other components have a structure that can be securely locked, such as being screwed together with a screw groove. In particular, a portion between the valve member 10 and the connector 12 and the like may be easily dislocated to other connection points or more due to its structure. Therefore, it is preferable to adopt a locking structure that is more secure than press-fitting.

【0021】次に、このバイパスチューブ1の使用方法
について、IABPバルーンカテーテルと併用する場合
を例にして説明する。バイパスチューブ1は、図3に示
す様に、IABPバルーンカテーテル30による治療を
受けている患者の左右両足の大腿動脈32L、32Rを
連絡するように装着される。
Next, a method of using the bypass tube 1 will be described by taking as an example a case where the bypass tube 1 is used in combination with an IABP balloon catheter. As shown in FIG. 3, the bypass tube 1 is attached so as to connect the femoral arteries 32L and 32R of both the left and right legs of the patient who is being treated with the IABP balloon catheter 30.

【0022】装着に当たっては、まず、図2(a)に示
した様に、挿入部材16及び穿刺針24が一体となって
いる状態のままで、穿刺針24を使って大腿動脈32L
(又は32R)を穿刺する。ここで、右足の大腿動脈3
2Rの穿刺位置については、IABPバルーンカテーテ
ル30の挿入位置(即ち、シース34の挿入位置)より
も僅かに末梢側とする。
In mounting, first, as shown in FIG. 2 (a), the femoral artery 32L is inserted using the puncture needle 24 while the insertion member 16 and the puncture needle 24 are integrated.
(Or 32R). Here, the right leg femoral artery 3
The puncture position of the 2R is slightly peripheral to the insertion position of the IABP balloon catheter 30 (that is, the insertion position of the sheath 34).

【0023】そして、挿入部材16の先端が十分に血管
内に入ったら、穿刺針24だけを引き抜き、挿入部材1
6にチューブ14を連結する。この時、バルブ部材10
のコック20は開放状態にされ、図示しない吸引器によ
って、チューブ14内には負圧がかけられる。これによ
り、バイパスチューブ1内の余分な空気は除去される。
When the distal end of the insertion member 16 has sufficiently entered the blood vessel, only the puncture needle 24 is withdrawn and the insertion member 1 is removed.
The tube 14 is connected to 6. At this time, the valve member 10
Is opened, and a negative pressure is applied to the inside of the tube 14 by a suction device (not shown). Thereby, excess air in the bypass tube 1 is removed.

【0024】最後に、バルブ部材10のコック20が閉
塞状態にされる。その結果、IABPバルーンカテーテ
ル30の挿入位置よりも末梢側への血流が阻害されてい
れば、左右の大腿動脈32L、32Rの圧力差によっ
て、左の大腿動脈32Lから右の大腿動脈32Rへ血液
が流れ、IABPバルーンカテーテル30の挿入位置よ
りも末梢側への血流が確保される。
Finally, the cock 20 of the valve member 10 is closed. As a result, if the blood flow to the peripheral side from the insertion position of the IABP balloon catheter 30 is obstructed, the pressure difference between the left and right femoral arteries 32L and 32R causes the blood to flow from the left femoral artery 32L to the right femoral artery 32R. Flows, and blood flow to the peripheral side from the insertion position of the IABP balloon catheter 30 is secured.

【0025】なお、バルブ部材10のコック20を開放
状態にすれば、ここから血管内に種々の薬液を投入する
ことも可能となる。また、圧力センサを接続することに
より、バイパスチューブ1が正常に機能しているか否か
を監視することもできる。以上説明した様に、上記バイ
パスチューブ1を用いれば、IABPバルーンカテーテ
ル30の挿入に伴う下肢虚血を未然に防止できるので、
IABPにおける安全性をより高くすることができる。
また、血管が細くて従来はIABPバルーンカテーテル
30の使用が困難であったような患者に対してでも、I
ABPを実施できるようになる。更に、バイパスチュー
ブ1で血流を確保できれば、従来よりも外径が太いカテ
ーテルやシースを使用することもできるので、例えば従
来は外径寸法との兼ね合いで断念せざるを得なかった様
なカテーテルの強度面や機能面での改良も可能となる。
If the cock 20 of the valve member 10 is opened, various chemicals can be introduced into the blood vessel from here. Also, by connecting a pressure sensor, it can be monitored whether the bypass tube 1 is functioning normally. As described above, if the bypass tube 1 is used, lower limb ischemia associated with the insertion of the IABP balloon catheter 30 can be prevented beforehand.
Security in IABP can be further improved.
Further, even for a patient whose blood vessels are thin and the use of the IABP balloon catheter 30 has been difficult in the past, the I
ABP can be implemented. Furthermore, if the blood flow can be secured by the bypass tube 1, a catheter or sheath having a larger outer diameter than before can be used. For example, a catheter which had to be abandoned in consideration of the outer diameter in the past. It is also possible to improve in terms of strength and function.

【0026】以上、本発明の実施形態について説明した
が、本発明の構成手段については上記実施形態以外にも
種々考えられる。例えば、上記バイパスチューブ1は、
コネクタ12によって各部が連結され、任意に分解可能
な構造となっていたが、必ずしも分解可能な構造となっ
ている必要はない。
Although the embodiments of the present invention have been described above, various constitutional means of the present invention can be considered in addition to the above embodiments. For example, the bypass tube 1
Although the components are connected by the connector 12 and have a structure that can be arbitrarily disassembled, it is not always necessary to have a structure that can be disassembled.

【0027】また、上記バイパスチューブ1には、バル
ブ部材10が設けてあったが、これも必須の構成ではな
い。また、バルブ部材10に代えて三方活栓等を設けて
もよい。
Although the bypass tube 1 is provided with the valve member 10, this is not essential. Further, a three-way cock may be provided instead of the valve member 10.

【図面の簡単な説明】[Brief description of the drawings]

【図1】 本発明のバイパスチューブの一例を示す正面
図である。
FIG. 1 is a front view showing an example of a bypass tube of the present invention.

【図2】 挿入部材及び穿刺針を示す正面図である。FIG. 2 is a front view showing an insertion member and a puncture needle.

【図3】 バイパスチューブの使用状態を示す模式図で
ある。
FIG. 3 is a schematic diagram showing a use state of a bypass tube.

【符号の説明】[Explanation of symbols]

1・・・バイパスチューブ、10・・・バルブ部材、1
2・・・コネクタ、14・・・チューブ、16・・・挿
入部材、20・・・コック、22・・・鍔、24・・・
穿刺針。
1 ... bypass tube, 10 ... valve member, 1
2 ... connector, 14 ... tube, 16 ... insertion member, 20 ... cock, 22 ... flange, 24 ...
Puncture needle.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 長尺で柔軟なチューブと、 該チューブの両端に設けられ、先端側は血管内へ挿入可
能な形状とされ、先端から前記チューブ内へ貫通する貫
通穴が形成された挿入部材とを備えたことを特徴とする
バイパスチューブ。
1. An insertion member provided with a long and flexible tube, provided at both ends of the tube, having a distal end formed into a shape capable of being inserted into a blood vessel, and having a through hole penetrating from the distal end into the tube. And a bypass tube comprising:
【請求項2】 請求項1記載のバイパスチューブにおい
て、 血液と接触する部分の一部又は全部が、抗血栓性材料に
よってコーティングされていることを特徴とするバイパ
スチューブ。
2. The bypass tube according to claim 1, wherein a part or all of a portion that comes into contact with blood is coated with an antithrombotic material.
【請求項3】 請求項1又は請求項2記載のバイパスチ
ューブにおいて、 前記チューブの両端間の所定位置に設けられ、該チュー
ブの内腔に連通する連通穴を有し、当該連通穴を開放又
は閉塞可能なバルブ部材を備えたことを特徴とするバイ
パスチューブ。
3. The bypass tube according to claim 1, further comprising a communication hole provided at a predetermined position between both ends of the tube and communicating with a lumen of the tube, wherein the communication hole is opened or A bypass tube comprising a valve member that can be closed.
【請求項4】 請求項1〜請求項3のいずれかに記載の
バイパスチューブにおいて、 前記チューブと前記挿入部材とが、コネクタを介して着
脱自在に連結されていることを特徴とするバイパスチュ
ーブ。
4. The bypass tube according to claim 1, wherein the tube and the insertion member are detachably connected via a connector.
【請求項5】 請求項4記載のバイパスチューブにおい
て、 前記挿入部材の貫通穴内に挿入した状態に配置され、該
挿入部材を血管内に挿入した後には、該挿入部材の後端
側から抜去可能な穿刺針を備えたことを特徴とするバイ
パスチューブ。
5. The bypass tube according to claim 4, wherein the bypass tube is arranged so as to be inserted into a through hole of the insertion member, and can be withdrawn from a rear end side of the insertion member after the insertion member is inserted into a blood vessel. A bypass tube comprising a puncture needle.
JP8190610A 1996-07-19 1996-07-19 Bypass tube Pending JPH1033666A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8190610A JPH1033666A (en) 1996-07-19 1996-07-19 Bypass tube

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8190610A JPH1033666A (en) 1996-07-19 1996-07-19 Bypass tube

Publications (1)

Publication Number Publication Date
JPH1033666A true JPH1033666A (en) 1998-02-10

Family

ID=16260942

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8190610A Pending JPH1033666A (en) 1996-07-19 1996-07-19 Bypass tube

Country Status (1)

Country Link
JP (1) JPH1033666A (en)

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