WO2018220818A1 - Ligature aid - Google Patents

Ligature aid Download PDF

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Publication number
WO2018220818A1
WO2018220818A1 PCT/JP2017/020598 JP2017020598W WO2018220818A1 WO 2018220818 A1 WO2018220818 A1 WO 2018220818A1 JP 2017020598 W JP2017020598 W JP 2017020598W WO 2018220818 A1 WO2018220818 A1 WO 2018220818A1
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WO
WIPO (PCT)
Prior art keywords
ligation
pair
protrusions
distal end
endoscope
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PCT/JP2017/020598
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French (fr)
Japanese (ja)
Inventor
孝侑 畠中
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オリンパス株式会社
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Application filed by オリンパス株式会社 filed Critical オリンパス株式会社
Priority to PCT/JP2017/020598 priority Critical patent/WO2018220818A1/en
Publication of WO2018220818A1 publication Critical patent/WO2018220818A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/04Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials

Definitions

  • the present invention relates to a ligation aid, and more particularly, to a ligation aid used when ligating a suture thread hung on a tissue.
  • a series of procedures of ligation includes an operation of applying a yarn to the tissue and an operation of forming a knot on the yarn so that the yarn applied to the tissue keeps applying a predetermined tension to the tissue.
  • the end of the thread hung on the tissue is pulled out of the body and the knot is made outside the body. After that, move the knot you made into the body and ligate.
  • a thread guide device attached to the distal end of the endoscope As a conventional technique related to ligation performed under an endoscope, a thread guide device attached to the distal end of the endoscope is disclosed (for example, see Patent Document 1).
  • This yarn guide device has a pair of yarn guide means formed in a tubular shape and extending into a tube wall. Both ends of the knotted thread are passed through each thread guiding means, and the thread guiding device is attached to the distal end of the endoscope. Thereafter, when the endoscope is advanced while holding both ends of the yarn, the knot can be moved to the vicinity of the portion where the yarn is hung.
  • an object of the present invention is to provide a ligation assisting tool that can be attached to an endoscope and that does not loosen the knot even if the endoscope is retracted after approaching the knot.
  • the present invention comprises a mounting portion that can be attached to and detached from the distal end portion of the endoscope, and a pair of projecting portions that are provided so as to protrude forward from the mounting portion and have a through-hole through which a thread can be inserted.
  • At least one of the pair of protrusions is a ligation aid in which the tip is configured to be accessible to the tip of the other protrusion by elastic deformation.
  • the mounting portion may be formed in a cylindrical shape or an annular shape having a central axis, and the pair of protrusions may extend in parallel with the central axis. At this time, the pair of protrusions may be formed so as to face each other with the central axis therebetween.
  • the pair of projecting portions may be configured such that the distal end portion is more easily elastically deformed than a region closer to the proximal end than the distal end portion.
  • the pair of protrusions may have a shape that gradually decreases in size as it approaches the tip.
  • the mounting portion is formed in a cylindrical shape or an annular shape having a central axis, and in the pair of projecting portions, an edge located on one side in the circumferential direction of the mounting portion is inclined with respect to the central axis. It may be located on a plane.
  • the ligation aid according to the present invention may further include a support member provided between the pair of protrusions.
  • the protrusion may have a groove extending from the through hole to the periphery of the protrusion.
  • the ligation aid according to the present invention may further include a threading member inserted into the through hole.
  • the ligation aid of the present invention can be attached to an endoscope, and even if the endoscope is retracted after the knot is brought close to the tissue, the knot is difficult to loosen.
  • Drawing 1 is a figure showing ligation auxiliary tool 1 of this embodiment, the left side is a front view and the right side is a side view.
  • the thread fixing device 1 includes a tubular mounting portion 10 and a pair of projecting portions 21 and 22 extending forward from the mounting portion 10.
  • the direction in which the pair of protrusions extend from the mounting portion 30 is referred to as the distal end side of the ligation aid 1
  • the side opposite to the direction in which the protrusion extends is referred to as the proximal end side of the ligation aid 1.
  • the mounting portion 10 is formed in a tubular shape or an annular shape with resin or the like, and is configured to be detachable from the distal end portion of the endoscope.
  • the inner diameter of the mounting portion 10 can be set as appropriate in consideration of the dimensions of the endoscope to be mounted.
  • the mounting portion 10 does not necessarily have to be tubular or annular as long as it can be securely mounted to such an extent that it does not fall off from the endoscope by an operation in use, which will be described later.
  • it may be a C-shape or U-shape that contacts only a part of the outer periphery of the insertion portion of the endoscope.
  • the protrusions 21 and 22 in the present embodiment have the same shape and size, and extend from the tip of the mounting part 10 in parallel with the central axis X1 of the mounting part 10.
  • the dimension D1 of the protrusions 21 and 22 in the circumferential direction of the mounting part 10 is the same from the base end connected to the mounting part 10 to the tip.
  • Through holes 21a and 22a are formed at the tip portions of the protrusions 21 and 22, respectively.
  • Each of the through holes 21 a and 22 a extends in a direction crossing the circumferential direction of the mounting portion 10. Since the through holes 21a and 22a face each other across the central axis X1, the line connecting the through hole 21a and the through hole 22a passes through the central axis X1.
  • the protrusions 21 and 22 in which the through holes 21a and 22a are formed also face each other across the central axis X1.
  • the mounting portion 10 and the projecting portions 21 and 22 are all integrally formed of an elastically deformable resin material.
  • the resin material include silicone and polytetrafluoroethylene (PTFE).
  • the forming method can be exemplified by integral molding using a resin material, but the attachment portion and the protruding portion are formed separately and joined together by adhesion, welding, or the like to produce the ligation aid 1. Good.
  • both the mounting portion 10 and the protruding portions 21 and 22 are formed to be transparent, but the mounting portion 10 is not necessarily transparent.
  • the operation at the time of use of the ligation aid 1 configured as described above will be described using an example of ligating a target site in the stomach.
  • the operator observes the target site with an endoscope using grasping forceps or the like passed through the treatment instrument channel of the endoscope and a curved needle to which a thread is connected. While threading the target part.
  • the operator removes the endoscope and the grasping forceps outside the body while holding the end of the thread that is not connected to the needle while holding the curved needle with the grasping forceps. Thereby, both ends of the thread hung on the target part are pulled out of the body.
  • the surgeon cuts the curved needle from the thread, holds the both ends of the thread, and forms it loose enough not to tighten the desired knot.
  • the end portions 101 and 102 of the thread 100 are passed through the through holes 21a and 22a from the lumen side of the attachment portion 10, respectively.
  • the surgeon attaches the ligation aid 1 through the thread 100 to the tip of the endoscope.
  • the mounting is performed by causing the endoscope to enter the mounting unit 10 from the proximal end side of the mounting unit 10.
  • the thread 100 may be passed through the ligation aid 1 after the ligation aid 1 has been attached to the endoscope in advance.
  • the surgeon inserts the endoscope into the patient's body while the end portions 101 and 102 are held so as not to move into the body, and as shown in FIG. Introduced until near.
  • the holding of the ends 101 and 102 may be performed by an operator or an assistant different from the operator.
  • the surgeon pulls the end portions 101 and 102 the knot approaches the target site T, and the target site is bound. Thereafter, when an operator or the like increases the pulling of the end portions 101 and 102 to increase the tension related to the thread 100, the protruding portions 21 and 22 through which the thread 100 is passed are elastically deformed by the tension applied to the thread 100. .
  • the tips of the protrusions 21 and 22 are deformed so as to approach the central axis X1.
  • the tip portions of the protrusions 21 and 22 provided with the through holes 21a and 22a approach the knot 110 while approaching each other, and the target site T is suitably temporarily ligated.
  • the protrusions 21 and 22 are parallel to the central axis X1 when the thread 100 is not tensioned.
  • the visual field of the endoscope 200 is not obstructed while maintaining the state.
  • the pair of protrusions 21 and 22 are elastically deformed, and through holes 21a and 22a are formed in the protrusions 21 and 22. The distal end is sufficiently close to the knot 110.
  • the protrusions 21 and 22 suitably hold the thread 100 extending from the knot 110 near the knot 110, and the knot 110 is less likely to loosen. Further, when the endoscope 200 is retracted for the main ligation, the state in which the tip portions of the projecting portions 21 and 22 are close to each other is maintained. For this reason, as shown in FIG. 5, the thread 100 is between the knot 110 and the protrusions 21 and 22 and is almost parallel to the axis X ⁇ b> 1 of the insertion portion of the endoscope 200. The direction in which the thread 100 moves backward substantially coincides with the direction in which the thread 100 is pulled. With these actions, it is possible to suitably prevent the knot 110 from being loosened when the endoscope 200 is removed.
  • the protrusions 21 and 22 are formed transparently, even when the protrusions are elastically deformed and move into the field of view of the endoscope 200, the state in front of the protrusions can be grasped through the protrusions. Can be performed smoothly.
  • the shape of the protruding portion can be variously changed.
  • the base end portion 21b may be formed narrower than the tip end portion provided with the through hole 21a, as in the protruding portion 21A of the modification shown in FIG.
  • the proximal end side is more easily elastically deformed than the distal end side.
  • FIG. 7 shows another modification example in which the base end side is more easily elastically deformed than the distal end side.
  • the protruding portion 21B of the modification shown in FIG. 7 has a base end portion 21b thinner than the distal end portion by reducing the dimension in the direction orthogonal to the circumferential direction of the mounting portion 10. Also in this case, in the protruding portion, the base end side is more easily elastically deformed than the distal end side.
  • the modification examples shown in FIGS. 6 and 7 can be appropriately used alone or in combination when it is desired to adjust the easiness (rigidity) of the elastic deformation of the protrusion to a desired value for each part. In order to make the distal end side more easily elastically deformed, the distal end side may be made thinner or thinner than the proximal end side.
  • the through-hole provided in the protrusion part may be configured to facilitate threading.
  • the threading member 40 is passed through the through hole 21a.
  • the through hole 21a is provided with a groove 21c extending to the periphery of the protruding portion. If it does in this way, the thread
  • the direction in which the groove 21c extends is not particularly limited, as shown in FIG. 9B, when the groove 21c extends toward the tip of the protruding portion 21, the thread is detached from the through hole 21a when the endoscope 200 is retracted. there is a possibility. Therefore, as shown in FIG. 9A, if the groove 21c extends in the circumferential direction of the mounting portion 10 or extends toward the proximal end side of the protrusion, such as extending toward the distal end, the passage through the through hole It is preferable because both ease and suppression of the yarn from coming off the through hole can be achieved.
  • the ligation aid of the present embodiment is different from the ligation aid 1 of the first embodiment in that it includes a support member that supports the knot.
  • components that are the same as those already described are assigned the same reference numerals and redundant description is omitted.
  • FIG. 10 is a front view of the ligation aid 51 of this embodiment
  • FIG. 11 is a cross-sectional view taken along the line II of FIG.
  • the ligation aid 51 includes a support member 52 provided between the protrusion 21 and the protrusion 22.
  • the support member 52 is a V-shaped member that is transparently formed of a resin material, glass, or the like. As shown in FIG. 11, the support member 52 is provided at the proximal end of each protrusion 21, 22 so as to protrude toward the distal end side of the protrusion 21, 22, that is, in the extending direction of the protrusion 21, 22. It is fixed. Of the support member, the convex bent portion 52a is located between the through hole 21a and the through hole 22a.
  • the ligation assisting tool 51 of the present embodiment configured as described above is also capable of elastically deforming the protruding portion to suitably prevent loosening of the knot when the endoscope is retracted. Can do. Further, by providing the support member 52, the knot can be pushed directly by the support member. As a result, the knot can be made sufficiently close to the tissue, and the knot can be pushed in with a smaller force, and the elastic deformation of the protrusions 21 and 22 can be controlled more reliably.
  • the knot 110 positioned between the pair of protrusions 21 and 22 is supported by the support member 52 so as not to be too close to the endoscope 200 as shown in FIG. . Therefore, even in a state before the protruding portion 21 is elastically deformed, it is possible to prevent a situation in which the knot is too close to the endoscope and difficult to observe.
  • the support member 52 is formed to be transparent, it is possible to check the situation in front of the support member 52 while preventing access to the knot endoscope.
  • the shape of the support member can be variously changed.
  • a U-shape or a C-shape in which a convex portion is formed in a curved shape may be used.
  • an L-shaped wire 53 may be used as a support member by disposing a part of the wire 53 between the through holes 21a and 22a.
  • the wire 53 is sufficiently thin with respect to the visual field of the endoscope 200, even if the wire 53 itself is not transparent, the knot can be supported almost without obstructing the observation of the endoscope 200. The same effect as 52 is produced.
  • FIG. 15 is a cross-sectional view taken along the line II-II in FIG. 14
  • FIG. 15 is a cross-sectional view taken along the line II-II in FIG. 14
  • the knot is supported by the peripheral portion of the window portion 54, and even if the support member 54 is not transparent, the endoscope 200 passes through the window portion 54a. Observation can be suitably performed.
  • the ligation aid of this embodiment differs from the ligation aid of each embodiment in the shape of the protrusions.
  • FIG. 16 is a side view showing the ligation aid 71 of the present embodiment.
  • the pair of protrusions 72 and 73 in the ligation assisting tool 71 are formed in a trapezoidal shape in a side view, and gradually become smaller as the dimension of the mounting portion 10 in the circumferential direction approaches the tip.
  • the protrusions 72 and 73 are formed by cutting off one end of the cylindrical member along straight lines L1 and L2 that are inclined with respect to the central axis X1. Accordingly, in the protrusions 72 and 73, one of the edges on both sides in the circumferential direction of the mounting portion 10 is located on the virtual plane P1 along the straight line L1, and the other is located on the virtual plane P2 along the straight line L2.
  • the operation when using the ligation aid 71 of the present embodiment configured as described above will be described.
  • the ligation assisting tool 71 is mounted on the endoscope 200 and introduced to the vicinity of the target site, as in the above-described embodiments. Thereafter, by pressing one of the edges of the protrusions 72 and 73 described above against the tissue, the protrusions 72 and 73 are approached from an oblique direction inclined with respect to the normal line N1 of the tissue surface Ts as shown in FIG. Can be made. Since the edges of the protrusions 72 and 73 are all on the same virtual plane, the posture after the ligation aid 71 is brought into contact with the tissue is stabilized.
  • the ligation aid 71 of the present embodiment can also prevent the knot from loosening when the projection is retracted by elastically deforming the protrusion. .
  • the protrusions 71 and 72 are gradually smaller as the circumferential dimension of the mounting portion 10 approaches the tip, that is, have a tapered shape. For this reason, the tip side of the protrusion is configured to be more easily deformed, and when tension is applied to the thread 100, the protrusions 71 and 72 first start elastic deformation from the tip side. As a result, the base of the protrusion is prevented from being bent sharply, and the knot behavior is stabilized.
  • the projecting portions 72 and 73 have a tapered shape, as described above, it is easy to approach the tissue from an oblique direction. This makes it possible to tighten the knot sufficiently close to the tissue even when it is difficult to approach the tissue from the normal direction due to the narrow internal space, such as the intestine. .
  • the angle formed by the straight line L2 with respect to the central axis X1 and the angle formed by the straight line L3 with respect to the central axis X1 are substantially the same.
  • the two angles may be different.
  • the angle at which the ligation assisting tool is attached to the endoscope can be changed to change the stable angle with respect to the tissue in accordance with the position of the target site.
  • one edge of the protruding portion may be parallel to the central axis as in the first embodiment, and only the other edge may be formed as in the present embodiment.
  • the proximal end side is made to be rigid by, for example, forming the proximal end side from another material, so that the central axis is substantially You may comprise the base end part of a protrusion part so that it may not elastically deform so that it may approach.
  • both of the pair of protrusions do not necessarily have to be elastically deformable. If at least one of the protrusions can be elastically deformed, the distal end side of the elastically deformed projecting portion approaches the other projecting portion, thereby providing the above-described effects.
  • the knot 110 is supported by the grasping forceps 205 or the like projected from the endoscope 200 as shown in FIG. May be.
  • the present invention can be applied to a ligation aid.

Abstract

This ligature aid comprises: a mounting part that can be attached to and detached from the distal end of an endoscope; and a pair of protrusions that are formed extending from the mounting part and include, in the distal ends thereof, through-holes into which a thread can be inserted. At least one of the pair of protrusions is configured such that the distal end thereof is capable of elastically deforming to approach the distal end of the other protrusion.

Description

結紮補助具Ligation aid
 本発明は、結紮補助具、より詳しくは、組織に掛けた縫合糸を結紮する際に用いる結紮補助具に関する。 The present invention relates to a ligation aid, and more particularly, to a ligation aid used when ligating a suture thread hung on a tissue.
 従来、消化管等の管腔臓器に挿入した軟性内視鏡を用いて、様々な処置が行われている。一般にこれらの処置は、内視鏡挿入部に設けられたチャンネルに内視鏡用処置具を挿通し、処置具の先端を内視鏡挿入部の先端から突出させて行われる。 Conventionally, various treatments have been performed using a flexible endoscope inserted into a luminal organ such as the digestive tract. In general, these treatments are performed by inserting an endoscope treatment tool through a channel provided in the endoscope insertion portion and projecting the distal end of the treatment tool from the distal end of the endoscope insertion portion.
 難度が高い処置の一つとして、縫合糸を用いた結紮がある。結紮という一連の手技は、組織に糸を掛ける動作と、組織に掛けた糸が、組織に所定のテンションを掛け続けるように糸に結び目を形成する動作とを含む。一般に、結び目を一つだけ有する単結紮を行う場合は、組織に掛けた糸の端部を体外に引き出して体外で結び目を作る。その後、作った結び目を体内に移動させて結紮を行う。 One of the difficult treatments is ligation using sutures. A series of procedures of ligation includes an operation of applying a yarn to the tissue and an operation of forming a knot on the yarn so that the yarn applied to the tissue keeps applying a predetermined tension to the tissue. In general, when performing single ligation with only one knot, the end of the thread hung on the tissue is pulled out of the body and the knot is made outside the body. After that, move the knot you made into the body and ligate.
 内視鏡下で行う結紮に関する従来技術として、内視鏡の先端に装着する糸案内装置が開示されている(例えば、特許文献1参照)。この糸案内装置は、管状に形成されて管壁内に延びる一対の糸案内手段を有する。結び目を作った糸の両端を各糸案内手段に通して糸案内装置を内視鏡の先端に装着する。その後、糸の両端を保持しつつ内視鏡を前進させると、糸が掛けられた部位の近くまで結び目を移動させることができる。 As a conventional technique related to ligation performed under an endoscope, a thread guide device attached to the distal end of the endoscope is disclosed (for example, see Patent Document 1). This yarn guide device has a pair of yarn guide means formed in a tubular shape and extending into a tube wall. Both ends of the knotted thread are passed through each thread guiding means, and the thread guiding device is attached to the distal end of the endoscope. Thereafter, when the endoscope is advanced while holding both ends of the yarn, the knot can be moved to the vicinity of the portion where the yarn is hung.
日本国特表平8-501001号公報Japanese National Table No. 8-501001
 特許文献1に記載の技術では、結び目を組織に接近させて仮結紮した後、本結紮のために内視鏡を後退させると、結び目が緩んでしまうことがある。結び目が緩んだ状態で本結紮を行うと、縫合部位が適切に結紮されない可能性がある。 In the technique described in Patent Document 1, when a knot is brought close to a tissue and temporarily ligated and then the endoscope is retracted for the main ligation, the knot may be loosened. If this ligation is performed with the knot loosened, the suture site may not be ligated properly.
 上記事情を踏まえ、本発明は、内視鏡に装着可能であり、結び目を組織に接近させた後に内視鏡を後退させても結び目が緩みにくい結紮補助具を提供することを目的とする。 In view of the above circumstances, an object of the present invention is to provide a ligation assisting tool that can be attached to an endoscope and that does not loosen the knot even if the endoscope is retracted after approaching the knot.
 本発明は、内視鏡の先端部に着脱可能な装着部と、前記装着部から前方に突出するよう設けられ、先端部に糸を挿通可能な貫通孔を有する一対の突出部とを備え、前記一対の突出部の少なくとも一方は、前記先端部が弾性変形により他方の突出部の先端部に接近可能に構成されている結紮補助具である。 The present invention comprises a mounting portion that can be attached to and detached from the distal end portion of the endoscope, and a pair of projecting portions that are provided so as to protrude forward from the mounting portion and have a through-hole through which a thread can be inserted. At least one of the pair of protrusions is a ligation aid in which the tip is configured to be accessible to the tip of the other protrusion by elastic deformation.
 前記装着部は、中心軸線を有する筒状または環状に形成され、前記一対の突出部は、前記中心軸線と平行に延びてもよい。
 このとき、前記一対の突出部は、前記中心軸線を挟んで対向するように形成されてもよい。
The mounting portion may be formed in a cylindrical shape or an annular shape having a central axis, and the pair of protrusions may extend in parallel with the central axis.
At this time, the pair of protrusions may be formed so as to face each other with the central axis therebetween.
 前記一対の突出部は、前記先端部が前記先端部より基端側の領域よりも弾性変形しやすく構成されてもよい。 The pair of projecting portions may be configured such that the distal end portion is more easily elastically deformed than a region closer to the proximal end than the distal end portion.
 前記一対の突出部は、先端に近づくにつれて徐々に寸法が小さくなる形状を有してもよい。
 このとき、前記装着部は、中心軸線を有する筒状または環状に形成され、前記一対の突出部において、前記装着部の周方向の一方に位置する縁が、前記中心軸線に対して傾斜する仮想平面上に位置してもよい。
The pair of protrusions may have a shape that gradually decreases in size as it approaches the tip.
At this time, the mounting portion is formed in a cylindrical shape or an annular shape having a central axis, and in the pair of projecting portions, an edge located on one side in the circumferential direction of the mounting portion is inclined with respect to the central axis. It may be located on a plane.
 本発明に係る結紮補助具は、前記一対の突出部の間に設けられた支持部材をさらに備えてもよい。 The ligation aid according to the present invention may further include a support member provided between the pair of protrusions.
 前記突出部は、前記貫通孔から前記突出部の周縁まで延びる溝を有してもよい。 The protrusion may have a groove extending from the through hole to the periphery of the protrusion.
 本発明に係る結紮補助具は、前記貫通孔に挿通された糸通し部材をさらに備えてもよい。 The ligation aid according to the present invention may further include a threading member inserted into the through hole.
 本発明の結紮補助具は、内視鏡に装着可能であり、結び目を組織に接近させた後に内視鏡を後退させても結び目が緩みにくい。 The ligation aid of the present invention can be attached to an endoscope, and even if the endoscope is retracted after the knot is brought close to the tissue, the knot is difficult to loosen.
本発明の第一実施形態に係る結紮補助具を示す図である。It is a figure which shows the ligation assistance tool which concerns on 1st embodiment of this invention. 同結紮補助具の使用時の一形態を示す図である。It is a figure which shows one form at the time of use of the ligation aid. 同結紮補助具の使用時の一形態を示す図である。It is a figure which shows one form at the time of use of the ligation aid. 同結紮補助具の使用時の一形態を示す図である。It is a figure which shows one form at the time of use of the ligation aid. 同結紮補助具の使用時の一形態を示す図である。It is a figure which shows one form at the time of use of the ligation aid. 同結紮補助具の変形例における突出部を示す図である。It is a figure which shows the protrusion part in the modification of the ligation aid. 同結紮補助具の変形例における突出部を示す図である。It is a figure which shows the protrusion part in the modification of the ligation aid. 同結紮補助具の変形例を示す部分拡大図である。It is the elements on larger scale which show the modification of the ligation aid. 同結紮補助具の変形例における突出部を示す図である。It is a figure which shows the protrusion part in the modification of the ligation aid. 同結紮補助具の変形例における突出部を示す図である。It is a figure which shows the protrusion part in the modification of the ligation aid. 本発明の第二実施形態に係る結紮補助具を示す正面図である。It is a front view which shows the ligation auxiliary tool which concerns on 2nd embodiment of this invention. 図10のI-I線における断面図である。It is sectional drawing in the II line | wire of FIG. 同結紮補助具の使用時の一形態を示す図である。It is a figure which shows one form at the time of use of the ligation aid. 同結紮補助具の変形例を示す図である。It is a figure which shows the modification of the ligation auxiliary tool. 同結紮補助具の変形例を示す図である。It is a figure which shows the modification of the ligation auxiliary tool. 図14のII-II線における断面図である。It is sectional drawing in the II-II line | wire of FIG. 本発明の第三実施形態に係る結紮補助具を示す図である。It is a figure which shows the ligation assistance tool which concerns on 3rd embodiment of this invention. 同結紮補助具の使用時の一形態を示す図である。It is a figure which shows one form at the time of use of the ligation aid. 本発明の変形例における結紮補助具を示す正面図である。It is a front view which shows the ligation assistance tool in the modification of this invention. 第一実施形態に係る結紮補助具の使用法の一例を示す図である。It is a figure which shows an example of the usage method of the ligation auxiliary tool which concerns on 1st embodiment.
 本発明の第一実施形態について、図1から図9Bを参照して説明する。
 図1は、本実施形態の結紮補助具1を示す図であり、左側が正面図、右側が側面図である。図1に示すように、糸固定具1は、管状の装着部10と、装着部10から前方に延びる一対の突出部21および22とを備えている。
 以降の説明において、一対の突出部が装着部30から延びる方向を結紮補助具1の先端側、突出部が延びる方向と反対の側を結紮補助具1の基端側と称する。
A first embodiment of the present invention will be described with reference to FIGS. 1 to 9B.
Drawing 1 is a figure showing ligation auxiliary tool 1 of this embodiment, the left side is a front view and the right side is a side view. As shown in FIG. 1, the thread fixing device 1 includes a tubular mounting portion 10 and a pair of projecting portions 21 and 22 extending forward from the mounting portion 10.
In the following description, the direction in which the pair of protrusions extend from the mounting portion 30 is referred to as the distal end side of the ligation aid 1, and the side opposite to the direction in which the protrusion extends is referred to as the proximal end side of the ligation aid 1.
 装着部10は、樹脂等で管状或いは環状に形成され、内視鏡の先端部に着脱できるように構成されている。装着部10の内径は、装着対象の内視鏡の寸法等を考慮して、適宜設定することができる。装着部10は、後述する使用時の動作により内視鏡から脱落しない程度に確実に装着できれば、必ずしも管状または環状でなくてもよい。例えば、内視鏡の挿入部外周の一部のみと接触する、C字状やU字状の形状であってもよい。 The mounting portion 10 is formed in a tubular shape or an annular shape with resin or the like, and is configured to be detachable from the distal end portion of the endoscope. The inner diameter of the mounting portion 10 can be set as appropriate in consideration of the dimensions of the endoscope to be mounted. The mounting portion 10 does not necessarily have to be tubular or annular as long as it can be securely mounted to such an extent that it does not fall off from the endoscope by an operation in use, which will be described later. For example, it may be a C-shape or U-shape that contacts only a part of the outer periphery of the insertion portion of the endoscope.
 本実施形態における突出部21、22は、同形同大であり、装着部10の先端から装着部10の中心軸線X1と平行に延びている。装着部10の周方向における突出部21、22の寸法D1は、装着部10と接続する基端から、先端まで同一である。 The protrusions 21 and 22 in the present embodiment have the same shape and size, and extend from the tip of the mounting part 10 in parallel with the central axis X1 of the mounting part 10. The dimension D1 of the protrusions 21 and 22 in the circumferential direction of the mounting part 10 is the same from the base end connected to the mounting part 10 to the tip.
 各突出部21、22の先端部には、それぞれ貫通孔21a、22aが形成されている。各貫通孔21a、22aは、装着部10の周方向と交差する方向に延びている。貫通孔21aと22aとは、中心軸線X1を挟んで正対しているため、貫通孔21aと貫通孔22aとを結ぶ線は、中心軸線X1を通る。貫通孔21a、22aが形成された突出部21および22も、中心軸線X1を挟んで正対している。 Through holes 21a and 22a are formed at the tip portions of the protrusions 21 and 22, respectively. Each of the through holes 21 a and 22 a extends in a direction crossing the circumferential direction of the mounting portion 10. Since the through holes 21a and 22a face each other across the central axis X1, the line connecting the through hole 21a and the through hole 22a passes through the central axis X1. The protrusions 21 and 22 in which the through holes 21a and 22a are formed also face each other across the central axis X1.
 本実施形態において、装着部10と突出部21、22とは、いずれも弾性変形可能な樹脂材料で一体に形成されている。樹脂材料としては、例えばシリコーンやポリテトラフルオロエチレン(PTFE)等を例示することができる。形成方法としては、樹脂材料を用いた一体成型を例示することができるが、装着部および突出部を別々に形成し、接着や溶着等により一体に接合して結紮補助具1が作製されてもよい。
 本実施形態の結紮補助具1では、装着部10および突出部21、22のいずれも透明に形成されているが、装着部10は、必ずしも透明でなくてもよい。
In the present embodiment, the mounting portion 10 and the projecting portions 21 and 22 are all integrally formed of an elastically deformable resin material. Examples of the resin material include silicone and polytetrafluoroethylene (PTFE). The forming method can be exemplified by integral molding using a resin material, but the attachment portion and the protruding portion are formed separately and joined together by adhesion, welding, or the like to produce the ligation aid 1. Good.
In the ligation aid 1 of the present embodiment, both the mounting portion 10 and the protruding portions 21 and 22 are formed to be transparent, but the mounting portion 10 is not necessarily transparent.
 上記のように構成された結紮補助具1の使用時の動作について、胃内の対象部位を結紮する例を用いて説明する。
 結紮補助具1を使用する前に、術者は、内視鏡の処置具チャンネルに通した把持鉗子等と、糸が接続された曲針等を用いて、内視鏡で対象部位を観察しながら対象部位に糸を掛ける。糸を掛けた後、術者は把持鉗子で曲針をつかんだまま、針と接続されていない側の糸の端部を体外で保持しつつ、内視鏡および把持鉗子を体外に抜去する。これにより、対象部位に掛けられた糸の両端が体外に引き出される。
The operation at the time of use of the ligation aid 1 configured as described above will be described using an example of ligating a target site in the stomach.
Before using the ligation aid 1, the operator observes the target site with an endoscope using grasping forceps or the like passed through the treatment instrument channel of the endoscope and a curved needle to which a thread is connected. While threading the target part. After applying the thread, the operator removes the endoscope and the grasping forceps outside the body while holding the end of the thread that is not connected to the needle while holding the curved needle with the grasping forceps. Thereby, both ends of the thread hung on the target part are pulled out of the body.
 次に、術者は、糸から曲針を切り離し、糸の両端を持って、所望の結び目を締め込まない程度に緩く形成する。その後、図2に示すように、糸100の端部101および102を、それぞれ装着部10の内腔側から貫通孔21aおよび22aに通す。 Next, the surgeon cuts the curved needle from the thread, holds the both ends of the thread, and forms it loose enough not to tighten the desired knot. Thereafter, as shown in FIG. 2, the end portions 101 and 102 of the thread 100 are passed through the through holes 21a and 22a from the lumen side of the attachment portion 10, respectively.
 術者は、糸100を通した結紮補助具1を内視鏡の先端に装着する。装着は、装着部10の基端側から内視鏡を装着部10内に進入させることにより行う。予め結紮補助具1を内視鏡に装着してから糸100を結紮補助具1に通してもよい。 The surgeon attaches the ligation aid 1 through the thread 100 to the tip of the endoscope. The mounting is performed by causing the endoscope to enter the mounting unit 10 from the proximal end side of the mounting unit 10. The thread 100 may be passed through the ligation aid 1 after the ligation aid 1 has been attached to the endoscope in advance.
 術者は、端部101、102が体内に移動しないように保持された状態で、内視鏡を患者の体内に挿入し、図3に示すように、内視鏡200の先端を対象部位Tの付近まで導入する。端部101、102の保持は、術者が行ってもよいし、術者と異なる補助者が行ってもよい。
 術者等が、端部101、102を牽引すると、結び目が対象部位Tに接近し、対象部位が緊縛される。その後、術者等が端部101、102の牽引を強めて糸100に係るテンションを増加させると、糸100が通された突出部21および22は、糸100に加えられたテンションにより弾性変形する。その結果、図4に示すように、突出部21、22の先端が、中心軸線X1に接近するように変形する。この弾性変形により、貫通孔21aおよび22aが設けられた突出部21、22の先端部は、互いに接近しながら結び目110に接近し、対象部位Tが好適に仮結紮された状態になる。
The surgeon inserts the endoscope into the patient's body while the end portions 101 and 102 are held so as not to move into the body, and as shown in FIG. Introduced until near. The holding of the ends 101 and 102 may be performed by an operator or an assistant different from the operator.
When the surgeon pulls the end portions 101 and 102, the knot approaches the target site T, and the target site is bound. Thereafter, when an operator or the like increases the pulling of the end portions 101 and 102 to increase the tension related to the thread 100, the protruding portions 21 and 22 through which the thread 100 is passed are elastically deformed by the tension applied to the thread 100. . As a result, as shown in FIG. 4, the tips of the protrusions 21 and 22 are deformed so as to approach the central axis X1. By this elastic deformation, the tip portions of the protrusions 21 and 22 provided with the through holes 21a and 22a approach the knot 110 while approaching each other, and the target site T is suitably temporarily ligated.
 術者は、仮結紮された状態を保持しつつ、本結紮を行う。本結紮の方法には特に制限はなく、公知の方法を適宜選択することができる。例えば、一旦内視鏡200を抜去して結紮補助具1から糸100を抜き、糸100に本結紮のための結び目を緩く形成してから再度結紮補助具1に糸100の端部を通す。その後、上述したのと同様の手順で本結紮のための結び目を対象部位Tの付近まで移動させればよい。他の方法として、内視鏡200から突出させた把持鉗子等を用いて本結紮を行ってもよい。
 本結紮後、糸100の余った部位を結び目から切り離して体外に除去すると、糸100を用いた対象部位Tの単結紮が完了する。単結紮を複数行う場合は、同様の手順を繰り返す。
The surgeon performs this ligation while maintaining the temporarily ligated state. There is no restriction | limiting in particular in the method of this ligation, A well-known method can be selected suitably. For example, once the endoscope 200 is removed, the thread 100 is removed from the ligation aid 1, a knot for the main ligation is loosely formed on the thread 100, and then the end of the thread 100 is passed through the ligation aid 1 again. Then, what is necessary is just to move the knot for this ligation to the vicinity of the object site | part T in the procedure similar to the above-mentioned. As another method, this ligation may be performed using a grasping forceps or the like protruding from the endoscope 200.
After the main ligation, when the remaining part of the thread 100 is separated from the knot and removed from the body, the single ligation of the target part T using the thread 100 is completed. Repeat the same procedure for multiple single ligations.
 本実施形態の結紮補助具1によれば、弾性変形可能な一対の突出部21、22を備えるため、糸100にテンションがかかっていないときは、突出部21、22が中心軸線X1と平行な状態を保って内視鏡200の視野を妨げない。一方、結び目110が対象部位Tの付近まで移動した状態で糸100にテンションを掛けると、一対の突出部21、22が弾性変形し、突出部21、22のうち貫通孔21a、22aが形成された先端部が結び目110に十分接近する。その結果、突出部21、22が結び目110から延びる糸100を結び目110の近くで好適に保持し、結び目110が緩みにくくなる。
 さらに、本結紮のために内視鏡200を後退させる際も、突出部21、22の先端部が互いに接近した状態が保持される。このため、図5に示すように、糸100は、結び目110と突出部21、22との間において、内視鏡200の挿入部の軸線X1に対して平行に近い状態となり、内視鏡200が後退する方向と糸100が牽引される方向とが概ね一致する。これらの作用により、内視鏡200を抜去する際に結び目110が緩むことを好適に防止することができる。
According to the ligation aid 1 of the present embodiment, since the pair of elastically deformable protrusions 21 and 22 are provided, the protrusions 21 and 22 are parallel to the central axis X1 when the thread 100 is not tensioned. The visual field of the endoscope 200 is not obstructed while maintaining the state. On the other hand, when tension is applied to the thread 100 with the knot 110 moved to the vicinity of the target site T, the pair of protrusions 21 and 22 are elastically deformed, and through holes 21a and 22a are formed in the protrusions 21 and 22. The distal end is sufficiently close to the knot 110. As a result, the protrusions 21 and 22 suitably hold the thread 100 extending from the knot 110 near the knot 110, and the knot 110 is less likely to loosen.
Further, when the endoscope 200 is retracted for the main ligation, the state in which the tip portions of the projecting portions 21 and 22 are close to each other is maintained. For this reason, as shown in FIG. 5, the thread 100 is between the knot 110 and the protrusions 21 and 22 and is almost parallel to the axis X <b> 1 of the insertion portion of the endoscope 200. The direction in which the thread 100 moves backward substantially coincides with the direction in which the thread 100 is pulled. With these actions, it is possible to suitably prevent the knot 110 from being loosened when the endoscope 200 is removed.
 加えて、突出部21、22が透明に形成されているため、突出部が弾性変形して内視鏡200の視野内に移動した場合も、突出部を通して突出部の前方の状態を把握することができ、円滑に手技を行うことができる。 In addition, since the protrusions 21 and 22 are formed transparently, even when the protrusions are elastically deformed and move into the field of view of the endoscope 200, the state in front of the protrusions can be grasped through the protrusions. Can be performed smoothly.
 本実施形態において、突出部の形状は、様々に変更することが可能である。
 例えば、図6に示す変形例の突出部21Aのように、貫通孔21aが設けられた先端部よりも基端部21bを細く形成してもよい。このように形成された突出部21Aにおいては、先端側よりも基端側がより弾性変形しやすくなる。
In the present embodiment, the shape of the protruding portion can be variously changed.
For example, the base end portion 21b may be formed narrower than the tip end portion provided with the through hole 21a, as in the protruding portion 21A of the modification shown in FIG. In the protruding portion 21A formed in this way, the proximal end side is more easily elastically deformed than the distal end side.
 先端側よりも基端側をより弾性変形しやすく構成する他の変形例を図7に示す。図7に示す変形例の突出部21Bは、装着部10の周方向に直交する方向における寸法を小さくすることにより、先端部よりも基端部21bを薄く形成している。この場合も、突出部において、先端側よりも基端側がより弾性変形しやすくなる。
 図6および図7に示した変形例は、突出部の弾性変形のしやすさ(剛性)を部位ごとに所望の値に調整したい場合に単独または組み合わせて適宜用いることができる。先端側をより弾性変形しやすくしたい場合は、先端側を、基端側より細くしたり薄くしたりすればよい。
FIG. 7 shows another modification example in which the base end side is more easily elastically deformed than the distal end side. The protruding portion 21B of the modification shown in FIG. 7 has a base end portion 21b thinner than the distal end portion by reducing the dimension in the direction orthogonal to the circumferential direction of the mounting portion 10. Also in this case, in the protruding portion, the base end side is more easily elastically deformed than the distal end side.
The modification examples shown in FIGS. 6 and 7 can be appropriately used alone or in combination when it is desired to adjust the easiness (rigidity) of the elastic deformation of the protrusion to a desired value for each part. In order to make the distal end side more easily elastically deformed, the distal end side may be made thinner or thinner than the proximal end side.
 また、突出部に設けられる貫通孔が、糸を通しやすく構成されてもよい。
 図8に示す変形例では、貫通孔21aに糸通し部材40が通されている。術者等が糸通し部材40に糸100を通して糸通し部材40を貫通孔21aから引き抜くと、糸100を容易に貫通孔21aに通すことができる。
Moreover, the through-hole provided in the protrusion part may be configured to facilitate threading.
In the modification shown in FIG. 8, the threading member 40 is passed through the through hole 21a. When an operator or the like passes the thread 100 through the threading member 40 and pulls out the threading member 40 from the through hole 21a, the thread 100 can be easily passed through the through hole 21a.
 図9Aおよび図9Bに示す変形例では、貫通孔21aに、突出部の周縁まで延びる溝21cが設けられている。このようにすると、糸100を溝21cに進入させて貫通孔内に移動させることにより、容易に糸100を貫通孔21aに通すことができる。
 溝21cの幅を糸100の直径よりもわずかに小さくすると、貫通孔21aに通した糸100が意図せず貫通孔21aから外れることが抑制されるため、好ましい。突出部21は弾性変形可能であるため、溝21cの幅が糸100の直径より狭くても、糸100を通すことができる。溝21cの延びる方向には特に制限はないが、図9Bに示すように、突出部21の先端に向かって溝21cが延びると、内視鏡200を後退させる際に糸が貫通孔21aから外れる可能性がある。したがって、図9Aに示すように、溝21cを装着部10の周方向に延ばしたり、突出部の基端側に向かって延ばしたりするなど、先端に向かわない方向に延ばすと、貫通孔への通しやすさと、糸が貫通孔から外れることの抑制とを両立することができ、好ましい。
In the modification shown in FIGS. 9A and 9B, the through hole 21a is provided with a groove 21c extending to the periphery of the protruding portion. If it does in this way, the thread | yarn 100 can be easily passed through the through-hole 21a by approaching the thread | yarn 100 to the groove | channel 21c, and moving it in a through-hole.
It is preferable to make the width of the groove 21c slightly smaller than the diameter of the thread 100 because the thread 100 that has passed through the through hole 21a is prevented from unintentionally coming off the through hole 21a. Since the protruding portion 21 can be elastically deformed, the yarn 100 can be passed even if the width of the groove 21 c is narrower than the diameter of the yarn 100. Although the direction in which the groove 21c extends is not particularly limited, as shown in FIG. 9B, when the groove 21c extends toward the tip of the protruding portion 21, the thread is detached from the through hole 21a when the endoscope 200 is retracted. there is a possibility. Therefore, as shown in FIG. 9A, if the groove 21c extends in the circumferential direction of the mounting portion 10 or extends toward the proximal end side of the protrusion, such as extending toward the distal end, the passage through the through hole It is preferable because both ease and suppression of the yarn from coming off the through hole can be achieved.
 次に、本発明の第二実施形態について、図10から図15を参照して説明する。本実施形態の結紮補助具と第一実施形態の結紮補助具1とは、結び目を支持する支持部材を備える点で異なっている。以降の説明において、既に説明したものと共通する構成については、同一の符号を付して重複する説明を省略する。 Next, a second embodiment of the present invention will be described with reference to FIGS. The ligation aid of the present embodiment is different from the ligation aid 1 of the first embodiment in that it includes a support member that supports the knot. In the following description, components that are the same as those already described are assigned the same reference numerals and redundant description is omitted.
 図10は、本実施形態の結紮補助具51の正面図であり、図11は、図10のI-I線における断面図である。結紮補助具51は、突出部21と突出部22との間に設けられた支持部材52を備えている。 FIG. 10 is a front view of the ligation aid 51 of this embodiment, and FIG. 11 is a cross-sectional view taken along the line II of FIG. The ligation aid 51 includes a support member 52 provided between the protrusion 21 and the protrusion 22.
 支持部材52は、樹脂材料やガラス等で透明に形成されたV字状の部材である。支持部材52は、図11に示すように、突出部21、22の先端側、すなわち突出部21、22の延びる方向に向かって凸となるように、各突出部21、22の基端部に固定されている。支持部材のうち、凸となる屈曲部52aは、貫通孔21aと貫通孔22aとの間に位置している。 The support member 52 is a V-shaped member that is transparently formed of a resin material, glass, or the like. As shown in FIG. 11, the support member 52 is provided at the proximal end of each protrusion 21, 22 so as to protrude toward the distal end side of the protrusion 21, 22, that is, in the extending direction of the protrusion 21, 22. It is fixed. Of the support member, the convex bent portion 52a is located between the through hole 21a and the through hole 22a.
 上記のように構成された本実施形態の結紮補助具51も、上述の結紮補助具1と同様に、突出部を弾性変形させて、内視鏡後退時の結び目の緩みを好適に防止することができる。
 また、支持部材52を備えることにより、結び目を直接支持部材で押すことができる。その結果、組織に結び目を十分に近づけることができるとともに、結び目の押し込みをより小さい力で確実に行って、突出部21、22の弾性変形をより確実に制御することができる。
Similarly to the above-described ligation assisting tool 1, the ligation assisting tool 51 of the present embodiment configured as described above is also capable of elastically deforming the protruding portion to suitably prevent loosening of the knot when the endoscope is retracted. Can do.
Further, by providing the support member 52, the knot can be pushed directly by the support member. As a result, the knot can be made sufficiently close to the tissue, and the knot can be pushed in with a smaller force, and the elastic deformation of the protrusions 21 and 22 can be controlled more reliably.
 さらに、糸100を通した際に、一対の突出部21、22間に位置する結び目110が、図12に示すように、支持部材52によって内視鏡200に接近しすぎないように支持される。したがって、突出部21が弾性変形する前の状態においても、結び目が内視鏡に接近しすぎて観察しにくくなる事態の発生を防止することができる。 Further, when the thread 100 is passed, the knot 110 positioned between the pair of protrusions 21 and 22 is supported by the support member 52 so as not to be too close to the endoscope 200 as shown in FIG. . Therefore, even in a state before the protruding portion 21 is elastically deformed, it is possible to prevent a situation in which the knot is too close to the endoscope and difficult to observe.
 さらに、支持部材52が透明に形成されているため、結び目の内視鏡への接近を防ぎつつ、支持部材52の前方の状況も確認することができる。 Furthermore, since the support member 52 is formed to be transparent, it is possible to check the situation in front of the support member 52 while preventing access to the knot endoscope.
 本実施形態において、支持部材の形状は様々に変更することができる。例えば、上述したV字状に代えて、凸となる部分が曲面状に形成されたU字状或いはC字状であってもよい。 In this embodiment, the shape of the support member can be variously changed. For example, instead of the V-shape described above, a U-shape or a C-shape in which a convex portion is formed in a curved shape may be used.
 また、図13に示すような、L字状のワイヤ53を一部が貫通孔21a、22a間に位置するように配置することにより支持部材として用いてもよい。この場合、内視鏡200の視野に対してワイヤ53が十分に細いため、ワイヤ53自体が透明でなくとも、内視鏡200の観察をほとんど妨げずに結び目を支持することができ、支持部材52と概ね同様の効果を奏する。 Alternatively, as shown in FIG. 13, an L-shaped wire 53 may be used as a support member by disposing a part of the wire 53 between the through holes 21a and 22a. In this case, since the wire 53 is sufficiently thin with respect to the visual field of the endoscope 200, even if the wire 53 itself is not transparent, the knot can be supported almost without obstructing the observation of the endoscope 200. The same effect as 52 is produced.
 さらに、図14および図15(図15は、図14のII-II線における断面図である。)に示す支持部材54のように、窓部54aを有する形状であってもよい。この場合、窓部54aには支持部材54の材料が存在しないため、窓部54の周縁部分で結び目を支持しつつ、支持部材54が透明でなくても、窓部54aを通して内視鏡200による観察を好適に行うことができる。 14 and 15 (FIG. 15 is a cross-sectional view taken along the line II-II in FIG. 14), and may have a shape having a window portion 54a. In this case, since the material of the support member 54 does not exist in the window portion 54a, the knot is supported by the peripheral portion of the window portion 54, and even if the support member 54 is not transparent, the endoscope 200 passes through the window portion 54a. Observation can be suitably performed.
 次に、本発明の第三実施形態について、図16および図17を参照して説明する。本実施形態の結紮補助具と各実施形態の結紮補助具とは、突出部の形状において異なっている。 Next, a third embodiment of the present invention will be described with reference to FIGS. The ligation aid of this embodiment differs from the ligation aid of each embodiment in the shape of the protrusions.
 図16は、本実施形態の結紮補助具71を示す側面図である。結紮補助具71における一対の突出部72、73は、側面視において台形状に形成されており、装着部10の周方向における寸法が先端に近づくにつれて徐々に小さくなっている。 FIG. 16 is a side view showing the ligation aid 71 of the present embodiment. The pair of protrusions 72 and 73 in the ligation assisting tool 71 are formed in a trapezoidal shape in a side view, and gradually become smaller as the dimension of the mounting portion 10 in the circumferential direction approaches the tip.
 突出部72、73は、筒状の部材の一方の端部を、中心軸線X1に対して傾斜する直線L1およびL2に沿って切り落とすことにより形成されている。したがって、突出部72、73において、装着部10の周方向両側の縁の一方は、直線L1に沿う仮想平面上P1に位置し、他方は直線L2に沿う仮想平面P2上に位置する。 The protrusions 72 and 73 are formed by cutting off one end of the cylindrical member along straight lines L1 and L2 that are inclined with respect to the central axis X1. Accordingly, in the protrusions 72 and 73, one of the edges on both sides in the circumferential direction of the mounting portion 10 is located on the virtual plane P1 along the straight line L1, and the other is located on the virtual plane P2 along the straight line L2.
 上記のように構成された本実施形態の結紮補助具71の使用時の動作について説明する。結紮補助具71は、上述の各実施形態同様、内視鏡200に装着して対象部位の付近まで導入される。その後、上述した突出部72、73の縁の一方を組織に押し当てることにより、図17に示すように、組織面Tsの法線N1に対して傾斜した斜め方向から突出部72、73を接近させることができる。突出部72、73の縁は、いずれも同一の仮想平面上に存在するため、結紮補助具71を組織に接触させた後の姿勢は安定する。 The operation when using the ligation aid 71 of the present embodiment configured as described above will be described. The ligation assisting tool 71 is mounted on the endoscope 200 and introduced to the vicinity of the target site, as in the above-described embodiments. Thereafter, by pressing one of the edges of the protrusions 72 and 73 described above against the tissue, the protrusions 72 and 73 are approached from an oblique direction inclined with respect to the normal line N1 of the tissue surface Ts as shown in FIG. Can be made. Since the edges of the protrusions 72 and 73 are all on the same virtual plane, the posture after the ligation aid 71 is brought into contact with the tissue is stabilized.
 本実施形態の結紮補助具71も、上述の各実施形態で説明した結紮補助具と同様に、突出部を弾性変形させて、内視鏡を後退させる際の結び目の緩みを防止することができる。 Similarly to the ligation aid described in the above embodiments, the ligation aid 71 of the present embodiment can also prevent the knot from loosening when the projection is retracted by elastically deforming the protrusion. .
 また、突出部71、72は、装着部10の周方向における寸法が先端に近づくにつれて徐々に小さく、すなわち先細り形状になっている。このため、突出部の中でも先端側がより変形しやすく構成されており、糸100にテンションを付加すると、突出部71、72はまず先端側から弾性変形を開始する。その結果、突出部の根元が急激に屈曲することが抑制され、結び目の挙動が安定する。 Further, the protrusions 71 and 72 are gradually smaller as the circumferential dimension of the mounting portion 10 approaches the tip, that is, have a tapered shape. For this reason, the tip side of the protrusion is configured to be more easily deformed, and when tension is applied to the thread 100, the protrusions 71 and 72 first start elastic deformation from the tip side. As a result, the base of the protrusion is prevented from being bent sharply, and the knot behavior is stabilized.
 さらに、突出部72、73が先細り形状であることにより、上述したように、組織に対して斜め方向からのアプローチが容易である。これにより、腸などのように、内部空間が狭いことにより組織に対して法線方向からのアプローチが困難である場合であっても、結び目を組織に十分接近させた状態で締め込むことができる。 Furthermore, since the projecting portions 72 and 73 have a tapered shape, as described above, it is easy to approach the tissue from an oblique direction. This makes it possible to tighten the knot sufficiently close to the tissue even when it is difficult to approach the tissue from the normal direction due to the narrow internal space, such as the intestine. .
 本実施形態では、図16に示したように、直線L2が中心軸線X1に対してなす角度と、直線L3が中心軸線X1に対してなす角度とが略同一である例を説明したが、二つの角度は異なっていてもよい。二つの角度を異ならせると、結紮補助具を内視鏡に装着する態様を変えることにより、組織に対して安定する角度を対象部位の位置等に応じて変更することができる。また、突出部の一方の縁を第一実施形態のように中心軸線と平行にし、他方の縁のみを本実施形態のように形成してもよい。 In the present embodiment, as shown in FIG. 16, an example has been described in which the angle formed by the straight line L2 with respect to the central axis X1 and the angle formed by the straight line L3 with respect to the central axis X1 are substantially the same. The two angles may be different. When the two angles are made different, the angle at which the ligation assisting tool is attached to the endoscope can be changed to change the stable angle with respect to the tissue in accordance with the position of the target site. Alternatively, one edge of the protruding portion may be parallel to the central axis as in the first embodiment, and only the other edge may be formed as in the present embodiment.
 以上、本発明の各実施形態について説明したが、本発明の技術範囲は上記実施形態に限定されるものではなく、本発明の趣旨を逸脱しない範囲において実施形態を超えて構成要素の組み合わせを変えたり、各構成要素に種々の変更を加えたり、削除したりすることが可能である。 The embodiments of the present invention have been described above. However, the technical scope of the present invention is not limited to the above-described embodiments, and the combination of components is changed beyond the embodiments without departing from the spirit of the present invention. It is possible to make various changes to each component or delete them.
 例えば、一対の突出部について、必ずしも装着部の中心軸線を挟むように配置されることは必須ではない。したがって、図18に示す変形例の突出部81、82のように、装着部の内部空間を挟んで対向するように配置されてもよい。 For example, it is not always necessary to arrange the pair of projecting portions so as to sandwich the central axis of the mounting portion. Therefore, like the protrusion parts 81 and 82 of the modification shown in FIG. 18, you may arrange | position so that it may oppose on both sides of the internal space of a mounting part.
 また、突出部は、少なくとも貫通孔が設けられた先端側のみが弾性変形できればよいため、基端側を別の材料で形成する等により基端側の剛性を高くして、実質的に中心軸線に接近するように弾性変形しないように突出部の基端部を構成してもよい。 In addition, since it is only necessary for the protruding portion to be elastically deformable at least only at the distal end side where the through hole is provided, the proximal end side is made to be rigid by, for example, forming the proximal end side from another material, so that the central axis is substantially You may comprise the base end part of a protrusion part so that it may not elastically deform so that it may approach.
 さらに、一対の突出部は、必ずしも両方が弾性変形可能でなくてもよい。少なくとも一方が弾性変形可能であれば、弾性変形した突出部の先端側が、他方の突出部に接近することにより、一定の上述した効果を奏する。 Furthermore, both of the pair of protrusions do not necessarily have to be elastically deformable. If at least one of the protrusions can be elastically deformed, the distal end side of the elastically deformed projecting portion approaches the other projecting portion, thereby providing the above-described effects.
 加えて、本発明の結紮補助具が第二実施形態で説明した支持部材を備えない場合は、図19に示すように、内視鏡200から突出させた把持鉗子205等により結び目110を支持してもよい。 In addition, when the ligation aid of the present invention does not include the support member described in the second embodiment, the knot 110 is supported by the grasping forceps 205 or the like projected from the endoscope 200 as shown in FIG. May be.
 本発明は、結紮補助具に適用することができる。 The present invention can be applied to a ligation aid.
 1、51、71 結紮補助具
 10 装着部
 21、21A、21B、22、72、73、81、82 突出部
 21a、22a 貫通孔
 21c 溝
 40 糸通し部材   
 52、54 支持部材
 53 ワイヤ(支持部材)
 40 操作ワイヤ(操作部材)
 45 制御シース(連結保持部材)
 200 内視鏡
 P1、P2 仮想平面
 X1 中心軸線
DESCRIPTION OF SYMBOLS 1, 51, 71 Ligation assist tool 10 Mounting part 21, 21A, 21B, 22, 72, 73, 81, 82 Protrusion part 21a, 22a Through- hole 21c Groove 40 Threading member
52, 54 Support member 53 Wire (support member)
40 Operation wire (operation member)
45 Control sheath (connection holding member)
200 Endoscope P1, P2 Virtual plane X1 Central axis

Claims (9)

  1.  内視鏡の先端部に着脱可能な装着部と、
     前記装着部から前方に突出するよう設けられ、先端部に糸を挿通可能な貫通孔を有する一対の突出部と、
     を備え、
     前記一対の突出部の少なくとも一方は、前記先端部が弾性変形により他方の突出部の先端部に接近可能に構成されている、
     結紮補助具。
    A mounting part detachable from the distal end of the endoscope;
    A pair of projecting portions provided to project forward from the mounting portion, and having a through-hole through which a thread can be inserted at the tip portion;
    With
    At least one of the pair of projecting portions is configured such that the distal end portion can approach the distal end portion of the other projecting portion by elastic deformation.
    Ligation aid.
  2.  前記装着部は、中心軸線を有する筒状または環状に形成され、
     前記一対の突出部は、前記中心軸線と平行に延びている、
     請求項1に記載の結紮補助具。
    The mounting portion is formed in a cylindrical or annular shape having a central axis,
    The pair of protrusions extend in parallel with the central axis.
    The ligation aid according to claim 1.
  3.  前記一対の突出部は、前記先端部が前記先端部より基端側の領域よりも弾性変形しやすく構成されている、請求項1に記載の結紮補助具。 The ligation assisting tool according to claim 1, wherein the pair of projecting portions are configured such that the distal end portion is more easily elastically deformed than a region closer to the proximal end than the distal end portion.
  4.  前記一対の突出部は、先端に近づくにつれて徐々に寸法が小さくなる形状を有する、請求項1に記載の結紮補助具。 The ligation assisting tool according to claim 1, wherein the pair of protrusions has a shape that gradually decreases in size as it approaches the tip.
  5.  前記装着部は、中心軸線を有する筒状または環状に形成され、
     前記一対の突出部において、前記装着部の周方向の一方に位置する縁が、前記中心軸線に対して傾斜する仮想平面上に位置する、請求項4に記載の結紮補助具。
    The mounting portion is formed in a cylindrical or annular shape having a central axis,
    The ligation assisting tool according to claim 4, wherein, in the pair of projecting portions, an edge located on one side in the circumferential direction of the mounting portion is located on a virtual plane inclined with respect to the central axis.
  6.  前記一対の突出部は、前記中心軸線を挟んで対向するように形成されている、請求項2に記載の結紮補助具。 The ligation aid according to claim 2, wherein the pair of projecting portions are formed so as to face each other with the central axis therebetween.
  7.  前記一対の突出部の間に設けられた支持部材をさらに備える、請求項1に記載の結紮補助具。 The ligation aid according to claim 1, further comprising a support member provided between the pair of protrusions.
  8.  前記突出部は、前記貫通孔から前記突出部の周縁まで延びる溝を有する、請求項1に記載の結紮補助具。 The ligation aid according to claim 1, wherein the protrusion has a groove extending from the through hole to a peripheral edge of the protrusion.
  9.  前記貫通孔に挿通された糸通し部材をさらに備える、請求項1に記載の結紮補助具。 The ligation aid according to claim 1, further comprising a threading member inserted through the through hole.
PCT/JP2017/020598 2017-06-02 2017-06-02 Ligature aid WO2018220818A1 (en)

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Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2131321A (en) * 1937-10-11 1938-09-27 Hart Wilber Ligator
US4018229A (en) * 1974-09-13 1977-04-19 Olympus Optical Co., Ltd. Apparatus for ligation of affected part in coeloma
US5281238A (en) * 1991-11-22 1994-01-25 Chin Albert K Endoscopic ligation instrument
WO1996041574A2 (en) * 1995-06-07 1996-12-27 Innovasive Devices, Inc. Surgical system and method for the reattachment of soft tissue to bone
US7270672B1 (en) * 2005-02-11 2007-09-18 Adam Joel Singer Rod for transferring and tightening knotted suture into patient's body
JP2007236679A (en) * 2006-03-09 2007-09-20 Olympus Medical Systems Corp Ligature device
JP2007244867A (en) * 2006-03-15 2007-09-27 Tyco Healthcare Group Lp Suture pushing apparatus
JP2012504482A (en) * 2008-10-06 2012-02-23 ウィルソン−クック・メディカル・インコーポレーテッド End cap for secure deployment of tissue anchors

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2131321A (en) * 1937-10-11 1938-09-27 Hart Wilber Ligator
US4018229A (en) * 1974-09-13 1977-04-19 Olympus Optical Co., Ltd. Apparatus for ligation of affected part in coeloma
US5281238A (en) * 1991-11-22 1994-01-25 Chin Albert K Endoscopic ligation instrument
WO1996041574A2 (en) * 1995-06-07 1996-12-27 Innovasive Devices, Inc. Surgical system and method for the reattachment of soft tissue to bone
US7270672B1 (en) * 2005-02-11 2007-09-18 Adam Joel Singer Rod for transferring and tightening knotted suture into patient's body
JP2007236679A (en) * 2006-03-09 2007-09-20 Olympus Medical Systems Corp Ligature device
JP2007244867A (en) * 2006-03-15 2007-09-27 Tyco Healthcare Group Lp Suture pushing apparatus
JP2012504482A (en) * 2008-10-06 2012-02-23 ウィルソン−クック・メディカル・インコーポレーテッド End cap for secure deployment of tissue anchors

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