JP5312868B2 - Endoscopic treatment tool - Google Patents

Endoscopic treatment tool Download PDF

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JP5312868B2
JP5312868B2 JP2008199765A JP2008199765A JP5312868B2 JP 5312868 B2 JP5312868 B2 JP 5312868B2 JP 2008199765 A JP2008199765 A JP 2008199765A JP 2008199765 A JP2008199765 A JP 2008199765A JP 5312868 B2 JP5312868 B2 JP 5312868B2
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forceps
treatment
opening
pair
forceps members
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JP2010035695A (en
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哲也 山本
啓太 鈴木
惠 木村
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Olympus Medical Systems Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a treatment tool for an endoscope which can be opened and closed while retaining sufficient open angle and width at a position near the front end of the endoscope. <P>SOLUTION: A high-frequency treatment tool 1, a treatment tool for an endoscope, includes: a treatment section 2 having a first forceps member 6 and a second forceps member 7 pivotably connected to each other by a rotation shaft 5, an urging member 11 attached so as to open the tips of the first forceps member 6 and the second forceps member 7 at a distance, and an open and close section 17 attached relatively movably in the longitudinal direction of the first forceps member 6 and the second forceps member 7. The open and close section 17 relatively moves back and forth in the open and close directions of the first forceps member 6 and the second forceps member 7, which pushes the first forceps member 6 and the second forceps member 7 against the biasing force of the urging member 11 to bring the tips of the first forceps member 6 and the second forceps member 7 into closer relationship and close them. <P>COPYRIGHT: (C)2010,JPO&amp;INPIT

Description

本発明は、経内視鏡的に体腔内に挿入されて組織に対して手技を行う内視鏡用処置具に関する。   The present invention relates to an endoscopic treatment tool that is inserted into a body cavity transendoscopically and performs a procedure on a tissue.

従来、経内視鏡的に体腔内に挿入され、患者の体腔内組織に対して様々な手技を行う内視鏡用処置具が知られている。
代表的な内視鏡用処置具として、特許文献1に記載の鉗子が知られている。この鉗子においては、回動自在に連結された一対の鉗子部材の基端側に設けられたピンが鉗子開閉部材に設けられたカム溝に挿通されている。そして、鉗子開閉部材が先端に取り付けられた操作ロッドを前進させると、上述したピンがカム溝に沿って移動することによって鉗子部材が開閉される。
2. Description of the Related Art Conventionally, an endoscopic treatment tool that is inserted into a body cavity by a transendoscope and performs various procedures on tissue in a body cavity of a patient is known.
As a typical endoscopic treatment tool, a forceps described in Patent Document 1 is known. In this forceps, a pin provided on the base end side of a pair of forceps members that are rotatably connected is inserted into a cam groove provided in a forceps opening / closing member. When the forceps opening / closing member advances the operation rod attached to the tip, the forceps member is opened / closed by moving the above-described pin along the cam groove.

また、内視鏡用処置具の他の例として、特許文献2に記載の鉗子を挙げることができる。この鉗子は、体内で処置を行うための一対の鉗子片の基端に接続された操作ワイヤを進退操作すると、鉗子片を開閉させることができるように構成されている。
特開平6−311986号公報 特開2005−58344号公報
Moreover, the forceps described in Patent Document 2 can be given as another example of the endoscope treatment tool. This forceps is configured to open and close the forceps piece when an operation wire connected to the proximal ends of a pair of forceps pieces for performing treatment in the body is advanced and retracted.
JP-A-6-311986 JP 2005-58344 A

しかしながら、特許文献1に記載の鉗子は、挿入した内視鏡の先端からあまり突出させずに鉗子部材の開閉を行うことができるものの、カム溝の形状に制限があるため、鉗子部材の開角度に限度がある。その結果、鉗子部材の充分な開き幅が得にくい。鉗子部材の長さを増大させればより大きな開き幅が確保できるが、そのために処置具としての挿入性や操作性が損なわれるという問題がある。   However, although the forceps described in Patent Document 1 can open and close the forceps member without protruding so much from the distal end of the inserted endoscope, the shape of the cam groove is limited. There is a limit. As a result, it is difficult to obtain a sufficient opening width of the forceps member. If the length of the forceps member is increased, a larger opening width can be ensured. However, there is a problem that insertability and operability as a treatment instrument are impaired.

一方、特許文献2に記載の鉗子は、鉗子片の開角度及び開き幅については特許文献1に記載の鉗子に比して良好であるものの、構造上、鉗子を充分に開く際に、鉗子片が内視鏡の先端から大きく離れることになる。その結果、内視鏡による患部の観察が困難になり、手技時の操作性が低下する等の問題がある。   On the other hand, although the forceps described in Patent Document 2 are better than the forceps described in Patent Document 1 in terms of the opening angle and opening width of the forceps pieces, the forceps pieces are structurally open when the forceps are sufficiently opened. Is far away from the tip of the endoscope. As a result, there are problems such as difficulty in observing the affected area with an endoscope and lowering operability during the procedure.

本発明は上記事情に鑑みて成されたものであり、内視鏡の先端に近い位置で、充分な開角度及び開き幅を確保しつつ開閉操作が行える内視鏡用処置具を提供することを目的とする。   The present invention has been made in view of the above circumstances, and provides an endoscope treatment tool that can be opened and closed while securing a sufficient opening angle and opening width at a position close to the distal end of the endoscope. With the goal.

本発明の内視鏡用処置具は、回動軸によって互いに回動可能に連結された一対の鉗子部材を有する処置部と、前記一対の鉗子部材の先端側が離間して開くように取り付けられた付勢部材と、前記一対の鉗子部材の長手方向に相対移動可能に取り付けられた開閉部と、前記一対の鉗子部材の少なくとも一方の外面に設けられた第1の電気接点と、前記開閉部の前記一対の鉗子部材に対向する面に設けられた第2の電気接点と、を備え、前記第2の電気接点は、高周波電源と電気的に接続可能に構成されており、前記開閉部は、前記一対の鉗子部材の開閉方向において重畳するように相対移動することによって、前記付勢部材の付勢力に抗して前記一対の鉗子部材を押圧し、前記一対の鉗子部材の前記先端側を接近させて閉じることができ、前記開閉部が前記一対の鉗子部材の長手方向に相対移動して前記第1の電気接点と前記第2の電気接点とが接触すると、前記高周波電源から前記第1の電気接点が設けられた前記鉗子部材に高周波電流が供給されることを特徴とする。 The endoscope treatment tool of the present invention is attached so that a treatment portion having a pair of forceps members connected to each other by a rotation shaft and a distal end side of the pair of forceps members are opened apart from each other. An urging member; an opening / closing portion attached to be movable relative to the longitudinal direction of the pair of forceps members; a first electrical contact provided on at least one outer surface of the pair of forceps members; A second electrical contact provided on a surface facing the pair of forceps members, the second electrical contact is configured to be electrically connectable to a high-frequency power source , The pair of forceps members are moved relative to each other so as to overlap each other, thereby pressing the pair of forceps members against the urging force of the urging member and approaching the distal ends of the pair of forceps members is not can be closed, the said When the closing portion relatively moves in the longitudinal direction of the pair of forceps members and the first electric contact and the second electric contact come into contact with each other, the forceps provided with the first electric contact from the high-frequency power source A high-frequency current is supplied to the member .

本発明の内視鏡用処置具によれば、付勢部材により、開閉することができ、かつ一対の鉗子部材の開角度が大きく保たれ、鉗子部材の長さが短くても大きな開き幅が確保される。そして、開閉部を鉗子部材に重畳するように相対移動させることによって、処置部をあまり突出させずに容易に処置部が開閉される。
さらにこの場合、処置具の一対の鉗子部材を閉じるときにだけ高周波電流を通電し、効率よく手技を行うことができる。
According to the endoscope treatment tool of the present invention, the biasing member can be opened and closed, the opening angle of the pair of forceps members is kept large, and a large opening width is obtained even when the forceps members are short. Secured. Then, by relatively moving the opening / closing part so as to overlap the forceps member, the treatment part can be easily opened / closed without causing the treatment part to protrude so much.
Furthermore, in this case, a high-frequency current can be applied only when the pair of forceps members of the treatment tool is closed, and the procedure can be performed efficiently.

本発明の内視鏡用処置具は、前記処置部が先端に設けられた第1のコイルシースと、前記第1のシースが挿通され、前記開閉部が先端側に設けられた第2のコイルシースとをさらに備えてもよい。このようにすると、処置部を開く際には第1コイルシースが圧縮され、第2コイルシースに引張張力が作用する。また、処置部が閉じられる際は、第1コイルシースに引張張力が作用し、第2コイルシースが圧縮される。したがって、圧縮及び引張張力に対する耐性を高めつつ、柔軟性をも確保することができる。   The endoscope treatment tool of the present invention includes a first coil sheath in which the treatment portion is provided at the distal end, a second coil sheath in which the first sheath is inserted, and the opening and closing portion is provided in the distal end side. May be further provided. If it does in this way, when opening a treatment part, the 1st coil sheath will be compressed and tensile tension will act on the 2nd coil sheath. Further, when the treatment portion is closed, tensile tension acts on the first coil sheath, and the second coil sheath is compressed. Therefore, flexibility can be ensured while enhancing resistance to compression and tensile tension.

本発明の内視鏡用処置具によれば、内視鏡の先端に近い位置で、充分な開角度及び開き幅を確保しつつ開閉操作を行うことができる。   According to the endoscope treatment tool of the present invention, the opening / closing operation can be performed at a position close to the distal end of the endoscope while ensuring a sufficient opening angle and opening width.

以下、図1から図5を参照して本発明の第1実施形態の内視鏡用処置具について説明する。本実施形態の内視鏡用処置具の一例である高周波処置具1は、図示しない電源から高周波電流が供給されて使用されるものであり、図1に示すように、体腔内組織に対して処置を行うための処置部2と、処置部2を操作するための操作部3と、処置部2と操作部3とを接続するための挿入部4とを備えて構成されている。   Hereinafter, an endoscope treatment tool according to a first embodiment of the present invention will be described with reference to FIGS. 1 to 5. A high-frequency treatment instrument 1 which is an example of an endoscopic treatment instrument of the present embodiment is used by being supplied with a high-frequency current from a power source (not shown). As shown in FIG. The treatment part 2 for performing a treatment, the operation part 3 for operating the treatment part 2, and the insertion part 4 for connecting the treatment part 2 and the operation part 3 are provided.

図2は、高周波処置具1の先端側を一部断面で示す拡大図である。図2に示すように、処置部2は、回動軸5で互いに回動自在に連結された第1鉗子部材6と第2鉗子部材7との一対の鉗子部材を備えている。   FIG. 2 is an enlarged view showing the distal end side of the high-frequency treatment instrument 1 in a partial cross section. As shown in FIG. 2, the treatment section 2 includes a pair of forceps members including a first forceps member 6 and a second forceps member 7 that are rotatably connected to each other by a rotation shaft 5.

図2において上側に位置する第1鉗子部材6は、アルミナやジルコニアといったセラミック部材、又はポリテトラフルオロエチレン(PTFE)、PEEK(登録商標)等の樹脂で構成されており、絶縁性を有している。なお、このような構成に代えてステンレス等の金属で構成されて表面に絶縁コーティングがなされたものでもよい。   The first forceps member 6 located on the upper side in FIG. 2 is made of a ceramic member such as alumina or zirconia, or a resin such as polytetrafluoroethylene (PTFE) or PEEK (registered trademark), and has an insulating property. Yes. In addition, it may replace with such a structure and may be comprised with metals, such as stainless steel, and the insulating coating was made | formed on the surface.

一方、下側の第2鉗子部材7は、ステンレス等の導電体で形成されており、第1鉗子部材6と対向する先端側の領域が処置時に体腔内組織に通電するための電極部8として機能する。第1鉗子部材6は、接続部材9を介して給電用のワイヤ10と接続されている。
なお、第2鉗子部材7は、電極部8以外の部分には絶縁処理が施されてもよい。当該絶縁処理においては、絶縁コーティングが用いられてもよいし、絶縁性の部材が接着等によって取り付けられてもよい。
On the other hand, the lower second forceps member 7 is formed of a conductive material such as stainless steel, and an electrode portion 8 for energizing the tissue in the body cavity at the distal end region facing the first forceps member 6 during treatment. Function. The first forceps member 6 is connected to a power supply wire 10 via a connection member 9.
Note that the second forceps member 7 may be subjected to an insulation process on portions other than the electrode portion 8. In the insulation process, an insulation coating may be used, or an insulating member may be attached by adhesion or the like.

図2及び図3に示すように、第1鉗子部材6及び第2鉗子部材7には、付勢部材11が取り付けられており、各鉗子部材6、7が回動軸5を中心として回動し、先端側が離間して開くように常に開付勢されている。付勢部材11による鉗子部材6、7の開角度は、手技を好適に行うために、例えば60度以上の大きな角度に設定されるのが好ましい。付勢部材11としては、図3に示すような棒状や、板状等の部材からなる各種のバネ等の弾性を有する部材を好適に採用することができる。   As shown in FIGS. 2 and 3, a biasing member 11 is attached to the first forceps member 6 and the second forceps member 7, and the forceps members 6 and 7 rotate around the rotation shaft 5. However, it is always urged to open so that the tip side is spaced apart. The opening angle of the forceps members 6 and 7 by the urging member 11 is preferably set to a large angle of, for example, 60 degrees or more in order to perform the procedure appropriately. As the urging member 11, a member having elasticity such as various springs made of a rod-like or plate-like member as shown in FIG. 3 can be suitably used.

図2に示すように、挿入部4は、先端に処置部2が取り付けられた第1コイルシース(第1のコイルシース)12と、第1コイルシース12が軸線方向に進退可能に挿通される被覆管部13とを備えている。
第1コイルシース12は金属等の素線が密に巻かれた公知の構成を有し、内部にワイヤ10が挿通されている。第1コイルシース12の先端には、連結部材14を介して処置部2が進退不能に取り付けられている。これによって、処置部2は第1コイルシース12と一体となって進退される。
As shown in FIG. 2, the insertion portion 4 includes a first coil sheath (first coil sheath) 12 having a treatment portion 2 attached to the tip, and a cladding tube portion through which the first coil sheath 12 is inserted so as to be able to advance and retract in the axial direction. 13.
The first coil sheath 12 has a known configuration in which a strand of metal or the like is tightly wound, and the wire 10 is inserted therein. The treatment section 2 is attached to the distal end of the first coil sheath 12 through a connecting member 14 so as not to advance or retreat. As a result, the treatment section 2 is advanced and retracted integrally with the first coil sheath 12.

被覆管部13は、第1コイルシースが挿通される第2コイルシース(第2のコイルシース)15と、第2コイルシース15の外面を絶縁被覆する絶縁チューブ16と、第2コイルシース15及び絶縁チューブ16の先端側に取り付けられた開閉部17とを備えて構成されている。第2コイルシース15及び絶縁チューブ16からなる被覆管部13の基本部分は、従来の絶縁被覆された内視鏡用処置具における可撓管とほぼ同様の構成である。   The cladding tube portion 13 includes a second coil sheath (second coil sheath) 15 through which the first coil sheath is inserted, an insulation tube 16 that insulates the outer surface of the second coil sheath 15, and tips of the second coil sheath 15 and the insulation tube 16. And an opening / closing part 17 attached to the side. The basic portion of the covering tube portion 13 composed of the second coil sheath 15 and the insulating tube 16 has substantially the same configuration as that of the flexible tube in the conventional treatment instrument for endoscope that is covered with insulation.

開閉部17は、略円筒状の部材であり、接続パイプ18を介して絶縁チューブ16と一体に取り付けられている。開閉部17は、後述する処置部2の開閉操作において、鉗子部材6、7を付勢部材11の付勢力に抗して閉じることができる程度の剛性を有する材料で形成されている。   The opening / closing part 17 is a substantially cylindrical member and is integrally attached to the insulating tube 16 via a connection pipe 18. The opening / closing part 17 is formed of a material having such a rigidity that the forceps members 6 and 7 can be closed against the urging force of the urging member 11 in the opening / closing operation of the treatment part 2 described later.

図1に戻って、操作部3は、細長の操作部本体18と、操作部本体18に対して軸線方向に相対移動可能に取り付けられたスライダ19とを備えている。操作部本体18には、挿入部4が挿通される挿入部用孔18Aが設けられており、被覆管部13が挿入部用孔18Aに挿通されてその基端が接続されている。挿入部4に挿通された第1コイルシース12及びワイヤ10の基端は、スライダ19に接続されている。操作部本体18の基端には、指掛用のハンドル20が設けられている。   Returning to FIG. 1, the operation unit 3 includes an elongated operation unit main body 18 and a slider 19 attached to the operation unit main body 18 so as to be relatively movable in the axial direction. The operation portion main body 18 is provided with an insertion portion hole 18A through which the insertion portion 4 is inserted, and the cladding tube portion 13 is inserted through the insertion portion hole 18A and the base end thereof is connected. The proximal ends of the first coil sheath 12 and the wire 10 inserted through the insertion portion 4 are connected to the slider 19. A finger-handle 20 is provided at the proximal end of the operation unit body 18.

スライダ19には、図示しない高周波電源と接続された図示しない電源ケーブルが接続されるプラグ21が取り付けられており、ワイヤ10と電気的に接続されている。したがって、電源ケーブルを介して高周波電源をプラグ21に接続して通電すると、高周波電流がワイヤ10及び接続部材9を通って電極部8を有する第2鉗子部材7に供給される。   A plug 21 to which a power cable (not shown) connected to a high frequency power source (not shown) is connected is attached to the slider 19 and is electrically connected to the wire 10. Therefore, when a high frequency power source is connected to the plug 21 via the power cable and energized, the high frequency current is supplied to the second forceps member 7 having the electrode portion 8 through the wire 10 and the connection member 9.

上記のように構成された高周波処置具1の使用時の動作について説明する。
まず、図示しない公知の対極板と接触させた患者の体内に図示しない内視鏡を挿入し、処置対象の体腔内組織付近まで当該内視鏡の先端を進める。
Operation during use of the high-frequency treatment instrument 1 configured as described above will be described.
First, an endoscope (not shown) is inserted into the body of a patient in contact with a known counter electrode plate (not shown), and the distal end of the endoscope is advanced to the vicinity of the tissue in the body cavity to be treated.

続いて、スライダ19を操作部本体18に対して後退させて一対の鉗子部材6、7を閉じた状態とし(この動作については後述)、内視鏡の図示しない鉗子チャンネルに処置部2及び挿入部4を挿入する。そして、処置部2を鉗子チャンネルから突出させた後、高周波電源とプラグ21とを電源ケーブルで接続する。   Subsequently, the slider 19 is moved backward with respect to the operation portion main body 18 to close the pair of forceps members 6 and 7 (this operation will be described later), and the treatment portion 2 and the insertion into the forceps channel (not shown) of the endoscope. Insert part 4. And after making the treatment part 2 protrude from a forceps channel, the high frequency power supply and the plug 21 are connected with a power cable.

処置を行う際には、スライダ19を操作部本体18に対して前進移動させる。すると、スライダ19に接続された第1コイルシース12及びワイヤ10が被覆管部13に対して前進する。これに連動して処置部2も被覆管部13に対して前進するように相対移動し、開閉部17の先端から突出する。処置部2の鉗子部材6、7が完全に開閉部17から露出すると、付勢部材11によって鉗子部材6、7の先端側が離間するように回動し、図4に示すように処置部2が開く。   When performing the treatment, the slider 19 is moved forward with respect to the operation unit main body 18. Then, the first coil sheath 12 and the wire 10 connected to the slider 19 advance with respect to the cladding tube portion 13. In conjunction with this, the treatment portion 2 also moves relative to the cladding tube portion 13 so as to advance, and protrudes from the tip of the opening / closing portion 17. When the forceps members 6 and 7 of the treatment part 2 are completely exposed from the opening / closing part 17, the urging member 11 is rotated so that the distal end sides of the forceps members 6 and 7 are separated from each other. As shown in FIG. open.

ユーザが対象組織を処置部2の開いた鉗子部材6、7間に位置させて、スライダ19を操作部本体18の基端側に引き戻すと、第1コイルシース12及びワイヤ10が被覆管部13に対して後退し、これと連動して処置部2が開閉部17に向かって移動する。開閉部17の先端と一対の鉗子部材6、7とが当接した後もさらにスライダ19を引き戻すと、開閉部17が鉗子部材6、7の開閉方向において鉗子部材6、7と重畳する。すなわち、挿入部4の長手方向において鉗子部材6、7と開閉部17との位置が略同一となる。そして、図5に示すように、開閉部17によって鉗子部材6、7が付勢部材11の付勢力に抗して押圧されて閉じるように回動される。このようにして処置部2に対象組織が挟み込まれる。そして、電極部8が処置対象である体内組織と接触する。   When the user places the target tissue between the open forceps members 6 and 7 of the treatment section 2 and pulls the slider 19 back to the proximal end side of the operation section main body 18, the first coil sheath 12 and the wire 10 are moved to the covering tube section 13. The treatment part 2 moves toward the opening / closing part 17 in conjunction with this. When the slider 19 is further pulled back after the tip of the opening / closing part 17 and the pair of forceps members 6, 7 contact each other, the opening / closing part 17 overlaps the forceps members 6, 7 in the opening / closing direction of the forceps members 6, 7. That is, the positions of the forceps members 6 and 7 and the opening / closing part 17 are substantially the same in the longitudinal direction of the insertion part 4. Then, as shown in FIG. 5, the forceps members 6 and 7 are rotated against the biasing force of the biasing member 11 by the opening / closing part 17 so as to be closed. In this way, the target tissue is sandwiched between the treatment sections 2. And the electrode part 8 contacts the body tissue which is a treatment object.

この状態で、ユーザが高周波電源から高周波電流を供給すると、高周波電流は上述の記経路を通って電極部8まで供給され、高周波電流によって対象組織が焼灼される。
処置終了後、ユーザがさらにスライダ19を後退させると、鉗子部材6、7が完全に閉じられて挿入部4内に収容される。高周波処置具1の先端をこのような状態にしてから、ユーザは高周波処置具1を鉗子チャンネルから抜去し、かつ、内視鏡を体外へ抜去させて手技を終了する。
In this state, when the user supplies a high-frequency current from the high-frequency power source, the high-frequency current is supplied to the electrode unit 8 through the above-described path, and the target tissue is cauterized by the high-frequency current.
When the user further retracts the slider 19 after the treatment is completed, the forceps members 6 and 7 are completely closed and accommodated in the insertion portion 4. After the distal end of the high-frequency treatment instrument 1 is in such a state, the user removes the high-frequency treatment instrument 1 from the forceps channel and removes the endoscope from the body to finish the procedure.

本実施形態の高周波処置具1によれば、スライダ19を操作して処置部2を開閉部17よりも先端側に移動させて露出させると、付勢部材11の付勢力によって、一対の第1鉗子部材6及び第2鉗子部材7が回動軸5を中心に回動し、各鉗子部材6、7の先端側が大きな開角度で直ちに開かれる。したがって、挿入される内視鏡の先端付近で、かつ大きな開角度で処置部を開閉することができる内視鏡用処置具とすることができる。   According to the high-frequency treatment instrument 1 of the present embodiment, when the treatment portion 2 is moved to the distal end side with respect to the opening / closing portion 17 by the operation of the slider 19 and exposed, the pair of first forces are applied by the biasing force of the biasing member 11. The forceps member 6 and the second forceps member 7 are rotated about the rotation shaft 5, and the distal ends of the forceps members 6 and 7 are immediately opened at a large opening angle. Therefore, it is possible to provide an endoscope treatment tool that can open and close the treatment portion near the distal end of the endoscope to be inserted and at a large opening angle.

また、挿入部4が第1コイルシース12と第2コイルシース15との2つのコイルシースを備えているので、処置部2の一対の鉗子部材6、7を開く際には第1コイルシースが圧縮され、第2コイルシースに引張張力が作用する。また、鉗子部材6、7が閉じられる際は、第1コイルシースに引張張力が作用し、第2コイルシースが圧縮される。したがって、圧縮及び引張張力に対する耐性を高めつつ、柔軟性をも確保することができる。   Further, since the insertion portion 4 includes two coil sheaths, the first coil sheath 12 and the second coil sheath 15, when the pair of forceps members 6 and 7 of the treatment portion 2 are opened, the first coil sheath is compressed, Tensile tension acts on the two-coil sheath. Further, when the forceps members 6 and 7 are closed, tensile tension acts on the first coil sheath, and the second coil sheath is compressed. Therefore, flexibility can be ensured while enhancing resistance to compression and tensile tension.

本実施形態においては、一対の鉗子部材のうち、一方の第2鉗子部材7のみに高周波電流が通電される、いわゆるモノポーラ式の高周波処置具の例を示したが、これに代えて、一対の鉗子部材の両方に処置電極が設けられた、いわゆるバイポーラ式の高周波処置具として本発明の高周波処置具を構成してもよい。この場合は、第1鉗子部材6についても第2鉗子部材7と同様の構成とすればよい。   In the present embodiment, an example of a so-called monopolar type high-frequency treatment instrument in which a high-frequency current is supplied to only one second forceps member 7 out of a pair of forceps members has been described. The high-frequency treatment device of the present invention may be configured as a so-called bipolar high-frequency treatment device in which treatment electrodes are provided on both forceps members. In this case, the first forceps member 6 may be configured similarly to the second forceps member 7.

また、ワイヤ10やプラグ21を備えず、処置部に通電を行わない単なる把持鉗子として本発明の内視鏡用処置具を構成してもよい。このようにしても、上述した処置部の開閉挙動に関する効果を同様に得ることができる。   Further, the endoscope treatment tool of the present invention may be configured as a simple grasping forceps that does not include the wire 10 or the plug 21 and does not energize the treatment portion. Even if it does in this way, the effect regarding the opening-and-closing behavior of the treatment part mentioned above can be acquired similarly.

続いて、本発明の第2実施形態について、図6から図8を参照して説明する。本実施形態の高周波処置具31と上述の高周波処置具1との異なるところは、第2鉗子部材とプラグとの接続態様である。
なお、上述の高周波処置具1と共通する構成については、同一の符号を付して重複する説明を省略する。
Next, a second embodiment of the present invention will be described with reference to FIGS. The difference between the high-frequency treatment instrument 31 of the present embodiment and the above-described high-frequency treatment instrument 1 is the connection mode between the second forceps member and the plug.
In addition, about the structure which is common in the above-mentioned high frequency treatment tool 1, the same code | symbol is attached | subjected and the overlapping description is abbreviate | omitted.

図6は、高周波処置具31の先端を一部断面で示す図である。図6に示すように、高周波処置具31にはワイヤ10は設けられておらず、その代わりに、開閉部17の先端付近の内面に電気接点(第2の電気接点)32が設けられている。電気接点32には、給電コード33が接続されており、給電コード33は、第1コイルシース12と第2コイルシース15との間を通ってプラグ21(不図示)に接続されている。
また、高周波処置具31においては、プラグ21は、スライダ19ではなく、操作部本体18に取り付けられている。したがって、給電コード33及びプラグ21は操作部本体18に対して摺動不能である。
FIG. 6 is a view showing a tip of the high-frequency treatment instrument 31 in a partial cross section. As shown in FIG. 6, the high-frequency treatment instrument 31 is not provided with the wire 10, and instead, an electrical contact (second electrical contact) 32 is provided on the inner surface near the distal end of the opening / closing part 17. . A power supply cord 33 is connected to the electrical contact 32, and the power supply cord 33 passes between the first coil sheath 12 and the second coil sheath 15 and is connected to the plug 21 (not shown).
Further, in the high-frequency treatment instrument 31, the plug 21 is attached not to the slider 19 but to the operation unit main body 18. Therefore, the power supply cord 33 and the plug 21 are not slidable with respect to the operation unit main body 18.

上記のように構成された高周波処置具31の使用時の動作について以下に説明する。
スライダ19を操作部本体18に対して前進させると処置部2が開く点は、第1実施形態の高周波処置具1と同様である。
処置部2を閉じるために、スライダ19を操作部本体18に対して後退させると、開閉部17と処置部2の鉗子部材6、7とが当接する。そして、鉗子部材6、7が閉じるにしたがって、まず第2鉗子部材7の一部(第1の電気接点)と電気接点32とが接触して導通状態となる。
図7に示すように、処置部2がさらに挿入部4内に引き込まれると、鉗子部材6、7が完全に閉じられる。
The operation at the time of use of the high-frequency treatment instrument 31 configured as described above will be described below.
The point that the treatment section 2 opens when the slider 19 is moved forward with respect to the operation section main body 18 is the same as the high-frequency treatment instrument 1 of the first embodiment.
When the slider 19 is retracted with respect to the operation unit main body 18 to close the treatment unit 2, the opening / closing unit 17 and the forceps members 6 and 7 of the treatment unit 2 come into contact with each other. Then, as the forceps members 6 and 7 are closed, first, a part (first electrical contact) of the second forceps member 7 and the electrical contact 32 come into contact with each other and become conductive.
As shown in FIG. 7, when the treatment portion 2 is further drawn into the insertion portion 4, the forceps members 6 and 7 are completely closed.

本実施形態の高周波処置具31によれば、処置部2が開いており、電気接点32と接触していない時には、処置部2に高周波電流が供給されないため、処置部2が処置対象でない体腔内組織等に接触して電流が漏れるのを好適に防止することができる。
一方、鉗子部材6、7が閉じられて、予め設定した所望の開角度となるときに電極部8に高周波電流が供給されるので、例えば組織を把持したときに、確実に電極部8に高周波電流が供給されて通電処置が行われるように調整することも可能である。したがって、処置部2に必要なときにだけ確実に高周波電流を供給して効率よく処置を行うことができる。
According to the high-frequency treatment tool 31 of the present embodiment, when the treatment unit 2 is open and not in contact with the electrical contact 32, no high-frequency current is supplied to the treatment unit 2, so that the treatment unit 2 is not a treatment target in a body cavity. It is possible to suitably prevent current from leaking in contact with tissue or the like.
On the other hand, since the high-frequency current is supplied to the electrode unit 8 when the forceps members 6 and 7 are closed and the desired opening angle is set in advance, for example, when the tissue is grasped, the high-frequency current is reliably applied to the electrode unit 8 It is also possible to adjust so that a current is supplied and an energization treatment is performed. Therefore, it is possible to perform the treatment efficiently by reliably supplying the high-frequency current only when necessary to the treatment section 2.

また、給電コード33が処置部2の開閉操作に伴って進退しないため、進退に伴う力量が作用しないので、給電コード33を、例えば0.1〜0.3ミリメートル(mm)程度の細径に構成することができる。したがって、給電コード33が第1コイルシース12と第2コイルシース15との間に配線されても、第1コイルシース12の被覆管部13内における摺動を妨げることがなく、良好な操作性を保持することができる。
なお、給電コード33は、第1コイルシース12内を通ってスライダ19に接続されてもよい。
In addition, since the power supply cord 33 does not advance or retreat in accordance with the opening / closing operation of the treatment section 2, the force associated with the advancement / retraction does not act. Can be configured. Therefore, even if the power supply cord 33 is wired between the first coil sheath 12 and the second coil sheath 15, it does not prevent the first coil sheath 12 from sliding in the cladding tube portion 13 and maintains good operability. be able to.
The power supply cord 33 may be connected to the slider 19 through the first coil sheath 12.

本実施形態においては、図8に示す変形例のように、第2鉗子部材7の外面の一部が絶縁部34によって絶縁被覆されてもよい。絶縁部34は、部分的に絶縁性の部材を貼りつけたり、絶縁コーティングを施したりすることによって形成することができる。
このようにすると、絶縁部34の位置により鉗子部材6、7が閉じたとき又は開いた時のいずれか一方のみにおいて、電極部8に高周波電流を供給することが可能となる。そして、高周波電流が電極部8に供給されるときの鉗子部材6、7の開角度等も絶縁部34を形成する位置や形状等を変えることによって適宜調整することができる。
なお、この場合は、第2鉗子部材7の絶縁部34よりも先端側の外面が、電気接点34と接触して電極部8に高周波電流を供給するための第1の電気接点として機能する。
In the present embodiment, as in the modification shown in FIG. 8, a part of the outer surface of the second forceps member 7 may be covered with an insulating portion 34. The insulating part 34 can be formed by attaching a partially insulating member or applying an insulating coating.
If it does in this way, it will become possible to supply a high frequency current to the electrode part 8 only when the forceps members 6 and 7 are closed or opened depending on the position of the insulating part 34. The opening angle of the forceps members 6 and 7 when the high-frequency current is supplied to the electrode unit 8 can be adjusted as appropriate by changing the position and shape of the insulating unit 34.
In this case, the outer surface of the second forceps member 7 on the distal end side with respect to the insulating portion 34 functions as a first electrical contact for contacting the electrical contact 34 and supplying a high-frequency current to the electrode portion 8.

さらに他の例として、第2鉗子部材7の基端側の外面を全体的に絶縁被覆し、一部だけ導電性の外面を露出させ、当該外面を第1の電気接点としてもよい。   As yet another example, the outer surface of the proximal end side of the second forceps member 7 may be entirely covered with insulation, and a part of the conductive outer surface may be exposed, and the outer surface may be used as the first electrical contact.

続いて、本発明の第3実施形態について、図9及び図10を参照して説明する。本実施形態の高周波処置具41と上述の高周波処置具1との異なるところは、開閉部の形状である。
なお、上述の各実施形態と共通する構成については、同一の符号を付して重複する説明を省略する。
Next, a third embodiment of the present invention will be described with reference to FIGS. The difference between the high-frequency treatment instrument 41 of the present embodiment and the above-described high-frequency treatment instrument 1 is the shape of the opening / closing part.
In addition, about the structure which is common in each above-mentioned embodiment, the same code | symbol is attached | subjected and the overlapping description is abbreviate | omitted.

図9は高周波処置具41の先端側の側面図であり、図10は、同先端側の使用時の動作を示す斜視図である。
図9及び図10に示すように、開閉部42には、先端側に処置部2を閉じるための開閉壁面43が軸線方向に突出して設けられている。
FIG. 9 is a side view of the distal end side of the high-frequency treatment instrument 41, and FIG. 10 is a perspective view showing an operation during use of the distal end side.
As shown in FIGS. 9 and 10, the opening / closing part 42 is provided with an opening / closing wall 43 for closing the treatment part 2 on the distal end side so as to protrude in the axial direction.

開閉壁面43は、各鉗子部材6、7の開閉方向における両端に、各鉗子部材6、7の開閉面Fに対して略直交するように、2箇所設けられている。電気接点32は、第2鉗子部材7に当接する開閉壁面43Aの内面に設けられている。   Two opening / closing wall surfaces 43 are provided at both ends in the opening / closing direction of the forceps members 6 and 7 so as to be substantially orthogonal to the opening / closing surface F of the forceps members 6 and 7. The electrical contact 32 is provided on the inner surface of the open / close wall surface 43 </ b> A that contacts the second forceps member 7.

本実施形態の高周波処置具41においては、図10に示すように、2箇所の開閉壁面43が、それぞれ第1鉗子部材6及び第2鉗子部材7と当接することによって押圧されて処置部2が閉じる。そして、第2鉗子部材7の外面と電気接点32とが接触することによって電極部8に高周波電流が供給される。   In the high-frequency treatment instrument 41 of the present embodiment, as shown in FIG. 10, the two openable / closable wall surfaces 43 are pressed by contacting the first forceps member 6 and the second forceps member 7, respectively, so that the treatment section 2 is pressed. close up. Then, when the outer surface of the second forceps member 7 and the electrical contact 32 come into contact with each other, a high frequency current is supplied to the electrode portion 8.

また、開閉壁面43は図10に示す上下方向にだけ形成されているので、図10に示す状態からさらにスライダ19を一定の長さ後退させても、処置部2の幅方向の外面は開閉部42によって覆われない。したがって、開閉部42が処置部2で組織を把持する際に邪魔にならず、各鉗子部材6、7の先端側領域を充分に使って、より好適に組織を把持しながら処置部2を閉じて処置等を行うことができる。   Since the open / close wall surface 43 is formed only in the vertical direction shown in FIG. 10, even if the slider 19 is further retracted by a certain length from the state shown in FIG. 42 is not covered. Therefore, the opening / closing part 42 does not get in the way when the treatment part 2 grasps the tissue, and the treatment part 2 is closed while more appropriately grasping the tissue by fully using the distal end side regions of the forceps members 6 and 7. Treatment can be performed.

以上、本発明の各実施形態について説明したが、本発明の技術範囲は上記実施形態に限定されるものではなく、本発明の趣旨を逸脱しない範囲において種々の変更を加えることが可能である。   Although the embodiments of the present invention have been described above, the technical scope of the present invention is not limited to the above embodiments, and various modifications can be made without departing from the spirit of the present invention.

例えば、上述の各実施形態においては、挿入部が、処置部の連結された第1コイルシースと、第1コイルシースが挿通された被覆管部とを備えている例を説明したが、これに代えて、一対の鉗子部材の基端に接続されたワイヤがコイル等からなるシースに挿通され、当該シースの先端側に上述したような円筒状又は開閉壁面のような構造を有する開閉部を設けて内視鏡用処置具を構成してもよい。この場合も、ワイヤを後退させて処置部をシースに対して相対移動させ、上述したのとほぼ同様に開閉部と一対の鉗子部材とを重畳させることによって処置部を閉じることが可能である。   For example, in each of the above-described embodiments, an example has been described in which the insertion portion includes the first coil sheath connected to the treatment portion and the cladding tube portion through which the first coil sheath is inserted. A wire connected to the proximal ends of the pair of forceps members is inserted through a sheath made of a coil or the like, and an opening / closing portion having a cylindrical shape or an opening / closing wall structure as described above is provided on the distal end side of the sheath. An endoscopic treatment tool may be configured. In this case as well, it is possible to close the treatment portion by retracting the wire, moving the treatment portion relative to the sheath, and overlapping the opening / closing portion and the pair of forceps members in substantially the same manner as described above.

本発明の第1実施形態の内視鏡用処置具である高周波処置具の全体図である。1 is an overall view of a high-frequency treatment tool that is a treatment tool for an endoscope according to a first embodiment of the present invention. 同高周波処置具の先端側を一部断面で示す側面図である。It is a side view which shows the front end side of the same high frequency treatment tool in a partial cross section. 同高周波処置具の処置部を示す図である。It is a figure which shows the treatment part of the high frequency treatment tool. 同高周波処置具の使用時の動作を示す図である。It is a figure which shows the operation | movement at the time of use of the high frequency treatment tool. 同高周波処置具の使用時の動作を示す図である。It is a figure which shows the operation | movement at the time of use of the high frequency treatment tool. 本発明の第2実施形態の高周波処置具の先端側を一部断面で示す図である。It is a figure which shows the front end side of the high frequency treatment tool of 2nd Embodiment of this invention in a partial cross section. 同高周波処置具の使用時の動作を示す図である。It is a figure which shows the operation | movement at the time of use of the high frequency treatment tool. 同実施形態の変形例の高周波処置具の先端側を一部断面で示す図である。It is a figure which shows the front end side of the high frequency treatment tool of the modification of the embodiment in a partial cross section. 本発明の第3実施形態の高周波処置具の先端側を一部断面で示す側面図である。It is a side view which shows the front end side of the high frequency treatment tool of 3rd Embodiment of this invention in a partial cross section. 同先端側の使用時の動作を示す図である。It is a figure which shows the operation | movement at the time of use of the front end side.

符号の説明Explanation of symbols

1、31、41 高周波処置具(内視鏡用処置具)
2 処置部
5 回動軸
6 第1鉗子部材
7 第2鉗子部材
10 ワイヤ
11 付勢部材
12 第1コイルシース(第1のコイルシース)
15 第2コイルシース(第2のコイルシース)
17、42 開閉部
32 電気接点(第2の電気接点)
1, 31, 41 High-frequency treatment tool (endoscopic treatment tool)
2 treatment section 5 rotating shaft 6 first forceps member 7 second forceps member 10 wire 11 biasing member 12 first coil sheath (first coil sheath)
15 Second coil sheath (second coil sheath)
17, 42 Opening / closing part 32 Electrical contact (second electrical contact)

Claims (2)

回動軸によって互いに回動可能に連結された一対の鉗子部材を有する処置部と、
前記一対の鉗子部材の先端側が離間して開くように取り付けられた付勢部材と、
前記一対の鉗子部材の長手方向に相対移動可能に取り付けられた開閉部と、
前記一対の鉗子部材の少なくとも一方の外面に設けられた第1の電気接点と、
前記開閉部の前記一対の鉗子部材に対向する面に設けられた第2の電気接点と、
を備え、
前記第2の電気接点は、高周波電源と電気的に接続可能に構成されており、
前記開閉部は、前記一対の鉗子部材の開閉方向において重畳するように相対移動することによって、前記付勢部材の付勢力に抗して前記一対の鉗子部材を押圧し、前記一対の鉗子部材の前記先端側を接近させて閉じることができ
前記開閉部が前記一対の鉗子部材の長手方向に相対移動して前記第1の電気接点と前記第2の電気接点とが接触すると、前記高周波電源から前記第1の電気接点が設けられた前記鉗子部材に高周波電流が供給される
ことを特徴とする内視鏡用処置具。
A treatment portion having a pair of forceps members coupled to each other by a pivot shaft;
An urging member attached so that the distal ends of the pair of forceps members are spaced apart; and
An opening / closing part attached to the longitudinal direction of the pair of forceps members so as to be relatively movable;
A first electrical contact provided on at least one outer surface of the pair of forceps members;
A second electrical contact provided on a surface of the opening / closing portion facing the pair of forceps members;
With
The second electrical contact is configured to be electrically connectable to a high frequency power source,
The opening / closing portion moves relative to each other so as to overlap in the opening / closing direction of the pair of forceps members, thereby pressing the pair of forceps members against the biasing force of the biasing members, The tip side can be approached and closed ,
When the opening / closing part relatively moves in the longitudinal direction of the pair of forceps members and the first electrical contact and the second electrical contact come into contact with each other, the first electrical contact is provided from the high-frequency power source. A treatment instrument for an endoscope , wherein a high-frequency current is supplied to a forceps member .
前記処置部が先端に設けられた第1のコイルシースと、
前記第1のシースが挿通され、前記開閉部が先端側に設けられた第2のコイルシースと、
をさらに備えることを特徴とする請求項1に記載の内視鏡用処置具。
A first coil sheath provided at the distal end with the treatment portion;
A second coil sheath in which the first sheath is inserted and the opening / closing portion is provided on a distal end side;
The endoscopic treatment tool according to claim 1, further comprising:
JP2008199765A 2008-08-01 2008-08-01 Endoscopic treatment tool Expired - Fee Related JP5312868B2 (en)

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US9072524B2 (en) * 2012-06-29 2015-07-07 Covidien Lp Surgical forceps
GB201322844D0 (en) * 2013-12-23 2014-02-12 Creo Medical Ltd Electrosurgical device
US9987076B2 (en) * 2014-09-17 2018-06-05 Covidien Lp Multi-function surgical instruments

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US5211655A (en) * 1992-05-08 1993-05-18 Hasson Harrith M Multiple use forceps for endoscopy
JP3354032B2 (en) * 1995-04-06 2002-12-09 オリンパス光学工業株式会社 Surgical forceps and ultrasonic coagulation and incision device
JP2002253563A (en) * 2001-03-02 2002-09-10 Olympus Optical Co Ltd Treatment instrument for endoscope

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