JPH10127643A - Medical treatment inserting tool - Google Patents
Medical treatment inserting toolInfo
- Publication number
- JPH10127643A JPH10127643A JP8290338A JP29033896A JPH10127643A JP H10127643 A JPH10127643 A JP H10127643A JP 8290338 A JP8290338 A JP 8290338A JP 29033896 A JP29033896 A JP 29033896A JP H10127643 A JPH10127643 A JP H10127643A
- Authority
- JP
- Japan
- Prior art keywords
- balloon
- cylindrical sheet
- tip
- branch tube
- medical treatment
- 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.)
- Granted
Links
Landscapes
- Surgical Instruments (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、内視鏡下手術にお
いて、気腹法を用いて、臓器を直接手で触れて処置する
ための処置挿入具に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a treatment insertion tool for performing treatment by directly touching an organ by an insufflation method in endoscopic surgery.
【0002】[0002]
【従来の技術】近年、低侵襲治療方法として、内視鏡下
手術が広く施行されるようになってきた。内視鏡下手術
は、主に腹部の諸臓器、例えば、胃、脾臓、腸、胆嚢等
の手術を行う際、腹壁に炭酸ガスを注入することにより
空間をつくり、そこへトラカール等の器具挿入用筒を複
数本刺入し、これより挿入された内視鏡の視野を見なが
ら、種々の処置具を挿入し、手術をする方法である。従
って、本法によると従来の開腹手術に比べ、切開創が極
めて小さく、患者へのダメージが少ないというメリット
がある。ここで、体内へ炭酸ガスを注入加圧し、腹腔内
等に必要な空間を形成せしめることを、気腹法と称せら
れる。一方、炭酸ガスの注入を行わず、皮下へ鋼線等を
刺し込んで腹壁を吊り上げる方法もあり、これを気腹法
に対し、吊り上げ法と呼ばれる。現状では、手術のし易
さなどから気腹法が多く使われている。しかしながら、
こうした内視鏡下手術、特に、気腹法においては、内視
鏡で映し出されたモニターの映像を見ながら、実際に手
で触れて処置を行っているのではなく、トラカール等の
挿入筒より鉗子類等を挿入しての遠隔操作で処置するた
めに、処置や操作が難しかったり、時間がかかるという
欠点があり、術者にとってはストレスの大きい術式であ
るといえる。また、万が一、術中に臓器や大血管を傷つ
けるような場合には、円筒状のトラカールしか処置ルー
トがないため、緊急のリカバリー処置が困難となる危険
もある。特に、大血管を傷つけた場合、瞬時の内に大出
血を引き起こし、最悪の結果となる可能性が高い。更
に、癌組織を体外に摘出する際に、腹壁に癌組織が付着
し、転移するという欠点もある。2. Description of the Related Art In recent years, endoscopic surgery has been widely practiced as a minimally invasive treatment method. Endoscopic surgery is mainly used when performing operations on various organs of the abdomen, such as the stomach, spleen, intestine, and gallbladder, by creating a space by injecting carbon dioxide into the abdominal wall and inserting instruments such as trocars into it. This is a method in which a plurality of use tubes are inserted, and various treatment tools are inserted and surgery is performed while viewing the field of view of the endoscope inserted therefrom. Therefore, according to the present method, there is an advantage that the incision is extremely small and damage to the patient is small as compared with the conventional laparotomy. Here, injecting and pressurizing carbon dioxide into the body to form a necessary space in the abdominal cavity or the like is referred to as insufflation. On the other hand, there is also a method of suspending the abdominal wall by inserting a steel wire or the like under the skin without injecting carbon dioxide gas, and this is called a lifting method, as opposed to an insufflation method. At present, pneumoperitoneum is often used due to ease of operation. However,
In such endoscopic surgery, especially in the pneumoperitoneum method, the procedure is not performed by actually touching with the hand while watching the image of the monitor projected on the endoscope, but from the insertion tube such as a trocar. Since the treatment is performed by remote operation with the insertion of forceps and the like, the treatment and operation are difficult and it takes time, which is a stressful operation for the surgeon. Also, in the unlikely event that an organ or a large blood vessel is damaged during the operation, there is a risk that an emergency recovery procedure may be difficult because only a cylindrical trocar has a procedure. In particular, when a large blood vessel is injured, a large bleeding is caused in an instant, and the worst result is likely to occur. Furthermore, when the cancer tissue is removed from the body, there is a disadvantage that the cancer tissue adheres to the abdominal wall and metastasizes.
【0003】[0003]
【発明が解決しようとする問題】本発明は、従来の内視
鏡下手術における臓器処置のこのような欠点を解決する
もので、その目的とするところは、気腹下で臓器処置を
行う際に、直接手で臓器に触れ、確実、安全に短時間で
処置でき、更に、気腹ガス漏れがなく、十分な視野の下
で処置できることにある。SUMMARY OF THE INVENTION The present invention solves such a drawback of the conventional organ treatment in endoscopic surgery, and an object thereof is to perform organ treatment under insufflation. In addition, it is possible to perform treatment in a short time by touching the organ directly with a hand, reliably, safely, and without pneumoperitoneum gas leakage, and with a sufficient visual field.
【0004】[0004]
【課題を解決するための手段】上記目的を達成するため
の本発明による医療用処置挿入具は、円筒状シート外周
に隣接して、先端側に先バルーン、後端側に後バルーン
を形成させ、該円筒状シートの該先バルーン下の周囲
に、気液不透過性手袋の袖の部分を気密的に隣接させて
付設し、更に、先端が該円筒状シートを通って該先バル
ーン内に連通した先枝チューブ、および先端部が該後バ
ルーンに連通した後枝チューブより構成され、該先枝チ
ューブと該後枝チューブの後端部には各々接続用コネク
ターを有する気液開閉装置を付設したことを構造上の特
徴とする。A medical treatment insert according to the present invention for achieving the above object has a front balloon formed on the front end side and a rear balloon formed on the rear end side adjacent to the outer periphery of the cylindrical sheet. A sleeve portion of a gas-liquid-impermeable glove is hermetically attached to a periphery of the cylindrical sheet below the tip balloon, and further, the leading end passes through the cylindrical sheet into the tip balloon. A gas-liquid opening / closing device having a connection connector is provided at the rear end of the front branch tube and the rear end of the rear branch tube. This is a structural feature.
【0005】[0005]
【発明の実施の形態】以下図面を用いて本発明を詳細に
説明する。図1は本発明による医療用処置挿入具の一実
施例を示す図であり、図1(a)は外観図、(b)は
(a)の断面図である。図2は他の実施例を示す外観図
であり、図3、図4は使用状態を示す概略図である。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail with reference to the drawings. FIG. 1 is a view showing one embodiment of a medical treatment insert according to the present invention, wherein FIG. 1 (a) is an external view and FIG. 1 (b) is a sectional view of FIG. FIG. 2 is an external view showing another embodiment, and FIGS. 3 and 4 are schematic diagrams showing a use state.
【0006】本発明による医療用処置挿入具は、図1
(a)のように、円筒状シート(3)外周に隣接して、
先端側に先バルーン(1)、後端側に後バルーン(2)
を形成させ、円筒状シート(3)外周の先端側に先バル
ーン(1)、後端側に後バルーン(2)を形成させ、該
円筒状シート(3)の該先バルーン(1)下の周囲に、
気液不透過性手袋(14)の袖の部分を気密的に隣接さ
せて付設し、更に、先端が該円筒状シート(3)を通っ
て該先バルーン内(1)に連通した先枝チューブ
(4)、および先端部が該後バルーン(2)に連通した
後枝チューブ(5)より構成され、該先枝チューブ
(4)と該後枝チューブ(5)の後端部には各々接続用
コネクターを有する気液開閉装置を付設している。[0006] The medical treatment insertion tool according to the present invention is shown in FIG.
As shown in (a), adjacent to the outer periphery of the cylindrical sheet (3),
Front balloon (1) at the front end, rear balloon (2) at the rear end
And a front balloon (1) is formed on the front end side of the outer periphery of the cylindrical sheet (3), and a rear balloon (2) is formed on the rear end side of the cylindrical sheet (3) under the front balloon (1). Around,
A forearm tube having a sleeve portion of a gas-liquid impermeable glove (14) airtightly adjoined and further having a leading end communicating with the inside of the tip balloon (1) through the cylindrical sheet (3). (4) and a rear branch tube (5) having a distal end communicating with the rear balloon (2). The rear branch tube (5) is connected to the front branch tube (4) and the rear end of the rear branch tube (5), respectively. A gas-liquid switchgear with a connector is provided.
【0007】先バルーン(1)、および後バルーン
(2)は、図1(b)の断面図のように、ドーナツ状で
中空の内腔を形成させたバルーンである。通常はブロー
成形、ディップ成形、フィルム加工、回転成形などの中
空成形等で作製される。それぞれが一体的に成形されて
も、当然ながら本特許範囲に含まれるものである。ま
た、円筒状シート(3)と先バルーン(1)及び後バル
ーン(2)が貼り合わされたり、一体化させて形成した
り、円筒状シート(3)を内筒とし、その外周に外筒と
して円筒状シートとを重ね合わせ、その先端部及び中央
部で内外筒を接着して、先バルーン(1)と後バルーン
(2)を形成させたものでも良い。先バルーン(1)、
後バルーン(2)共に、バルーン肉厚は0.1〜2mm
程度の薄肉が好ましく、特に先バルーン(1)は腹壁
(7)の3〜10cm程度の切開口より体内(6)に挿
入するため、薄肉でかさばらない方が有利であり、バル
ーン内に空気を注入した場合でも、実使用の2倍以上の
量を注入しても破裂しない程度の最低限の肉厚が好まし
い。円筒状シート(3)の内径は、後バルーン(2)と
先バルーン(1)内を通して手、腕(15)を挿入して
処置を行うため、手、腕(15)が挿入できる程度の径
が好ましく、60〜90mm程度が適当である。最外径
は90〜200mm程度で、特に先バルーン(1)は体
内(6)挿入時かさばらない程度の外径にするのが好ま
しい。バルーン材質については、例えば、軟質塩化ビニ
ル樹脂、ポリウレタン樹脂、ポリエチレン樹脂、ポリプ
ロピレン樹脂、ポリエステル樹脂、シリコーンゴム、天
然ゴムのような適度な柔軟性をもつ材料が好ましいが必
ずしもそのような材質に限定する必要はない。先バルー
ン(1)が空気を注入しない状態で、かさばらず切開口
より体内(6)に簡単に挿入でき、体組織を傷つけない
程度の柔軟性をもち、また、空気、あるいは水を注入し
た場合にも実使用の2倍以上の量を注入しても破裂しな
い程度の十分な破裂強度及び引裂強度をもつ材質を選択
することが肝要である。[0007] The front balloon (1) and the rear balloon (2) are donut-shaped hollow lumens as shown in the sectional view of FIG. 1 (b). Usually, it is produced by blow molding, dip molding, film processing, or hollow molding such as rotational molding. Even if each is integrally formed, it is naturally included in the scope of the present patent. Further, the cylindrical sheet (3) and the front balloon (1) and the rear balloon (2) are bonded or formed integrally, or the cylindrical sheet (3) is formed as an inner cylinder and the outer cylinder is formed as an outer cylinder on its outer periphery. A cylindrical sheet may be superimposed, and the inner and outer cylinders may be bonded at the tip and the center to form a front balloon (1) and a rear balloon (2). Balloon (1),
Both the rear balloon (2) and the balloon have a wall thickness of 0.1 to 2 mm.
In order to insert the tip balloon (1) into the body (6) through an incision of about 3 to 10 cm into the abdominal wall (7), it is advantageous that the balloon is thin and not bulky. Even in the case of injection, a minimum wall thickness that does not rupture even if the amount is twice or more than that of actual use is preferable. The inside diameter of the cylindrical sheet (3) is such that the hand and arm (15) are inserted through the rear balloon (2) and the front balloon (1) to perform the treatment, so that the hand and arm (15) can be inserted. Is preferable, and about 60 to 90 mm is appropriate. The outermost diameter is about 90 to 200 mm, and it is particularly preferable that the balloon (1) has an outer diameter that is not bulky when the body (6) is inserted. As the balloon material, for example, a material having appropriate flexibility such as a soft vinyl chloride resin, a polyurethane resin, a polyethylene resin, a polypropylene resin, a polyester resin, a silicone rubber, and a natural rubber is preferable, but is not necessarily limited to such a material. No need. When the balloon (1) does not inject air, it is not bulky, can be easily inserted into the body (6) through the incision, has enough flexibility not to damage body tissues, and when air or water is injected. In addition, it is important to select a material having a sufficient burst strength and a sufficient tear strength so that the material does not burst even if the amount is twice or more than that of the actual use.
【0008】円筒状シート(3)は肉厚0.1〜2mm
の円筒状のシート部材であり、通常、インフレーション
成形等で作製されるが特に、これに限定されない。使用
上、そのシート内に手、腕(15)を挿入し、また、切
開口で固定されるため、材質は、かさばらず、適度な柔
軟性をもつ材質がよく、例えば、軟質塩化ビニル樹脂、
ポリウレタン樹脂、ポリエチレン樹脂、ポリプロピレン
樹脂、ポリエステル樹脂、シリコーンゴム、天然ゴムの
ような材料が好ましい。また、内径も50〜100mm
程度が適切である。そのシートの外周に、先バルーン
(1)と後バルーン(2)を貼り合わせるが、先バルー
ン(1)と後バルーン(2)の間隔は患者の腹壁(7)
の厚さに対応するもので通常10〜15mm程度である
が、特に個人差のある皮下脂肪層の厚みを考慮して5〜
30mmの間で数種準備しておくのが好ましい。そのた
め、円筒状シート(3)長さは5〜20cm程度が適切
である。The cylindrical sheet (3) has a thickness of 0.1 to 2 mm.
And is usually produced by inflation molding or the like, but is not particularly limited thereto. In use, the hand and the arm (15) are inserted into the sheet and fixed by the incision. Therefore, the material is not bulky, and a material having appropriate flexibility is preferable. For example, soft vinyl chloride resin,
Materials such as polyurethane resin, polyethylene resin, polypropylene resin, polyester resin, silicone rubber and natural rubber are preferred. The inner diameter is also 50-100mm
The degree is appropriate. The front balloon (1) and the rear balloon (2) are bonded to the outer periphery of the sheet, and the distance between the front balloon (1) and the rear balloon (2) is set to the abdominal wall (7) of the patient.
The thickness is usually about 10 to 15 mm corresponding to the thickness of the subcutaneous fat layer, which has individual differences.
It is preferable to prepare several types between 30 mm. Therefore, the length of the cylindrical sheet (3) is suitably about 5 to 20 cm.
【0009】図1(a)断面のように、先枝チューブ
(4)は、先端部が円筒状シート(3)内を通って、先
バルーン(1)内に開口し、後枝チューブ(5)は先端
部が後バルーン(2)内に開口し、各々そこからバルー
ン部の後端側へ気液流通のために導き出されたチューブ
である。先枝チューブ(4)は先端部が円筒状シート
(3)の内側あるいは外側のどちらを通っても、先バル
ーン(1)に開口していれば良い。また、先枝チューブ
(4)及び後枝チューブ(5)は、図1(a)のように
各々独立したチューブでも良いが、図2に示すようにバ
ルーン後端部近傍は互いに一体化されたチューブで2つ
の流通路をもつ2腔チューブ(8)を用い、後方の位置
に分岐部(9)を設けて枝分かれしても良い。材質とし
ては、例えば、軟質塩化ビニル樹脂、ウレタン樹脂、シ
リコーンゴム、天然ゴムのような適度な柔軟性と硬度を
もつ材料を使用し、押出成形された内径0.3〜3m
m、肉厚0.3〜2mmのチューブが好ましい。また、
枝チューブ(4)(5)の長さは、術者が様々な処置具
を使用するのに支障にならないように、30〜300m
m程度が適当である。As shown in the cross section of FIG. 1 (a), the leading branch tube (4) has a distal end portion that passes through the cylindrical sheet (3) and opens into the leading balloon (1), and the trailing branch tube (5). ) Are tubes each having a distal end opening into the rear balloon (2) and being led out therefrom to the rear end side of the balloon for gas-liquid circulation. Regardless of whether the distal end portion of the leading tube (4) passes through the inside or outside of the cylindrical sheet (3), it is sufficient that the leading end tube (4) is open to the leading balloon (1). Further, the leading branch tube (4) and the trailing branch tube (5) may be independent tubes as shown in FIG. 1 (a), but as shown in FIG. 2, the vicinity of the balloon rear end is integrated with each other. It is also possible to use a two-chamber tube (8) having two flow passages and provide a branch (9) at the rear position to branch the tube. As the material, for example, a material having an appropriate flexibility and hardness such as a soft vinyl chloride resin, a urethane resin, a silicone rubber, and a natural rubber is used.
m, a tube having a wall thickness of 0.3 to 2 mm is preferable. Also,
The length of the branch tubes (4) and (5) is set to 30 to 300 m so as not to hinder the operator from using various treatment tools.
About m is appropriate.
【0010】更に、先枝チューブ(4)および後枝チュ
ーブ(5)の後端部には、それぞれ気液開閉装置(1
0)(11)であるコネクターを有する逆止弁、2方コ
ック、もしくは3方コック等が連結されており一般的な
バルーンの膨張注入器具である注射筒の着脱により、簡
便に開閉できる構造となっている。また、枝チューブ
(4)(5)と気液開閉装置(10)(11)の間には
パイロットバルーン(12)(13)が連結されても良
く、この場合、パイロットバルーン(12)(13)
は、バルーン部(1)(2)のバルーン膨張状況のモニ
ターができるように、例えば、軟質塩化ビニル樹脂、ウ
レタン樹脂、シリコーンゴム、天然ゴム等の適度な柔軟
性と弾力性を有する材料で成形されている。Further, the rear ends of the leading branch tube (4) and the trailing branch tube (5) have gas-liquid opening / closing devices (1), respectively.
0) A check valve having a connector as described in (11), a two-way cock, a three-way cock, or the like is connected, and a structure that can be easily opened and closed by attaching and detaching a syringe which is a general balloon inflation and injection device. Has become. Further, pilot balloons (12) and (13) may be connected between the branch tubes (4) and (5) and the gas-liquid switching devices (10) and (11). In this case, the pilot balloons (12) and (13) )
Is molded from a material having appropriate flexibility and elasticity, such as a soft vinyl chloride resin, urethane resin, silicone rubber, or natural rubber, so that the balloon inflation status of the balloon portions (1) and (2) can be monitored. Have been.
【0011】手袋(14)は腹壁(16)の切開口より
先バルーン(1)と一緒に体内(6)に挿入されるた
め、かさばらない方が有利であり、0.1〜2mm程度
の肉薄のシートが好ましい。また、この仕様は気腹下で
使用され、体内(6)の気密を保つため、手袋(14)
には気密性が必要であり、手袋(14)は先バルーン
(1)内壁外周、あるいは円筒状シート(3)下部に手
袋(14)の袖の部分を気密的に隣接させて使用され
る。手袋(14)と円筒状シート(3)が貼り合わされ
たり、一体化されて形成しても良い。材質については、
例えば、軟質塩化ビニル樹脂、ポリウレタン樹脂、ポリ
エチレン樹脂、ポリプロピレン樹脂、ポリエステル樹
脂、シリコーンゴム、天然ゴムのような適度な柔軟性を
もつ材料が好ましいが必ずしもこの限りでない。手袋
(14)が直接臓器に触れることがあるため、臓器に傷
をつけず、また、通常の使用で裂けたり、穴が開いて気
腹ガスが漏れない程度の引裂強度を持つ材質を選択する
ことが肝要である。Since the glove (14) is inserted into the body (6) together with the balloon (1) beyond the incision in the abdominal wall (16), it is advantageous that the glove is not bulky, and it is as thin as about 0.1 to 2 mm. Sheets are preferred. In addition, this specification is used under the stomach and gloves (14) to keep the body (6) airtight.
The glove (14) is used with the sleeve portion of the glove (14) air-tightly adjacent to the inner wall of the balloon (1) or the lower part of the cylindrical sheet (3). The glove (14) and the cylindrical sheet (3) may be laminated or integrated. For material,
For example, a material having appropriate flexibility such as a soft vinyl chloride resin, a polyurethane resin, a polyethylene resin, a polypropylene resin, a polyester resin, a silicone rubber, and a natural rubber is preferable, but not necessarily limited thereto. Since the gloves (14) may come into direct contact with the organ, select a material that does not damage the organ, and has a tearing strength such that the glove (14) does not tear or puncture due to normal use and does not leak gas. It is important.
【0012】本発明による医療用処置挿入具の使用に当
たっては、例えば、図3に示すように腹壁(7)の切開
口から、先バルーン(1)を手で小さくし、体内(6)
に挿入する。挿入後、気液開閉装置(10)(11)か
ら、シリンジ等を用いて空気または水を注入することに
より先バルーン(1)を膨張させる。ここで、この医療
用処置挿入具を引いて腹壁(7)内側に先バルーン
(1)を密着させた後、後バルーン(2)を同様にして
体外で膨張させ、腹壁(7)を先バルーン(1)と後バ
ルーン(2)の2つのバルーン膨張部で挟み込むように
して、気密的に医療用処置挿入具を体表に固定する。円
筒状シート(3)及び手袋(14)により、体内の気密
が保たれ、手袋(14)のシート1枚を介した状態で、
体外と体内(6)の挿入路が通じ、手、腕(15)を円
筒状シート(3)に通して手袋(14)に装着した後に
手袋(14)を介して手で直接、処置を行うことができ
る。また、切除した臓器を手袋(14)の中に入れ、ひ
っくり返して、体外に摘出することにより、腹壁に癌組
織が付着せずに摘出が行うことが出来、癌組織の転移を
予防することが出来る。In using the medical treatment insertion tool according to the present invention, for example, as shown in FIG. 3, the balloon (1) is made smaller by hand through an incision in the abdominal wall (7), and the body (6) is cut.
Insert After the insertion, the balloon (1) is inflated by injecting air or water from the gas-liquid opening / closing device (10) (11) using a syringe or the like. Here, after pulling this medical treatment insertion tool and bringing the front balloon (1) into close contact with the inside of the abdominal wall (7), the rear balloon (2) is similarly expanded outside the body, and the abdominal wall (7) is inflated outside the body. The medical treatment insertion tool is airtightly fixed to the body surface so as to be sandwiched between two balloon inflatable portions of (1) and the rear balloon (2). The airtightness in the body is maintained by the cylindrical sheet (3) and the gloves (14), and the gloves (14) pass through one sheet.
The insertion path between the outside of the body and the inside of the body (6) communicates, the hand and the arm (15) are passed through the cylindrical sheet (3) and attached to the glove (14), and then the treatment is performed directly by hand through the glove (14). be able to. In addition, by putting the resected organ in gloves (14), turning it over, and removing it outside the body, it can be removed without attaching cancerous tissue to the abdominal wall, and preventing metastasis of cancerous tissue. Can be done.
【0013】[0013]
【発明の効果】本発明の医療用処置挿入具は腹壁の切開
口より挿入する時、かさばりがなく、また、バルーンの
適度な柔軟性のため、安全に容易に挿入できる。また、
2個のバルーン膨張部をもち、体内と体外表面でバルー
ンを膨張させることにより、切開口を体内外から挟み込
むように固定でき、医療用処置挿入具を気密的に確実に
固定することができる。バルーンが柔軟なため、小切開
口についても損傷する恐れがない。膨張したバルーン内
部で、体外と体内が通じるため、体外から体内に手を容
易に挿入して直接手で臓器処置あるいは摘出を行え、確
実、安全に短時間で処置することができる。また、膨張
バルーンは操作角度に追随して自由に変形し、臓器処置
を容易に行うことができる。更に、癌組織を体外に取り
出すときにも腹壁に付着することがなく取り出すことが
出来るため、転移の心配がない。気密性に関しても、円
筒状シートの先バルーン下の周囲に気液不透過性の手袋
を気密的に隣接させて付設することにより気腹ガス漏れ
がなく、十分な空間を体内に保て、良好な視野の下で安
全、短時間で処置が行うことができ、内視鏡下手術で処
置を行う場合、極めて有用である。The medical treatment insert of the present invention has no bulk when inserted through an incision in the abdominal wall, and can be safely and easily inserted because of the appropriate flexibility of the balloon. Also,
By having two balloon inflatable portions and inflating the balloon on the inside and outside of the body, the incision can be fixed so as to be sandwiched from inside and outside the body, and the medical treatment insertion tool can be securely fixed in an airtight manner. Because the balloon is flexible, there is no risk of damage to the small opening. Since the inside of the inflated balloon communicates with the outside of the body, the hand can be easily inserted into the body from outside the body, and the organ can be directly treated or extracted by hand, and the treatment can be performed reliably, safely, and in a short time. Further, the inflation balloon is freely deformed according to the operation angle, so that organ treatment can be easily performed. Furthermore, even when the cancer tissue is taken out of the body, it can be taken out without adhering to the abdominal wall, so that there is no fear of metastasis. As for airtightness, gas-liquid-impermeable gloves are provided airtightly adjacent to the cylindrical sheet below the tip of the balloon, so that there is no insufflation gas leak, sufficient space can be kept in the body, and good The procedure can be performed safely and in a short time under a wide field of view, and is extremely useful when performing the procedure by endoscopic surgery.
【図1】(a)気腹法で目的を達成するための本発明に
よる医療用処置挿入具の一実施例を示す図である。 (b)気腹法で目的を達成するための本発明による医療
用処置挿入具の一実施例を示す断面図である。FIG. 1 (a) is a view showing one embodiment of a medical treatment insert according to the present invention for achieving an object by an insufflation method. (B) It is sectional drawing which shows one Example of the medical treatment insertion tool by this invention for achieving the objective by the insufflation method.
【図2】気腹法で目的を達成するための本発明による医
療用処置挿入具の他の実施例を示す図である。FIG. 2 is a view showing another embodiment of the medical treatment insertion tool according to the present invention for achieving the purpose of insufflation.
【図3】本発明による医療用処置挿入具の使用状態を示
す概略図である。FIG. 3 is a schematic view showing a use state of the medical treatment insertion tool according to the present invention.
【図4】本発明による医療用処置挿入具の手を挿入した
ときの使用状態を示す概略図である。FIG. 4 is a schematic view showing a use state when a hand of the medical treatment insertion tool according to the present invention is inserted.
1.先バルーン 2.後バルーン 3.円筒状シート 4.先枝チューブ 5.後枝チューブ 6.体内 7.腹壁 8.2腔チューブ 9.分岐部 10.11.気液開閉装置 12.13.パイロットバルーン 14.手袋 15.手、腕 1. Tip balloon 2. Rear balloon 3. 3. cylindrical sheet Branch tube 5. Rear branch tube 6. Inside the body 7. 8. Abdominal wall 8.2 cavity tube Branch 10.11. Gas-liquid switching device 12.13. Pilot balloon 14. Gloves 15. Hands, arms
Claims (5)
先バルーン、後端側に後バルーンを形成させ、該円筒状
シートの該先バルーン下の周囲に、気液不透過性手袋の
袖の部分を気密的に隣接させて付設し、更に、先端が該
円筒状シートを通って該先バルーン内に連通した先枝チ
ューブ、および先端部が該後バルーンに連通した後枝チ
ューブより構成され、該先枝チューブと該後枝チューブ
の後端部には各々接続用コネクターを有する気液開閉装
置を付設したことを特徴とする医療用処置挿入具。1. A front balloon is formed on the front end side and a rear balloon is formed on the rear end side adjacent to the outer periphery of the cylindrical sheet, and a gas-liquid impermeable glove is formed around the cylindrical sheet below the front balloon. A sleeve portion is provided so as to be airtightly adjacent to the sleeve portion, and further comprises a front branch tube having a leading end communicating with the front balloon through the cylindrical sheet and a rear branch tube having a leading end communicating with the rear balloon. A medical treatment insert, wherein a gas-liquid opening / closing device having a connector for connection is provided at a rear end portion of each of the leading branch tube and the trailing branch tube.
合わされて形成した請求項1の医療用処置挿入具。2. The medical treatment insert according to claim 1, wherein the cylindrical sheet and the gas-liquid impermeable glove are bonded to each other.
ンが貼り合わされて形成した請求項1の医療用処置挿入
具。3. The medical treatment insertion tool according to claim 1, wherein the cylindrical sheet, the front balloon, and the rear balloon are bonded to each other.
筒として円筒状シートとを重ね合わせ、その先端部及び
中央部で内外筒を接着して、先バルーンと後バルーンを
形成させた請求項1の医療用処置挿入具。4. An inner cylinder is used as a cylindrical sheet, and a cylindrical sheet is superimposed on an outer cylinder as an outer cylinder, and the inner and outer cylinders are adhered at a tip portion and a central portion to form a front balloon and a rear balloon. The medical treatment insert according to claim 1.
筒状シート内径が5〜10cmである請求項1の医療用
処置挿入具。5. The medical treatment insert according to claim 1, wherein the length of the cylindrical sheet is 5 to 20 cm and the inner diameter of the cylindrical sheet is 5 to 10 cm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29033896A JP3614259B2 (en) | 1996-10-31 | 1996-10-31 | Medical treatment insert |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29033896A JP3614259B2 (en) | 1996-10-31 | 1996-10-31 | Medical treatment insert |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH10127643A true JPH10127643A (en) | 1998-05-19 |
JP3614259B2 JP3614259B2 (en) | 2005-01-26 |
Family
ID=17754774
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP29033896A Expired - Fee Related JP3614259B2 (en) | 1996-10-31 | 1996-10-31 | Medical treatment insert |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3614259B2 (en) |
-
1996
- 1996-10-31 JP JP29033896A patent/JP3614259B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP3614259B2 (en) | 2005-01-26 |
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