JPS6324886Y2 - - Google Patents
Info
- Publication number
- JPS6324886Y2 JPS6324886Y2 JP1983090233U JP9023383U JPS6324886Y2 JP S6324886 Y2 JPS6324886 Y2 JP S6324886Y2 JP 1983090233 U JP1983090233 U JP 1983090233U JP 9023383 U JP9023383 U JP 9023383U JP S6324886 Y2 JPS6324886 Y2 JP S6324886Y2
- Authority
- JP
- Japan
- Prior art keywords
- tube
- coil body
- treatment instrument
- section
- instrument insertion
- 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
Links
Landscapes
- Instruments For Viewing The Inside Of Hollow Bodies (AREA)
Description
【考案の詳細な説明】
本考案は内視鏡の処置具挿通管の改良に関す
る。[Detailed Description of the Invention] The present invention relates to an improvement of a treatment instrument insertion tube of an endoscope.
内視鏡において鉗子等の処置具を挿通するた
め、その内視鏡の挿入部内には挿通用チヤンネル
を形成する可撓性の挿通管が配設されている。と
ころで、この挿通管として単にプラスチツク製の
チユーブを使用すると、湾曲させたときに腰折れ
(チユーブの一部が扁平になつて急角度で折れる
現象)が激しく、これを防ぐため壁厚の大きなも
のを採用せざるを得ない。しかし、内視鏡の処置
具挿通管としてはできるだけその外径を小さくす
る必要がある。そこで、処置具挿通管の外周にコ
イルを巻装する方式として未公開ではあるが本件
出願人実願昭57−131015号(実開昭59−36302号
公報)に示されるものを提案した。この出願に示
された方式によれば、確かにチユーブが腰折れし
ずらくなる。しかしながら、この方式は上記チユ
ーブに素線の断面形状を改良したコイル体を単に
巻装しているだけである。そのため、上記チユー
ブを大きな湾曲角度、または小さな曲率半径に曲
げたときに、その湾曲部分の外側壁に大きな引張
力が発生し、内側壁に大きな圧縮力が発生する
と、これらの力によつて上記チユーブに腰折れが
生じるということがあつた。とくに、上記チユー
ブの内径が大きい場合にはこのような現象が顕著
になる傾向がある。 In order to insert a treatment instrument such as forceps into an endoscope, a flexible insertion tube forming an insertion channel is disposed within the insertion portion of the endoscope. By the way, if you simply use a plastic tube as the insertion tube, it will easily bend at the waist (a phenomenon in which a part of the tube becomes flattened and breaks at a steep angle), so to prevent this, use one with a thick wall. I have no choice but to adopt it. However, it is necessary to make the outer diameter of the treatment instrument insertion tube of an endoscope as small as possible. Therefore, we have proposed a method for winding a coil around the outer periphery of the treatment instrument insertion tube, which has not yet been published, but is shown in Utility Model Application No. 57-131015 (Japanese Utility Model Application No. 59-36302) filed by the present applicant. According to the method shown in this application, the tube is certainly less likely to buckle. However, in this method, a coil body having an improved cross-sectional shape of the wire is simply wound around the tube. Therefore, when the tube is bent to a large bending angle or a small radius of curvature, a large tensile force is generated on the outer wall of the curved portion and a large compressive force is generated on the inner wall. There was an incident where Tube broke his back. Particularly, when the inner diameter of the tube is large, this phenomenon tends to become noticeable.
本考案は上記事情にもとづきなされたもので、
その目的とするところは、チユーブを大きな湾曲
角度で曲げた場合でも、上記チユーブに腰折れが
生じないようにした内視鏡の処置具挿通管を提供
することにある。 This idea was made based on the above circumstances,
The object thereof is to provide a treatment instrument insertion tube for an endoscope in which the tube does not bend at the waist even when the tube is bent at a large angle of curvature.
以下、本考案の一実施例を図面を参照して説明
する。第1図中11は内視鏡の挿入部であり、こ
の挿入部11の基端は図示しない操作部に連結さ
れている。この挿入部11は基端側に位置する可
撓管部12と、この可撓管部12の先端に連結さ
れた湾曲管部13と、この湾曲管部13の先端に
連結された先端硬性部14とから構成されてい
る。上記可撓管部12は外力によつて湾曲される
よう構成されている。また、上記湾曲管部13は
複数の湾曲駒15を互いに回動自在に連結した湾
曲芯16の外周に外皮17を被覆してなる。この
湾曲管部13は、上記挿入部11内に挿通され先
端を上記先端硬性部14に連結した複数の操作ワ
イヤ18を上記操作部側で押し引きすることによ
り強制的に湾曲させられるようになつている。上
記先端硬性部14には外部に開口する通孔19が
形成され、またこの他には対物レンズ系21など
内視鏡に必要なものが設けられている。さらに、
上記挿入部11内にはイメージガイドフアイバ2
2および処置具挿通管23などが挿通されてい
る。そして、上記イメージガイドフアイバ22の
先端は先端硬性部14に取付固定され、上記対物
レンズ系21に対し光学的に接続されている。ま
た、上記処置具挿通管23の先端は上記通孔19
に連通するよう先端硬性部14に取付固定されて
いる。さらに、この処置具挿通管23の基端側は
上記操作部に導かれ、この操作部に形成された処
置具挿入口部(図示せず)に連結されている。す
なわち、上記処置具挿通管23は鉗子、カテーテ
ル、高周波治療具などの処置具30(第4図に示
す)を体腔内へ挿通するための挿通用チヤンネル
24を形成している。また、この挿通用チヤンネ
ル24を利用して吸引を行なうこともできる。 An embodiment of the present invention will be described below with reference to the drawings. Reference numeral 11 in FIG. 1 is an insertion section of the endoscope, and the proximal end of this insertion section 11 is connected to an operation section (not shown). The insertion section 11 includes a flexible tube section 12 located on the proximal side, a curved tube section 13 connected to the distal end of the flexible tube section 12, and a rigid distal end section connected to the distal end of the curved tube section 13. It consists of 14. The flexible tube section 12 is configured to be bent by external force. Further, the bending tube portion 13 is formed by covering the outer periphery of a bending core 16 in which a plurality of bending pieces 15 are rotatably connected to each other with an outer skin 17. The bending tube section 13 can be forcibly bent by pushing and pulling a plurality of operation wires 18 inserted into the insertion section 11 and having their tips connected to the rigid tip section 14 on the operation section side. ing. A through hole 19 that opens to the outside is formed in the rigid tip portion 14, and other components necessary for the endoscope, such as an objective lens system 21, are provided. moreover,
An image guide fiber 2 is provided inside the insertion section 11.
2 and a treatment instrument insertion tube 23 are inserted therethrough. The tip of the image guide fiber 22 is attached and fixed to the rigid tip portion 14, and is optically connected to the objective lens system 21. Further, the tip of the treatment instrument insertion tube 23 is connected to the through hole 19.
It is attached and fixed to the tip rigid portion 14 so as to communicate with the tip. Further, the proximal end side of the treatment instrument insertion tube 23 is guided to the operation section and connected to a treatment instrument insertion opening (not shown) formed in the operation section. That is, the treatment instrument insertion tube 23 forms an insertion channel 24 through which a treatment instrument 30 (shown in FIG. 4) such as forceps, a catheter, or a high-frequency treatment instrument is inserted into the body cavity. In addition, suction can also be performed using this insertion channel 24.
上記処置具挿通管23は第2図に示すように構
成されている。すなわち、この処置具挿通管23
は、たとえば沸素樹脂材などで成形された可撓性
を有するチユーブ25の外周のほぼ上記湾曲管部
13内に位置する部分にだけコイル体26を嵌挿
するとともに、上記チユーブ25には上記コイル
体26の素線27間に位置する部分を径方向外方
へ隆起させた隆起部28を形成してなる。この隆
起部28は、たとえばチユーブ25を成形すると
きに同時に成形するなどして設ける。また、上記
チユーブ25は全長にわたつて内径寸法がdで、
コイル体26が巻装された部分の肉厚tは他の部
分の肉厚t1に比べて薄く形成されている。つま
り、肉厚tの部分は、肉厚t1の部分に比べて外径
寸法が小さく形成されている。さらに、上記コイ
ル体26はその素線27の断面形状が第3図に示
すように長軸方向の寸法がa、短軸方向の寸法が
bの長円形状、つまり断面円形状の線材を押し潰
すことによつて長軸方向両端が半円形となつた長
円形状に形成されていて、その長軸方向をチユー
ブ25の軸方向に沿わせている。そして、この素
線27を所定のピツチpで螺旋状に巻くことによ
り上記コイル体26が形成されている。このコイ
ル体26の内径寸法は上記チユーブ25のコイル
体26が巻装される部分が外径寸法とほぼ等しく
設定される。 The treatment instrument insertion tube 23 is constructed as shown in FIG. That is, this treatment instrument insertion tube 23
In this case, the coil body 26 is inserted only into a portion of the outer periphery of a flexible tube 25 made of, for example, a fluorine resin material, which is located approximately inside the curved tube portion 13, and the coil body 26 is inserted into the tube 25. A raised portion 28 is formed by raising a portion of the coil body 26 between the strands 27 radially outward. This raised portion 28 is provided, for example, by being molded simultaneously when the tube 25 is molded. Further, the inner diameter of the tube 25 is d over the entire length,
The wall thickness t of the portion where the coil body 26 is wound is formed to be thinner than the wall thickness t 1 of the other portion. In other words, the portion with the wall thickness t is formed to have a smaller outer diameter than the portion with the wall thickness t1 . Furthermore, the coil body 26 has a cross-sectional shape of the wire 27, which is an oval shape with a dimension a in the major axis direction and a dimension b in the minor axis direction, as shown in FIG. By crushing it, it is formed into an elliptical shape with semicircular ends at both ends in the longitudinal direction, and the longitudinal direction is aligned along the axial direction of the tube 25. The coil body 26 is formed by spirally winding this wire 27 at a predetermined pitch p. The inner diameter of the coil body 26 is set to be approximately equal to the outer diameter of the portion of the tube 25 around which the coil body 26 is wound.
なお、本実施例においては、チユーブ25に沸
素樹脂を用い、dは1.5〜3mm、tは0.1〜0.3mm、
aは0.2〜0.8mm、bは0.1〜0.3mm、pはaの1.5〜
3倍とした。また、(p−a)の寸法、すなわち
コイル体26の素線27間の寸法はtの2倍より
大きく5倍より小さい寸法とした。 In this example, fluororesin is used for the tube 25, d is 1.5 to 3 mm, t is 0.1 to 0.3 mm,
a is 0.2 to 0.8 mm, b is 0.1 to 0.3 mm, p is 1.5 to a
It was tripled. Further, the dimension (p-a), that is, the dimension between the strands 27 of the coil body 26, was set to be larger than twice t and smaller than 5 times t.
しかして、上記構成によれば、チユーブ25の
コイル体26を巻装した部分は、湾曲管部13が
強制的に湾曲させられたとき、それに応じて第4
図に示すように湾曲する。このとき、上記コイル
体26が適度な剛性を示すとともに、この剛性に
よつてチユーブ25の径方向の形状が全体にわた
つて円形に保持されるから、上記チユーブ25が
腰折れを起こすことがほとんどない。またチユー
ブ25が湾曲させられたとき、このチユーブ25
の湾曲部分の外側になる部分の隆起部28が伸
び、ここに加わる引張力を分散し、内側になる部
分の隆起部28が圧縮されてここに加わる圧縮力
を吸収する。したがつて、上記チユーブ25をと
くに大きな湾曲角度で曲げても、上記チユーブ2
5には腰折れが生じることがほとんどない。ま
た、コイル体26の素線27間の寸法、つまり
(p−a)をチユーブ25のコイル体26が巻装
される部分の肉厚tの2倍〜5倍の範囲にしたか
ら、上記チユーブ25が湾曲させられたときにそ
の湾曲部分の隣り合う素線27が互いに接触する
のが防げる。したがつて、湾曲部分の内側になる
部分の隆起部28が上記素線27間に突出して確
実に圧縮変形するから、このことによつてもチユ
ーブ25の腰折れを防ぐことになる。さらに、チ
ユーブ25を湾曲して処置具30を挿通する場
合、この処置具30の先端部は上記チユーブ25
の湾曲部分の隆起部28が伸びた外側の内面に沿
つて案内されるから、上記隆起部28に処置具3
0が引掛り、その挿通が円滑に行なえなくなると
いうことがない。 According to the above configuration, when the curved tube portion 13 is forcibly bent, the portion of the tube 25 around which the coil body 26 is wound is arranged in the fourth position.
Curve as shown. At this time, the coil body 26 exhibits appropriate rigidity, and this rigidity maintains the entire radial shape of the tube 25 in a circular shape, so that the tube 25 hardly bends at the waist. . Also, when the tube 25 is bent, this tube 25
The ridges 28 on the outside of the curved portion extend to disperse the tensile force applied thereto, and the ridges 28 on the inside are compressed to absorb the compressive force applied thereto. Therefore, even if the tube 25 is bent at a particularly large bending angle, the tube 2
5 has almost no chance of buckling. Moreover, since the dimension between the wires 27 of the coil body 26, that is, (p-a), is set in the range of 2 to 5 times the wall thickness t of the portion of the tube 25 where the coil body 26 is wound, the tube When the wire 25 is bent, adjacent wires 27 in the curved portion are prevented from coming into contact with each other. Therefore, the raised portion 28 on the inside of the curved portion protrudes between the strands 27 and is reliably compressed and deformed, which also prevents the tube 25 from buckling. Furthermore, when the tube 25 is curved and the treatment instrument 30 is inserted, the distal end of the treatment instrument 30 is inserted into the tube 25.
The treatment instrument 3 is guided along the outer inner surface of the curved portion of the curved portion 28, so that the treatment instrument 3
There is no possibility that the 0 will get caught and the insertion will not be carried out smoothly.
また、上記チユーブ25は、コイル体26が巻
装される部分の肉厚tを他の部分に比べて薄くし
たから、それだけコイル体26の径方向外方への
突出を小さくできる。つまり、処置具挿通管23
を全長にわたつて細くすることができる。 Furthermore, since the tube 25 has a wall thickness t thinner at the portion around which the coil body 26 is wound than other portions, the radial outward protrusion of the coil body 26 can be reduced accordingly. In other words, the treatment instrument insertion tube 23
can be made thinner over its entire length.
なお、上記一実施例ではコイル体25の素線2
7の断面形状を長円形としたが、その断面形状は
長方形や円形などであつてもよい。 In addition, in the above embodiment, the strands 2 of the coil body 25
Although the cross-sectional shape of No. 7 is oval, the cross-sectional shape may be rectangular, circular, or the like.
また、チユーブ25に形成する隆起部28は、
コイル体26が嵌挿される部分の全体に形成して
もよくあるいは一部分にだけ形成してもよい。一
部分にだけ隆起部28を形成する場合、上記チユ
ーブ25が最も大きな湾曲角度で湾曲される湾曲
管部13の軸方向中央部分に対応する個所に形成
するのが効果的である。 Moreover, the raised portion 28 formed on the tube 25 is
The coil body 26 may be formed over the entire portion into which the coil body 26 is inserted, or may be formed only on a portion thereof. When the raised portion 28 is formed only in one portion, it is effective to form it at a location corresponding to the axial center portion of the curved tube portion 13 where the tube 25 is curved at the largest bending angle.
以上述べたように本考案は、可撓性チユーブの
少なくとも湾曲管部と対応する部分の外周にコイ
ル体を嵌挿する処置具挿通管において、上記チユ
ーブの上記コイル体が嵌挿される部分の肉厚を他
の部分に比べて薄くするとともに、上記チユーブ
の素線間に位置する部分を径方向外方に隆起させ
た隆起部に形成した。したがつて、チユーブが湾
曲させられたときに、その湾曲部分の外側に位置
する隆起部が伸びて引張力を分散し、内側に位置
する隆起部が圧縮されて圧縮力を吸収するから、
上記引張力や圧縮力によつてチユーブが腰折れす
ることがほとんどなく、とくに湾曲させたときに
大きな引張力や圧縮力が発生する内径が大きなチ
ユーブには極めて有効である。また、チユーブの
コイル体が嵌挿される部分の肉厚を他の部分より
も薄くしたので、それだけ処置具挿通管の外径を
細くし、挿入部のとくに湾曲管部の細径化による
挿入性の向上を計ることができ、さらにチユーブ
の外側にだけコイル体が設けられるため、使用後
におけるチユーブ内面の洗浄を容易かつ確実に行
なうことができる。 As described above, the present invention provides a treatment instrument insertion tube in which a coil body is inserted into the outer periphery of at least the portion corresponding to the curved tube portion of the flexible tube. The thickness was made thinner than other parts, and the part of the tube located between the strands was formed into a raised part raised outward in the radial direction. Therefore, when the tube is bent, the ridges located on the outside of the curved portion stretch to disperse the tensile force, and the ridges located on the inside are compressed and absorb the compressive force.
The tube hardly bends due to the above-mentioned tensile force or compressive force, and is particularly effective for tubes with a large inner diameter that generate large tensile force or compressive force when curved. In addition, since the wall thickness of the part where the coil body of the tube is inserted is made thinner than other parts, the outer diameter of the treatment instrument insertion tube is made thinner accordingly, and the insertion part, especially the curved tube part, is made thinner to facilitate insertion. Furthermore, since the coil body is provided only on the outside of the tube, the inner surface of the tube can be easily and reliably cleaned after use.
図面は本考案の一実施例を示し、第1図は内視
鏡挿入部の側断面図、第2図は処置具挿通管の側
断面図、第3図はコイル体の素線の断面図、第4
図は上記処置具挿通管を湾曲させたときの側断面
図である。
25……チユーブ、26……コイル体、27…
…コイル体の素線、28……隆起部。
The drawings show one embodiment of the present invention, in which Fig. 1 is a side sectional view of the endoscope insertion section, Fig. 2 is a side sectional view of the treatment instrument insertion tube, and Fig. 3 is a sectional view of the strands of the coil body. , 4th
The figure is a side sectional view when the treatment instrument insertion tube is curved. 25...tube, 26...coil body, 27...
...Line wire of coil body, 28...Protuberance.
Claims (1)
のチユーブの少なくとも上記湾曲管部と対応す
る部分の外周にコイル体を嵌挿した内視鏡の処
置具挿通管において、上記チユーブの上記コイ
ル体が嵌挿される部分の肉厚を他の部分に比べ
て薄くするとともに、上記チユーブの上記コイ
ル体の素線間に位置する部分を径方向外方へ隆
起させた隆起部に形成したことを特徴とする内
視鏡の処置具挿通管。 (2) 上記隆起部は上記可撓性チユーブのコイル体
が嵌挿された部分の少なくとも一部に形成した
ことを特徴とする実用新案登録請求の範囲第1
項記載の内視鏡の処置具挿通管。 (3) 上記コイル体の素線間の間隔は、上記チユー
ブのコイル体が嵌挿された部分の肉厚の2倍以
上5倍以下であることを特徴とする実用新案登
録請求の範囲第1項記載の内視鏡の処置具挿通
管。 (4) 上記コイル体の素線の断面形状はほぼ長円形
もしくは長方形であることを特徴とする実用新
案登録請求の範囲第1項記載の内視鏡の処置具
挿通管。[Claims for Utility Model Registration] (1) An endoscope in which a coil body is fitted around at least the outer periphery of a flexible tube inserted into an insertion section having a curved tube section, at least in a portion corresponding to the curved tube section. In the treatment instrument insertion tube, the wall thickness of the portion of the tube into which the coil body is inserted is made thinner than other portions, and the portion of the tube located between the wires of the coil body is made radially outward. A treatment instrument insertion tube for an endoscope, characterized in that the treatment instrument insertion tube is formed in a raised part. (2) Utility model registration claim 1, characterized in that the raised portion is formed on at least a part of the portion of the flexible tube into which the coil body is inserted.
Endoscope treatment instrument insertion tube as described in section. (3) Utility model registration claim 1, characterized in that the distance between the strands of the coil body is between two times and five times the wall thickness of the portion of the tube into which the coil body is inserted. Endoscope treatment instrument insertion tube as described in section. (4) The treatment instrument insertion tube for an endoscope according to claim 1, wherein the cross-sectional shape of the wire of the coil body is approximately oval or rectangular.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9023383U JPS59196206U (en) | 1983-06-13 | 1983-06-13 | Endoscope treatment instrument tube |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9023383U JPS59196206U (en) | 1983-06-13 | 1983-06-13 | Endoscope treatment instrument tube |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59196206U JPS59196206U (en) | 1984-12-27 |
JPS6324886Y2 true JPS6324886Y2 (en) | 1988-07-07 |
Family
ID=30220138
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9023383U Granted JPS59196206U (en) | 1983-06-13 | 1983-06-13 | Endoscope treatment instrument tube |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59196206U (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0733764Y2 (en) * | 1987-05-20 | 1995-08-02 | オリンパス光学工業株式会社 | Endoscope |
JP2009254798A (en) * | 2008-03-28 | 2009-11-05 | Olympus Medical Systems Corp | Tube for endoscope |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5099515U (en) * | 1974-01-12 | 1975-08-18 | ||
JPS50122911U (en) * | 1974-03-23 | 1975-10-07 | ||
JPS5940002Y2 (en) * | 1976-12-28 | 1984-11-12 | 株式会社メドス研究所 | Bending device in endoscope |
JPS56125580U (en) * | 1980-02-26 | 1981-09-24 | ||
JPS57136432A (en) * | 1981-02-19 | 1982-08-23 | Olympus Optical Co | Tube for endoscope |
-
1983
- 1983-06-13 JP JP9023383U patent/JPS59196206U/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS59196206U (en) | 1984-12-27 |
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