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WO2018062415A1 - Endoscopic treatment tool and production method for endoscopic treatment tool - Google Patents

Endoscopic treatment tool and production method for endoscopic treatment tool Download PDF

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Publication number
WO2018062415A1
WO2018062415A1 PCT/JP2017/035311 JP2017035311W WO2018062415A1 WO 2018062415 A1 WO2018062415 A1 WO 2018062415A1 JP 2017035311 W JP2017035311 W JP 2017035311W WO 2018062415 A1 WO2018062415 A1 WO 2018062415A1
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WIPO (PCT)
Prior art keywords
treatment tool
wire
operation wire
snare
endoscope
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Ceased
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PCT/JP2017/035311
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French (fr)
Japanese (ja)
Inventor
隆充 岩浪
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Olympus Corp
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Olympus Corp
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Publication date
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Publication of WO2018062415A1 publication Critical patent/WO2018062415A1/en
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/012Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor characterised by internal passages or accessories therefor
    • A61B1/018Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor characterised by internal passages or accessories therefor for receiving instruments
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods
    • A61B17/22Implements for squeezing-off ulcers or the like on inner organs of the body; Implements for scraping-out cavities of body organs, e.g. bones; for invasive removal or destruction of calculus using mechanical vibrations; for removing obstructions in blood vessels, not otherwise provided for
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods
    • A61B17/32Surgical cutting instruments

Definitions

  • the present invention relates to a treatment tool for endoscope and a method for manufacturing a treatment tool for endoscope.
  • a treatment tool used in medical endoscopes it is inserted into the lumen from the distal end of the endoscope insertion portion, and the internal tissues such as polyps are bound by excision with a snare which is a loop-like wire
  • the treatment tool to do is known (for example, refer to patent documents 1).
  • a high frequency snare hot snare
  • cauterizes and excises the tied internal tissues by supplying a high frequency current to the snare.
  • a method called a cold snare has been widely spread, in which a body tissue is ablated only by binding with a wire without flowing a high frequency current through the snare.
  • Excision of internal tissues with a cold snare is accompanied by bleeding because hemostasis due to heat coagulation can not be expected like high frequency snares, but its influence is limited to the excision site, and therefore the invasiveness is low.
  • cold snares do not require complicated preoperative preparation as in the case of high frequency snares.
  • the diameter of the wire forming the snare is reduced, the difference in outer diameter from the operation wire becomes large, which makes it difficult to connect the snare and the operation wire, and various problems may occur.
  • the gap between the connecting member and the snare is large, so air bubbles (voids) and holes (insertion voids) are generated and the brazing material is not sufficiently filled.
  • the bonding strength tends to vary.
  • the present invention has been made in view of the above, and it is possible to join operation wires and wire treatment tools having a large difference in outer diameter without causing variations in joint strength or deterioration of product performance, and additionally, conventionally It is an object of the present invention to provide a method of manufacturing a treatment tool for an endoscope which can significantly reduce the length of the rigid portion and a treatment tool for an endoscope manufactured thereby.
  • a treatment tool for an endoscope comprises: a metal operation wire; a wire treatment tool formed by bundling the end portions of the metal wire; A connecting portion formed by twisting a plurality of metal wires constituting the proximal end portion of the wire treatment tool and having an outer diameter equal to the outer diameter of the operating wire;
  • the end faces of the parts are characterized in that they are joined by upset resistance welding in a state where they are butted to each other.
  • the endoscope treatment tool according to the present invention is characterized in that, in the above invention, the wire treatment tool is a loop snare.
  • a method of manufacturing a treatment tool for an endoscope is a wire treatment tool formed by bundling an operation wire made of metal and an end portion of the metal wire And a connecting portion having an outer diameter equal to the outer diameter of the operation wire, in the method of manufacturing a treatment tool for an endoscope, the plurality of metal wires constituting the proximal end portion of the wire treatment device being the operation.
  • the upset resistance welding is performed in a state where the end of the operation wire and the end face of the connection part are butted against each other, and the end of the operation wire and the end face of the connection part are abutted with each other. And welding.
  • the method for manufacturing a treatment tool for an endoscope according to the present invention further includes, in the above-mentioned invention, a detent step of melting and cutting the connection portion at a predetermined position between the twisting step and the welding step. It is characterized by
  • the welding is performed by arc welding.
  • the method may further include a detent step of melting the cut portion of the connection portion.
  • the proximal end portion of the wire treatment tool is twisted to form a connection portion, and the operation wire and the wire treatment device are joined via the connection portion, leading to variations in bonding strength and a decrease in product performance. Therefore, the operation wire and the wire treatment tool having a large difference in outer diameter can be joined. Further, since the operation wire and the wire treatment tool are joined without using the connecting member, the length of the hard portion can be significantly shortened as compared with the conventional case, and the degree of freedom in product design is expanded.
  • FIG. 1 is a view showing a configuration of an endoscope including a treatment tool for an endoscope according to an embodiment of the present invention.
  • FIG. 2 is a cross-sectional view showing the configuration of the operation part and the insertion part in the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 3 is a view showing the configuration of the insertion portion in the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 4 is a flowchart showing an example of a method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 5 is a view showing a twisting step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 6 is a view showing a twisting step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 7 is a view showing a twisting step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 8 is a view showing a welding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 9 is a view showing a welding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 10 is a view showing a polishing step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 11 is a view showing the unfolding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 12 is a view showing the unfolding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 13 is a view showing a state in which the end surface of the distal end portion of the operation wire and the end surface of the connecting portion are abutted after the unfolding stop step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention It is.
  • FIG. 14 is a view showing the unfolding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 15 is a view showing the unfolding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 16 is a view showing the unfolding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention.
  • FIG. 17 is a view showing a modified example of the wire treatment tool in the endoscope treatment tool according to the embodiment of the present invention.
  • FIG. 18 is a view showing a modified example of the wire treatment tool in the endoscope treatment tool according to the embodiment of the present invention.
  • FIG. 19 is a view showing a modified example of the wire treatment tool in the endoscope treatment tool according to the embodiment of the present invention.
  • the configuration of the endoscope treatment tool according to the present embodiment will be described with reference to FIGS. 1 to 3.
  • the endoscope treatment tool 1 constitutes a part of the endoscope 100 as shown in FIG. 1, and is specifically used in a cold snare system.
  • the endoscope treatment tool 1 includes an operation unit 10 and an insertion unit 20 provided on the distal end side of the operation unit 10.
  • the operation unit 10 is for operating the snare 23 provided on the distal end side of the insertion unit 20.
  • the operation unit 10 includes a main body portion 11, a connection cap 12, a fold prevention portion 13, a slider 14, and a stopper pipe 15.
  • the main body portion 11 is formed in an elongated cylindrical shape. Inside the main body portion 11, a guide groove 11a is formed along the direction of the axis (see the dashed line in FIG. 2). The guide groove 11a accommodates the projection 143 of the slider 14 and the operation wire 22 connected to the projection 143, as described later.
  • a ring portion 111 for a user who manipulates the endoscope 100 to insert and hook a thumb is formed on the proximal end side of the main body portion 11.
  • a connection cap 12 is fixed to the tip end side of the main body portion 11.
  • the main body 11 and the connection cap 12 are made of a synthetic resin material (for example, an ABS resin) which can be freely processed into a desired shape at low cost.
  • connection cap 12 is connected to a proximal end portion 131 of the fold prevention portion 13 and a proximal end portion 211 of the flexible sheath 21 described later.
  • the anti-folding portion 13 is formed in an elongated cylindrical shape, and is made of a flexible material (for example, a fluorine resin such as Teflon (registered trademark) resin, polyethylene, etc.) like the flexible sheath 21 described later. It is configured.
  • the slider 14 is attached to the main body 11 and is configured to be movable back and forth along the axial direction.
  • the slider 14 includes a pair of ring portions 141 and 142 for the user to insert and hook two fingers other than the thumb.
  • the ring portions 141 and 142 are provided at positions on both sides of the main body portion 11, that is, in symmetrical positions with respect to the axial direction.
  • the slider 14 is provided with a projection 143 which is inserted into the guide groove 11 a of the main body 11.
  • An engaging member 144 is embedded in the projection 143, and a proximal end 221 of an operation wire 22 described later is engaged with the engaging member 144.
  • the operation wire 22 advances and retracts in conjunction with the advancing and retracting operation of the slider 14.
  • the stopper pipe 15 is formed in an elongated cylindrical shape, and is disposed so as to cover a part of the operation wire 22.
  • the stopper pipe 15 restricts the drawing-in position of the operation wire 22 by coming into contact with the projection 143 when the slider 14 is slid to the base end side (ring portion 111 side).
  • the stopper pipe 15 is made of, for example, a conductive material such as a stainless steel pipe material.
  • the insertion portion 20 is inserted in a treatment channel 102 formed in the insertion portion 101 of the endoscope 100 so as to be able to move forward and backward, and is inserted into the body via the treatment channel 102.
  • the insertion portion 20 includes a flexible sheath 21, an operation wire 22, a snare 23, and a connection portion 24.
  • the flexible sheath 21 constitutes an outer cover of the insertion portion 20, and accommodates the operation wire 22, the snare 23, and the connection portion 24 in a retractable manner.
  • the flexible sheath 21 has a small friction and an excellent ability to transmit force, in order to improve the insertion of the endoscope 100 into the treatment instrument channel 102 and the operability of the operation wire 22 advancing and retracting the inside.
  • the distal end of the flexible sheath 21 is inclined at an angle of 45 ° with respect to the axial direction. As a result, the flexible sheath 21 can be prevented from collapsing when the body tissue is bound by the snare 23.
  • the operation wire 22 is accommodated inside the flexible sheath 21.
  • the operation wire 22 is made of a large diameter metal wire excellent in operability, and is formed of, for example, a stranded wire of a metal wire such as stainless steel SUS304.
  • the metal wire that constitutes the operation wire 22 have a force transmission that can reliably deploy the snare 23 from the flexible sheath 21 under any circumstances. Further, the metal wire that constitutes the operation wire 22 is also in a situation that is disadvantageous for the deployment of the snare 23, as in the case where the snare 23 is located at the curved portion of the insertion portion 101 of the endoscope 100, for example. It is desirable that the snare 23 has a force transferability that enables the snare 23 to be deployed from the distal end of the flexible sheath 21 with certainty.
  • the snare (wire treatment tool) 23 is formed by bundling the end portions of a thin metal wire excellent in excision, and, like the operation wire 22, for example, by a stranded wire of a metal wire such as stainless steel SUS304. It is configured.
  • the snare 23 includes a pair of elliptical loop portions 231 and 232, and an end portion 233 formed by bending a metal wire in a U shape at one end of the loop portions 231 and 232, And 24.
  • the connecting portion 24 is joined to the distal end portion 222 of the operation wire 22 via the welding portion 25.
  • the connection portion 24 is formed by twisting a plurality of metal wires constituting the proximal end 234 of the snare 23, as shown in FIGS. 5 and 6 described later.
  • the connecting portion 24 has an outer diameter substantially equal to the outer diameter of the distal end portion 222 of the operation wire 22.
  • the welding portion 25 is formed when the distal end portion 222 of the operation wire 22 and the connection portion 24 are joined by upset resistance welding as described later, and the metal wire constituting the operation wire 22 and the connection portion 24 are It is comprised from the metal structure which the metal wire to comprise mixed.
  • step S 1 A method of manufacturing the endoscope treatment tool 1 according to the present embodiment will be described with reference to FIGS. 4 to 16.
  • a twisting step step S 1 of twisting the proximal end 234 of the snare 23 to form the connecting portion 24, and the operation wire 22
  • a welding step step S2 of joining the connecting portion 24 by upset resistance welding is performed in this order. The details of each step will be described below.
  • ⁇ Twisting step> a plurality of metal wires constituting the proximal end 234 of the snare 23 are twisted so as to be substantially equal to the outer diameter of the distal end 222 of the operation wire 22 to form the connecting part 24.
  • the chuck 31 sandwiches from the vicinity of the start end 234a of the proximal end 234 of the snare 23 where the metal wires are arranged in parallel to the vicinity of the end of the loop portions 231 and 232. Fix it. Subsequently, the vicinity of the end 234 b of the base end 234 of the snare 23 is sandwiched and fixed by the chuck 32.
  • the coupling portion 24 is formed by rotating the chuck 32 about the axis and twisting so that two metal wires constituting the proximal end portion 234 become one. Subsequently, as shown in FIG. 7, the formed connection portion 24 is cut into a predetermined length by a cutting tool (nipper or the like) to form an end surface 242.
  • the outer diameter of the proximal end 234 of the snare 23 shown in FIG. 5 is smaller than the outer diameter of the distal end 222 of the operation wire 22.
  • the outer diameter of the metal wire constituting the snare 23 Assuming that r is the outer diameter of the metal wire constituting the operation wire 22 is R, the outer diameter r of the metal wire constituting the snare 23 is 1/2 or less of the outer diameter R of the metal wire constituting the operation wire 22. It is desirable that (0 ⁇ r ⁇ R / 2), and 1/3 or less (0 ⁇ r ⁇ R / 3) is more preferable because excisability of internal tissues is improved.
  • the proximal end 234 of the snare 23 and the distal end 222 of the operation wire 22 originally have a large difference in outer diameter
  • the snare 23 is obtained.
  • the proximal end 234 is processed into the connecting portion 24 having the same outer diameter as the distal end 222 of the operation wire 22.
  • ⁇ Welding step> As shown in FIGS. 8 and 9, the end surface 223 of the distal end portion 222 of the operation wire 22 and the end surface 242 of the connection portion 24 are joined by upset resistance welding in a state where they abut each other.
  • the connecting portion 24 is attached to the stationary chuck 41 of the upset resistance welding device 40. At this time, positioning is performed so that the end surface 242 of the connecting portion 24 is positioned at the center of the gap between the fixed chuck 41 and the movable chuck 42.
  • the size d 1 of the gap between the fixed-side chuck 41 and the moving-side chuck 42 is almost equal to the outer diameter of the generally bonded members is a measure.
  • the end surface 223 of the operation wire 22 is abutted against the end surface 242 of the connection portion 24 and fixed to the moving chuck 42.
  • the end surface 223 of the operation wire 22 and the end surface 242 of the connection portion 24 be in close contact with each other without a gap and be abutted.
  • each end surface 223, 242 It is desirable to finish it at right angles.
  • the operation wire 22 when the operation wire 22 is easily broken, the operation wire 22 may be melted or cut off and welded to the operation wire 22, and then a right angle finish with a file, a grinder or the like may be performed.
  • the stopper (not shown) of the movable chuck 42 is released, the movable chuck 42 is pressed by the pressure spring 43, and the end surface 223 of the operation wire 22 is The end face 242 is pressurized with a predetermined force.
  • a predetermined current is applied to the fixed chuck 41 and the movable chuck 42, and the member to be joined between the fixed chuck 41 and the movable chuck 42, that is, the end surface 223 of the operation wire 22 and the end surface 242 of the connecting portion 24.
  • the metal structure around the butting part A is heated by resistance (Joule) and melted.
  • the molten metal structure is set up by the upset pressure (set-up pressure), and as shown in FIG. 9, the operation wire 22 and the connecting portion 24 set up while extruding the molten excess metal structure. It is pushed to the center B.
  • the size of the gap between the fixed-side chuck 41 and the moving-side chuck 42 is reduced from d 1 to d 2.
  • the moving amount (d 1 ⁇ d 2 ) of the moving side chuck 42 at that time, that is, the length (quantity) of pushing out the molten metal structure becomes the upset amount (defensing amount).
  • a polishing step is performed to finish the extra metal structure pushed out to the outer periphery with a file, a grinder or the like to complete the bonding.
  • the upset resistance welding heats the members to be joined by resistance heating (Joule heat), so if the shapes and dimensions of the members to be joined differ greatly, the difference in resistance value causes a large difference in heat generation. It can not be made stable welding.
  • the proximal end 234 of the snare 23 is twisted, and a connecting portion having an outer diameter substantially equal to the outer diameter of the distal end 222 of the operation wire 22.
  • the difference in outer diameter between the operation wire 22 and the proximal end 234 of the snare 23 is compensated. Therefore, the difference in cross-sectional area between the members to be joined becomes smaller, and the amount of heat generated between the members to be joined becomes equal, so stable welding becomes possible.
  • the unwrapping step for preventing the unraveling of the metal wire forming the connecting portion 24 is performed between the twisting step and the welding step. May be
  • the anti-rolling step can use, for example, a method of melting the connecting portion 24 at a predetermined position. That is, after forming the connecting portion 24 in the above-described twisting step, as shown in FIG. 11, one side of the connecting portion 24 is sandwiched and fixed by the chuck 51 of the fusing apparatus 50, and the other side of the connecting portion 24 is It clamps with a chuck
  • connection part 24 can be cut
  • connection portion 24 is formed in the above-described twisting step, the connection portion 24 is cut at a predetermined position. Subsequently, as shown in FIG. 14, the connecting portion 24 is sandwiched and fixed by the chuck 61 of the arc welding apparatus 60 so that the cutting portion 243 of the connecting portion 24 protrudes from the end surface 611 of the chuck 61 to the arc electrode 62 side. Do. Subsequently, when arc welding is performed in this state, the cut portion 243 of the connection portion 24 melts, and as shown in FIG. 15, a molten ball 25A is formed. Subsequently, as shown in FIG.
  • the melting spheres 25A are attached to form a vertical end face 242B. Then, in the same manner as in FIG. 13 described above, the welding step is performed in a state where the end surface 223 of the distal end portion 222 of the operation wire 22 butts against the end surface 242B of the connecting portion 24 formed by melting. The distal end portion 222 and the connecting portion 24 are joined.
  • the proximal end 234 of the snare 23 is twisted to form the connecting portion 24, and the operation wire is connected via the connecting portion 24.
  • the operation wire 22 and the snare 23 can be joined at low cost without causing variations in joining strength or deterioration in product performance and without using advanced skills.
  • the operation wire 22 and the snare 23 are joined without using the connecting member, the length of the hard portion can be considerably shortened as compared with the conventional case, and the degree of freedom in product design is expanded.
  • the metal wire which comprises the operation wire 22 or the snare 23 twists a thin metal wire together, a clearance gap exists between wires. Therefore, as in the general welding method, if only melting and solidifying the metal structure of the joint, the metal structure corresponding to the gap volume between the strands runs short, and the joint is extremely thinly constricted. And defects tend to occur in the metal structure of the joint.
  • the endoscope treatment tool 1 according to the present embodiment can obtain a large bonding strength as a whole, and sufficiently satisfy the bonding strength required for the cold snare type endoscope treatment tool 1 as well. Can.
  • the wire treatment tool in the endoscopic treatment tool 1 is not limited to the snare 23 shown in FIG.
  • the endoscope treatment tool 1 may use, as a wire treatment tool, for example, as shown in FIG. 17, a snare 23A including polygonal loop portions 231A and 232A made of metal wires.
  • the endoscope treatment tool 1 may use, as a wire treatment tool, for example, as shown in FIG. 18, a snare 23B including asymmetrically shaped loop portions 231B and 232B made of metal wires.
  • the endoscope treatment tool 1 is a wire treatment tool, for example, as shown in FIG. 19, polygonal loop portions 231C, 232C, 233C, and 234C consisting of four metal wires, and these loop portions 231C, And a tip cap 235C for bundling 232C, 233C, and 234C, and may use a basket 23C.
  • connection structure of the operation wire 22 and the snare 23 in the endoscopic treatment tool 1 used in the cold snare method has been described, but the connection structure is the endoscope used in the hot snare method. It is applicable also to a treatment tool.
  • a metal terminal is fixed to the slider 14 of the operation unit 10
  • the proximal end 221 of the operation wire 22 is connected to one end of the terminal
  • the high frequency generator is connected to the other end.
  • the other structure required for the treatment tool for endoscopes used by such a hot snare system is disclosed by above-mentioned patent document 1, detailed description is abbreviate
  • omitted since the other structure required for the treatment tool for endoscopes used by such a hot snare system is disclosed by above-mentioned patent document 1, detailed description is abbreviate

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Abstract

An endoscopic treatment tool 1 that comprises: a metal operation wire 22; a snare 23 that is formed by bundling end parts of a metal wire; and a connection part 24 that has the same outer diameter as the operation wire 22 and is formed by twisting together a plurality of metal wires that constitute a base end part 234 of the snare 23. An end surface of the operation wire 22 abuts and is joined by upset resistance welding to an end surface of the connection part 24.

Description

内視鏡用処置具および内視鏡用処置具の製造方法Treatment tool for endoscope and method of manufacturing treatment tool for endoscope

 本発明は、内視鏡用処置具および内視鏡用処置具の製造方法に関する。 The present invention relates to a treatment tool for endoscope and a method for manufacturing a treatment tool for endoscope.

 従来、医療用の内視鏡で使用される処置具として、内視鏡挿入部の先端部から管腔内に挿入され、ポリープ等の体内組織をループ状のワイヤであるスネアによって緊縛して切除する処置具が知られている(例えば、特許文献1を参照)。このような処置具では、スネアに高周波電流を流すことにより、緊縛した体内組織を焼灼切除する高周波スネア(ホットスネア)を用いるのが一般的である。 Conventionally, as a treatment tool used in medical endoscopes, it is inserted into the lumen from the distal end of the endoscope insertion portion, and the internal tissues such as polyps are bound by excision with a snare which is a loop-like wire The treatment tool to do is known (for example, refer to patent documents 1). In such a treatment tool, it is general to use a high frequency snare (hot snare) which cauterizes and excises the tied internal tissues by supplying a high frequency current to the snare.

 高周波スネアでは、焼灼によって体内組織を熱凝固(止血)しながら切除するため、術中の出血を抑えることができる一方、術後に切除部の深層組織から大きな出血を伴う場合もある。また、高周波スネアでは、高周波電源の準備や患者への対極板の取り付け等が必要であるため、術前の準備が煩雑である。加えて、高周波スネアの場合、術中も患者や術者の熱傷等に注意する必要がある。 In high-frequency snares, ablation is performed while cauterizing the body tissue while performing thermal coagulation (hemostasis), so that bleeding during operation can be suppressed, but in some cases, deep bleeding from the deep tissue of the resected site may be accompanied by surgery. Further, in the high frequency snare, preparation for the operation is complicated because preparation of the high frequency power source and attachment of the return electrode plate to the patient are required. In addition, in the case of a high frequency snare, it is necessary to pay attention to burns and the like of the patient and the operator during the operation.

 このような背景の下、近年、スネアに高周波電流を流すことなく、ワイヤによる緊縛のみで体内組織を切除するコールドスネアと呼ばれる手法が普及しつつある。コールドスネアによる体内組織の切除は、高周波スネアのように熱凝固作用による止血が期待できないため出血を伴うものの、その影響は切除部に限られるため侵襲性が低い。また、コールドスネアは、高周波スネアの場合のように煩雑な術前の準備を必要としない。 Under such circumstances, in recent years, a method called a cold snare has been widely spread, in which a body tissue is ablated only by binding with a wire without flowing a high frequency current through the snare. Excision of internal tissues with a cold snare is accompanied by bleeding because hemostasis due to heat coagulation can not be expected like high frequency snares, but its influence is limited to the excision site, and therefore the invasiveness is low. In addition, cold snares do not require complicated preoperative preparation as in the case of high frequency snares.

 その一方で、コールドスネアの場合、体内の出血を最小限に抑えて体内組織を切除するためには、切れ味のよいスネアを用いることが必須である。切れ味のよいスネアを形成するためには、径が小さいワイヤを用いてスネアを形成するのが最も効果的である。これにより、体内組織を緊縛した際にスネアが体内組織に切り込みやすくなり、少ない出血で体内組織を切除することができる。 On the other hand, in the case of cold snares, it is essential to use sharp snares in order to remove body tissue with minimal bleeding in the body. In order to form a sharp snare, it is most effective to form a snare using a small diameter wire. This makes it easier for the snare to cut into the body tissue when the body tissue is tied up, and the body tissue can be removed with less bleeding.

特開2001-218771号公報Japanese Patent Application Publication No. 2001-218771 特許第5325520号公報Patent No. 5325520

 しかしながら、スネアを形成するワイヤの径が小さくなると、操作ワイヤとの外径寸法差が大きくなってスネアと操作ワイヤとの接続が困難になるだけでなく、様々な不具合が生じるおそれがある。例えば、連結部材を介してスネアと操作ワイヤをロウ付けする場合、連結部材とスネアとの隙間が大きいため、気泡(ボイド)や孔(挿通ボイド)が発生してロウ材が十分に充填されず、接合強度にばらつきが生じやすい。 However, if the diameter of the wire forming the snare is reduced, the difference in outer diameter from the operation wire becomes large, which makes it difficult to connect the snare and the operation wire, and various problems may occur. For example, when the snare and the operation wire are brazed through the connecting member, the gap between the connecting member and the snare is large, so air bubbles (voids) and holes (insertion voids) are generated and the brazing material is not sufficiently filled. The bonding strength tends to vary.

 この問題を解決するために、例えば特許文献2に示すように、連結部材とスネアをカシメによって接続することが考えられる。しかしながらこの場合には、スネアの基端部の連結部材との隙間が大きいことに起因して、スネアを構成する撚り線が解れやねじれを生じた状態で接合されてしまうことがある。スネアを構成する撚り線が解れやねじれを生じた結果、処置具の挿入部の先端からスネアを展開する際にループが同一の平面内に広がらず、体内組織に引っ掛けにくくなったり、緊縛時にスネアが体内組織から外れやすくなったりして、製品性能が低下してしまうおそれがある。 In order to solve this problem, for example, as shown in Patent Document 2, it is conceivable to connect the connecting member and the snare by caulking. However, in this case, due to the large gap between the proximal end portion of the snare and the connecting member, the twisted wires constituting the snare may be joined in a state where the snare is broken or twisted. As a result of the twisted wire constituting the snare being untwisted or twisted, the loop does not spread in the same plane when deploying the snare from the distal end of the insertion portion of the treatment tool, making it difficult to hook on body tissue, or snare during tightening. Can easily come off internal tissues, and product performance may be degraded.

 また、特許文献1,2では、スネアの基端部と操作ワイヤとを、連結部材を介して接続するため、硬質部長が長くなるという問題がある。硬質部長が長くなると、内視鏡用処置具を内視鏡の処置具チャンネルを介して体内に挿入する際に、挿入力量の増大や、処置具チャンネル内での引っ掛かりが発生しやすくなり、ユーザの操作性を損なうおそれがあった。 Moreover, in patent document 1, 2, in order to connect the proximal end part of a snare, and an operation wire via a connection member, there exists a problem that hard part length becomes long. When the length of the hard part is increased, when inserting the endoscope treatment tool into the body through the treatment channel of the endoscope, an increase in the amount of insertion force and catching in the treatment channel are likely to occur. There was a risk that the operability of the

 本発明は、上記に鑑みてなされたものであって、接合強度のばらつきや製品性能の低下を招くことなく、外径差の大きい操作ワイヤおよびワイヤ処置具を接合することができ、加えて従来よりも硬質部長を大幅に短縮することができる内視鏡用処置具の製造方法およびそれにより製造された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, and it is possible to join operation wires and wire treatment tools having a large difference in outer diameter without causing variations in joint strength or deterioration of product performance, and additionally, conventionally It is an object of the present invention to provide a method of manufacturing a treatment tool for an endoscope which can significantly reduce the length of the rigid portion and a treatment tool for an endoscope manufactured thereby.

 上述した課題を解決し、目的を達成するために、本発明に係る内視鏡用処置具は、金属製の操作ワイヤと、金属ワイヤの端部を束ねて形成されたワイヤ処置具と、前記ワイヤ処置具の基端部を構成する複数の金属ワイヤが撚り込まれることにより形成され、前記操作ワイヤの外径と等しい外径を有する連結部と、を備え、前記操作ワイヤの端面と前記連結部の端面とは、互いに突き合わされた状態で、アップセット抵抗溶接により接合されていることを特徴とする。 In order to solve the problems described above and to achieve the object, a treatment tool for an endoscope according to the present invention comprises: a metal operation wire; a wire treatment tool formed by bundling the end portions of the metal wire; A connecting portion formed by twisting a plurality of metal wires constituting the proximal end portion of the wire treatment tool and having an outer diameter equal to the outer diameter of the operating wire; The end faces of the parts are characterized in that they are joined by upset resistance welding in a state where they are butted to each other.

 また、本発明に係る内視鏡用処置具は、上記発明において、前記ワイヤ処置具は、ループ状のスネアであることを特徴とする。 The endoscope treatment tool according to the present invention is characterized in that, in the above invention, the wire treatment tool is a loop snare.

 上述した課題を解決し、目的を達成するために、本発明に係る内視鏡用処置具の製造方法は、金属製の操作ワイヤと、金属ワイヤの端部を束ねて形成されたワイヤ処置具と、前記操作ワイヤの外径と等しい外径を有する連結部と、を備える内視鏡用処置具の製造方法において、前記ワイヤ処置具の基端部を構成する複数の金属ワイヤを、前記操作ワイヤの外径と等しくなるように撚り込んで前記連結部を形成する撚り込み加工ステップと、前記操作ワイヤの端面と前記連結部の端面とを、互いに突き当てた状態で、アップセット抵抗溶接により接合する溶接ステップと、を含むことを特徴とする。 In order to solve the problems described above and to achieve the object, a method of manufacturing a treatment tool for an endoscope according to the present invention is a wire treatment tool formed by bundling an operation wire made of metal and an end portion of the metal wire And a connecting portion having an outer diameter equal to the outer diameter of the operation wire, in the method of manufacturing a treatment tool for an endoscope, the plurality of metal wires constituting the proximal end portion of the wire treatment device being the operation The upset resistance welding is performed in a state where the end of the operation wire and the end face of the connection part are butted against each other, and the end of the operation wire and the end face of the connection part are abutted with each other. And welding.

 また、本発明に係る内視鏡用処置具の製造方法は、上記発明において、前記撚り込み加工ステップと前記溶接ステップとの間に、前記連結部を所定位置で溶断する解れ止めステップをさらに含むことを特徴とする。 Further, the method for manufacturing a treatment tool for an endoscope according to the present invention further includes, in the above-mentioned invention, a detent step of melting and cutting the connection portion at a predetermined position between the twisting step and the welding step. It is characterized by

 また、本発明に係る内視鏡用処置具の製造方法は、上記発明において、前記撚り込み加工ステップと前記溶接ステップとの間に、前記連結部を所定位置で切断した後、アーク溶接により前記連結部の切断部を溶融させる解れ止めステップをさらに含むことを特徴とする。 In the method for manufacturing a treatment tool for an endoscope according to the present invention, in the above-mentioned invention, after cutting the connecting portion at a predetermined position between the twisting step and the welding step, the welding is performed by arc welding. The method may further include a detent step of melting the cut portion of the connection portion.

 本発明によれば、ワイヤ処置具の基端部を撚り込んで連結部とし、当該連結部を介して操作ワイヤおよびワイヤ処置具を接合することにより、接合強度のばらつきや製品性能の低下を招くことなく、外径差の大きい操作ワイヤおよびワイヤ処置具を接合することができる。また、連結部材を用いずに操作ワイヤおよびワイヤ処置具を接合するため、従来よりも硬質部長を大幅に短縮することができ、製品設計の自由度が拡大する。 According to the present invention, the proximal end portion of the wire treatment tool is twisted to form a connection portion, and the operation wire and the wire treatment device are joined via the connection portion, leading to variations in bonding strength and a decrease in product performance. Therefore, the operation wire and the wire treatment tool having a large difference in outer diameter can be joined. Further, since the operation wire and the wire treatment tool are joined without using the connecting member, the length of the hard portion can be significantly shortened as compared with the conventional case, and the degree of freedom in product design is expanded.

図1は、本発明の実施の形態に係る内視鏡用処置具を含む内視鏡の構成を示す図である。FIG. 1 is a view showing a configuration of an endoscope including a treatment tool for an endoscope according to an embodiment of the present invention. 図2は、本発明の実施の形態に係る内視鏡用処置具における操作部および挿入部の構成を示す断面図である。FIG. 2 is a cross-sectional view showing the configuration of the operation part and the insertion part in the endoscopic treatment tool according to the embodiment of the present invention. 図3は、本発明の実施の形態に係る内視鏡用処置具における挿入部の構成を示す図である。FIG. 3 is a view showing the configuration of the insertion portion in the endoscopic treatment tool according to the embodiment of the present invention. 図4は、本発明の実施の形態に係る内視鏡用処置具の製造方法の一例を示すフローチャートである。FIG. 4 is a flowchart showing an example of a method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention. 図5は、本発明の実施の形態に係る内視鏡用処置具の製造方法における撚り込み加工ステップを示す図である。FIG. 5 is a view showing a twisting step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention. 図6は、本発明の実施の形態に係る内視鏡用処置具の製造方法における撚り込み加工ステップを示す図である。FIG. 6 is a view showing a twisting step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention. 図7は、本発明の実施の形態に係る内視鏡用処置具の製造方法における撚り込み加工ステップを示す図である。FIG. 7 is a view showing a twisting step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention. 図8は、本発明の実施の形態に係る内視鏡用処置具の製造方法における溶接ステップを示す図である。FIG. 8 is a view showing a welding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention. 図9は、本発明の実施の形態に係る内視鏡用処置具の製造方法における溶接ステップを示す図である。FIG. 9 is a view showing a welding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention. 図10は、本発明の実施の形態に係る内視鏡用処置具の製造方法における研磨ステップを示す図である。FIG. 10 is a view showing a polishing step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention. 図11は、本発明の実施の形態に係る内視鏡用処置具の製造方法における解れ止めステップを示す図である。FIG. 11 is a view showing the unfolding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention. 図12は、本発明の実施の形態に係る内視鏡用処置具の製造方法における解れ止めステップを示す図である。FIG. 12 is a view showing the unfolding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention. 図13は、本発明の実施の形態に係る内視鏡用処置具の製造方法における解れ止めステップの後に、操作ワイヤの先端部の端面と、連結部の端面とを突き当てた状態を示す図である。FIG. 13 is a view showing a state in which the end surface of the distal end portion of the operation wire and the end surface of the connecting portion are abutted after the unfolding stop step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention It is. 図14は、本発明の実施の形態に係る内視鏡用処置具の製造方法における解れ止めステップを示す図である。FIG. 14 is a view showing the unfolding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention. 図15は、本発明の実施の形態に係る内視鏡用処置具の製造方法における解れ止めステップを示す図である。FIG. 15 is a view showing the unfolding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention. 図16は、本発明の実施の形態に係る内視鏡用処置具の製造方法における解れ止めステップを示す図である。FIG. 16 is a view showing the unfolding step in the method of manufacturing the endoscopic treatment tool according to the embodiment of the present invention. 図17は、本発明の実施の形態に係る内視鏡用処置具において、ワイヤ処置具の変形例を示す図である。FIG. 17 is a view showing a modified example of the wire treatment tool in the endoscope treatment tool according to the embodiment of the present invention. 図18は、本発明の実施の形態に係る内視鏡用処置具において、ワイヤ処置具の変形例を示す図である。FIG. 18 is a view showing a modified example of the wire treatment tool in the endoscope treatment tool according to the embodiment of the present invention. 図19は、本発明の実施の形態に係る内視鏡用処置具において、ワイヤ処置具の変形例を示す図である。FIG. 19 is a view showing a modified example of the wire treatment tool in the endoscope treatment tool according to the embodiment of the present invention.

 以下、本発明の実施の形態に係る内視鏡用処置具および内視鏡用処置具の製造方法について、図面を参照しながら説明する。なお、本発明は以下の実施の形態に限定されるものではなく、以下の実施の形態における構成要素には、当業者が置換可能かつ容易なもの、あるいは実質的に同一のものも含まれる。また、以下で参照する各図面において、同一部分には同一の符号を付して示している。 Hereinafter, a treatment tool for an endoscope and a method of manufacturing the treatment tool for an endoscope according to the embodiment of the present invention will be described with reference to the drawings. The present invention is not limited to the following embodiments, and the constituent elements in the following embodiments include those that can be easily replaced by persons skilled in the art or those that are substantially the same. In each drawing referred to in the following, the same parts are indicated by the same reference numerals.

[内視鏡用処置具]
 本実施の形態に係る内視鏡用処置具の構成について、図1~図3を参照しながら説明する。内視鏡用処置具1は、図1に示すように、内視鏡100の一部を構成するものであり、具体的にはコールドスネア方式で用いられる。内視鏡用処置具1は、操作部10と、当該操作部10の先端側に設けられた挿入部20と、を備えている。
[Treatment tool for endoscope]
The configuration of the endoscope treatment tool according to the present embodiment will be described with reference to FIGS. 1 to 3. The endoscope treatment tool 1 constitutes a part of the endoscope 100 as shown in FIG. 1, and is specifically used in a cold snare system. The endoscope treatment tool 1 includes an operation unit 10 and an insertion unit 20 provided on the distal end side of the operation unit 10.

 操作部10は、挿入部20の先端側に設けられたスネア23を操作するためのものである。操作部10は、具体的には図2に示すように、本体部11と、連結用キャップ12と、折れ止め部13と、スライダ14と、ストッパパイプ15と、を備えている。 The operation unit 10 is for operating the snare 23 provided on the distal end side of the insertion unit 20. Specifically, as shown in FIG. 2, the operation unit 10 includes a main body portion 11, a connection cap 12, a fold prevention portion 13, a slider 14, and a stopper pipe 15.

 本体部11は、細長い筒状に形成されている。本体部11の内部には、軸線(図2の一点鎖線参照)方向に沿ってガイド溝11aが形成されている。このガイド溝11aには、後記するように、スライダ14の突起部143および当該突起部143に接続された操作ワイヤ22が収容されている。 The main body portion 11 is formed in an elongated cylindrical shape. Inside the main body portion 11, a guide groove 11a is formed along the direction of the axis (see the dashed line in FIG. 2). The guide groove 11a accommodates the projection 143 of the slider 14 and the operation wire 22 connected to the projection 143, as described later.

 本体部11の基端側には、内視鏡100を扱うユーザが親指を挿入して引っ掛けるためのリング部111が形成されている。また、本体部11の先端側には、連結用キャップ12が固定されている。なお、本体部11および連結用キャップ12は、低コストで、所望の形状へと自由に加工することが可能な合成樹脂材料(例えばABS樹脂)により構成されている。 On the proximal end side of the main body portion 11, a ring portion 111 for a user who manipulates the endoscope 100 to insert and hook a thumb is formed. In addition, a connection cap 12 is fixed to the tip end side of the main body portion 11. The main body 11 and the connection cap 12 are made of a synthetic resin material (for example, an ABS resin) which can be freely processed into a desired shape at low cost.

 連結用キャップ12には、折れ止め部13の基端部131と、後記する可撓性シース21の基端部211とが連結されている。折れ止め部13は、細長い筒状に形成されており、後記する可撓性シース21と同様に、可撓性のある材料(例えばテフロン(登録商標)樹脂等のフッ素系樹脂やポリエチレン等)により構成されている。 The connection cap 12 is connected to a proximal end portion 131 of the fold prevention portion 13 and a proximal end portion 211 of the flexible sheath 21 described later. The anti-folding portion 13 is formed in an elongated cylindrical shape, and is made of a flexible material (for example, a fluorine resin such as Teflon (registered trademark) resin, polyethylene, etc.) like the flexible sheath 21 described later. It is configured.

 スライダ14は、本体部11に取り付けられており、軸線方向に沿って進退自在に構成されている。スライダ14は、ユーザが親指以外の2本の指をそれぞれ挿入して引っ掛けるための一対のリング部141,142を備えている。リング部141,142は、本体部11の両側の位置、すなわち軸線方向に対して対称な位置に設けられている。 The slider 14 is attached to the main body 11 and is configured to be movable back and forth along the axial direction. The slider 14 includes a pair of ring portions 141 and 142 for the user to insert and hook two fingers other than the thumb. The ring portions 141 and 142 are provided at positions on both sides of the main body portion 11, that is, in symmetrical positions with respect to the axial direction.

 また、スライダ14は、本体部11のガイド溝11a内に挿入される突起部143を備えている。この突起部143には係合部材144が埋設されており、当該係合部材144に、後記する操作ワイヤ22の基端部221が係合されている。これにより、スライダ14の進退動作に連動して操作ワイヤ22が進退する。 Further, the slider 14 is provided with a projection 143 which is inserted into the guide groove 11 a of the main body 11. An engaging member 144 is embedded in the projection 143, and a proximal end 221 of an operation wire 22 described later is engaged with the engaging member 144. Thereby, the operation wire 22 advances and retracts in conjunction with the advancing and retracting operation of the slider 14.

 すなわち、スライダ14を基端側(リング部111側)にスライド操作すると、スネア23の一対のループ部231,232(図3参照)が直線状に延ばされ、可撓性シース21の内側に引き込まれて収容される。一方、スライダ14を先端側(連結用キャップ12側)にスライド操作すると、可撓性シース21の外側にスネア23が突き出され、スネア23の一対のループ部231,232(図3参照)がループ状に展開する。 That is, when the slider 14 is operated to slide to the base end side (ring portion 111 side), the pair of loop portions 231, 232 (see FIG. 3) of the snare 23 are linearly extended, and the flexible sheath 21 is It is drawn in and accommodated. On the other hand, when the slider 14 is operated to slide to the tip side (the connection cap 12 side), the snare 23 is protruded to the outside of the flexible sheath 21 and the pair of loop portions 231 and 232 (see FIG. 3) of the snare 23 are looped. Expand into a shape.

 ストッパパイプ15は、細長い筒状に形成されており、操作ワイヤ22の一部を覆うように配置されている。ストッパパイプ15は、スライダ14が基端側(リング部111側)にスライド操作された際に、突起部143に当接することにより、操作ワイヤ22の引き込み位置を規制する。なお、ストッパパイプ15は、例えばステンレス鋼パイプ材等の導電材により構成されている。 The stopper pipe 15 is formed in an elongated cylindrical shape, and is disposed so as to cover a part of the operation wire 22. The stopper pipe 15 restricts the drawing-in position of the operation wire 22 by coming into contact with the projection 143 when the slider 14 is slid to the base end side (ring portion 111 side). The stopper pipe 15 is made of, for example, a conductive material such as a stainless steel pipe material.

 挿入部20は、図1に示すように、内視鏡100の挿入部101に形成された処置具チャンネル102に進退自在に挿通されており、当該処置具チャンネル102を介して体内に挿入される。挿入部20は、具体的には図3に示すように、可撓性シース21と、操作ワイヤ22と、スネア23と、連結部24と、を備えている。 As shown in FIG. 1, the insertion portion 20 is inserted in a treatment channel 102 formed in the insertion portion 101 of the endoscope 100 so as to be able to move forward and backward, and is inserted into the body via the treatment channel 102. . Specifically, as shown in FIG. 3, the insertion portion 20 includes a flexible sheath 21, an operation wire 22, a snare 23, and a connection portion 24.

 可撓性シース21は、挿入部20の外皮を構成しており、操作ワイヤ22、スネア23および連結部24を進退自在に収容する。可撓性シース21は、内視鏡100の処置具チャンネル102への挿通性や、内部を進退する操作ワイヤ22の操作性を良好にするために、摩擦が小さく、かつ力量伝達性に優れた剛性を有する材料で構成されることが望ましく、例えばテフロン(登録商標)樹脂等のフッ素系樹脂やポリエチレン等により構成される。 The flexible sheath 21 constitutes an outer cover of the insertion portion 20, and accommodates the operation wire 22, the snare 23, and the connection portion 24 in a retractable manner. The flexible sheath 21 has a small friction and an excellent ability to transmit force, in order to improve the insertion of the endoscope 100 into the treatment instrument channel 102 and the operability of the operation wire 22 advancing and retracting the inside. It is desirable to be made of a material having rigidity, and it is made of, for example, a fluorine-based resin such as Teflon (registered trademark) resin or polyethylene.

 なお、可撓性シース21の先端は、軸線方向に対して斜め45°に傾斜している。これにより、スネア23によって体内組織を緊縛する際に可撓性シース21がつぶれることを防止することができる。 The distal end of the flexible sheath 21 is inclined at an angle of 45 ° with respect to the axial direction. As a result, the flexible sheath 21 can be prevented from collapsing when the body tissue is bound by the snare 23.

 操作ワイヤ22は、可撓性シース21の内部に収容されている。操作ワイヤ22は、操作性に優れた太径の金属ワイヤからなり、例えばステンレス鋼SUS304等の金属素線の撚り線により構成されている。 The operation wire 22 is accommodated inside the flexible sheath 21. The operation wire 22 is made of a large diameter metal wire excellent in operability, and is formed of, for example, a stranded wire of a metal wire such as stainless steel SUS304.

 操作ワイヤ22を構成する金属ワイヤは、いかなる状況においても、可撓性シース21からスネア23を確実に展開させることができる力量伝達性を有していることが望ましい。また、操作ワイヤ22を構成する金属ワイヤは、例えば内視鏡100の挿入部101の湾曲している部分にスネア23が位置している場合のように、スネア23の展開に不利な状況においても、スネア23を可撓性シース21の先端から確実に展開させることができる力量伝達性を有していることが望ましい。 It is desirable that the metal wire that constitutes the operation wire 22 have a force transmission that can reliably deploy the snare 23 from the flexible sheath 21 under any circumstances. Further, the metal wire that constitutes the operation wire 22 is also in a situation that is disadvantageous for the deployment of the snare 23, as in the case where the snare 23 is located at the curved portion of the insertion portion 101 of the endoscope 100, for example. It is desirable that the snare 23 has a force transferability that enables the snare 23 to be deployed from the distal end of the flexible sheath 21 with certainty.

 操作ワイヤ22の先端部222の端面223と、連結部24の端面242とは、互いに突き合わされた状態で、アップセット抵抗溶接により接合されている。なお、アップセット抵抗溶接の詳細については後記する。 The end surface 223 of the distal end portion 222 of the operation wire 22 and the end surface 242 of the connection portion 24 are joined together by upset resistance welding. The details of upset resistance welding will be described later.

 スネア(ワイヤ処置具)23は、切除性に優れた細径の金属ワイヤの端部を束ねて形成されており、操作ワイヤ22と同様に、例えばステンレス鋼SUS304等の金属素線の撚り線により構成されている。 The snare (wire treatment tool) 23 is formed by bundling the end portions of a thin metal wire excellent in excision, and, like the operation wire 22, for example, by a stranded wire of a metal wire such as stainless steel SUS304. It is configured.

 スネア23は、具体的には、楕円状をなす一対のループ部231,232と、当該ループ部231,232の一端側において、金属ワイヤがU字状に折り返されてなる先端部233と、連結部24と、を備えている。 Specifically, the snare 23 includes a pair of elliptical loop portions 231 and 232, and an end portion 233 formed by bending a metal wire in a U shape at one end of the loop portions 231 and 232, And 24.

 連結部24は、溶接部25を介して操作ワイヤ22の先端部222と接合されている。連結部24は、後記する図5および図6に示すように、スネア23の基端部234を構成する複数の金属ワイヤが撚り込まれることにより形成されている。連結部24は、操作ワイヤ22の先端部222の外径と略等しい外径を有している。 The connecting portion 24 is joined to the distal end portion 222 of the operation wire 22 via the welding portion 25. The connection portion 24 is formed by twisting a plurality of metal wires constituting the proximal end 234 of the snare 23, as shown in FIGS. 5 and 6 described later. The connecting portion 24 has an outer diameter substantially equal to the outer diameter of the distal end portion 222 of the operation wire 22.

 溶接部25は、後記するように、操作ワイヤ22の先端部222と連結部24とがアップセット抵抗溶接により接合された際に形成され、操作ワイヤ22を構成する金属ワイヤと、連結部24を構成する金属ワイヤとが混ざり合った金属組織から構成される。 The welding portion 25 is formed when the distal end portion 222 of the operation wire 22 and the connection portion 24 are joined by upset resistance welding as described later, and the metal wire constituting the operation wire 22 and the connection portion 24 are It is comprised from the metal structure which the metal wire to comprise mixed.

[内視鏡用処置具の製造方法]
 本実施の形態に係る内視鏡用処置具1の製造方法について、図4~図16を参照しながら説明する。内視鏡用処置具1の製造方法は、図4に示すように、スネア23の基端部234を撚り込んで連結部24を形成する撚り込み加工ステップ(ステップS1)と、操作ワイヤ22と連結部24とを、アップセット抵抗溶接により接合する溶接ステップ(ステップS2)と、をこの順で行う。以下、各ステップの詳細について説明する。
[Method of manufacturing treatment tool for endoscope]
A method of manufacturing the endoscope treatment tool 1 according to the present embodiment will be described with reference to FIGS. 4 to 16. In the method of manufacturing the endoscopic treatment tool 1, as shown in FIG. 4, a twisting step (step S 1) of twisting the proximal end 234 of the snare 23 to form the connecting portion 24, and the operation wire 22 A welding step (step S2) of joining the connecting portion 24 by upset resistance welding is performed in this order. The details of each step will be described below.

<撚り込み加工ステップ>
 本ステップでは、スネア23の基端部234を構成する複数の金属ワイヤを、操作ワイヤ22の先端部222の外径と略等しくなるように撚り込んで連結部24を形成する。具体的には、図5に示すように、金属ワイヤの両端を並列に並べたスネア23の基端部234の始端234a付近から、ループ部231,232の終端部付近までをチャック31で挟んで固定する。続いて、スネア23の基端部234の終端234b付近をチャック32で挟んで固定する。
<Twisting step>
In this step, a plurality of metal wires constituting the proximal end 234 of the snare 23 are twisted so as to be substantially equal to the outer diameter of the distal end 222 of the operation wire 22 to form the connecting part 24. Specifically, as shown in FIG. 5, the chuck 31 sandwiches from the vicinity of the start end 234a of the proximal end 234 of the snare 23 where the metal wires are arranged in parallel to the vicinity of the end of the loop portions 231 and 232. Fix it. Subsequently, the vicinity of the end 234 b of the base end 234 of the snare 23 is sandwiched and fixed by the chuck 32.

 続いて、図6に示すように、チャック32を軸線周りに回転させて基端部234を構成する2本の金属ワイヤが1本になるように撚り込むことにより、連結部24を形成する。続いて、図7に示すように、形成した連結部24を、切断工具(ニッパ等)で所定の長さに切断し、端面242を形成する。 Subsequently, as shown in FIG. 6, the coupling portion 24 is formed by rotating the chuck 32 about the axis and twisting so that two metal wires constituting the proximal end portion 234 become one. Subsequently, as shown in FIG. 7, the formed connection portion 24 is cut into a predetermined length by a cutting tool (nipper or the like) to form an end surface 242.

 なお、図5で示したスネア23の基端部234の外径は、操作ワイヤ22の先端部222の外径よりも小径に形成されており、例えばスネア23を構成する金属ワイヤの外径をrとし、操作ワイヤ22を構成する金属ワイヤの外径をRとした場合、スネア23を構成する金属ワイヤの外径rは、操作ワイヤ22を構成する金属ワイヤの外径Rの1/2以下(0<r≦R/2)とすることが望ましく、1/3以下(0<r≦R/3)とすると、体内組織の切除性がよくなるため、より望ましい。 The outer diameter of the proximal end 234 of the snare 23 shown in FIG. 5 is smaller than the outer diameter of the distal end 222 of the operation wire 22. For example, the outer diameter of the metal wire constituting the snare 23 Assuming that r is the outer diameter of the metal wire constituting the operation wire 22 is R, the outer diameter r of the metal wire constituting the snare 23 is 1/2 or less of the outer diameter R of the metal wire constituting the operation wire 22. It is desirable that (0 <r ≦ R / 2), and 1/3 or less (0 <r ≦ R / 3) is more preferable because excisability of internal tissues is improved.

 このように、スネア23の基端部234と、操作ワイヤ22の先端部222とは、元々は大きな外径差を有しているが、前記した撚り込み加工ステップを行うことにより、スネア23の基端部234が、操作ワイヤ22の先端部222と同等の外径を有する連結部24へと加工される。 As described above, although the proximal end 234 of the snare 23 and the distal end 222 of the operation wire 22 originally have a large difference in outer diameter, by performing the above-described twisting step, the snare 23 is obtained. The proximal end 234 is processed into the connecting portion 24 having the same outer diameter as the distal end 222 of the operation wire 22.

<溶接ステップ>
 本ステップでは、図8および図9に示すように、操作ワイヤ22の先端部222の端面223と、連結部24の端面242とを、互いに突き当てた状態で、アップセット抵抗溶接により接合する。
<Welding step>
In this step, as shown in FIGS. 8 and 9, the end surface 223 of the distal end portion 222 of the operation wire 22 and the end surface 242 of the connection portion 24 are joined by upset resistance welding in a state where they abut each other.

 具体的には、図8に示すように、まず連結部24を、アップセット抵抗溶接装置40の固定側チャック41に取り付ける。その際、連結部24の端面242が、固定側チャック41と移動側チャック42との間の隙間の中央に位置するように位置決めを行う。なお、固定側チャック41と移動側チャック42との間の隙間の大きさdは、一般的に被接合部材の外径寸法と同等程度が目安とされている。 Specifically, as shown in FIG. 8, first, the connecting portion 24 is attached to the stationary chuck 41 of the upset resistance welding device 40. At this time, positioning is performed so that the end surface 242 of the connecting portion 24 is positioned at the center of the gap between the fixed chuck 41 and the movable chuck 42. The size d 1 of the gap between the fixed-side chuck 41 and the moving-side chuck 42 is almost equal to the outer diameter of the generally bonded members is a measure.

 続いて、操作ワイヤ22の端面223を、連結部24の端面242に突き当て、移動側チャック42に固定する。その際、操作ワイヤ22の端面223と、連結部24の端面242との間に隙間があると、アップセット抵抗溶接の際にアーク放電が発生するおそれがある。従って、操作ワイヤ22の端面223と、連結部24の端面242とは、隙間なく密着させて突き当てることが望ましく、例えば本ステップを実施する前に、予め各端面223,242をヤスリやグラインダー等により直角に仕上げておくことが望ましい。 Subsequently, the end surface 223 of the operation wire 22 is abutted against the end surface 242 of the connection portion 24 and fixed to the moving chuck 42. At that time, if there is a gap between the end face 223 of the operation wire 22 and the end face 242 of the connecting portion 24, there is a possibility that arc discharge may occur at the time of upset resistance welding. Therefore, it is desirable that the end surface 223 of the operation wire 22 and the end surface 242 of the connection portion 24 be in close contact with each other without a gap and be abutted. For example, before performing this step, each end surface 223, 242 It is desirable to finish it at right angles.

 また、例えば操作ワイヤ22に解れが発生しやすい場合は、操作ワイヤ22を溶断、または操作ワイヤ22に対して解れ止め溶接を施した後に、ヤスリやグラインダー等による直角仕上げを施してもよい。 Further, for example, when the operation wire 22 is easily broken, the operation wire 22 may be melted or cut off and welded to the operation wire 22, and then a right angle finish with a file, a grinder or the like may be performed.

 続いて、アップセット抵抗溶接装置40が起動すると、移動側チャック42の図示しないストッパーが解除され、移動側チャック42が加圧バネ43によって押圧され、操作ワイヤ22の端面223が、連結部24の端面242を所定の力で加圧する。そして、固定側チャック41および移動側チャック42に所定の電流が印加され、固定側チャック41および移動側チャック42の間の被接合部材、つまり操作ワイヤ22の端面223と、連結部24の端面242との突き当て部A周辺の金属組織が抵抗(ジュール)加熱されて溶融する。 Subsequently, when the upset resistance welding apparatus 40 is activated, the stopper (not shown) of the movable chuck 42 is released, the movable chuck 42 is pressed by the pressure spring 43, and the end surface 223 of the operation wire 22 is The end face 242 is pressurized with a predetermined force. Then, a predetermined current is applied to the fixed chuck 41 and the movable chuck 42, and the member to be joined between the fixed chuck 41 and the movable chuck 42, that is, the end surface 223 of the operation wire 22 and the end surface 242 of the connecting portion 24. The metal structure around the butting part A is heated by resistance (Joule) and melted.

 そして、溶融した金属組織は、アップセット圧力(据え込み圧力)により据え込まれ、図9に示すように、操作ワイヤ22と連結部24とが、溶融した余分な金属組織を押し出しながら、据え込み中心Bまで押し込まれる。これにより、固定側チャック41と移動側チャック42との間の隙間の大きさが、dからdへと縮小される。なお、その際の移動側チャック42の移動量(d‐d)、つまり溶融した金属組織を押し出した長さ(量)が、アップセット量(据え込み量)となる。 Then, the molten metal structure is set up by the upset pressure (set-up pressure), and as shown in FIG. 9, the operation wire 22 and the connecting portion 24 set up while extruding the molten excess metal structure. It is pushed to the center B. Thus, the size of the gap between the fixed-side chuck 41 and the moving-side chuck 42 is reduced from d 1 to d 2. The moving amount (d 1 −d 2 ) of the moving side chuck 42 at that time, that is, the length (quantity) of pushing out the molten metal structure becomes the upset amount (defensing amount).

 続いて、電流の印加を停止すると、溶融した金属組織が冷却され、操作ワイヤ22の先端部222と連結部24とが、一体となって接合される。そして最後に、図10に示すように、外周に押し出された余分な金属組織をヤスリやグラインダー等により仕上げ加工する研磨ステップを行い、接合が完了する。 Subsequently, when the application of the current is stopped, the molten metal structure is cooled, and the distal end portion 222 of the operation wire 22 and the connecting portion 24 are integrally joined. Finally, as shown in FIG. 10, a polishing step is performed to finish the extra metal structure pushed out to the outer periphery with a file, a grinder or the like to complete the bonding.

 ここで、アップセット抵抗溶接は、抵抗加熱(ジュール熱)によって被接合部材を加熱するため、接合する被接合部材同士の形状や寸法が大きく異なると、抵抗値の違いによって発熱量に大きな差が生じ、安定した溶接をすることができない。一方、本実施の形態に係る内視鏡用処置具1の製造方法では、スネア23の基端部234を撚り込み、操作ワイヤ22の先端部222の外径と略等しい外径を有する連結部24を形成することにより、操作ワイヤ22とスネア23の基端部234との間の外径差を補っている。従って、被接合部材間における断面積の差が小さくなって、被接合部材間における発熱量が均等になるため、安定した溶接が可能となる。 Here, the upset resistance welding heats the members to be joined by resistance heating (Joule heat), so if the shapes and dimensions of the members to be joined differ greatly, the difference in resistance value causes a large difference in heat generation. It can not be made stable welding. On the other hand, in the method of manufacturing the endoscopic treatment tool 1 according to the present embodiment, the proximal end 234 of the snare 23 is twisted, and a connecting portion having an outer diameter substantially equal to the outer diameter of the distal end 222 of the operation wire 22. By forming 24, the difference in outer diameter between the operation wire 22 and the proximal end 234 of the snare 23 is compensated. Therefore, the difference in cross-sectional area between the members to be joined becomes smaller, and the amount of heat generated between the members to be joined becomes equal, so stable welding becomes possible.

<解れ止めステップ>
 本実施の形態に係る内視鏡用処置具1の製造方法では、撚り込み加工ステップと溶接ステップとの間に、連結部24を構成する金属ワイヤの解れを防止するための解れ止めステップを行ってもよい。
<Dissolving step>
In the method of manufacturing the endoscope treatment tool 1 according to the present embodiment, the unwrapping step for preventing the unraveling of the metal wire forming the connecting portion 24 is performed between the twisting step and the welding step. May be

 解れ止めステップは、例えば連結部24を所定位置で溶断する方法を利用することができる。すなわち、前記した撚り込み加工ステップで連結部24を形成した後、図11に示すように、連結部24の一方側を溶断装置50のチャック51で挟んで固定し、連結部24の他方側をチャック52で挟んで固定する。続いて、この状態で電流を印加することにより、チャック51,52間の連結部24を加熱し、図12に示すように、加熱部を焼滅して切断し、端面242Aを形成する。 The anti-rolling step can use, for example, a method of melting the connecting portion 24 at a predetermined position. That is, after forming the connecting portion 24 in the above-described twisting step, as shown in FIG. 11, one side of the connecting portion 24 is sandwiched and fixed by the chuck 51 of the fusing apparatus 50, and the other side of the connecting portion 24 is It clamps with a chuck | zipper 52 and fixes. Subsequently, by applying a current in this state, the connecting portion 24 between the chucks 51 and 52 is heated, and as shown in FIG. 12, the heating portion is burned out and cut to form an end face 242A.

 これにより、連結部24を構成する金属ワイヤの解れを防止しつつ、当該連結部24を切断することができる。そして、図13に示すように、操作ワイヤ22の先端部222の端面223と、溶断により形成した連結部24の端面242Aとを、突き当てた状態で、前記した溶接ステップを行い、操作ワイヤ22の先端部222と連結部24とを接合する。 Thereby, the said connection part 24 can be cut | disconnected, preventing the metal wire which comprises the connection part 24 loosening. Then, as shown in FIG. 13, with the end face 223 of the distal end portion 222 of the operation wire 22 butting against the end face 242A of the connecting portion 24 formed by melting, the welding step described above is carried out. The distal end portion 222 and the connecting portion 24 are joined.

 また、解れ止めステップは、溶断の他にも、アーク溶接を利用して行うことも可能である。すなわち、前記した撚り込み加工ステップで連結部24を形成した後、連結部24を所定位置で切断する。続いて、図14に示すように、連結部24の切断部243がチャック61の端面611からアーク電極62側に突出するように、当該連結部24をアーク溶接装置60のチャック61で挟んで固定する。続いて、この状態でアーク溶接を実施すると、連結部24の切断部243が溶融し、図15に示すように、溶融球25Aが形成される。続いて、図16に示すように、溶融球25Aをヤスリ掛けし、垂直な端面242Bを形成する。そして、前記した図13と同様に、操作ワイヤ22の先端部222の端面223と、溶断により形成した連結部24の端面242Bとを突き当てた状態で、前記した溶接ステップを行い、操作ワイヤ22の先端部222と連結部24とを接合する。 In addition to melting, it is also possible to carry out the anti-rolling step using arc welding. That is, after the connection portion 24 is formed in the above-described twisting step, the connection portion 24 is cut at a predetermined position. Subsequently, as shown in FIG. 14, the connecting portion 24 is sandwiched and fixed by the chuck 61 of the arc welding apparatus 60 so that the cutting portion 243 of the connecting portion 24 protrudes from the end surface 611 of the chuck 61 to the arc electrode 62 side. Do. Subsequently, when arc welding is performed in this state, the cut portion 243 of the connection portion 24 melts, and as shown in FIG. 15, a molten ball 25A is formed. Subsequently, as shown in FIG. 16, the melting spheres 25A are attached to form a vertical end face 242B. Then, in the same manner as in FIG. 13 described above, the welding step is performed in a state where the end surface 223 of the distal end portion 222 of the operation wire 22 butts against the end surface 242B of the connecting portion 24 formed by melting. The distal end portion 222 and the connecting portion 24 are joined.

 以上のように、本実施の形態に係る内視鏡用処置具1の製造方法によれば、スネア23の基端部234を撚り込んで連結部24とし、当該連結部24を介して操作ワイヤ22およびスネア23を接合することにより、操作ワイヤ22およびスネア23を、接合強度のばらつきや製品性能の低下を招くことなく、かつ高度な技能を用いることなく、低コストで接合することができる。また、連結部材を用いずに操作ワイヤ22およびスネア23を接合するため、従来よりも硬質部長を大幅に短縮することができ、製品設計の自由度が拡大する。 As described above, according to the method of manufacturing the endoscope treatment tool 1 according to the present embodiment, the proximal end 234 of the snare 23 is twisted to form the connecting portion 24, and the operation wire is connected via the connecting portion 24. By joining 22 and snare 23, the operation wire 22 and the snare 23 can be joined at low cost without causing variations in joining strength or deterioration in product performance and without using advanced skills. In addition, since the operation wire 22 and the snare 23 are joined without using the connecting member, the length of the hard portion can be considerably shortened as compared with the conventional case, and the degree of freedom in product design is expanded.

 また、操作ワイヤ22やスネア23を構成する金属ワイヤは、細い金属素線を撚り合わせたものであるため、素線間に隙間が存在する。そのため、一般的な溶接方法のように、接合部の金属組織を溶融して固化するだけであると、素線間の隙間容積に相当する金属組織が不足して、接合部が極度に細く括れたり、あるいは接合部の金属組織に欠損が発生しやすくなる。 Moreover, since the metal wire which comprises the operation wire 22 or the snare 23 twists a thin metal wire together, a clearance gap exists between wires. Therefore, as in the general welding method, if only melting and solidifying the metal structure of the joint, the metal structure corresponding to the gap volume between the strands runs short, and the joint is extremely thinly constricted. And defects tend to occur in the metal structure of the joint.

 一方、本実施の形態に係る内視鏡用処置具1の製造方法では、アップセット抵抗溶接により操作ワイヤ22とスネア23の連結部24とを溶接するため、図9に示すように、据え込みにより素線間において不足する金属組織が補充され、接合部の括れや組織の欠損が防止される。特に、素線が太く、撚り本数の少ない金属ワイヤによって操作ワイヤ22やスネア23が構成されている場合は素線間の隙間も大きくなるため、アップセット抵抗溶接を利用することによる効果が大きくなる。 On the other hand, in the method of manufacturing the endoscopic treatment tool 1 according to the present embodiment, as shown in FIG. 9, since the operation wire 22 and the connecting portion 24 of the snare 23 are welded by upset resistance welding, As a result, the metal structure lacking between the strands is replenished, and joint constriction and tissue loss are prevented. In particular, when the operation wire 22 and the snare 23 are formed of thick wires and metal wires with a small number of twists, the gaps between the wires are also large, so the effect of using upset resistance welding is enhanced. .

 さらに、本実施の形態に係る内視鏡用処置具1は、全体として大きな接合強度を得ることができ、コールドスネア方式の内視鏡用処置具1に要求される接合強度も十分に満たすことができる。 Furthermore, the endoscope treatment tool 1 according to the present embodiment can obtain a large bonding strength as a whole, and sufficiently satisfy the bonding strength required for the cold snare type endoscope treatment tool 1 as well. Can.

 以上、本発明に係る内視鏡用処置具および内視鏡用処置具の製造方法について、発明を実施するための形態により具体的に説明したが、本発明の趣旨はこれらの記載に限定されるものではなく、請求の範囲の記載に基づいて広く解釈されなければならない。また、これらの記載に基づいて種々変更、改変等したものも本発明の趣旨に含まれることはいうまでもない。 As mentioned above, although the manufacturing method of the treatment tool for endoscopes and the treatment tool for endoscopes concerning the present invention was concretely explained by the form for carrying out the invention, the meaning of the present invention is limited to these statements. It should be interpreted broadly based on the statement of the claims, not Further, it is needless to say that various changes, modifications and the like based on these descriptions are included in the spirit of the present invention.

 例えば、前記した実施の形態において、内視鏡用処置具1におけるワイヤ処置具は、図3等に示したスネア23に限定されない。内視鏡用処置具1は、ワイヤ処置具として、例えば図17に示すように、金属ワイヤからなる多角形状のループ部231A,232Aを備えるスネア23Aを用いてもよい。また、内視鏡用処置具1は、ワイヤ処置具として、例えば図18に示すように、金属ワイヤからなる非対称形状のループ部231B,232Bを備えるスネア23Bを用いてもよい。 For example, in the embodiment described above, the wire treatment tool in the endoscopic treatment tool 1 is not limited to the snare 23 shown in FIG. The endoscope treatment tool 1 may use, as a wire treatment tool, for example, as shown in FIG. 17, a snare 23A including polygonal loop portions 231A and 232A made of metal wires. The endoscope treatment tool 1 may use, as a wire treatment tool, for example, as shown in FIG. 18, a snare 23B including asymmetrically shaped loop portions 231B and 232B made of metal wires.

 また、内視鏡用処置具1は、ワイヤ処置具として、例えば図19に示すように、4本の金属ワイヤからなる多角形状のループ部231C,232C,233C,234Cと、これらループ部231C,232C,233C,234Cを束ねる先端キャップ235Cと、を備えるバスケット23Cを用いてもよい。 The endoscope treatment tool 1 is a wire treatment tool, for example, as shown in FIG. 19, polygonal loop portions 231C, 232C, 233C, and 234C consisting of four metal wires, and these loop portions 231C, And a tip cap 235C for bundling 232C, 233C, and 234C, and may use a basket 23C.

 また、前記した実施の形態では、コールドスネア方式で用いられる内視鏡用処置具1における操作ワイヤ22とスネア23の接続構造について説明したが、当該接続構造はホットスネア方式で用いられる内視鏡用処置具にも適用可能である。この場合、操作部10のスライダ14に金属製の端子が固定され、当該端子の一端側に操作ワイヤ22の基端部221が、他端側に高周波発生装置が接続される。なお、このようなホットスネア方式で用いられる内視鏡用処置具に必要なその他の構成は、例えば前記した特許文献1に開示されているため、詳細な説明は省略する。 In the above-described embodiment, the connection structure of the operation wire 22 and the snare 23 in the endoscopic treatment tool 1 used in the cold snare method has been described, but the connection structure is the endoscope used in the hot snare method. It is applicable also to a treatment tool. In this case, a metal terminal is fixed to the slider 14 of the operation unit 10, the proximal end 221 of the operation wire 22 is connected to one end of the terminal, and the high frequency generator is connected to the other end. In addition, since the other structure required for the treatment tool for endoscopes used by such a hot snare system is disclosed by above-mentioned patent document 1, detailed description is abbreviate | omitted.

 1 内視鏡用処置具
 10 操作部
 11 本体部
 11a ガイド溝
 111 リング部
 12 連結用キャップ
 13 折れ止め部
 131 基端部
 14 スライダ
 141,142 リング部
 143 突起部
 144 係合部材
 15 ストッパパイプ
 20 挿入部
 21 可撓性シース
 211 基端部
 22 操作ワイヤ
 221 基端部
 222 先端部
 223 端面
 23,23A,23B スネア
 23C バスケット
 231,232,231A,232A,231B,232B,231C,232C,233C,234C ループ部
 233 先端部
 234 基端部
 234a 始端
 234b 終端
 235C 先端キャップ
 24 連結部
 242,242A,242B 端面
 243 切断部
 25 溶接部
 25A 溶融球
 31,32 チャック
 40 アップセット抵抗溶接装置
 41 固定側チャック
 42 移動側チャック
 43 加圧バネ
 50 溶断装置
 51,52 チャック
 60 アーク溶接装置
 61 チャック
 611 端面
 62 アーク電極
 100 内視鏡
 101 挿入部
 102 処置具チャンネル
 A 突き当て部
 B 据え込み中心
DESCRIPTION OF SYMBOLS 1 Treatment tool for endoscopes 10 Operation part 11 Body part 11a Guide groove 111 Ring part 12 Cap for joint 13 Breaking part 131 Base end part 14 Slider 141, 142 Ring part 143 Protrusion part 144 Engagement member 15 Stopper pipe 20 insertion Section 21 flexible sheath 211 proximal end 22 operation wire 221 proximal end 222 distal end 223 end face 23, 23A, 23B snare 23C basket 231, 232, 231A, 232A, 231B, 232B, 231C, 232C, 233C, 234C loop Part 233 Tip part 234 Base end 234a Leading end 234b End 235C Tip cap 24 Connection part 242, 242A, 242B End face 243 Cutting part 25 Welded part 25A Melt ball 31, 32 Chuck 40 Upset resistance welding device 41 Fixed side cha Click 42 movable chuck 43 pressure spring 50 fusing device 51 chucks 60 arc welding apparatus 61 chuck 611 end face 62 around the arc electrode 100 endoscope 101 insertion portion 102 upsetting treatment instrument channel A butting portion B

Claims (5)

 金属製の操作ワイヤと、
 金属ワイヤの端部を束ねて形成されたワイヤ処置具と、
 前記ワイヤ処置具の基端部を構成する複数の金属ワイヤが撚り込まれることにより形成され、前記操作ワイヤの外径と等しい外径を有する連結部と、
 を備え、
 前記操作ワイヤの端面と前記連結部の端面とは、互いに突き合わされた状態で、アップセット抵抗溶接により接合されていることを特徴とする内視鏡用処置具。
Metal operation wire,
A wire treatment tool formed by bundling ends of metal wires;
A connecting portion formed by twisting a plurality of metal wires constituting the proximal end portion of the wire treatment tool and having an outer diameter equal to the outer diameter of the operation wire;
Equipped with
An endoscope treatment tool characterized in that an end face of the operation wire and an end face of the connection portion are joined by upset resistance welding in a state where the end face of the operation wire and the end face of the connection portion are butted to each other.
 前記ワイヤ処置具は、ループ状のスネアであることを特徴とする請求項1に記載の内視鏡用処置具。 The endoscope treatment tool according to claim 1, wherein the wire treatment tool is a loop snare.  金属製の操作ワイヤと、金属ワイヤの端部を束ねて形成されたワイヤ処置具と、前記操作ワイヤの外径と等しい外径を有する連結部と、を備える内視鏡用処置具の製造方法において、
 前記ワイヤ処置具の基端部を構成する複数の金属ワイヤを、前記操作ワイヤの外径と等しくなるように撚り込んで前記連結部を形成する撚り込み加工ステップと、
 前記操作ワイヤの端面と前記連結部の端面とを、互いに突き当てた状態で、アップセット抵抗溶接により接合する溶接ステップと、
 を含むことを特徴とする内視鏡用処置具の製造方法。
A method of manufacturing a treatment tool for an endoscope, comprising a metal operation wire, a wire treatment tool formed by bundling end portions of the metal wire, and a connecting portion having an outer diameter equal to the outer diameter of the operation wire. In
A twisting step of twisting a plurality of metal wires forming the proximal end of the wire treatment tool so as to be equal to the outer diameter of the operation wire to form the connecting portion;
A welding step of joining by upset resistance welding in a state in which the end face of the operation wire and the end face of the connecting portion abut each other;
A method of manufacturing a treatment tool for an endoscope, comprising:
 前記撚り込み加工ステップと前記溶接ステップとの間に、前記連結部を所定位置で溶断する解れ止めステップをさらに含むことを特徴とする請求項3に記載の内視鏡用処置具の製造方法。 The method for manufacturing a treatment tool for an endoscope according to claim 3, further comprising a anti-breaking step of melting and cutting the connection portion at a predetermined position between the twisting step and the welding step.  前記撚り込み加工ステップと前記溶接ステップとの間に、前記連結部を所定位置で切断した後、アーク溶接により前記連結部の切断部を溶融させる解れ止めステップをさらに含むことを特徴とする請求項3に記載の内視鏡用処置具の製造方法。 The method according to claim 1, further comprising: a detent step of cutting the connection portion at a predetermined position and melting the cut portion of the connection portion by arc welding after the twisting step and the welding step. The manufacturing method of the treatment tool for endoscopes of 3.
PCT/JP2017/035311 2016-09-30 2017-09-28 Endoscopic treatment tool and production method for endoscopic treatment tool Ceased WO2018062415A1 (en)

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS623882A (en) * 1985-06-27 1987-01-09 Nissan Motor Co Ltd Joining method for welding wire
JP2001198139A (en) * 2000-01-24 2001-07-24 Asahi Optical Co Ltd Wire loop type treatment instrument for endoscope
US20020010485A1 (en) * 2000-06-02 2002-01-24 John Griego Medical device having linear to rotation control
JP2012192177A (en) * 2011-02-28 2012-10-11 Sumitomo Bakelite Co Ltd Medical equipment and method of manufacturing the same

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS623882A (en) * 1985-06-27 1987-01-09 Nissan Motor Co Ltd Joining method for welding wire
JP2001198139A (en) * 2000-01-24 2001-07-24 Asahi Optical Co Ltd Wire loop type treatment instrument for endoscope
US20020010485A1 (en) * 2000-06-02 2002-01-24 John Griego Medical device having linear to rotation control
JP2012192177A (en) * 2011-02-28 2012-10-11 Sumitomo Bakelite Co Ltd Medical equipment and method of manufacturing the same

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