WO1996035377A1 - Materiau de suture medicale - Google Patents

Materiau de suture medicale Download PDF

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Publication number
WO1996035377A1
WO1996035377A1 PCT/JP1996/001220 JP9601220W WO9635377A1 WO 1996035377 A1 WO1996035377 A1 WO 1996035377A1 JP 9601220 W JP9601220 W JP 9601220W WO 9635377 A1 WO9635377 A1 WO 9635377A1
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WO
WIPO (PCT)
Prior art keywords
suture
suture material
medical
main
shape
Prior art date
Application number
PCT/JP1996/001220
Other languages
English (en)
French (fr)
Inventor
Keiji Igaki
Original Assignee
Kabushikikaisha Igaki Iryo Sekkei
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kabushikikaisha Igaki Iryo Sekkei filed Critical Kabushikikaisha Igaki Iryo Sekkei
Priority to EP96913704A priority Critical patent/EP0770356B1/en
Priority to CA002194170A priority patent/CA2194170C/en
Priority to KR1019960707423A priority patent/KR100289262B1/ko
Priority to DE69629263T priority patent/DE69629263T2/de
Priority to AT96913704T priority patent/ATE245944T1/de
Priority to AU56589/96A priority patent/AU709545B2/en
Priority to US08/765,942 priority patent/US5766188A/en
Publication of WO1996035377A1 publication Critical patent/WO1996035377A1/ja

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/068Surgical staplers, e.g. containing multiple staples or clamps
    • A61B17/072Surgical staplers, e.g. containing multiple staples or clamps for applying a row of staples in a single action, e.g. the staples being applied simultaneously
    • A61B17/07207Surgical staplers, e.g. containing multiple staples or clamps for applying a row of staples in a single action, e.g. the staples being applied simultaneously the staples being applied sequentially
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/00234Surgical instruments, devices or methods, e.g. tourniquets for minimally invasive surgery
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/068Surgical staplers, e.g. containing multiple staples or clamps
    • A61B17/072Surgical staplers, e.g. containing multiple staples or clamps for applying a row of staples in a single action, e.g. the staples being applied simultaneously
    • A61B17/07292Reinforcements for staple line, e.g. pledgets
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B2017/00004(bio)absorbable, (bio)resorbable, resorptive
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B90/00Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
    • A61B90/08Accessories or related features not otherwise provided for
    • A61B2090/0815Implantable devices for insertion in between organs or other soft tissues
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/0063Implantable repair or support meshes, e.g. hernia meshes

Definitions

  • suture Technical Field The present invention for the name medical invention relates suture material for medical use is stitched to the ablation site or the like of a living tissue, particularly suture material for medical use is used by attaching the stapler Related. Scientific techniques are generally used to remove lesions that have occurred in living tissues, but endoscopic surgery has been performed to reduce the burden on patients. ing.
  • an automatic suture device for example, resection using an automatic suture device is one example.
  • the automatic suturing device is introduced into a living body through a perforation and suturing an affected part and suturing a resected part at the same time.
  • the use of the automatic suturing apparatus eliminates the need for incision of the affected part. Therefore, the automatic suturing device has a suturing mechanism at the distal end for sandwiching the resected portion of the living tissue, and the suturing mechanism further includes a plurality of step lines for suturing.
  • a cutting mechanism such as a knife is provided.
  • the use of the automatic suturing device is advantageous for shortening the suturing and incision time and simplifying the operation.
  • a suture material has been attached to the automatic suturing device, and the suture material has been sewn to a resection site of a living tissue with a step.
  • a felt-like suture material is overlaid with an elastic knit fabric, It has been proposed that these are sewn along both side edges with temporary sewing threads to form a tube.
  • the suture material in which an elastic knit fabric is sewn with a suture thread and can be attached to the automatic suture device, the suture material is inserted when the automatic suture device is inserted into a living body and introduced into an affected part.
  • There are inconveniences such as shrinking in the direction, biasing toward the proximal end of the automatic suture device, and rotating around the automatic suture device, that is, twisting.
  • the present invention has been proposed in view of such circumstances. Therefore, it is an object of the present invention to provide a medical suture material that does not cause displacement or rotation when an automatic suture device is inserted, and that can reliably prevent air leakage when used for a lung operation, for example. Aim.
  • the medical suture material of the present invention has a shape-sustaining support member made of a film or a sheet having rigidity over the main suture material, and these main suture materials are overlapped with each other.
  • the material and the shape maintaining property are sewn along the width direction both side edges using the suture thread, and formed into a tubular body so that it can be attached to an automatic suturing machine having a stable line. .
  • the main suturing material may be of any form as long as it has a certain degree of flexibility and elasticity, such as non-woven cloth such as felt, woven cloth, and knit fabric. It can be used, and any known materials can be used.However, considering the postoperative condition, a bioabsorbable polymer such as polyglycolic acid or a part of a living tissue, for example, an organ protective membrane such as a pericardial membrane. It is desirable to use
  • the shape-retaining support material a material having rigidity that does not deform even when a slight force is applied is used.
  • a sheet-like or film-like material such as plastic, metal, or paper is used. Is used.
  • the shape-retaining support material is not deformed even when an external force is applied, and therefore, the suture material formed into a tubular shape is skewed due to contraction in the insertion direction when the automatic suture device is inserted. I will not.
  • the suture material is shaped according to the shape of the automatic suturing device by the shape-maintaining support material, and the state is maintained by the rigidity of the shape-maintaining support material. I will not. BRIEF DESCRIPTION OF THE DRAWINGS FIG.
  • FIG. 1 is a schematic perspective view showing an example of a suture material according to the present invention.
  • FIG. 2 is a schematic perspective view showing another example of the suture material according to the present invention.
  • FIG. 3 is a schematic perspective view showing an example of an automatic suture device using the above-mentioned suture material.
  • Fig. 4 is a schematic plan view of a main part of a suturing mechanism of the automatic suturing device.
  • Fig. 5 is a schematic perspective view showing a state in which a suture material is attached to the automatic suturing device.
  • FIG. 6 is a schematic perspective view showing a suturing operation state by the automatic suturing device.
  • FIG. 7 is a schematic perspective view showing a state where the suturing procedure has been completed.
  • FIG. 8 is a schematic perspective view showing still another example of the suture material according to the present invention with one end closed.
  • the medical suture material 1 of the present embodiment has a single main suture made of, for example, felt of absorbent polyglycolic acid (eg, Neobel, trade name, manufactured by Gunze Co., Ltd.). Material 2 and a form-retaining support material 3 made of a plastic sheet are stitched together using a suture thread. It is.
  • felt of absorbent polyglycolic acid eg, Neobel, trade name, manufactured by Gunze Co., Ltd.
  • a material conventionally used as a suturing material can be used.
  • a part of a living tissue such as an organ protective membrane such as a pericardium.
  • the shape-sustaining support material 3 is not limited to the plastic sheet, and any material having a certain degree of rigidity, such as a metal sheet or paper, can be used.
  • the main suturing material 2 and the shape maintaining support material 3 are formed in a strip shape having a length substantially equal to the length of a mounting portion of an automatic suturing device to be described later, and two suture yarns are provided along both side edges in the width direction. Sewn together by 4, 5 ⁇
  • the sutures 4 and 5 are preferably so-called monofilaments in consideration of ease of removal, and their material is arbitrary.
  • a bioabsorbable polymer yarn, a polyamide yarn having good slipperiness (a so-called Nymouth yarn) and the like are suitable.
  • suture threads 4 and 5 may be left as they are, and may be individually removed from the main suture material 2 or the shape-retaining support material 3 after completion of the suture, or the shape-retaining material 3
  • a structure may be provided such that a knot or the like is provided at the end on the side so that the shape-maintaining support material 3 is withdrawn at the same time as the sutures 4 and 5 are withdrawn after the suturing.
  • the width of the main suture 2 is Wl and the width of the shape-maintaining support 3 is W2, W1 ⁇ W2. That is, the shape-retaining support material 3 is wider than the main suture material 2.
  • the shape-maintaining support material 3 made of a plastic sheet is bent to have a shape that matches the external shape of the mounting site of the automatic suture machine, the mounting state is extremely stable In other words, the rotation can be reliably prevented.
  • the width of the main suture material 2 may be made larger than the width of the shape-maintaining support member 3 so as to cover the shape-maintaining support member 3 to some extent.
  • the medical suture material having the above configuration is used by being attached to an automatic suture instrument. Therefore, the structure of the automatic suture instrument and the method of using the medical suture material of the present embodiment will be described next.
  • the automatic suturing device has a self-sealing portion 2 which is closed at the distal end of the shaft 11 and an operation for grasping and operating at the proximal end. Section 13 is provided.
  • the suturing portion 12 includes a force cartridge containing a stable, a suturing mechanism portion 12a into which a knife blade is loaded, and a jaw portion 12b for sandwiching living tissue.
  • This automatic suturing device is introduced into a living body through an attachment called a surge boat. That is, first, a hole is provided in the body —Attach a boat and insert the automatic suturing device shaft 11 into the body through this surge port. Thereby, the hermetic seal of the perforation provided in the living body is maintained.
  • FIG. 5 shows a state in which the suturing material 1 is mounted on the suturing portion 12 of the automatic suturing device.
  • the suturing material 1 is attached to the suturing mechanism 12a and the jaw 12b, respectively.
  • the attachment of the suture material 1 to the suture portion 12 can be performed smoothly by sliding the suture portion 12 along the shape-maintaining support material 3 made of a plastic sheet.
  • the suture portion 12 When bent into a rectangular shape in accordance with the shape of the sewn portion 12, it can be easily mounted using the flat surface on the back side.
  • the automatic suturing device is inserted into the living body through the surge port and reaches the affected part as described above.
  • the suture material 1 attached to the automatic suturing device has a shape maintaining property. Since the shape is reinforced by the support material 3, there is no occurrence of biased waste due to shrinkage.
  • the suturing portion 12 is introduced into the affected area, as shown in FIG. 6, the cut portion of the living tissue 20 is sandwiched between the suturing mechanism portion 12a and the jaw portion 12b. Thereby, the resection site is covered with the main suture 2.
  • the operating lever 13a provided on the operating portion 13 of the automatic suture device is operated, and the staple is driven from the staple line 13 by the staple.
  • the stable is stapled along the resected portion of the living tissue 20 and a suturing procedure is performed.
  • the main suturing material of the suturing material 1 simultaneously attached to the suturing portion 12 is applied. 2 is pressed against the resection site of the living tissue 20 And stitched by the staple.
  • the main suture 2 functions as a reinforcing material at the time of suturing.
  • the main suture 2 By cutting a cut portion of the living tissue 20 through the main suture 2, rupture of the tissue is prevented, for example, a giant lung cyst. Air leakage is prevented during resection of the stomach.
  • the knife provided on the suturing mechanism 12a is scanned along the scanning line 15 to cut the living tissue 20 and the main suture material 2.
  • the automatic suturing device is withdrawn, and an extra member, that is, the shape maintaining support material 3 is removed from the living body.
  • the main suture material 2 and the shape-maintaining support material 3 are pulled out of the suture threads 4 and 5, which are sewn together. What is necessary is just to remove the maintenance support material 3 from the living body.
  • the suture thread 4, 5 is simultaneously pulled out of the shape-maintenance support material 3 after the suturing is completed. Can also be extracted.
  • FIG. 7 shows a state where the suturing is completed.
  • the main suturing material 2 is sewn to the suturing site of the living tissue 20 so that the suturing state is extremely stable.
  • both ends of the suture material 1 obtained by sewing the main suture material 2 and the shape-maintaining support material 3 are open, As shown in FIG. 8, the end of the main suture material 2 or the shape-maintaining support material 3 may be folded back and sewn in a bag shape whose tip is closed by one suture thread 4.
  • the suture material 1 is pushed by the automatic suture device when the device is inserted into the living body by attaching it to the automatic suture device, and the displacement of the suture material 1 is prevented.
  • the suture material of the present invention since the main suture material having flexibility is supported by a support material having a certain degree of rigidity, it is generated when the automatic suture device is inserted. It is possible to prevent a side twist or the like due to shrinkage.
  • the suturing site can be reliably reinforced, and it is possible to suppress tissue tearing and air leakage.

Description

明細 : 発明の名称 医療用の縫合材 技術分野 本発明は、 生体組織の切除部位等に縫い合わされる医療用の縫合 材に関し、 特に自動縫合器に装着して使用される医療用の縫合材に 関する。 景技術 生体組織に生じた病巣の切除は、 外科的手術によるのが一般的で あるが、 患者に対する負担の軽減などを目的に、 内視鏡下での手術 等が施術されるようになってきている。
例えば、 自動縫合器を用いた切除術等は、 その一例である。 自動 縫合器は、 穿孔から生体内へ導入され、 患部を切除すると同時に切 除部位の縫合を行うものであり、 これを用いることで患部の切開が 不要となるという利点がある。 したがって、 上記自動縫合器は、 先 端に生体組織の切除部位を挟み込む縫合機構部を有し、 さらにこの 縫合機構部には、 縫合のための複数のステ一プルラインゃ生体組織 を切断するためのナイフ等の切断機構が設けられている。 もちろん、 外科的手術においても、 前記自動縫合器の使用は、 縫 合、 切開時間の短縮や、 施術の簡便化に有利である。
ところで、 肺、 気管支、 肝臓、 消化管等の脆弱な組織に対して前 述の自動縫合器で施術する場合、 ステ一プルによる縫合のみでは、 組織の断裂の皮があり、 また、 例えば肺の手術においては、 空気漏 れが発生する虞がある。 前記空気漏れは、 患者にとって致命的であ り、 これを確実に防止することが望まれる。
そこで従来、 前記自動縫合器に縫合材を装着しておき、 これを生 体組織の切除部位にステ一プルで縫い合わせるということが行われ ている。
この場合、 縫合材を自動縫合器に装着可能とし、 確実に患部に到 達させるためには、 何らかの工夫が必要であり、 例えば、 フェルト 状の縫合材に伸縮性を有するニッ ト地を重ね、 これらを仮縫い糸で 両側縁に沿って縫い付け、 筒状にしたものが提案されている。
しかしながら、 伸縮性を有するニッ ト地を縫合用の糸により縫い 付けて自動縫合器への装着を可能とした縫合材では、 自動縫合器を 生体内に挿入して患部へ導入する際に、 挿入方向で収縮し自動縫合 器の基端側に片寄ったり、 自動縫合器の周囲で回転する、 すなわち ヅイストする等の不都合が発生している。
縫合材に片寄りや回転が生ずると、 的確な処置が難しく、 特に内 視鏡下のような限られた視野での施術の際に、 大きな問題となる。 発明の開示 そこで本発明は、 このような実情に鑑みて提案されたものであつ て、 自動縫合器の挿入時に片寄りや回転が発生することがなく、 例 えば肺の手術に用いた場合に空気漏れを確実に防止することが可能 な医療用の縫合材を提供することを目的とする。
前述の目的を達成するために、 本発明の医療用の縫合材は、 主縫 合材に対して剛性を有するフィルムまたはシ一トよりなる形態維持 性支持材が重ね合わされるとともに、 これら主縫合材と形態維持性 支持材とが幅方向両側縁に沿って縫合用の糸を用いて縫い合わされ てなり、 ステーブルラインを有する自動縫合器に装着可能なように 筒状体に形成されている。
本発明の縫合材において、 主縫合材には、 フェル トのような不織 布や、 織布、 ニッ ト地等、 ある程度の柔軟性、 伸縮性を有するもの であれば任意の形態のものが使用でき、 その材質も公知のものがい ずれも使用できるが、 術後を考えると、 ポリグリコール酸のような 生体吸収性高分子や生体組織の一部、 例えば心のう膜等の臓器保護 膜を用いることが望ましい。
また、 形態維持性支持材には、 多少の力が加わっても変形するこ とのない剛性を有する材料が用いられ、 例えばプラスチックや金属、 紙等のシ一ト状あるいはフィルム状の材料の一種が用いられる。 形態維持性支持材は、 外力が加わっても変形することがなく、 し たがってこれを縫い合わせ筒状にした縫合材は、 自動縫合器挿入の 際に挿入方向に収縮することによる片寄りが発生することはない。 また、 前記縫合材は、 形態維持性支持材によって自動縫合器の形 状に沿った形とされ、 その状態が形状維持性支持材の剛性によって 維持されることから、 不用意に回転 (ツイスト) することはない。 図面の簡単な説明 図 1は、 本発明に係る縫合材の一例を示す概略斜視図である。 図 2は、 本発明に係る縫合材の他の例を示す概略斜視図である。 図 3は、 上記縫合材が用いられる自動縫合器の一例を示す概略斜 視図である。
図 4は、 上記自動縫合器の縫合機構部の要部概略平面図である. 図 5は、 縫合材の上記自動縫合器への装着状態を示す概略斜視図 である。
図 6は、 上記自動縫合器による縫合操作状態を示す概略斜視図で あ o
図 7は、 縫合処置終了状態を示す概略斜視図である。
図 8は、 一端を閉塞状態とした本発明に係る縫合材のさらに他の 例を示す概略斜視図である。 発明を実施するための最良の形態 以下、 本発明を適用した具体的な実施例について、 図面を参照し ながら詳細に説明する。
¾M 1
本実施例の医療用の縫合材 1は、 図 1に示すように、 例えば吸収 性ポリグリコール酸のフェルト (例えば、 グンゼ株式会社製、 商品 名ネオべ一ル等) よりなる 1枚の主縫合材 2と、 プラスチヅクシ一 卜よりなる形態維持性支持材 3とを縫合用の糸を用いて縫い合わせ てなるものである。
主縫合材 2には、 前記吸収性ポリグリコール酸のような生体吸収 性高分子の他、 従来縫合材として用いられているものが使用可能で ある。 例えば、 心のう膜等の臓器保護膜のような生体組織の一部を 使用することも可能である。
また、 形態維持性支持材 3も、 前記プラスチックシートに限らず、 金属シート、 紙など、 ある程度剛性を有する材料であれば、 いずれ も使用可能である。
これら主縫合材 2及び形態維持性支持材 3は、 後述の自動縫合器 の装着部位の長さとほぼ等しい長さを有する短冊状とされ、 幅方向 両側縁に沿って 2本の縫合用の糸 4、 5によって縫い合わされてい ο
前記縫合用の糸 4、 5は、 抜取り易さを考慮すると、 いわゆるモ ノフィラメントがよく、 その材質は任意である。 例えば、 生体吸収 性ポリマーの糸や、 滑り性の良好なポリアミ ド糸 (いわゆるナイ口 ン糸) 等が好適である。
これら縫合用の糸 4、 5の末端は、 そのままの状態としておき、 縫合終了後に主縫合材 2や形態維持性支持材 3から個々に抜き取る ようにしてもよいし、 あるいは形態維持性支持材 3側で末端に結び 目等の抜け止めを設け、 縫合終了後に形態維持性支持材 3を抜き取 ると同時にこれら縫合用の糸 4、 5が抜き取られるような構成とし てもよい。
また、 本例においては、 前記主縫合材 2の幅を W l、 形態維持性 支持材 3の幅を W 2としたときに、 W 1 < W 2とされている。 すな わち、 形態維持性支持材 3の方が主縫合材 2よりも幅広とされてい る。
これは、 自動縫合器の挟み込み面に主縫合材 2を配し、 背面側を 形態維持性支持材 3で覆って装着状態を安定なものとするためで、 このような設定とすることで、 自動縫合器装着時の回転が防止され o
特に、 図 2に示すように、 プラスチックシートよりなる形態維持 性支持材 3に対して折り曲げ加工を施し、 自動縫合器の装着部位の 外形形状に合わせた形状にしておけば、 装着状態が極めて安定なも のとなり、 前記回転を確実に防止することができる。
もちろん、 これに限らず、 例えば主縫合材 2の幅を形態維持性支 持材 3の幅よりも大として、 形態維持性支持材 3をある程度覆うよ うな構成とすることも可能である。
上述の構成を有する医療用の縫合材は、 自動縫合器に装着して使 用される。 そこで次に、 自動縫合器の構造、 並びに本実施例の医療 用の縫合材の使用方法について説明する。
自動縫合器は、 図 3に示すように、 シャフ ト 1 1の先端に閧閉自 在な縫合部ェ 2を有してなるものであって、 基端部には把持 ·操作 するための操作部 1 3が設けられている。
前記縫合部 1 2は、 図 4に示すように、 ステーブルが収容された 力一トリッジゃナイフブレードが装填される縫合機構部 1 2 a及び 生体組織を挟み込むための顎部 1 2 bとからなり、 縫合機構部 1 2 aの挟み込み面には、 複数 (本例では、 3列 X 3列 = 6列) のステ 一プルライン 1 4やナイフの走査ライン 1 5が臨んでいる。
この自動縫合器は、 サージボートと称されるアタッチメントを介 して生体内に導入される。 すなわち、 まず、 生体に設けた穿孔にサ —ジボートを装着し、 このサージポートを通して自動縫合器のシャ フ ト 1 1を生体内へと挿入する。 これによつて、 生体に設けた穿孔 の密閉が保たれる。
先の医療用の縫合材 1は、 前記自動縫合器の縫合部 1 2に装着し て使用される。 図 5は、 縫合材 1を自動縫合器の縫合部 1 2に装着 した状態を示すもので、 縫合機構部 1 2 a及び顎部 1 2 bにそれぞ れ縫合材 1が取り付けられる。
縫合材 1の縫合部 1 2への装着は、 ブラスチックシートよりなる 形態維持性支持材 3に沿って縫合部 1 2を滑らすことで円滑に行う ことができ、 特に形態維持性支持材 3を縫合部 1 2の形状に合わせ て矩形に折り曲げ加工した場合には、 背面側の平坦面を利用して、 容易に装着することができる。
この状態で、 先に述べたようにサージポートを介して自動縫合器 を生体内へと挿入し、 患部へと到達させる. このとき、 自動縫合器 に装着される縫合材 1は、 形態維持性支持材 3によって補強された かたちになっているので、 収縮による片寄りゃッイス 卜が発生する ことはない。
縫合部 1 2を患部へ導入した後、 図 6に示すように、 生体組織 2 0の切除部位を縫合機構部 1 2 a及び顎部 1 2 bによって挟み込む。 これによつて、 前記切除部位は主縫合材 2で覆われることになる。 次に、 自動縫合器の操作部 1 3に設けられた操作レバー 1 3 aを 操作し、 前記ステ一プルライン 1 3からステ一プルを打針する。 これによつて、 生体組織 2 0の切除部位に沿ってステーブルが打 針され、 縫合処置が施されるが、 このとき、 同時に縫合部 1 2に装 着された縫合材 1の主縫合材 2が生体組織 2 0の切除部位に押し当 てられ、 前記ステ一プルによって縫合される。
前記主縫合材 2は、 縫合の際の補強材として機能し、 生体組織 2 0の切断部分をこの主縫合材 2を介して縫合することで、 組織の断 裂が防止され、 例えば巨大肺のう胞の切除術等においては、 空気漏 れが防止される。
次いで、 縫合機構部 1 2 aに設けられたナイフを走査ライン 1 5 に沿って走査し、 生体組織 2 0及び主縫合材 2を切断する。
上述の縫合操作後、 自動縫合器を抜き取り、 余分な部材、 すなわ ち形態維持性支持材 3を生体内から除去する。 この形態維持性支持 材 3を除去するには、 主縫合材 2と形態維持性支持材 3とを縫い合 わせている縫合用の糸 4、 5を引き抜いてこれらを分離した後、 前 記形態維持性支持材 3を生体内から取り出せばよい。 あるいは、 前 述のように形態維持性支持材 3側の末端に結び目等の抜け止めを設 けた場合には、 縫合終了後に形態維持性支持材 3を抜き取ると同時 に縫合用の糸 4、 5を抜き取ることも可能である。
以上によって縫合処置が完了するが、 本例の縫合材 1を用いるこ とによって、 縫合操作を円滑に進めることができ、 しかも確実に縫 合部位の補強、 空気漏れの防止を行うことができる。 図 7は、 縫合 終了状態を示すものであり、 生体組織 2 0の縫合部位には、 主縫合 材 2が縫い合わされ、 縫合状態が極めて安定なものとなっている。 以上、 本発明の具体的な実施例について説明してきたが、 本発明 がこの実施例に限られるものではなく、 材質、 形状等において種々 の変形が可能であることは言うまでもない。
例えば、 上述の実施例においては、 主縫合材 2と形態維持性支持 材 3とを縫い合わせた縫合材 1の両端部を開放した状態としたが、 図 8に示すように、 主縫合材 2あるいは形態維持性支持材 3の端部 を折り返し、 1本の縫合用の糸 4によって先端が閉塞された袋状に 縫い合わせてもよい。 このように先端を閉塞した場合には、 自動縫 合器に装着して生体内に挿入する際に、 縫合材 1を自動縫合器で押 し込むことになり、 縫合材 1の片寄り防止は一層確実なものとなる ( 産業上の利用可能性 本発明の縫合材においては、 柔軟性を有する主縫合材をある程度 剛性のある支持材によって支持するようにしているので、 自動縫合 器挿入時に発生する縮みによる片寄りゃッイスト等を防止すること ができる。
したがって、 本発明の縫合材を用いることによって、 縫合部位の 補強を確実に行うことができ、 組織の断裂や空気漏れを抑えること が可能である。

Claims

請求の範囲
1 . ステーブルラインを有する自動縫合器に装着されて用いられる 医療用縫合材であり、
主縫合材に対して剛性を有するフィルムまたはシ一トょりなる形 態維持性支持材が重ね合わされるとともに、 これら主縫合材と形態 維持性支持材とが幅方向両側縁に沿って縫合用の糸によって縫い合 わされてなり、 ステーブルラインを有する自動縫合器に装着可能な ように筒状体とされている医療用の縫合材。
2 . 上記主縫合材が不織布、 織布、 ニット地から選ばれる少なくと も 1種よりなることを特徴とする請求の範囲第 1項記載の医療用の
3 . 上記主縫合材が合成高分子よりなることを特徴とする請求の範 囲第 2項記載の医療用の縫合材。
. 上記合成高分子が生体吸収性商分子であることを特徴とする請 求の範囲第 3項記載の医療用の縫合材。
5 . 上記生体吸収性高分子がポリグリコール酸であることを特徴と する請求の範囲第 4項記載の医療用の縫合材。
6 . 上記主縫合材が生体組織の一部よりなることを特徴とする請求 の範囲第 1項記載の医療用の縫合材。
7 . 上記生体組織が臓器保護膜であることを特徴とする請求の範囲 第 6項記載の医療用の縫合材。
8 . 上記生体組織が心のう膜であることを特徴とする請求の範囲第 7項記載の医療用の縫合材。
9 . 上記形態維持性支持材がプラスチック、 金属、 紙から選ばれる 少なく とも 1種よりなることを特徴とする請求の範囲第 1項記載の 医療用の縫合材。
1 0 . 上記形態維持性支持材が自動縫合器の装着部位の形状に合わ せて成形されていることを特徴とする請求の範囲第 1項記載の医療 用の縫合材。
1 1 . ステ一プルラインを有する自動縫合器に装着されて用いられ る医療用縫合材であり、
不織布、 織布、 ニッ ト地から選ばれる少なく とも 1種よりなる主 縫合材に対して剛性を有するフィルムまたはシ一トよりなる形態維 持性支持材が重ね合わされるとともに、 これら主縫合材と形態維持 性支持材とが単一の縫合用の糸によって袋状に縫い合わされ、 上記 , ステ一プルラインを有する自動縫合器に装着可能なように先端側が 閉塞された筒状体とされている医療用の縫合材。
1 2 . 上記主縫合材が生体吸収性高分子であることを特徴とする請 求の範囲第 1 1項記載の医療用の縫合材。
1 3 . 上記生体吸収性高分子がポリグリコール酸であることを特徴 とする請求の範囲第 1 2項記載の医療用の縫合材。
1 4 . 上記主縫合材が生体組織の一部よりなることを特徴とする請 求の範囲第 1 1項記載の医療用の縫合材。
1 5 . 上記生体組織が臓器保護膜であることを特徴とする請求の範 囲第 1 1項記載の医療用の縫合材。
PCT/JP1996/001220 1995-05-08 1996-05-08 Materiau de suture medicale WO1996035377A1 (fr)

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EP96913704A EP0770356B1 (en) 1995-05-08 1996-05-08 Medical suture material
CA002194170A CA2194170C (en) 1995-05-08 1996-05-08 Medical suturing material
KR1019960707423A KR100289262B1 (ko) 1995-05-08 1996-05-08 의료용봉합재
DE69629263T DE69629263T2 (de) 1995-05-08 1996-05-08 Medizinisches nähmaterial
AT96913704T ATE245944T1 (de) 1995-05-08 1996-05-08 Medizinisches nähmaterial
AU56589/96A AU709545B2 (en) 1995-05-08 1996-05-08 Medical suturing material
US08/765,942 US5766188A (en) 1995-05-08 1996-05-08 Medical suturing material

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JP7/109833 1995-05-08
JP10983395A JP3526487B2 (ja) 1995-05-08 1995-05-08 医療用縫合材

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CA (1) CA2194170C (ja)
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EP0770356A1 (en) 1997-05-02
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ATE245944T1 (de) 2003-08-15
US5766188A (en) 1998-06-16
AU709545B2 (en) 1999-09-02
EP0770356B1 (en) 2003-07-30
DE69629263D1 (de) 2003-09-04
EP0770356A4 (en) 1998-02-11
JP3526487B2 (ja) 2004-05-17
CA2194170A1 (en) 1996-11-14
CA2194170C (en) 2007-03-27
JPH08299427A (ja) 1996-11-19

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