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JP2013158492A - Tool for high frequency wave treatment - Google Patents

Tool for high frequency wave treatment Download PDF

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JP2013158492A
JP2013158492A JP2012023285A JP2012023285A JP2013158492A JP 2013158492 A JP2013158492 A JP 2013158492A JP 2012023285 A JP2012023285 A JP 2012023285A JP 2012023285 A JP2012023285 A JP 2012023285A JP 2013158492 A JP2013158492 A JP 2013158492A
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flexible tube
treatment
operation wire
high frequency
distal end
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JP5884534B2 (en
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Yasuhisa Ishii
靖久 石井
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Sumitomo Bakelite Co Ltd
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Sumitomo Bakelite Co Ltd
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Abstract

PROBLEM TO BE SOLVED: To provide a tool for a high frequency wave treatment making the treatment easy irrespective of the position of an affected part, and without having any bad effect on his healthy area other than the affected part.SOLUTION: A tool for a high frequency wave treatment includes a treatment section, an operation wire having the treatment section at its leading end, and a first flexible tube where the operation wire is slidably inserted through. A second flexible tube for adjusting the operation conditions of the treatment section is detachably extending from the first flexible tube. As the operation conditions of the treatment section can be adjusted by such structure, treatment can become easier, regardless of the position of an affected region. Further the treatment tool reduces the possibility of having any harmful effect on regions other than the affected part.

Description

本発明は高周波処置具に関する。   The present invention relates to a high-frequency treatment instrument.

高周波処置具は、体内の病変部位において高周波電流を利用して行う処置に用いられる。一般的に高周波処置具は、体腔内に挿入される可撓管と、可撓管内に進退自在に挿通された操作ワイヤと、操作ワイヤ先端部に配置され高周波電流の印加により患部を処置する処置部と、操作ワイヤに当接して高周波電流を印加する高周波印加部と、可撓管の基端部に付設され操作ワイヤを介して処置部を操作する操作部で構成されている。   The high-frequency treatment tool is used for treatment performed using a high-frequency current at a lesion site in the body. Generally, a high-frequency treatment instrument is a treatment that treats an affected area by applying a high-frequency current to a flexible tube that is inserted into a body cavity, an operation wire that is inserted into the flexible tube so as to freely advance and retract, and a distal end portion of the operation wire. A high-frequency application unit that applies a high-frequency current in contact with the operation wire, and an operation unit that is attached to the proximal end of the flexible tube and operates the treatment unit via the operation wire.

この高周波処置具は、外部の高周波電源装置から高周波電源接続コードを介して操作ワイヤおよび操作ワイヤの先端部に付設された処置部に高周波電流を流すことで患部の切離・止血等の処置を行うものである。   This high-frequency treatment instrument performs treatment such as separation and hemostasis of an affected part by flowing a high-frequency current from an external high-frequency power supply device to the operation wire and a treatment part attached to the distal end of the operation wire via a high-frequency power supply connection cord. Is what you do.

このような高周波処置具として、処置部に針状電極を有し、この針状電極を可撓管本体から任意の長さに突出させてから患部の切離等の処置を行うものが開示されている(例えば、特許文献1参照)。   As such a high-frequency treatment instrument, there is disclosed a device having a needle-like electrode in a treatment portion, and protruding the needle-like electrode from the flexible tube main body to an arbitrary length and then performing a treatment such as separation of the affected portion. (For example, refer to Patent Document 1).

特許文献1の高周波処置具では、可撓管本体から針状電極を一度突出させ、その後処置部位に応じて突出長を調整する作業が必要となる。このような作業では所望の長さだけ針状電極を突出させることは困難である。そのため、針状電極を突出させすぎてしまい、患部の処置を行う際に患部を正確に狙うことが困難であるという課題があった。   In the high-frequency treatment instrument of Patent Document 1, it is necessary to make the needle-like electrode protrude once from the flexible tube main body and then adjust the protrusion length according to the treatment site. In such an operation, it is difficult to protrude the needle electrode by a desired length. For this reason, there is a problem that the needle-shaped electrode is protruded too much, and it is difficult to accurately aim at the affected part when the affected part is treated.

このような課題を解決するために、電気絶縁性の可撓性シースの先端付近の側面部から高周波電極を外面に露出させて配置したり(特許文献2)、電極棒の表面の金属露出部以外の部分をすべて電気絶縁性コーティングするといった高周波処置具が提案されている(特許文献3)。   In order to solve such a problem, the high-frequency electrode is exposed from the side surface near the tip of the electrically insulating flexible sheath (Patent Document 2), or the metal exposed portion on the surface of the electrode rod There has been proposed a high-frequency treatment instrument in which all other parts are electrically insulatively coated (Patent Document 3).

特開平4−329944号公報JP-A-4-329944 特許第4275004号公報Japanese Patent No. 4275004 特許第4725808号公報Japanese Patent No. 4725808

しかしながら、特許文献2の高周波処置具では、患部以外の健康組織の損傷を防止することはできるものの、患部に合せて処置部を回転させる必要が生じる。また、組織に対して水平方向に処置を行う場合は問題ないが、組織に対して垂直方向に処置を行う場合、患部によっては処置を行いにくい場合がある。   However, although the high-frequency treatment tool of Patent Document 2 can prevent damage to healthy tissues other than the affected part, it is necessary to rotate the treatment part according to the affected part. Further, there is no problem when the treatment is performed in the horizontal direction with respect to the tissue, but when the treatment is performed in the vertical direction with respect to the tissue, the treatment may be difficult depending on the affected part.

また、特許文献3の高周波処置具では、金属露出部に高周波電流が集中するため、漏れ電流による患部以外の健康組織の損傷を防止することができる。しかし、高周波電流を連続的に金属部に通電すると熱エネルギーが発生し、電気絶縁性コーティングをしても患部以外の健康組織に悪影響を及ぼすおそれがある。   Moreover, in the high frequency treatment tool of patent document 3, since a high frequency current concentrates on a metal exposure part, damage to healthy tissues other than the affected part by a leakage current can be prevented. However, if high-frequency current is continuously applied to the metal part, heat energy is generated, and even if the electrically insulating coating is applied, there is a possibility of adversely affecting healthy tissues other than the affected part.

本発明はこのような課題に鑑みなされたものであり、患部の位置によらず処置が容易となる高周波処置具を提供するものである。また、患部以外の健康組織に悪影響を及ぼすことのない高周波処置具を提供するものである。   This invention is made | formed in view of such a subject, and provides the high frequency treatment tool which a treatment becomes easy irrespective of the position of an affected part. Moreover, the high frequency treatment tool which does not have a bad influence on healthy tissues other than an affected part is provided.

このような目的は、以下に記載の本発明により達成される。   Such an object is achieved by the present invention described below.

本発明は、処置部と、前記処置部を先端に有する操作ワイヤと、前記操作ワイヤを摺動自在に挿通する第1可撓管と、を備える高周波処置具であって、
前記第1可撓管には、前記処置部の作動状態を調整する第2可撓管が着脱自在に突設されていることを特徴とする。
The present invention is a high-frequency treatment instrument comprising a treatment portion, an operation wire having the treatment portion at a tip, and a first flexible tube through which the operation wire is slidably inserted.
The first flexible tube is detachably provided with a second flexible tube that adjusts the operating state of the treatment portion.

第2可撓管は、外周に表面を貫通するスリットまたは貫通しない凹部を有していてもよい。   The second flexible tube may have a slit that penetrates the surface or a recess that does not penetrate on the outer periphery.

前記処置部の基端部または前記操作ワイヤの先端部の少なくともいずれか一方は、絶縁コーティングされていてもよい。   At least one of the proximal end portion of the treatment portion and the distal end portion of the operation wire may be insulated.

前記第1可撓管の先端は、前記第2可撓管の前進を防止する形状をなしていてもよい。   The tip of the first flexible tube may have a shape that prevents the second flexible tube from moving forward.

前記第2可撓管の後端に、前記第2可撓管の前進を防止する第1ストッパーを有していてもよい。   A rear end of the second flexible tube may have a first stopper that prevents the second flexible tube from moving forward.

前記操作ワイヤに、前記処置部及び前記操作ワイヤの前進を防止する第2ストッパーを有していてもよい。   The operation wire may include a second stopper that prevents the treatment portion and the operation wire from moving forward.

前記第2可撓管の先端は、前記処置部の後退を防止する形状をなしていてもよい。   The distal end of the second flexible tube may have a shape that prevents the treatment portion from retreating.

前記処置部の後端の径は前記処置部の先端側の径よりも小さくてもよい。   The diameter of the rear end of the treatment part may be smaller than the diameter of the treatment part on the front end side.

本発明によれば、処置部の作動状態が調整可能であることから、患部の位置によらず処置を容易にすることが可能である。また、患部以外の健康組織への悪影響を低減することができる。   According to the present invention, since the operating state of the treatment part can be adjusted, it is possible to facilitate the treatment regardless of the position of the affected part. In addition, adverse effects on healthy tissues other than the affected area can be reduced.

本発明の実施形態に係る高周波処置具の正面図である。It is a front view of the high frequency treatment tool concerning the embodiment of the present invention. 本発明の実施形態に係る高周波処置具の側面図である。It is a side view of the high frequency treatment tool concerning the embodiment of the present invention. 本発明の実施形態に係る高周波処置具の処置部を突出させた第1状態を示す拡大図である。(a)は第1状態における高周波処置具の先端部の正面図であり、(b)は第1可撓管内部を示した一部縦断面図である。It is an enlarged view which shows the 1st state which protruded the treatment part of the high frequency treatment tool which concerns on embodiment of this invention. (A) is a front view of the front-end | tip part of the high frequency treatment tool in a 1st state, (b) is a partial longitudinal cross-sectional view which showed the inside of the 1st flexible tube. 本発明の実施形態に係る高周波処置具の処置部先端が第2可撓管から突出した第2状態を示す拡大図である。(a)は第2状態における高周波処置具の先端部の正面図であり、(b)は第1可撓管内部を示した一部縦断面図である。It is an enlarged view which shows the 2nd state which the treatment part front-end | tip of the high frequency treatment tool which concerns on embodiment of this invention protruded from the 2nd flexible tube. (A) is a front view of the front-end | tip part of the high frequency treatment tool in a 2nd state, (b) is a partial longitudinal cross-sectional view which showed the inside of the 1st flexible tube. 本発明の実施形態に係る高周波処置具の処置部を第2可撓管に収納した第3状態を示す拡大図である。(a)は第3状態における高周波処置具の先端部の正面図であり、(b)は第1可撓管内部を示した一部縦断面図である。It is an enlarged view which shows the 3rd state which accommodated the treatment part of the high frequency treatment tool which concerns on embodiment of this invention in the 2nd flexible tube. (A) is a front view of the front-end | tip part of the high frequency treatment tool in a 3rd state, (b) is a partial longitudinal cross-sectional view which showed the inside of the 1st flexible tube. 本発明の実施形態に係る高周波処置具の第2可撓管が第1可撓管に収納された第4状態を示す拡大図である。(a)は第4状態における高周波処置具の先端部の正面図であり、(b)は第1可撓管内部を示した一部縦断面図である。It is an enlarged view which shows the 4th state by which the 2nd flexible tube of the high frequency treatment tool which concerns on embodiment of this invention was accommodated in the 1st flexible tube. (A) is a front view of the front-end | tip part of the high frequency treatment tool in a 4th state, (b) is a partial longitudinal cross-sectional view which showed the inside of the 1st flexible tube.

以下、本発明の高周波処置具の好適な実施形態について、図面を参照しつつ詳細に説明する。   Hereinafter, preferred embodiments of the high-frequency treatment device of the present invention will be described in detail with reference to the drawings.

本実施形態の高周波処置具1は、内視鏡のルーメン(内腔)に挿通して用いられ、高周波電流の印加により患部を処置するための器具である。   The high-frequency treatment instrument 1 of this embodiment is an instrument that is used by being inserted through a lumen (lumen) of an endoscope and treating an affected area by applying a high-frequency current.

図1及び図2に示すように、本実施形態の高周波処置具1は、体腔内に挿入される第1可撓管2と、第1可撓管2に進退自在に挿通された導電性の操作ワイヤ3と、操作ワイヤ3の先端部に配置され高周波電流の印加により患部を処置する処置部4と、第1可撓管2の基端部に付設された操作部5とを有している。   As shown in FIGS. 1 and 2, the high-frequency treatment device 1 of the present embodiment includes a first flexible tube 2 inserted into a body cavity, and an electrically conductive material inserted through the first flexible tube 2 so as to freely advance and retract. It has an operation wire 3, a treatment portion 4 disposed at the distal end portion of the operation wire 3 and treating the affected area by applying a high frequency current, and an operation portion 5 attached to the proximal end portion of the first flexible tube 2. Yes.

第1可撓管2は、高周波処置具1の全長の大部分を占める長尺管である。第1可撓管2は、操作部5と処置部4を接続し、処置部4の病変部位へのアクセスを可能とする。   The first flexible tube 2 is a long tube that occupies most of the entire length of the high-frequency treatment instrument 1. The first flexible tube 2 connects the operation unit 5 and the treatment unit 4 and enables access to a lesion site of the treatment unit 4.

第1可撓管2としては、可撓性を有していればいかなるものを用いてもよい。第1可撓管2の材料としては、例えば、ステンレス鋼のような導電性材料、フッ素系樹脂、ポリエチレンやポリプロピレンのようなポリオレフィン系樹脂、ポリアミド系樹脂、ポリイミド系樹脂、ポリウレタン系樹脂、ポリカーボネート系樹脂等が挙げられる。中でもフッ素系樹脂を用いる場合、第1可撓管2が挿通される内視鏡の鉗子孔との摺動性に優れるため好ましい。
また、導電性材料を用いる場合には、第1可撓管2の内表面には絶縁性材料を薄膜コーティングすることが好ましい。
Any first flexible tube 2 may be used as long as it has flexibility. Examples of the material of the first flexible tube 2 include a conductive material such as stainless steel, a fluorine resin, a polyolefin resin such as polyethylene and polypropylene, a polyamide resin, a polyimide resin, a polyurethane resin, and a polycarbonate resin. Examples thereof include resins. Among these, the use of a fluororesin is preferable because it is excellent in slidability with the forceps hole of the endoscope through which the first flexible tube 2 is inserted.
When using a conductive material, it is preferable to coat the inner surface of the first flexible tube 2 with an insulating material.

第1可撓管2の寸法は、使用する内視鏡により異なるが、例えば、長さが1500〜2500mm、外径が1.5〜3mmの範囲にあることが好ましい。長さが上記範囲内にあれば、高周波処置具1を内視鏡のルーメン(内腔)に挿通して使用することができる。また、外径が上記上限以下であれば、内視鏡の鉗子孔への挿通性がより良好となる。   Although the dimension of the 1st flexible tube 2 changes with endoscopes to be used, for example, it is preferable that a length is 1500-2500 mm and an outer diameter is in the range of 1.5-3 mm. If the length is within the above range, the high-frequency treatment instrument 1 can be used by being inserted into the lumen (lumen) of the endoscope. Moreover, if an outer diameter is below the said upper limit, the penetration property to the forceps hole of an endoscope will become more favorable.

第1可撓管2の先端21は、後述する第2可撓管6の前進を防止する形状をなしている。第1可撓管2の先端21に第2可撓管6の前進を防止する形状を有することにより、操作部5を過剰に前進させても、第2可撓管6が第1可撓管2から逸脱しなくなる。   The tip 21 of the first flexible tube 2 has a shape that prevents the advancement of the second flexible tube 6 described later. By having the shape which prevents the advance of the 2nd flexible tube 6 in the front-end | tip 21 of the 1st flexible tube 2, even if the operation part 5 is advanced too much, the 2nd flexible tube 6 is a 1st flexible tube. No deviation from 2.

本実施形態では、第1可撓管2の先端21は開口径が第1可撓管2の内径よりも小さくなるように形成されている。すなわち、図3から図6に示すように、第1可撓管2の先端21は軸方向に直角に延出して形成されている。そして、この先端21に後に説明する第1ストッパー62が係止されることで第2可撓管6の第1可撓管2からの前進を阻止できる。なお、本実施形態では、先端21が軸方向に直角に延出していることを説明したが、本発明はこれに限られず、例えば、第1可撓管の内径が先端に向かって漸減するようにしてもよい。   In the present embodiment, the tip 21 of the first flexible tube 2 is formed so that the opening diameter is smaller than the inner diameter of the first flexible tube 2. That is, as shown in FIGS. 3 to 6, the tip 21 of the first flexible tube 2 is formed to extend perpendicular to the axial direction. And the advancement from the 1st flexible tube 2 of the 2nd flexible tube 6 can be prevented because the 1st stopper 62 demonstrated later by this front-end | tip 21 is latched. In the present embodiment, it has been described that the tip 21 extends at right angles to the axial direction. However, the present invention is not limited to this. For example, the inner diameter of the first flexible tube gradually decreases toward the tip. It may be.

操作ワイヤ3は、第1可撓管2の管腔に挿通されるワイヤ線である。操作ワイヤ3の先端は、処置部4と接続されている。また、操作ワイヤ3の基端は、操作部5と接続されている。これによって、後に説明するように、操作部5を操作することで操作ワイヤ3を介して処置部4を駆動操作することができる。   The operation wire 3 is a wire line inserted through the lumen of the first flexible tube 2. The distal end of the operation wire 3 is connected to the treatment unit 4. The proximal end of the operation wire 3 is connected to the operation unit 5. Thus, as will be described later, the treatment section 4 can be driven and operated via the operation wire 3 by operating the operation section 5.

操作ワイヤ3の材料としては、例えば、ステンレス鋼、チタンやチタン合金などの金属材料や、ポリ(パラフェニレンベンゾビスオキサゾール)(PBO)、ポリエーテルエーテルケトン(PEEK)、ポリフェニレンスルフィド(PPS)、ポリブチレンテレフタレート(PBT)、ポリイミド(PI)またはポリテトラフルオロエチレン(PTFE)などの高分子ファイバーが挙げられる。   Examples of the material of the operation wire 3 include metal materials such as stainless steel, titanium and titanium alloys, poly (paraphenylenebenzobisoxazole) (PBO), polyetheretherketone (PEEK), polyphenylene sulfide (PPS), poly Examples thereof include polymer fibers such as butylene terephthalate (PBT), polyimide (PI), and polytetrafluoroethylene (PTFE).

操作ワイヤ3の寸法は、例えば、長さが1600〜2600mmの範囲にあることが好ましい。長さが上記範囲内にあれば、操作部5を操作することで操作ワイヤ3を介して処置部4を駆動操作することができる。   For example, the length of the operation wire 3 is preferably in the range of 1600 to 2600 mm. If the length is within the above range, the treatment section 4 can be driven and operated via the operation wire 3 by operating the operation section 5.

操作ワイヤ3は、処置部4及び操作ワイヤ3の前進を防止する第2ストッパー31を有している。処置部4及び操作ワイヤ3の前進を防止する第2ストッパー31を有することにより、操作部5を過剰に前進操作させても、処置部4及び操作ワイヤ3が所定の長さより前進しなくなる。また、第2ストッパー31を設けることにより、操作部5を前進操作させた際に第2可撓管6を前進させることが可能となる。   The operation wire 3 has a second stopper 31 that prevents the treatment section 4 and the operation wire 3 from moving forward. By having the second stopper 31 that prevents the treatment section 4 and the operation wire 3 from moving forward, the treatment section 4 and the operation wire 3 do not advance more than a predetermined length even if the operation section 5 is excessively advanced. In addition, by providing the second stopper 31, the second flexible tube 6 can be advanced when the operation unit 5 is operated to advance.

本実施形態では、第2ストッパー31の外径は、第2可撓管6の基端側の内径よりも大きく形成されている。すなわち、図3から図6に示すように、第2ストッパー31は操作ワイヤ3の先端部において環状凸部状をなしている。このため、操作ワイヤ3の第2ストッパー31よりも基端側の部分は第2可撓管6の内腔内に侵入することはない。したがって、操作ワイヤ3を前進させると、まず、第2ストッパー31が第2可撓管6の基端部に当接し、第2可撓管6を前進させる。第2可撓管6は、上述のように、第1ストッパー62が第1可撓管2の先端21に係止されることで前進を阻止される。このため操作ワイヤ3の前進も阻止されることとなる。なお、本実施形態では第2ストッパーは環状凸部状であることを説明したが、本発明はこれに限られず、例えば、操作ワイヤの基端部に複数の凸部が形成されていてもよい。   In the present embodiment, the outer diameter of the second stopper 31 is formed larger than the inner diameter on the proximal end side of the second flexible tube 6. That is, as shown in FIGS. 3 to 6, the second stopper 31 has an annular convex shape at the distal end portion of the operation wire 3. For this reason, the portion of the operation wire 3 closer to the proximal end than the second stopper 31 does not enter the lumen of the second flexible tube 6. Therefore, when the operation wire 3 is advanced, first, the second stopper 31 comes into contact with the proximal end portion of the second flexible tube 6 to advance the second flexible tube 6. As described above, the second flexible tube 6 is prevented from advancing when the first stopper 62 is locked to the tip 21 of the first flexible tube 2. For this reason, the advance of the operation wire 3 is also prevented. In addition, although this embodiment demonstrated that the 2nd stopper was cyclic | annular convex shape, this invention is not limited to this, For example, the some convex part may be formed in the base end part of the operation wire. .

処置部4は、第1可撓管2の先端に配置され、操作ワイヤ3の進退により駆動する。処置部4は、高周波電流の印加により患部を処置するデバイスである。処置部4に高周波電流を印加するために、高周波電流コード(図示せず)が装着される電源端子7が高周波処置具1に突出して設けられている。   The treatment section 4 is disposed at the distal end of the first flexible tube 2 and is driven by the advancement / retraction of the operation wire 3. The treatment section 4 is a device that treats an affected area by applying a high-frequency current. In order to apply a high frequency current to the treatment section 4, a power supply terminal 7 to which a high frequency current cord (not shown) is attached is provided protruding from the high frequency treatment instrument 1.

処置部4の具体的な構成は特に限定されないが、本実施形態では処置部4は最先端の球状部41、球状部41の基端側に接続される棒状部42、棒状部42の基端側に接続される絶縁部43より構成される。そして絶縁部43の基端が操作ワイヤ3の先端に接続されている。操作ワイヤ3の前進によって処置部4が突出し、処置部4を患部に押し当て、患部に高周波電流を印加しつつこれを切開する。なお、処置部の形状はこれに限られず、例えば、針状や、鉤状などであってもよい。   Although the specific configuration of the treatment portion 4 is not particularly limited, in the present embodiment, the treatment portion 4 includes the most advanced spherical portion 41, a rod-like portion 42 connected to the proximal end side of the spherical portion 41, and a proximal end of the rod-like portion 42. It is comprised from the insulation part 43 connected to the side. The proximal end of the insulating portion 43 is connected to the distal end of the operation wire 3. As the operation wire 3 advances, the treatment section 4 protrudes, presses the treatment section 4 against the affected area, and incises this while applying high-frequency current to the affected area. The shape of the treatment portion is not limited to this, and may be, for example, a needle shape or a hook shape.

処置部4の材料としては、ステンレス鋼のような導電性材料が挙げられる。特に処置部4を通じて組織に高周波電流を通電する処置部部分は電気伝導率が高い材質を使用することが好ましい。   Examples of the material for the treatment section 4 include conductive materials such as stainless steel. In particular, it is preferable to use a material having a high electrical conductivity for the treatment portion that supplies high-frequency current to the tissue through the treatment portion 4.

本実施形態では処置部4の絶縁部43は、棒状部42の基端側の部分が絶縁チューブで被覆されて構成されている。処置部4の基端側に絶縁部43を設けることで、後に説明するように、処置部4をすべて突出させた時に、第2可撓管6の外周の表面を貫通するスリット61から金属部分が露出することがなくなる。第2可撓管6の外周に表面を貫通するスリット61から金属部分が露出しなくなることにより、第2可撓管6より前にある処置部4のみに通電することができる。また図4に示すように、処置部4を第2可撓管6に収納した場合、絶縁部43が後退するため、第2可撓管6の貫通するスリット61の部分に位置する部分から組織に通電することができるようになる。   In the present embodiment, the insulating portion 43 of the treatment portion 4 is configured by covering the proximal end portion of the rod-like portion 42 with an insulating tube. By providing the insulating portion 43 on the proximal end side of the treatment portion 4, as will be described later, when the treatment portion 4 is entirely projected, the metal portion is formed from the slit 61 penetrating the outer peripheral surface of the second flexible tube 6. Will not be exposed. Since the metal portion is not exposed from the slit 61 penetrating the surface of the outer periphery of the second flexible tube 6, it is possible to energize only the treatment portion 4 in front of the second flexible tube 6. As shown in FIG. 4, when the treatment portion 4 is housed in the second flexible tube 6, the insulating portion 43 retreats, so that the tissue is removed from the portion located in the slit 61 portion that penetrates the second flexible tube 6. Can be energized.

棒状部42の外径は球状部41の外径よりも小さい。棒状部42の外径が球状部41の外径よりも小さいことにより、球状部41を第2可撓管6に嵌合させることができ、操作ワイヤ3を後退させた際に、第2可撓管6を第1可撓管2に収納することが可能となる。   The outer diameter of the rod-shaped part 42 is smaller than the outer diameter of the spherical part 41. Since the outer diameter of the rod-shaped portion 42 is smaller than the outer diameter of the spherical portion 41, the spherical portion 41 can be fitted into the second flexible tube 6, and the second possible portion can be obtained when the operation wire 3 is retracted. The flexible tube 6 can be stored in the first flexible tube 2.

操作部5は、第1可撓管2の基端部に設けられ、処置部4の突出長を調整する。操作部5は、軸部51と軸部51に摺動自在に係合するスライダ部52を備える。   The operation unit 5 is provided at the proximal end of the first flexible tube 2 and adjusts the protruding length of the treatment unit 4. The operation unit 5 includes a shaft portion 51 and a slider portion 52 that is slidably engaged with the shaft portion 51.

軸部51は、筒状をなしている。軸部51の先端部には第1可撓管2の基端が接続されている。また、軸部51の内部には操作ワイヤ3が挿通されている。   The shaft portion 51 has a cylindrical shape. The proximal end of the first flexible tube 2 is connected to the distal end portion of the shaft portion 51. Further, the operation wire 3 is inserted into the shaft portion 51.

スライダ部52は、操作ワイヤ3及び処置部4を進退操作する部材である。本実施形態では、図1に示すように、スライダ部52は長手方向中央の外周が凹没した円筒状をなしている。スライダ部52は軸部51に装着されており、軸部51の長手方向に摺動する。スライダ部52には操作ワイヤ3の基端部が固定されている。したがって、スライダ部52を軸部51に対して前後方向に摺動させると、操作ワイヤ3が進退する。   The slider portion 52 is a member that moves the operation wire 3 and the treatment portion 4 forward and backward. In the present embodiment, as shown in FIG. 1, the slider portion 52 has a cylindrical shape in which the outer periphery at the center in the longitudinal direction is recessed. The slider portion 52 is attached to the shaft portion 51 and slides in the longitudinal direction of the shaft portion 51. A proximal end portion of the operation wire 3 is fixed to the slider portion 52. Therefore, when the slider portion 52 is slid in the front-rear direction with respect to the shaft portion 51, the operation wire 3 moves back and forth.

図3から図6に示すように、本実施形態の第1可撓管2には、処置部4の作動状態を調整する第2可撓管6が着脱自在に突設されている。第1可撓管2に第2可撓管6を設けることで、第2可撓管6で処置部4を進退自由に覆うことが可能となり、術者が所望する処置部4の長さに調節することができる。   As shown in FIG. 3 to FIG. 6, a second flexible tube 6 that adjusts the operating state of the treatment section 4 is detachably protruded from the first flexible tube 2 of the present embodiment. By providing the second flexible tube 6 on the first flexible tube 2, the treatment portion 4 can be covered freely with the second flexible tube 6, and the length of the treatment portion 4 desired by the operator can be obtained. Can be adjusted.

ここで、処置部の作動状態を調整することには、処置部の突出長を調整することや、処置部のうち外部に露出する部分の範囲を調整することが含まれる。   Here, adjusting the operating state of the treatment section includes adjusting the protrusion length of the treatment section and adjusting the range of the portion of the treatment section exposed to the outside.

第2可撓管6としては、可撓性を有していればいかなるものを用いてもよい。第2可撓管6の材料としては、例えば、フッ素系樹脂、ポリエチレンやポリプロピレンのようなポリオレフィン系樹脂、ポリアミド系樹脂、ポリイミド系樹脂、ポリウレタン系樹脂、ポリカーボネート系樹脂等が挙げられる。   Any second flexible tube 6 may be used as long as it has flexibility. Examples of the material of the second flexible tube 6 include fluorine resins, polyolefin resins such as polyethylene and polypropylene, polyamide resins, polyimide resins, polyurethane resins, and polycarbonate resins.

また、第2可撓管6の寸法は処置部4の形状、寸法により異なるが、例えば、長さが2〜5mm、外径が1.5〜2.5mmの範囲にあることが好ましい。   Moreover, although the dimension of the 2nd flexible tube 6 changes with shapes and dimensions of the treatment part 4, for example, it is preferable that length is in the range of 2-5 mm and an outer diameter is 1.5-2.5 mm.

本実施形態では、第2可撓管6は外周に表面を貫通するスリット61を有する。第2可撓管6の外周に表面を貫通するスリット61を有することで、処置部4を第2可撓管6に収納した場合でも、第2可撓管6の貫通するスリット61の部分に位置する部分から組織に通電することができ、患部を処置することができる。すなわち、第2可撓管3のスリット61は、処置部4のうち外部に露出する部分の大きさを調整する役割を果たす。   In this embodiment, the 2nd flexible tube 6 has the slit 61 which penetrates the surface on an outer periphery. By having the slit 61 penetrating the surface on the outer periphery of the second flexible tube 6, even when the treatment section 4 is stored in the second flexible tube 6, the slit 61 passing through the second flexible tube 6 The tissue can be energized from the position where it is located, and the affected area can be treated. That is, the slit 61 of the second flexible tube 3 serves to adjust the size of the portion of the treatment portion 4 exposed to the outside.

なお、本実施形態では第2可撓管の外周に表面を貫通するスリットを設けたが、貫通しない凹部を設けるようにしてもよい。この場合には、処置部は外部に露出することはないが、凹部の形成された部分は薄肉となっているため、組織に通電することが可能である。   In the present embodiment, a slit that penetrates the surface is provided on the outer periphery of the second flexible tube, but a recess that does not penetrate may be provided. In this case, the treatment portion is not exposed to the outside, but the portion where the recess is formed is thin, so that the tissue can be energized.

第2可撓管6の後端には、第2可撓管6の前進を防止する第1ストッパー62を有している。第2可撓管6の前進を防止する第1ストッパー62を有することにより、操作部5を過剰に前進させても、第2可撓管6が第1可撓管2から逸脱しなくなる。   A rear end of the second flexible tube 6 has a first stopper 62 that prevents the second flexible tube 6 from moving forward. By having the first stopper 62 that prevents the second flexible tube 6 from moving forward, the second flexible tube 6 does not deviate from the first flexible tube 2 even if the operation portion 5 is excessively advanced.

本実施形態では、第1ストッパー62は第2可撓管6の基端部の外径を先端部の外径よりも大きく形成されている。すなわち、図3から図6に示すように、第1ストッパー62は第2可撓管6の基端部をフランジ状に形成してなる。この第1ストッパー62は前述した第1可撓管2の先端21と当接し係止されることで第2可撓管6が第1可撓管2から脱落することを防止する。なお、第1ストッパーの形状はこれに限られず、例えば、第2可撓管6の外径を基端に向かって漸増するように形成してもよい。   In the present embodiment, the first stopper 62 is formed so that the outer diameter of the proximal end portion of the second flexible tube 6 is larger than the outer diameter of the distal end portion. That is, as shown in FIGS. 3 to 6, the first stopper 62 is formed by forming the base end portion of the second flexible tube 6 in a flange shape. The first stopper 62 is in contact with and locked with the tip 21 of the first flexible tube 2 described above, thereby preventing the second flexible tube 6 from dropping from the first flexible tube 2. The shape of the first stopper is not limited to this, and for example, it may be formed so that the outer diameter of the second flexible tube 6 gradually increases toward the base end.

次に本実施形態の高周波処置具1の使用方法について説明する。まず、内視鏡の鉗子孔から高周波処置具1を挿入する。そして内視鏡の画像を観察しながら、第1可撓管2の先端21を患部の近傍へと誘導する。   Next, the usage method of the high frequency treatment tool 1 of this embodiment is demonstrated. First, the high-frequency treatment tool 1 is inserted from the forceps hole of the endoscope. Then, the distal end 21 of the first flexible tube 2 is guided to the vicinity of the affected part while observing the image of the endoscope.

高周波処置具1の先端21を患部へと誘導したのち、手元の操作部5を前進操作させ、処置部4を図3に示す状態(第1状態)とする。すなわち、球状部41および棒状部42を第1可撓管2および第2可撓管6の先端から突出させる。このような第1状態は病変周囲の粘膜組織を切開するような処置に適している。   After guiding the distal end 21 of the high-frequency treatment instrument 1 to the affected area, the operation section 5 at the hand is operated forward, and the treatment section 4 is set to the state shown in FIG. 3 (first state). That is, the spherical portion 41 and the rod-shaped portion 42 are projected from the tips of the first flexible tube 2 and the second flexible tube 6. Such a first state is suitable for a treatment such as incising mucosal tissue around the lesion.

第1状態においては第2可撓管6内には絶縁部43が位置している。このためスリット61から高周波電流が漏れ出ることはなく、処置部4の先端部のみで処置が可能である。   In the first state, the insulating portion 43 is located in the second flexible tube 6. For this reason, the high frequency current does not leak from the slit 61, and the treatment can be performed only by the distal end portion of the treatment portion 4.

また、スライダ52を基端側に摺動させて処置部4を第1状態から図4に示す状態(第2状態)とする。すなわち、球状部41の先端側の略半分のみが第2可撓管6の先端から露出するまで処置部4を突出させる。このような第2状態は病変切除範囲の粘膜下層を剥離するような処置に適している。   Further, the slider 52 is slid to the proximal end side to change the treatment section 4 from the first state to the state shown in FIG. 4 (second state). That is, the treatment section 4 is protruded until only approximately half of the distal end side of the spherical section 41 is exposed from the distal end of the second flexible tube 6. Such a second state is suitable for a treatment in which the submucosal layer in the lesion excision range is peeled off.

さらに、スライダ52を摺動させて処置部4を第2状態から図5に示す状態(第3状態)とする。すなわち、処置部4の球状部41の先端が第2可撓管6の先端と一致し、第2可撓管6の先端からは処置部4が突出しない状態とする。この状態で高周波電流を印加すると、スリット72から第2可撓管表面に高周波電流が漏れ出る。このような第3状態は病変切除範囲の目安をつけるマーキングのような処置に適している。   Further, the slider 52 is slid to change the treatment section 4 from the second state to the state shown in FIG. 5 (third state). That is, the distal end of the spherical portion 41 of the treatment section 4 is aligned with the distal end of the second flexible tube 6, and the treatment section 4 does not protrude from the distal end of the second flexible tube 6. When a high frequency current is applied in this state, the high frequency current leaks from the slit 72 to the surface of the second flexible tube. Such a third state is suitable for a treatment such as marking for indicating the extent of the lesion excision range.

このように本実施形態の高周波処置具1は処置部4の第2可撓管6からの突出長を調整でき、突出状態(作動状態)の違いにより患部の種々の状況に適した処置を選択することができる。   As described above, the high-frequency treatment instrument 1 of the present embodiment can adjust the protrusion length of the treatment portion 4 from the second flexible tube 6 and select treatments suitable for various situations of the affected portion depending on the difference of the protrusion state (operation state). can do.

さらに、高周波処置具1を内視鏡の鉗子孔に挿抜する際には図6に示すように、処置部4および第2可撓管6が第1可撓管2に収納された状態(第4状態)とすることで、挿抜等の取り扱い時に処置部4を保護することができる。   Further, when the high-frequency treatment instrument 1 is inserted into and removed from the forceps hole of the endoscope, the treatment section 4 and the second flexible tube 6 are housed in the first flexible tube 2 as shown in FIG. 4 state), the treatment section 4 can be protected during handling such as insertion / extraction.

以上、本発明を実施形態に基づいて説明した。これらの実施形態はあくまで例示であり、種々の変形例が可能なこと、またそうした変形例も本発明の範囲にあることは当業者に理解されるところである。   The present invention has been described based on the embodiments. It is to be understood by those skilled in the art that these embodiments are merely examples, and that various modifications are possible and that such modifications are within the scope of the present invention.

1 高周波処置具
2 第1可撓管
21 第1可撓管の先端
3 操作ワイヤ
31 第2ストッパー
4 処置部
41 球状部
42 棒状部
43 絶縁チューブ
5 操作部
51 軸部
52 スライダ部
6 第2可撓管
61 スリット
62 第1ストッパー
7 電源端子
DESCRIPTION OF SYMBOLS 1 High frequency treatment tool 2 1st flexible tube 21 The front-end | tip of 1st flexible tube 3 Operation wire 31 2nd stopper 4 Treatment part 41 Spherical part 42 Rod-shaped part 43 Insulation tube 5 Operation part 51 Shaft part 52 Slider part 6 2nd possible Flexible tube 61 Slit 62 First stopper 7 Power supply terminal

Claims (8)

処置部と、前記処置部を先端に有する操作ワイヤと、前記操作ワイヤを摺動自在に挿通する第1可撓管と、を備える高周波処置具であって、
前記第1可撓管には、前記処置部の作動状態を調整する第2可撓管が着脱自在に突設されていることを特徴とする高周波処置具。
A high-frequency treatment instrument comprising a treatment part, an operation wire having the treatment part at a distal end, and a first flexible tube through which the operation wire is slidably inserted,
A high-frequency treatment instrument, wherein a second flexible tube for adjusting an operating state of the treatment portion is detachably provided on the first flexible tube.
前記第2可撓管は、外周に表面を貫通するスリットまたは貫通しない凹部を有する請求項1に記載の高周波処置具。   The high-frequency treatment instrument according to claim 1, wherein the second flexible tube has a slit that penetrates the surface or a recess that does not penetrate on the outer periphery. 前記処置部の基端部または前記操作ワイヤの先端部の少なくともいずれか一方は、絶縁コーティングされている請求項1又は2に記載の高周波処置具。   The high-frequency treatment tool according to claim 1 or 2, wherein at least one of a proximal end portion of the treatment portion and a distal end portion of the operation wire is coated with insulation. 前記第1可撓管の先端は、前記第2可撓管の前進を防止する形状をなしている請求項1乃至3のいずれか一項に記載の高周波処置具。   The high-frequency treatment instrument according to any one of claims 1 to 3, wherein a distal end of the first flexible tube has a shape that prevents the second flexible tube from moving forward. 前記第2可撓管の後端に、前記第2可撓管の前進を防止する第1ストッパーを有している請求項1乃至4のいずれか一項に記載の高周波処置具。 5. The high-frequency treatment device according to claim 1, further comprising a first stopper that prevents the second flexible tube from advancing at a rear end of the second flexible tube. 前記操作ワイヤに、前記処置部及び前記操作ワイヤの前進を防止する第2ストッパーを有している請求項1乃至4のいずれか一項に記載の高周波処置具。 The high frequency treatment tool according to any one of claims 1 to 4, wherein the operation wire includes a second stopper that prevents the treatment portion and the operation wire from moving forward. 前記第2可撓管の先端は、前記処置部の後退を防止する形状をなしている請求項1乃至6のいずれか一項に記載の高周波処置具   The high-frequency treatment instrument according to any one of claims 1 to 6, wherein a distal end of the second flexible tube has a shape that prevents the treatment portion from retreating. 前記処置部の後端の径は前記処置部の先端側の径よりも小さい請求項1乃至7のいずれか一項に記載の高周波処置具。   The high frequency treatment tool according to any one of claims 1 to 7, wherein a diameter of a rear end of the treatment portion is smaller than a diameter of a distal end side of the treatment portion.
JP2012023285A 2012-02-06 2012-02-06 High frequency treatment tool Expired - Fee Related JP5884534B2 (en)

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JP2009240380A (en) * 2008-03-28 2009-10-22 Fujifilm Corp High-frequency knife and high-frequency knife system
JP2010179009A (en) * 2009-02-09 2010-08-19 Hoya Corp High-frequency treatment tool for endoscope
JP2010268845A (en) * 2009-05-19 2010-12-02 Hoya Corp High frequency knife for endoscope
JP2010284244A (en) * 2009-06-10 2010-12-24 Hoya Corp High frequency knife for endoscope
JP2011078549A (en) * 2009-10-07 2011-04-21 Hoya Corp High frequency knife for endoscope
JP2011142995A (en) * 2010-01-13 2011-07-28 Hoya Corp High frequency treatment instrument for endoscope

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JP2006326157A (en) * 2005-05-30 2006-12-07 Olympus Corp Treatment instrument for endoscope and treatment instrument system for endoscope
JP2008000386A (en) * 2006-06-23 2008-01-10 Fujinon Corp High frequency treatment instrument
JP2009240380A (en) * 2008-03-28 2009-10-22 Fujifilm Corp High-frequency knife and high-frequency knife system
JP2010179009A (en) * 2009-02-09 2010-08-19 Hoya Corp High-frequency treatment tool for endoscope
JP2010268845A (en) * 2009-05-19 2010-12-02 Hoya Corp High frequency knife for endoscope
JP2010284244A (en) * 2009-06-10 2010-12-24 Hoya Corp High frequency knife for endoscope
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