JP2016064130A - Surgical tool and vasodilatation device - Google Patents

Surgical tool and vasodilatation device Download PDF

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JP2016064130A
JP2016064130A JP2015187425A JP2015187425A JP2016064130A JP 2016064130 A JP2016064130 A JP 2016064130A JP 2015187425 A JP2015187425 A JP 2015187425A JP 2015187425 A JP2015187425 A JP 2015187425A JP 2016064130 A JP2016064130 A JP 2016064130A
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clamping member
blood vessel
surgical instrument
recess
insertion tube
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伊藤 学
Manabu Ito
学 伊藤
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Saga University NUC
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Abstract

PROBLEM TO BE SOLVED: To provide a surgical tool capable of safely and securely preventing leakage of fluid under pressure without damaging a blood vessel in a vasodilation surgery, and a vasodilatation device composed of the surgical tool and an insertion tube.SOLUTION: A vasodilatation device includes an insertion tube 10 and a surgical tool 20. The insertion tube 10 includes a step formed in a shape that a connection 15 is smaller in diameter than that of an insertion tip 11. The surgical tool 20 includes a first recess 26a recessed in an arc shape formed on a first holding member 26, a second recess 27a recessed in an arc shape formed at a position corresponding to the first recess 26a on a second holding member 27, a retention mechanism 24 to keep a closed state of the first holding member 26 and the second holding member 27. In the state where the first holding member 26 and the second holding member 27 are closed, a diameter of a blood vessel holder 23 formed with the first recess 26a and the second recess 27a is substantially equal to that of the connection 15 at the step.SELECTED DRAWING: Figure 4

Description

本発明は、剥離採取した血管を血管拡張する場合に用いられる手術器具、並びにこの手術器具及び挿入管からなる血管拡張器具に関する。   The present invention relates to a surgical instrument used for vasodilation of a blood vessel that has been exfoliated and collected, and a vasodilator comprising the surgical instrument and an insertion tube.

例えば、末期腎不全患者における透析用ブラッドアクセス作製術において、血行再建のために剥離採取した自己血管(自家静脈)を拡張させる必要がある、この場合、剥離した自家静脈(橈側皮静脈や尺側皮静脈)の吻合部位から、それより中枢の剥離していない前腕部から上腕部にかけての広範囲の静脈を確実且つ損傷なく安全に拡張させる必要がある。   For example, in blood access preparation for dialysis in patients with end-stage renal failure, it is necessary to expand the detached blood vessels (autologous veins) for blood circulation reconstruction. There is a need to securely and safely expand a wide range of veins from the anastomosis site of the skin vein) to the central arm where the central arm is not separated from the forearm to the upper arm.

同様に、虚血性心疾患に対する冠動脈バイパス手術、下肢閉塞性動脈硬化症に対する下肢血行再建術、頭頸部領域の血行再建術等でも、剥離採取した血管(大伏在静脈や橈骨動脈)の分枝の処理や損傷部の確認、修復の際に血管を拡張させる必要がある。   Similarly, in the coronary artery bypass surgery for ischemic heart disease, lower limb revascularization for lower limb obstructive arteriosclerosis, head and neck revascularization, etc. It is necessary to dilate blood vessels during treatment, confirmation of damaged parts, and repair.

上記のような血管拡張は、具体的には先端がテーパ状の挿入管(カニューレ)又は球状になったカニューレを挿入し、ヘパリン入り生理食塩水等を内腔に注入し、血管を内側から加圧して拡張させる。カニューレ挿入部からの液体の漏れをコントロールする際には、ストレート型の鉗子を利用する場合があるが、鉗子とカニューレが接する部分が限局しており、それ以外の部分からの漏れが生じて血管拡張作業が不十分になってしまう。このような問題点があるため、臨床現場では、漏れを制御するために細い絹糸で血管の外側から結紮することを余儀なくされていることが多い。結紮する作業は人手と時間を要するだけでなく、血管拡張後に結紮糸を取り除く際にも手間が生じる。また外側からの結紮により血管結紮部分が破損したり、結紮糸を取り除く際に血管が破損する危険がある。血管の破損部分は切除せざるを得なくなり、結果的にバイパスグラフト(特に透析用ブラッドアクセス作成術の際)としての適正な長さを維持できなくなってしまうという欠点がある。   Specifically, vascular dilation as described above is performed by inserting a tapered insertion tube (cannula) or a spherical cannula, injecting heparin-containing physiological saline into the lumen, and adding the blood vessel from the inside. Press to expand. In order to control the leakage of liquid from the cannula insertion part, straight forceps may be used, but the part where the forceps and the cannula are in contact is limited, and leakage from other parts causes blood vessels. Expansion work becomes insufficient. Because of these problems, in clinical practice, it is often forced to ligate from the outside of the blood vessel with a thin silk thread to control leakage. The work of ligating not only requires manpower and time, but also takes time to remove the ligature after vasodilation. Further, there is a risk that the blood vessel ligation part is damaged by ligation from the outside, or the blood vessel is damaged when the ligature is removed. The damaged portion of the blood vessel has to be excised, and as a result, there is a drawback that it is impossible to maintain an appropriate length as a bypass graft (particularly in the case of blood access for dialysis).

また、手術中に被把持対象物を安定して把持するための技術として、例えば特許文献1、2に示す技術が開示されている。特許文献1に示す技術は、管状シャフト11先端に可動ジョー12と固定ジョー13から構成したクリップ保持部18を有するクリップ操作用鉗子10と、管状シャフト21先端に可動ジョー22と固定ジョー23から構成したクリップ挟持部28を有するクリップ着脱用鉗子20と、クリップ30から構成される内視鏡下外科手術器具セットであって、クリップ操作用鉗子は、クリップを保持したときに常に管状シャフトの軸方向に対し一定の向きで保持されるように保持用凹部16,17が形成され、クリップ着脱用鉗子は、クリップを挟持したときに常に管状シャフトの軸方向に対し同一の角度で挟持されるように挟持用凹部26,27が形成され、前記クリップは、クリップ操作用鉗子の可動ジョーと固定ジョーで保持される被保持部と、クリップ着脱用鉗子の可動ジョーと固定ジョーで挟持される被挟持部が形成されているものである。   Further, for example, techniques disclosed in Patent Documents 1 and 2 are disclosed as techniques for stably grasping an object to be grasped during surgery. The technique shown in Patent Document 1 includes a clip-operating forceps 10 having a clip holding portion 18 constituted by a movable jaw 12 and a fixed jaw 13 at the distal end of a tubular shaft 11, and a movable jaw 22 and a fixed jaw 23 at the distal end of the tubular shaft 21. An endoscopic surgical instrument set including a clip attaching / detaching forceps 20 having a clip holding portion 28 and a clip 30, and the clip operating forceps is always in the axial direction of the tubular shaft when holding the clip. The holding recesses 16 and 17 are formed so as to be held in a fixed direction, and the clip attaching / detaching forceps are always held at the same angle with respect to the axial direction of the tubular shaft when the clip is held. The holding recesses 26 and 27 are formed, and the clip is held by the movable jaw and the fixed jaw of the clip operation forceps. When, in which clamped portion sandwiched by the movable jaw and the fixed jaw of the clip removable forceps are formed.

特許文献2に示す技術は、体腔内に導入した内視鏡を体腔内の切込み開口部に誘導するための誘導補助器具1において、挿入部用シース2に進退自在に装着された操作ロッド5の先端に鉤状の把持部材6を連接し、前記シース2の先端位置には前記把持部材6内に取り込んだ前記内視鏡の被把持部分を受けて前記鉤状部6との間に前記内視鏡の被把持部分を挟み込む弾性部材7を設け、前記シース2の基端側には前記操作ロッド5を介して前記把持部材6を進退操作する操作部3とを具備するものである。   The technique disclosed in Patent Document 2 is a guide assisting instrument 1 for guiding an endoscope introduced into a body cavity to a notch opening in the body cavity. A hook-shaped gripping member 6 is connected to the tip, and the sheath 2 receives the gripped portion of the endoscope taken into the gripping member 6 at the tip position of the sheath 2, and the inner portion is interposed between the hook-shaped portion 6. An elastic member 7 that sandwiches a grasped portion of the endoscope is provided, and an operation portion 3 that moves the grasping member 6 forward and backward via the operation rod 5 is provided on the proximal end side of the sheath 2.

特開2012−232066号公報JP 2012-232066 A 特開平10−272139号公報JP-A-10-272139

しかしながら、上記各特許文献に示す技術は、あくまで被把持対象物を安定して把持するものであり、加圧された液体を漏れを発生させることなく強固に且つ安全に挟持して保持できるものではない。すなわち、上記に示したような血管拡張における問題点を解決できる技術ではない。   However, the techniques shown in the above-mentioned patent documents only hold the object to be gripped stably, and cannot hold the pressurized liquid firmly and safely without causing leakage. Absent. That is, it is not a technique that can solve the problems in vascular dilation as described above.

本発明は、血管拡張の手術において、血管を損傷させることなく安全で確実に加圧による液体の漏れを防ぐことができる手術器具、並びにこの手術器具及び挿入管からなる血管拡張器具を提供する。   The present invention provides a surgical instrument capable of safely and reliably preventing leakage of liquid due to pressurization without damaging a blood vessel in a vasodilation operation, and a vasodilator comprising the surgical instrument and an insertion tube.

本発明は、血管の内部に挿入される挿入先端部、及び液体注入器具(注射器)が接続される接続部を有する筒状の挿入管と、第1挟持部材、第2挟持部材、及び該第1挟持部材と該第2挟持部材とを開閉可能に連結する連結部を有し、血管に挿入された前記挿入先端部を挟持する手術器具と、を備える血管拡張器具であって、前記挿入管は、前記挿入先端部の外面に設けられ、該挿入先端部側の外径よりも前記接続部側の外径が小さく形成された段差部を備え、前記手術器具は、前記第1挟持部材における前記第2挟持部材に対向する面に形成される円弧状に凹んだ第1凹部と、前記第2挟持部材における前記第1挟持部材に対向する面の前記第1凹部に対応する位置に形成される円弧状に凹んだ第2凹部と、前記第1挟持部材及び前記第2挟持部材の閉状態を保持する保持機構と、を備え、前記第1挟持部材及び前記第2挟持部材の閉状態において前記第1凹部及び前記第2凹部により形成される血管挟持部の径は、前記段差部における前記接続部側の外径と略等しく形成される血管拡張器具に関する。   The present invention provides a cylindrical insertion tube having an insertion tip portion to be inserted into a blood vessel, a connection portion to which a liquid injection device (syringe) is connected, a first clamping member, a second clamping member, and the first A vascular dilator having a connecting part that connects the first holding member and the second holding member so as to be openable and closable, and a surgical instrument that holds the insertion tip inserted into a blood vessel. Is provided on the outer surface of the insertion tip portion, and includes a stepped portion having an outer diameter on the connection portion side smaller than the outer diameter on the insertion tip portion side, and the surgical instrument in the first clamping member A first recess recessed in an arc shape formed on a surface facing the second clamping member, and a position corresponding to the first recess on the surface facing the first clamping member in the second clamping member. A second recess recessed in a circular arc shape, the first clamping member and the second A holding mechanism for holding the holding member in a closed state, and the diameter of the blood vessel holding portion formed by the first recess and the second recess in the closed state of the first holding member and the second holding member is The present invention relates to a vasodilator that is formed substantially equal to the outer diameter of the stepped portion on the connection portion side.

また、本発明は、第1挟持部材、第2挟持部材、及び前記第1挟持部材と第2挟持部材とを開閉可能に連結する連結部を有し、先端部が血管の内部に挿入された挿入管を挟持する手術器具であって、前記第1挟持部材における前記第2挟持部材に対向する面に複数形成され、それぞれ異なる径で円弧状に凹んだ複数の第1凹部と、前記第2挟持部材における前記第1挟持部材に対向する面の複数の前記第1凹部それぞれに対応する位置に形成され、円弧状に凹んだ複数の第2凹部と、をさらに備える手術器具に関する。   Further, the present invention has a first clamping member, a second clamping member, and a connecting portion that connects the first clamping member and the second clamping member so as to be openable and closable, and the distal end portion is inserted into the blood vessel. A surgical instrument for clamping an insertion tube, wherein a plurality of first recesses formed on a surface of the first clamping member facing the second clamping member, each having a different diameter and recessed in an arc shape, and the second The present invention relates to a surgical instrument further comprising a plurality of second recesses that are formed in positions corresponding to the plurality of first recesses on the surface of the sandwiching member that faces the first clamping member and are recessed in an arc shape.

また、前記第1挟持部材における複数の前記第1凹部が形成される面と複数の該第1凹部との境界部分、及び前記第2挟持部材における複数の前記第2凹部が形成される面と複数の該第2凹部との境界部分は、曲面により構成されることが好ましい。   In addition, a boundary portion between a plurality of the first recesses and a surface of the first clamping member where the plurality of first recesses are formed, and a surface of the second clamping member where the plurality of second recesses are formed. It is preferable that the boundary part with several this 2nd recessed part is comprised by a curved surface.

また、複数の前記第1凹部の円弧の中心角は、複数の前記第2凹部の円弧の中心角よりも大きく構成されることが好ましい。   Moreover, it is preferable that the center angle of the arcs of the plurality of first recesses is configured to be larger than the center angle of the arcs of the plurality of second recesses.

また、本発明は、弾性変形可能な樹脂部材により構成される第1挟持部材及び第2挟持部材と、前記第1挟持部材及び前記第2挟持部材の先端側を開閉可能に該第1挟持部材及び前記第2挟持部材の基端側を連結する連結部と、を有し、血管の内部に挿入された挿入管を挟持する手術器具であって、前記第1挟持部材における前記第2挟持部材に対向する面に形成される円弧状に凹んだ第1凹部と、前記第2挟持部材における前記第1挟持部材に対向する面の前記第1凹部に対応する位置に形成される円弧状に凹んだ第2凹部と、前記第1挟持部材及び前記第2挟持部材の先端側において該第1挟持部材及び前記第2挟持部材を係合させて閉状態を保持する係合部と、前記第1挟持部材及び前記第2挟持部材それぞれの基端側の外面が凹んで形成される係合解除部と、を備える手術器具に関する。   In addition, the present invention provides a first clamping member and a second clamping member that are made of an elastically deformable resin member, and the first clamping member that can open and close the front end sides of the first clamping member and the second clamping member. And a connecting part for connecting the proximal end side of the second clamping member, and a surgical instrument for clamping an insertion tube inserted into a blood vessel, wherein the second clamping member in the first clamping member A first recess recessed in an arc shape formed on a surface facing the first recess, and an arcuate recess formed in a position corresponding to the first recess on the surface facing the first clamping member in the second clamping member A second recess, an engagement portion for engaging the first clamping member and the second clamping member on the front end side of the first clamping member and the second clamping member, and holding the closed state; The outer surface of the base end side of each of the holding member and the second holding member is recessed. A disengagement section to be made relates to surgical instruments comprising a.

また、本発明は、血管の内部に挿入される挿入先端部、及び液体注入器具が接続される接続部を有する筒状の挿入管と、上述のいずれかに記載の手術器具と、を備える血管拡張器具であって、前記挿入管は、前記挿入先端部の外面に設けられ、該挿入先端部側の外径よりも前記接続部側の外径が小さく形成された段差部を備え、前記第1挟持部材及び前記第2挟持部材の閉状態において前記第1凹部及び前記第2凹部により形成される血管挟持部の径は、前記段差部における前記接続部側の外径と略等しく形成される血管拡張器具に関する。   In addition, the present invention provides a blood vessel comprising an insertion tip portion inserted into a blood vessel, a cylindrical insertion tube having a connection portion to which a liquid injection device is connected, and the surgical instrument described above. In the expansion device, the insertion tube is provided on an outer surface of the insertion tip portion, and includes a stepped portion having an outer diameter on the connection portion side smaller than an outer diameter on the insertion tip portion side. In the closed state of the first clamping member and the second clamping member, the diameter of the blood vessel clamping portion formed by the first recess and the second recess is formed substantially equal to the outer diameter of the stepped portion on the connection portion side. The present invention relates to a vasodilator.

本発明によれば、血管拡張の手術において、血管を損傷させることなく、血管に挿入された挿入管の抜去を防止し、安全で確実に加圧による液体の漏れを防ぐことができる手術器具及びこの手術器具及び挿入管からなる血管拡張器具を提供できる。   According to the present invention, in a vasodilation operation, a surgical instrument capable of preventing removal of an insertion tube inserted into a blood vessel without damaging the blood vessel and preventing leakage of liquid due to pressurization safely and reliably. A vasodilator comprising the surgical instrument and an insertion tube can be provided.

本発明の血管拡張器具を構成する、血管内に挿入する挿入管の構造を示す図である。It is a figure which shows the structure of the insertion pipe | tube inserted in the blood vessel which comprises the vasodilator of this invention. 血管内に挿入先端部が挿入された場合の断面図である。It is sectional drawing when an insertion front-end | tip part is inserted in the blood vessel. 第1の実施形態に係る手術器具の外観図である。It is an external view of the surgical instrument which concerns on 1st Embodiment. 実際の手術において挿入管及び手術器具(血管拡張器具)を利用する場合の利用形態を示す図である。It is a figure which shows the utilization form in the case of utilizing an insertion tube and a surgical instrument (vasodilator) in actual surgery. 血管、手術器具の内壁部材及び挿入管の外周部材の硬度の関係を示す図である。It is a figure which shows the relationship of the hardness of the blood vessel, the inner wall member of a surgical instrument, and the outer peripheral member of an insertion tube. 第1の実施形態に係る手術器具の第1の応用例を示す図である。It is a figure which shows the 1st application example of the surgical instrument which concerns on 1st Embodiment. 第1の実施形態に係る手術器具の第2の応用例を示す図である。It is a figure which shows the 2nd application example of the surgical instrument which concerns on 1st Embodiment. 第2の実施形態に係る手術器具の構成を示す第1の図である。It is a 1st figure which shows the structure of the surgical instrument which concerns on 2nd Embodiment. 第2の実施形態に係る手術器具の構成を示す第2の図である。It is a 2nd figure which shows the structure of the surgical instrument which concerns on 2nd Embodiment. 第2の実施形態に係る手術器具の構成を示す第3の図である。It is a 3rd figure which shows the structure of the surgical instrument which concerns on 2nd Embodiment.

以下、本発明の実施の形態を説明する。本発明は多くの異なる形態で実施可能である。また、本実施形態の全体を通して同じ要素には同じ符号を付けている。   Embodiments of the present invention will be described below. The present invention can be implemented in many different forms. Also, the same reference numerals are given to the same elements throughout the present embodiment.

(本発明の第1の実施形態)
本実施形態に係る手術器具及び血管拡張器具について、図1ないし図7を用いて説明する。本実施形態に係る手術器具は、血行再建において剥離採取した血管(自家静脈又は自家動脈)を拡張する際に利用するものであり、血管内に挿入する挿入管と当該挿入管が挿入された血管とを同時に挟み込んで固定するものである。また、本実施形態に係る血管拡張器具は、挿入管と手術器具とがセットになって構成されるものである。
(First embodiment of the present invention)
A surgical instrument and a vasodilator according to this embodiment will be described with reference to FIGS. The surgical instrument according to the present embodiment is used when expanding a blood vessel (autologous vein or autologous artery) obtained by exfoliation in revascularization, and an insertion tube to be inserted into the blood vessel and a blood vessel in which the insertion tube is inserted Are sandwiched and fixed at the same time. In addition, the vasodilator according to the present embodiment is configured by a set of an insertion tube and a surgical instrument.

図1は、血管内に挿入する挿入管の構造を示す図である。挿入管10は、挿入先端部11を血管内に挿入され、中心を貫通し血管内に液体を流入するための流路12が形成された導管部13と、血管内に流入する液体を貯留する貯留部14と、挿入管10を介して血管の内部に液体を注入するための液体注入器具としての注射器17の先端部16が挿入されることで、注射器17と挿入管10を接続する接続部15とを備える。注射器17から排出された液体は、その先端部16、接続部15、貯留部14、流路12、挿入先端部11を介して血管内に流入される。この挿入管10は、血管の太さに応じて異なる規格で用意されており、例えば、挿入先端部11の凸部の径が2mm、3mm、4mmといった規格のものがある。
また、挿入管10は、挿入先端部11の外面に設けられ、挿入先端部11側の外径よりも接続部15側の外径が小さく形成された段差部を有して構成される。
FIG. 1 is a diagram showing a structure of an insertion tube to be inserted into a blood vessel. The insertion tube 10 has an insertion tip portion 11 inserted into a blood vessel, and stores a conduit portion 13 in which a flow path 12 for penetrating the center and flowing liquid into the blood vessel is formed, and liquid flowing into the blood vessel. The connecting portion that connects the syringe 17 and the insertion tube 10 by inserting the storage portion 14 and the distal end portion 16 of the syringe 17 as a liquid injection device for injecting liquid into the blood vessel via the insertion tube 10. 15. The liquid discharged from the syringe 17 flows into the blood vessel through the distal end portion 16, the connection portion 15, the storage portion 14, the flow path 12, and the insertion distal end portion 11. The insertion tube 10 is prepared in accordance with different standards depending on the thickness of the blood vessel. For example, there are standards in which the diameter of the convex portion of the insertion tip portion 11 is 2 mm, 3 mm, and 4 mm.
The insertion tube 10 is provided on the outer surface of the insertion tip portion 11 and has a stepped portion having an outer diameter on the connection portion 15 side that is smaller than the outer diameter on the insertion tip portion 11 side.

図2は、血管内に挿入先端部11が挿入された場合の断面図である。剥離採取された血管Sに挿入先端部11より少し深い位置(導管部13が太くなる方を深い位置とする)までの部分が挿入される。すなわち、挿入先端部11+αの領域が血管Sで覆われる状態となる。この+αの領域は、後述する本実施形態の手術器具20により血管Sを締め付けて固定する領域として利用される。なお、図2(B)に示すように、挿入先端部11と導管部13との間に形成されている段差部を利用し、この段差部による凸部18と手術器具20とが血管Sを介して嵌合するように、手術器具20の締め込み部分に凹部19を形成するようにしてもよい。図2(A)、(B)のいずれの場合であっても、挿入先端部11と導管部13との問の段差を利用して、挿入管10と手術器具20とのズレを防止することができる。   FIG. 2 is a cross-sectional view when the insertion tip 11 is inserted into the blood vessel. A portion up to a position slightly deeper than the insertion tip portion 11 (the thicker portion of the conduit portion 13 is defined as a deep position) is inserted into the blood vessel S that has been separated and collected. That is, the region of the insertion tip 11 + α is covered with the blood vessel S. This + α region is used as a region where the blood vessel S is fastened and fixed by the surgical instrument 20 of the present embodiment described later. As shown in FIG. 2 (B), a step formed between the insertion tip 11 and the conduit 13 is used, and the convex portion 18 and the surgical instrument 20 formed by this step form the blood vessel S. The recessed portion 19 may be formed in the tightened portion of the surgical instrument 20 so as to be fitted through. In any case of FIGS. 2A and 2B, the gap between the insertion tube 10 and the surgical instrument 20 can be prevented by utilizing the difference in level between the insertion tip portion 11 and the conduit portion 13. Can do.

また、図1において、注射器17の先端部16は、例えば弾性体等の弾性力を利用して接続部15に密着固定されており、注射器17内の液体を導管部13に注入する。注入された液体は、導管部13を通り抜けて血管S内に流入される。挿入管10と血管Sは、図2に示したように、手術器具(詳細は後述する)により締め付けて固定されているため隙間なく密閉され、注射器17内の液体を加圧状態で血管内に送り込むことができる。加圧状態で液体が流入されることで血管Sが十分に拡張される。   Further, in FIG. 1, the distal end portion 16 of the syringe 17 is tightly fixed to the connection portion 15 using an elastic force such as an elastic body, and injects the liquid in the syringe 17 into the conduit portion 13. The injected liquid passes through the conduit portion 13 and flows into the blood vessel S. As shown in FIG. 2, the insertion tube 10 and the blood vessel S are tightly fixed by a surgical instrument (details will be described later), so that the insertion tube 10 and the blood vessel S are sealed without gaps, and the liquid in the syringe 17 is pressed into the blood vessel in a pressurized state. Can be sent. The blood vessel S is sufficiently expanded by inflowing the liquid under pressure.

次に、挿入管10と血管Sとを固定する本実施形態に係る手術器具について説明する。図3は、本実施形態に係る手術器具の外観図である。図3(A)は締め込み部分が閉じた状態(挿入管10と血管Sとを締め付けた状態)、図3(B)は締め込み部分が開いた状態(挿入管10と血管Sとを締め付けていない状態)を示している。   Next, a surgical instrument according to this embodiment for fixing the insertion tube 10 and the blood vessel S will be described. FIG. 3 is an external view of the surgical instrument according to the present embodiment. FIG. 3A shows a state in which the tightening portion is closed (state in which the insertion tube 10 and the blood vessel S are tightened), and FIG. 3B shows a state in which the tightening portion is open (in which the insertion tube 10 and the blood vessel S are tightened). State).

手術器具20は、第1挟持部材としての第1締込部材26と第2挟持部材としての第2締込部材27とが連結部24において連結されたクリップ構造となっており、手元での開閉操作部21の操作に応じて締込部22の開閉状態を制御して血管Sを締め付ける。つまり、開閉操作部21の幅を狭めると締込部22の幅が広がり、開閉操作部21の幅を広げると締込部22の幅が狭まる。開閉操作部21には、その開閉方向に弾性力が作用するようにバネ状の弾性部29を有しており、外部からの力が加わっていない状態では、弾性部29の作用により開閉操作部21が開いた状態、すなわち締込部22が閉じた状態で保持される。すなわち、弾性部29は、締込部22(第1締込部材26及び第2挟持部材27)の閉状態を保持する保持機構として機能する。また、血管Sを挟み込んで締め付ける際には、外側から矢印Aの方向に応力をかけて開閉操作部21を閉じ、同時に締込部22を開く。そして、所望の締込孔23aないし23cに血管Sが嵌入されると、矢印Aの方向にかけていた応力を解放することで締込部22を閉じて血管Sが固定される。上述したように、例えば挿入管10に3つの規格がある場合は、その規格に合わせて締込孔23a(2mmφ)、23b(3mmφ)、23c(4mmφ)が形成される。   The surgical instrument 20 has a clip structure in which a first clamping member 26 as a first clamping member and a second clamping member 27 as a second clamping member are coupled at a coupling portion 24, and can be opened and closed at hand. The open / close state of the tightening portion 22 is controlled according to the operation of the operation portion 21 to tighten the blood vessel S. That is, when the width of the opening / closing operation part 21 is reduced, the width of the tightening part 22 is increased, and when the width of the opening / closing operation part 21 is increased, the width of the tightening part 22 is reduced. The opening / closing operation portion 21 has a spring-like elastic portion 29 so that an elastic force acts in the opening / closing direction. When no external force is applied, the opening / closing operation portion 21 is operated by the elastic portion 29. 21 is held in an open state, that is, in a state in which the tightening portion 22 is closed. That is, the elastic portion 29 functions as a holding mechanism that holds the closed state of the tightening portion 22 (the first tightening member 26 and the second clamping member 27). When the blood vessel S is sandwiched and tightened, stress is applied from the outside in the direction of arrow A to close the opening / closing operation unit 21 and simultaneously open the tightening unit 22. When the blood vessel S is inserted into the desired tightening holes 23a to 23c, the tightening portion 22 is closed by releasing the stress applied in the direction of the arrow A, and the blood vessel S is fixed. As described above, for example, when the insertion tube 10 has three standards, the tightening holes 23a (2 mmφ), 23b (3 mmφ), and 23c (4 mmφ) are formed in accordance with the standards.

各締込孔23a〜23cは、第1締込部材26と第2締込部材27とが合わさることで円形状に形成されるようになっている。すなわち、第1締込部材26には、第2締込部材27に対向する面に形成され円弧状に凹んだ複数の第1凹部としての半円形状の切欠部26a〜26cが配置される。また、第2締込部材27には、第1挟持部材26に対向する面の複数の切欠部26a〜26cそれぞれに対応する位置に形成され円弧状に凹んだ複数の第2凹部としての半円形状の切欠部27a〜27cが配置される。そして、第1締込部材26及び第2締込部材27の閉状態において、切欠部26a〜26cと、切欠部27a〜27cとが合わさることで、円形の血管挟持部としての締込孔23a〜23cが形成される。そして、図2に示したように、これら締込孔23a〜23cにより断面が円形状の血管Sを周方向から包み込むように締め込むことができる。本実施形態では、複数の切欠部26a〜26cはそれぞれ異なる径に形成され、複数の切欠部27a〜27cもそれぞれ異なる径に形成される。また、対応する切欠部26aと切欠部27a、切欠部26bと切欠部27b、切欠部26cと切欠部27cは、同じ径に形成される。   Each tightening hole 23a-23c is formed in a circular shape by combining the first tightening member 26 and the second tightening member 27. In other words, the first tightening member 26 is provided with a plurality of semicircular cutouts 26 a to 26 c as first recesses formed on the surface facing the second tightening member 27 and recessed in an arc shape. The second tightening member 27 has a semicircle as a plurality of second recesses formed in positions corresponding to the plurality of notches 26a to 26c on the surface facing the first clamping member 26 and recessed in an arc shape. Shaped notches 27a-27c are arranged. And in the closed state of the 1st clamping member 26 and the 2nd clamping member 27, the notch parts 26a-26c and the notch parts 27a-27c match | combine, and the clamping holes 23a- as a circular blood vessel clamping part are combined. 23c is formed. Then, as shown in FIG. 2, these tightening holes 23 a to 23 c can tighten the blood vessel S having a circular cross section so as to wrap from the circumferential direction. In the present embodiment, the plurality of notches 26a to 26c are formed with different diameters, and the plurality of notches 27a to 27c are also formed with different diameters. Further, the corresponding notch 26a and notch 27a, the notch 26b and notch 27b, and the notch 26c and notch 27c are formed to have the same diameter.

図4は、実際の手術において挿入管10及び手術器具20を利用する場合の利用形態を示す図である。腕の先端部分から剥離採取した血管Sに挿入管10が挿入され、その挿入部分を手術器具20で締め込んで、注射器17からヘパリン入り生理食塩水等の液体を加圧状態で注入する。注入された液体は、血管S内を高圧で流通し血管拡張がなされる。   FIG. 4 is a diagram showing a usage pattern when the insertion tube 10 and the surgical instrument 20 are used in actual surgery. The insertion tube 10 is inserted into the blood vessel S peeled and collected from the tip of the arm, the insertion portion is tightened with the surgical instrument 20, and a liquid such as physiological saline containing heparin is injected from the syringe 17 in a pressurized state. The injected liquid circulates in the blood vessel S at a high pressure and undergoes vasodilation.

なお、本実施形態においては、血管Sの硬度に対して、手術器具20における血管Sと接触する内壁部材、及び、挿入管10における血管Sと接触する外周部材の硬度が適正に調整されていることが望ましい。図5は、血管、手術器具の内壁部材51及び挿入管10の外周部材52の硬度の関係を示す図である。図5において、各部位の硬度が、(1)手術器具20における血管Sと接触する内壁部材51の硬度>血管Sの硬度>挿入管10における血管Sと接触する外周部材52の硬度、又は、(2)外周部材52の硬度>血管Sの硬度>内壁部材51の硬度という関係を保って形成されていることが望ましい。すなわち、血管Sを硬い部材と柔らかい部材で挟むことにより、硬い部材により強固な締め付けと柔らかい部材による血管損傷の防止を同時に実現することができる。   In the present embodiment, the hardness of the inner wall member in contact with the blood vessel S in the surgical instrument 20 and the hardness of the outer peripheral member in contact with the blood vessel S in the insertion tube 10 are appropriately adjusted with respect to the hardness of the blood vessel S. It is desirable. FIG. 5 is a diagram showing the relationship between the hardness of the blood vessel, the inner wall member 51 of the surgical instrument, and the outer peripheral member 52 of the insertion tube 10. 5, the hardness of each part is (1) hardness of the inner wall member 51 in contact with the blood vessel S in the surgical instrument 20> hardness of the blood vessel S> hardness of the outer peripheral member 52 in contact with the blood vessel S in the insertion tube 10, or (2) It is desirable that the outer peripheral member 52 be formed so as to maintain a relationship of hardness> blood vessel S hardness> inner wall member 51 hardness. That is, by sandwiching the blood vessel S between a hard member and a soft member, it is possible to simultaneously realize strong tightening by the hard member and prevention of blood vessel damage by the soft member.

また、図2(B)において示したように、内壁部材51及び外周部材52に凹凸部を形成することで、手術中の挿入管10及び手術器具20のズレを防止することができるが、血管損傷の可能性がある揚合には、図2(A)のように、内壁部材51及び外周部材52における血管Sと接触する表面が平滑であることが望ましい。   In addition, as shown in FIG. 2B, by forming the concavo-convex portions on the inner wall member 51 and the outer peripheral member 52, it is possible to prevent the insertion tube 10 and the surgical instrument 20 from being displaced during the operation. For lifting that may be damaged, it is desirable that the surfaces of the inner wall member 51 and the outer peripheral member 52 that are in contact with the blood vessel S are smooth as shown in FIG.

また、第1締込部材26及び第2締込部材27の閉状態において切欠部26a〜26c及び切欠部27a〜27cにより形成される締込孔23a〜23cの径は、挿入管10の段差部における接続部15側の外径と略等しく形成されることが好ましい。すなわち、手術器具20と挿入管10とをセットにして血管拡張器具を構成する場合、挿入管10の段差部における小径部分の径が、締込孔23a〜23cのいずれかの径と略等しく構成された挿入管10と手術器具20とをセットにすることで、血管を好適に締め込むことができ、また、締め込んだ血管を外れにくくできる。   The diameters of the tightening holes 23 a to 23 c formed by the notches 26 a to 26 c and the notches 27 a to 27 c in the closed state of the first tightening member 26 and the second tightening member 27 are the stepped portions of the insertion tube 10. It is preferable that the outer diameter on the side of the connecting portion 15 is substantially equal. That is, when configuring the vascular dilator with the surgical instrument 20 and the insertion tube 10 as a set, the diameter of the small diameter portion of the step portion of the insertion tube 10 is configured to be approximately equal to the diameter of any of the tightening holes 23a to 23c. By setting the inserted insertion tube 10 and the surgical instrument 20 as a set, the blood vessel can be suitably tightened, and the tightened blood vessel can be hardly detached.

さらに、挿入管10の外周寸法に対する手術器具20の締込孔23aないし23cの内径が、血管Sの塑性変形率に応じて形成されていることが望ましい。すなわち、血管Sが変形する際の許容量を考慮した締め付けの力になるように、挿入管10の外周寸法と締込孔23aないし23cの内径が形成されていることが望ましい。   Furthermore, it is desirable that the inner diameters of the tightening holes 23 a to 23 c of the surgical instrument 20 with respect to the outer circumference of the insertion tube 10 are formed according to the plastic deformation rate of the blood vessel S. That is, it is desirable that the outer peripheral dimensions of the insertion tube 10 and the inner diameters of the tightening holes 23a to 23c are formed so that the tightening force takes into account the allowable amount when the blood vessel S is deformed.

さらにまた、図6に示すように、切欠部26a,26b、27a,27bから平坦部61a〜61c、62a〜62cに連接する箇所におけるエッジ部分63a〜63d、64a〜64d(第1締込部材26における複数の切欠部26a,26bが形成される面61a〜61cと複数の切欠部26a,26bとの境界部分及び第2締込部材27における複数の切欠部27a,27bが形成される面62a〜62cと複数の切欠部27a,27bとの境界部分)が曲面に形成されることが望ましい。そうすることで、エッジ部分63a〜63d、64a〜64dが血管Sを挟み込んで損傷させてしまうことを防止することができる。なお、このとき、手術器具20による締め付けが不十分にならないように、血管の塑性変形率を考慮したエッジ部の曲面のアールが設定されているものとする。   Furthermore, as shown in FIG. 6, edge portions 63a to 63d, 64a to 64d (first tightening members 26) at locations where the flat portions 61a to 61c and 62a to 62c are connected from the notches 26a, 26b, 27a and 27b. Boundary surfaces between the plurality of notches 26a and 26b and the plurality of notches 26a and 26b, and the surfaces 62a to 62b on the second tightening member 27 where the plurality of notches 27a and 27b are formed. 62c and a plurality of notches 27a and 27b) are preferably formed on a curved surface. By doing so, it can prevent that the edge parts 63a-63d and 64a-64d pinch the blood vessel S and damage it. At this time, it is assumed that the curvature of the curved surface of the edge portion in consideration of the plastic deformation rate of the blood vessel is set so that the surgical instrument 20 is not sufficiently tightened.

さらにまた、図7に示すように、切欠部26a,26b,27a,27bを半円形状に切り欠く必要はなく、中心角が異なる扇形の円弧状に切り欠くようにしてもよい。こうすることで、血管Sを大きい切欠部27a,27b(切り欠きの円弧が大きい側、つまり中心角が大きい側)に安定して固定することができると共に、挟み込む際のエッジ部63a〜63d(血管Sが設置されていない挟み込みに向かう側のエッジ部)におけるエッジ角を大きくすることができ、血管の損傷を防止することができる。   Furthermore, as shown in FIG. 7, the notches 26a, 26b, 27a, and 27b do not have to be cut into a semicircular shape, and may be cut into a fan-shaped arc having a different central angle. By doing so, the blood vessel S can be stably fixed to the large notches 27a and 27b (the side where the arc of the notch is large, that is, the side where the central angle is large), and the edge portions 63a to 63d ( The edge angle in the edge portion on the side facing the sandwiching where the blood vessel S is not installed) can be increased, and damage to the blood vessel can be prevented.

このように、本実施形態に係る手術器具20及び血管拡張器具においては、手術器具20を挿入管10の外周にフィットさせて加圧による液体の漏れを防止することができ、結紮等を行うことなく安全で確実に血管拡張を行うことが可能になる。   Thus, in the surgical instrument 20 and the vasodilator according to the present embodiment, the surgical instrument 20 can be fitted to the outer periphery of the insertion tube 10 to prevent liquid leakage due to pressurization, and ligation or the like can be performed. It is possible to perform vascular dilation safely and reliably.

(本発明の第2の実施形態)
本実施形態に係る手術器具について、図8ないし図10を用いて説明する。本実施形態に係る手術器具は、1つの締込孔23のみを有し、半円形状の締込部材を先端部で係合させて固定することで円形状の血管の締め込みを行う。締込孔を1つにしたことと、締込部材を係合させて固定することで、サイズや質量を軽量化させることができ手術作業への影響を最小限に抑えることができる。
(Second embodiment of the present invention)
A surgical instrument according to this embodiment will be described with reference to FIGS. The surgical instrument according to the present embodiment has only one tightening hole 23, and tightens a circular blood vessel by engaging and fixing a semicircular tightening member at the tip. By making the tightening hole one and engaging and fixing the tightening member, the size and mass can be reduced, and the influence on the surgical operation can be minimized.

図8ないし図10は、本実施形態に係る手術器具の構成を示す図である。図8に示す手術器具20は、血管Sを挟み込む前の状態を示したものであり、図9に示す手術器具20は、血管Sを挟み込んで固定した状態を示したものであり、図10(A)に示す手術器具20は、血管Sを挟み込んだ状態から手術器具を解放する際の状態を示したものである。   8 to 10 are diagrams showing a configuration of the surgical instrument according to the present embodiment. The surgical instrument 20 shown in FIG. 8 shows a state before the blood vessel S is sandwiched, and the surgical instrument 20 shown in FIG. 9 shows a state where the blood vessel S is sandwiched and fixed, and FIG. A surgical instrument 20 shown in A) shows a state when the surgical instrument is released from a state in which the blood vessel S is sandwiched.

図8に示すように、本実施形態に係る手術器具20は、前記第1の実施形態の場合と同様に血管Sを挟み込んで挿入管10と共に固定するものであり、血管拡張器具は、この手術器具20と挿入管10とのセットにより構成されるが、図3に示したような開閉操作部21を備えておらず、また、1つの締込孔23しか備えていない。すなわち、図3の構造に比べて汎用性は低下するものの、小型化及び軽量化を図ることができ、手術の邪魔にもならない。また、合成樹脂等の素材を用いて大量生産を図ることで、使い捨ての手術器具20として使用することができ、衛生面でも向上を図ることができる。   As shown in FIG. 8, the surgical instrument 20 according to the present embodiment sandwiches the blood vessel S and fixes it together with the insertion tube 10 as in the case of the first embodiment. Although it is configured by a set of the instrument 20 and the insertion tube 10, it does not include the opening / closing operation unit 21 as shown in FIG. 3, and includes only one tightening hole 23. That is, although versatility is reduced as compared with the structure of FIG. 3, it can be reduced in size and weight, and does not interfere with the operation. Further, mass production using a material such as a synthetic resin can be used as a disposable surgical instrument 20, and improvement in hygiene can be achieved.

図8において、手術器具20は可擁性且つ弾性力を有する(弾性変形可能な)例えば合成樹脂等で形成されており、半円状の開口を有する第1締込部材26及び第2締込部材27を連結部としての基部81で連結して構成されている。各第1締込部材26及び第2締込部材27は基部81を基点として開閉自在に固定されており、血管Sを挟み込んだり、血管Sから取り外す際には各第1締込部材26及び第2締込部材27を図8及び図9の矢印A方向に動作させる。第1締込部材26及び第2締込部材27の先端部(基部81と対向する位置)には、一方の係合凸部82と他方の係合凹部83からなる係合部が設けられており、図9に示すように、係合凸部82と係合凹部83とが係合して円形の締込孔23が形成される。   In FIG. 8, the surgical instrument 20 is made of, for example, a synthetic resin or the like having a supportive and elastic force (elastically deformable) and having a semicircular opening and a second tightening member. The member 27 is connected by a base portion 81 as a connecting portion. The first tightening member 26 and the second tightening member 27 are fixed to be openable and closable with the base 81 as a base point. When the blood vessel S is sandwiched or removed from the blood vessel S, the first tightening member 26 and the second tightening member 27 are fixed. 2 The tightening member 27 is moved in the direction of arrow A in FIGS. An engaging portion including one engaging convex portion 82 and the other engaging concave portion 83 is provided at the distal end portions (positions facing the base portion 81) of the first tightening member 26 and the second tightening member 27. As shown in FIG. 9, the engagement convex portion 82 and the engagement concave portion 83 are engaged to form a circular tightening hole 23.

また、図10(A)に示すように、第1締込部材26及び第2締込部材27における基部81近傍にはそれぞれ、第1締込部材26及び第2締込部材27の外面が凹んで形成される係止凹部84,85からなる係合解除部が配置されており、この係止凹部84,85の配置部分における第1締込部材26及び第2締込部材27の肉厚が薄く形成されることで大きな可擁性を生じる。この各係止凹部84,85に押圧力を加えると締込孔23の円形が崩れ、係合凹部83から係合凸部82が離脱して手術器具20を開放状態にすることができる。   Further, as shown in FIG. 10A, the outer surfaces of the first tightening member 26 and the second tightening member 27 are recessed in the vicinity of the base 81 in the first tightening member 26 and the second tightening member 27, respectively. The disengagement part which consists of the latching recessed parts 84 and 85 formed in this is arrange | positioned, and the thickness of the 1st clamping member 26 and the 2nd clamping member 27 in the arrangement | positioning part of this latching recessed part 84 and 85 is the same. Forming a thin film creates great absorbability. When a pressing force is applied to each of the locking recesses 84 and 85, the circular shape of the tightening hole 23 is broken, and the engagement projection 82 is detached from the engagement recess 83, so that the surgical instrument 20 can be opened.

なお、係止凹部84,85に押圧力を加える際は指で行ってもよいが、締込孔23の径は2〜4mmと非常に小さく指ではうまく押圧力を加えることができない場合がある。そのような揚合は、例えば、図10(B)に示すようなペンチ状の専用器具89により係止凹部84,85に押圧力を加えるようにしてもよい。すなわち、専用器具89の先端部86,87を係止凹部84,85に当接させ、矢印Bの方向に加力することで係合凹部83から係合凸部82を離脱させるようにしてもよい。また、必ずしも係止凹部84,85に押圧力を加えなくても、爪等で係合凹部83を外側方向に引っ掻くように変形させることで、係合凹部83から係合凸部82を離脱させるようにしてもよい。   In addition, when applying a pressing force to the locking recesses 84 and 85, it may be performed with a finger, but the diameter of the tightening hole 23 is as very small as 2 to 4 mm, and the pressing force may not be applied well with a finger. . Such lifting may be performed, for example, by applying a pressing force to the locking recesses 84 and 85 with a pliers-like dedicated instrument 89 as shown in FIG. That is, the front end portions 86 and 87 of the dedicated instrument 89 are brought into contact with the locking concave portions 84 and 85, and the engaging convex portion 82 is detached from the engaging concave portion 83 by applying force in the direction of arrow B. Good. Further, the engaging protrusion 82 is detached from the engaging recess 83 by deforming the engaging recess 83 so as to be scratched outward by a claw or the like without necessarily applying a pressing force to the locking recesses 84 and 85. You may do it.

このように、本実施形態に係る手術器具においては、血管を加圧状態で確実に締め込んで血管拡張を安全且つ確実に実施することを可能にすると同時に、小型で量産可能な構造とすることで衛生面での向上を図ると共に、手術の阻害を最小限に抑えることを可能としている。   As described above, in the surgical instrument according to the present embodiment, it is possible to securely tighten the blood vessel in a pressurized state and perform the blood vessel expansion safely and reliably, and at the same time, to have a small and mass-produced structure. This makes it possible to improve the hygiene and minimize the hindrance to the operation.

また、本実施形態においても、第1の実施形態と同様に、第1締込部材26及び第2締込部材27の閉状態において締込孔23の径は、挿入管10の段差部における接続部15側の外径と略等しく形成されることが好ましい。すなわち、手術器具20と挿入管10とをセットにして血管拡張器具を構成する場合、挿入管10の段差部における小径部分の径が、締込孔23の径と略等しく構成された挿入管10と手術器具20とをセットにすることで、血管を好適に締め込むことができ、また、締め込んだ血管を外れにくくできる。   Also in the present embodiment, as in the first embodiment, the diameter of the tightening hole 23 in the closed state of the first tightening member 26 and the second tightening member 27 is the connection at the step portion of the insertion tube 10. It is preferable that the outer diameter on the part 15 side is substantially equal. That is, when the vascular dilator is configured by setting the surgical instrument 20 and the insertion tube 10 as a set, the diameter of the small diameter portion of the step portion of the insertion tube 10 is configured to be substantially equal to the diameter of the tightening hole 23. And the surgical instrument 20 as a set, the blood vessel can be suitably tightened, and the tightened blood vessel can be hardly detached.

以上、本発明の好ましい各実施形態につき説明したが、本発明は、以下のような特徴を有するとも言える。   The preferred embodiments of the present invention have been described above, but it can be said that the present invention has the following characteristics.

(1)本発明に係る手術器具は、剥離採取した血管内に挿入管を挿入し、当該挿入管が挿入された血管を挟んで血管拡張する手術器具であって、前記挿入管の外周径に略等しい開口孔を有し、当該開口孔の外周の一部を支点として週方向に開閉自在に形成され、前記挿入管が挿入された血管を外側から前記開口孔の内壁で挟み込む血管挟持部からなるものである。   (1) A surgical instrument according to the present invention is a surgical instrument that inserts an insertion tube into a peeled and collected blood vessel, and expands the blood vessel across the blood vessel into which the insertion tube is inserted. From a blood vessel holding portion that has substantially the same opening hole, is formed to be openable and closable in a weekly direction with a part of the outer periphery of the opening hole as a fulcrum, and sandwiches the blood vessel into which the insertion tube is inserted from the inner wall of the opening hole It will be.

このように、本発明に係る手術器具においては、剥離採取した血管内に挿入した挿入管の外周径に略等しい開口孔を有し、当該開口孔の外周の一部を支点として周方向に開閉自在に形成され、前記挿入管が挿入された血管を外側から前記開口孔の内壁で挟み込む血管挟持部からなるため、血管挟持部を挿入管の外周にフィットさせて加圧による液体の漏れを防止することができ、結紮等を行うことなく安全で確実に血管拡張を行うことが可能になるという効果を奏する。   As described above, the surgical instrument according to the present invention has an opening hole that is substantially equal to the outer diameter of the insertion tube inserted into the peeled and collected blood vessel, and is opened and closed in the circumferential direction using a part of the outer periphery of the opening hole as a fulcrum. Since it is formed freely and consists of a blood vessel clamping part that sandwiches the blood vessel in which the insertion tube is inserted from the outside with the inner wall of the opening hole, the blood vessel clamping unit is fitted to the outer periphery of the insertion tube to prevent liquid leakage due to pressurization It is possible to perform vasodilation safely and reliably without ligation or the like.

(2)本発明に係る手術器具は、前記血管挟持部が、半円状の第1部材及び第2部材からなり、当該第1部材及び第2部材が合わさった状態で円形の前記開口孔が形成されるものである。   (2) In the surgical instrument according to the present invention, the blood vessel clamping portion is composed of a semicircular first member and a second member, and the circular opening hole is formed in a state where the first member and the second member are combined. Is formed.

このように、本発明に係る手術器具においては、血管挟持部が、半円状の第1部材及び第2部材からなり、当該第1部材及び第2部材が合わさった状態で円形の前記開口孔が形成されるため、血管に挿入された挿入管を外側から挟み込むことができ、血管を傷つけることなく安全で確実に血管拡張を行うことができるという効果を奏する。   As described above, in the surgical instrument according to the present invention, the blood vessel clamping portion includes the semicircular first member and the second member, and the circular opening hole in a state where the first member and the second member are combined. Therefore, the insertion tube inserted into the blood vessel can be sandwiched from the outside, and the blood vessel can be safely and reliably expanded without damaging the blood vessel.

(3)本発明に係る手術器具は、前記血管挟持部の少なくとも内壁が、平滑に形成されているものである。   (3) In the surgical instrument according to the present invention, at least the inner wall of the blood vessel clamping portion is formed smoothly.

このように、本発明に係る手術器具においては、血管挟持部の少なくとも内壁が、平滑に形成されているため、血管を損傷することなく安全で確実に血管拡張を行うことができるという効果を奏する。   Thus, in the surgical instrument according to the present invention, since at least the inner wall of the blood vessel clamping portion is formed smoothly, there is an effect that the blood vessel can be expanded safely and reliably without damaging the blood vessel. .

(4)本発明に係る手術器具は、前記血管の硬度に対して、前記血管挟持部における前記血管と接触する内壁部材の硬度が小さく、且つ、前記挿入管における前記血管と接触する外周部材の硬度が大きい、又は、前記血管挟持部における前記血管と接触する内壁部材の硬度が大きく、且つ、前記挿入管における前記血管と接触する外周部材の硬度が小さいものである。   (4) In the surgical instrument according to the present invention, the hardness of the inner wall member in contact with the blood vessel in the blood vessel clamping portion is smaller than the hardness of the blood vessel, and the outer peripheral member in contact with the blood vessel in the insertion tube Hardness is large, or the hardness of the inner wall member in contact with the blood vessel in the blood vessel clamping portion is large, and the hardness of the outer peripheral member in contact with the blood vessel in the insertion tube is small.

このように、本発明に係る手術器具においては、血管の硬度に対して、血管挟持部における血管と接触する内壁部材の硬度が小さく、且つ、挿入管における血管と接触する外周部材の硬度が大きい、又は、血管挟持部における血管と接触する内壁部材の硬度が大きく、且つ、挿入管における血管と接触する外周部材の硬度が小さいため、血管を損傷させることなく安全で確実に血管拡張を行うことができるという効果を奏する。すなわち、血管を内側と外側から挟み込む場合に、血管の硬度に対して内側又は外側のいずれか一方の硬度が小さく、いずれか他方の硬度が大きくなっているため、血管に掛かる圧力を硬度が小さい方の素材が吸収し、強めに挟み込んでも血管を損傷することなく確実に血管拡張を行うことができるという効果を奏する。   Thus, in the surgical instrument according to the present invention, the hardness of the inner wall member in contact with the blood vessel in the blood vessel clamping portion is small and the hardness of the outer peripheral member in contact with the blood vessel in the insertion tube is large relative to the hardness of the blood vessel. Or, since the hardness of the inner wall member in contact with the blood vessel in the blood vessel clamping portion is large and the hardness of the outer peripheral member in contact with the blood vessel in the insertion tube is small, the blood vessel can be expanded safely and reliably without damaging the blood vessel. There is an effect that can be. That is, when the blood vessel is sandwiched from the inside and the outside, either the inside or outside hardness is small relative to the blood vessel hardness, and either one is high, so the pressure applied to the blood vessel is small. Even if the material of the other side absorbs it, it has an effect that the blood vessel can be surely expanded without damaging the blood vessel even if it is sandwiched strongly.

(5)本発明に係る手術器具は、前記血管挟持部の内壁形状が、前記挿入管の外周辺に形成された凹部及び/又は凸部に嵌合する凸部及び/又は凹部で形成されるものである。   (5) In the surgical instrument according to the present invention, the inner wall shape of the blood vessel clamping portion is formed by a convex portion and / or a concave portion that fits into the concave portion and / or the convex portion formed on the outer periphery of the insertion tube. Is.

このように、本発明に係る手術器具においては、血管挟持部の内壁形状が、前記挿入管の外周辺に形成された凹部及び/又は凸部に嵌合する凸部及び/又は凹部で形成されるため、挿入管と血管挟持部とがずれるのを防止して強固に固定することができるという効果を奏する。   Thus, in the surgical instrument according to the present invention, the inner wall shape of the blood vessel sandwiching portion is formed by the convex portion and / or the concave portion that fits into the concave portion and / or the convex portion formed on the outer periphery of the insertion tube. Therefore, there is an effect that the insertion tube and the blood vessel clamping portion can be prevented from being displaced and can be firmly fixed.

(6)本発明に係る手術器具は、前記挿入管の外周寸法に対する前記血管挟持部の開口孔における内周寸法が、前記血管の塑性変形率に基づいた寸法差で形成されるものである。   (6) In the surgical instrument according to the present invention, the inner peripheral dimension in the opening hole of the blood vessel clamping portion with respect to the outer peripheral dimension of the insertion tube is formed by a dimensional difference based on the plastic deformation rate of the blood vessel.

このように、本発明に係る手術器具においては、挿入管の外周寸法に対する前記血管挟持部の開口孔における内周寸法が、前記血管の塑性変形率に基づいた寸法差で形成されるため、血管の塑性変形率に基づいて血管を損傷させることなく、加圧による液体の漏れを防止した血管拡張が可能になるという効果を奏する。   As described above, in the surgical instrument according to the present invention, the inner peripheral dimension in the opening hole of the blood vessel clamping portion with respect to the outer peripheral dimension of the insertion tube is formed with a dimensional difference based on the plastic deformation rate of the blood vessel. Based on the plastic deformation rate, the blood vessel can be expanded without damaging the blood vessel and preventing leakage of liquid due to pressurization.

以上、本発明の手術器具及び血管拡張器具の好ましい各実施形態につき説明したが、本発明は、上述の実施形態に制限されるものではなく、適宜変更が可能である。
例えば、第1の実施形態では、手術器具20を、3つの締込孔23a〜23cを含んで構成したが、これに限らない。すなわち、第1の実施形態の手術器具を1つの締込孔により構成してもよい。
The preferred embodiments of the surgical instrument and vasodilator of the present invention have been described above. However, the present invention is not limited to the above-described embodiments, and can be modified as appropriate.
For example, in the first embodiment, the surgical instrument 20 includes the three tightening holes 23a to 23c, but is not limited thereto. That is, you may comprise the surgical instrument of 1st Embodiment by one clamping hole.

10 挿入管
11 挿入先端部
12 流路
13 導管部
14 貯留部
15 接続部
16 先端部
17 注射器(液体注入器具)
20 手術器具
21 開閉操作部
22 締込部
23(23a〜23c) 締込孔
26 第1締込部材(第1挟持部材)
26a〜26c 切欠部(第1凹部)
27 第2締込部材(第2挟持部材)
27a〜27c 切欠部(第2凹部)
29 弾性部
51 内壁部材
52 外周部材
61a〜61d 平坦部
62a〜62d 平坦部
63a〜63f エッジ部
64a〜64f エッジ部
81 基部
82 係合凸部
83 係合凹部
84,85 係止凹部
DESCRIPTION OF SYMBOLS 10 Insertion tube 11 Insertion front-end | tip part 12 Flow path 13 Conduit part 14 Storage part 15 Connection part 16 Tip part 17 Syringe (liquid injection | pouring instrument)
DESCRIPTION OF SYMBOLS 20 Surgical instrument 21 Opening-closing operation part 22 Tightening part 23 (23a-23c) Tightening hole 26 1st fastening member (1st clamping member)
26a-26c Notch (first recess)
27 Second tightening member (second clamping member)
27a-27c Notch (second recess)
DESCRIPTION OF SYMBOLS 29 Elastic part 51 Inner wall member 52 Outer peripheral member 61a-61d Flat part 62a-62d Flat part 63a-63f Edge part 64a-64f Edge part 81 Base 82 Engagement convex part 83 Engagement recessed part 84,85 Engagement recessed part

Claims (6)

血管の内部に挿入される挿入先端部、及び液体注入器具が接続される接続部を有する筒状の挿入管と、
第1挟持部材、第2挟持部材、及び該第1挟持部材と該第2挟持部材とを開閉可能に連結する連結部を有し、血管に挿入された前記挿入先端部を挟持する手術器具と、を備える血管拡張器具であって、
前記挿入管は、前記挿入先端部の外面に設けられ、該挿入先端部側の外径よりも前記接続部側の外径が小さく形成された段差部を備え、
前記手術器具は、
前記第1挟持部材における前記第2挟持部材に対向する面に形成される円弧状に凹んだ第1凹部と、
前記第2挟持部材における前記第1挟持部材に対向する面の前記第1凹部に対応する位置に形成される円弧状に凹んだ第2凹部と、
前記第1挟持部材及び前記第2挟持部材の閉状態を保持する保持機構と、を備え、
前記第1挟持部材及び前記第2挟持部材の閉状態において前記第1凹部及び前記第2凹部により形成される血管挟持部の径は、前記段差部における前記接続部側の外径と略等しく形成される血管拡張器具。
A cylindrical insertion tube having an insertion tip portion to be inserted into the blood vessel and a connection portion to which a liquid injection device is connected;
A surgical instrument that has a first clamping member, a second clamping member, and a connecting part that connects the first clamping member and the second clamping member so as to be openable and closable, and clamps the insertion tip inserted into a blood vessel; A vasodilator comprising:
The insertion tube is provided on an outer surface of the insertion tip portion, and includes a step portion formed with an outer diameter on the connection portion side smaller than an outer diameter on the insertion tip portion side,
The surgical instrument is:
A first recess recessed in an arc shape formed on a surface of the first clamping member facing the second clamping member;
A second recess recessed in an arc shape formed at a position corresponding to the first recess on a surface of the second sandwiching member facing the first sandwiching member;
A holding mechanism for holding a closed state of the first clamping member and the second clamping member,
In the closed state of the first clamping member and the second clamping member, the diameter of the blood vessel clamping portion formed by the first recess and the second recess is substantially equal to the outer diameter of the stepped portion on the connection portion side. Vasodilator.
第1挟持部材、第2挟持部材、及び前記第1挟持部材と第2挟持部材とを開閉可能に連結する連結部を有し、先端部が血管の内部に挿入された挿入管を挟持する手術器具であって、
前記第1挟持部材における前記第2挟持部材に対向する面に複数形成され、それぞれ異なる径で円弧状に凹んだ複数の第1凹部と、
前記第2挟持部材における前記第1挟持部材に対向する面の複数の前記第1凹部それぞれに対応する位置に形成され、円弧状に凹んだ複数の第2凹部と、をさらに備える手術器具。
Surgery that has a first clamping member, a second clamping member, and a connecting portion that connects the first clamping member and the second clamping member so as to be openable and closable, and clamps an insertion tube having a distal end inserted into a blood vessel. An instrument,
A plurality of first concave portions formed on a surface of the first clamping member facing the second clamping member, each of which has a different diameter and is recessed in an arc shape;
A surgical instrument further comprising: a plurality of second recesses formed in positions corresponding to the plurality of first recesses on a surface of the second holding member facing the first clamping member and recessed in an arc shape.
前記第1挟持部材における複数の前記第1凹部が形成される面と複数の該第1凹部との境界部分、及び前記第2挟持部材における複数の前記第2凹部が形成される面と複数の該第2凹部との境界部分は、曲面により構成される請求項2に記載の手術器具。   A boundary portion between a plurality of first recesses in the first clamping member and a plurality of first recesses, and a surface in the second clamping member on which the second recesses are formed and a plurality of The surgical instrument according to claim 2, wherein a boundary portion with the second recess is configured by a curved surface. 複数の前記第1凹部の円弧の中心角は、複数の前記第2凹部の円弧の中心角よりも大きく構成される請求項2又は3に記載の手術器具。   The surgical instrument according to claim 2 or 3, wherein a center angle of the arcs of the plurality of first recesses is configured to be larger than a center angle of the arcs of the plurality of second recesses. 弾性変形可能な樹脂部材により構成される第1挟持部材及び第2挟持部材と、前記第1挟持部材及び前記第2挟持部材の先端側を開閉可能に該第1挟持部材及び前記第2挟持部材の基端側を連結する連結部と、を有し、血管の内部に挿入された挿入管を挟持する手術器具であって、
前記第1挟持部材における前記第2挟持部材に対向する面に形成される円弧状に凹んだ第1凹部と、
前記第2挟持部材における前記第1挟持部材に対向する面の前記第1凹部に対応する位置に形成される円弧状に凹んだ第2凹部と、
前記第1挟持部材及び前記第2挟持部材の先端側において該第1挟持部材及び前記第2挟持部材を係合させて閉状態を保持する係合部と、
前記第1挟持部材及び前記第2挟持部材それぞれの基端側の外面が凹んで形成される係合解除部と、を備える手術器具。
A first clamping member and a second clamping member configured by an elastically deformable resin member, and the first clamping member and the second clamping member so as to be able to open and close the front ends of the first clamping member and the second clamping member. A surgical instrument that sandwiches an insertion tube inserted into a blood vessel,
A first recess recessed in an arc shape formed on a surface of the first clamping member facing the second clamping member;
A second recess recessed in an arc shape formed at a position corresponding to the first recess on a surface of the second sandwiching member facing the first sandwiching member;
An engagement portion that engages the first clamping member and the second clamping member on the front end side of the first clamping member and the second clamping member, and holds the closed state;
A surgical instrument comprising: a disengagement portion formed by recessing an outer surface on a proximal end side of each of the first clamping member and the second clamping member.
血管の内部に挿入される挿入先端部、及び液体注入器具が接続される接続部を有する筒状の挿入管と、請求項5に記載の手術器具と、を備える血管拡張器具であって、
前記挿入管は、前記挿入先端部の外面に設けられ、該挿入先端部側の外径よりも前記接続部側の外径が小さく形成された段差部を備え、
前記第1挟持部材及び前記第2挟持部材の閉状態において前記第1凹部及び前記第2凹部により形成される血管挟持部の径は、前記段差部における前記接続部側の外径と略等しく形成される血管拡張器具。
A vascular dilation device comprising: an insertion tip portion inserted into a blood vessel; a cylindrical insertion tube having a connection portion to which a liquid injection device is connected; and the surgical instrument according to claim 5,
The insertion tube is provided on an outer surface of the insertion tip portion, and includes a step portion formed with an outer diameter on the connection portion side smaller than an outer diameter on the insertion tip portion side,
In the closed state of the first clamping member and the second clamping member, the diameter of the blood vessel clamping portion formed by the first recess and the second recess is substantially equal to the outer diameter of the stepped portion on the connection portion side. Vasodilator.
JP2015187425A 2014-09-24 2015-09-24 Surgical tool and vasodilatation device Pending JP2016064130A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019156176A1 (en) * 2018-02-08 2019-08-15 株式会社ジェイ・エム・エス Blood vessel expanding tool
CN112880559A (en) * 2021-01-12 2021-06-01 吉林大学 Dedicated intraoperative positioning and measuring device of vascular surgeon

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019156176A1 (en) * 2018-02-08 2019-08-15 株式会社ジェイ・エム・エス Blood vessel expanding tool
JPWO2019156176A1 (en) * 2018-02-08 2021-03-04 株式会社ジェイ・エム・エス Vasodilator
JP7154526B2 (en) 2018-02-08 2022-10-18 株式会社ジェイ・エム・エス Vasodilator
CN112880559A (en) * 2021-01-12 2021-06-01 吉林大学 Dedicated intraoperative positioning and measuring device of vascular surgeon

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