JP2015006262A - Positioning medical apparatus - Google Patents

Positioning medical apparatus Download PDF

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JP2015006262A
JP2015006262A JP2013133063A JP2013133063A JP2015006262A JP 2015006262 A JP2015006262 A JP 2015006262A JP 2013133063 A JP2013133063 A JP 2013133063A JP 2013133063 A JP2013133063 A JP 2013133063A JP 2015006262 A JP2015006262 A JP 2015006262A
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bending direction
medical device
bending
tubular
surface continuous
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JP6276522B2 (en
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清明 本間
Kiyoaki Honma
清明 本間
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Abstract

PROBLEM TO BE SOLVED: To provide a positioning medical apparatus which makes it possible to easily position a tip at an intended position in bending a bend unit by drawing an operation wire by operation at an operation unit, and has excellent operability.SOLUTION: A positioning medical apparatus 1 includes an operation unit 3 and a flexible sheath 2 in a tubular shape connected to the operation unit 3. The flexible sheath 2 is composed of: a tubular flexible unit 5 extending from the operation unit 3 side; a bend unit 6 which is connected to the tubular flexible unit 5 and is bent by operation at the operation unit 3; and a tip side tubular unit 7 which is connected to the bend unit 6 and has an action site for acting on a treatment target. Drawing the operation wire 4 arranged in the flexible sheath 2 by operation at the operation unit 3 makes the tip side tubular unit 7 be drawn to bend the bend unit 6. The tubular flexible unit 5 is configured so that deformation easiness of a face connected to the inside in a bending direction of the bend unit 6 is different from that of a face connected to the outside in the bending direction over a predetermined length.

Description

本発明は、人体内に挿入され、遠隔操作によって任意に湾曲させることのできる位置決め医療機器に関する。   The present invention relates to a positioning medical device that is inserted into a human body and can be arbitrarily bent by a remote operation.

一般に、位置決め医療機器は内視鏡や高周波治療用カテーテルとして、または内視鏡や高周波治療用カテーテルを体内に導入するためのガイドチューブ等として用いられる。そして、このような位置決め医療機器は、体内において先端を所望の方向に向けることができるように、基端側に設けられた操作部からの遠隔操作によって湾曲自在な湾曲部が先端に設けられている。
このような従来の位置決め医療機器としては、例えば特許文献1に記載のものがある。
Generally, the positioning medical device is used as an endoscope or a high-frequency treatment catheter, or as a guide tube for introducing the endoscope or the high-frequency treatment catheter into the body. Such a positioning medical device is provided with a bending portion at the tip that can be bent by a remote operation from an operation portion provided on the proximal end side so that the tip can be directed in a desired direction in the body. Yes.
As such a conventional positioning medical device, there exists a thing of patent document 1, for example.

特開2007−29120号公報JP 2007-29120 A

特許文献1に記載された位置決め医療機器である医療用カテーテルチューブは、内層管、補強材層、X線不透過性を有した金属からなるマーカー、そして補強材層とマーカーを覆い柔軟性を有する樹脂管からなる外層樹脂が一体となった医療用カテーテルチューブであって、補強材層として内層管上にタングステン素線とこれに同径のステンレス素線で編組し、該タングステン素線の数は少なくとも1本以上、全素線数の半数以下とし、補強材層、マーカーが存在しない最先端部を有し、該外層樹脂の存在により、基部から先端部にかけての曲げ剛性が段階的に小さくなるように構成することにより、高い柔軟性をもち、かつトルク伝達の異方性のない医療用カテーテルチューブとなっている。   A medical catheter tube which is a positioning medical device described in Patent Document 1 has an inner layer tube, a reinforcing material layer, a marker made of a metal having radiopacity, and a flexibility covering the reinforcing material layer and the marker. A medical catheter tube in which an outer layer resin made of a resin tube is integrated, and braided with a tungsten wire and a stainless steel wire of the same diameter on the inner layer tube as a reinforcing material layer, and the number of tungsten wires is At least one and not more than half of the total number of strands, and has the most advanced part where the reinforcing material layer and marker do not exist, and the bending rigidity from the base part to the tip part gradually decreases due to the presence of the outer layer resin. With this configuration, the medical catheter tube has high flexibility and no torque transmission anisotropy.

しかしながら、特許文献1記載のカテーテルチューブのような従来技術によるものにおいては、手元操作部による操作で先端側を湾曲させるときに、意図しない湾曲が起こり、機器の作用部位である先端部が、操作者の意図した位置から離れてしまう事があり、正確で手早い操作の妨げとなるという課題があった。
詳述すると、図5に示すように、操作部3と、操作部3から延伸する管状の可撓性シース200を有し、この可撓性シース200が操作部3側から、管状可撓部50と、操作部3の操作により湾曲する湾曲部60と、先端側管状部70とからなる位置決め医療機器において、操作部3の操作によって、可撓性シース200内に配置された操作ワイヤを牽引することにより先端を牽引して湾曲部60を湾曲させた場合、湾曲部60が可撓性シース200の中心軸Nよりも湾曲方向内側(図中X方向)の反対側である湾曲方向外側(図矢印Y方向)へ後退してのけぞるような形状となる。
すなわち、牽引された操作ワイヤの力によって先端側管状部70と湾曲部60は湾曲するが、先端側管状部70のポリマー等が受けた圧縮力を解放するために管状可撓部50が可撓性シース200の中心軸Nよりも湾曲方向外側へのけぞるように曲がり、全体としてS字状に湾曲してしまうため、操作者が意図した先端位置よりも距離L分だけずれてしまう事になり、操作量の予測が困難となり操作性が低下する。
However, in the case of the conventional technique such as the catheter tube described in Patent Document 1, when the distal end side is bent by the operation by the hand operation section, an unintended bending occurs, and the distal end section, which is the working part of the device, is operated. There is a problem that it may be away from the position intended by the person, which hinders accurate and quick operation.
More specifically, as shown in FIG. 5, an operation unit 3 and a tubular flexible sheath 200 extending from the operation unit 3 are provided, and the flexible sheath 200 is connected to the tubular flexible unit from the operation unit 3 side. 50, a bending medical unit 60 that is bent by the operation of the operation unit 3, and a distal medical tubular unit 70, the operation wire disposed in the flexible sheath 200 is pulled by the operation of the operation unit 3. Thus, when the bending portion 60 is bent by pulling the tip, the bending portion 60 is outside the bending direction (the X direction in the drawing) opposite to the central axis N of the flexible sheath 200 (the X direction in the drawing). It has a shape that slides back in the direction of the arrow Y).
That is, the distal tubular portion 70 and the bending portion 60 are bent by the force of the pulled operation wire, but the tubular flexible portion 50 is flexible to release the compressive force received by the polymer or the like of the distal tubular portion 70. Since it bends to the outside in the bending direction from the central axis N of the sheath 200 and is curved in an S shape as a whole, it will be displaced by a distance L from the tip position intended by the operator. The amount of operation is difficult to predict and the operability is reduced.

このような課題に鑑みて、本発明は、操作部の操作により操作ワイヤ牽引して湾曲部を湾曲させるときに、意図した位置に容易に先端を位置させることができて操作性の良い位置決め医療機器を提供することを目的とする。   In view of such a problem, the present invention is a positioning medical device that can easily position the tip at an intended position and has good operability when the operation wire is pulled by the operation of the operation unit to bend the bending portion. The purpose is to provide equipment.

前記目的を達成するために本発明は、操作部と、該操作部に連結される管状の可撓性シースを有し、該可撓性シースが、前記操作部側から延伸する管状可撓部と、該管状可撓部に接合され前記操作部の操作により湾曲する湾曲部と、該湾曲部に接合され処置対象に働きかける作用部位を有する先端側管状部とからなり、前記操作部の操作によって、前記可撓性シース内に配置された操作ワイヤを牽引することにより前記先端側管状部を牽引して前記湾曲部を湾曲させる位置決め医療機器であって、前記管状可撓部を、前記湾曲部と隣接する位置から所定の長さに亘って前記湾曲部の湾曲方向内側に連続する面と湾曲方向外側に連続する面との変形容易性が異なるよう構成したことを第1の特徴とする。   In order to achieve the above object, the present invention has an operation portion and a tubular flexible sheath connected to the operation portion, and the flexible sheath extends from the operation portion side. A bending portion that is joined to the tubular flexible portion and is bent by the operation of the operation portion, and a distal-side tubular portion that is joined to the bending portion and has an action portion that acts on a treatment target, and is operated by the operation of the operation portion. A positioning medical device that pulls the distal tubular portion by bending an operation wire disposed in the flexible sheath to bend the bending portion, wherein the tubular flexible portion is connected to the bending portion. The first feature is that the surface of the bending portion that is continuous on the inner side in the bending direction and the surface that is continuous on the outer side of the bending direction are different from each other in a predetermined length from the adjacent position.

また、前記第1の特徴の位置決め医療機器において、前記所定の長さは、少なくとも前記湾曲部と前記先端側管状部とを合わせた長さと同程度であることを第2の特徴とし、前記第1または2の特徴の位置決め医療機器において、前記管状可撓部は、前記湾曲方向内側に連続する面の硬度を前記湾曲方向外側に連続する面の硬度よりも高くすることにより前記変形容易性が異なるよう構成したことを第3の特徴とする。   Further, in the positioning medical device according to the first feature, the predetermined length is approximately the same as a length obtained by combining at least the curved portion and the distal tubular portion, In the positioning medical device according to the first or second feature, the tubular flexible portion has the ease of deformation by increasing the hardness of the surface continuous on the inner side in the bending direction than the hardness of the surface continuous on the outer side in the bending direction. The third feature is that they are configured differently.

さらに、前記第1乃至3のいずれかの特徴の位置決め医療機器において、前記管状可撓部は、前記湾曲方向内側に連続する面に架橋性物質を含浸し架橋させ、前記湾曲方向内側に連続する面の弾性率を前記湾曲方向外側に連続する面の弾性率よりも大きくすることにより前記変形容易性が異なるよう構成したことを第4の特徴とし、前記第1乃至4のいずれかの特徴の位置決め医療機器において、前記管状可撓部は、前記湾曲方向内側に連続する面の壁厚を前記湾曲方向外側に連続する面の壁厚よりも厚くすることにより前記変形容易性が異なるよう構成したことを第5の特徴とし、前記第1乃至5のいずれかの特徴の位置決め医療機器において、前記可撓性シースには、前記作用部位に連結するリードワイヤ等の内蔵物が配置され、該内蔵物を前記可撓性シース内の前記湾曲方向内側に偏在させることにより前記変形容易性が異なるように構成したことを第6の特徴とする。   Furthermore, in the positioning medical device according to any one of the first to third features, the tubular flexible portion is impregnated with a crosslinkable substance on a surface continuous on the inner side in the bending direction, and is continuous on the inner side in the bending direction. The fourth feature is that the ease of deformation is different by making the elastic modulus of the surface larger than the elastic modulus of the surface continuous to the outside in the bending direction, and the feature of any one of the first to fourth features In the positioning medical device, the tubular flexible portion is configured such that the ease of deformation is different by making the wall thickness of the surface continuous in the bending direction thicker than the wall thickness of the surface continuous in the bending direction outer side. In the positioning medical device according to any one of the first to fifth features, a built-in object such as a lead wire connected to the working site is disposed in the flexible sheath. A and sixth characteristic of said deformation easiness was configured differently by unevenly distributed in the curved inward in the flexible sheath.

また、前記第1または2の特徴の位置決め医療機器において、前記管状可撓部は、前記湾曲方向外側に連続する面の硬度を前記湾曲方向内側に連続する面の硬度よりも高くすることにより前記変形容易性が異なるよう構成したことを第7特徴とし、前記第1、2、7のいずれかの特徴の位置決め医療機器において、前記管状可撓部は、前記湾曲方向外側に連続する面に架橋性物質を含浸し架橋させ、前記湾曲方向外側に連続する面の弾性率を前記湾曲方向内側に連続する面の弾性率よりも大きくすることにより前記変形容易性が異なるよう構成したことを第8の特徴とし、前記第1、2、7、8のいずれかの特徴の位置決め医療機器において、前記管状可撓部は、前記湾曲方向外側に連続する面の壁厚を前記湾曲方向内側に連続する面の壁厚よりも厚くすることにより前記変形容易性が異なるよう構成したことを第9の特徴とし、前記第1、2、7、8、9のいずれかの特徴の位置決め医療機器において、前記可撓性シースには、前記作用部位に連結するリードワイヤ等の内蔵物が配置され、該内蔵物を前記可撓性シース内の前記湾曲方向外側に偏在させることにより前記変形容易性が異なるように構成したことを第10の特徴とする。   Further, in the positioning medical device according to the first or second feature, the tubular flexible portion is configured such that the hardness of the surface continuous on the outer side in the bending direction is higher than the hardness of the surface continuous on the inner side in the bending direction. In the positioning medical device according to any one of the first, second, and seventh features, the tubular flexible portion is cross-linked to a surface continuous outward in the bending direction. In the eighth aspect, the deformability is made different by impregnating and cross-linking the active substance so that the elastic modulus of the surface continuous on the outer side in the bending direction is larger than the elastic modulus of the surface continuous on the inner side in the bending direction. In the positioning medical device according to any one of the first, second, seventh, and eighth features, the tubular flexible portion has a wall thickness of a surface that continues to the outside in the bending direction and continues to the inside in the bending direction. Face wall thickness In the positioning medical device according to any one of the first, second, seventh, eighth, and ninth features, the flexible sheath is configured such that the ease of deformation is different by increasing the thickness. Is configured such that a built-in object such as a lead wire connected to the working site is arranged, and the deformability is different by unevenly distributing the built-in object to the outside in the bending direction in the flexible sheath. Is a tenth feature.

したがって、上記説明から、本発明による位置決め医療機器によれば、管状可撓部を、湾曲部と隣接する位置から所定の長さに亘って前記湾曲部の湾曲方向内側に連続する面と湾曲方向外側に連続する面との変形容易性を異なるよう構成し、この変形容易性について、湾曲方向内側に連続する面を湾曲方向外側に連続する面よりも硬度を高くしたり、弾性率を大きくしたり、壁厚を厚くする等により、湾曲方向内側に連続する面を変形し難くすれば、管状可撓部が可撓性シース中心軸よりも湾曲方向と反対側へのけぞりにくくなる為、意図した位置に容易に先端部を位置させることができて操作性が良い。
また、逆に湾曲方向外側に連続する面を湾曲方向内側に連続する面よりも硬度を高くしたり、弾性率を大きくしたり、壁厚を厚くする等により、湾曲方向外側に連続する面を変形し難くすれば、管状可撓部が可撓性シース中心軸よりも湾曲方向と反対側へ大きくのけぞるため、先端環状体の先端がシースの中心軸の延長上に直行する方向に向き(すなわち先端が側方を向き)、処置対象に先端を当接させ易くなる。
Therefore, from the above description, according to the positioning medical device according to the present invention, the tubular flexible portion is formed in a curved direction and a surface continuous from the position adjacent to the curved portion to the inside of the curved direction of the curved portion over a predetermined length. It is configured so that the deformability is different from the surface that is continuous on the outside, and the surface that is continuous on the inside in the bending direction is made harder than the surface that is continuous on the outside in the bending direction, or the elastic modulus is increased. If it is difficult to deform the surface continuous in the bending direction by increasing the wall thickness, etc., the tubular flexible part is less likely to slide in the direction opposite to the bending direction than the central axis of the flexible sheath. The tip can be easily positioned at the position, and the operability is good.
Conversely, by increasing the hardness of the surface continuous in the bending direction outside the surface continuous in the bending direction, increasing the elastic modulus, or increasing the wall thickness, the surface continuous in the bending direction is changed. If it is difficult to deform, the tubular flexible portion is greatly displaced to the opposite side of the bending direction from the flexible sheath central axis, so that the distal end of the distal annular body is directed in a direction perpendicular to the extension of the central axis of the sheath (i.e. The tip is directed to the side), and the tip is easily brought into contact with the treatment target.

本発明の位置決め医療機器の全体を示す図。The figure which shows the whole positioning medical device of this invention. 本発明の第1実施形態の先端側を示す断面図。Sectional drawing which shows the front end side of 1st Embodiment of this invention. 本発明の第2実施形態の先端側を示す断面図。Sectional drawing which shows the front end side of 2nd Embodiment of this invention. 本発明の効果を説明するための図The figure for demonstrating the effect of this invention 従来の位置決め医療機器を説明するための図。The figure for demonstrating the conventional positioning medical device.

[第1実施形態]
以下、本発明の第1実施形態による位置決め医療機器を図面を参照して詳細に説明する。図1は本発明の位置決め医療機器の全体を示す図である。
本発明による位置決め医療機器1は、例えば診断や治療を行うためのカテーテルであり、概略構造は、図1及び図2に示すように、体内に挿入するための樹脂等からなる円筒状の可撓性シース2と、可撓性シース2の先端側を湾曲させるための操作部3とを備え、可撓性シース2内に挿通されると共に可撓性シース2の内部先端側と操作部3内部に固着され、撚り線からなる操作ワイヤ4を有し、操作部3の湾曲ノブ3aを操作することによって、操作ワイヤ4を操作部3側である基端側に牽引することにより、可撓性シース2の先端側が牽引されて湾曲するよう構成されている。
[First Embodiment]
Hereinafter, a positioning medical device according to a first embodiment of the present invention will be described in detail with reference to the drawings. FIG. 1 is a diagram showing the entire positioning medical device of the present invention.
The positioning medical device 1 according to the present invention is, for example, a catheter for performing diagnosis or treatment, and the schematic structure thereof is a cylindrical flexible made of resin or the like for insertion into the body as shown in FIGS. The flexible sheath 2 and an operation portion 3 for bending the distal end side of the flexible sheath 2 are inserted into the flexible sheath 2, and the inner distal end side of the flexible sheath 2 and the inside of the operation portion 3 are provided. The operation wire 4 is made of a stranded wire, and is flexible by pulling the operation wire 4 to the proximal end side which is the operation unit 3 side by operating the bending knob 3a of the operation unit 3. The distal end side of the sheath 2 is pulled and curved.

可撓性シース2は、操作部3側から延伸する比較的高硬度の管状可撓部5と、管状可撓部5よりも低硬度で、管状可撓部5に接合され操作部3の操作により湾曲する湾曲部6と、湾曲部6より高硬度かつ管状可撓部5よりも低硬度であって、湾曲部6に接合され処置対象に働きかける作用部位を有する先端側管状部7とからなる。
可撓性シース2(符号2aは外被)には、先端部近傍にプラチナリング11が取り付けられ、可撓性シース2の先端にはプラチナ電極からなる先端キャップ10が溶接され、図示しない電気導線等により印加して患部を診断等することができる作用部位となっている。また、この先端キャップ10の内側には、可撓性シース2の内部の軸方向に沿う中心に面を捩じらずに配置される平板15が接着材21で接着されている。
平板15で仕切られた可撓性シース2の内腔には、それぞれPTFE等の樹脂からなるチューブ13が配置され、このチューブ13は、可撓性シース2の内壁に接着されている。そして、各チューブ13内部に挿通された操作ワイヤ4が、平板15の先端近傍に取り付けられた平板貫通部材16の両端及び、操作部3に固定さていることにより、操作部3の操作により湾曲方向内側(図中X方向)に配置された操作ワイヤ4を操作部3側に牽引すると、可撓性シース2の先端側が湾曲するよう構成されている。
The flexible sheath 2 has a relatively flexible tubular flexible portion 5 extending from the operation portion 3 side, and has a lower hardness than the tubular flexible portion 5 and is joined to the tubular flexible portion 5 to operate the operation portion 3. And the distal end side tubular portion 7 having an action portion that is higher in hardness than the bending portion 6 and lower in hardness than the tubular flexible portion 5 and that acts on the treatment target. .
A platinum ring 11 is attached to the flexible sheath 2 (symbol 2a is a jacket) in the vicinity of the distal end portion, and a distal end cap 10 made of a platinum electrode is welded to the distal end of the flexible sheath 2, and an electric conductor (not shown) It is an action site that can be applied by, for example, diagnosis of the affected area. A flat plate 15 disposed without twisting the surface at the center along the axial direction inside the flexible sheath 2 is bonded to the inner side of the distal end cap 10 with an adhesive 21.
Tubes 13 made of resin such as PTFE are disposed in the lumens of the flexible sheath 2 partitioned by the flat plate 15, and the tubes 13 are bonded to the inner wall of the flexible sheath 2. The operation wire 4 inserted into each tube 13 is fixed to both ends of the flat plate penetrating member 16 attached in the vicinity of the distal end of the flat plate 15 and the operation unit 3, so that the bending direction is obtained by the operation of the operation unit 3. When the operation wire 4 arranged on the inner side (X direction in the drawing) is pulled toward the operation unit 3, the distal end side of the flexible sheath 2 is configured to bend.

また、管状可撓部5を、湾曲部6と隣接する位置から所定の長さ、具体的には、少なくとも湾曲部6と先端側管状部7とを合わせた長さと同程度(通常湾曲部6と先端側管状部7の長さを合わせると30cm程度、管状可撓部5の長さは80〜120cm程度である為、この管状可撓部5の長さのうち、湾曲部6と隣接する位置から30cm程度)に亘って、湾曲部6の湾曲方向内側(X方向側)に連続する面と湾曲方向外側(Y方向側)に連続する面との変形容易性が異なるよう構成する。
詳述すると、図2の(a)の管状可撓部5の断面を表す図(b)に示すように、管状可撓部5を、平板15を中心として、湾曲方向内側(図中X方向)半部5aを、湾曲方向外側(図中Y方向)半部5bに比べて硬度の高い樹脂により構成する。
なお、診断治療の安全性、効率を上げるため、造影性等の付与が必要な場合には、上記構成に加え、湾曲方向内側半部5aに、例えば造影剤として硫酸バリウム、次炭酸ビスマス、タングステン、酸化バリウム、リン酸バリウム、酸化ビスマス、硫化ビスマス、チタン酸ビスマス、酸化モリブデン、三酸化タングステン等を含む化合物を用いることが可能である。
このとき、
In addition, the tubular flexible portion 5 has a predetermined length from a position adjacent to the bending portion 6, specifically, at least as long as the combined length of the bending portion 6 and the distal tubular portion 7 (normally the bending portion 6 The length of the tubular flexible portion 5 is about 30 cm and the length of the tubular flexible portion 5 is about 80 to 120 cm. Therefore, the length of the tubular flexible portion 5 is adjacent to the curved portion 6. The surface of the bending portion 6 that is continuous on the inner side in the bending direction (X direction side) and the surface that is continuous on the outer side of the bending direction (Y direction side) are configured so that the deformability is different.
Specifically, as shown in FIG. 2B, which shows a cross section of the tubular flexible portion 5 in FIG. 2A, the tubular flexible portion 5 is bent inward in the bending direction with the flat plate 15 as the center (X direction in the figure). ) The half part 5a is made of a resin having higher hardness than the outer half part 5b in the bending direction (Y direction in the figure).
In addition, in order to increase the safety and efficiency of diagnostic treatment, in the case where it is necessary to provide contrast, etc., in addition to the above configuration, for example, barium sulfate, bismuth subcarbonate, tungsten as a contrast agent in the bending direction inner half 5a. It is possible to use a compound containing barium oxide, barium phosphate, bismuth oxide, bismuth sulfide, bismuth titanate, molybdenum oxide, tungsten trioxide, or the like.
At this time,

このように構成された位置決め医療機器1は、管状可撓部5の湾曲方向内側半部5aと湾曲方向外側半部5bそれぞれを違う硬度の樹脂により構成し、湾曲方向内側半部5aを、湾曲方向外側半部5bに比べて硬度を高くすることによって、操作ワイヤ4による牽引力を受けたときに、湾曲方向内側半部5aが湾曲方向外側半部5bよりも牽引力に対する抵抗力が大きくなり圧縮され難くなる為、従来技術のような、管状可撓部の湾曲方向外側へののけぞりを回避することができ、操作者が意図した位置に容易に先端を位置させることができて操作性が良い。   The positioning medical device 1 configured in this way is configured such that the bending direction inner half 5a and the bending direction outer half 5b of the tubular flexible portion 5 are made of resins of different hardness, and the bending direction inner half 5a is bent. By making the hardness higher than that of the outer half portion 5b, the bending direction inner half portion 5a becomes more resistant to traction force than the bending direction outer half portion 5b when compressed by the operation wire 4, and is compressed. Since it becomes difficult, it is possible to avoid the sliding of the tubular flexible portion to the outside in the bending direction as in the prior art, and the tip can be easily positioned at the position intended by the operator, and the operability is good.

なお、上述のように管状可撓部5の湾曲方向内側半部5aと湾曲方向外側半部5bそれぞれを違う硬度の樹脂とするのに代えて、または併用して、湾曲方向内側半部5aに対してイソシアナート化合物やエポキシ化合物などの架橋性物質などを含浸して架橋させ、弾性率を湾曲方向外側半部5bよりも大きくしてもよく、また管状可撓部5のチューブを押し出し成形する際に湾曲方向内側半部5aを湾曲方向外側半部5bよりも肉厚に押し出してもよい。   As described above, the bending direction inner half 5a and the bending direction outer half 5b of the tubular flexible portion 5 are replaced with or combined with the resins having different hardnesses. On the other hand, a crosslinkable substance such as an isocyanate compound or an epoxy compound may be impregnated to crosslink, and the elastic modulus may be larger than that of the outer half portion 5b in the bending direction, and the tube of the tubular flexible portion 5 is extruded. At this time, the inner half 5a in the bending direction may be pushed out more thickly than the outer half 5b in the bending direction.

また、本実施形態では、湾曲方向内側半部5aを、湾曲方向外側半部5bに比べて硬度の高い樹脂により構成し、または、湾曲方向内側半部5aを架橋させ、弾性率を湾曲方向外側半部5bよりも大きくし、また管状可撓部5のチューブを押し出し成形する際に湾曲方向内側半部5aを湾曲方向外側半部5bよりも肉厚にする例を説明したが、逆に、湾曲方向外側半部5bを、湾曲方向内側半部5aに比べて硬度の高い樹脂により構成し、または、湾曲方向外側半部5bに対して架橋性物質などを含浸して架橋させて弾性率を湾曲方向内側半部5aよりも大きくし、また管状可撓部5のチューブを押し出し成形する際に湾湾曲方向外側半部5bを湾曲方向内側半部5aよりも肉厚にした場合には、従来技術よりも操作ワイヤ4の牽引時に管状可撓部5が湾曲方向外側へ大きくのけぞるため、図4に示すように、先端側管状部7の先端(本実施形態においては先端キャップ10)が、湾曲前と中心軸Nに対する距離がほぼ変化せずに中心軸Nに直交する方向に向き(すなわち先端が側方を向き)、このことから処置対象に先端を当接させ易くなり、この場合においても操作者が意図した位置に先端を位置させることができて操作性が良い。   Further, in the present embodiment, the bending direction inner half 5a is made of a resin having higher hardness than the bending direction outer half 5b, or the bending direction inner half 5a is cross-linked to change the elastic modulus to the bending direction outer side. Although an example in which the inner half 5a in the bending direction is made thicker than the outer half 5b in the bending direction when the tube of the tubular flexible portion 5 is extruded and formed larger than the half 5b, The bending direction outer half part 5b is made of a resin having a higher hardness than the bending direction inner half part 5a, or the bending direction outer half part 5b is impregnated with a crosslinkable substance or the like to be crosslinked. When the bay curve direction outer half part 5b is thicker than the curve direction inner half part 5a when extruding the tube of the tubular flexible part 5 to be larger than the curve direction inner half part 5a, Tubing when pulling operation wire 4 rather than technology Since the bending portion 5 is greatly bent outward in the bending direction, as shown in FIG. 4, the distance between the distal end of the distal end side tubular portion 7 (the distal end cap 10 in the present embodiment) and the central axis N changes substantially. Therefore, the tip is oriented in a direction perpendicular to the central axis N (that is, the tip is directed sideways), which makes it easy to contact the treatment target, and in this case also, the tip is positioned at the position intended by the operator. It is easy to operate.

[第2実施形態]
次に本発明の第2実施形態を説明する。図3は本発明の第2の実施形態の位置決め医療機器の断面図である。
前述の実施形態においては、管状可撓部5の、湾曲部6の湾曲方向内側(X方向)に連続する面と湾曲方向外側(Y方向)に連続する面との変形容易性が異なるよう構成するために、管状可撓部5の湾曲方向内側半部5aと湾曲方向外側半部5bの硬度を変える等したが、本発明はこれに限られず、図3に示すように、管状可撓部5の湾曲方向内側(X方向)と湾曲方向外側(Y方向)の材質を同一とし、操作ワイヤ4の通路をチューブ13とチューブ13の先端側に配置される密着コイル23、24とから構成し、湾曲方向外側に配置される密着コイル24を湾曲部6から管状可撓部5の一部まで配置される初張力ゼロの密着コイルとし、湾曲方向内側に配置される密着コイル23を湾曲部6内に配置される初張力の大きい密着コイルとして、管状可撓部5の湾曲方向内側と湾曲方向外側とで変形容易性が異なるようにしても良い。
なお、その他の構成については、第1の実施形態と同様である。
[Second Embodiment]
Next, a second embodiment of the present invention will be described. FIG. 3 is a sectional view of a positioning medical device according to the second embodiment of the present invention.
In the above-described embodiment, the tubular flexible portion 5 is configured such that the deformability of the surface continuous in the bending direction (X direction) of the bending portion 6 and the surface continuous in the bending direction outer side (Y direction) are different. In order to achieve this, the hardness of the bending direction inner half part 5a and the bending direction outer half part 5b of the tubular flexible part 5 is changed. However, the present invention is not limited to this, and as shown in FIG. 5 is made of the same material on the inside in the bending direction (X direction) and the outside in the bending direction (Y direction), and the passage of the operation wire 4 is composed of the tube 13 and the close contact coils 23 and 24 arranged on the distal end side of the tube 13. The close contact coil 24 disposed on the outer side in the bending direction is a close contact coil with zero initial tension disposed from the bending portion 6 to a part of the tubular flexible portion 5, and the close contact coil 23 disposed on the inner side in the bending direction is the bending portion 6. Adhesion coil with high initial tension placed inside , It may be different deformation ease with curved inwardly curved outward of the tubular flexible portion 5.
Other configurations are the same as those in the first embodiment.

第2実施形態による位置決め医療機器は、操作ワイヤ4の通路に張力の異なる密着コイルを使用したことにより、第1実施形態と同様に、操作ワイヤ4による牽引力を受けたときに、湾曲方向内側が湾曲方向外側よりも牽引力に対する抵抗力が大きくなり圧縮され難くなる為、管状可撓部5の湾曲方向外側へののけぞりを回避することができ、操作者が意図した位置に容易に先端を位置させることができて操作性が良い。   Since the positioning medical device according to the second embodiment uses a close-contact coil having different tension in the passage of the operation wire 4, when receiving the traction force by the operation wire 4, the inner side in the bending direction is the same as in the first embodiment. Since the resistance force to the traction force is larger than the outer side in the bending direction and it is difficult to compress, the sliding of the tubular flexible portion 5 to the outer side in the bending direction can be avoided, and the tip can be easily positioned at the position intended by the operator. It is easy to operate.

なお、本実施形態においては、操作ワイヤ4の通路に張力の異なる密着コイルを用いる例を示したが、これに限られず、密着コイルに代えて、湾曲方向内側には摩擦係数の高い樹脂からなるチューブを用い、湾曲方向外側には摩擦係数の低い樹脂からなるチューブを用いる構成としても良い。
また、操作ワイヤ4の通路に使用する密着コイル、または上記摩擦係数の異なるチューブの配置を湾曲方向内側と湾曲方向外側とで逆にした場合には、従来技術よりも操作ワイヤ4の牽引時に管状可撓部5湾曲方向外側へ大きくのけぞるため、図4に示すように、先端側管状部7の先端(本実施形態においては先端キャップ10)が、湾曲前と中心軸Nに対する距離がほぼ変化せずに可撓性シース2の中心軸Nに直交する方向に向き(すなわち先端が側方を向き)、このことから処置対象に先端を当接させ易くなり、この場合においておも操作者が意図した位置に先端を位置させることができて操作性が良い。
In the present embodiment, an example in which a contact coil having different tension is used in the passage of the operation wire 4 is shown. However, the present invention is not limited to this, and instead of the contact coil, the inside of the bending direction is made of a resin having a high friction coefficient. A tube may be used, and a tube made of a resin having a low friction coefficient may be used on the outer side in the bending direction.
Further, when the arrangement of the close contact coils used in the passage of the operation wire 4 or the tubes having different friction coefficients is reversed between the inside in the bending direction and the outside in the bending direction, the tube is more tubular when the operation wire 4 is pulled than in the prior art. As shown in FIG. 4, the distance between the distal end of the distal end side tubular portion 7 (the distal end cap 10 in this embodiment) and the center axis N changes substantially as shown in FIG. Without being oriented in the direction perpendicular to the central axis N of the flexible sheath 2 (that is, the distal end faces sideways), which makes it easier to bring the distal end into contact with the treatment target. The tip can be positioned at the position where it is placed, and operability is good.

また、本発明は、上記実施形態に限られず、上記構成に代えて、または併用して、電極やセンサーなどに接続するリードワイヤ(図示せず)等の内蔵物を湾曲方向内側または湾曲方向外側に偏在させることにより、偏在した側に変形抵抗性をもたせることができ、上記実施形態と同様の効果を発生させることもできる。   Further, the present invention is not limited to the above-described embodiment, and instead of or in combination with the above-described configuration, a built-in object such as a lead wire (not shown) connected to an electrode, a sensor, or the like is bent inward or outward in the bending direction. By being unevenly distributed, deformation resistance can be given to the unevenly distributed side, and the same effect as in the above embodiment can be generated.

1 位置決め医療機器
2 可撓性シース
3 操作部
4 操作ワイヤ
5 管状可撓部
5a 湾曲方向内側半部
5b 湾曲方向外側半部
6 湾曲部
7 先端側管状部
X 湾曲方向内側
Y 湾曲方向外側
DESCRIPTION OF SYMBOLS 1 Positioning medical device 2 Flexible sheath 3 Operation part 4 Operation wire 5 Tubular flexible part 5a Curve direction inner side half part 5b Curve direction outer side half part 6 Curve part 7 Tip side tubular part X Curve direction inner side Y Curve direction outer side

Claims (10)

操作部と、該操作部に連結される管状の可撓性シースを有し、該可撓性シースが、前記操作部側から延伸する管状可撓部と、該管状可撓部に接合され前記操作部の操作により湾曲する湾曲部と、該湾曲部に接合され処置対象に働きかける作用部位を有する先端側管状部とからなり、前記操作部の操作によって、前記可撓性シース内に配置された操作ワイヤを牽引することにより前記先端側管状部を牽引して前記湾曲部を湾曲させる位置決め医療機器であって、
前記管状可撓部を、前記湾曲部と隣接する位置から所定の長さに亘って前記湾曲部の湾曲方向内側に連続する面と湾曲方向外側に連続する面との変形容易性が異なるよう構成したことを特徴とする位置決め医療機器。
An operation portion; and a tubular flexible sheath connected to the operation portion, the flexible sheath extending from the operation portion side, and the tubular flexible portion joined to the tubular flexible portion. A bending portion that is bent by the operation of the operation portion and a distal-side tubular portion that is joined to the bending portion and has an action portion that acts on a treatment target, and is disposed in the flexible sheath by the operation of the operation portion. A positioning medical device that pulls the distal tubular portion by pulling an operation wire to bend the bending portion,
The tubular flexible portion is configured so that the deformability of a surface continuous on the inside in the bending direction of the bending portion and a surface continuous on the outside in the bending direction are different from each other for a predetermined length from a position adjacent to the bending portion. Positioning medical device characterized by that.
前記所定の長さは、少なくとも前記湾曲部と前記先端側管状部とを合わせた長さと同程度であることを特徴とする請求項1に記載の位置決め医療機器。   The positioning medical device according to claim 1, wherein the predetermined length is at least as long as a combined length of the bending portion and the distal tubular portion. 前記管状可撓部は、前記湾曲方向内側に連続する面の硬度を前記湾曲方向外側に連続する面の硬度よりも高くすることにより前記変形容易性が異なるよう構成したことを特徴とする請求項1または2に記載の位置決め医療機器。   The tubular flexible portion is configured such that the ease of deformation is different by making the hardness of a surface continuous on the inner side in the bending direction higher than the hardness of a surface continuous on the outer side in the bending direction. The positioning medical device according to 1 or 2. 前記管状可撓部は、前記湾曲方向内側に連続する面に架橋性物質を含浸し架橋させ、前記湾曲方向内側に連続する面の弾性率を前記湾曲方向外側に連続する面の弾性率よりも大きくすることにより前記変形容易性が異なるよう構成したことを特徴とする請求項1乃至3のいずれかに記載の位置決め医療機器。   The tubular flexible portion is formed by impregnating a cross-linking substance into a surface continuous on the inside in the bending direction and cross-linking the surface, and the elastic modulus of the surface continuous on the inside in the bending direction is higher than the elastic modulus of the surface continuous on the outside in the bending direction. The positioning medical device according to any one of claims 1 to 3, wherein the ease of deformation is changed by increasing the size. 前記管状可撓部は、前記湾曲方向内側に連続する面の壁厚を前記湾曲方向外側に連続する面の壁厚よりも厚くすることにより前記変形容易性が異なるよう構成したことを特徴とする請求項1乃至4のいずれかに記載の位置決め医療機器。   The tubular flexible portion is configured such that the ease of deformation is different by making the wall thickness of the surface continuous on the inside in the bending direction thicker than the wall thickness of the surface continuous on the outside in the bending direction. The positioning medical device according to any one of claims 1 to 4. 前記可撓性シースには、前記作用部位に連結するリードワイヤ等の内蔵物が配置され、該内蔵物を前記可撓性シース内の前記湾曲方向内側に偏在させることにより前記変形容易性が異なるように構成したことを特徴とする請求項1乃至5のいずれかに記載の位置決め医療機器。   The flexible sheath is provided with a built-in object such as a lead wire connected to the working site, and the deformability is different by making the built-in object unevenly distributed in the bending direction inside the flexible sheath. The positioning medical device according to any one of claims 1 to 5, wherein the positioning medical device is configured as described above. 前記管状可撓部は、前記湾曲方向外側に連続する面の硬度を前記湾曲方向内側に連続する面の硬度よりも高くすることにより前記変形容易性が異なるよう構成したことを特徴とする請求項1または2に記載の位置決め医療機器。   The tubular flexible portion is configured such that the ease of deformation is different by making the hardness of the surface continuous on the outside in the bending direction higher than the hardness of the surface continuous on the inside in the bending direction. The positioning medical device according to 1 or 2. 前記管状可撓部は、前記湾曲方向外側に連続する面に架橋性物質を含浸し架橋させ、前記湾曲方向外側に連続する面の弾性率を前記湾曲方向内側に連続する面の弾性率よりも大きくすることにより前記変形容易性が異なるよう構成したことを特徴とする請求項1、2、7のいずれかに記載の位置決め医療機器。   The tubular flexible portion is formed by impregnating a cross-linkable substance into a surface continuous on the outside in the bending direction and cross-linking the surface, so that the elastic modulus of the surface continuous on the outside in the bending direction is higher than the elastic modulus of the surface continuous on the inside in the bending direction. The positioning medical device according to any one of claims 1, 2, and 7, wherein the deformability is changed by increasing the size. 前記管状可撓部は、前記湾曲方向外側に連続する面の壁厚を前記湾曲方向内側に連続する面の壁厚よりも厚くすることにより前記変形容易性が異なるよう構成したことを特徴とする請求項1、2、7、8のいずれかに記載の位置決め医療機器。   The tubular flexible part is configured such that the ease of deformation is different by making the wall thickness of the surface continuous to the outside in the bending direction thicker than the wall thickness of the surface continuous to the inside of the bending direction. The positioning medical device according to any one of claims 1, 2, 7, and 8. 前記可撓性シースには、前記作用部位に連結するリードワイヤ等の内蔵物が配置され、該内蔵物を前記可撓性シース内の前記湾曲方向外側に偏在させることにより前記変形容易性が異なるように構成したことを特徴とする請求項1、2、7、8、9のいずれかに記載の位置決め医療機器。   The flexible sheath is provided with a built-in object such as a lead wire connected to the action site, and the deformability is different by making the built-in object unevenly distributed outside the bending direction in the flexible sheath. The positioning medical device according to any one of claims 1, 2, 7, 8, and 9, wherein the positioning medical device is configured as described above.
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WO2017013908A1 (en) * 2015-07-21 2017-01-26 オリンパス株式会社 Endoscope

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