JP2002301088A - Endoscopic treatment device - Google Patents
Endoscopic treatment deviceInfo
- Publication number
- JP2002301088A JP2002301088A JP2001107442A JP2001107442A JP2002301088A JP 2002301088 A JP2002301088 A JP 2002301088A JP 2001107442 A JP2001107442 A JP 2001107442A JP 2001107442 A JP2001107442 A JP 2001107442A JP 2002301088 A JP2002301088 A JP 2002301088A
- Authority
- JP
- Japan
- Prior art keywords
- tip
- probe
- electrode
- frequency
- endoscope
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 238000012277 endoscopic treatment Methods 0.000 title abstract 3
- 239000000523 sample Substances 0.000 claims abstract description 66
- 238000011282 treatment Methods 0.000 claims abstract description 36
- 239000011261 inert gas Substances 0.000 claims abstract description 14
- 239000000615 nonconductor Substances 0.000 claims description 5
- 230000015271 coagulation Effects 0.000 abstract description 28
- 238000005345 coagulation Methods 0.000 abstract description 28
- 230000023597 hemostasis Effects 0.000 abstract description 26
- 230000007159 enucleation Effects 0.000 abstract 1
- 238000009413 insulation Methods 0.000 abstract 1
- 238000003780 insertion Methods 0.000 description 22
- 230000037431 insertion Effects 0.000 description 22
- 230000000740 bleeding effect Effects 0.000 description 21
- 210000004400 mucous membrane Anatomy 0.000 description 20
- 239000011347 resin Substances 0.000 description 17
- 229920005989 resin Polymers 0.000 description 17
- 239000000463 material Substances 0.000 description 15
- 238000000034 method Methods 0.000 description 15
- 239000012530 fluid Substances 0.000 description 13
- 210000001519 tissue Anatomy 0.000 description 9
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 8
- 230000002439 hemostatic effect Effects 0.000 description 8
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 7
- 229910052737 gold Inorganic materials 0.000 description 7
- 239000010931 gold Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 238000010586 diagram Methods 0.000 description 6
- 238000012986 modification Methods 0.000 description 6
- 230000004048 modification Effects 0.000 description 6
- 229910001220 stainless steel Inorganic materials 0.000 description 6
- 239000010935 stainless steel Substances 0.000 description 6
- 239000008280 blood Substances 0.000 description 5
- 210000004369 blood Anatomy 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 229910052786 argon Inorganic materials 0.000 description 4
- 239000000919 ceramic Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000003825 pressing Methods 0.000 description 4
- 238000002271 resection Methods 0.000 description 4
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 4
- 229910052721 tungsten Inorganic materials 0.000 description 4
- 239000010937 tungsten Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000003779 heat-resistant material Substances 0.000 description 3
- 210000000056 organ Anatomy 0.000 description 3
- 229940030225 antihemorrhagics Drugs 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 239000002874 hemostatic agent Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 210000002808 connective tissue Anatomy 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 210000004877 mucosa Anatomy 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 230000003387 muscular Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
Landscapes
- Surgical Instruments (AREA)
- Endoscopes (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、経内視鏡的に使用
され、高周波電流を流すことにより、生体組織を切開し
たり、出血部などの生体の処置対象部位を止血または凝
固したりする内視鏡用治療装置に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention is used endoscopically to cut a living tissue or to stop or coagulate a treatment target site of a living body such as a bleeding part by applying a high-frequency current. The present invention relates to a treatment device for an endoscope.
【0002】[0002]
【従来の技術】出血部に高周波電流を流すことによって
止血を行う内視鏡用高周波凝固装置は、特開平9-164149
号公報等に開示されている。2. Description of the Related Art A high-frequency coagulation apparatus for an endoscope which stops hemostasis by supplying a high-frequency current to a bleeding part is disclosed in Japanese Patent Application Laid-Open No. 9-164149.
No. 6,009,036.
【0003】また、アルゴン・ビーム・コアギュレータ
ーとして知られている特開平9-164149号公報に開示され
た装置は、イオン化可能なガス(アルゴンなどの不活性
ガス)を供給するためのガス供給手段と、HF源と、H
F源からガス中にHF電流を導く1つのエレメントとを
備える。これは、ガス供給手段によって出血部に向けて
噴射されたガスを媒体としてHF電流を出血部に流し、
これによって、非接触で一度に広範囲の止血を行うこと
ができる。An apparatus disclosed in Japanese Patent Application Laid-Open No. Hei 9-164149, known as an argon beam coagulator, uses a gas supply for supplying an ionizable gas (an inert gas such as argon). Means, HF source, H
One element for conducting an HF current from the F source into the gas. This means that the HF current is caused to flow through the bleeding part using the gas injected toward the bleeding part by the gas supply means as a medium,
Thus, a wide range of hemostasis can be performed at once without contact.
【0004】一方、経内視鏡的に患部の粘膜の切除を行
うようにした内視鏡用処置装置は、特開平8-299355号公
報等に開示されている。この特開平8-299355号公報に開
示された内視鏡用処置装置は、針状の高周波ナイフと、
高周波ナイフの先端に設けられた、高周波ナイフよりも
大径の電気的絶縁チップとを備えたものである。これに
よると、絶縁部を患部に押し当てながら切開するため、
粘膜の切開中において、切開すべきでない深部組織への
刺入や不要な焼灼を防止し得る。On the other hand, a treatment apparatus for an endoscope in which a mucous membrane of an affected part is resected endoscopically is disclosed in Japanese Patent Application Laid-Open No. 8-299355. The treatment apparatus for an endoscope disclosed in this Japanese Patent Application Laid-Open No. 8-299355 discloses a needle-shaped high-frequency knife,
An electric insulating tip provided at the tip of the high-frequency knife and having a diameter larger than that of the high-frequency knife. According to this, because the incision is made while pressing the insulating part against the affected part,
During incision of the mucous membrane, penetration into deep tissue that should not be incised and unnecessary cauterization can be prevented.
【0005】[0005]
【発明が解決しようとする課題】ところで、従来、粘膜
の切開後に止血を行う際、特開平8-299355号公報等に開
示された内視鏡用処置装置により、粘膜に切開を加えた
後、特開平9-164149号公報等に開示された別の内視鏡用
高周波凝固装置に入れ替えていた。By the way, conventionally, when hemostasis is performed after incision of the mucous membrane, after the incision is made in the mucous membrane by a treatment device for an endoscope disclosed in Japanese Patent Application Laid-Open No. 8-299355, It has been replaced with another high-frequency coagulation device for endoscopes disclosed in Japanese Patent Application Laid-Open No. 9-164149.
【0006】この従来の場合、処置具の入れ替えを行う
必要があり、その入れ替えの手間と時間が必要になり、
術者や患者の負担が大きい。In the case of this conventional technique, it is necessary to replace the treatment tool, which requires labor and time for replacement.
The burden on the surgeon and patient is large.
【0007】更に、特開平9-164149号公報等に開示され
た内視鏡用高周波凝固装置を用いて止血を行う際にあっ
ては、その装置先端部分に粘膜が接触すると、プローブ
先端に粘膜がこびり付くことがあり、このような場合
は、本来の処置機能を充分に果たせなくなり、プローブ
自体を交換するなど、手間と時間がかかるという欠点が
あった。Further, when hemostasis is performed using a high-frequency coagulation device for an endoscope disclosed in Japanese Patent Application Laid-Open No. 9-164149, etc., when a mucous membrane comes into contact with the distal end of the device, the mucosa contacts the distal end of the probe. In such a case, the original treatment function cannot be sufficiently performed, and there is a disadvantage that it takes time and effort such as replacing the probe itself.
【0008】本発明は前述した事情に着目してなされた
もので、その目的とするところは、内視鏡の処置具挿通
孔に異なる機能の処置具を入れ替えて処置する必要がな
く、病変組織の切除と止血とに至る一連の作業を迅速に
行うことができる内視鏡用治療装置を提供することと、
患部の粘膜が装置先端に接触しても粘膜が電極にこびり
付くことが防げる内視鏡用治療装置を提供することにあ
る。SUMMARY OF THE INVENTION The present invention has been made in view of the above-mentioned circumstances. It is an object of the present invention to replace a treatment tool having a different function in a treatment tool insertion hole of an endoscope and perform treatment. To provide an endoscope treatment device that can quickly perform a series of operations leading to resection and hemostasis,
An object of the present invention is to provide a treatment device for an endoscope which can prevent the mucous membrane from sticking to the electrode even when the mucous membrane of the affected part contacts the distal end of the device.
【0009】[0009]
【課題を解決するための手段】前記目的を達成すべく、
本発明は、経内視鏡的に使用でき、生体の処置対象部位
に高周波電流を流すことによって処置対象部位を切開・
止血・凝固する内視鏡用治療装置において、経内視鏡的
に体内に挿入可能で、且つ先端で開口する通孔を有する
長尺なプローブと、前記プローブの先端付近に設けら
れ、前記プローブの先端より突没可能で、且つ高周波電
流を通電可能な電極と、前記電極の先端に設けられた、
前記電極より大径の電気絶縁体と、前記電極に高周波電
流を供給する高周波電源と、前記プローブが有する前記
通孔に不活性ガスを供給する手段と前記電極に高周波電
流を供給する手段とを有する制御装置とを具備したこと
を特徴とする。In order to achieve the above object,
INDUSTRIAL APPLICABILITY The present invention can be used endoscopically.
In a treatment device for an endoscope that stops and coagulates blood, a long probe that can be inserted into a body transendoscopically and has a through hole that opens at the tip, and the probe that is provided near the tip of the probe, An electrode which can be protruded and retracted from the tip of the electrode, and which can supply a high-frequency current, provided at the tip of the electrode,
An electrical insulator having a diameter larger than that of the electrode, a high-frequency power supply for supplying a high-frequency current to the electrode, a means for supplying an inert gas to the through hole of the probe, and a means for supplying a high-frequency current to the electrode. And a control device having the same.
【0010】本発明によれば、ひとつの処置具に切開す
る機能と、止血する機能が備わっているため、処置具の
入れ替えが不要になる。また、電極先端に設けた電気絶
縁体を患部に当てることにより、プローブの電極先端と
粘膜との距離が保たれる。このため、粘膜が電極先端に
付着することを防止する。[0010] According to the present invention, there is provided a function of incising a single treatment tool and a function of stopping blood, so that it is not necessary to replace the treatment tool. In addition, the distance between the electrode tip of the probe and the mucous membrane is maintained by applying the electrical insulator provided at the electrode tip to the affected part. This prevents the mucous membrane from adhering to the electrode tip.
【0011】[0011]
【発明の実施の形態】(第1実施形態)図1〜図14を
参照しながら、本発明の第1実施形態について説明す
る。本実施形態に係る内視鏡用高周波凝固装置は、図1
に示されるように、後述する内視鏡1(図8を参照)の処
置具挿通孔2に挿入可能で長尺なプローブ(処置用プロ
ーブ本体)3と、このプローブ3の手元側操作部4にそ
れぞれ接続される通電ケーブル(高周波供給手段)5及
び流体供給チューブ(流体供給手段)6と、前記通電ケ
ーブル5と前記流体供給チューブ6を介して前記プロー
ブ3が接続される制御装置7と、術者が制御装置7を操
作するためのフットスイッチ8とを備える。DESCRIPTION OF THE PREFERRED EMBODIMENTS (First Embodiment) A first embodiment of the present invention will be described with reference to FIGS. The high-frequency coagulation apparatus for an endoscope according to the present embodiment is shown in FIG.
As shown in FIG. 1, a long probe (treatment probe main body) 3 that can be inserted into a treatment tool insertion hole 2 of an endoscope 1 (see FIG. 8) described later, and a hand-side operation unit 4 of the probe 3 A control device 7 to which the probe 3 is connected via the current supply cable 5 and the fluid supply tube 6; A foot switch 8 for an operator to operate the control device 7.
【0012】前記プローブ3は、図2に示すように、挿
入部9と、これに挿通される高周波ナイフ13と、前記
制御装置7からの高周波電流を高周波ナイフ13に伝え
るための導電ワイヤ21と、前記手元側操作部4とによ
って構成されている。As shown in FIG. 2, the probe 3 includes an insertion portion 9, a high-frequency knife 13 inserted therein, and a conductive wire 21 for transmitting a high-frequency current from the control device 7 to the high-frequency knife 13. , And the near-side operation unit 4.
【0013】図3に示すように、前記プローブ3の挿入
部9は、樹脂チューブ15と、これの先端に取り付けら
れる先端チップ10とからなり、先端チップ10はリン
グ状の仲介具19を介して前記樹脂チューブ15に連結
されている。前記樹脂チューブ15は、中心に形成され
る比較的大きな径の管路48と、その周囲に少なくとも
1つ以上設けられた比較的小さな径の管路16を形成し
た、いわゆるマルチルーメンチューブからなるものであ
る。また、樹脂チューブ15は、例えばPTFE等の可
撓性に優れる材質で作られていることが望ましい。ま
た、樹脂チューブ15の外径は、φ1.5mm〜φ6mmで
あるが、特にφ2mm〜3.5mmであることが望ましい。
また、樹脂チューブ15の長さは内視鏡1の処置具挿通
孔2の全長よりも長い。As shown in FIG. 3, the insertion portion 9 of the probe 3 comprises a resin tube 15 and a tip 10 attached to the tip of the resin tube 15. The tip 10 is connected via a ring-shaped intermediary tool 19. It is connected to the resin tube 15. The resin tube 15 is a so-called multi-lumen tube in which a relatively large-diameter pipe line 48 formed at the center and at least one or more relatively small-diameter pipe lines 16 provided around the pipe 48 are formed. It is. The resin tube 15 is desirably made of a material having excellent flexibility such as PTFE. Further, the outer diameter of the resin tube 15 is φ1.5 mm to φ6 mm, and particularly preferably φ2 mm to 3.5 mm.
The length of the resin tube 15 is longer than the entire length of the treatment instrument insertion hole 2 of the endoscope 1.
【0014】樹脂チューブ15の径が大きい方の管路4
8の径は、高周波ナイフ13と導電ワイヤ21が進退し
ても、適量の不活性ガスが流れるのに十分な大きさであ
る。The pipe 4 having the larger diameter of the resin tube 15
The diameter of 8 is large enough to allow an appropriate amount of inert gas to flow even when the high-frequency knife 13 and the conductive wire 21 advance and retreat.
【0015】また、小さな径の方の管路16には操作ワ
イヤ18が挿通されており、操作ワイヤ18の一端は管
路16の先端部分で樹脂チューブ15に接着固定されて
いる。操作ワイヤ18のもう一端側は樹脂チューブ15
の基端部分まで伸び、図5に示すように、樹脂チューブ
15の基端部分に形成したスリット54から外へ伸び出
している。操作ワイヤ18は手元側で押し引き操作する
ことにより進退が可能なものである。An operation wire 18 is inserted through the smaller diameter pipe 16, and one end of the operation wire 18 is adhesively fixed to the resin tube 15 at a tip end of the pipe 16. The other end of the operation wire 18 is a resin tube 15
5 and extends out from a slit 54 formed in the base end portion of the resin tube 15 as shown in FIG. The operation wire 18 can be advanced and retracted by performing a push-pull operation on the hand side.
【0016】図3に示すように、樹脂チューブ15の小
さな径の方の管路16の先端側部分には矩形状に形成さ
れた複数のスリット(孔)17が設けられている。この
ようにスリット17を形成したことにより、小さな径の
管路16に挿通している操作ワイヤ18を手元側に引い
た際、樹脂チューブ15の先端が手元側に引き寄せら
れ、前記スリット17を形成した部分から湾曲するよう
になる。これを利用して、プローブ3先端の向きを自由
に調節することができる(図8を参照)。As shown in FIG. 3, a plurality of rectangular slits (holes) 17 are provided in the distal end portion of the smaller diameter pipe 16 of the resin tube 15. By forming the slit 17 in this manner, when the operation wire 18 inserted into the small-diameter conduit 16 is pulled toward the hand, the tip of the resin tube 15 is drawn toward the hand, and the slit 17 is formed. The curved portion starts to curve. By utilizing this, the direction of the tip of the probe 3 can be freely adjusted (see FIG. 8).
【0017】なお、前記スリット17の幅は、1mm〜1
0mmであり、特に3mm〜6mmであることが望ましい。ス
リット17の間隔は、1mm〜100mmであり、特に2mm
〜5mmであることが望ましい。スリット17の数は図に
示される個数に限らない。The width of the slit 17 is 1 mm to 1 mm.
0 mm, and particularly desirably 3 mm to 6 mm. The interval between the slits 17 is 1 mm to 100 mm, particularly 2 mm
Desirably, it is about 5 mm. The number of slits 17 is not limited to the number shown in the figure.
【0018】樹脂チューブ15の管路48における先端
側内面には前記仲介具19が接合されて接着固定されて
いる。前記仲介具19は、例えばセラミック等の比較的
硬質で耐熱性を有する材料で作られている。前記仲介具
19の中心部には通孔47が設けられている。また、こ
の通孔47の径は高周波ナイフ13が進退し、且つ適量
の不活性ガスが流れるのに十分な大きさである。The intermediary tool 19 is bonded and fixed to the inner surface of the resin tube 15 at the distal end of the conduit 48. The intermediary device 19 is made of a relatively hard and heat-resistant material such as a ceramic, for example. A through hole 47 is provided in the center of the mediating tool 19. The diameter of the through hole 47 is large enough for the high-frequency knife 13 to advance and retreat, and to allow an appropriate amount of inert gas to flow.
【0019】前記仲介具19の先端側外周部分にはねじ
部22が形成され、このねじ部22には先端チップ10
がねじ込まれている。先端チップ10は例えばセラミッ
ク等の比較的硬質で耐熱性を有する材料で作られてい
る。先端チップ10の外径はφ1.5mm〜φ6mmである
が、特にφ2mm〜φ3.5mmであることが望ましい。A screw portion 22 is formed on the outer peripheral portion on the distal end side of the intermediary tool 19.
Is screwed. The tip 10 is made of a relatively hard and heat-resistant material such as ceramic. The outer diameter of the distal end tip 10 is φ1.5 mm to φ6 mm, and particularly preferably φ2 mm to φ3.5 mm.
【0020】先端チップ10の中心部には通孔14が設
けられており、この通孔14の径は、高周波ナイフ13
が進退し、不活性ガスが流れるのに十分な大きさであ
る。A through hole 14 is provided at the center of the tip 10. The diameter of the through hole 14 is
Are large enough to advance and retreat, and to flow the inert gas.
【0021】先端チップ10の基端側内表面にはねじ部
22が設けられている。これにより、先端チップ10は
前記仲介具19に固定的に取り付けられるが、着脱自在
でもある。また、先端チップ10と仲介具19との接続
手段は、着脱自在であればどのような接続方式でもよ
く、ねじ方式のものだけに限らない。A screw portion 22 is provided on the proximal inner surface of the distal tip 10. As a result, the distal tip 10 is fixedly attached to the intermediary tool 19, but is also detachable. The connection means between the tip 10 and the intermediary tool 19 may be of any type as long as it is detachable, and is not limited to the screw type.
【0022】高周波ナイフ13は前記プローブ3の先端
より突没可能で、且つ高周波電流を通電可能な電極とし
てのナイフ部11と、これの先端に設けられる電気絶縁
体としての先端絶縁部12とからなる。前記ナイフ部1
1は、例えばタングステン、ステンレス、金等の導電性
に優れる材質からできている。また、ナイフ部11の長
さは、3mm〜20mmであるが、特に5mm〜10mmである
ことが望ましい。また、ナイフ部11は先端チップ10
の通孔14より突没自在であり、このときの突出長さは
1mm〜7mmであるが、特に2mm〜5mmであることが望ま
しい。The high-frequency knife 13 is composed of a knife section 11 as an electrode which can be protruded and retracted from the tip of the probe 3 and which can supply a high-frequency current, and a tip insulating section 12 as an electrical insulator provided at the tip of the knife section 11. Become. The knife unit 1
1 is made of a material having excellent conductivity, such as tungsten, stainless steel, and gold. In addition, the length of the knife portion 11 is 3 mm to 20 mm, and particularly preferably 5 mm to 10 mm. In addition, the knife portion 11 has the tip 10
The protrusion length at this time is from 1 mm to 7 mm, but is preferably from 2 mm to 5 mm.
【0023】ナイフ部11の先端に取り付けられる先端
絶縁部12は、電極としてのナイフ部11の外径よりも
大径である。また、先端絶縁部12は、例えばセラミッ
クなどの電気的絶縁性及び耐熱性に優れる材料で作られ
ている。また、先端絶縁部12の表面には粘膜のこびり
つき防止のために、例えばフッ素コート等が薄くコーテ
ィングされている。The tip insulating section 12 attached to the tip of the knife section 11 has a diameter larger than the outer diameter of the knife section 11 as an electrode. Further, the distal end insulating portion 12 is made of a material having excellent electrical insulation properties and heat resistance, such as ceramics, for example. Further, the surface of the distal end insulating portion 12 is thinly coated with, for example, a fluorine coat or the like in order to prevent sticking of the mucous membrane.
【0024】ナイフ部11の基端側には接続パイプ20
を介して前記導電ワイヤ21の先端が接続されている。
接続パイプ20はステンレスや金などの導電性に優れる
材質で作られている。A connecting pipe 20 is provided at the base end side of the knife portion 11.
The distal end of the conductive wire 21 is connected via the.
The connection pipe 20 is made of a material having excellent conductivity, such as stainless steel or gold.
【0025】前記手元側操作部4は、図5に示すよう
に、パイプ状の本体49と、口金部材(流体供給接続手
段)50と、通電コネクタ(高周波供給接続手段)23と
を備えてなる。本体49は内部管路51を有しており、
この内部管路51の内径は口金部材50の先端側部分が
挿通するのに十分な大きさである。As shown in FIG. 5, the hand-side operation section 4 includes a pipe-shaped main body 49, a base member (fluid supply connection means) 50, and a current-carrying connector (high-frequency supply connection means) 23. . The main body 49 has an internal conduit 51,
The inner diameter of the internal conduit 51 is large enough to allow the distal end portion of the base member 50 to pass therethrough.
【0026】本体49における内部管路51内表面の一
部と、口金部材50の先端付近の外表面には、それそれ
半円状の突起28,27が設けられている。また、それ
ぞれの突起28,27の位置関係は、図5に示すよう
に、高周波ナイフ13を最も突き出したとき、突起27
が突起28よりも先端側に位置するようになっている。
これにより、突起27,28は、故意に口金部材50を
動かさない限りは移動しないようにするストッパ代わり
になる。Semi-circular projections 28 and 27 are provided on a part of the inner surface of the inner conduit 51 of the main body 49 and on the outer surface near the tip of the base member 50, respectively. As shown in FIG. 5, when the high-frequency knife 13 is most protruded, the protrusions 27 and 27 are positioned relative to each other.
Are located on the distal end side of the protrusion 28.
As a result, the projections 27 and 28 serve as stoppers that do not move unless the base member 50 is intentionally moved.
【0027】よって、高周波ナイフ13を、最も突き出
した位置に固定できる。このとき、口金部材50の凸部
61が本体49の開口端を封する役割をしている。この
ため、内部管路51内は気密が保たれている。また、そ
れぞれの突起27,28の表面は十分に滑らかなため、
故意に口金部材50を動かそうとするときには比較的容
易に動かすことができる。また、突起27,28の形状
は図のものに限らず、楕円形でも台形でも三角形等でも
よい。また、ストッパ機構は突起のものに限らず、ねじ
などで固定する方式のものとしてもよい。Thus, the high-frequency knife 13 can be fixed at the most protruding position. At this time, the convex portion 61 of the base member 50 has a role of sealing the open end of the main body 49. Therefore, the inside of the internal conduit 51 is kept airtight. Also, since the surfaces of the projections 27 and 28 are sufficiently smooth,
When the cap member 50 is intentionally moved, it can be moved relatively easily. Further, the shapes of the protrusions 27 and 28 are not limited to those shown in the drawings, and may be elliptical, trapezoidal, triangular, or the like. Further, the stopper mechanism is not limited to the protrusion mechanism, and may be a method of fixing with a screw or the like.
【0028】図5に示すように、口金部材50には不活
性ガスを流入させるための管路25が貫通するように形
成され、また、凸部61よりも手元側壁部には通電コネ
クタ23が設けられている。通電コネクタ23はカバー
部24と接続端子26とが設けられている。接続端子2
6はカバー部24内に位置し、L字パイプ52を介して
前記導電ワイヤ21と電気的に接続されている。L字パ
イプ52は例えばステンレスや金などの導電性に優れる
材質で作られている。これにより、口金部材50の進退
操作で高周波ナイフ13の進退操作が可能である。As shown in FIG. 5, a pipe 25 for flowing an inert gas is formed through the base member 50 so as to penetrate therethrough. Is provided. The current-carrying connector 23 is provided with a cover 24 and a connection terminal 26. Connection terminal 2
6 is located in the cover part 24 and is electrically connected to the conductive wire 21 via an L-shaped pipe 52. The L-shaped pipe 52 is made of a material having excellent conductivity such as stainless steel or gold. This allows the high-frequency knife 13 to move forward and backward by moving the base member 50 forward and backward.
【0029】次に、図6〜図14を参照しながら、本実
施形態に係る内視鏡用高周波凝固装置の作用を説明す
る。まず、図6に示すように、図示しない局注針を用い
て粘膜29と筋層31との間の結合組織30に生理食塩
水を注入し、粘膜29を膨瘤させる。また、予め、電極
(Pプレート)を患者の体外に張っておく。Next, the operation of the high-frequency coagulation apparatus for an endoscope according to the present embodiment will be described with reference to FIGS. First, as shown in FIG. 6, physiological saline is injected into the connective tissue 30 between the mucous membrane 29 and the muscular layer 31 using a local injection needle (not shown), and the mucous membrane 29 is bulged. Also, in advance,
(P plate) is stretched outside the patient's body.
【0030】次に、高周波ナイフ13の切開部11で、
膨瘤した粘膜29に小切開53を加えた後、高周波ナイ
フ13の先端絶縁部12を粘膜29の下に差し入れる。
この状態で粘膜29を切除することにより、筋層31へ
の通電を防ぎながら粘膜29の切開を行なう。Next, at the incision 11 of the high-frequency knife 13,
After making a small incision 53 on the swollen mucous membrane 29, the tip insulating portion 12 of the high-frequency knife 13 is inserted under the mucous membrane 29.
By cutting off the mucous membrane 29 in this state, the mucous membrane 29 is incised while preventing power supply to the muscle layer 31.
【0031】次に、粘膜切除を行っている間、もしくは
切除完了後における出血部位の止血操作について説明す
る。図7に示すように、内視鏡1で観察しながら出血部
位に対して高周波ナイフ13を向ける。高周波ナイフ1
3を先端チップ10の通孔14より突出させ、出血部位
に高周波ナイフ13の先端絶縁部12を押し当てる。Next, a description will be given of a hemostatic operation at a bleeding site during or after mucosal resection. As shown in FIG. 7, the high-frequency knife 13 is turned to the bleeding site while observing with the endoscope 1. High frequency knife 1
3 is made to protrude from the through hole 14 of the tip 10, and the tip insulating portion 12 of the high-frequency knife 13 is pressed against the bleeding site.
【0032】次に、不活性ガスの放出と高周波通電を行
う。これによってナイフ部11とこれに隣接する生体組
織との間でプラズマ反応を引き起こし、出血部位を焼灼
して止血を行う。このとき、電極としてのナイフ部11
を突き立てているため、プローブ10のナイフ部11が
粘膜に接触することがない。Next, discharge of an inert gas and high-frequency current supply are performed. As a result, a plasma reaction is caused between the knife portion 11 and a living tissue adjacent to the knife portion 11, and the bleeding site is cauterized to stop bleeding. At this time, the knife portion 11 as an electrode
, The knife portion 11 of the probe 10 does not contact the mucous membrane.
【0033】更に、手元側の操作で、操作ワイヤ18を
引っ張り、図8に示すように、挿入部9の先端部分を湾
曲させることで、内視鏡1の方を湾曲できないような狭
い管腔臓器内でも、挿入部9の先端部分と止血部位とを
容易に正対させて止血を行うことができる。Further, by pulling the operation wire 18 by the operation on the hand side and bending the distal end portion of the insertion portion 9 as shown in FIG. 8, a narrow lumen which cannot bend the endoscope 1 is used. Even in an organ, the hemostasis can be performed by easily facing the distal end portion of the insertion portion 9 and the hemostasis site.
【0034】このとき、図9に示すように、内視鏡1の
挿入部55に導電体の被覆32を施し、手元側で制御装
置7に接続するようにした場合には、内視鏡1の挿入部
55が人体側の電極(Pプレート)の代わりとなり、人体
内で、図9に示すように電流の受け渡しを行える。これ
により、人体側の電極(Pプレート)を患者の体外に張る
手間が省ける。At this time, as shown in FIG. 9, when the insertion portion 55 of the endoscope 1 is covered with a conductor 32 and is connected to the control device 7 at hand, the endoscope 1 The insertion portion 55 is used in place of the electrode (P plate) on the human body side, and the current can be transferred within the human body as shown in FIG. This saves the labor of extending the electrode (P plate) on the human body side outside the patient's body.
【0035】また、内視鏡1に被覆を施さずに、図10
に示すように、オーバーチューブ33に導電体の被覆3
4を施し、接続具36及び接続コード37を介して、制
御装置7に接続してもよい。このときは、あらかじめ体
内に挿入されたオーバーチューブ33内に手元口金35
より内視鏡1を挿入して使用する。Further, without coating the endoscope 1, FIG.
As shown in FIG.
4 and may be connected to the control device 7 via the connection tool 36 and the connection cord 37. At this time, the hand base 35 is inserted into the overtube 33 inserted in the body in advance.
The endoscope 1 is inserted and used.
【0036】さらに、先端チップ10は取替え可能であ
るため、用途によって様々な種類のチップに交換して使
い分けることができる。以下に、いくつかの先端チップ
10の例を挙げ、それらの説明する。Furthermore, since the tip 10 is replaceable, it can be replaced with various types of tips depending on the application and used properly. Hereinafter, some examples of the tip 10 will be described and described.
【0037】(1)図11に示すものは、先端が閉じた
形状の先端チップ10であり、先端チップ10の側面に
側口37を備える。この先端チップ10によれば、内視
鏡1を湾曲できないような狭い管腔臓器内の止血を行う
際、操作ワイヤ18の進退操作を必要としないため、よ
り容易に止血を行うことができる。側口37の大きさは
流体が流出するのに十分な大きさである。また、側口3
7の形状は図11のものに限らない。(1) The tip shown in FIG. 11 is a tip 10 having a closed tip, and a side port 37 is provided on a side surface of the tip 10. According to the distal tip 10, when performing hemostasis in a narrow luminal organ in which the endoscope 1 cannot be bent, the operation wire 18 does not need to be advanced or retracted, so that hemostasis can be performed more easily. The size of the side port 37 is large enough for the fluid to flow out. In addition, side mouth 3
The shape of 7 is not limited to that of FIG.
【0038】(2)図12に示すものは、先端チップ1
0の軸中心に設けられた、電極挿通孔38と、先端チッ
プ10の側壁に設けられた複数の流体挿通孔39とを備
えたものである。(2) The tip shown in FIG.
It has an electrode insertion hole 38 provided at the center of the 0 axis and a plurality of fluid insertion holes 39 provided on the side wall of the distal end tip 10.
【0039】この先端チップ10によれば、図13に示
すように、同時に多方向へ流体及び高周波電流を流すこ
とができるため、一度に広範囲の止血が可能である。特
に凹状になっている患部の止血に有効である。また、電
極挿通孔38の大きさは、高周波ナイフ13が進退し、
流体が流出するのに十分な大きさである。流体挿通孔3
9の大きさは、流体が流出するのに十分な大きさであ
る。流体挿通孔39の数は図12及び図13に示すもの
に限らない。また、流体挿通孔39の形状は図12及び
図13のものに限らず、楕円形でも、三角形でも、四角
形でもよい。According to the tip 10, as shown in FIG. 13, fluid and high-frequency current can be simultaneously passed in multiple directions, so that a wide range of hemostasis can be achieved at once. It is particularly effective for hemostasis of a concave affected part. In addition, the size of the electrode insertion hole 38 is such that the high-frequency knife 13 advances and retreats,
It is large enough for the fluid to escape. Fluid insertion hole 3
The size of 9 is large enough for the fluid to flow out. The number of fluid insertion holes 39 is not limited to those shown in FIGS. Further, the shape of the fluid insertion hole 39 is not limited to those shown in FIGS. 12 and 13, and may be elliptical, triangular, or square.
【0040】(3)図14に示す先端チップ10は先端
が閉じた形状のものであり、軸方向に前記側孔37を複
数個並べている。この先端チップ10によれば、軸方向
に長く高周波電流を流すことができるため、一度に広範
囲の止血が可能になる。特に細長い管腔臓器の止血に有
効である。なお、側孔37の数は図14に示すものに限
らない。(3) The tip 10 shown in FIG. 14 has a closed end, and a plurality of the side holes 37 are arranged in the axial direction. According to the tip 10, a high-frequency current can be passed in the axial direction for a long time, so that hemostasis over a wide area can be achieved at once. It is particularly effective for hemostasis of elongated hollow organs. The number of side holes 37 is not limited to that shown in FIG.
【0041】本実施形態のものによれば、内視鏡1の処
置具挿通孔(チャンネル)2に異なる機能の処置具を入
れ替えることなく、病変組織の切除と止血とに至る一連
の作業を連続して容易に行うことができ、結果的に手術
時間の短縮を図ることができる。According to the present embodiment, a series of operations from resection of diseased tissue to hemostasis can be continuously performed without replacing a treatment tool having a different function in the treatment tool insertion hole (channel) 2 of the endoscope 1. The operation can be easily performed, and as a result, the operation time can be reduced.
【0042】また、高周波ナイフ13の先端絶縁部12
を患部に押し当てることで、プローブ3の先端チップ1
0と粘膜29との距離を適度に離すことができる。した
がって、先端チップ10に粘膜29が付着して、不活性
ガスが流れにくくなり、出血部周辺に対して均等に止血
を行えなくなるといった事態を防ぐことができる。Also, the tip insulating portion 12 of the high-frequency knife 13
Is pressed against the diseased part, so that the tip 1 of the probe 3
The distance between 0 and the mucous membrane 29 can be appropriately set apart. Therefore, it is possible to prevent a situation in which the mucous membrane 29 adheres to the distal end tip 10, making it difficult for the inert gas to flow, and making it impossible to uniformly stop bleeding around the bleeding part.
【0043】(第2実施形態)図15及び図16を参照
しながら、本発明の第2実施形態について説明する。本
実施形態に係る内視鏡用高周波凝固装置は、切開の機能
と広範囲止血の機能に加え、局所止血の機能も加えたも
のであり、大まかな構成は前術した第1実施形態のもの
と同じである。(Second Embodiment) A second embodiment of the present invention will be described with reference to FIGS. The high-frequency coagulation apparatus for an endoscope according to the present embodiment has a function of local hemostasis in addition to a function of incision and a function of wide-range hemostasis, and a rough configuration is the same as that of the first embodiment which was previously performed. Is the same.
【0044】挿入部9は、先端チップ10と、接続具1
9と、シングルルーメンチューブ56と、保護部材41
とを備えたものである。先端チップ10は、例えばタン
グステン、ステンレス、金などの導電性に優れる材質で
作られている。先端チップ10の表面には焦げ付き防止
のために、例えばフッ素樹脂などを薄くコーティングし
ている。また、接続具19は、例えばタングステン、ス
テンレス、金などの導電性に優れる材質で作られてい
る。接続具19の通孔47の大きさはこの後に説明する
高周波ナイフ13のナイフ部11の先端側端部に設けら
れた突起40の径よりも小さい。The insertion portion 9 includes the tip 10 and the connecting tool 1.
9, the single lumen tube 56, the protection member 41
It is provided with. The tip 10 is made of a material having excellent conductivity, such as tungsten, stainless steel, or gold. The surface of the tip 10 is coated with a thin film of, for example, a fluororesin to prevent scorching. Further, the connection tool 19 is made of a material having excellent conductivity such as tungsten, stainless steel, and gold. The size of the through hole 47 of the connector 19 is smaller than the diameter of a projection 40 provided at the distal end of the knife portion 11 of the high-frequency knife 13 described later.
【0045】また、シングルルーメンチューブ56は、
例えばPTFE等の可撓性に優れる材質で作られてい
る。また、保護部材41は例えばセラミック等の比較的
硬質で耐熱性を有する材料で作られている。また、保護
部材41は先端チップ10の通孔14内で、高周波ナイ
フ13と先端チップ10との間に割って入るように配設
されている。保護部材41は止血時のプラズマ反応によ
って先端チップ10が溶けないように保護する役割をす
る。The single lumen tube 56 is
For example, it is made of a material having excellent flexibility such as PTFE. The protection member 41 is made of a relatively hard and heat-resistant material such as a ceramic. The protection member 41 is disposed so as to be cut between the high-frequency knife 13 and the tip 10 in the through hole 14 of the tip 10. The protection member 41 serves to protect the tip 10 from being melted by the plasma reaction during hemostasis.
【0046】また、高周波ナイフ13のナイフ部11に
おける先端部分にはそのナイフ部11よりも大径であ
り、且つ先端絶縁部12よりも小径である円盤状の突起
40を設けた。突起40は例えばタングステン、ステン
レス、金などの導電性に優れる材料で作られている。な
お、上記突起40の断面形状は円に限らず、楕円形でも
四角形でも三角形でもよい。At the tip of the knife portion 11 of the high-frequency knife 13, a disk-shaped projection 40 having a diameter larger than that of the knife portion 11 and smaller than the tip insulating portion 12 is provided. The protrusion 40 is made of a material having excellent conductivity, such as tungsten, stainless steel, and gold. The cross-sectional shape of the projection 40 is not limited to a circle, but may be an ellipse, a square, or a triangle.
【0047】上述のように、突起40の径は仲介具19
の通孔47よりも大きいため、図16に示すように、高
周波ナイフ13を収納した際には突起40が仲介具19
に接触するようになっている。As described above, the diameter of the protrusion 40 is
As shown in FIG. 16, when the high-frequency knife 13 is stored, the projection 40 is
It comes in contact with.
【0048】次に、本実施形態に係る内視鏡用高周波凝
固装置の作用について説明する。まず、切開を行なう方
法については、前述した第1実施形態の場合と同じであ
る。なお、突起40の径は先端絶縁部12よりも十分に
小さいため、切開時に突起40が意図しない部分を切開
することはない。また、広範囲にわたり止血する方法に
ついても前述した第1実施形態の場合と同じである。Next, the operation of the high-frequency coagulation apparatus for an endoscope according to this embodiment will be described. First, the method of making the incision is the same as in the case of the first embodiment described above. Since the diameter of the projection 40 is sufficiently smaller than the diameter of the distal end insulating portion 12, an unintended portion of the projection 40 is not cut at the time of cutting. Also, the method of stopping blood over a wide range is the same as in the first embodiment described above.
【0049】局所的な止血方法については、図16に示
すように、内視鏡1で観察しながらプローブ3の先端チ
ップ10を出血部位に押し当てる。このとき、高周波ナ
イフ13をいっぱいに引き込み、突起40と仲介具19
を接触させておく。そして、先端チップ10を出血部位
に押し当てた後、制御装置7よりHF電流を供給する。
すると、供給された高周波電流は、導電ワイヤ21→ナ
イフ部11→突起40→仲介具19→先端チップ10の
順に伝わっていき、出血部位を直接焼灼することにより
止血を行う。この際、先端チップ10には焦げ付き防止
用のコーティングを施しているため、粘膜がこびり付い
て通孔14を塞ぐこともない。As for the local hemostasis method, as shown in FIG. 16, the distal tip 10 of the probe 3 is pressed against the bleeding site while observing with the endoscope 1. At this time, the high-frequency knife 13 is fully pulled in, and the projection 40 and the intermediate tool 19 are
Contact. Then, after pressing the tip 10 against the bleeding site, the controller 7 supplies an HF current.
Then, the supplied high-frequency current is transmitted in the order of the conductive wire 21 → the knife portion 11 → the protrusion 40 → the mediation tool 19 → the distal tip 10 to perform hemostasis by directly cauterizing the bleeding site. At this time, since the tip tip 10 is provided with a coating for preventing burning, the mucous membrane does not stick and does not block the through hole 14.
【0050】本実施形態によれば、前述した第1実施形
態の効果に加えて、処置具の入れ替えを行わずに、比較
的勢いのある出血(アルゴン・ビーム・コアギュレータ
ーの不得意としている)にも対応できる。According to the present embodiment, in addition to the effects of the above-described first embodiment, relatively vigorous bleeding (which is not good at argon beam coagulators) without changing the treatment tool is performed. ) Can also be supported.
【0051】(他の止血プローブの例)ここで、出血部
の他の止血プローブの別例を示す。図17に示すもの
は、高周波ナイフ13の代わりに渦巻き状に形成した電
極42を用いてプローブ3を構成する。このプローブ3
によれば、第1実施形態に記載した場合のように、不活
性ガス中にプラズマを発生させて止血する方法も可能で
あると同時に、止血剤をプローブ3内の管路から散布す
ることも可能である。このとき、前記電極42は、ねじ
のように渦巻状に溝43を設けているため、流体を霧状
にして、広範囲に止血剤を散布することが可能である。(Example of Another Hemostatic Probe) Here, another example of another hemostatic probe of the bleeding part is shown. In the probe shown in FIG. 17, the probe 3 is constituted by using a spirally formed electrode 42 instead of the high-frequency knife 13. This probe 3
According to the method, as in the case of the first embodiment, a method of stopping blood by generating plasma in an inert gas is also possible, and at the same time, a hemostatic agent can be sprayed from a conduit in the probe 3. It is possible. At this time, since the electrode 42 is provided with the spiral groove 43 like a screw, it is possible to spray the hemostatic agent over a wide area by atomizing the fluid.
【0052】図18に示すものは高周波ナイフ13の代
わりに高周波スネア44を用いてプローブ3を構成し
た。このプローブ3によれば、例えばポリペクトミーな
どの病変部を高周波スネア44で切除後、第1実施形態
に記載したように不活性ガス中にプラズマを発生させて
止血するといった一連の操作を、処置具の入れ替えを行
うことなくできる。In the probe shown in FIG. 18, the probe 3 was constituted by using a high-frequency snare 44 instead of the high-frequency knife 13. According to the probe 3, a series of operations such as generating a plasma in an inert gas to stop blood bleeding as described in the first embodiment after excision of a lesion such as polypectomy with a high-frequency snare 44 are performed by a treatment tool. Can be done without replacing
【0053】また、図19に示すものは、軸方向に対
し、中心に設けられた電極用通孔45と、その周囲に設
けられた複数個の流体用通孔46とを持つ先端チップ1
0を備えたプローブ3とした。このプローブ3によれ
ば、電極45が常に中心の位置に固定されるため、電極
45を中心にしてプラズマを電極45の周囲に均等に発
生させることができる。これにより、止血状態のムラが
なくなる。FIG. 19 shows a tip 1 having an electrode through-hole 45 provided at the center in the axial direction and a plurality of fluid through-holes 46 provided therearound.
Probe 3 provided with 0. According to the probe 3, since the electrode 45 is always fixed at the center position, plasma can be uniformly generated around the electrode 45 around the electrode 45. This eliminates unevenness in the hemostatic state.
【0054】(第3実施形態)図20及び図21を参照
しながら、本発明の第3実施形態について説明する。本
実施形態は、前述した第2実施形態における局所止血の
機能を持つプローブにおいて、バイポーラ高周波を用い
た例と、その製造方法であり、これらを以下に説明する
が、概略の構成は前述した第2実施形態と同じであり、
異なる構成部を中心に説明する。(Third Embodiment) A third embodiment of the present invention will be described with reference to FIGS. The present embodiment is an example using a bipolar high frequency in the probe having the function of local hemostasis in the above-described second embodiment and a method of manufacturing the same. These will be described below. Same as the second embodiment,
The description will focus on the different components.
【0055】図20及び図21に示すように、プローブ
3の挿入部9は、先端チップ10が電気的絶縁性の樹脂
チューブ15と導線59を備えてなり、先端チップ10
の表面には2本の独立したらせん電極57および58を
設けている。らせん電極57は樹脂チューブ15内に内
蔵された導線59と接続され、らせん電極58は先端チ
ップ10に内蔵された仲介具19と接続されている。よ
って、高周波ナイフ13を基端側に引き込み、高周波ナ
イフ13を仲介具19に当て付けることで、らせん電極
58に通電させることが可能となるように構成されてい
る。As shown in FIGS. 20 and 21, the insertion portion 9 of the probe 3 has a distal tip 10 provided with an electrically insulating resin tube 15 and a conducting wire 59.
Are provided with two independent spiral electrodes 57 and 58. The helical electrode 57 is connected to a conducting wire 59 built in the resin tube 15, and the helical electrode 58 is connected to the intermediary tool 19 built in the tip 10. Therefore, the high-frequency knife 13 is pulled toward the base end, and the high-frequency knife 13 is applied to the intermediary tool 19 so that the spiral electrode 58 can be energized.
【0056】ここで、らせん電極57および58は先端
チップ10の外表面上に凹凸なく同一平面に形成されい
る。また、らせん電極57および58は導電性の素材で
あれば、同一の素材でも、異なる素材でも構わないが、
耐熱性を考慮すると、銀や金といった素材よりも白金等
の融点が高い素材の方が好ましい。Here, the spiral electrodes 57 and 58 are formed on the outer surface of the tip chip 10 without any irregularities and on the same plane. The spiral electrodes 57 and 58 may be the same material or different materials as long as they are conductive materials.
In consideration of heat resistance, a material having a higher melting point, such as platinum, is preferable to a material such as silver or gold.
【0057】次に、先端チップ10の製造方法につい
て、図20乃至図25を参照して説明する。まず、図2
2及び図23に示すように、先端チップ10の外表面に
予め2本のらせん溝60を形成する(らせん溝形成工
程)。Next, a method of manufacturing the tip 10 will be described with reference to FIGS. First, FIG.
As shown in FIGS. 2 and 23, two spiral grooves 60 are previously formed on the outer surface of the distal end tip 10 (spiral groove forming step).
【0058】次に、図24に示すように、先端チップ1
0の外表面を完全に被覆するようにらせん電極57およ
び58となる素材を形成する(電極素材となる被覆形成
工程)。Next, as shown in FIG.
A material to be the spiral electrodes 57 and 58 is formed so as to completely cover the outer surface of No. 0 (coating forming process to be an electrode material).
【0059】最後に、図25に示すように、らせん電極
57および58となる素材によって被覆された先端チッ
プ10の外表面を均等に研磨もしくは研削することによ
り、らせん状電極57および58を独立的に露出させる
(らせん状電極露出形成工程)。Finally, as shown in FIG. 25, the outer surfaces of the distal end tip 10 covered with the materials to be the spiral electrodes 57 and 58 are uniformly polished or ground to separate the spiral electrodes 57 and 58 independently. (Spiral electrode exposure forming step).
【0060】本実施形態のプローブ3を用いて切開する
方法は前述した第1実施形態のものに同じである。ま
た、広範囲の止血方法も第1実施形態の場合に同じであ
る。The method of incising using the probe 3 of this embodiment is the same as that of the first embodiment described above. Further, the method for stopping hemostasis over a wide range is the same as in the case of the first embodiment.
【0061】局所的な止血方法は内視鏡1で観察しなが
らプローブ3の先端チップ10を出血部位に押し当て
る。また、このとき、高周波ナイフ13を一杯まで引き
込み、突起40と接続パイプ19を接触させておく。先
端チップ10を出血部位に押し当てた後、制御装置7よ
り凝固電流を供給する。すると、供給された高周波電流
は、導電ワイヤ21→ナイフ部11→突起40→仲介具
19→らせん電極58の順に伝わり、押し当てられた出
血部位を経て、らせん電極57→導線59から供給源に
戻り、出血部位を直接焼灼することにより止血を行う。In the local hemostasis method, the tip 10 of the probe 3 is pressed against the bleeding site while observing with the endoscope 1. At this time, the high-frequency knife 13 is fully pulled in, and the projection 40 and the connection pipe 19 are kept in contact. After pressing the tip 10 against the bleeding site, the controller 7 supplies a coagulation current. Then, the supplied high-frequency current is transmitted in the order of the conductive wire 21 → the knife portion 11 → the protrusion 40 → the mediator 19 → the spiral electrode 58, and passes through the pressed bleeding site, and the spiral electrode 57 → the conducting wire 59 to the supply source. Return, and perform hemostasis by directly cauterizing the bleeding site.
【0062】本実施形態の効果は、前述した第2実施形
態の効果に加えて、次のような効果が得られる。The effects of the present embodiment have the following effects in addition to the effects of the above-described second embodiment.
【0063】まず、先端チップ10の外表面に設けられ
た止血用高周波電極(らせん電極)57,58がバイポ
ーラ電極であるため、人体側の電極(Pプレート)を必要
とせず、簡便に処置が行える。First, since the hemostatic high-frequency electrodes (spiral electrodes) 57 and 58 provided on the outer surface of the distal end tip 10 are bipolar electrodes, a treatment on the human body side (P plate) is not required and the treatment can be performed easily. I can do it.
【0064】また、らせん電極57および58が先端チ
ップ10の外表面に凹凸無く同一面に形成されているの
で、先端チップ10の外表面がフラットであり、内視鏡
1の処置具挿通孔2内をスムーズに挿通させることがで
きる。Further, since the spiral electrodes 57 and 58 are formed on the outer surface of the distal tip 10 without any irregularities on the same surface, the outer surface of the distal tip 10 is flat, and the treatment tool insertion hole 2 of the endoscope 1 is provided. The inside can be smoothly inserted.
【0065】さらに、らせん溝60を設けた後、らせん
電極57および58を形成しているため、らせん電極5
7および58の幅を高精度に均一に形成することがで
き、均一な高周波凝固能を発揮できる。Further, after the spiral groove 60 is provided, the spiral electrodes 57 and 58 are formed.
The widths of 7 and 58 can be formed uniformly with high precision, and uniform high-frequency solidification ability can be exhibited.
【0066】尚、本発明は前述した各実施形態に限定さ
れるものではなく、他の形態にも適用が可能である。The present invention is not limited to the above embodiments, but can be applied to other embodiments.
【0067】前述した説明によれば、以下に列挙する事
項および以下に列挙した事項のものを任意に組み合わせ
た事項のものが得られる。According to the above description, the following items and items obtained by arbitrarily combining the items listed below can be obtained.
【0068】1.経内視鏡的に使用でき、生体の処置対
象部位に高周波電流を流すことによって処置対象部位を
止血・凝固する内視鏡用高周波凝固装置において、経内
視鏡的に体内に挿入可能で、且つ先端で開口する通孔を
有する長尺なプローブと、前記プローブの先端付近に設
けられた、高周波電流を通電可能な電極と、前記電極の
先端に設けられた、前記電極より大径の電気絶縁体と、
前記電極に高周波電源を供給するための高周波電源装置
と、前記プローブが有する前記通孔に不活性ガスを供給
する手段及び前記電極に高周波電流を供給する手段とを
有した制御部とからなることを特徴とする内視鏡用高周
波凝固装置。1. In a high-frequency coagulation device for an endoscope that can be used endoscopically and stops and coagulates a treatment target site by flowing a high-frequency current to a treatment target site of a living body, it can be inserted into the body transendoscopically, A long probe having a through-hole opening at the tip, an electrode provided near the tip of the probe and capable of conducting a high-frequency current, and an electricity provided at the tip of the electrode and having a larger diameter than the electrode. An insulator,
A high frequency power supply for supplying high frequency power to the electrode, and a control unit having means for supplying an inert gas to the through hole of the probe and means for supplying a high frequency current to the electrode. A high-frequency coagulation device for an endoscope, comprising:
【0069】2.第1項において、前記プローブは、前
記先端チップと前記樹脂チューブとを着脱自在に取り付
けられる取付機構を持つことを特徴とするもの。2. 3. The probe according to claim 1, wherein the probe has an attachment mechanism for detachably attaching the distal end tip and the resin tube.
【0070】3.第1項において、前記電極は前記プロ
ーブ先端において突没自在であり、その突出量が1mm〜
7mmに設定されていることを特徴とするもの。3. In the first aspect, the electrode can be freely protruded and retracted at the probe tip, and the protruding amount is 1 mm to
It is characterized by being set to 7 mm.
【0071】4.第3項において、前記プローブは、前
記電極が最も突出した位置で固定される固定機構をもつ
ことを特徴とするもの。4. 3. The probe according to claim 3, wherein the probe has a fixing mechanism for fixing the electrode at a position where the electrode protrudes most.
【0072】[0072]
【発明の効果】以上説明したように本発明によれば、切
開機能と凝固機能を併せ持たせたことにより、内視鏡の
処置具挿通孔に異なる機能の処置具を入れ替えることな
く、病変組織の切除と止血とに至る一連の作業を行うこ
とができ、その結果、手技が簡便になると共に手技時間
の短縮が図れる。また、電極の先端に設けた電気絶縁体
を組織に押し当てることで、アルゴン・ビーム・コアギ
ュレーターのプローブ先端と組織とを確実に適正な距離
に離した状態に保てるため、電極先端が組織に触れて電
極に組織が焦げ付いて付着してしまい、不活性ガスが流
れなくなるという問題を生じさせない。その結果、手技
中に本来の機能を損なうことなく、組織を凝固できると
共に、治療装置のメンテナンスが不要であり、また、短
期間の使用で廃棄してしまうことがなくなり、医療費の
削減にもつながる。As described above, according to the present invention, by having both the incision function and the coagulation function, the diseased tissue can be replaced without changing the treatment tool having a different function into the treatment tool insertion hole of the endoscope. A series of operations from resection to hemostasis can be performed, and as a result, the procedure becomes simpler and the procedure time can be shortened. In addition, pressing the electrical insulator provided at the tip of the electrode against the tissue ensures that the tip of the probe of the argon beam coagulator and the tissue are kept at an appropriate distance. Does not cause the problem that the tissue is scorched and adhered to the electrode and the inert gas stops flowing. As a result, the tissue can be coagulated without impairing the original function during the procedure, and maintenance of the treatment device is not required. Connect.
【図1】本発明の第1実施形態に係る内視鏡用高周波凝
固装置の概略的な説明図。FIG. 1 is a schematic explanatory view of a high-frequency coagulation device for an endoscope according to a first embodiment of the present invention.
【図2】第1実施形態に係る内視鏡用高周波凝固装置の
プローブの先端部付近の斜視図。FIG. 2 is a perspective view of the vicinity of a distal end of a probe of the high-frequency coagulation device for an endoscope according to the first embodiment.
【図3】第1実施形態に係る内視鏡用高周波凝固装置の
プローブの先端部付近の縦断面図。FIG. 3 is a longitudinal sectional view of the vicinity of a distal end of a probe of the high-frequency coagulation apparatus for an endoscope according to the first embodiment.
【図4】第1実施形態に係る内視鏡用高周波凝固装置の
プローブの手元側部分の斜視図。FIG. 4 is a perspective view of a proximal portion of a probe of the high-frequency coagulation apparatus for an endoscope according to the first embodiment.
【図5】第1実施形態に係る内視鏡用高周波凝固装置の
プローブの手元側部分の縦断面図。FIG. 5 is a longitudinal sectional view of a proximal portion of a probe of the high-frequency coagulation apparatus for an endoscope according to the first embodiment.
【図6】第1実施形態に係る内視鏡用高周波凝固装置の
作用の説明図。FIG. 6 is an explanatory diagram of the operation of the high-frequency coagulation device for an endoscope according to the first embodiment.
【図7】第1実施形態に係る内視鏡用高周波凝固装置の
作用の説明図。FIG. 7 is an explanatory diagram of the operation of the high-frequency coagulation device for an endoscope according to the first embodiment.
【図8】第1実施形態に係る内視鏡用高周波凝固装置の
作用の説明図。FIG. 8 is an explanatory diagram of the operation of the high-frequency coagulation device for an endoscope according to the first embodiment.
【図9】第1実施形態に係る内視鏡用高周波凝固装置の
変形例における作用説明図。FIG. 9 is an operation explanatory view of a modification of the high-frequency coagulation device for an endoscope according to the first embodiment.
【図10】第1実施形態に係る内視鏡用高周波凝固装置
の他の変形例における作用説明図。FIG. 10 is an operation explanatory view of another modification of the high-frequency coagulation device for an endoscope according to the first embodiment.
【図11】第1実施形態に係る内視鏡用高周波凝固装置
の先端チップの変形例の使用状態の斜視図。FIG. 11 is a perspective view of a usage state of a modification of the distal end tip of the high-frequency coagulation device for an endoscope according to the first embodiment.
【図12】第1実施形態に係る内視鏡用高周波凝固装置
の先端チップの他の変形例の説明図。FIG. 12 is an explanatory view of another modification of the distal end tip of the high-frequency coagulation device for an endoscope according to the first embodiment.
【図13】第1実施形態に係る内視鏡用高周波凝固装置
の先端チップの他の変形例の作用説明図。FIG. 13 is an operation explanatory view of another modification of the distal end tip of the high-frequency coagulation device for an endoscope according to the first embodiment.
【図14】第1実施形態に係る内視鏡用高周波凝固装置
の先端チップの他の変形例の作用説明図。FIG. 14 is an operation explanatory view of another modification of the distal end tip of the high-frequency coagulation device for an endoscope according to the first embodiment.
【図15】第2実施形態に係る内視鏡用高周波凝固装置
のプローブの先端部付近の縦断面図。FIG. 15 is a longitudinal sectional view of the vicinity of a distal end of a probe of the high-frequency coagulation apparatus for an endoscope according to the second embodiment.
【図16】第2実施形態に係る内視鏡用高周波凝固装置
のプローブの先端部付近の使用状態での縦断面図。FIG. 16 is a vertical cross-sectional view of the probe of the high-frequency coagulation apparatus for an endoscope according to the second embodiment in the use state near the distal end thereof.
【図17】止血プローブの別例を示す先端部付近の縦断
面図。FIG. 17 is a longitudinal sectional view showing the vicinity of a distal end portion of another example of the hemostatic probe.
【図18】止血プローブの他の例を示す先端部付近の縦
断面図。FIG. 18 is a vertical cross-sectional view showing the vicinity of the distal end of another example of the hemostatic probe.
【図19】止血プローブのさらに他の例を示す先端部付
近の縦断面図。FIG. 19 is a vertical cross-sectional view of the vicinity of a distal end showing still another example of the hemostatic probe.
【図20】本発明の第3実施形態に係るプローブにおけ
る先端部の側面図。FIG. 20 is a side view of the distal end of the probe according to the third embodiment of the present invention.
【図21】本発明の第3実施形態に係るプローブにおけ
る先端部の縦断面図。FIG. 21 is a longitudinal sectional view of a distal end portion of a probe according to a third embodiment of the present invention.
【図22】本発明の第3実施形態に係るプローブにおけ
る先端チップの製造方法の手順の説明図。FIG. 22 is an explanatory diagram of a procedure of a method of manufacturing a tip in a probe according to a third embodiment of the present invention.
【図23】本発明の第3実施形態に係るプローブにおけ
る先端チップの製造方法の説明図。FIG. 23 is an explanatory diagram of a method of manufacturing a tip in a probe according to a third embodiment of the present invention.
【図24】本発明の第3実施形態に係るプローブにおけ
る先端チップの製造方法の手順の説明図。FIG. 24 is an explanatory view of a procedure of a method of manufacturing a tip in a probe according to a third embodiment of the present invention.
【図25】本発明の第3実施形態に係るプローブにおけ
る先端チップの製造方法の手順の説明図。FIG. 25 is an explanatory diagram of a procedure of a method of manufacturing a tip in a probe according to a third embodiment of the present invention.
1…内視鏡、2…処置具挿通孔、3…プローブ、4…手
元側操作部、5…通電ケーブル、6…流体供給チュー
ブ、7…制御装置、9…挿入部、10…先端チップ、1
1…ナイフ部、12…先端絶縁部、13…高周波ナイ
フ、23…通電コネクタ、26…接続端子、48…管
路、49…本体、50…口金部材。DESCRIPTION OF SYMBOLS 1 ... Endoscope, 2 ... Treatment tool insertion hole, 3 ... Probe, 4 ... Hand side operation part, 5 ... Electrification cable, 6 ... Fluid supply tube, 7 ... Control device, 9 ... Insertion part, 10 ... Tip, 1
DESCRIPTION OF SYMBOLS 1 ... Knife part, 12 ... Insulated tip part, 13 ... High frequency knife, 23 ... Power supply connector, 26 ... Connection terminal, 48 ... Pipe line, 49 ... Main body, 50 ... Base member.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 木村 耕 東京都渋谷区幡ヶ谷2丁目43番2号 オリ ンパス光学工業株式会社内 Fターム(参考) 4C060 FF10 FF19 KK03 KK04 KK05 KK06 KK09 KK10 KK13 KK17 KK20 4C061 GG15 ────────────────────────────────────────────────── ─── Continuing on the front page (72) Inventor Kou Kimura 2-43-2 Hatagaya, Shibuya-ku, Tokyo F-term in Olympus Optical Co., Ltd. 4C060 FF10 FF19 KK03 KK04 KK05 KK06 KK09 KK10 KK13 KK17 KK20 4C061 GG15
Claims (1)
位に高周波電流を流すことによって処置対象部位を切開
・止血・凝固する内視鏡用治療装置において、 経内視鏡的に体内に挿入可能で、且つ先端で開口する通
孔を有する長尺なプローブと、 前記プローブの先端付近に設けられ、前記プローブの先
端より突没可能で、且つ高周波電流を通電可能な電極
と、 前記電極の先端に設けられた、前記電極より大径の電気
絶縁体と、 前記電極に高周波電流を供給する高周波電源と、 前記プローブが有する前記通孔に不活性ガスを供給する
手段と前記電極に高周波電流を供給する手段とを有する
制御装置とを具備したことを特徴とする内視鏡用治療装
置。1. A treatment apparatus for an endoscope which can be used endoscopically and incises, stops, and coagulates a treatment target site by flowing a high-frequency current to a treatment target site in a living body. A long probe that can be inserted into the body and has a through hole that opens at the tip, and an electrode that is provided near the tip of the probe and that can protrude and sink from the tip of the probe and that can pass a high-frequency current, An electrical insulator provided at the tip of the electrode, having a larger diameter than the electrode; a high-frequency power supply for supplying a high-frequency current to the electrode; a means for supplying an inert gas to the through hole of the probe; and the electrode And a control device having means for supplying a high-frequency current to the endoscope.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001107442A JP2002301088A (en) | 2001-04-05 | 2001-04-05 | Endoscopic treatment device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001107442A JP2002301088A (en) | 2001-04-05 | 2001-04-05 | Endoscopic treatment device |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2002301088A true JP2002301088A (en) | 2002-10-15 |
Family
ID=18959766
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001107442A Withdrawn JP2002301088A (en) | 2001-04-05 | 2001-04-05 | Endoscopic treatment device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2002301088A (en) |
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| A300 | Withdrawal of application because of no request for examination |
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