WO1991006260A1 - Prosthesis of the hip- or knee-joint anchored with a prestressing element - Google Patents

Prosthesis of the hip- or knee-joint anchored with a prestressing element Download PDF

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Publication number
WO1991006260A1
WO1991006260A1 PCT/GR1990/000006 GR9000006W WO9106260A1 WO 1991006260 A1 WO1991006260 A1 WO 1991006260A1 GR 9000006 W GR9000006 W GR 9000006W WO 9106260 A1 WO9106260 A1 WO 9106260A1
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WO
WIPO (PCT)
Prior art keywords
bone
prestressing
anchorage
prosthesis
tendons
Prior art date
Application number
PCT/GR1990/000006
Other languages
French (fr)
Inventor
Constantin Protogirou
Original Assignee
Constantin Protogirou
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 Constantin Protogirou filed Critical Constantin Protogirou
Publication of WO1991006260A1 publication Critical patent/WO1991006260A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/064Surgical staples, i.e. penetrating the tissue
    • A61B17/0642Surgical staples, i.e. penetrating the tissue for bones, e.g. for osteosynthesis or connecting tendon to bone
    • 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
    • A61F2/32Joints for the hip
    • 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
    • A61F2/38Joints for elbows or knees
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16BDEVICES FOR FASTENING OR SECURING CONSTRUCTIONAL ELEMENTS OR MACHINE PARTS TOGETHER, e.g. NAILS, BOLTS, CIRCLIPS, CLAMPS, CLIPS OR WEDGES; JOINTS OR JOINTING
    • F16B35/00Screw-bolts; Stay-bolts; Screw-threaded studs; Screws; Set screws
    • F16B35/04Screw-bolts; Stay-bolts; Screw-threaded studs; Screws; Set screws with specially-shaped head or shaft in order to fix the bolt on or in an object
    • F16B35/041Specially-shaped shafts
    • F16B35/042Specially-shaped shafts for retention or rotation by a tool, e.g. of polygonal cross-section
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • 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, setting implements or the like
    • A61B17/68Internal fixation devices, including fasteners and spinal fixators, even if a part thereof projects from the skin
    • A61B17/84Fasteners therefor or fasteners being internal fixation devices
    • A61B17/86Pins or screws or threaded wires; nuts therefor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B17/00Surgical instruments, devices or methods, e.g. tourniquets
    • A61B17/064Surgical staples, i.e. penetrating the tissue
    • A61B2017/0647Surgical staples, i.e. penetrating the tissue having one single leg, e.g. tacks
    • A61B2017/0648Surgical staples, i.e. penetrating the tissue having one single leg, e.g. tacks threaded, e.g. tacks with a screw thread
    • 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
    • A61F2/08Muscles; Tendons; Ligaments
    • A61F2/0811Fixation devices for tendons or ligaments

Definitions

  • prostheses As substitution for hip -and knee joints, artificial joints (prostheses) have been in use, which were caulked in the bone with the help of bone cement. After a certain period of time, an aseptic loosening of both components of the hip as well as the knee joint prostheses is obse ⁇ rved. This is due to the weakness of bone cement to cope with traction forces (mechanical weakness). To overcome this specific weakness, prostheses which do not use bone cement have been in use for a number of years.
  • the suitable time to charge the artificial joint as well as its life ⁇ pan depend on a number of factors, for example : -The material and surface of the prosthesis. -The joining between prosthesis and bone. -The way of transfer of forces between prosthesis and bone. -The spreading and uniform distribution of forces on the bone.
  • cementles ⁇ endoprostheses require the following: Biological harmonization between bone and prosthesis, and minimization of the consequenses caused by mechanical forces at points of contact between bone and prosthesis, so as to avoid or to reduce small movements between bone and prosthesis, which lead to loosening and rejection of the prosthesis.
  • the density of trabecular bone depends on the forces, which are received by the bone. On artificial joints, a certain portion of the to ⁇ tal forces are received by the prosthesis.
  • the time needed for biological harmonization between prosthesis and bone is so shorter as smaller are the movements between prosthesis and bone.
  • the lifespan of the artificial joints depends on the small movements between prosthesis and bone as well as on the osteopo ⁇ rosis caused by the discharge of the trabecular bone by the prosthesis.
  • the prosthesis is loaded eccentrically with regard to the theoretical axis of the femur, creating a curving momentum, which affects the bone negatively, causing osteolysis, principally to the Adams arc and the femur diaphysis. Attempts of neutralization of this curving momentum with the use of screws from the prosthesis towards the area of the major trochanter have failed, because of the metal's weariness and breaking.
  • This articulating joint receives the small movements, which continue, even diminished, to occur and prevents weariness and bending of the metal (it acts as a guide for the small movements).
  • the anchorage of the prestressing tendon as far away as possible from the prosthesis causes pressure forces on the bone, which in turn cause osteogenesis.
  • This • anchorage is applied as peripherally as possible (Fig. I B) for the following two reasons: first because the 5 pressure forces, which cause osteogenesis, are directed towards a greater part of the bone, and second because the difference " in E-Module between the system prosthe- sis-prestre ⁇ sing tendon and the bone diminishes.
  • the anchorage securing of the prestressing tendon is effe- 0 ctuated with the help of a " washer (Fig. Ill 8), and the anchorage itself by the special cone (Fig.Ill 7) .
  • the outer part of the anchorage cone is used as a lever for the protection of the bone (Fig. Ill 6).
  • 25 means of wire tendons, made either of the same material as the prosthesis, or carbon fibres, or carbon fibre plastics. They have a diameter of I.2-1.8 mm and are of differing length and processing, depending on the way of application of prestressing, of adaptation to the
  • the other part of the hip joint prosthesis receives pressure forces on its DC ⁇ ling and the small movements are neutralized or minimi ⁇ zed whith the application of prestressing on the pubis, ischium and ilium.
  • the acetabulum consists of two parts, the inner one, which is made of plastic material, with a spherical cavity for the formation of an articulation with the femur head of the prosthesis, and the outer part, made of metal, which is anchored into the bone of the pelvis with prestressing tendons and whose surface, which comes in contact with the bone, is of ellipsoidal shape for the enlargement of the area of distribution of forces.
  • the anchorage in the pelvis which is spongy, is effectuated with the special screws for anchorage into spongy bone (Fig.V 13).
  • the screws are set with the help of a flexible tap (Fig.V 12), which is guided for ⁇ ward within the spongy matter of the pelvis respecting the cortical bone, and are screwed with the help of the special screwdriver (Fig.V II).
  • the work is done as follows: A model acetabulum is applied on the preparated bone. This model bears guiding tubes towards the pubis, ischium and ilium, through which we place the anchorage screws of (Fig.V 13) with the help of the special, flexible screwdriver (Fig.V II), just under the bony surface.
  • both the fe ⁇ moral component as well as the tibial component receive pressure forces which are interchangeable, i.e. when the medial condyle of the prosthesis is under pressure, the lateral condyle of the prosthesis has the tendency to distance itself from its contact with the bony surfa ⁇ ce of the lateral condyle of the femoral bone. Because of this, traction (prestressed) forces have to be applied
  • the direction of the prestressing application must be vertical to the plane created by the application of the prosthesis, and eventually, two or three prestressing tendons can be used for each condyle.
  • the prestressing tendons cross each other and are anchored on the inferior third of the fe ⁇ moral bone.
  • the bisector of the angle, which they form, must coincide with the axi ⁇ of the femoral bone.
  • the junction of the prestressing tendon with the prosthesis is done with a hook, which is part of a concave sphere, is by construction part of the prosthesis, and on which the sphere of the prestressing tendon is adapted.
  • the tendons are anchored with the help of the distribution washer (Fig.Ill 8) and the lever for bone protection (Fig.1116), and the application of prestressing is achi- eved with dynamometers, and must be simultaneous and of the same tension for all prestressing tendons. They are finally anchored with the cone (Fig.Ill 7) or the tracti ⁇ on screw (Fig.V 10).
  • the knee joint prostheses have to be supplied with hooks (Fig.IV A) for the adaptation of the prestressing tendons, on the part of the prostheses, which receives the greatest traction forces.
  • the prestressing tendons are anchored by the traction screw (Fig.V 10) or by the cone (Fig.Ill 7) -and number from two to four.
  • two holes are made by means of a long drill, as follows: one is made from the medial condyle to the lateral hyper- condylial surface of the femoral cortex, and the other is made * from the lateral condyle to the medial femoral cortex. Two prestressing tendons are introduced through these holes.
  • prestre ⁇ ssing is applied with the help of two dynamometers si- multaneously to both tendons, which are then anchored to the medial and lateral hypercondylial cortex either by means of the cone or the traction (prestressing) screw.
  • the lever for bone protection as well as the surfa ⁇ ces which are subject to contact and friction, are covered with hard plastic material. The Material in use.
  • the prostheses must be fitted up with sockets to receive the sphere of the prestressing ten ⁇ ons on the appropriate place.
  • these sockets are built on the oppo ⁇ site side of the head itself, on the place of the major trochanter, as eccentrically as possible, and if nece ⁇ sa- ry, by modification of the shape of the prostheses. (The protrusion of this side of the prostheses like a double Z inside the mass of the major trochanter is desirable).
  • the prestressing tendons are separated according to their length, and are of specified and of unspecified length. The one end of the tendon of unspecified length forms a sphere for the creation of a joint with the so ⁇ cket on the prosthesis. Its other end is free, and after application of prestressing, is anchored within the bone through the cone.
  • Prestressing tendons of specified length are used in instances, where their exact length is known in advance. They have a length of 3 to 20 cm. The one end is cochle- ated (male screw), so that the traction (prestressing) screw (female screw) can be used, and the other end is either a sphere, so that they can adapt to the appropri ⁇ ate socket of the prosthesis, or it forms the head of a screw with wide spiral, suitable for anchoring into spongy bone (Fig.V 13) • (Eg. Acetabulum anchorage). These screws are very short, 5-8mm, and have a hole in the centre for the appropriate screwdriver (Fig.V II). They are put in place with the help of the special tap (Fig.
  • V 12 which has the shape of a rounded, truncated cone, and has at its base a short articulated cutter mill for the use of the screwdriver.
  • This screwdriver is short and flexible, with a central opening as receptor for the prestressing tendon.
  • the outer part of the anchorage cone (Fig.Ill) forms a joint with the washer and is used as a lever for bone protection.
  • the traction (prestressing) screw (Fig.V 10) can be put instead of the cone inside the above mentioned outer part of the cone, and forms a joint with the washer.

Abstract

Prostheses of the hip and the knee joint, of which both components are anchored into the bone with prestressing tendons (5) and by interposition of a joint. The anchorage system of the prostheses for the femoral part of the hip joint prosthesis and for both parts of the knee joint prosthesis consists of: (a) the sockets (3, 6) for the spheric end of the prestressing tendons on both components of the prostheses for the neutralization of tension forces, (b) the prestressing tendons, (c) the mechanism for bone protection, anchorage and fixing of the prestressing. The acetabulum part of the hip joint prosthesis is anchored into the bone of the pelvis with prestressing tendons.

Description

Prosthesis of the hip-or knee-joint anchored with a prestressing element.
As substitution for hip -and knee joints, artificial joints (prostheses) have been in use, which were caulked in the bone with the help of bone cement. After a certain period of time, an aseptic loosening of both components of the hip as well as the knee joint prostheses is obse¬ rved. This is due to the weakness of bone cement to cope with traction forces (mechanical weakness). To overcome this specific weakness, prostheses which do not use bone cement have been in use for a number of years.
Several attempts have also been made with modifica¬ tions in the__shape and the stem of the prostheses, which attempts aimed at the early charge and longer lifespan of the prostheses (main problems).
The suitable time to charge the artificial joint as well as its lifeεpan, depend on a number of factors, for example : -The material and surface of the prosthesis. -The joining between prosthesis and bone. -The way of transfer of forces between prosthesis and bone. -The spreading and uniform distribution of forces on the bone.
-The mechanical conditions created during the ini¬ tial placing of the prostheses, to which the bone will adapt accordingly. As opposed to the prostheses for which bone cement is used, cementlesε endoprostheses require the following: Biological harmonization between bone and prosthesis, and minimization of the consequenses caused by mechanical forces at points of contact between bone and prosthesis, so as to avoid or to reduce small movements between bone and prosthesis, which lead to loosening and rejection of the prosthesis. Moreover, the density of trabecular bone depends on the forces, which are received by the bone. On artificial joints, a certain portion of the to¬ tal forces are received by the prosthesis. This discha¬ rge of the trabecular bone leads to osteoporosis, which is another cause of loosening of the prosthesis. The bone is capable of receiving great and continual pressure forces and adapt to them. In contrast, small, sudden and on a small area exercised pressure forces lead to excessive stress on the bone and to its atrophy. This results to bone absorption and loosening of the prosthesis.
The time needed for biological harmonization between prosthesis and bone is so shorter as smaller are the movements between prosthesis and bone. The lifespan of the artificial joints depends on the small movements between prosthesis and bone as well as on the osteopo¬ rosis caused by the discharge of the trabecular bone by the prosthesis.
The attempts made sofar concerned the stem of the prostheses. In the case of the hip joint, for example, (for the femur part of the prosthesis), the efforts were towards the creation of a counterbalancing traction zone . The prosthesis is loaded eccentrically with regard to the theoretical axis of the femur, creating a curving momentum, which affects the bone negatively, causing osteolysis, principally to the Adams arc and the femur diaphysis. Attempts of neutralization of this curving momentum with the use of screws from the prosthesis towards the area of the major trochanter have failed, because of the metal's weariness and breaking. As for the stem of the prostheses in the case of the knee artificial joint, either plastic material has been placed on the extremity of the stem (attempt to diminish the small movements of the prosthesis), or the stem has been cut off alltogether. During walking, the momentary and on part of the prosthesis exercised force is great and the only force that can compensate it, is a counter-force on the oppo¬ site paxt of the prosthesis. This eccentric force is more effective if prestressing is used. The firmness of this prestressed force is achieved through the interpo¬ sition of an articulating joint (one part of which is covered with plastic material) between the prosthesis 5 and the prestressing bearer (commonly called tendon'). This articulating joint receives the small movements, which continue, even diminished, to occur and prevents weariness and bending of the metal (it acts as a guide for the small movements). 0 The anchorage of the prestressing tendon as far away as possible from the prosthesis, causes pressure forces on the bone, which in turn cause osteogenesis.'This anchorage is applied as peripherally as possible (Fig. I B) for the following two reasons: first because the 5 pressure forces, which cause osteogenesis, are directed towards a greater part of the bone, and second because the difference "in E-Module between the system prosthe- sis-prestreεsing tendon and the bone diminishes. The anchorage securing of the prestressing tendon is effe- 0 ctuated with the help of a" washer (Fig. Ill 8), and the anchorage itself by the special cone (Fig.Ill 7) . The outer part of the anchorage cone is used as a lever for the protection of the bone (Fig. Ill 6).
The application of prestressing is effectuated by
25 means of wire tendons, made either of the same material as the prosthesis, or carbon fibres, or carbon fibre plastics. They have a diameter of I.2-1.8 mm and are of differing length and processing, depending on the way of application of prestressing, of adaptation to the
30 joint and of anchorage within the bone. Their course is endomyelic (Fig. I) between the prosthesis and the lever for bone protection, and they are lying like tightened chords inside the femoral lumen.
For the neutralization of forces in the sagittal
■z r plane, the prestressing tendons are anchored frontally and laterally, dorsally and laterally respectively, as near to the knee joint as possible (Fig. I). With this .anchorage techniqμe of the prostheses in the bone we achieve the following:
-The counterbalance of the pressure forces on the prosthesis by counterlateral traction forces on the pro¬ sthesis. -The neutralization of the small movements of the prosthesis by the above mentioned counterlateral traction forces.
-The sufficiency of the traction forces on the pro¬ sthesis because of the application of prestressing. -Bone osteogenesis because of the continual pressure forces on the bone, created by the application of pre¬ stressing.
-Minimization of the difference in E- odule between bone and prosthesis because of the application of pre- stressing on a large bone area.
Way of working.
-(Femoral prosthesis of the hip joint) .
After the usual preparation of the femur to receive the prosthesis, on which the one end of the prestressing tendon is articulated, we introduce the other end of the tendon intramedularly through a plastic conducting tube to its anchorage place (lateral corticalis of the femur) .
-(Acetabulu prosthesis, of the hip joint) .
The other part of the hip joint prosthesis, the ace- tabulum (Fig.VI), receives pressure forces on its cei¬ ling and the small movements are neutralized or minimi¬ zed whith the application of prestressing on the pubis, ischium and ilium. The acetabulum consists of two parts, the inner one, which is made of plastic material, with a spherical cavity for the formation of an articulation with the femur head of the prosthesis, and the outer part, made of metal, which is anchored into the bone of the pelvis with prestressing tendons and whose surface, which comes in contact with the bone, is of ellipsoidal shape for the enlargement of the area of distribution of forces. The anchorage in the pelvis, which is spongy, is effectuated with the special screws for anchorage into spongy bone (Fig.V 13). The screws are set with the help of a flexible tap (Fig.V 12), which is guided for¬ ward within the spongy matter of the pelvis respecting the cortical bone, and are screwed with the help of the special screwdriver (Fig.V II). The work is done as follows: A model acetabulum is applied on the preparated bone. This model bears guiding tubes towards the pubis, ischium and ilium, through which we place the anchorage screws of (Fig.V 13) with the help of the special, flexible screwdriver (Fig.V II), just under the bony surface. These screws serve as an- chorage and at the same time as prestressing bearers. The other ends of these screws are accessible after the metal part of the double acetabulum is put in place . The pre¬ stressing is_applied with the traction screws of (Fig. V 10) by screwing gradually and alternatively. The ace¬ tabulum serves as joint as well as resting point of the prestressing (i.e. the metal part of the double aceta¬ bulum). It serves as a joint (articulation) because the holes it bears for the traction screws for'.n part of a concave sphere, whereas the base of the screws (Fig.V 10) are part of a sphere. This construction allows for small corrections and forms a joint at the same time.
The possibility of anchorage far away from the ace¬ tabulum, as well as the flexibility of the prestressing -tendons and the existence of a joint between them and the acetabulum, secure solidity and elasticity for the system anonym bone-acetabulu , which allow early charge and a longer lifespan of the prosthesis. -(Knee joint prosthesis). As regards the knee joint prosthesis, both the fe¬ moral component as well as the tibial component receive pressure forces which are interchangeable, i.e. when the medial condyle of the prosthesis is under pressure, the lateral condyle of the prosthesis has the tendency to distance itself from its contact with the bony surfa¬ ce of the lateral condyle of the femoral bone. Because of this, traction (prestressed) forces have to be applied
• to both condyles. For the femoral condyles, the direction of the prestressing application must be vertical to the plane created by the application of the prosthesis, and eventually, two or three prestressing tendons can be used for each condyle. The prestressing tendons cross each other and are anchored on the inferior third of the fe¬ moral bone. The bisector of the angle, which they form, must coincide with the axiε of the femoral bone. The junction of the prestressing tendon with the prosthesis is done with a hook, which is part of a concave sphere, is by construction part of the prosthesis, and on which the sphere of the prestressing tendon is adapted. The tendons are anchored with the help of the distribution washer (Fig.Ill 8) and the lever for bone protection (Fig.1116), and the application of prestressing is achi- eved with dynamometers, and must be simultaneous and of the same tension for all prestressing tendons. They are finally anchored with the cone (Fig.Ill 7) or the tracti¬ on screw (Fig.V 10).
In the case of the tibial condyles, we take into con- sideration the vertical to the plane formed by them, be¬ cause of the inclination this plane has from upper fron- tally towards lower dorsally. This vertical does not follow the axis of the tibial bone but is in front of it and in this case, the intersection of the prestressing tendons must form an angle, whose bisector coincides with the axis of the tibial bone and is parallel to the above mentioned vertical-. The knee joint prostheses have to be supplied with hooks (Fig.IV A) for the adaptation of the prestressing tendons, on the part of the prostheses, which receives the greatest traction forces. The prestressing tendons are anchored by the traction screw (Fig.V 10) or by the cone (Fig.Ill 7) -and number from two to four.
For the knee joint, after the preparation of the con¬ dyles of the femur for the insertion of the prosthesis, two holes are made by means of a long drill, as follows: one is made from the medial condyle to the lateral hyper- condylial surface of the femoral cortex, and the other is made* from the lateral condyle to the medial femoral cortex. Two prestressing tendons are introduced through these holes. After the prosthesis has been positioned by means of a hammer, and is perfectly in place, prestre¬ ssing is applied with the help of two dynamometers si- multaneously to both tendons, which are then anchored to the medial and lateral hypercondylial cortex either by means of the cone or the traction (prestressing) screw. We repeate the process for the tibial part of the pro¬ sthesis. The lever for bone protection as well as the surfa¬ ces which are subject to contact and friction, are covered with hard plastic material. The Material in use. First of all, the prostheses must be fitted up with sockets to receive the sphere of the prestressing tenαons on the appropriate place. For the femur head of the pro¬ sthesis, for example, these sockets are built on the oppo¬ site side of the head itself, on the place of the major trochanter, as eccentrically as possible, and if neceεsa- ry, by modification of the shape of the prostheses. (The protrusion of this side of the prostheses like a double Z inside the mass of the major trochanter is desirable). The prestressing tendons are separated according to their length, and are of specified and of unspecified length. The one end of the tendon of unspecified length forms a sphere for the creation of a joint with the so¬ cket on the prosthesis. Its other end is free, and after application of prestressing, is anchored within the bone through the cone. Prestressing tendons of specified length are used in instances, where their exact length is known in advance. They have a length of 3 to 20 cm. The one end is cochle- ated (male screw), so that the traction (prestressing) screw (female screw) can be used, and the other end is either a sphere, so that they can adapt to the appropri¬ ate socket of the prosthesis, or it forms the head of a screw with wide spiral, suitable for anchoring into spongy bone (Fig.V 13) • (Eg. Acetabulum anchorage). These screws are very short, 5-8mm, and have a hole in the centre for the appropriate screwdriver (Fig.V II). They are put in place with the help of the special tap (Fig. V 12), which has the shape of a rounded, truncated cone, and has at its base a short articulated cutter mill for the use of the screwdriver. This screwdriver is short and flexible, with a central opening as receptor for the prestressing tendon. The outer part of the anchorage cone (Fig.Ill) forms a joint with the washer and is used as a lever for bone protection. The traction (prestressing) screw (Fig.V 10) can be put instead of the cone inside the above mentioned outer part of the cone, and forms a joint with the washer. With the~above described way of anchorage of the prostheses, i.e. with prestressing and interposition of a joint at the points of anchorage and fixing of the pre¬ stressing tendons, we achieve stability and elasticity for the whole system prosthesis-prestressing tendons-bone, which ensure the early charge and a longer lifespan of the prostheses by the creation of ideal mechanical con¬ ditions, and ameliorate the walking quality.

Claims

C L A I M S
1. Prostheses of the hip joint and the knee joint, of which both components are anchored into the bone with prestressing tendons and by interposition of a joint.
The anchorage system of the prostheses for the femoral part of the hip joint prosthesis and for both parts of the knee joint prosthesis consists of: a) the sockets for the spheric end of the prestressing tendons on both components of the prostheses for the neutrali¬ zation of tension forces, b) the prestressing tendons, c) the mechanism for bone protection, anchorage and fixing of the prestressing.
The acetabulum part of the hip joint prosthesis consists of two parts, the inner one, which is made of plastic material, with a spherical cavity for the forma- tion of an articulation with the femur head of the pro¬ sthesis, and the outer part, made of metal, which is anchored into the bone of the pelvis whith prestressing tendons and its surface, which comes in contact with the bone, is of ellipsoidal shape for the enlargement of the area of distribution of forces.
2. Prostheses of the hip joint and the knee joint, according to claim I, whose components bear sockets, which are either cavities, or openings, or hooks, all of hemispherical shape, for the housing and anchorage of the spheric end of the prestressing tendons, which form articulations inside the sockets.(Figures I,II,IV,VI);
3. Prostheses of the knee joint, according to claim I, whose both components, the femoral as well as the tibial, bear 2-4 sockets for the articulated anchorage of the prestressing tendons. The other end of the prestressing tendons is anchored in the bone cortex far away from the prosthesis, into the mechanism for bone protection and for anchorage.(Fig.IV) .
4. The tendons for the application of prestressing, according to claim I, are thin metal wires, or branchy wire (in which case they are covered with plastic mate¬ rial), or other materials with the same mechanical pro- perties (carbon fibres or carbon fibre plastics,e.t.c.) . Their one end either forms a sphere for their articula¬ ted anchorage into the appropriate sockets of the pro¬ stheses, or is adjusted to the head of the anchorage screw with wide spiral, suitable for anchoring into spongy bone, in which case their other end forms an external screw for the traction screw. (Figures II,V).
5. The mechanism for bone protection, anchorage and fixing of the prestressing, according to claim I, con¬ sists of: a)~*the fulcrum for bone protection, cylindri- cal body with a conical cavity for the anchorage of the prestressing tendons through a cone, whose base is of semicircular cross-section for the formation of a joint with the washer, and b) the washer for fixing of the prestressing and distribution of forces, whose side coming in contact with the bone has a concave or a con¬ vex shape depending on the bone surface and bears small dents, and whose aperture is of semicircular cross- section for the formation of an articulation with the base of the fulcrum for bone protection.(Fig res I,III,VI).
6. The acetabulum part of the hip joint prosthesis, according to claim I, consists of two parts, the me¬ tallic one (outer part) and the plastic one (inner part). The metallic part is of ellipsoidal shape as concerns its surface which comes in contact with the bone aceta- bulum, and of hemispherical shape as concerns its sur¬ face which comes in contact with the plastic part of the acetabulum, and bears openings of hemispherical cross- section for the articulated anchorage of the prestressing tendons. (Figure VI). II
7. Anchorage screw, according to claim 4, which is fit for the anchorage into spongy bone. It has the sha¬ pe of a rounded, truncated cone so as to avoid .piercing the cortical bone. It bears the prestressing tendon and the housing of the appropriate screwdriver at its head. For its screwing we use a special flexible tap, which also respects the cortical bone and a special flexible screwdriver. This screwdriver has a central opening as receptor for the prestressing tendon. (Figure V) .
8. The application and fixing of the prestressing are effectuated with the help of the traction (female) screw, which is screwed around the prestressing tendon (male screw), and whose head forms an .articulation with the metallic pas* of the acetabulum prosthesis.(Figures V,VI),
PCT/GR1990/000006 1989-10-31 1990-10-30 Prosthesis of the hip- or knee-joint anchored with a prestressing element WO1991006260A1 (en)

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AU (1) AU6541790A (en)
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US5931871A (en) * 1993-10-21 1999-08-03 Allo Pro Ag Kit of parts for a modular femur head prosthesis, in particular, a reoperation prosthesis, and a femur head prosthesis from such a kit of parts
EP1550419A3 (en) * 2003-12-30 2005-07-27 Zimmer Technology, Inc. Tethered implant systems with fastener for mounting on an articulation surface of an orthopedic joint
US7172595B1 (en) 2000-10-03 2007-02-06 Medicinelodge, Inc. Bone fixation systems and related methods
EP1838224A1 (en) * 2005-01-21 2007-10-03 Medicinelodge, Inc. Trochlear groove implants and related methods and instruments
US7462199B2 (en) 2003-12-30 2008-12-09 Medicinelodge, Inc. Methods for mounting a tibial condylar implant
US7578824B2 (en) 2003-12-30 2009-08-25 Zimmer, Inc. Methods and apparatus for forming a tunnel through a proximal end of a tibia
US7695477B2 (en) 2005-05-26 2010-04-13 Zimmer, Inc. Milling system and methods for resecting a joint articulation surface
US7727239B2 (en) 2005-06-10 2010-06-01 Zimmer Technology, Inc. Milling system with guide paths and related methods for resecting a joint articulation surface
US7806898B2 (en) 2004-07-09 2010-10-05 Zimmer, Inc. Modular guide systems and related rasps and methods for resecting a joint articulation surface
US7819878B2 (en) 2003-12-30 2010-10-26 Zimmer, Inc. Tibial condylar hemiplasty tissue preparation instruments and methods
US20110093091A1 (en) * 2004-03-16 2011-04-21 Tensegrity Prosthetics, Inc. Tensegrity Joints for Prosthetic, Orthotic, and Robotic Devices
US8048163B2 (en) 2002-02-20 2011-11-01 Zimmer, Inc. Knee arthroplasty prosthesis
US8157867B2 (en) 2004-07-09 2012-04-17 Zimmer, Inc. Trochlear groove implants and related methods and instruments
US8287538B2 (en) 2008-01-14 2012-10-16 Conventus Orthopaedics, Inc. Apparatus and methods for fracture repair
US8562608B2 (en) 2008-09-19 2013-10-22 Zimmer, Inc. Patello-femoral milling system
US8821589B2 (en) 2008-05-13 2014-09-02 Jerome R. Rifkin Joints for prosthetic, orthotic and/or robotic devices
US8906022B2 (en) 2010-03-08 2014-12-09 Conventus Orthopaedics, Inc. Apparatus and methods for securing a bone implant
US8961518B2 (en) 2010-01-20 2015-02-24 Conventus Orthopaedics, Inc. Apparatus and methods for bone access and cavity preparation
EP2967888A4 (en) * 2013-03-15 2016-11-16 Smed Ta Td Llc Fixation of bone implants
US9730739B2 (en) 2010-01-15 2017-08-15 Conventus Orthopaedics, Inc. Rotary-rigid orthopaedic rod
US10022132B2 (en) 2013-12-12 2018-07-17 Conventus Orthopaedics, Inc. Tissue displacement tools and methods
US10918426B2 (en) 2017-07-04 2021-02-16 Conventus Orthopaedics, Inc. Apparatus and methods for treatment of a bone

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US5931871A (en) * 1993-10-21 1999-08-03 Allo Pro Ag Kit of parts for a modular femur head prosthesis, in particular, a reoperation prosthesis, and a femur head prosthesis from such a kit of parts
US7172595B1 (en) 2000-10-03 2007-02-06 Medicinelodge, Inc. Bone fixation systems and related methods
US8048163B2 (en) 2002-02-20 2011-11-01 Zimmer, Inc. Knee arthroplasty prosthesis
US9072605B2 (en) 2002-02-20 2015-07-07 Zimmer, Inc. Knee arthroplasty prosthesis
US7578824B2 (en) 2003-12-30 2009-08-25 Zimmer, Inc. Methods and apparatus for forming a tunnel through a proximal end of a tibia
US7462199B2 (en) 2003-12-30 2008-12-09 Medicinelodge, Inc. Methods for mounting a tibial condylar implant
EP1550419A3 (en) * 2003-12-30 2005-07-27 Zimmer Technology, Inc. Tethered implant systems with fastener for mounting on an articulation surface of an orthopedic joint
US7867236B2 (en) 2003-12-30 2011-01-11 Zimmer, Inc. Instruments and methods for preparing a joint articulation surface for an implant
US7819878B2 (en) 2003-12-30 2010-10-26 Zimmer, Inc. Tibial condylar hemiplasty tissue preparation instruments and methods
US7771483B2 (en) 2003-12-30 2010-08-10 Zimmer, Inc. Tibial condylar hemiplasty implants, anchor assemblies, and related methods
US20110093091A1 (en) * 2004-03-16 2011-04-21 Tensegrity Prosthetics, Inc. Tensegrity Joints for Prosthetic, Orthotic, and Robotic Devices
US7806898B2 (en) 2004-07-09 2010-10-05 Zimmer, Inc. Modular guide systems and related rasps and methods for resecting a joint articulation surface
US8852195B2 (en) 2004-07-09 2014-10-07 Zimmer, Inc. Guide templates for surgical implants and related methods
US8157867B2 (en) 2004-07-09 2012-04-17 Zimmer, Inc. Trochlear groove implants and related methods and instruments
EP1838224A4 (en) * 2005-01-21 2010-03-17 Medicinelodge Inc Trochlear groove implants and related methods and instruments
GB2437659B (en) * 2005-01-21 2009-07-15 Medicinelodge Inc Trochlear groove implants and related methods and instruments
EP1838224A1 (en) * 2005-01-21 2007-10-03 Medicinelodge, Inc. Trochlear groove implants and related methods and instruments
US7695477B2 (en) 2005-05-26 2010-04-13 Zimmer, Inc. Milling system and methods for resecting a joint articulation surface
US7727239B2 (en) 2005-06-10 2010-06-01 Zimmer Technology, Inc. Milling system with guide paths and related methods for resecting a joint articulation surface
US8287538B2 (en) 2008-01-14 2012-10-16 Conventus Orthopaedics, Inc. Apparatus and methods for fracture repair
US11399878B2 (en) 2008-01-14 2022-08-02 Conventus Orthopaedics, Inc. Apparatus and methods for fracture repair
US10603087B2 (en) 2008-01-14 2020-03-31 Conventus Orthopaedics, Inc. Apparatus and methods for fracture repair
US9517093B2 (en) 2008-01-14 2016-12-13 Conventus Orthopaedics, Inc. Apparatus and methods for fracture repair
US9788870B2 (en) 2008-01-14 2017-10-17 Conventus Orthopaedics, Inc. Apparatus and methods for fracture repair
US8821589B2 (en) 2008-05-13 2014-09-02 Jerome R. Rifkin Joints for prosthetic, orthotic and/or robotic devices
US8562608B2 (en) 2008-09-19 2013-10-22 Zimmer, Inc. Patello-femoral milling system
US9314255B2 (en) 2008-09-19 2016-04-19 Zimmer, Inc. Patello-femoral milling system
US9730739B2 (en) 2010-01-15 2017-08-15 Conventus Orthopaedics, Inc. Rotary-rigid orthopaedic rod
US8961518B2 (en) 2010-01-20 2015-02-24 Conventus Orthopaedics, Inc. Apparatus and methods for bone access and cavity preparation
US9848889B2 (en) 2010-01-20 2017-12-26 Conventus Orthopaedics, Inc. Apparatus and methods for bone access and cavity preparation
US9993277B2 (en) 2010-03-08 2018-06-12 Conventus Orthopaedics, Inc. Apparatus and methods for securing a bone implant
US8906022B2 (en) 2010-03-08 2014-12-09 Conventus Orthopaedics, Inc. Apparatus and methods for securing a bone implant
US9681906B2 (en) 2013-03-15 2017-06-20 SMcd-TA/TD, LLC Fixation of bone implants
US10194963B2 (en) 2013-03-15 2019-02-05 Smed-Ta/Td, Llc Fixation of bone implants
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US11051865B2 (en) 2013-03-15 2021-07-06 Smed-Ta/Td, Llc Fixation of bone implants
US10022132B2 (en) 2013-12-12 2018-07-17 Conventus Orthopaedics, Inc. Tissue displacement tools and methods
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Also Published As

Publication number Publication date
EP0458914A1 (en) 1991-12-04
GR890100704A (en) 1992-03-20
AU6541790A (en) 1991-05-31
GR1000872B (en) 1993-03-16

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