JPH06189987A - Joint constitution material - Google Patents

Joint constitution material

Info

Publication number
JPH06189987A
JPH06189987A JP34814592A JP34814592A JPH06189987A JP H06189987 A JPH06189987 A JP H06189987A JP 34814592 A JP34814592 A JP 34814592A JP 34814592 A JP34814592 A JP 34814592A JP H06189987 A JPH06189987 A JP H06189987A
Authority
JP
Japan
Prior art keywords
joint
bone
joint component
distal
constitution
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP34814592A
Other languages
Japanese (ja)
Other versions
JP3164675B2 (en
Inventor
Noriyuki Ishida
典之 石田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kyocera Corp
Original Assignee
Kyocera Corp
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 Kyocera Corp filed Critical Kyocera Corp
Priority to JP34814592A priority Critical patent/JP3164675B2/en
Publication of JPH06189987A publication Critical patent/JPH06189987A/en
Application granted granted Critical
Publication of JP3164675B2 publication Critical patent/JP3164675B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • 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
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/42Joints for wrists or ankles; for hands, e.g. fingers; for feet, e.g. toes
    • A61F2/4241Joints for wrists or ankles; for hands, e.g. fingers; for feet, e.g. toes for hands, e.g. fingers
    • 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
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof

Landscapes

  • Health & Medical Sciences (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Cardiology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Transplantation (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Prostheses (AREA)

Abstract

PURPOSE:To enable a simple joint replacement operation to be undertaken, and provide a large joint moving area by forming a joint constitution material having a bone tissue, at a proxal end adjacent to a bone tissue at a distal end, in such a way as having at least one surfaces sliding on the surface of at least one bone edge section. CONSTITUTION:This joint constitution material 1 made of sapphire or the like has a spherical outer surface 1a, and this surface 1a is mirror finished, for example, to 0.05 or less with surface roughness of Ra via chemical treatment. When this material 1 is used to replace a thumb CM joint, each of bone edges P2 and D2 of a broken proximal lateral bone D and a broken distal lateral bone D are so made as to smoothly slide on the outer surface 1a of the material 1. According to this construction, a problem regarding a complication due to a dislocation between a stem and a bone as seen in an artificial joint fitted with a stem and fixed in a myeloid cavity can be eliminated, and a very large joint moving area can be provided.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、母指CM関節やMP関
節などの手足の指関節の他、肩関節、股関節、脊椎など
の人体の関節を形成する主要部位において、変形性関節
症、リウマチ関節、外傷などの疾患による破壊で機能が
十分に果たせなくなった関節、すなわち、直接的には関
節軟骨の損傷によって発生し、次第に関節面の変形が顕
著となり、それに伴って関節機能の低下や関節の疼痛な
どを誘発し、やがて日常生活にも支障をきたすようにな
った重度疾患の関節の機能を復元し疾患を治癒するた
め、関節を置換する関節構成物体に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to osteoarthritis in major parts that form joints of the human body such as shoulder joints, hip joints, and spines, in addition to finger joints such as thumb CM joints and MP joints. Rheumatoid joints, joints that have been unable to function satisfactorily due to destruction due to diseases such as trauma, that is, directly caused by damage to the articular cartilage, gradually deforming the joint surface, resulting in deterioration of joint function and The present invention relates to a joint component that replaces a joint in order to restore the function of a severely diseased joint that induces joint pain or the like and eventually impairs daily life and cures the disease.

【0002】[0002]

【従来の技術】何らかの原因で機能が十分に果たせなく
なった関節を置換する関節構成物体の形状及び材質は、
人体の関節の元来の形状や軟部組織を含めた構造、関節
周囲の筋肉やじん帯の配置に依存する生体力学的なバラ
ンス、関節に要求される様々な方向の可動性、更に、そ
れらの動きにおける関節荷重の大きさや方向に依存し、
総合的な適合性を鑑みて決定される。
2. Description of the Related Art The shape and material of a joint-constituting object that replaces a joint whose function cannot be sufficiently fulfilled for some reason is as follows.
The structure of the human body joint including its original shape and soft tissue, the biomechanical balance depending on the arrangement of muscles and ligaments around the joint, the mobility in various directions required for the joint, and their movement. Depending on the size and direction of the joint load at
It is decided in consideration of overall suitability.

【0003】従来用いられた関節構成物体として、例え
ば米国特許第4,242,757 号の発明の如く、近位側骨髄腔
内に挿入する髄腔支持部を備える近位側骨部材と遠位側
骨髄腔内に挿入する髄腔支持部を備える遠位側骨部材に
より構成され、この2つの部材は、互いに髄腔支持部を
髄腔に挿入固定することにより骨組織に固着され、かつ
髄腔支持部と反対側に位置する関節部の先端に形成し
た、それぞれの関節摺動面で、周囲の軟部組織の圧迫力
や支持性によりそれぞれの部材が生体力学的にバランス
し、該関節摺動面に様々な形状を与えることで元の関節
の機能に近い機能を与え、これにより関節機能が再建し
ようとするものがあった。
As a joint component used conventionally, for example, as in the invention of US Pat. No. 4,242,757, a proximal bone member having a medullary cavity support portion to be inserted into a proximal medullary cavity and a distal medullary cavity are provided. A distal bone member having a medullary cavity support portion to be inserted into the medullary cavity, and these two members are fixed to bone tissue by inserting and fixing the medullary cavity support portion into the medullary cavity, and At each joint sliding surface formed at the tip of the joint located on the opposite side, each member biomechanically balances due to the compression force and support of the surrounding soft tissue, and various joint sliding surfaces are formed. There is a thing which gives a function close to the function of the original joint by giving such a shape, and thereby the joint function is reconstructed.

【0004】また、米国特許第4,367,562 号の発明の如
く、近位側骨髄腔に挿入する髄腔支持部と近位側骨髄腔
内に挿入する髄腔支持部を具備し、シリコンより一体成
形されてなる関節構造物体があった。これは関節摺動面
を持たない一体形の関節構成物体としたもので、シリコ
ンの弾性を利用して関節機能を復元しようとするもので
あった。
Further, as in the invention of US Pat. No. 4,367,562, it comprises a medullary cavity support portion to be inserted into the proximal side bone marrow cavity and a medullary cavity support portion to be inserted into the proximal side bone marrow cavity, and is integrally molded from silicon. There was an articulated structure object. This is an integrated joint component that does not have a joint sliding surface, and was designed to restore the joint function by utilizing the elasticity of silicon.

【0005】[0005]

【従来技術の課題】しかしながら、上記の従来技術には
以下のような問題があった。
However, the above-mentioned prior art has the following problems.

【0006】すなわち、近位側骨部材と遠位側骨部材か
ら構成され、近位側骨髄腔と遠位側骨髄腔にそれぞれ挿
入する髄腔支持部を具備する関節構成物体において、該
髄腔内支持部材は、元来両部材のアンカーとして機能す
るのであるが、関節内で発生する荷重を骨組織に伝達す
る作用も有し、時として過度の荷重が骨に伝達してい
た。また、関節摺動面の機能を追求し、回転方向や回転
角度を制限することによるデザイン上の要求から関節部
が大きめとなってしまい、それに伴い骨切除量も多くな
った。
[0006] That is, in a joint component comprising a proximal side bone member and a distal side bone member and having a medullary cavity support portion inserted into the proximal side bone marrow cavity and the distal side bone marrow cavity, respectively, The inner support member originally functions as an anchor for both members, but also has a function of transmitting the load generated in the joint to the bone tissue, and sometimes an excessive load is transmitted to the bone. In addition, the joint part has become large due to the design requirement by pursuing the function of the joint sliding surface and limiting the rotation direction and the rotation angle, and the bone resection amount has also increased accordingly.

【0007】このように、力学的要因である生体内での
過度な応力伝達と、関節構造物体のデザインによる不必
要な骨切除によって引き起こされる骨組織の関節構造物
体を受容する支持性能の低下があると、これらが原因と
なり骨吸収や、部材と骨とのルーズニングなどを起こ
り、人工関節置換術を施行したのち長期間が経過するに
つれ、周囲の骨組織の局部的な破壊が始まり、破壊の範
囲が広がるにつれ、改善していた疼痛が再び出現した
り、関節の機能が手術前のレベルに戻ってしまうことが
あった。
As described above, the excessive stress transmission in the body which is a mechanical factor and the deterioration of the supporting ability of the bone tissue for receiving the joint structure object caused by the unnecessary bone resection due to the design of the joint structure object are caused. If so, these causes bone resorption, loosening between the member and the bone, etc., and as a long time elapses after the artificial joint replacement operation is performed, local destruction of surrounding bone tissue begins and destruction occurs. As the range of pain increased, pain that had improved could reappear and joint function could return to pre-operative levels.

【0008】このような状態を引き起こしてしまうと、
再度、関節構成物体置換術を施行することが必要り、こ
の際には初回の手術よりも広範囲に破壊され消失した骨
組織に関節構造物体をインプラントしなければならず、
より困難な技術が要求されるとともに患者に多大な苦痛
を経験させてしまう。
If such a situation is caused,
Again, it is necessary to perform joint component replacement surgery, in which case the joint structure body must be implanted in the bone tissue that has been destroyed and lost more extensively than the first surgery,
More difficult techniques are required and the patient experiences great pain.

【0009】加えて、人工材料よりなる両部材を摺動面
において摺動させることから、摩耗によって部材の摩滅
が起こり、摩耗片が生体に取り込まれることなどがあ
り、生体にさまざまな悪影響を及ぼしていた。
In addition, since both members made of an artificial material are slid on the sliding surface, the members may wear due to wear and the wear pieces may be taken into the living body, which has various adverse effects on the living body. Was there.

【0010】次に、シリコンより一体的に形成される関
節構成物体においては、関節の屈曲、伸展に従い、関節
構成物体も屈曲、伸展するのであるが、生体内での反復
的な屈曲、伸展により比較的短期に関節構成物体を構成
するシリコンが劣化してしまい、すぐに関節構成物体の
置換術を行わなければならないという不具合があった。
Next, in the joint component formed integrally from silicon, the joint component also bends and extends in accordance with the bending and extension of the joint, but by repeated bending and extension in the living body. There has been a problem that the silicon constituting the joint component deteriorates in a relatively short period of time and the joint component replacement operation must be performed immediately.

【0011】[0011]

【課題を解決するための手段】上記の課題に対して、本
発明は生体の関節を構成し、近位端側の骨組織と遠位端
側の骨組織に隣接する関節構成物体であって、少なくと
も一方の骨端部表面にて摺動するよう少なくとも一つ以
上の曲面により形成され、生体内で安定でかつ異害性を
示さない材料からなることを特徴とする関節構成物体を
提供するものである。
In order to solve the above-mentioned problems, the present invention provides a joint component which constitutes a joint of a living body and is adjacent to bone tissue on the proximal end side and bone tissue on the distal end side. And a joint component characterized by being formed of at least one curved surface so as to slide on at least one epiphyseal surface and made of a material that is stable in vivo and does not show any harm. It is a thing.

【0012】[0012]

【実施例】以下、本発明実施例を図面に基づいて具体的
に詳述する。
Embodiments of the present invention will be described in detail below with reference to the drawings.

【0013】図1には、サファイアからなり、球状の外
表面1aを有する本発明実施例の関節構成物体1を示
し、該外表面1aは化学的な処理により面粗さRaで
0.05以下の鏡面に仕上げられている。また、図2に
はこの関節構成物体1で母指CM関節Jを置換したとこ
ろを示し、後述する方法で球面に骨切りした近位側骨P
と遠位側骨Dの骨端面P2 、D2 と上記関節構成物体1
の外表面1aが滑らかに摺動するようになっている。
FIG. 1 shows a joint component 1 of a preferred embodiment of the present invention, which is made of sapphire and has a spherical outer surface 1a. The outer surface 1a has a surface roughness Ra of 0.05 or less by chemical treatment. It is finished to the mirror surface. Further, FIG. 2 shows that the thumb CM joint J is replaced with this joint component 1, and the proximal bone P is cut into a spherical surface by the method described later.
And the end face P 2 , D 2 of the distal bone D and the joint component 1
The outer surface 1a of the above slides smoothly.

【0014】このような関節構成物体1は、ステムを備
えず、したがってステムを骨髄腔内に固定する人工関節
にしばしば見られる、ステムと骨とのズレより生じる合
併症の問題が発生することがない。さらに、この関節構
成物体1で置換した母指CM関節Jの屈曲、伸展等の動
きは、関節構成物体1の球状の外表面1aが上記骨端面
2 、D2 と摺動することによって行われるため、非常
に広い可動域を有する。
Such a joint-constituting object 1 does not have a stem, and therefore, a problem of complication caused by a deviation between the stem and the bone, which is often seen in an artificial joint for fixing the stem in the bone marrow cavity, may occur. Absent. Further, the flexion, extension, and other movements of the thumb CM joint J replaced with the joint component 1 are performed by sliding the spherical outer surface 1a of the joint component 1 with the epiphyses P 2 and D 2. Therefore, it has a very wide range of motion.

【0015】なお、機械的処理のみで関節構成物体1を
作製する場合、微小凹凸が外表面に存在してしまうこと
もあり、摺動特性上好ましくないことがある。
When the joint-constituting object 1 is produced only by mechanical treatment, fine irregularities may be present on the outer surface, which is not preferable in terms of sliding characteristics.

【0016】上述の関節構成物体1の材質としては、ア
ルミナやジルコニアなどの多結晶セラミックス、単結晶
サファイア、などのセラミック材料、生体ガラス、カー
ボンなどの無機材料、或いはコバルト/クロム合金など
生体親和性を有する金属材料、又は超高分子量ポリエチ
レン、ポリウレタン、PVAなどの有機材料等の生体為
害性を示さない材料を用いることができる。但し、シリ
コンなどのようにたとえ医用材料であっても、生体内で
の耐久性に乏しい材料は好ましくない。
As the material of the joint component 1, the polycrystal ceramics such as alumina and zirconia, the ceramic material such as single crystal sapphire, the inorganic material such as bioglass and carbon, or the biocompatibility such as cobalt / chromium alloy is used. It is possible to use a metal material having the above or an organic material such as ultra-high molecular weight polyethylene, polyurethane, PVA, or the like, which does not show biotoxicity. However, even if it is a medical material such as silicon, a material having poor durability in a living body is not preferable.

【0017】この、関節構成物体1を用いた上記母指C
M関節Jの置換術では、まず関節構成物体1として直径
8mm〜11mmまでのものを1mmごとに用意してお
き、またこれらの関節構成物体と同寸法、同形状の部分
を有する指摘(不図示)とこれらに対応する掘削用リー
マー(不図示)を用意した。次に、適当な寸法の掘削用
リーマーを選択し、これを用いて母指CM関節J部分を
掘削し、近位側骨Pの骨遠位端P1 と遠位側骨Dの骨近
位端D1 に、曲面をなした骨端面P2 、D2 を形成し
た。この骨掘削の作業の後、上記指摘を用いて関節を置
換する関節構成物体1の最も適した寸法を確認した上
で、その寸法の関節構成物体1を近位側骨Pと遠位部骨
Dの間に設置してその安定性を最終的に確認し、最後
に、APLの半切腱を用いて関節包の補強を行った。
The thumb C using the joint component 1
In the replacement operation of the M joint J, first, the joint component 1 having a diameter of 8 mm to 11 mm is prepared for each 1 mm, and the joint component has the same size and shape (not shown). ) And a reamer for excavation (not shown) corresponding to these are prepared. Next, an reamer for excavation having an appropriate size is selected, and the CM joint J portion of the thumb is excavated by using the reamer, and the bone distal end P 1 of the proximal bone P and the bone proximal of the distal bone D are proximally excavated. Curved bone end faces P 2 and D 2 were formed at the end D 1 . After this bone excavation work, the most suitable size of the joint component 1 for replacing the joint is confirmed using the above-mentioned indication, and then the joint component 1 of that size is used for the proximal bone P and the distal bone. It was placed between D and its stability was finally confirmed, and finally, the joint capsule was reinforced using a half-section tendon of APL.

【0018】本置換術は、上述のように近位側骨Pと遠
位側骨Dについて骨髄腔の掘削を行う必要がなく、両骨
のそれぞれ骨遠位端P1 と骨近位端D1 に、わずかな骨
掘削量で曲面をなした骨端面P2 、D2 を形成するの
で、手術時間の大幅な短縮と、出血量の大幅な減少が実
現し、患者にとって非常に安全である。また、一般に手
や足の指の関節置換術は周囲のじん帯や関節包みの機能
を損なうと関節構成物体の支持性能が低下してしまうの
で、置換術を非常に慎重に執り行う必要があり、熟練が
要求されるものであるが、本置換術においては手術手技
が簡便であり特に熟練を必要とするものではないため安
全である。
In this replacement operation, it is not necessary to excavate the bone marrow cavity in the proximal bone P and the distal bone D as described above, and the bone distal end P 1 and the bone proximal end D of both bones are respectively removed. In addition , since the curved end faces P 2 and D 2 are formed with a small amount of bone excavation, the operation time is greatly shortened and the bleeding amount is significantly reduced, which is very safe for the patient. . In addition, joint replacement of the hands and toes generally impairs the ability to support joint components when the functions of the surrounding ligaments and joint wraps are impaired, so replacement must be performed very carefully. However, it is safe because the surgical procedure is simple and does not require special skill in this replacement surgery.

【0019】また、上述の置換術後、3〜4週間は患部
に固定用装具(不図示)を装着し、その後可動域ROM
を増やす訓練を行った。置換例20件につき術後1年の
経過では、疼痛の大幅な軽減、可動域ROM及びピンチ
力の改善が確認され、また亜脱臼や脱臼は生じておら
ず、術後の経過は良好である。
After the above-mentioned replacement, the fixing device (not shown) is attached to the affected area for 3 to 4 weeks, and then the range of motion ROM is set.
I trained to increase. One year after the operation for 20 replacement cases, the pain was significantly reduced, the ROM of range of motion and the pinch force were improved, and subluxation and dislocation did not occur. The postoperative course is good. .

【0020】上述の実施例は本発明の範囲を限定するも
のではなく、例えば、足の指関節、肩関節など、その他
の応用部位があり、また関節の破壊状態には様々な様態
なものがあるため、関節を置換する関節構成物体1とし
ては症例に応じた形状、大きさのものが必要になってく
る。
The above-described embodiments do not limit the scope of the present invention, and there are other application parts such as a toe joint, a shoulder joint, and the like, and various states of destruction of joints are possible. Therefore, the joint-constituting object 1 that replaces the joint needs to have a shape and size according to the case.

【0021】図3には、他の形状を有する本発明の関節
構成物体を示し、(a)は先端に球面1を具備した略三
角錐形状をなす関節構成物体1、(b)は楕円球状をな
す関節構成物体1、(c)は瓢箪型をした関節構成物体
1、(d)には中央が略円筒形状をなし、両端が半球状
である関節構成物体1であり、これらの関節構成物体1
は、球面1bが遠位部側骨Pの骨端面P2 あるいは近位
部側骨Dの骨端面D2と摺動するようになっている。な
お、骨端面P2 、D2 と摺動する面の形状は球面1bに
限られるわけではなく曲面であればよい。
FIG. 3 shows a joint-constituting object of the present invention having another shape. (A) is a joint-constituting object 1 having a substantially triangular pyramid shape having a spherical surface 1 at its tip, and (b) is an elliptic sphere. Is a gourd-shaped joint constituent object 1, and (d) is a joint constituent object 1 having a substantially cylindrical center and hemispherical ends. Object 1
The spherical surface 1b slides on the epiphyseal surface P 2 of the distal bone B or the epiphysial surface D 2 of the proximal bone D. The shape of the surface that slides on the bone end faces P 2 and D 2 is not limited to the spherical surface 1b and may be a curved surface.

【0022】また本発明の関節構成物体1は、単独で関
節部分を置換するものの他に、図4に示すように、複数
の球状の関節構成物体1でもって、関節部分を置換する
ものであってもよい。
Further, the joint-constituting object 1 of the present invention replaces the joint portion alone, and as shown in FIG. 4, it replaces the joint portion with a plurality of spherical joint-constituting objects 1. May be.

【0023】[0023]

【発明の効果】本発明の関節構成物体は、髄腔支持部を
手術時間の短縮、出血量の低減を伴うより簡便な関節置
換術が可能であり、さらにステムを備えた関節構成物体
の如く骨とのズレによつ合併症等を引きを越すことがな
いため患者にとってより安全な関節構成物体の設置が実
現し、さらに本関節構成物体によって、より大きな関節
の可動域が実現した。
EFFECTS OF THE INVENTION The joint component of the present invention is capable of performing a simpler joint replacement operation that shortens the operation time of the medullary cavity support portion and reduces the amount of bleeding, and is like a joint component having a stem. Since the complications caused by the displacement with the bone are not exceeded, it is possible to install the joint component more safely for the patient, and the joint component realizes a larger range of motion of the joint.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明実施例の関節構成物体の斜視図である。FIG. 1 is a perspective view of a joint component according to an embodiment of the present invention.

【図2】本発明実施例の関節構成物体を示す斜視図であ
る。
FIG. 2 is a perspective view showing a joint component according to an embodiment of the present invention.

【図3】本発明の関節構成物体の斜視図であり、(a)
は先端に球面を有する略三角錐形状をなす関節構成物
体、(b)は楕円球状をなす関節構成物体1、(c)に
は瓢箪型をした関節構成物体1、(d)は中央が略円筒
形状をなし、両端が半球状である関節構成物体1であ
る。
FIG. 3 is a perspective view of a joint component of the present invention, (a)
Is a joint component having a substantially triangular pyramid shape with a spherical tip, (b) is an ellipsoidal joint component 1, (c) is a gourd-shaped joint component 1, and (d) has a substantially central portion. The joint component 1 has a cylindrical shape and both ends are hemispherical.

【図4】複数を同一箇所に用いた関節構成物体を示す斜
視図である。
FIG. 4 is a perspective view showing a joint-constituting object using a plurality of joints at the same location.

【符号の説明】[Explanation of symbols]

1 関節構成物体 1a 外表面 1b 球面 P 近位側骨 D 遠位側骨 P1 骨遠位端 D1 骨近位端 P2 骨端面 D2 骨端面 J 母指CM関節1 glenoid object 1a outer surface 1b spherical P proximal bone D distal bone P 1 Bone distal end D 1 Bone proximal end P 2 epiphyseal face D 2 epiphyseal surface J thumb CM joint

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 生体の関節を構成し、近位端側の骨組織
と遠位端側の骨組織に隣接する関節構成物体であって、
少なくとも一方の骨端部表面にて摺動するよう少なくと
も一つ以上の曲面により形成され、生体内で安定でかつ
異害性を示さない材料からなることを特徴とする関節構
成物体。
1. A joint component that constitutes a joint of a living body and is adjacent to bone tissue on the proximal end side and bone tissue on the distal end side,
A joint component, which is formed of at least one curved surface so as to slide on at least one epiphyseal surface and is made of a material that is stable in the body and does not show harm.
JP34814592A 1992-12-28 1992-12-28 Joint component Expired - Fee Related JP3164675B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP34814592A JP3164675B2 (en) 1992-12-28 1992-12-28 Joint component

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP34814592A JP3164675B2 (en) 1992-12-28 1992-12-28 Joint component

Publications (2)

Publication Number Publication Date
JPH06189987A true JPH06189987A (en) 1994-07-12
JP3164675B2 JP3164675B2 (en) 2001-05-08

Family

ID=18395055

Family Applications (1)

Application Number Title Priority Date Filing Date
JP34814592A Expired - Fee Related JP3164675B2 (en) 1992-12-28 1992-12-28 Joint component

Country Status (1)

Country Link
JP (1) JP3164675B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2018530397A (en) * 2015-10-15 2018-10-18 ジンマー,インコーポレイティド Stemless shoulder joint implant
US10687949B2 (en) 2012-12-27 2020-06-23 Zimmer Gmbh Shoulder prosthesis and components thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10687949B2 (en) 2012-12-27 2020-06-23 Zimmer Gmbh Shoulder prosthesis and components thereof
US10828169B2 (en) 2013-12-19 2020-11-10 Zimmer, Inc. Stemless shoulder implant
JP2018530397A (en) * 2015-10-15 2018-10-18 ジンマー,インコーポレイティド Stemless shoulder joint implant
US11666450B2 (en) 2015-10-15 2023-06-06 Zimmer, Inc. Method for installing a stemless shoulder implant

Also Published As

Publication number Publication date
JP3164675B2 (en) 2001-05-08

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