JPH0362112B2 - - Google Patents

Info

Publication number
JPH0362112B2
JPH0362112B2 JP62331512A JP33151287A JPH0362112B2 JP H0362112 B2 JPH0362112 B2 JP H0362112B2 JP 62331512 A JP62331512 A JP 62331512A JP 33151287 A JP33151287 A JP 33151287A JP H0362112 B2 JPH0362112 B2 JP H0362112B2
Authority
JP
Japan
Prior art keywords
catheter
opening
main body
balloon
needle
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.)
Expired - Lifetime
Application number
JP62331512A
Other languages
Japanese (ja)
Other versions
JPH01171569A (en
Inventor
Akira Igarashi
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.)
Fuji Systems Corp
Original Assignee
Fuji Systems Corp
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 Fuji Systems Corp filed Critical Fuji Systems Corp
Priority to JP62331512A priority Critical patent/JPH01171569A/en
Publication of JPH01171569A publication Critical patent/JPH01171569A/en
Publication of JPH0362112B2 publication Critical patent/JPH0362112B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M39/00Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
    • A61M39/02Access sites
    • A61M39/0208Subcutaneous access sites for injecting or removing fluids

Landscapes

  • Health & Medical Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pulmonology (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Infusion, Injection, And Reservoir Apparatuses (AREA)
  • Media Introduction/Drainage Providing Device (AREA)

Description

【発明の詳細な説明】 (1) 産業上の利用分野 この発明は、切除不能な進行性悪性腫瘍患者の
血管系へ制癌剤などの薬液を繰り返し注入するの
に用いられる皮下埋込み型薬液注入用カテーテル
に関するものである。
[Detailed Description of the Invention] (1) Industrial Application Field The present invention relates to a subcutaneously implantable drug solution injection catheter used for repeatedly injecting a drug solution such as an anticancer drug into the vascular system of a patient with an unresectable advanced malignant tumor. It is related to.

(2) 従来の技術 従来この種カテーテルとして、第8図に示すも
のが知られている。101は上端開口の内腔10
3を有し、皮下に埋め込まれたプラスチツク製の
略円錐形本体で、該本体101には内腔103の
下部と連通する水平の連通孔104が側面に開口
して形成され、かつ連通孔104の開口部にはシ
リコーンゴムからなる所定長さのカテーテルチユ
ーブ105の後端開口部が接続されている。内腔
103の上部に形成された大径凹所にはシリコー
ンゴム製の穿刺部110が圧縮状態で嵌着されて
いる。
(2) Prior Art As a conventional catheter of this type, the one shown in FIG. 8 is known. 101 is a lumen 10 with an opening at the upper end.
3, and is a generally conical main body made of plastic that is implanted subcutaneously, and the main body 101 has a horizontal communication hole 104 opened on the side that communicates with the lower part of the inner cavity 103, and the communication hole 104 A rear end opening of a catheter tube 105 of a predetermined length made of silicone rubber is connected to the opening. A puncture part 110 made of silicone rubber is fitted in a compressed state into a large diameter recess formed in the upper part of the inner cavity 103.

そして、前記において薬液を患部へ注入するに
は、注射針111を本体101の穿刺部110に
刺突し、注射器内の薬液をその針先から内腔10
3の下部へ、さらに内腔103の下部からカテー
テルチユーブ105を経て該チユーブの先端開口
部が位置する患部へ流すことにより行なつてい
る。
In order to inject the medicinal solution into the affected area, the injection needle 111 is pierced into the puncture part 110 of the main body 101, and the medicinal solution in the syringe is injected into the lumen 10 from the needle tip.
3 and further from the lower part of the lumen 103 through the catheter tube 105 to the affected area where the distal opening of the tube is located.

(3) 発明が解決しようとする課題 ところで、前記従来のカテーテルの場合、薬液
を患部へ注入する際に、薬液の濃度が血液でかな
り薄くなつてしまうことを否めず、これを防止す
るような手段もないために患部の効果的な治療を
行なえないという問題点があつた。
(3) Problems to be Solved by the Invention By the way, in the case of the conventional catheter described above, it is undeniable that the concentration of the medicinal solution becomes considerably diluted with blood when the medicinal solution is injected into the affected area. The problem was that effective treatment of the affected area could not be performed because there was no means available.

そこで、この発明は前記従来のカテーテルのも
つ問題点を排除し、注入される薬液の濃度が血液
で薄くなるのを防止できて、患部のより効果的な
治療を行なえるカテーテルを提供することを目的
とする。
SUMMARY OF THE INVENTION Therefore, the present invention aims to provide a catheter that eliminates the problems of the conventional catheters, prevents the concentration of the injected drug solution from diluting with blood, and allows more effective treatment of the affected area. purpose.

(4) 課題を解決するための手段 前記目的を達成するため、この発明のカテーテ
ルは、上端開口の内腔を2個有する本体を具え、
この本体の各内腔には剛性材料からなる上端開口
の針受け容器が嵌合され、これら針受け容器の上
部には自己閉塞性を有する弾性材料からなる穿刺
部が嵌合され、これら穿刺部より下方の針受け容
器の側壁に通孔が穿設され、これら通孔を介して
穿刺部より下方の針受け容器内とそれぞれ連通す
るように第1、第2カテーテルチユーブの後端開
口部が前記本体に接続され、かつ第1カテーテル
チユーブの先端開口部に血管閉塞用のバルーンが
取付けられていることを特徴とするものである。
(4) Means for Solving the Problems In order to achieve the above object, the catheter of the present invention includes a main body having two lumens with an upper end opening,
A needle receiving container made of a rigid material and having an open top is fitted into each lumen of this main body, and puncture parts made of an elastic material having self-closing properties are fitted into the upper part of these needle receiving containers. Through holes are formed in the side wall of the needle receiving container located lower below, and the rear end openings of the first and second catheter tubes communicate with the interior of the needle receiving container below the puncture portion through these holes. The present invention is characterized in that a balloon for occluding blood vessels is connected to the main body and attached to the opening at the distal end of the first catheter tube.

(5) 作用 薬液を患部に注入する際に、第1カテーテルチ
ユーブの先端開口部に取付けたバルーンで患部を
養う近くの血管を圧迫して閉塞することが可能と
なるので、注入される薬液の濃度が血液で薄くな
ることがなくなる。
(5) Effect When injecting the medicinal solution into the affected area, the balloon attached to the opening at the tip of the first catheter tube can compress and occlude the blood vessels near the affected area, so the injected medicinal solution can be The concentration will no longer be diluted by blood.

(6) 実施例 第1図は血管閉塞用バルーン付き薬液注入用カ
テーテルの平面図を示す。同図で下側のカテーテ
ル部分Aが薬液の注入を行ない、上側のカテーテ
ル部分Bが血管閉塞を行なうように構成されてい
る。薬液の注入を行なうカテーテル部分Aの構成
は第2図のようになつている。1は上端開口の内
腔3を有するシリコーンゴム製の略円錐形本体
で、該本体1には内腔3の下部と連通する水平の
連通孔4が側面に開口して形成されている。本体
1の内腔3にはステンレス製の針受け容器5が内
腔3の回りの本体1で固定されて抜き出し不能に
嵌合されている。針受け容器5が嵌合された内腔
3の上端開口の回りには触指部6が設けられてい
る。触指部6は本体1が皮下に埋め込まれた状態
で、皮膚の上から内腔3の上端開口を確認できる
ように凸状の肉盛りとなつている。針受け容器5
は内腔3の下部に嵌合された円筒部5aと、該円
筒部の上端から上向きに徐々に大径となつて拡開
状に連設され、内腔3の上部に嵌合された拡開筒
部5bとからなり、円筒部5aの側壁には連通孔
4と連通する通孔7が穿設され、拡開筒部5bの
頂壁には内腔3の上端開口と連通する開口部8が
穿設されている。拡開筒部5b内にはシリコーン
ゴム製の穿刺部10が圧縮状態で嵌合され、穿刺
部10は抜け出ないようにその上端外周面が拡開
筒部5bの開口部8の回りのフランジ11で押え
られている。そして、穿刺部10はシリコーンゴ
ムからなつているため、注射針の何回もの刺突が
可能で、かつ刺突した注射針を抜いた場合に自ら
の弾力性によつて該抜いた針の通路を閉鎖し、薬
液の漏れが起らない自己閉塞性がよいものとなつ
ている。穿刺部10より下方の容器5内の従来の
カテーテルの内腔下部のように、薬液が一時貯留
可能なリザーバー13になつている。
(6) Embodiment FIG. 1 shows a plan view of a drug solution injection catheter with a blood vessel occlusion balloon. In the figure, the lower catheter section A is configured to inject a medical solution, and the upper catheter section B is configured to occlude blood vessels. The structure of the catheter section A through which the drug is injected is as shown in FIG. Reference numeral 1 denotes a substantially conical main body made of silicone rubber having a lumen 3 with an open upper end, and a horizontal communication hole 4 that communicates with the lower part of the lumen 3 is formed in the main body 1 and opens on the side surface. A needle receiving container 5 made of stainless steel is fixed to the inner cavity 3 of the main body 1 by the main body 1 around the inner cavity 3 and is fitted in a manner that cannot be removed. A tactile section 6 is provided around the upper end opening of the inner cavity 3 into which the needle receiving container 5 is fitted. The tactile part 6 has a convex padding so that the upper end opening of the inner cavity 3 can be confirmed from above the skin when the main body 1 is implanted subcutaneously. Needle receiver container 5
The cylindrical portion 5a is fitted into the lower part of the inner cavity 3, and the expanded cylindrical part 5a is connected to the upper end of the cylindrical part in an enlarged shape with the diameter gradually increasing upward from the upper end of the cylindrical part, and which is fitted into the upper part of the inner cavity 3. A through hole 7 communicating with the communication hole 4 is bored in the side wall of the cylindrical part 5a, and an opening communicating with the upper end opening of the inner cavity 3 is formed in the top wall of the expanding cylindrical part 5b. 8 is drilled. A puncture part 10 made of silicone rubber is fitted into the expansion tube part 5b in a compressed state, and the outer peripheral surface of the upper end of the puncture part 10 has a flange 11 around the opening 8 of the expansion tube part 5b so that the puncture part 10 does not slip out. is being held down. Since the puncture part 10 is made of silicone rubber, it can be punctured with the injection needle many times, and when the punctured needle is removed, its own elasticity allows the needle to pass through. It has good self-closing properties to prevent leakage of chemical solution. Like the lower part of the lumen of a conventional catheter in the container 5 below the puncture part 10, there is a reservoir 13 in which a medicinal solution can be temporarily stored.

連通孔4の開口部にはシリコーンゴムからなる
所定長さのカテーテルチユーブ15の後端開口部
が接続され、該チユーブ15の先端開口部には同
様の所定長さのカテーテルチユーブ16の後端開
口部がコネクタ17を介して連通可能に接続され
ている。カテーテルチユーブ16の先端開口部
(流出口)近くには該先端部を固定するための環
状突条18が設けられている。20はカテーテル
チユーブ15,16より血液がリザーバー13側
へ逆流するのを防止する逆止弁で、連通孔4内に
嵌着されている。21は本体1の下部周縁に穿設
され、本体1を皮下組織の筋膜に縫いつけて固定
するための縫合ホール、22は縫合ホール21を
含む本体1の底面に貼着されたホール補強用のポ
リエステルメツシユである。
The rear end opening of a catheter tube 15 of a predetermined length made of silicone rubber is connected to the opening of the communication hole 4, and the rear end opening of a catheter tube 16 of a similar predetermined length is connected to the distal end opening of the tube 15. The parts are communicatively connected via a connector 17. An annular protrusion 18 is provided near the tip opening (outlet) of the catheter tube 16 for fixing the tip. Reference numeral 20 denotes a check valve that prevents blood from flowing back toward the reservoir 13 from the catheter tubes 15 and 16, and is fitted into the communication hole 4. Reference numeral 21 indicates a suture hole drilled in the lower periphery of the main body 1 for sewing and fixing the main body 1 to the fascia of the subcutaneous tissue. Reference numeral 22 indicates a reinforcing hole attached to the bottom of the main body 1 including the suture hole 21. It is polyester mesh.

一方、血管の閉塞を行なうカテーテル部分Bの
構成は第3図のようになつている。このカテーテ
ル部分Bの構成は逆止弁20がない以外、前記し
たカテーテル部分Aの構成と基本的には同様とな
つている。そのため、同様の部分には同一符号に
ダツシユを付して詳細な説明を省略し、以下には
異なる構成について説明することとなる。連通孔
4′の開口部に後端開口部が接続されたシリコー
ンゴムからなる所定長さのカテーテルチユーブ2
4の先端開口部は、チユーブを切り裂いて加工し
た屈曲可能な外側サポート部25と、該サポート
部の内周面に周縁部が接着された薄いシート状の
内側バルーン部26からなるシリコーンゴム製バ
ルーン27のサポート部25にバルーン27内と
連通して固着されている。バルーン27のバルー
ン部26はカテーテルチユーブ24から生理食塩
水など液体がバルーン27内に注入されると、第
3図の屈曲した状態から第4図に示すようにサポ
ート部25を押し広げて膨らむようになつてい
る。28はサポート部25の両端部の外周面に設
けられた突条で、バルーン27を血管に固定する
際、サポート部25に巻き付ける糸がずれ落ちな
いようにするためのものである。
On the other hand, the configuration of the catheter portion B that performs occlusion of the blood vessel is as shown in FIG. The configuration of this catheter section B is basically the same as the configuration of the catheter section A described above, except that the check valve 20 is not provided. Therefore, similar parts will be given the same reference numerals with dashes, detailed explanations will be omitted, and different configurations will be explained below. A catheter tube 2 of a predetermined length made of silicone rubber and whose rear end opening is connected to the opening of the communication hole 4'.
The tip opening of No. 4 is a silicone rubber balloon consisting of a bendable outer support part 25 made by cutting out a tube, and a thin sheet-like inner balloon part 26 whose peripheral edge is adhered to the inner peripheral surface of the support part. It is fixed to the support part 25 of 27 in communication with the inside of the balloon 27. When a liquid such as physiological saline is injected into the balloon 27 from the catheter tube 24, the balloon portion 26 of the balloon 27 expands by pushing the support portion 25 apart from the bent state shown in FIG. 3 as shown in FIG. It's getting old. Reference numeral 28 denotes protrusions provided on the outer circumferential surface of both ends of the support section 25 to prevent the threads wound around the support section 25 from slipping off when the balloon 27 is fixed to the blood vessel.

前記のような薬液注入用カテーテルは使用し易
いように本体1,1′部分が、カテーテルチユー
ブ15,16とカテーテルチユーブ24がほぼ平
行となるように接着剤等を用いて並列状に一体固
着されている。また、血管の閉塞を行なうカテー
テル部分Bの本体1′の触指部6′の表面には第1
図に示すようにカテーテル部分Aの本体1との識
別を行なう標示部31が付されている。
In order to facilitate use of the above-mentioned drug solution injection catheter, the main bodies 1 and 1' are fixed together in parallel using an adhesive or the like so that the catheter tubes 15 and 16 and the catheter tube 24 are approximately parallel to each other. ing. In addition, a first contact portion 6′ of the main body 1′ of the catheter portion B for occluding blood vessels is provided with a first contact portion 6′.
As shown in the figure, a marking part 31 is attached to the catheter part A to identify it from the main body 1.

次に、前記実施例の作用を説明する。 Next, the operation of the above embodiment will be explained.

カテーテルを皮下に埋込み設置するには、第5
図に示すようにカテーテルチユーブ16をその先
端側から例えば肝臓80の肝動脈81の末梢より
血管内部に差し込み、先端開口部を治療を施す患
部まで進めて固定した状態で、カテーテルチユー
ブ24のバルーン27を目的とする肝動脈81に
位置させ、バルーン部26を内側にして第6図の
ように糸82を巻き付け固定する。
To implant the catheter subcutaneously, step 5
As shown in the figure, the catheter tube 16 is inserted into the blood vessel from the distal end of the hepatic artery 81 of the liver 80, for example, and the distal opening is advanced to the affected area to be treated and fixed, and the balloon 27 of the catheter tube 24 is inserted into the blood vessel. The tube is placed in the intended hepatic artery 81, and the string 82 is wound and fixed with the balloon portion 26 facing inside as shown in FIG.

一方、本体1,1′も縫合ホール21,21′を
介して皮下組織の筋膜に縫いつけて固定する。
On the other hand, the main bodies 1 and 1' are also sewn and fixed to the fascia of the subcutaneous tissue through the suture holes 21 and 21'.

前記により皮下に埋め込んだカテーテルにおい
て、薬液として制癌剤を患部へ注入するには、標
示部31により識別した本体1の触指部6に軽く
指を当てて内腔3の上端開口を確認したうえ、第
7図に示すように注射針83を穿刺部10に刺突
し、注射器内の制癌剤をその針先からリザーバー
13に注入する。この注射針83の刺突に際し、
注射針83がほぼ垂直に刺突されなくともその針
先が針受け容器5の拡開筒部5bの内面のテーパ
面に当つたのち、該テーパ面によつてリザーバー
13へ案内され、針先がひつかかつてしまうこと
がない。また、針受け容器5がステンレスからな
つているため、針先がこれを貫通してしまうこと
もない。リザーバー13に注入された制癌剤は通
孔7、連通孔4内の逆止弁20、カテーテルチユ
ーブ15,16を経てチユーブ16の先端開口部
から患部へ流れる。
In order to inject an anticancer drug as a medicinal solution into an affected area in the catheter implanted subcutaneously as described above, lightly place a finger on the tactile part 6 of the main body 1 identified by the marking part 31 to confirm the upper end opening of the lumen 3, As shown in FIG. 7, an injection needle 83 is inserted into the puncture section 10, and the anticancer agent in the syringe is injected into the reservoir 13 from the needle tip. When piercing this injection needle 83,
Even if the injection needle 83 is not inserted almost perpendicularly, the needle tip hits the tapered surface on the inner surface of the expanding tube portion 5b of the needle receiving container 5, and then is guided to the reservoir 13 by the tapered surface, and the needle tip I never get tired of it. Furthermore, since the needle receiving container 5 is made of stainless steel, the needle tip will not penetrate through it. The anticancer drug injected into the reservoir 13 passes through the through hole 7, the check valve 20 in the communicating hole 4, and the catheter tubes 15 and 16, and flows from the distal opening of the tube 16 to the affected area.

このようにして制癌剤の患部への流入が行なわ
れる。
In this way, the anticancer drug flows into the affected area.

そして、この患部への制癌剤の注入に際して
は、制癌剤の濃度が薄くなるのを防ぐために事前
に本体1′の穿刺部10に図示しない別の注射針
を刺突してリザーバー13′に生理食塩水など液
体を注入し、カテーテルチユーブ24を通してバ
ルーン27内に入れてバルーン部26を膨らま
せ、肝動脈81を圧迫してここを閉塞し血流を一
時的に遮断する。これにより、患部へ流れる制癌
剤の濃度は薄薄くなることがなく、濃度の高い制
癌剤によつて患部のより効果的な治療が可能とな
る。このような閉塞用バルーン27によつて血流
を遮断する方法は、従来のBOAI(Balloon
occlusion arterial infusion)という血管内に入
れたバルーンカテーテルによる血流の遮断法に比
し、肝動脈内に血栓などができることがなく、極
めて有効的な方法である。
When injecting the anticancer drug into the affected area, in order to prevent the concentration of the anticancer drug from becoming diluted, another injection needle (not shown) is inserted into the puncture part 10 of the main body 1' in advance, and physiological saline is injected into the reservoir 13'. The liquid is injected into the balloon 27 through the catheter tube 24, and the balloon portion 26 is inflated, compressing the hepatic artery 81 to occlude it and temporarily cutting off blood flow. As a result, the concentration of the anticancer agent flowing to the affected area does not become diluted, making it possible to treat the affected area more effectively with a highly concentrated anticancer agent. A method of blocking blood flow using such an occlusion balloon 27 is the conventional BOAI (Balloon Balloon 27).
Compared to a method called occlusion arterial infusion, which blocks blood flow using a balloon catheter inserted into a blood vessel, this method does not cause the formation of blood clots in the hepatic artery and is extremely effective.

前記流入した生理食塩水など液体は使用後に再
び注射針を穿刺部10′に刺突して抜き取る。
After use, the injected liquid such as physiological saline is drawn out by inserting the injection needle into the puncture portion 10' again.

尚、前記各実施例においては針受け容器5,
5′をステンレスとしたが、刺突に際し注射針が
貫通しないものであれば、ほかにステンレス以外
の金属、セラミツク、又は硬質プラスチツクなど
の比較的軽くて剛性のある材質としてもよい。ま
た、2個の内腔3,3′をそれぞれ別々の本体1,
1′に形成したが、1個の本体に形成してもよい。
In each of the above embodiments, the needle receiving container 5,
Although 5' is made of stainless steel, it may be made of a relatively light and rigid material other than stainless steel, such as metal, ceramic, or hard plastic, as long as it does not allow the injection needle to penetrate upon piercing. In addition, the two inner cavities 3 and 3' are connected to separate bodies 1 and 3' respectively.
1', but it may be formed into one body.

(7) 発明の効果 この発明は前記のような構成からなり、薬液の
注入に際し、第1カテーテルチユーブの先端開口
部に設けたバルーンで患部を養う近くの血管を閉
塞することが可能なので、患部へ注入される薬液
の濃度が薄くなるのを防止でき、したがつて濃度
の高い薬液によつて患部のより効果的な治療が可
能となる。また、この薬液の注入と血管閉塞を
別々のカテーテルで行なう必要がなく、これら両
機能をもつた1つのカテーテルで行なえるので、
薬液の注入および血管閉塞の取扱い作業が極めて
容易であるのに加え、皮下組織への埋込み設置に
際しても本体の縫い付け固定作業が1回ですみ、
作業性がよい等の優れた効果がある。
(7) Effects of the Invention This invention has the above-mentioned configuration, and when injecting a drug solution, it is possible to occlude a blood vessel near the affected area with the balloon provided at the opening at the tip of the first catheter tube. It is possible to prevent the concentration of the medicinal solution injected into the patient from becoming diluted, thus making it possible to treat the affected area more effectively with a highly concentrated medicinal solution. In addition, there is no need to use separate catheters for injecting the drug and occluding the blood vessel; it is possible to use a single catheter that has both functions.
In addition to being extremely easy to inject medical fluids and handle vascular occlusion, the main body only needs to be sewn and fixed once when implanted into subcutaneous tissue.
It has excellent effects such as good workability.

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

第1図はこの発明の一実施例を示す薬液注入用
カテーテルの一部省略の平面図、第2図は同上の
薬液の注入を行なうカテーテル部分の一部省略の
縦断正面図、第3図は同上の血管閉塞を行なうカ
テーテル部分の一部省略の縦断正面図、第4図は
同上のバルーン部の部分斜視図、第5図は作用説
明図、第6図は同上でバルーン部を固定する状態
を示す部分斜視図、第7図は同上で注射器により
薬液を注入している状態を示す斜視図、第8図は
従来例を示す縦断正面図である。 1,1′……本体、3,3′……内腔、4,4′
……連通孔、5,5′……針受け容器、6,6′…
…触指部、7,7′……通孔、8,8′……開口
部、10,10′……穿刺部、15,16……カ
テーテルチユーブ、20……逆止弁、25……サ
ポート部、26……バルーン部、27……バルー
ン、31……標示部。
FIG. 1 is a partially omitted plan view of a catheter for injecting a drug solution according to an embodiment of the present invention, FIG. A partially omitted longitudinal sectional front view of the catheter section for occluding the blood vessel as above, Fig. 4 is a partial perspective view of the balloon section as above, Fig. 5 is an explanatory view of the operation, and Fig. 6 is a state in which the balloon section is fixed as above. FIG. 7 is a perspective view showing a state in which a drug solution is being injected using a syringe in the same device as above, and FIG. 8 is a longitudinal sectional front view showing a conventional example. 1, 1'...Main body, 3, 3'...Inner cavity, 4, 4'
...Communication hole, 5,5'...Needle receiver container, 6,6'...
...Touch portion, 7,7'...Through hole, 8,8'...Opening, 10,10'...Puncture portion, 15,16...Catheter tube, 20...Check valve, 25... Support part, 26...Balloon part, 27...Balloon, 31...Indication part.

Claims (1)

【特許請求の範囲】 1 上端開口の内腔を2個有する本体を具え、こ
の本体の各内腔には剛性材料からなる上端開口の
針受け容器が嵌合され、これら針受け容器の上部
には自己閉塞性を有する弾性材料からなる穿刺部
が嵌合され、これら穿刺部より下方の針受け容器
の側壁に通孔が穿設され、これら通孔を介して穿
刺部より下方の針受け容器内とそれぞれ連通する
ように第1、第2カテーテルチユーブの後端開口
部が前記本体に接続され、かつ第1カテーテルチ
ユーブの先端開口部に血管閉塞用のバルーンが取
付けられていることを特徴とする皮下埋込み型薬
液注入用カテーテル。 2 第2カテーテルチユーブの後端開口部と通孔
間に、該カテーテルチユーブより血液が通孔側へ
逆流するのを防ぐ逆止弁が配設されている特許請
求の範囲第1項記載の皮下埋込み型注入用カテー
テル。
[Scope of Claims] 1. A main body having two lumens with an opening at the top, a needle receiving container made of a rigid material and having an opening at the top fitted into each lumen of the main body, and a needle receiving container made of a rigid material and having an opening at the top. Puncture parts made of an elastic material with self-closing properties are fitted, and through holes are made in the side wall of the needle receiver container below the puncture parts, and through these holes, the needle receiver container below the puncture part is inserted. The rear end openings of the first and second catheter tubes are connected to the main body so as to communicate with the inside of the body, and a balloon for occluding blood vessels is attached to the front end opening of the first catheter tube. A subcutaneously implantable drug injection catheter. 2. The subcutaneous device according to claim 1, wherein a check valve is provided between the rear end opening of the second catheter tube and the through hole to prevent blood from flowing backward from the catheter tube toward the through hole. Implantable infusion catheter.
JP62331512A 1987-12-26 1987-12-26 Subcutaneous burying type catheter for injecting medical solution Granted JPH01171569A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62331512A JPH01171569A (en) 1987-12-26 1987-12-26 Subcutaneous burying type catheter for injecting medical solution

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62331512A JPH01171569A (en) 1987-12-26 1987-12-26 Subcutaneous burying type catheter for injecting medical solution

Publications (2)

Publication Number Publication Date
JPH01171569A JPH01171569A (en) 1989-07-06
JPH0362112B2 true JPH0362112B2 (en) 1991-09-24

Family

ID=18244471

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62331512A Granted JPH01171569A (en) 1987-12-26 1987-12-26 Subcutaneous burying type catheter for injecting medical solution

Country Status (1)

Country Link
JP (1) JPH01171569A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH063613Y2 (en) * 1989-11-08 1994-02-02 株式会社八光電機製作所 Implantable reservoir
DE202004021447U1 (en) * 2004-08-31 2008-02-28 Steco-System-Technik Gmbh & Co.Kg Subcutaneously implantable infusion port

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6359972A (en) * 1986-08-21 1988-03-15 ベ−・ブラウン・メルズンゲン・アクチエンゲゼルシャフト Catheter apparatus for embedding

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6359972A (en) * 1986-08-21 1988-03-15 ベ−・ブラウン・メルズンゲン・アクチエンゲゼルシャフト Catheter apparatus for embedding

Also Published As

Publication number Publication date
JPH01171569A (en) 1989-07-06

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