Abstract:
A replacement system for a joint including a first cup member having an interior lining material and forming a hemispherical cavity therein, a ball member received within the hemispherical cavity and being cantable within the cavity, a securing member connected to the first cup member for affixing the first cup member within an acetabulum area of the pelvic bone of a human joint, and an affixing member interconnected to the ball member for affixing the ball member against the femoral head area of the femur of a human joint. The ball has an outer diameter of no more than one inch. The securing member is a screw having one end embedded into the first cup member and extending through the pelvic bone. The affixing member is a shaft connected at one end to the ball member and extends into the femur bone. The affixing member further includes a nail extending through a portion of the femur and engaged with the shaft distal the ball member. This nail is secured to the femur through the use of surgical screws.
Abstract:
In a total hip replacement, a stem of a femoral component is disposed in a patient's thigh bone with a ball extending in such femoral component above the stem. The ball is disposed in a hemispherical cup positioned in the patient's pelvis and enveloping the ball for frontal movement of the ball relative to the cup. A low-friction liner (e.g., plastic or ceramic) is disposed at the bottom of the cup. To determine whether the ball is properly positioned in the cup, a first member (e.g., a coil) is disposed on the bottom of the liner. A second member (e.g., a patch defining a loop) is disposed on the patient's thigh in operatively coupled (e.g. magnetic) relationship to the first member. The operative coupling between the members is variable in accordance with variations in the disposition of the ball in the cup. When the first and second members are respectively a coil and a patch, the coil and a capacitance may be fixed in the patient's body in a circuit resonant at a particular frequency. The patch may be included in electrical circuity disposed externally on the patient's body and energizable by a source (e.g., a battery) disposed externally on the patient's body. This circuity may be resonant at a frequency variable in accordance with variations in the magnetic coupling between the coil and the patch. A sensory indication may be provided when the resonant frequency of the circuity varies outside of particular limits. This indicates that the hip replacement may not be functioning properly in regard to subluxation, dislocation, or excessive material wear.
Abstract:
This invention relates to a biojoint prosthesis comprising:a) a prosthetic comprising a first component having an outer surface comprising at least 90 mol% zirconia, andb) a second component having a surface shaped to receive the outer surface of the first component,wherein the outer surface of the first component is received on the surface of the second component, andwherein a) at least a portion of the surface of the second component receiving the first component comprises a ceramic having a surface roughness of no more than 100 nm, and b) the outer surface of the first component has a surface roughness of no more than 100 nm.
Abstract:
An acetabular cup assembly for use with a femoral implant. The cup assembly includes an outer shell, a bearing liner configured to fit into a cavity in the shell, a generally annular retaining ring and a locking ring configured to hold the retaining ring in the shell adjacent the bearing liner. The locking ring is slidable between locked and free configurations, with at least part of the locking ring being formed as a closed loop to prevent radial contraction of the locking ring inner surface as the locking ring is slid between the free and locked configurations. At least one small circumferential rib is formed on the outer surface of the locking ring to engage a corresponding circumferential groove in the shell when the locking ring is installed therein in the locked configuration.
Abstract:
This is basically an Engineering design of a means to control the stability and or resistivity of certain materials subject to Cold Flow without materially decreasing the material's normal function. This does not require additional thickness and/or hardening which may increase the resistance of the material. This method overcomes these limitations. This is accomplished by my development of a system of encapsulation, adding certain types of fibers, or both as may be required. The subject material using this method can then be processed to meet specific pressures and resistivity. There are many uses for this method, for example this method can be used for constructing the cartilage for an artificial joint where it is desired to have a predetermined force for separation and yet have low resistivity to normal motion. Another example is to apply this method to plastic bearings and bushings in order to reduce cold flow with little or no change in resistivity.
Abstract:
An acetabular cup assembly 10 that uses the mating contour of its bearing component 20 and its shell component 30 to provide a reliable interlocking engagement to secure the bearing component to the shell component is disclosed. Bearing component 20 includes end surface 24 and a convex spherical surface 22, which extends beyond its lateral diametrical plane 23, making the shape of the bearing component slightly greater than a hemisphere. Shell component 30 includes a concave inner surface 36 defining an open cavity 37 for receiving bearing component 20. Concave shell surface 36 has a diametrical recess 40, and surface 36 is complimentary and approximately the same in contour and radial dimension to convex bearing surface 22. Concave shell surface 36 includes an annular portion 38, which extends beyond its lateral diametrical plane 39. Consequently, bearing component 30 can not be inserted directly into the shell cavity, because its lateral diameter is greater than the diameter at the mouth of the shell cavity. Recess 40 in concave shell surface 36 allows bearing component 20 to be inserted into shell cavity 37 in a sideways position. Once inserted in shell cavity 37 in a sideways position, bearing component 20 can be rotated back 90.degree. within the shell cavity so that convex bearing surface 22 is seated concentrically over concave shell surface 36. In this rotated position, annular portion 38 of concave shell surface 36 converges partially over bearing component 20 to secure the bearing component within shell cavity 37.
Abstract:
A bipolar endoprosthesis assembly which provides for a wide-range of motion between a bone and a socket (e.g., a femur and an acetabular socket), comprising a metal outer shell element, a ultra-high molecular weight, low-friction insert formed to fit within the shell element, and a locking ring designed to lock the assembly together with a femoral head prosthesis. The outer shell has a generally spherical shape on its outer surface to be received by a human socket such as the acetabulum. The inner surface of the outer shell is faceted to inhibit rotation of a correspondingly shaped inner insert. The insert has an outside surface shaped to mate with the inside surface of the outer shell element. The locking ring is slotted to facilitate insertion of a femoral head prosthesis. The locking ring also has dual sets of locking barbs shaped to mate with recesses on the inner surface of the outer shell element. The redundant locking mechanism of the locking ring inhibits accidental in vivo disassembly of the device yet allows for relatively easy intraoperative disassembly without specialty tools or fixtures.
Abstract:
A joint prosthesis and a joint prosthesis organ comprising a cup-shaped element having two parts. One part (1) is a ring which may be connected to the cup-shaped second part (2) with use of click-joint elements (2',2") which are such that ring and cup-shaped part are allowed to rotate freely relative to each other. Described is that said ring may be formed such as to hamper luxation; the ring therefore may partially have an enlarged height. The surgeon using a joint prosthesis according to the invention on a patient has the possibility to rotate the ring with respect to the cup-shaped part until an optimal position is reached. If necessary the two parts may then be fixed to each other using separate means for fixation.
Abstract:
A ball and socket joint for implating in the body is provided wherein the socket portion of the joint can have various orientations with respect to the patient's anatomy, and the orientation used for a particular patient can be selected and/or changed in situ, that is, during or after implantation of the joint. In addition, the configuration of the joint, e.g., constrained versus semi-constrained, as well as the materials making up the socket portion of the joint, e.g., plastic versus metal, can be selected and/or changed in situ.
Abstract:
A liquid chamber (3) arranged in the bottom of the socket cavity (2) is latitudinally sealed by the engaging ball head (4) of the femoral prosthesis shaft. The ball head (4) of the hip joint prosthesis is supported hydrostatically by the liquid chamber (3) filled with synovia and sealed by the ball head following a deformation of the elastic sealing edge (5). By means of the hydrostatic support, the friction moment increases only a little when the load becomes higher and approaches a constant value which is considerably lower than in conventional hip joint sockets.