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WO2016013123A1 - Bone binding braid, and method for producing bone binding braid - Google Patents

Bone binding braid, and method for producing bone binding braid Download PDF

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Publication number
WO2016013123A1
WO2016013123A1 PCT/JP2014/069755 JP2014069755W WO2016013123A1 WO 2016013123 A1 WO2016013123 A1 WO 2016013123A1 JP 2014069755 W JP2014069755 W JP 2014069755W WO 2016013123 A1 WO2016013123 A1 WO 2016013123A1
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WO
WIPO (PCT)
Prior art keywords
cord
bone
binding
wire
basic
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Ceased
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PCT/JP2014/069755
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French (fr)
Japanese (ja)
Inventor
加納川 快明
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Osaka Coat Rope Co ltd
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Osaka Coat Rope Co ltd
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Priority to PCT/JP2014/069755 priority Critical patent/WO2016013123A1/en
Publication of WO2016013123A1 publication Critical patent/WO2016013123A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods
    • A61B17/56Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor
    • A61B17/58Surgical instruments or methods for treatment of bones or joints; Devices specially adapted therefor for osteosynthesis, e.g. bone plates, screws or setting implements

Definitions

  • the present invention relates to a bundling cord used for bundling longitudinally torn bones, and a method for producing a bundling cord.
  • a bone called the sternum in the center of the chest is cut open in the longitudinal direction, and the prescribed treatment is performed. Finally, the cut sternum is used as a binding thread. The technique of uniting is performed.
  • a single thin thread or wire is used alone, or a single wire or a plurality of loops are formed by interweaving and knitting a wire and a wire.
  • the wire is straight and has a feature that it is easy to fasten by using a hole in the ring at the time of knotting (bundling), and a straight needle or a curved needle that penetrates the sternum is connected to both ends or one end.
  • a material for suture of the sternum has been developed in which only the end to which is connected is squeezed and knitted narrower than the central portion (for example, see Patent Document 1 below).
  • those made of a single wire stainless steel wire have an advantage that the risk of tissue damage when passing around the sternum during sternum bundling work is reduced because the cross-sectional shape is a striate having a circular shape.
  • those made of a belt-shaped stainless steel plate can be tied around the sternum while being in surface contact with the outer peripheral surface of the sternum, so that the sternum can be fixed relatively stably.
  • the binding yarn made of a belt-like stainless steel plate is curved only in the surface direction and not curved in the edge direction, so that it is inferior in workability when passing around the sternum when binding the sternum.
  • tissue damage around the sternum is likely to occur at the edge during hand movement, and the hemostatic treatment tends to increase the operation time.
  • the binding yarn made of a single wire stainless steel wire or a belt-like stainless steel plate is not stretchable, loosening may occur after binding, and the sternum may be insufficiently bound.
  • the bone fastening hollow cable described in Patent Document 2 has a circular cross-sectional shape at the time of hand movement, reduces the risk of tissue damage, and is deformed into a band shape at the time of binding, so that bone collapse and damage are less likely to occur.
  • the hollow cable for bone fastening described in Patent Document 2 is braided by plain weave or oblique weave, there is almost no stretchability in the length direction, and a single wire stainless steel wire or strip As in the case of the binding yarn made of a stainless steel plate, loosening may occur after binding, and the sternum may be insufficiently bound.
  • the present invention has been developed in view of the above technical problem, and can reduce the risk of damage to the tissue existing around the bone when passing around the bone at the time of hand movement, and can stably bind the bone.
  • An object of the present invention is to provide a novel bone binding cord and a method for producing the bone binding cord.
  • the bone uniting cord of the present invention is a bone uniting cord used when bundling longitudinally torn bones, and is a single wire of a metal filament or a metal filament
  • the cord body is knitted into the basic line so that it can be expanded and contracted in the length direction and flatly deformed into a flat plate shape when the bones are bound, so that it can come into surface contact with the surface of the bone.
  • a hollow braided body having a net-like peripheral wall configured by the above-described structure, and each of the basic lines constituting the peripheral wall is spirally arranged along the peripheral wall (hereinafter referred to as the present invention cord). Called the body).
  • the basic line is preferably a parallel arrangement type converging line in which a plurality of metal filaments are adjacent to each other along the length direction (hereinafter referred to as this mode). This is called the first cord of the present invention).
  • the basic line is preferably a parallel-arranged convergent line in which two or three metal filaments are adjacent to each other along the length direction. .
  • the metal filament has a wire diameter of 9 to 300 ⁇ m.
  • the basic wire is preferably a twisted wire-type converging wire formed by twisting a plurality of metal filaments (this mode is hereinafter referred to as the second embodiment of the present invention). It is called a cord.)
  • the basic wire is a cored twisted wire type converging wire formed by winding a plurality of metal filaments around a single metal filament as a core material Is a preferred embodiment.
  • the metal filament having a wire diameter of 3 to 150 ⁇ m is a preferred embodiment.
  • the basic line does not have a twist that twists about the virtual axis of the basic line.
  • a tensile stress required to pull at least 2 mm is 15 N or less.
  • ⁇ Test> The cord body is held at a chuck distance of 200 mm, and the tensile stress is measured while pulling the cord body in the length direction at a tensile speed of 5 mm per minute.
  • the cord body when the cord body is pulled according to the test conditions, if the tensile stress is 100 N or less, then the stretchability is restored when the test force is not applied.
  • the tensile stress is 100 N or less, then the stretchability is restored when the test force is not applied.
  • the method for manufacturing a bundling cord of the present invention is a method of manufacturing the second cord of the present invention, and before braiding the basic line, the basic line is twisted around the axis. A twist is imparted, and the basic line is braided in a direction in which the twist is unwound.
  • the bone when passing around the bone at the time of hand movement, there is little risk of damage to the tissue existing around the bone, and the bone can be stably bound.
  • FIG. 1 (a) is a perspective view showing an outline of the overall configuration of the cord of the present invention according to Embodiment 1
  • FIG. 1 (b) is a cross section showing a stretched state of the cord body in the cord of the present invention.
  • Fig. 1 (c) is a plan view showing a stretched state of the cord body in the cord of the present invention
  • Fig. 1 (d) is a flat deformation of the cord body of the cord of the present invention. It is sectional drawing which shows a state.
  • FIG. 2 (a) is a plan view showing a state in which the sternum is bound by the cord of the present invention.
  • FIG. 2 (b) is a diagram before the cord of the present invention is wound around the sternum and bound.
  • FIG. 1 (a) is a perspective view showing an outline of the overall configuration of the cord of the present invention according to Embodiment 1
  • FIG. 1 (b) is a cross section showing a stretched state of the cord body in the cord of the present
  • FIG. 2C is a cross-sectional view showing a state in which the sternum is bound by the cord of the present invention.
  • FIG. 3 is a graph showing the expansion and contraction characteristics of the cord of the present invention.
  • FIG. 4 is a graph showing the expansion / contraction characteristics of a conventional tying yarn.
  • FIG. 5 is a perspective view showing an outline of the overall configuration of the cord of the present invention (the first cord of the present invention) according to Embodiment 2.
  • FIG. 6A is a perspective view showing an outline of the overall configuration of the cord of the present invention (second cord of the present invention) according to Embodiment 3, and
  • FIG. 6B shows the configuration of the cord of the present invention. It is a sectional view showing a basic line.
  • FIG. 1A shows an outline of the overall configuration of the cord 1 of the present invention according to the first embodiment.
  • the cable body 1 of the present invention includes a cable body 2, a penetrating blade 3 provided on one end side of the cable body 2, and a buckle 4 provided on the other end side of the cable body 2. To do.
  • the cord body 2 is a single wire of a metal filament (in this embodiment, a stainless steel filament).
  • a plurality of basic lines 21 (48 in this embodiment) are braided so as to cross each other.
  • the cord body 2 is formed by knitting each of the basic wires 21 into a net-like peripheral wall by arranging each of the basic wires 21 in a spiral shape, thereby forming a hollow braided body as a whole. It is.
  • tubular knitting is a knitting method called warp knitting that does not distinguish between warp and weft, and each basic line 21 constituting the cord body 2 is connected to the cord body 2.
  • the cord body 2 braided by the tubular knitting has an axis of the cord body 2 and a running direction of each basic line 21 running spirally with respect to the length direction of the cord body 2.
  • the formed angles are equal at any position of the cord body 1.
  • the wire diameter ( ⁇ ) of the basic line (in the case of the present embodiment, a single filament wire) 21 constituting the cord body 2 is used as the strength and thickness required for the cord body 2 or used. What is necessary is just to determine suitably according to the number of the basic lines 21, and it does not specifically limit.
  • the wire diameter ( ⁇ ) of the basic wire 21 is preferably 9 to 300 ⁇ m (more preferably 15 to 150 ⁇ m).
  • the basic wire 21 is made of stainless steel, but the basic wire 21 is preferably made of a corrosion-resistant metal such as nickel titanium alloy or titanium alloy in addition to stainless steel. Used.
  • the peripheral wall of the cord body 2 is constituted by 48 basic lines 21 for convenience, but the number of the basic lines 21 constituting the peripheral wall is 30 to 100. (More preferably, it is in the range of 36 to 96).
  • the length of the cord body 2 is not particularly limited as long as the cord body 2 has a length that can circulate around the outer circumference of the bone to be bound in a state where the tightening allowance at the time of binding is left.
  • the length of the cord body 2 is preferably 10 to 100 cm (more preferably 15 to 65 cm).
  • the cord body 2 having such a structure has a length while contracting its wire diameter when a tensile stress is applied along the length direction. When stretched in the direction and then released from the tensile stress along the length direction, it has a property (stretchability) that elastically recovers to its original state. Further, as shown in FIG. 1 (d), when it is wound around a certain object, it has a property of flattening while maintaining stretchability and deforming into a flat plate shape (flat deformation).
  • the wire diameter of the cord body 2 itself is indefinite because it changes according to the tensile stress, but the cord body 2 when a tensile stress (about 20 to 100 N) is applied along the length direction.
  • the wire diameter ( ⁇ ) of itself is within a range of 0.5 to 10 mm (more preferably 1 to 5 mm), and the wire body 2 itself has a wire diameter ( ⁇ 0 ) is preferably 1 to 20 mm (more preferably 2 to 10 mm).
  • the width when the cord body 2 is deformed into a flat plate shape is preferably 0.75 to 15 mm (more preferably 1.5 to 7.5 mm).
  • the penetrating blade 3 is for piercing a living tissue existing around a bone to be bound, and for incising a passage for circling the cord body 2, and a blade 31 having a sharp tip end side; A curved body part 32 and a proximal end part 33 on the distal side are provided.
  • the penetrating blade 3 is welded and fixed to the cord body 2 in a state where the base end portion 33 is inserted into one end side of the cord body 2, and at this time, one end side of the cord body 2. Is in a state where the wire diameter is contracted according to the outer diameter of the base end portion 33.
  • the buckle 4 is a flat metal plate material, and is fixed to the cord body 2 by welding.
  • the buckle 4 is provided with two long holes 41 and 42 into which the cable body 2 can be inserted, and each of the long holes 41 and 42 has a saw blade that can mesh with the cable body 2.
  • Shaped return portions 41a and 42a are provided. It is preferable that the buckle 4 is configured to have a thickness of 2 mm or less in a state where the buckle 4 is welded and fixed to the cord body 2 so that the buckle 4 does not cause a sense of foreign matter during bone fixation. .
  • the chest is cut and opened in the longitudinal direction at the center of the sternum 5, and after necessary treatment, the cut sternum 5 is approached and temporarily closed.
  • the penetrating blade 3 existing at one end of the cord 1 of the present invention is pierced between the ribs 51, and the cord body 2 following the penetrating blade 3 is inserted into the sternum 5 while incising the tissue existing around the sternum 5. Orbit around.
  • the buckle 4 existing on the other end side of the cord body 2 is positioned at the center of the sternum 5, Is passed through the elongated hole 41 in the buckle 4 and the subsequent cord body 2 is inserted into the elongated hole 41 (FIG. 2B). )reference).
  • the cord body 2 is pulled in this state, the cord body 2 is pressed around the sternum 5 while being stretched to be flattened into a flat shape (see FIG. 2C).
  • the cord body 2 that has been stretched and flattened into a flat plate shape is still stretchable, so that the cord body 2 is urged in a contracting direction. Since the net
  • the penetrating blade 3 is another part of the buckle 4. Passing through the elongated hole 42, the subsequent cord body 2 is inserted into the elongated hole 42. Thereafter, after confirming that the cord body 2 is not loosened, an excessive portion on one end side of the cord body 2 is cut to separate the penetrating blade 3 from the cord body 2 (FIG. 2 (a )reference).
  • the cord 1 of the present invention has a circular or oval striated shape while the cord body 2 expands and contracts in the length direction in response to the operator's pulling and the cross-sectional shape is contracted during hand movement. To prevent damage to the tissue around the bone more than necessary. Further, after the bones are bound, since the binding state can be maintained by the contraction force of the cord body 2, the cords of the present invention 1 are used when the bones are bound by a plurality of cords of the present invention 1. Even if there is a slight difference in the binding force in each of these, looseness and play do not occur, and a good binding state can be maintained.
  • the cord 1 of the present invention is deformed into a flat plate shape when wound around the bone, it is fixed in a state of surface contact with the outer peripheral surface of the bone. Therefore, it does not bite into the bone and does not give the patient a feeling of discomfort or tenderness after the operation.
  • the cord 1 of the present invention is fixed to the bone by the contraction force of the cord body 2, even if a patient sneezes or crushes after the operation and an instantaneous force is applied, the cord is flexible. It can be expanded and contracted to reduce the risk of damaging bone.
  • the graph of FIG. 3 is a chart showing the expansion and contraction characteristics of the cord body 2 in the cord of the present invention 1 under the following test conditions, and the vertical axis indicates the tensile stress applied to the cord body 2. The horizontal axis indicates the tensile distance (stroke).
  • ⁇ Test> Grasping the cable body 2 at a chuck distance of 200 mm, and measuring the tensile stress when the cable body 2 is stretched in the length direction at a tensile speed of 5 mm per minute (Testing machine: SHIMADZU AG-IS 50 kN ).
  • stage (A) in the figure is a stage in which the spiral radius of each of the basic lines 21 constituting the peripheral wall of the cord body 2 is reduced and the helical pitch is increased by tension, and the basic lines arranged in a spiral shape are formed. This is because the linear elastic force of 21 and the frictional force generated at the intersection of the basic lines 21 do not resist tensile stress.
  • the stage (A) in this figure continues at least until the cord body 2 is pulled 2 mm (more preferably 2.5 mm), and the tensile stress required at that time is 15 N or less. (More preferably 10N or less).
  • This numerical target is achieved mainly by appropriately selecting the number and diameter of the basic lines 21 constituting the peripheral wall of the cord body 2 and the spiral radius and spiral pitch of the basic lines 21 in a steady state. be able to.
  • the cord body 21 When the cord body 21 is released from the tensile stress at the stage (B) in the figure, the cross-sectional shape is somewhat reduced (the wire diameter is reduced), but the original state is almost restored.
  • the tensile stress is 100 N or less (more preferably, 200 N or less), it belongs to the stage (B) in this figure.
  • This numerical target can be achieved by appropriately selecting the number, the wire diameter, the tensile strength, and the like of the basic wires 21 mainly constituting the peripheral wall of the cord body 2.
  • stage (B) in the figure If a tensile stress is further applied beyond the stage (B) in the figure, unrecoverable elongation occurs in the basic line 21 constituting the cord body 2 (stage (c) in the figure). ) Eventually, the cord body 2 is disconnected (stage (D) in the figure), but the cord body 2 is not connected to the cord body 2 during actual binding work or in a state of being fixed to the bone. It is unlikely that the stage (C) or the stage (D) in the figure occurs.
  • the cord 1 of the present invention has a stage of (A) in the figure that can be easily pulled and a stage of (B) in the figure that can restore the stretchability.
  • a stable binding state can be achieved.
  • FIG. 5 shows an outline of the overall configuration of the first rope body 11 of the present invention according to the second embodiment.
  • the first cable body 11 of the present invention includes a cable body 2, a penetrating blade 3 provided on one end side of the cable body 2, a buckle 4 provided on the other end side of the cable body 2, It comprises.
  • the cord body 2 is of a parallel arrangement type in which a plurality (two in the present embodiment) of metal filaments (stainless steel filaments in the present embodiment) F are adjacent to each other along the length direction.
  • a plurality of basic lines 21 composed of convergent lines (48 in the present embodiment) are braided so as to cross each other by cylindrical knitting (see an enlarged view of FIG. 5).
  • the cord body 2 has the same configuration as that of the first embodiment except that a parallel arrangement type convergence line is used as the basic line 21.
  • the wire diameter of the metal filament F constituting the basic wire 21 is preferably 9 to 300 ⁇ m (more preferably 15 to 150 ⁇ m).
  • the penetrating blade 3 and the buckle 4 are the same as those used in the first embodiment, and are fixed to the cord body 2 by the same means as in the first embodiment.
  • the first cable body 11 of the present invention having such a configuration uses a parallel arrangement type converging line as the basic line 21, when it is wound around some object and deformed into a flat plate shape, a metal filament The sharpness of the edge portion is reduced as compared with the cord 1 of the present invention according to the first embodiment created using the basic line 21 made of a single wire.
  • This provides the advantage of less risk of damaging the bone and tissue surrounding the bone when it is wound around the bone.
  • the first cord 11 of the present invention created with the parallel arrangement type convergence line as the basic line 21 is wound around a certain object as the number of metal filaments F constituting the convergence line increases. It has been confirmed that the sharpness of the edge portion tends to be more relaxed when flattened into a flat plate shape.
  • the metal filaments F constituting the convergence line have almost no stretchability, it is very difficult to bundle all the metal filaments F under the same conditions.
  • a parallel arrangement type converging line in which a number of metallic filaments F are adjacent to each other is likely to be bent or the like in a part of the metallic filaments F constituting the converging line.
  • the bent metal filament F is easily broken by itself, and the broken metal filament F becomes a cause of raising on the peripheral wall of the first cord body 1 of the present invention.
  • a parallel arrangement type convergence line as the basic line 21
  • a parallel arrangement type convergence line in which two or three metal filaments F are adjacent to each other in the length direction is used. It is preferable to use it.
  • FIG. 6A shows an outline of the overall configuration of the second cord 12 of the present invention according to the third embodiment.
  • the second cord body 12 of the present invention includes a cord body 2, a penetrating blade 3 provided on one end side of the cord body 2, a buckle 4 provided on the other end side of the cord body 2, It comprises.
  • the cord body 2 is composed of a twisted wire-type converging wire formed by twisting a plurality of (seven in this embodiment) metal filaments (stainless steel filaments in this embodiment) F.
  • a plurality of the basic lines 21 (48 in the present embodiment) are braided so as to cross each other by cylindrical knitting (see an enlarged view of FIG. 6A).
  • the cord body 2 has the same configuration as that of the first embodiment except that a twisted-type converging wire is used as the basic wire 21.
  • the wire diameter of the metal filament F used for the basic wire 21 is preferably 3 to 150 ⁇ m (more preferably 9 to 100 ⁇ m).
  • the penetrating blade 3 and the buckle 4 are the same as those used in the first embodiment, and are fixed to the cord body 2 by the same means as in the first embodiment.
  • the second cord 12 of the present invention having such a configuration uses a twisted-type converging wire as the basic wire 21, when it is wound around some object and flattened into a flat plate shape, a metal filament The sharpness of the edge portion is reduced as compared with the cord 1 of the present invention according to the first embodiment created using the basic line 21 made of a single wire.
  • This provides the advantage of less risk of damaging the bone and tissue surrounding the bone when it is wound around the bone.
  • the twisted wire type converging wire has a higher physical strength against tensile stress than a single-filament metal filament having the same wire diameter, the maximum value of the tensile stress at the stage (b) in FIG. There is also an advantage of higher.
  • the twisting method of the metal filament F constituting the basic wire 21 is not particularly limited.
  • a twisting method of the metal filament F constituting the basic wire 21 for example, a twisting method called Z twisting or a twisting method called S twisting can be suitably used.
  • a stranded wire-type converging wire when used as the basic wire 21, a plurality of metal filaments are disposed around one metal filament FO as a core as shown in FIG. It is preferable to use a cored strand type converging wire formed by winding F.
  • This cored stranded wire type converging wire is compared with a stranded wire type converging wire without a core material because a single metal filament FO as a core material is arranged along the axis of the converging wire.
  • a single metal filament FO as a core material is arranged along the axis of the converging wire.
  • the peripheral wall of the cord body 2 is spirally formed.
  • a twist that twists around the virtual axis is generated. This twist causes the metal filament F constituting the basic wire 21 to be broken. Then, the broken metal filament F becomes a cause to cause a scissors on the peripheral wall of the cord 1 of the present invention.
  • the basic line 21 is formed before the basic line 21 is braided.
  • the number of twists applied in advance to the basic line 21 may be determined according to the number of times the basic line 21 is spirally wound during braiding.
  • the thus produced cord body 2 is not twisted in the basic line 21 constituting the peripheral wall, and the risk of the metal filament F constituting the basic line 21 is reduced.
  • the cord of the present invention is used for bundling vertically fractured bones, and particularly suitable for bundling sternum cut in thoracotomy.

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Abstract

A bone binding braid (1, 11, 12) has a braid main body (2). The braid main body (2) is composed of multiple base wires (21). The base wires (21) are woven to form the hollow braid main body (2). Each of the base wires (21) is composed of one or multiple metallic filaments. A penetrating blade (3) is provided at one end of the braid main body (2), and a buckle (4) is provided at the other end of the braid main body (2). When it is intended to bind a breast bone (5) which has been cut, a physician allows the braid main body (2) to pass around the breast bone (5) while incising tissues surrounding the breast bone (5) with the penetrating blade (3). At this time, the braid main body (2) extends in the length direction while keeping the cross-sectional shape of the braid main body (2) in a circular or oval shape. Therefore, the braid main body (2) hardly damages the tissues. Thereafter, when the physician allows one end of the braid main body (2) to pass through a long hole (41) in the buckle (4) and then pulls the one end, the braid main body (2) is pushed against the periphery of the breast bone (5) while further extending, resulting in the deformation of the braid main body (2) into a flat plate-like shape. In this manner, the breast bone (5) can be bound stably.

Description

骨結束用索体、及び骨結束用索体の製造方法Bone uniting cord and method for producing bone uniting cord

 本発明は、縦断裂した骨の結束時に使用する骨結束用索体、及び骨結束用索体の製造方法に関する。 The present invention relates to a bundling cord used for bundling longitudinally torn bones, and a method for producing a bundling cord.

 例えば、開胸を要する外科手術を行うにあたっては、胸部中央に存する胸骨と称される骨を縦方向に切断して開いたうえで所定の処置を行い、最後に、切断した胸骨を結束糸にて結束する術式が行われる。 For example, when performing a surgical operation that requires thoracotomy, a bone called the sternum in the center of the chest is cut open in the longitudinal direction, and the prescribed treatment is performed. Finally, the cut sternum is used as a binding thread. The technique of uniting is performed.

 従来、このような開胸手術の際に使用される前記結束糸としては、単線のステンレスワイヤや平板帯状のステンレス板が用いられていた。 Conventionally, as the tying yarn used in such a thoracotomy, a single wire stainless steel wire or a plate-like stainless steel plate has been used.

 最近では、単線の細い糸又はワイヤを糸単独、ワイヤ単独或いは糸とワイヤを交織し編みこむことにより、一個あるいは鎖状の複数の輪を形成し、縫合時(運針時)には緊張により糸又はワイヤが直線状となり、結節時(結束時)には輪の穴を利用し締結しやすいという特徴を持ち、両端又は片端に胸骨を貫通させる直針又は湾曲した針が接続されており、針が接続している端部だけが中央部分より細く絞られて編みこまれている胸骨縫合用材料が開発されている(例えば、下記特許文献1参照。)。 Recently, a single thin thread or wire is used alone, or a single wire or a plurality of loops are formed by interweaving and knitting a wire and a wire. Or, the wire is straight and has a feature that it is easy to fasten by using a hole in the ring at the time of knotting (bundling), and a straight needle or a curved needle that penetrates the sternum is connected to both ends or one end. A material for suture of the sternum has been developed in which only the end to which is connected is squeezed and knitted narrower than the central portion (for example, see Patent Document 1 below).

 又、繊維を編組して断面概略円形の管状に形成してなる骨締結用中空ケーブルも開発されている(例えば、下記特許文献2参照。)。 In addition, a bone fastening hollow cable formed by braiding fibers into a tubular shape having a substantially circular cross section has been developed (for example, see Patent Document 2 below).

 これらの結束糸は、いずれも胸骨外周に沿って巻き回された後、端部間が締結されることによって胸骨を結束するものである。 These tying yarns are all wound around the outer circumference of the sternum, and then the ends are fastened to bind the sternum.

特開2003‐79632号公報JP 2003-79632 A 特開2008‐43431号公報JP 2008-43431 A

 前記結束糸のうち、単線のステンレスワイヤからなるものは、断面形状が円形の線条体であることから、胸骨結束作業時における胸骨周りに通過させる際の組織損傷リスクが少なくなるといった利点がある反面、胸骨周りに縛り付ける際の力加減が難しく、胸骨に対して線接触する前記結束糸が胸骨に食い込み、患者に違和感や圧痛を生じさせる場合があった。 Among the tying yarns, those made of a single wire stainless steel wire have an advantage that the risk of tissue damage when passing around the sternum during sternum bundling work is reduced because the cross-sectional shape is a striate having a circular shape. On the other hand, it is difficult to adjust the force when tying around the sternum, and the tying thread that makes a line contact with the sternum bites into the sternum and sometimes causes the patient to feel uncomfortable or tender.

 一方、前記結束糸のうち、帯状のステンレス板からなるものは、胸骨の外周面と面接触した状態にて胸骨周りに縛り付けることができることから、胸骨の固定は比較的安定的に行い得る。しかしながら、帯状のステンレス板からなる前記結束糸は、面方向にのみ湾曲し、エッジ方向へ湾曲しないものであることから、胸骨結束時に胸骨周りに通過させる際の作業性に劣る。しかも運針時にエッジにて胸骨周りの組織損傷を起こし易く、その止血処置により、手術時間が長くなる傾向があった。 On the other hand, among the tying yarns, those made of a belt-shaped stainless steel plate can be tied around the sternum while being in surface contact with the outer peripheral surface of the sternum, so that the sternum can be fixed relatively stably. However, the binding yarn made of a belt-like stainless steel plate is curved only in the surface direction and not curved in the edge direction, so that it is inferior in workability when passing around the sternum when binding the sternum. In addition, tissue damage around the sternum is likely to occur at the edge during hand movement, and the hemostatic treatment tends to increase the operation time.

 又、単線のステンレスワイヤや帯状のステンレス板からなる前記結束糸は、いずれも伸縮性がないため、結束後に緩みが生じ、胸骨の結束が不十分となる場合もある。 In addition, since the binding yarn made of a single wire stainless steel wire or a belt-like stainless steel plate is not stretchable, loosening may occur after binding, and the sternum may be insufficiently bound.

 この点につき、前記特許文献1に記載の胸骨縫合用材料は、伸縮性があることから、結束後の緩みの発生は比較的少なくなる利点がある。しかしながら、前記特許文献1に記載の胸骨縫合用材料は、結束時にテンションがかけられると線条体となるため、前述の単線のステンレスワイヤからなるものと同様、胸骨に対して線接触し、胸骨に食い込む場合がある。 In this regard, since the material for suturing the sternum described in Patent Document 1 is stretchable, there is an advantage that the occurrence of loosening after binding is relatively reduced. However, since the material for suturing the sternum described in Patent Document 1 becomes a striatum when tension is applied at the time of tying, it makes line contact with the sternum as in the case of the aforementioned single wire stainless steel wire, and the sternum May bite into.

 なお、前記特許文献1には、胸骨内に位置する中央部分をテープ状の平織りとする旨も開示されているが、このような形状とした場合にあっては、前述の帯状のステンレス板からなるものと同様、運針時にエッジにて組織損傷を起こし易いものとなる。 In addition, although the patent document 1 discloses that the central portion located in the sternum is a tape-shaped plain weave, in the case of such a shape, the above-described belt-shaped stainless steel plate is used. Like this, tissue damage is likely to occur at the edge during hand movement.

 一方、前記特許文献2に記載の骨締結用中空ケーブルは、運針時において円形の断面形状となり、組織損傷のリスクを小さくすると共に、結束時において帯状に変形し、骨の陥没や損傷を生じ難くする利点がある。しかしながら、前記特許文献2に記載の骨締結用中空ケーブルは、平織、又は斜文織によって、繊維を編組していることから、長さ方向への伸縮性が殆ど無く、単線のステンレスワイヤや帯状のステンレス板からなる前記結束糸と同様、結束後に緩みが生じ、胸骨の結束が不十分となる場合がある。 On the other hand, the bone fastening hollow cable described in Patent Document 2 has a circular cross-sectional shape at the time of hand movement, reduces the risk of tissue damage, and is deformed into a band shape at the time of binding, so that bone collapse and damage are less likely to occur. There are advantages to doing. However, since the hollow cable for bone fastening described in Patent Document 2 is braided by plain weave or oblique weave, there is almost no stretchability in the length direction, and a single wire stainless steel wire or strip As in the case of the binding yarn made of a stainless steel plate, loosening may occur after binding, and the sternum may be insufficiently bound.

 本発明は前記技術的課題に鑑みて開発されたものであり、運針時における骨周りに通過させる際に骨周囲に存する組織に対する損傷のリスクが少なく、且つ骨の結束を安定的に行うことができる新規な骨結束用索体、及び骨結束用索体の製造方法を提供することを目的とする。 The present invention has been developed in view of the above technical problem, and can reduce the risk of damage to the tissue existing around the bone when passing around the bone at the time of hand movement, and can stably bind the bone. An object of the present invention is to provide a novel bone binding cord and a method for producing the bone binding cord.

 前記技術的課題を解決するために、本発明の骨結束用索体は、縦断裂した骨を結束する際に用いられる骨結束用索体であって、金属製フィラメントの単線、又は金属製フィラメントの収束線からなる基本線が複数本、互いに交差された状態にて編組された索体本体を具備してなり、運針時には、前記索体本体の断面形状が円形又は楕円形を維持した状態にて長さ方向に伸縮し、且つ、骨の結束時には平板状に偏平変形し、もって前記骨の表面に対して面接触し得るように、前記索体本体が、前記基本線を筒編みすることによって構成された網状の周壁を有する中空の編組体となされ、前記周壁を構成する前記基本線の各々が前記周壁に沿って螺旋状に配されてなることを特徴とする(以下、本発明索体と称する。)。 In order to solve the above technical problem, the bone uniting cord of the present invention is a bone uniting cord used when bundling longitudinally torn bones, and is a single wire of a metal filament or a metal filament A plurality of basic lines composed of convergent lines, comprising a cord body that is braided in a state of crossing each other, and during handling, the cross-sectional shape of the cord body maintains a circular or elliptical shape. The cord body is knitted into the basic line so that it can be expanded and contracted in the length direction and flatly deformed into a flat plate shape when the bones are bound, so that it can come into surface contact with the surface of the bone. A hollow braided body having a net-like peripheral wall configured by the above-described structure, and each of the basic lines constituting the peripheral wall is spirally arranged along the peripheral wall (hereinafter referred to as the present invention cord). Called the body).

 本発明索体においては、前記基本線が、複数本の金属製フィラメントを各々長さ方向に沿って隣接させた並列配置型の収束線となされたものが好ましい態様となる(以下、この態様を本発明第一索体と称する。)。 In the cord of the present invention, the basic line is preferably a parallel arrangement type converging line in which a plurality of metal filaments are adjacent to each other along the length direction (hereinafter referred to as this mode). This is called the first cord of the present invention).

 本発明第一索体においては、前記基本線が、二本、又は三本の金属製フィラメントを各々長さ方向に沿って隣接させた並列配置型の収束線となされたものが好ましい態様となる。 In the first cord of the present invention, the basic line is preferably a parallel-arranged convergent line in which two or three metal filaments are adjacent to each other along the length direction. .

 本発明第一索体においては、前記金属製フィラメントが、9~300μmの線径を有するものが好ましい態様となる。 In the first cord of the present invention, it is preferable that the metal filament has a wire diameter of 9 to 300 μm.

 本発明索体においては、前記基本線が、複数本の金属製フィラメントを撚ることによって形成された撚線型の収束線となされたものが好ましい態様となる(以下、この態様を本発明第二索体と称する。)。 In the cord of the present invention, the basic wire is preferably a twisted wire-type converging wire formed by twisting a plurality of metal filaments (this mode is hereinafter referred to as the second embodiment of the present invention). It is called a cord.)

 本発明第二索体においては、前記基本線が、芯材となる一本の金属製フィラメントの周囲に複数本の金属製フィラメントを巻き付けて形成された有芯撚線型の収束線となされたものが好ましい態様となる。 In the second cord of the present invention, the basic wire is a cored twisted wire type converging wire formed by winding a plurality of metal filaments around a single metal filament as a core material Is a preferred embodiment.

 本発明第二索体においては、前記金属製フィラメントが、3~150μmの線径を有するものが好ましい態様となる。 In the second cord of the present invention, the metal filament having a wire diameter of 3 to 150 μm is a preferred embodiment.

 本発明第二索体においては、前記基本線に、前記基本線の仮想軸芯を中心として捻転するねじれが無いものが好ましい態様となる。 In the second cord of the present invention, it is preferable that the basic line does not have a twist that twists about the virtual axis of the basic line.

 本発明索体においては、下記試験条件によって前記索体本体が引張された際、少なくとも2mm引張するまでに要する引張応力が、15N以下であるものが好ましい態様となる。 In the cord of the present invention, when the cord body is pulled under the following test conditions, a tensile stress required to pull at least 2 mm is 15 N or less.

<試験>
 チャック間距離200mmにて前記索体本体をつかみ、毎分5mmの引張速度で前記索体本体を長さ方向に引張させながら引張応力を測定する。
<Test>
The cord body is held at a chuck distance of 200 mm, and the tensile stress is measured while pulling the cord body in the length direction at a tensile speed of 5 mm per minute.

 本発明索体においては、前記試験条件によって前記索体本体が引張された際、引張応力が100N以下であれば、その後、試験力が付与されない状態とされた際に伸縮性を回復するものが好ましい態様となる。 In the cord of the present invention, when the cord body is pulled according to the test conditions, if the tensile stress is 100 N or less, then the stretchability is restored when the test force is not applied. This is a preferred embodiment.

 本発明の骨結束用索体の製造方法は、前記本発明第二索体を製造する方法であって、前記基本線を編組するに先立ち、前記基本線に対し、軸芯を中心として捻転するねじれを付与し、前記ねじれがほどける方向に向かって前記基本線を編組することを特徴とする。 The method for manufacturing a bundling cord of the present invention is a method of manufacturing the second cord of the present invention, and before braiding the basic line, the basic line is twisted around the axis. A twist is imparted, and the basic line is braided in a direction in which the twist is unwound.

 本発明によれば、運針時における骨周りに通過させる際に骨周囲に存する組織に対する損傷のリスクが少なく、且つ骨の結束を安定的に行うことができる。 According to the present invention, when passing around the bone at the time of hand movement, there is little risk of damage to the tissue existing around the bone, and the bone can be stably bound.

図1(a)は、実施形態1に係る本発明索体の全体構成の概略を示す斜視図  であり、図1(b)は、前記本発明索体における索体本体の伸縮状態を示す断面図で  あり、図1(c)は、前記本発明索体における索体本体の伸縮状態を示す平面図であ  り、図1(d)は、前記本発明索体の索体本体の偏平変形状態を示す断面図である。FIG. 1 (a) is a perspective view showing an outline of the overall configuration of the cord of the present invention according to Embodiment 1, and FIG. 1 (b) is a cross section showing a stretched state of the cord body in the cord of the present invention. Fig. 1 (c) is a plan view showing a stretched state of the cord body in the cord of the present invention, and Fig. 1 (d) is a flat deformation of the cord body of the cord of the present invention. It is sectional drawing which shows a state. 図2(a)は、前記本発明索体にて胸骨を結束した状態を示す平面図であり  、図2(b)は、前記本発明索体を胸骨の周囲に周回させて結束する前の状態を示す  断面図であり、図2(c)は、前記本発明索体にて胸骨を結束する様子を示す断面図  である。FIG. 2 (a) is a plan view showing a state in which the sternum is bound by the cord of the present invention. FIG. 2 (b) is a diagram before the cord of the present invention is wound around the sternum and bound. FIG. 2C is a cross-sectional view showing a state in which the sternum is bound by the cord of the present invention. 図3は、前記本発明索体の伸縮特性を示すグラフである。FIG. 3 is a graph showing the expansion and contraction characteristics of the cord of the present invention. 図4は、従来の結束糸の伸縮特性を示すグラフである。FIG. 4 is a graph showing the expansion / contraction characteristics of a conventional tying yarn. 図5は、実施形態2に係る本発明索体(本発明第一索体)の全体構成の概略  を示す斜視図である。FIG. 5 is a perspective view showing an outline of the overall configuration of the cord of the present invention (the first cord of the present invention) according to Embodiment 2. 図6(a)は、実施形態3に係る本発明索体(本発明第二索体)の全体構成  の概略を示す斜視図であり、図6(b)は、前記本発明索体を構成する基本線を示す  断面図である。FIG. 6A is a perspective view showing an outline of the overall configuration of the cord of the present invention (second cord of the present invention) according to Embodiment 3, and FIG. 6B shows the configuration of the cord of the present invention. It is a sectional view showing a basic line.

 以下、本発明の実施形態を図面を参照して説明するが、本発明はこれらの実施形態に限定されるものではない。 Hereinafter, embodiments of the present invention will be described with reference to the drawings, but the present invention is not limited to these embodiments.

<実施形態1>
 図1(a)は、実施形態1に係る本発明索体1の全体構成の概略を示すものである。この本発明索体1は、索体本体2と、前記索体本体2の一端側に設けられた貫通刃3と、前記索体本体2の他端側に設けられたバックル4と、を具備する。
<Embodiment 1>
FIG. 1A shows an outline of the overall configuration of the cord 1 of the present invention according to the first embodiment. The cable body 1 of the present invention includes a cable body 2, a penetrating blade 3 provided on one end side of the cable body 2, and a buckle 4 provided on the other end side of the cable body 2. To do.

 図1(a)の拡大図(前記索体本体2の中ほどの部分の拡大図)に示すように前記索体本体2は、金属製フィラメント(本実施形態においては、ステンレス製フィラメント)の単線からなる基本線21が複数本(本実施形態においては48本)、互いに交差された状態にて編組されたものである。前記索体本体2は、前記基本線21の各々を筒編みし、前記基本線21の各々が螺旋状に配置されることによって網状の周壁となり、もって、全体として中空の編組体となされたものである。本発明において「筒編み」とは、「輪編み」とも称される縦糸と横糸の区別が無い編み方であり、前記索体本体2を構成する各基本線21を、前記索体本体2の軸芯周りにおいて、同一の螺旋ピッチにて螺旋状に走るように配置しながら各々を互い違いに交差させて編組する編み方を意味する。係る筒編みにて編組された前記索体本体2は、前記索体本体2の軸芯と、前記索体本体2の長さ方向に対して螺旋状に走る各基本線21の走行方向とがなす角が、前記索体本体1のいずれの位置においても等しくなる。 As shown in the enlarged view of FIG. 1 (a) (enlarged view of the middle portion of the cord body 2), the cord body 2 is a single wire of a metal filament (in this embodiment, a stainless steel filament). A plurality of basic lines 21 (48 in this embodiment) are braided so as to cross each other. The cord body 2 is formed by knitting each of the basic wires 21 into a net-like peripheral wall by arranging each of the basic wires 21 in a spiral shape, thereby forming a hollow braided body as a whole. It is. In the present invention, “tubular knitting” is a knitting method called warp knitting that does not distinguish between warp and weft, and each basic line 21 constituting the cord body 2 is connected to the cord body 2. It means a knitting method in which braiding is performed by alternately intersecting each other while being arranged so as to run spirally at the same spiral pitch around the axis. The cord body 2 braided by the tubular knitting has an axis of the cord body 2 and a running direction of each basic line 21 running spirally with respect to the length direction of the cord body 2. The formed angles are equal at any position of the cord body 1.

 前記索体本体2を構成する前記基本線(本実施形態の場合、フィラメントの単線)21の線径(φ)としては、前記索体本体2に要求される強度や太さ、或いは使用される基本線21の本数に応じて適宜決定すれば良く、特に限定されるものではない。前記基本線21の線径(φ)としては、9~300μm(より好ましくは、15~150μm)のものを用いることが好ましい。 The wire diameter (φ) of the basic line (in the case of the present embodiment, a single filament wire) 21 constituting the cord body 2 is used as the strength and thickness required for the cord body 2 or used. What is necessary is just to determine suitably according to the number of the basic lines 21, and it does not specifically limit. The wire diameter (φ) of the basic wire 21 is preferably 9 to 300 μm (more preferably 15 to 150 μm).

 本実施形態においては、前記基本線21としてステンレス製のものが用いられているが、前記基本線21の素材としては、ステンレスの他、例えば、ニッケルチタン合金やチタン合金などの耐食性金属が好適に用いられる。 In the present embodiment, the basic wire 21 is made of stainless steel, but the basic wire 21 is preferably made of a corrosion-resistant metal such as nickel titanium alloy or titanium alloy in addition to stainless steel. Used.

 又、本実施形態においては、都合48本の前記基本線21にて前記索体本体2の周壁を構成しているが、前記周壁を構成する前記基本線21の本数としては、30~100本(より好ましくは、36~96本)の範囲内とすることが好ましい。 Further, in this embodiment, the peripheral wall of the cord body 2 is constituted by 48 basic lines 21 for convenience, but the number of the basic lines 21 constituting the peripheral wall is 30 to 100. (More preferably, it is in the range of 36 to 96).

 前記索体本体2は、結束時の締め付け代を残した状態にて結束対象の骨の外周を周回することができる長さがあれば、その長さについて特に限定されるものではない。前記索体本体2の長さとしては、10~100cm(より好ましくは、15~65cm)とすることが好ましい。 The length of the cord body 2 is not particularly limited as long as the cord body 2 has a length that can circulate around the outer circumference of the bone to be bound in a state where the tightening allowance at the time of binding is left. The length of the cord body 2 is preferably 10 to 100 cm (more preferably 15 to 65 cm).

 図1(b)、(c)に示すように、このような構成を有する前記索体本体2は、長さ方向に沿って引張応力が付加されると、その線径を委縮させながら長さ方向に伸長し、その後、長さ方向に沿う引張応力から解放されると、ほぼ元の状態に弾性的に回復する性質(伸縮性)を有する。又、何らかの対象物に巻き付けられると、図1(d)に示すように、伸縮性を維持したまま偏平し、平板状に変形する性質(偏平変形性)も有する。 As shown in FIGS. 1 (b) and 1 (c), the cord body 2 having such a structure has a length while contracting its wire diameter when a tensile stress is applied along the length direction. When stretched in the direction and then released from the tensile stress along the length direction, it has a property (stretchability) that elastically recovers to its original state. Further, as shown in FIG. 1 (d), when it is wound around a certain object, it has a property of flattening while maintaining stretchability and deforming into a flat plate shape (flat deformation).

 従って、前記索体本体2自体の線径は引張応力に応じて変化するため不定であるが、長さ方向に沿って引張応力(20~100N程度)が付加された際の前記索体本体2自体の線径(Φ)は、0.5~10mm(より好ましくは、1~5mm)の範囲内、引張応力から解放された際(定常時)の前記索体本体2自体の線径(Φ)は、1~20mm(より好ましくは、2~10mm)となるようにすることが好ましい。 Accordingly, the wire diameter of the cord body 2 itself is indefinite because it changes according to the tensile stress, but the cord body 2 when a tensile stress (about 20 to 100 N) is applied along the length direction. The wire diameter (Φ) of itself is within a range of 0.5 to 10 mm (more preferably 1 to 5 mm), and the wire body 2 itself has a wire diameter (Φ 0 ) is preferably 1 to 20 mm (more preferably 2 to 10 mm).

 又、前記索体本体2が平板状に変形された際の幅長としては、0.75~15mm(より好ましくは、1.5~7.5mm)となるようにすることが好ましい。 In addition, the width when the cord body 2 is deformed into a flat plate shape is preferably 0.75 to 15 mm (more preferably 1.5 to 7.5 mm).

 前記貫通刃3は、結束対象たる骨の周囲に存する生体組織に突き刺して、前記索体本体2を周回させるための通路を切開するためのものであり、先端側が鋭利となされた刃31と、湾曲する胴体部32と、末端側の基端部33とを具備する。前記貫通刃3は、前記基端部33が前記索体本体2の一端側に挿入された状態にて前記索体本体2に溶接固定されており、この際、前記索体本体2の一端側は、前記基端部33の外径に応じて線径を委縮させた状態となされている。 The penetrating blade 3 is for piercing a living tissue existing around a bone to be bound, and for incising a passage for circling the cord body 2, and a blade 31 having a sharp tip end side; A curved body part 32 and a proximal end part 33 on the distal side are provided. The penetrating blade 3 is welded and fixed to the cord body 2 in a state where the base end portion 33 is inserted into one end side of the cord body 2, and at this time, one end side of the cord body 2. Is in a state where the wire diameter is contracted according to the outer diameter of the base end portion 33.

 前記バックル4は、平板状の金属製板材であり、前記索体本体2に溶接固定されている。前記バックル4には、前記索体本体2が挿通可能となされた二つの長穴41、42が設けられており、各長穴41、42には、前記索体本体2に噛合し得るノコギリ刃状の返し部41a、42aが設けられている。骨固定時において、このバックル4が異物感の原因とならないように、前記バックル4は、前記索体本体2と溶接固定された状態にて、厚さ2mm以下となるように構成することが好ましい。 The buckle 4 is a flat metal plate material, and is fixed to the cord body 2 by welding. The buckle 4 is provided with two long holes 41 and 42 into which the cable body 2 can be inserted, and each of the long holes 41 and 42 has a saw blade that can mesh with the cable body 2. Shaped return portions 41a and 42a are provided. It is preferable that the buckle 4 is configured to have a thickness of 2 mm or less in a state where the buckle 4 is welded and fixed to the cord body 2 so that the buckle 4 does not cause a sense of foreign matter during bone fixation. .

 次に、図2を参照しながら、前記本発明索体1の使用方法について、開胸手術時において切断された胸骨5の結束作業を例に挙げて説明する。 Next, with reference to FIG. 2, a method of using the above-described cord 1 of the present invention will be described by taking as an example a binding operation of the sternum 5 cut during the thoracotomy.

 開胸手術においては、まず、胸部を胸骨5の中央にて縦方向に切断して開き、必要な処置を行った後、切断した胸骨5を接近させて仮閉じする。 In the thoracotomy, first, the chest is cut and opened in the longitudinal direction at the center of the sternum 5, and after necessary treatment, the cut sternum 5 is approached and temporarily closed.

 次に、前記本発明索体1の一端に存する前記貫通刃3を肋骨51間に突き刺し、胸骨5の周囲に存する組織を切開しながら、前記貫通刃3に続く前記索体本体2を胸骨5の周囲に周回させる。 Next, the penetrating blade 3 existing at one end of the cord 1 of the present invention is pierced between the ribs 51, and the cord body 2 following the penetrating blade 3 is inserted into the sternum 5 while incising the tissue existing around the sternum 5. Orbit around.

 前記本発明索体1における前記索体本体2を胸骨5の周囲に周回した後は、前記索体本体2の他端側に存する前記バックル4を胸骨5の中央に位置させ、胸骨5の周囲を周回して術者の手元側に戻ってきた前記貫通刃3を前記バックル4に存する前記長穴41に通過させ、続く前記索体本体2を前記長穴41に挿通させる(図2(b)参照)。この状態で前記索体本体2の一端側を引っ張ると、前記索体本体2が伸長しながら胸骨5の周囲に押し付けられて平板状に偏平変形する(図2(c)参照)。引き伸ばされて平板状に偏平変形した前記索体本体2は、依然伸縮性を有していることから、収縮する方向に付勢されているが、前記索体本体2は、前記長穴41に設けられた前記返し部41aに周壁を構成する網が引掛かかるため、胸骨5の周囲に巻き付けられた状態にて固定される。 After the cord body 2 in the cord 1 of the present invention circulates around the sternum 5, the buckle 4 existing on the other end side of the cord body 2 is positioned at the center of the sternum 5, Is passed through the elongated hole 41 in the buckle 4 and the subsequent cord body 2 is inserted into the elongated hole 41 (FIG. 2B). )reference). When one end side of the cord body 2 is pulled in this state, the cord body 2 is pressed around the sternum 5 while being stretched to be flattened into a flat shape (see FIG. 2C). The cord body 2 that has been stretched and flattened into a flat plate shape is still stretchable, so that the cord body 2 is urged in a contracting direction. Since the net | network which comprises a surrounding wall is hooked in the said return part 41a provided, it is fixed in the state wound around the sternum 5.

 患者の骨密度や年齢に応じて、適当な弾性力を保った状態にて前記本発明索体1を胸骨5の周囲に固定した後は、前記貫通刃3を前記バックル4に存するもう一つの長穴42に通過させ、続く前記索体本体2を前記長穴42に挿通する。その後、前記索体本体2が緩まないことを確認したうえで、前記索体本体2の一端側の余分な部分を切断して前記貫通刃3を前記索体本体2から切り離す(図2(a)参照)。 After fixing the cord 1 of the present invention around the sternum 5 while maintaining an appropriate elastic force according to the bone density and age of the patient, the penetrating blade 3 is another part of the buckle 4. Passing through the elongated hole 42, the subsequent cord body 2 is inserted into the elongated hole 42. Thereafter, after confirming that the cord body 2 is not loosened, an excessive portion on one end side of the cord body 2 is cut to separate the penetrating blade 3 from the cord body 2 (FIG. 2 (a )reference).

 本発明索体1は、運針時において、術者の引っ張りに応じて前記索体本体2が長さ方向に伸縮し、且つ、その断面形状が委縮しつつ、円形若しくは楕円形の線条体形状を維持するため、骨周囲に存する組織に必要以上の損傷を与えない。又、骨の結束後は、前記索体本体2の収縮力によってその結束状態を維持することができるため、骨を複数本の本発明索体1にて結束する際に、本発明索体1の各々において結束力に多少の差が生じていても、緩みやガタが生じることがなく、良好な結束状態を維持することができる。 The cord 1 of the present invention has a circular or oval striated shape while the cord body 2 expands and contracts in the length direction in response to the operator's pulling and the cross-sectional shape is contracted during hand movement. To prevent damage to the tissue around the bone more than necessary. Further, after the bones are bound, since the binding state can be maintained by the contraction force of the cord body 2, the cords of the present invention 1 are used when the bones are bound by a plurality of cords of the present invention 1. Even if there is a slight difference in the binding force in each of these, looseness and play do not occur, and a good binding state can be maintained.

 又、本発明索体1は、骨の周囲に巻き付けられた際に、平板状に変形するため、骨の外周面に対して面接触した状態にて固定される。そのため、骨に対して食い込んだりすることがなく、術後の違和感や圧痛を患者に与えることがない。 Moreover, since the cord 1 of the present invention is deformed into a flat plate shape when wound around the bone, it is fixed in a state of surface contact with the outer peripheral surface of the bone. Therefore, it does not bite into the bone and does not give the patient a feeling of discomfort or tenderness after the operation.

 更に、本発明索体1は、前記索体本体2の収縮力によって骨に固定されるため、術後に患者がくしゃみしたりせきしたりして瞬発的な力が加えられても、柔軟に伸縮して対応することができ、骨を損傷するリスクが少ないものとなる。 Furthermore, since the cord 1 of the present invention is fixed to the bone by the contraction force of the cord body 2, even if a patient sneezes or crushes after the operation and an instantaneous force is applied, the cord is flexible. It can be expanded and contracted to reduce the risk of damaging bone.

 図3のグラフは、下記試験条件によって、前記本発明索体1における前記索体本体2の伸縮特性をチャートにて示したものであり、縦軸が前記索体本体2に付加された引張応力、横軸が引張距離(ストローク)を示す。 The graph of FIG. 3 is a chart showing the expansion and contraction characteristics of the cord body 2 in the cord of the present invention 1 under the following test conditions, and the vertical axis indicates the tensile stress applied to the cord body 2. The horizontal axis indicates the tensile distance (stroke).

<試験>
 チャック間距離200mmにて前記索体本体2をつかみ、毎分5mmの引張速度で前記索体本体2を長さ方向に伸長させた際の引張応力を測定する(試験機:SHIMADZU  AG‐IS 50kN)。
<Test>
Grasping the cable body 2 at a chuck distance of 200 mm, and measuring the tensile stress when the cable body 2 is stretched in the length direction at a tensile speed of 5 mm per minute (Testing machine: SHIMADZU AG-IS 50 kN ).

 図3のグラフに示すように、前記索体本体2は、長さ方向に沿って引張応力が付加されると、引張の初期段階(図中(A)の段階)において、ほとんど抵抗なく引き伸ばされる。この段階は、引張によって、前記索体本体2の周壁を構成する前記基本線21の各々の螺旋半径が小さくなると共に螺旋ピッチが長くなっている段階であり、螺旋状に配された前記基本線21の線形弾性力、及び各基本線21の交点において生じる摩擦力以外は、引張応力に対して抗しないためである。本発明においては、この図中(A)の段階が、少なくとも前記索体本体2を2mm(より好ましくは、2.5mm)引張するまで継続し、且つ、その際に要する引張応力が、15N以下(より好ましくは10N以下)であることが好ましい。この数値目標は、主に前記索体本体2の周壁を構成する前記基本線21の本数や線径、及び定常時における前記基本線21の螺旋半径や螺旋ピッチなどを適宜選択することによって達成することができる。 As shown in the graph of FIG. 3, when a tensile stress is applied along the length direction, the cord body 2 is stretched with almost no resistance in the initial stage of tension (stage (A) in the figure). . This stage is a stage in which the spiral radius of each of the basic lines 21 constituting the peripheral wall of the cord body 2 is reduced and the helical pitch is increased by tension, and the basic lines arranged in a spiral shape are formed. This is because the linear elastic force of 21 and the frictional force generated at the intersection of the basic lines 21 do not resist tensile stress. In the present invention, the stage (A) in this figure continues at least until the cord body 2 is pulled 2 mm (more preferably 2.5 mm), and the tensile stress required at that time is 15 N or less. (More preferably 10N or less). This numerical target is achieved mainly by appropriately selecting the number and diameter of the basic lines 21 constituting the peripheral wall of the cord body 2 and the spiral radius and spiral pitch of the basic lines 21 in a steady state. be able to.

 図中(A)の段階を超えて、引張応力が付加されると、引張応力に対する伸長度が低下し、引張応力が増加してもほとんど前記索体本体2は伸長しなくなる(図中(B)の段階)。これは、前記索体本体2が引張されて、前記索体本体2の周壁を構成する前記基本線21の各々の螺旋半径が小さくなると共に螺旋ピッチが長くなると、隣接する前記基本線21同志が近接し、接触し始め、前記基本線21の自由度が喪失されるためである。この際、引張応力に抗する力は、主に前記基本線21各々が有する引張強度の総和となる。なお、図中(B)の段階で、前記索体本体21を引張応力から解放すると、多少の断面形状の委縮(線径の減少)は生じるが、ほぼ元の状態を回復する。本発明においては、少なくとも引張応力が100N以下(より好ましくは、200N以下)の間は、この図中(B)の段階に属していることが好ましい。この数値目標は、主に前記索体本体2の周壁を構成する前記基本線21の本数や線径、引張強度などを適宜選択することによって達成することができる。 If tensile stress is applied beyond the stage (A) in the figure, the elongation with respect to the tensile stress decreases, and the cord body 2 hardly expands even if the tensile stress increases ((B in the figure) ) Stage). This is because when the cord body 2 is pulled and the spiral radius of each of the basic lines 21 constituting the peripheral wall of the cord body 2 is reduced and the spiral pitch is increased, the adjacent basic lines 21 are This is because the proximity of the base line 21 is lost due to the approach and contact. At this time, the force against the tensile stress is mainly the sum of the tensile strengths of the basic lines 21. When the cord body 21 is released from the tensile stress at the stage (B) in the figure, the cross-sectional shape is somewhat reduced (the wire diameter is reduced), but the original state is almost restored. In the present invention, it is preferable that at least when the tensile stress is 100 N or less (more preferably, 200 N or less), it belongs to the stage (B) in this figure. This numerical target can be achieved by appropriately selecting the number, the wire diameter, the tensile strength, and the like of the basic wires 21 mainly constituting the peripheral wall of the cord body 2.

 なお、図中(B)の段階を超えて、更に引張応力が付加されると、前記索体本体2を構成する前記基本線21に回復不可能な伸びが生じ(図中(c)の段階)、最終的には、前記索体本体2が断線する(図中(D)の段階)が、実際の結束作業時や骨に固定された状態において、前記索体本体2に対し、図中(C)の段階や図中(D)の段階が生じることは考え難い。 If a tensile stress is further applied beyond the stage (B) in the figure, unrecoverable elongation occurs in the basic line 21 constituting the cord body 2 (stage (c) in the figure). ) Eventually, the cord body 2 is disconnected (stage (D) in the figure), but the cord body 2 is not connected to the cord body 2 during actual binding work or in a state of being fixed to the bone. It is unlikely that the stage (C) or the stage (D) in the figure occurs.

 即ち、本発明索体1は、容易に引張することができる図中(A)の段階と、伸縮性を回復し得る図中(B)の段階を有することから、作業性が良好で、且つ、安定的な結束状態を達成することができるのである。 That is, the cord 1 of the present invention has a stage of (A) in the figure that can be easily pulled and a stage of (B) in the figure that can restore the stretchability. Thus, a stable binding state can be achieved.

 参考として、同試験条件下で測定した、従来の結束糸(ステンレス製の帯状平板タイプ)の伸縮特性を図4に示す。図4のチャートに示すように、従来の結束糸は、長さ方向に引張されるとすぐさま回復不可能な延伸を生じ、伸縮性をほとんど示さないことが認められた。 As a reference, the expansion and contraction characteristics of a conventional tying yarn (stainless steel belt-like flat plate type) measured under the same test conditions are shown in FIG. As shown in the chart of FIG. 4, it was recognized that the conventional tying yarn produced an unrecoverable stretch as soon as it was pulled in the length direction, and showed almost no stretchability.

<実施形態2>
 図5は、実施形態2に係る本発明第一索体11の全体構成の概略を示すものである。この本発明第一索体11は、索体本体2と、前記索体本体2の一端側に設けられた貫通刃3と、前記索体本体2の他端側に設けられたバックル4と、を具備する。
<Embodiment 2>
FIG. 5 shows an outline of the overall configuration of the first rope body 11 of the present invention according to the second embodiment. The first cable body 11 of the present invention includes a cable body 2, a penetrating blade 3 provided on one end side of the cable body 2, a buckle 4 provided on the other end side of the cable body 2, It comprises.

 前記索体本体2は、複数本(本実施形態においては二本)の金属製フィラメント(本実施形態においては、ステンレス製のフィラメント)Fを互いに長さ方向に沿って隣接させた並列配置型の収束線からなる基本線21が複数本(本実施形態においては48本)、筒編みによって、互いに交差された状態にて編組されたものである(図5の拡大図参照)。前記索体本体2は、基本線21として並列配置型の収束線を用いた以外は、前記実施形態1と同様の構成を有する。 The cord body 2 is of a parallel arrangement type in which a plurality (two in the present embodiment) of metal filaments (stainless steel filaments in the present embodiment) F are adjacent to each other along the length direction. A plurality of basic lines 21 composed of convergent lines (48 in the present embodiment) are braided so as to cross each other by cylindrical knitting (see an enlarged view of FIG. 5). The cord body 2 has the same configuration as that of the first embodiment except that a parallel arrangement type convergence line is used as the basic line 21.

 前記基本線21を構成する金属製フィラメントFの線径としては、9~300μm(より好ましくは、15~150μm)のものを用いることが好ましい。 The wire diameter of the metal filament F constituting the basic wire 21 is preferably 9 to 300 μm (more preferably 15 to 150 μm).

 前記貫通刃3、及び前記バックル4は、前記実施形態1において用いたものと同様のものであり、前記実施形態1と同様の手段にて前記索体本体2に固定されている。 The penetrating blade 3 and the buckle 4 are the same as those used in the first embodiment, and are fixed to the cord body 2 by the same means as in the first embodiment.

 このような構成を有する本発明第一索体11は、前記基本線21として並列配置型の収束線を用いているため、何らかの対象物に巻き付けられて平板状に変形された際、金属製フィラメント単線からなる基本線21を用いて作成された前記実施形態1に係る本発明索体1と比較して、エッジ部分の鋭利さが緩和される。 Since the first cable body 11 of the present invention having such a configuration uses a parallel arrangement type converging line as the basic line 21, when it is wound around some object and deformed into a flat plate shape, a metal filament The sharpness of the edge portion is reduced as compared with the cord 1 of the present invention according to the first embodiment created using the basic line 21 made of a single wire.

 これにより、骨の周囲に巻き回された際に、骨や骨周囲に存する組織に対して損傷を与えるリスクがより小さくなる利点が生じる。 This provides the advantage of less risk of damaging the bone and tissue surrounding the bone when it is wound around the bone.

 ところで、並列配置型の収束線を基本線21として作成された本発明第一索体11は、係る収束線を構成する金属製フィラメントFの数が多くなればなるほど、何らかの対象物に巻き付けられて平板状に偏平変形された際に、エッジ部分の鋭利さがより緩和される傾向があることが確認されている。 By the way, the first cord 11 of the present invention created with the parallel arrangement type convergence line as the basic line 21 is wound around a certain object as the number of metal filaments F constituting the convergence line increases. It has been confirmed that the sharpness of the edge portion tends to be more relaxed when flattened into a flat plate shape.

 但し、係る収束線を構成する金属製フィラメントF自体には伸縮性がほとんどないため、数多くの金属製フィラメントFを全て同一条件下で束ねることは非常に困難となる。言い換えれば、数多くの金属製フィラメントFを隣接させた並列配置型の収束線には、係る収束線を構成する金属製フィラメントFの一部に撓み等が生じ易くなる。撓んだ金属製フィラメントFは単独で断裂し易く、断裂した金属製フィラメントFは本発明第一索体1の周壁においてささくれを生じさせる原因となる。 However, since the metal filaments F constituting the convergence line have almost no stretchability, it is very difficult to bundle all the metal filaments F under the same conditions. In other words, a parallel arrangement type converging line in which a number of metallic filaments F are adjacent to each other is likely to be bent or the like in a part of the metallic filaments F constituting the converging line. The bent metal filament F is easily broken by itself, and the broken metal filament F becomes a cause of raising on the peripheral wall of the first cord body 1 of the present invention.

 そのため、本発明において、並列配置型の収束線を基本線21として用いるにあたっては、二本、又は三本の金属製フィラメントFを各々長さ方向に沿って隣接させた並列配置型の収束線を用いることが好ましい。 Therefore, in the present invention, when using a parallel arrangement type convergence line as the basic line 21, a parallel arrangement type convergence line in which two or three metal filaments F are adjacent to each other in the length direction is used. It is preferable to use it.

 その余は、前記実施形態1において説明した事項と同様のため、繰り返しの説明を避けるべく、ここでは説明を省略する。 Since the remainder is the same as that described in the first embodiment, the description is omitted here to avoid repeated description.

<実施形態3>
  図6(a)は、実施形態3に係る本発明第二索体12の全体構成の概略を示すものである。この本発明第二索体12は、索体本体2と、前記索体本体2の一端側に設けられた貫通刃3と、前記索体本体2の他端側に設けられたバックル4と、を具備する。
<Embodiment 3>
FIG. 6A shows an outline of the overall configuration of the second cord 12 of the present invention according to the third embodiment. The second cord body 12 of the present invention includes a cord body 2, a penetrating blade 3 provided on one end side of the cord body 2, a buckle 4 provided on the other end side of the cord body 2, It comprises.

 前記索体本体2は、複数本(本実施形態においては七本)の金属製フィラメント(本実施形態においては、ステンレス製のフィラメント)Fを撚ることによって形成された撚線型の収束線からなる基本線21が複数本(本実施形態においては48本)、筒編みによって、互いに交差された状態にて編組されたものである(図6(a)の拡大図参照)。前記索体本体2は、基本線21として撚線型の収束線を用いた以外は、前記実施形態1と同様の構成を有する。 The cord body 2 is composed of a twisted wire-type converging wire formed by twisting a plurality of (seven in this embodiment) metal filaments (stainless steel filaments in this embodiment) F. A plurality of the basic lines 21 (48 in the present embodiment) are braided so as to cross each other by cylindrical knitting (see an enlarged view of FIG. 6A). The cord body 2 has the same configuration as that of the first embodiment except that a twisted-type converging wire is used as the basic wire 21.

 前記基本線21に用いられる金属製フィラメントFの線径としては、3~150μm(より好ましくは、9~100μm)のものを用いることが好ましい。 The wire diameter of the metal filament F used for the basic wire 21 is preferably 3 to 150 μm (more preferably 9 to 100 μm).

 前記貫通刃3、及び前記バックル4は、前記実施形態1において用いたものと同様のものであり、前記実施形態1と同様の手段にて前記索体本体2に固定されている。 The penetrating blade 3 and the buckle 4 are the same as those used in the first embodiment, and are fixed to the cord body 2 by the same means as in the first embodiment.

 このような構成を有する本発明第二索体12は、前記基本線21として撚線型の収束線を用いているため、何らかの対象物に巻き付けられて平板状に偏平変形された際、金属製フィラメント単線からなる基本線21を用いて作成された前記実施形態1に係る本発明索体1と比較して、エッジ部分の鋭利さが緩和される。 Since the second cord 12 of the present invention having such a configuration uses a twisted-type converging wire as the basic wire 21, when it is wound around some object and flattened into a flat plate shape, a metal filament The sharpness of the edge portion is reduced as compared with the cord 1 of the present invention according to the first embodiment created using the basic line 21 made of a single wire.

 これにより、骨の周囲に巻き回された際に、骨や骨周囲に存する組織に対して損傷を与えるリスクがより小さくなる利点が生じる。 This provides the advantage of less risk of damaging the bone and tissue surrounding the bone when it is wound around the bone.

 又、撚線型の収束線は、線径が同じ単線の金属製フィラメントと比較して引張応力に対する物理的強度が高くなるため、前述した図3における(b)の段階における引張応力の最大値が高くなる利点もある。 In addition, since the twisted wire type converging wire has a higher physical strength against tensile stress than a single-filament metal filament having the same wire diameter, the maximum value of the tensile stress at the stage (b) in FIG. There is also an advantage of higher.

 なお、本発明において、前記基本線21を構成する金属製フィラメントFの撚糸方法としては、特に限定されるものではない。前記基本線21を構成する金属製フィラメントFの撚糸方法としては、例えば、Z撚りと称される撚糸方法や、S撚りと称される撚糸方法を好適に用いることができる。 In the present invention, the twisting method of the metal filament F constituting the basic wire 21 is not particularly limited. As a twisting method of the metal filament F constituting the basic wire 21, for example, a twisting method called Z twisting or a twisting method called S twisting can be suitably used.

 特に、本発明において、前記基本線21として撚線型の収束線を用いるにあたっては、図6(b)に示すような、芯材となる一本の金属製フィラメントFOの周囲に複数の金属製フィラメントFを巻き付けて形成された有芯撚線型の収束線を用いることが好ましい。 In particular, in the present invention, when a stranded wire-type converging wire is used as the basic wire 21, a plurality of metal filaments are disposed around one metal filament FO as a core as shown in FIG. It is preferable to use a cored strand type converging wire formed by winding F.

 この有芯撚線型の収束線は、収束線の軸芯に沿って、芯材となる一本の金属製フィラメントFOが配置されていることから、芯材の無い撚線型の収束線と比較して、引張応力に対する物理的強度がより高くなる利点がある。 This cored stranded wire type converging wire is compared with a stranded wire type converging wire without a core material because a single metal filament FO as a core material is arranged along the axis of the converging wire. Thus, there is an advantage that the physical strength against tensile stress is higher.

 ところで、本発明第二索体12のように、前記基本線21として撚線型の収束線を、筒編みによって編組して前記索体本体2を作成すると、前記索体本体2の周壁に螺旋状に配置される前記基本線21において、その仮想軸芯を中心として捻転するねじれが生じる。このねじれは、前記基本線21を構成する金属フィラメントFの断裂の原因となる。そして、断裂した金属製フィラメントFは本発明索体1の周壁においてささくれを生じさせる原因となる。 By the way, like the second cord body 12 of the present invention, when the cord body 2 is created by braiding a twisted-type converging wire as the basic wire 21 by tubular knitting, the peripheral wall of the cord body 2 is spirally formed. In the basic line 21 arranged at the center, a twist that twists around the virtual axis is generated. This twist causes the metal filament F constituting the basic wire 21 to be broken. Then, the broken metal filament F becomes a cause to cause a scissors on the peripheral wall of the cord 1 of the present invention.

 そこで、本発明においては、前記基本線21として撚線型の収束線を筒編みによって編組して前記索体本体2を作成するにあたり、前記基本線21を編組するに先立って、前記基本線21に対し、軸芯を中心として捻転するねじれを付与し、前記ねじれがほどける方向に向かって前記基本線21を編組することが好ましい。 Therefore, in the present invention, when creating the cord body 2 by braiding a twisted-wire-type converging line as the basic line 21 by tubular knitting, the basic line 21 is formed before the basic line 21 is braided. On the other hand, it is preferable to impart a twist that twists about the axis, and braid the basic line 21 in a direction in which the twist is unwound.

 前記基本線21に対して前もって付与されるねじれの回数は、編組の際に、前記基本線21が螺旋状に巻き回される回数に応じて決定すれば良い。 The number of twists applied in advance to the basic line 21 may be determined according to the number of times the basic line 21 is spirally wound during braiding.

 このようにして作成された前記索体本体2は、その周壁を構成する前記基本線21においてねじれがなくなり、前記基本線21を構成する金属フィラメントFの断裂のリスクが小さくなる。 The thus produced cord body 2 is not twisted in the basic line 21 constituting the peripheral wall, and the risk of the metal filament F constituting the basic line 21 is reduced.

 その余は、前記実施形態1において説明した事項と同様のため、繰り返しの説明を避けるべく、ここでは説明を省略する。 Since the remainder is the same as that described in the first embodiment, the description is omitted here to avoid repeated description.

 なお、本発明は、その精神又は主要な特徴から逸脱することなく、他のいろいろな形態で実施することができる。そのため、上述の実施形態はあらゆる点で単なる例示に過ぎず、限定的に解釈してはならない。本発明の範囲は特許請求の範囲によって示すものであって、明細書本文には何ら拘束されない。更に、特許請求の範囲の均等範囲に属する変形や変更は、すべて本発明の範囲内のものである。 Note that the present invention can be implemented in various other forms without departing from the spirit or main features thereof. Therefore, the above-mentioned embodiment is only a mere illustration in all points, and should not be interpreted limitedly. The scope of the present invention is indicated by the claims, and is not restricted by the text of the specification. Further, all modifications and changes belonging to the equivalent scope of the claims are within the scope of the present invention.

 本発明索体は、縦に断裂した骨の結束に用いられるものであり、特に、開胸手術において切断された胸骨の結束に好適に用いられる。 The cord of the present invention is used for bundling vertically fractured bones, and particularly suitable for bundling sternum cut in thoracotomy.

1 本発明索体(骨結束用索体)
11 本発明第一索体(骨結束用索体)
12 本発明第二索体(骨結束用索体)
2 索体本体
21 基本線
3 貫通刃
31 刃
32 胴体部
33 基端部
4 バックル
41 長穴
42 長穴
5 胸骨
51 肋骨
F 金属製フィラメント
F0 金属製フィラメント(芯材)
 
1 Present invention cord (bone binding cord)
11 First cord body of the present invention (bone binding cord)
12 The second cord of the present invention (the cord for bundling)
2 Cord body 21 Basic line 3 Penetrating blade 31 Blade 32 Body portion 33 Base end portion 4 Buckle 41 Long hole 42 Long hole 5 Sternal bone 51 Rib F Metal filament F0 Metal filament (core material)

Claims (11)

 縦断裂した骨を結束する際に用いられる骨結束用索体であって、
 金属製フィラメントの単線、又は金属製フィラメントの収束線からなる基本線が、複数本、互いに交差された状態にて編組された索体本体を具備してなり、
 運針時には、前記索体本体の断面形状が円形又は楕円形を維持した状態にて長さ方向に伸縮し、且つ、骨の結束時には平板状に偏平変形し、もって前記骨の表面に対して面接触し得るように、
 前記索体本体が、前記基本線を筒網することによって構成された網状の周壁を有する中空の編組体となされ、前記周壁を構成する前記基本線の各々が前記周壁に沿って螺旋状に配されてなることを特徴とする骨結束用索体。
A bundling cord used for bundling longitudinally fractured bones,
A single wire of a metal filament, or a basic wire composed of a convergent wire of a metal filament, comprising a plurality of cord bodies that are braided in a state of crossing each other,
When operating the hand, the cord body expands and contracts in the length direction while maintaining a circular or elliptical cross-sectional shape, and when the bone is bound, it flattenes into a flat plate shape, so that it faces the surface of the bone. So that you can contact
The cord body is formed as a hollow braided body having a net-like peripheral wall formed by connecting the basic lines, and each of the basic lines constituting the peripheral wall is spirally arranged along the peripheral wall. A bone uniting cord body characterized by being made.
 請求項1に記載の骨結束用索体において、
 前記基本線が、複数本の金属製フィラメントを各々長さ方向に沿って隣接させた並列配置型の収束線となされた骨結束用索体。
In the bone binding cord according to claim 1,
The bone binding cord, wherein the basic line is a parallel arrangement type converging line in which a plurality of metal filaments are adjacent to each other along the length direction.
 請求項2に記載の骨結束用索体において、
 前記基本線が、二本、又は三本の金属製フィラメントを各々長さ方向に沿って隣接させた並列配置型の収束線となされた骨結束用索体。
The cord for binding bone according to claim 2,
A bone binding rope in which the basic line is a converging line of a parallel arrangement type in which two or three metal filaments are adjacent to each other along the length direction.
 請求項2又は3に記載の骨結束用索体において、
 前記金属製フィラメントが、9~300μmの線径を有する骨結束用索体。
The cord for binding bone according to claim 2 or 3,
A bone binding cord having a wire diameter of 9 to 300 μm.
 請求項1に記載の骨結束用索体において、
 前記基本線が、複数本の金属製フィラメントを撚ることによって形成された撚線型の収束線となされた骨結束用索体。
In the bone binding cord according to claim 1,
A bone binding rope in which the basic wire is a twisted-type convergent wire formed by twisting a plurality of metal filaments.
 請求項5に記載の骨結束用索体において、
 前記基本線が、芯材となる一本の金属製フィラメントの周囲に複数本の金属製フィラメントを巻き付けて形成された有芯撚線型の収束線となされた骨結束用索体。
The cord for binding bone according to claim 5,
A bone binding cord in which the basic wire is a cored strand type converging wire formed by winding a plurality of metal filaments around one metal filament as a core material.
 請求項5又は6に記載の骨結束用索体において、
 前記金属製フィラメントが、3~150μmの線径を有する骨結束用索体。
The bone binding cord according to claim 5 or 6,
A bone binding cord having a wire diameter of 3 to 150 μm.
 請求項5ないし7のいずれか1項に記載の骨結束用索体において、
 前記基本線には、前記基本線の仮想軸芯を中心として捻転するねじれが無い骨結束用索体。
In the bone unity rope according to any one of claims 5 to 7,
The bone binding cord having no twist that twists around the virtual axis of the basic line.
 請求項1ないし8のいずれか1項に記載の骨結束用索体において、
 下記試験条件によって前記索体本体が引張された際、少なくとも2mm引張するまでに要する引張応力が、15N以下である骨結束用索体。
<試験>
 チャック間距離200mmにて前記索体本体をつかみ、毎分5mmの引張速度で前記索体本体を長さ方向に引張させながら引張応力を測定する。
The bone unity rope according to any one of claims 1 to 8,
A bone binding rope having a tensile stress of 15 N or less required to pull at least 2 mm when the cord body is pulled under the following test conditions.
<Test>
The cord body is held at a chuck distance of 200 mm, and the tensile stress is measured while pulling the cord body in the length direction at a tensile speed of 5 mm per minute.
 請求項9に記載の骨結束用索体において、
 前記試験条件によって前記索体本体が引張された際、引張応力が100N以下であれば、その後、試験力が付与されない状態とされた際に伸縮性を回復する骨結束用索体。
In the bone unity cord according to claim 9,
When the cord body is pulled according to the test conditions, if the tensile stress is 100 N or less, then the cord for cord binding that recovers stretchability when the test force is not applied.
 請求項8に記載の骨結束用索体の製造方法であって、
 前記基本線を編組するに先立ち、前記基本線に対し、軸芯を中心として捻転するねじれを付与し、前記ねじれがほどける方向に向かって前記基本線を編組することを特徴とする骨結束用索体の製造方法。
 
It is a manufacturing method of the rope for bone unity according to claim 8,
Prior to braiding the basic line, the basic line is imparted with a twist that twists about an axis, and the basic line is braided in a direction in which the twist is unwound. A manufacturing method of a cord.
PCT/JP2014/069755 2014-07-25 2014-07-25 Bone binding braid, and method for producing bone binding braid Ceased WO2016013123A1 (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113712656A (en) * 2021-09-13 2021-11-30 上海火点医疗器械有限公司 Sternum fixing system

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Publication number Priority date Publication date Assignee Title
JPS5817282A (en) * 1981-07-13 1983-02-01 ストレトフレツクス・インコ−ポレイテツド Hose reinforced by braided wire and its manufacture
JPH1033683A (en) * 1996-04-30 1998-02-10 Target Therapeutics Inc Superelastic alloy braided structure
WO2008018412A1 (en) * 2006-08-11 2008-02-14 Alfresa Pharma Corporation Bone fastening hollow cable
US20080119892A1 (en) * 2004-12-06 2008-05-22 Socovar Societe En Commandite Binding Component
JP2012232027A (en) * 2011-05-06 2012-11-29 Osaka Coat Rope Kk Wire for sternum suture

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5817282A (en) * 1981-07-13 1983-02-01 ストレトフレツクス・インコ−ポレイテツド Hose reinforced by braided wire and its manufacture
JPH1033683A (en) * 1996-04-30 1998-02-10 Target Therapeutics Inc Superelastic alloy braided structure
US20080119892A1 (en) * 2004-12-06 2008-05-22 Socovar Societe En Commandite Binding Component
WO2008018412A1 (en) * 2006-08-11 2008-02-14 Alfresa Pharma Corporation Bone fastening hollow cable
JP2012232027A (en) * 2011-05-06 2012-11-29 Osaka Coat Rope Kk Wire for sternum suture

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113712656A (en) * 2021-09-13 2021-11-30 上海火点医疗器械有限公司 Sternum fixing system
CN113712656B (en) * 2021-09-13 2023-08-08 上海火点医疗器械有限公司 Sternum fixation system

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