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JPS6216102B2 - - Google Patents

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Publication number
JPS6216102B2
JPS6216102B2 JP57029753A JP2975382A JPS6216102B2 JP S6216102 B2 JPS6216102 B2 JP S6216102B2 JP 57029753 A JP57029753 A JP 57029753A JP 2975382 A JP2975382 A JP 2975382A JP S6216102 B2 JPS6216102 B2 JP S6216102B2
Authority
JP
Japan
Prior art keywords
surgical instrument
abrasive element
abrasive
tubular member
outer tubular
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.)
Expired
Application number
JP57029753A
Other languages
Japanese (ja)
Other versions
JPS57156753A (en
Inventor
Eru Jonson Ranii
Ii Buritsusetsute Robaato
Jei Bonneru Reonaado
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.)
Dionics Inc
Original Assignee
Dionics Inc
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 Dionics Inc filed Critical Dionics Inc
Publication of JPS57156753A publication Critical patent/JPS57156753A/en
Publication of JPS6216102B2 publication Critical patent/JPS6216102B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/313Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor for introducing through surgical openings, e.g. laparoscopes
    • A61B1/317Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor for introducing through surgical openings, e.g. laparoscopes for bones or joints, e.g. osteoscopes, arthroscopes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/04Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor combined with photographic or television appliances
    • A61B1/042Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor combined with photographic or television appliances characterised by a proximal camera, e.g. a CCD camera
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods
    • A61B17/32Surgical cutting instruments
    • A61B17/320016Endoscopic cutting instruments, e.g. arthroscopes, resectoscopes
    • A61B17/32002Endoscopic cutting instruments, e.g. arthroscopes, resectoscopes with continuously rotating, oscillating or reciprocating cutting instruments

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Surgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Medical Informatics (AREA)
  • Molecular Biology (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physics & Mathematics (AREA)
  • Biophysics (AREA)
  • Optics & Photonics (AREA)
  • Pathology (AREA)
  • Radiology & Medical Imaging (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Surgical Instruments (AREA)

Description

【発明の詳細な説明】 本発明は整形外科器具に関し、特に関節鏡使用
の目視による関節内関節形成術を行ない得る器具
に関する。関節内とは生体の関節例えば膝を意味
し、関節形成術とは関節面の成形又は修正を意味
し、関節鏡使用とは開口を通して関節部内に挿入
した深針による目視であつて関節を外科的に切開
しない。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to orthopedic instruments, and more particularly to instruments capable of performing arthroscopic visual intra-articular joint arthroplasty. Intra-articular refers to a living joint such as a knee, arthroplasty refers to shaping or modifying the joint surface, and arthroscopy refers to visual observation using a deep needle inserted into the joint through an opening, and surgical treatment of the joint. Do not make any incisions.

数十年前から、人体関節は目視深針即ち内視鏡
を挿入すれば目視可能であることは知られている
が、関節手術は主として開放外科によつて行なわ
れている。標準の膝手術において、手術目的は少
量の軟骨又は骨を除去することであつても、比較
的大きな切開が必要とされた。これは手術自体が
外傷を生ずるため、長い治療期間と、不愉快と、
運動制限とを招く。
Although it has been known for several decades that joints in the human body can be visualized through the insertion of a deep needle or endoscope, joint surgeries are primarily performed by open surgery. In standard knee surgery, relatively large incisions are required, even when the purpose of the surgery is to remove small amounts of cartilage or bone. This is because the surgery itself causes trauma, resulting in a long treatment period and discomfort.
This can lead to exercise restrictions.

膝又は他の関節スペースの閉鎖外科によつて関
節形成術を企画する場合には、多くの要件、互に
矛盾した要件が生ずる。例えば、器具は小型で操
作性が良く、関節部に入る必要があり、しかも、
力の伝達と除去物質の導出のための大きさを必要
とする。関節面に対する不時の作用を行なわない
安全性と、所要の時の強い切削作用とを必要とす
る。尚、信頼性高く、各種の熟練度の整形外科医
が安全に使用し得る必要がある。
When planning an arthroplasty by closed surgery of the knee or other joint spaces, many and sometimes contradictory requirements arise. For example, the device must be small, maneuverable, enter the joint, and
Requires size for force transmission and removal material extraction. It requires safety to avoid unintentional action on the joint surface, and strong cutting action when required. Additionally, it must be highly reliable and safe to use by orthopedic surgeons of various levels of skill.

関節鏡使用外科器具の既知の例は米国特許第
4203444号があり、使用目的には著しく有効な関
節内削成装置であるが骨の除去を必要とする関節
形成術には使用できない。
A known example of an arthroscopic surgical instrument is U.S. Pat.
No. 4203444, which is an extremely effective intra-articular ablation device for its intended use, but cannot be used in joint arthroplasty procedures that require the removal of bone.

関節面の再生については、脛骨及び大腿骨の軟
骨面上の低摩擦負荷支持面として作用する関節軟
骨の薄い被覆が変性した時、例えば退行性関節点
の場合には、選択された互に離れた複数の点で軟
骨下の骨まで3〜4mmの深さに穿孔し、脈管床を
露出させて線維軟骨の生成を促して関節面を再生
する提案がある。
For regeneration of articular surfaces, when the thin covering of articular cartilage that acts as a low-friction load-bearing surface on the cartilaginous surfaces of the tibia and femur degenerates, e.g. in the case of degenerative joint points, There is a proposal to drill holes to a depth of 3 to 4 mm into the subchondral bone at multiple points, expose the vascular bed, and promote the production of fibrocartilage to regenerate the joint surface.

他の例では同じ目的のために掻把が使用される
が面形状に悪い変化がある。
In other examples, scrapers are used for the same purpose, but with negative changes in surface shape.

本発明によつて、既知の深い離れた穿孔や強い
掻把に代えて関節面を広い範囲に深さ0.5〜1mm
程度に、関節鏡を外科医が直視して回転半遮蔽軟
骨及び骨磨削吸取り器具を使用して除去即ち磨削
することによつて良い結果が得られる。
With the present invention, instead of the known deep and distant drilling and strong scraping, the articular surface can be drilled over a wide area with a depth of 0.5 to 1 mm.
To some extent, good results are obtained by removing or ablating the arthroscope in direct view of the surgeon using a rotating semi-shielded cartilage and bone ablation instrument.

本発明による関節鏡使用磨削器具は、関節鏡の
制御の下で関節形成術を可能にし、器具は小型で
操作性が良く狭い関節部内に入ることができ、軟
骨と骨とを磨削除去するに必要な力を伝達でき、
除去物質を取出可能であり、小さな穿孔のみを経
て関節形成術を可能とする。
The arthroscopic abrasion instrument of the present invention enables arthroplasty under arthroscopic control, the instrument is small and maneuverable, and can enter narrow joints to abrade cartilage and bone. can transmit the force necessary to
The removed material is removable, allowing arthroplasty through only a small puncture.

詳細に述べれば、本発明は関節鏡使用関節形成
術用の外科器具であつて、穿孔を経て関節内に挿
入され、関節鏡による外科医の直接目視制御下で
負荷支持関節面の変性した軟骨と骨を除去して、
硬化した骨の面の下の豊富な脈管を露出させて、
脈管床の供給する血液による線維生成と治ゆとを
可能にし、かくして負荷支持関節面を覆う線維軟
骨の生成を可能にする。この器具は外側管状シー
スと、シースを固着する支持部材と、外側シース
内を延長する内側管状軸とを備え、内側管状軸の
前端に支持した磨削素子の面は回転によつて関節
面を磨削するようにし、外側シースの形状は磨削
素子の限定部分を露出して磨削作用を行なわせ、
外側シースは保護シールドの役割として磨削素子
の関節面内に限定した深さの切込みを補助すると
共に磨削素子が他の方向から関節面に接触するの
を防ぐシールドとなり、内側管状軸は後端を真空
源に連結可能として液と随伴磨削物質とを管状軸
を通つて排出し、内側管状軸を回転させる装置を
備え、軸を外側シースに対して少なくとも1個の
中空の環状前部軸受部材を設け、磨削素子は関節
面との磨削係合間横方向の負荷を受け、内側管状
軸は軸受を通つて軸受部材より前方の液開口に連
通して液と随判磨削物質とを軸受内を通つて排出
可能とする。
Specifically, the present invention is a surgical instrument for arthroscopic arthroplasty that is inserted into a joint through a drill hole and, under direct visual control of the arthroscopic surgeon, removes the degenerated cartilage of a load-bearing articular surface. remove the bone,
By exposing the rich vasculature beneath the hardened bone surface,
It allows fibrosis and healing by the blood supplied by the vascular bed, thus allowing the production of fibrocartilage covering the load-bearing articular surfaces. The instrument includes an outer tubular sheath, a support member for securing the sheath, and an inner tubular shaft extending within the outer sheath, wherein the surface of the abrasive element supported at the front end of the inner tubular shaft rotates to rotate the articular surface. The shape of the outer sheath exposes a limited portion of the abrasive element to perform the abrasive action;
The outer sheath acts as a protective shield, helping the grinding element to cut to a limited depth within the articular surface, and also serves as a shield to prevent the grinding element from coming into contact with the articular surface from other directions. at least one hollow annular front portion, the end being connectable to a vacuum source to expel liquid and entrained abrasive material through the tubular shaft, and having a device for rotating the inner tubular shaft, the shaft relative to the outer sheath; A bearing member is provided, the abrasive element receives a lateral load during abrasive engagement with the articular surface, and the inner tubular shaft communicates through the bearing to a fluid opening anterior to the bearing member to receive fluid and abrasive material. and can be discharged through the bearing.

好適な実施例は次の通りである。互に離れた前
部後部軸受面を設け、前部軸受部材は半径方向に
延長し内側管状軸と共に回転する環状面とし;外
側シースの形状は磨削素子の一側の限定部分を露
出するようにし;外側シースの形状は磨削素子の
端部の限定部分を露出させ;外側シースの形状は
磨削素子の磨削作用のための一側の限定部分と端
部の限定部分を露出させ;外側シースの前端部を
一側に沿つて斜方向に切取つて磨削素子の磨削面
の一側を次第に露出させ;軸の前端部を磨削素子
の端面に近接した位置とし;磨削素子の露出側は
外側シースの骨状壁にほぼ一致させ;外側シース
をシース軸線に対して30゜の角度の面内の線に沿
つて切取り;器具を外部真空源に連結して内側管
状軸は液と随伴磨削組織と骨とを関節部から少な
くとも100c.c./分の流量で排出させ;磨削素子の
一端に駆動スプールを形成させ、駆動スプールを
軸線方向に内側管状軸の前端に取外可能に支持
し;内側管状軸の前端をチヤツク部材とし、チヤ
ツク部材は中空として磨削素子の関節面係合間駆
動スプールを受入固着する受入装置を設け;前端
軸受をチヤツク部材の受入装置付近の外壁から環
状に延長させ、チヤツク部材の環状壁に孔を設
け、孔を受入装置に近接して軸受の前方とし、チ
ヤツク部材は液と随伴磨削組織の導管として前部
軸受とチヤツク部材内を通つて内側管状軸導管に
連通して液を体内から排出させ;内側環状軸にロ
ツク装置を設けて磨削素子駆動スプールの前端を
受けて係止し手術間の駆動スプールの抜け出しを
防ぎ;磨削素子と駆動スプールとを一体に形成
し;外側管状シースを約50mm以上の長さで約4mm
以上の直径とし;内側管状軸は500rpm乃至3000
の回転とし;回転装置は外科医の制御で反転可能
とし;磨削素子は反転に際して正転よりは小さな
切込みとする。
A preferred embodiment is as follows. Spaced apart front and rear bearing surfaces are provided, the front bearing member being a radially extending annular surface that rotates with the inner tubular shaft; the outer sheath is shaped to expose a limited portion of one side of the abrasive element. the shape of the outer sheath exposes a limited portion of the end of the abrasive element; the shape of the outer sheath exposes a limited portion of one side and a limited portion of the end for the abrasive action of the abrasive element; The front end of the outer sheath is cut diagonally along one side to gradually expose one side of the abrasive surface of the abrasive element; the front end of the shaft is located proximate the end surface of the abrasive element; the exposed side of the outer sheath approximately coincides with the bony wall of the outer sheath; cut the outer sheath along a line in the plane at a 30° angle to the sheath axis; connect the instrument to an external vacuum source and the inner tubular shaft Fluid and accompanying abrasive tissue and bone are expelled from the joint at a flow rate of at least 100 c.c./min; a drive spool is formed at one end of the abrasive element, and the drive spool is axially attached to the anterior end of the inner tubular shaft. The front end of the inner tubular shaft is removably supported; the chuck member is hollow and has a receiving device for receiving and fixing the driving spool between the articulating surfaces of the grinding element; the front end bearing is provided near the receiving device of the chuck member; extending annularly from the outer wall of the chuck member and providing a hole in the annular wall of the chuck member, with the hole proximate the receiving device and forward of the bearing, and the chuck member serving as a conduit for fluid and entrained abrasive tissue within the front bearing and the chuck member. through the inner tubular shaft to communicate with the inner tubular shaft conduit for draining fluid from the body; a locking device is provided on the inner annular shaft to receive and lock the front end of the abrasive element drive spool to prevent the drive spool from slipping out during surgery; The grinding element and the drive spool are integrally formed; the outer tubular sheath has a length of about 4 mm with a length of about 50 mm or more.
The diameter of the inner tubular shaft should be between 500rpm and 3000rpm.
The rotating device is reversible under the surgeon's control; the abrasive element makes a smaller cut when reversing than when rotating forward.

上述の特定の関節形成術以外にも本発明の器具
は使用可能である。例えば関節の軟骨が面の欠陥
又は不整面がある場合、又は他の関節内外科に際
して軟骨に不整形が形成された場合等である。本
発明の器具は面の欠陥不整を平滑にし整形して患
者の苦痛を減少し、患者の関節運動性を向上する
のに有効である。
The device of the present invention can be used in addition to the specific arthroplasty procedures described above. For example, this may occur when the articular cartilage has a defective or irregular surface, or when an irregularity is formed in the cartilage during other intra-articular surgery. The devices of the present invention are effective in smoothing and shaping surface imperfections to reduce patient pain and improve patient joint mobility.

全く異なる分野で、人体から物体を除去するた
めに、特に目の中の物体例えば白内障のレンズを
除去するために、磨削器具に調整可能の管状装置
を設けて磨削切刃の露出を制御することが米国特
許第3937222号に記述してある。
In a completely different field, for removing objects from the human body, especially for removing objects in the eye, such as cataract lenses, the abrasive instrument is provided with an adjustable tubular device to control the exposure of the abrasive cutting edge. This is described in US Pat. No. 3,937,222.

本発明の構造と作動とを好適な例示とした実施
例並びに図面について説明する。
Embodiments and drawings illustrating the structure and operation of the present invention will be described.

第1,2図に示す器具10は、膝関節内に挿入
されて脛骨6と大腿骨8との低摩擦負荷支持関節
面に作用する。同時にフアイバーオプテイツクス
装置4は光を光源12から関節内に導き、別の光
経路に沿つて可視像を戻す。像は外科医の接眼鏡
及び記録カメラに導くこともできるが、図示の好
適な実施例では像をテレビジヨンカメラ16に導
いて表示18を生じ、この表示を外科医が見て手
術運動を制御する。スクリーンを見て器具を操作
することによつて、器具は関節面に沿つて動き、
関節面を磨削し、これがテレビ画面に示される。
面画の詳細は第10,11図について後述する。
The instrument 10 shown in FIGS. 1 and 2 is inserted into the knee joint and acts on the low-friction, load-bearing articular surfaces of the tibia 6 and femur 8. At the same time, fiber optic device 4 directs light from light source 12 into the joint and returns a visible image along another light path. Although the image could be directed to the surgeon's eyepiece and recording camera, in the preferred embodiment shown, the image is directed to a television camera 16 to produce a display 18 that is viewed by the surgeon to control surgical movements. By looking at the screen and operating the device, the device moves along the joint surface.
The joint surfaces are ground and this is shown on the television screen.
Details of the screen will be described later with reference to FIGS. 10 and 11.

手術間、生理的食塩水を制御された水圧で給水
源2から供給して関節を膨張させる。
During surgery, physiological saline is supplied from water source 2 at controlled water pressure to inflate the joint.

器具の成功は前述した通り本発明による構造の
重要な特長によつて定まる。第2,2a,3図に
示す通り、好適な実施例による器具10の外管2
0は外径7.5mm、内径6.4mmとし、外管20内に伸
縮可能に挿入した内管24は外径5.2mm、内径4.4
mmとした。内管24は外管20に対して回転さ
せ、駆動装置は第1図に示し、電池駆動モータ1
54はハンドル50内に取付けて第2図に示す駆
動突起28に係合する。モータ54は足踏みスイ
ツチ55等を外科医が制御して逆転可能である。
モータ54の生ずるトルク値は2.88Kg・cm程度と
し、磨削素子を通常の骨磨削負荷で約500rpm、
最大約3000rpmで回転させる。
The success of the device depends on the important features of the structure according to the invention, as mentioned above. As shown in FIGS. 2, 2a and 3, an outer tube 2 of a device 10 according to a preferred embodiment
0 has an outer diameter of 7.5 mm and an inner diameter of 6.4 mm, and the inner tube 24, which is extendably inserted into the outer tube 20, has an outer diameter of 5.2 mm and an inner diameter of 4.4 mm.
mm. The inner tube 24 is rotated relative to the outer tube 20, and the drive device is shown in FIG.
54 is mounted within the handle 50 and engages the drive projection 28 shown in FIG. The motor 54 can be reversed by controlling a foot switch 55 or the like by the surgeon.
The torque value generated by the motor 54 is approximately 2.88 kg cm, and the grinding element is rotated at approximately 500 rpm under normal bone grinding load.
Rotate at a maximum of approximately 3000 rpm.

第2a,3,4,5図において、内管24の先
端にチヤツク30を固着する。チヤツク30は別
個に成型したユニツトとし、内管24にエポキシ
接着剤によつて軸線方向に固着する。チヤツク3
0は磨削素子40の駆動スプール42を受入保持
し、器具を関節面に係合させる間に作用する力に
確実に抗し得る保持とする。このためには、熱処
理ステンレス鋼製のチヤツク30の壁部32に軸
線に沿つた切断部34を形成し、板ばね状係止部
36を永久的に形成する。壁部32に変形部38
を形成してアライメント案内とする。磨削素子4
0に磨削ヘツド44を設け、図示の例では直径
5.5mmとし、磨削面には12本のらせん状の溝とし
た切刃を設ける。ヘツド44の駆動スプール42
は直径2.4mm長さ10.3mmとした。らせん状切刃の
構成は、正回転の時に磨削素子の切込量が大き
く、逆回転の時は少なくなるようにする。ヘツド
44とスプール42とは熱処理ステンレス鋼の一
体の部材から加工し、外科手術間の作用力例えば
横方向曲げ圧力170〜340Kg/cm2程度の作用下で破
断するのを防ぐ。この磨削素子は一回限り使用と
し、手術毎に新しい鋭い刃を使用できる。駆動ス
プール42に軸線方向の切込みを設け、この切込
み部は第6,7図に示す通り、アライメント平面
部52、係止平面部54及びアライメント案内用
間隙56とする。スプール42に環状切込み58
を自由端に形成してチヤツクへの挿入を容易にす
る。器具を使用可能状態とするには、駆動スプー
ル42をチヤツク30の端部に軽く挿入し、磨削
素子を緩やかに回転してアライメント案内38を
アライメント平面部52に一致させ、スプール4
2をチヤツク30内に押しこむ。磨削素子40を
軸線方向にチヤツク内に押込み、係止部36を係
止平面部54内とし、この時はチヤツク30の肩
部が磨削素子40の肩部に接触する。この位置
で、磨削ヘツド44は内側軸24上に固定され、
外科手術間に作用するすべての力に耐える。磨削
ヘツドを取外すには、第9図に示す工具を使用す
る必要がある。磨削ヘツド44を開口62内に通
し、開口64はチヤツク30の周囲に接触する。
矢印Aに示す方向に力を作用し、スプール42を
チヤツク30から引抜く。磨削素子は廃棄し、新
しい素子を挿入する。内管24と外管20とは通
常は分解して磨削素子の取付取外を行なう。
In Figures 2a, 3, 4 and 5, a chuck 30 is fixed to the tip of the inner tube 24. The chuck 30 is a separately molded unit and is axially secured to the inner tube 24 by epoxy adhesive. Check 3
0 receives and holds the drive spool 42 of the abrasive element 40, providing a secure hold against the forces exerted during engagement of the instrument with the articular surface. To this end, an axial cut 34 is formed in the wall 32 of the chuck 30 made of heat-treated stainless steel to permanently form a leaf spring-like lock 36. Deformed portion 38 on wall portion 32
is formed to serve as an alignment guide. Grinding element 4
A grinding head 44 is provided at 0, and in the example shown, the diameter
The diameter is 5.5 mm, and the cutting edge has 12 spiral grooves on the ground surface. Drive spool 42 of head 44
The diameter was 2.4 mm and the length was 10.3 mm. The configuration of the helical cutting edge is such that the depth of cut of the abrasive element is large when rotating in the forward direction, and small when rotating in the reverse direction. The head 44 and spool 42 are fabricated from a single piece of heat-treated stainless steel to resist rupture under the forces exerted during surgical procedures, such as lateral bending pressures on the order of 170-340 kg/cm 2 . This abrasive element is for one-time use and a new sharp blade can be used for each surgery. The drive spool 42 is provided with an axial notch, which serves as an alignment flat portion 52, a locking flat portion 54, and an alignment guide gap 56, as shown in FIGS. Annular notch 58 in spool 42
is formed at the free end to facilitate insertion into the chuck. To prepare the instrument for use, the drive spool 42 is lightly inserted into the end of the chuck 30, the abrasive element is gently rotated to align the alignment guide 38 with the alignment flat 52, and the spool 4 is
2 into the chuck 30. The abrasive element 40 is pushed axially into the chuck so that the catch 36 is within the catch flat 54, with the shoulder of the chuck 30 contacting the shoulder of the abrasive element 40. In this position, the grinding head 44 is fixed on the inner shaft 24 and
Withstands all forces acting during surgical procedures. To remove the grinding head it is necessary to use the tool shown in FIG. The abrasive head 44 is passed through the aperture 62 and the aperture 64 contacts the circumference of the chuck 30.
A force is applied in the direction shown by arrow A to pull the spool 42 out of the chuck 30. The abrasive element is discarded and a new element inserted. The inner tube 24 and the outer tube 20 are normally disassembled to attach and remove the grinding elements.

組立てた時には磨削ヘツド44は軸線方向に外
管20の前端から約1mm突出する。外管20は標
準として長さ少なくとも50mmとする。外管20の
前端は一側に沿つて管の軸線に対してある角度、
図示の例では24゜に切取り、外管外壁82と一致
した位置で摩削ヘツド44の側面80を順次露出
させる。この順次のテーパを第12〜12b図の
断面として示す。
When assembled, the grinding head 44 axially projects approximately 1 mm from the front end of the outer tube 20. As standard, the outer tube 20 has a length of at least 50 mm. The front end of the outer tube 20 is at an angle to the axis of the tube along one side;
In the illustrated example, the cut is made at 24 degrees to sequentially expose the side surface 80 of the grinding head 44 at a position that coincides with the outer wall 82 of the outer tube. This sequential taper is shown in cross section in Figures 12-12b.

磨削素子44に対してある角度即ち実質上駆動
軸線に対して直角方向に作用する力によつて、骨
の磨削負荷の下で半径方向の曲りを生じないよう
に内軸24を支持する必要がある。この支持を行
なう前端環状軸受90は外管20の前端に近い位
置でチヤツク30の外壁31に固着し、後端は後
端環状軸受92を内軸24の壁部に固着して支持
する。両軸受は内軸24と共に回転し外管20の
内壁に対して軸24を支持する。更に、上述の軸
受を設けることによつて器具の摩擦抗力は低く、
所要のトルク即ち約2.88Kg・cmを磨削素子に供給
し得る。このトルクは故意に上限を定めて過負荷
条件の危険を避ける。
A force acting on the abrasive element 44 at an angle, substantially perpendicular to the drive axis, supports the inner shaft 24 against radial bending under bone abrasive loads. There is a need. A front end annular bearing 90 that provides this support is fixed to the outer wall 31 of the chuck 30 at a position near the front end of the outer tube 20, and a rear end annular bearing 92 is fixed to the wall of the inner shaft 24 and supported at the rear end. Both bearings rotate together with the inner shaft 24 and support the shaft 24 against the inner wall of the outer tube 20. Furthermore, by providing the above-mentioned bearing, the frictional drag of the instrument is low.
The required torque, approximately 2.88 Kg·cm, can be supplied to the grinding element. This torque is intentionally capped to avoid the risk of overload conditions.

チヤツク30の壁部の駆動スプール係止部36
に近接して孔70を設け、中空チヤツク30から
前端軸受90を経て内軸24に達する通路に孔7
0を連結し、真空源45に連通して関節から磨削
された組織を全部取除く。真空源45は器具外と
し、通常は外科用器材中の壁取付真空装置とし、
通常は水銀柱350〜400mm程度とする。真空値は弁
43によつて手許で制御する。
Drive spool locking portion 36 on the wall of chuck 30
A hole 70 is provided in the vicinity of the hollow chuck 30, and the hole 70 is provided in a passage from the hollow chuck 30 to the inner shaft 24 via the front end bearing 90.
0 and communicates with a vacuum source 45 to remove any abraded tissue from the joint. The vacuum source 45 is external to the instrument, typically a wall-mounted vacuum device in the surgical equipment;
Normally, the mercury column is about 350 to 400 mm. The vacuum value is controlled manually by valve 43.

同じ構成の他の実施例として、外管20の外径
5.7mm内径4.7mmとし、この中を滑動可能とした内
管24は外径4.2mm内径3.8mmとし、磨削素子外径
4.0とする。
As another example of the same configuration, the outer diameter of the outer tube 20
The inner diameter of the grinding element is 5.7mm and the inner diameter is 4.7mm, and the inner tube 24 that can slide inside it has an outer diameter of 4.2mm and an inner diameter of 3.8mm.
Set it to 4.0.

作動について説明する。 The operation will be explained.

第1図に示す手術過程間、患者は全身麻酢し、
患者の筋肉の関節付近の選定点にトロアカールカ
ニユーレによつて所要の孔あけを行なう。液を供
給源2から1本のカニユーレ内に僅かに高い圧力
で導入して関節を膨脹させ、関節を経て器具10
の吸入ポート70に流れる流れを生じさせる。流
量は100c.c./分以上を必要とし、関節から磨削さ
れたすべての物質が器具10内に吸込まれて関節
から取除かれるのを確実にする。更に関節内液を
清澄にして器具の目視案内を容易にする。
During the surgical process shown in Figure 1, the patient was given hemp vinegar all over the body,
The required holes are made with a trocar cannula at selected points near the joints of the patient's muscles. Fluid is introduced from source 2 into one cannula at slightly higher pressure to inflate the joint, passing through the joint to instrument 10.
This causes a flow to flow into the suction port 70 of the. The flow rate should be greater than 100 c.c./min to ensure that all material abraded from the joint is sucked into the instrument 10 and removed from the joint. Additionally, intra-articular fluid is clarified to facilitate visual guidance of instruments.

目視器具4を他のカニユーレを経て関節内に挿
入する。第2図に示す器具10は第3のカニユー
レ内に挿入する。
Visual instrument 4 is inserted into the joint via another cannula. The instrument 10 shown in FIG. 2 is inserted into the third cannula.

関節腔内に液供給源2から供給された液は磨削
素子面を通つてチヤツク30と外管20の前端と
の間の環状スペース21に流入し、ここからチヤ
ツク30の壁部の開口70を通る。チヤツク30
の内部スペース71は液を前端軸受を通つて流れ
させ、内管24の形成する通路72に入り、後端
軸受92を通つて排液室74に排出する。室74
はハウジング42内で真空源45に連結する。排
液室74の形状によつて、磨削素子40の回転間
は吸込みが連続的に保たれる。
The fluid supplied from the fluid source 2 into the joint cavity flows through the abrasive element surface into the annular space 21 between the chuck 30 and the front end of the outer tube 20 and from there through the opening 70 in the wall of the chuck 30. pass through. Check 30
The internal space 71 allows the liquid to flow through the front end bearing, enter the passage 72 formed by the inner tube 24 and discharge through the rear end bearing 92 into the drainage chamber 74 . room 74
is connected within housing 42 to a vacuum source 45 . Due to the shape of the drainage chamber 74, suction is maintained continuously during the rotation of the abrasive element 40.

外科医はモータを止めたまゝ器具を関節内に挿
入する。液供給源2と真空源45とを釣合せて関
節内に導入した液量と同量が器具を通つて排出さ
れ、流入圧力を僅に高い圧力に保ち、関節を所要
程度に膨脹させる。
The surgeon inserts the instrument into the joint with the motor stopped. The fluid source 2 and vacuum source 45 are balanced so that the same amount of fluid introduced into the joint is expelled through the instrument, keeping the inlet pressure at a slightly higher pressure and inflating the joint to the desired degree.

流通路と器具の作動部分とは器具を吸込負圧源
(水銀柱約350〜400mm)に連結した時に所要作動
を行なう構造とする。
The flow path and the operating part of the device are designed to perform the required operation when the device is connected to a suction negative pressure source (approximately 350 to 400 mm of mercury).

第10図に示す通り、器具を脛骨6と大腿骨8
の顆面間の狭いスペース100(即ち寸法Bは約
8mm)内に挿入し、軟骨の薄い層102及びその
下の顆骨を磨削する。図示の例では1回のパスで
薄い軟骨層と骨のある深さとを磨削するが、外管
20の底部82を制御支点として使用して1回の
パスでは更に浅い組織を磨削するように制御する
こともできる。磨削ヘツド44の一側と端部との
一部のみが外管20のテーパ端から露出して軟骨
面102に接触し、磨削面の側部後部部分は外管
によつて遮蔽されて周囲の関節組織に不時に接触
するのを防ぐ。
As shown in Figure 10, the instrument is inserted into the tibia 6 and femur 8.
into the narrow space 100 between the condylar surfaces (i.e., dimension B is approximately 8 mm) and abrades the thin layer of cartilage 102 and the underlying condylar bone. Although the illustrated example abrades a thin cartilage layer and bone depth in one pass, the bottom 82 of the outer tube 20 can be used as a control fulcrum to abrade shallower tissue in a single pass. It can also be controlled. Only one side and a portion of the end of the abrasive head 44 are exposed from the tapered end of the outer tube 20 and contact the cartilage surface 102, and the rear side portion of the abrasive surface is shielded by the outer tube. Prevents accidental contact with surrounding joint tissue.

かくして、関節の負荷支持軟骨が変性して回転
半シールド軟骨となつた時に器具の骨磨削ヘツド
44は焦点部位、即ち疾患部分で関節面を動き、
関節軟骨の薄い被覆層と薄い骨の層とを除去し、
軟骨下の骨を深さ約0.5〜1.0mm除去する。これに
よつて平滑な面104を生じ、脈管床が通常露出
し、関節面上に線維軟骨の均等な生成を可能にす
る。
Thus, as the load-bearing cartilage of the joint degenerates into rotating semi-shielded cartilage, the bone abrasive head 44 of the instrument moves across the articular surface at the focal site, i.e. the diseased area.
removing the thin covering layer of articular cartilage and the thin layer of bone;
Remove the subchondral bone to a depth of approximately 0.5-1.0 mm. This creates a smooth surface 104 that normally exposes the vascular bed and allows even production of fibrocartilage over the articular surface.

本発明は種々の変型が可能である。例えば、磨
削素子の形状を楕円形、円筒形等の形状とするこ
ともでき、図示以外の磨削面、比較的平滑な面と
することもできる。
The present invention is capable of various modifications. For example, the shape of the grinding element may be an ellipse, a cylinder, or the like, and the grinding element may have a grinding surface other than that shown, or a relatively smooth surface.

本発明の器具は関節形式術用の他の外科手術例
えば他の軟骨面の損傷又は不整部の平滑化用とし
て使用することができる。
The instruments of the invention can be used in other surgical procedures for arthroplasty, such as smoothing defects or irregularities in other cartilage surfaces.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は膝の関節内関節形成術を行なうための
器材と本発明器具とを示す斜視図、第2図は第1
図の器具の後端部の拡大縦断面図、第2a図は同
じく前端部の拡大縦断面図、第3図は第2a図の
底面側から見た縦断面図、第4図は第2a図の拡
大部分断面図、第5図は第3図の拡大部分断面
図、第6図は器具に使用する磨削素子の側面図、
第7図は第6図の右端面図、第8図は第6図の平
面図、第9図は第6図の磨削素子を取外す工具の
側面図、第10図は本発明器具による関節内の面
に対する脈管床の関節形成術を行なう斜視図、第
11図は第10図の平面図、第12図、第12a
図、第12b図はそれぞれ第5図の12−12
線、12a−12a線、12b−12b線に沿う
断面図である。 6……脛骨、8……大腿骨、10……外科器
具、2……液供給源、20……外側シース、24
……管状軸、40……磨削素子、45……真空
源、70……開口、80……磨削面、90,92
……軸受、102……関節面、140……関節
鏡、154……モータ。
FIG. 1 is a perspective view showing an instrument for performing intra-articular arthroplasty of the knee and the device of the present invention, and FIG.
Figure 2a is an enlarged vertical cross-sectional view of the rear end of the instrument, Figure 3 is a longitudinal cross-sectional view of the front end as seen from the bottom side of Figure 2a, and Figure 4 is Figure 2a. 5 is an enlarged partial sectional view of FIG. 3; FIG. 6 is a side view of the abrasive element used in the instrument;
7 is a right end view of FIG. 6, FIG. 8 is a plan view of FIG. 6, FIG. 9 is a side view of a tool for removing the grinding element of FIG. 6, and FIG. 10 is a joint formed by the instrument of the present invention. 11 is a plan view of FIG. 10; FIG. 12, FIG. 12a;
Figures 12b and 12b are 12-12 of Figure 5, respectively.
12a-12a and 12b-12b; FIG. 6... Tibia, 8... Femur, 10... Surgical instrument, 2... Fluid source, 20... Outer sheath, 24
... Tubular shaft, 40 ... Grinding element, 45 ... Vacuum source, 70 ... Opening, 80 ... Grinding surface, 90, 92
... Bearing, 102 ... Articular surface, 140 ... Arthroscope, 154 ... Motor.

Claims (1)

【特許請求の範囲】 1 先端部側が側方支持されていて、端部に摩削
素子40を有している内側の駆動軸24と、この
駆動軸を包囲し、軸受領域において該駆動軸に対
する前記側方支持を提供する固定の外側管状部材
20とを備えて成る外科用器具であつて、前記摩
削素子の1部に対する遮蔽を提供する前記外側管
状部材の先端延長部と、前記摩削素子の領域から
前記軸受領域を通つて後端部側へ伸び後端部側の
真空連結部に連通する真空通路とを包含してお
り、これによつて、前記駆動軸を駆動しかつ前記
連結部を介して負圧を導入すると、駆動される前
記摩削素子によつて除去された部片が前記軸受領
域を通つて該器具から排出されるようになされた
ことを特徴とする外科用器具。 2 特許請求の範囲第1項に記載の外科用器具に
おいて、前記駆動軸は中空の内側チユーブであ
り、また前記摩削素子を取外し可能に把持しかつ
これを駆動するようになされた中空の内側チユー
ブの先端部に取付けられたチヤツク部材30と、
前記チヤツク部材の先端部に設けられ前記内側チ
ユーブの中への部片の侵入を許容する入口装置7
0とを包含しており、前記内側チユーブの内側の
先端部分が前記真空連結部と連通していることを
特徴とする外科用器具。 3 特許請求の範囲第2項に記載の外科用器具に
おいて、前記入口装置が前記軸受領域の先端部側
に設けられることを特徴とする外科用器具。 4 特許請求の範囲第1項に記載の外科用器具に
おいて、前記外側管状部材の管状の延長部および
前記摩削素子は、生体の肉に設けられる開口を通
して外部から挿入されるような寸法で、かつ、該
器具が可視装置によつて案内される間に、前記摩
削素子が作用する表面の位置に伸長するのに十分
な長さを有するようになされることを特徴とする
外科用器具。 5 特許請求の範囲第1項に記載の外科用器具に
おいて、該器具は、外部真空源に連結されるよう
になされ、かつ、前記領域から摩削された組織を
運ぶ流体を少くとも1分間当り100立方センチメ
ートル程度の流量で排出する能力を有するように
なされたことを特徴とする外科用器具。 6 特許請求の範囲第1項に記載の外科用器具に
おいて、前記駆動軸が、通常の負荷において、少
くとも500rpm程度の速度で回転するようになさ
れたことを特徴とする外科用器具。 7 特許請求の範囲第1項に記載の外科用器具に
おいて、前記駆動軸は外科医の操作により順方向
および逆方向に回転するようになされ、また前記
摩削素子は前記順方向におけるよりも逆方向にお
ける方がより消極的に摩削するようになされてい
ることを特徴とする外科用器具。 8 特許請求の範囲第1項に記載の外科用器具に
おいて、前記外側管状部材の先端部の延長部分は
一側部に沿つて漸次減少して前記摩削素子の表面
を1側部から漸次露呈しており、該外側管状部材
の先端部は前記摩削素子の端面よりも後端側で終
端となつていることを特徴とする外科用器具。 9 特許請求の範囲第8項に記載の外科用器具に
おいて、前記外側管状部材がこの管状部材の軸線
に対して30゜またはそれより小さな角度をもつて
配設される平面内を延在する線に沿つて漸次減少
していることを特徴とする外科用器具。
Claims: 1. An inner drive shaft 24 which is laterally supported on its tip side and has an abrasive element 40 at its end; a fixed outer tubular member 20 providing lateral support; a distal extension of the outer tubular member providing shielding for a portion of the abrasive element; a vacuum passageway extending from the region of the element through the bearing region toward the rear end and communicating with the vacuum connection at the rear end, thereby driving the drive shaft and connecting the Surgical instrument characterized in that upon introduction of negative pressure through the section, the parts removed by the driven abrasive element are ejected from the instrument through the bearing area. . 2. The surgical instrument of claim 1, wherein the drive shaft is a hollow inner tube, and a hollow inner tube adapted to removably grip and drive the abrasive element. a chuck member 30 attached to the tip of the tube;
an inlet device 7 provided at the distal end of the chuck member for allowing entry of the piece into the inner tube;
0, wherein an inner tip portion of the inner tube communicates with the vacuum connection. 3. The surgical instrument according to claim 2, wherein the inlet device is provided on the distal end side of the bearing region. 4. The surgical instrument of claim 1, wherein the tubular extension of the outer tubular member and the abrasive element are dimensioned to be inserted externally through an opening in the flesh of a living body; Surgical instrument, characterized in that the abrasive element is of sufficient length to extend into the position of the working surface while the instrument is guided by a visual device. 5. A surgical instrument according to claim 1, wherein the instrument is adapted to be connected to an external vacuum source and to deliver a fluid carrying ablated tissue from the region at least per minute. A surgical instrument characterized in that it has the ability to discharge at a flow rate of about 100 cubic centimeters. 6. The surgical instrument according to claim 1, wherein the drive shaft rotates at a speed of at least about 500 rpm under normal load. 7. The surgical instrument of claim 1, wherein the drive shaft is rotated in forward and reverse directions by operation of the surgeon, and the abrasive element rotates in the reverse direction more than in the forward direction. 1. A surgical instrument characterized by being adapted to be more passively abrasive. 8. The surgical instrument according to claim 1, wherein the extension of the distal end of the outer tubular member gradually decreases along one side to gradually expose the surface of the abrasive element from one side. A surgical instrument characterized in that the distal end of the outer tubular member terminates on the rear end side of the end surface of the abrasive element. 9. The surgical instrument of claim 8, wherein a line extends in a plane in which the outer tubular member is disposed at an angle of 30° or less to the axis of the tubular member. A surgical instrument characterized in that it gradually decreases along the line.
JP57029753A 1981-02-25 1982-02-25 Surgical device for joint formation Granted JPS57156753A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US23789581A 1981-02-25 1981-02-25

Publications (2)

Publication Number Publication Date
JPS57156753A JPS57156753A (en) 1982-09-28
JPS6216102B2 true JPS6216102B2 (en) 1987-04-10

Family

ID=22895691

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57029753A Granted JPS57156753A (en) 1981-02-25 1982-02-25 Surgical device for joint formation

Country Status (5)

Country Link
JP (1) JPS57156753A (en)
CA (1) CA1175725A (en)
DE (1) DE3206782C2 (en)
FR (1) FR2500292B1 (en)
GB (1) GB2093353B (en)

Families Citing this family (104)

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Publication number Publication date
GB2093353B (en) 1984-09-19
FR2500292A1 (en) 1982-08-27
FR2500292B1 (en) 1986-10-10
JPS57156753A (en) 1982-09-28
DE3206782A1 (en) 1982-10-28
GB2093353A (en) 1982-09-02
DE3206782C2 (en) 1983-01-13
CA1175725A (en) 1984-10-09

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