This invention relates to orthopedic surgery, particularly to minimally invasive bi-compartmental partial knee replacement, inclusive of instrumentation and methods therefore.
Total knee replacement is a conventional surgical approach for treatment of trauma and disease of the knee involving more than one of the three compartments of the joint. The traditional total knee replacement starts with a 10 to 12 inch incision over the knee, the quadriceps muscle is split or moved to one side disrupting the patella, the ends of the femur and tibia are re-shaped removing all the cartilage, and matching femoral and tibial implants are driven into the shaped ends. Polyethylene inserts in the tibial implant articulates with the polished femoral component and replaced cartilage. The patella is reshaped and a prosthesis added to smoothly slide over the femoral implant. The muscle, tendons and ligaments are reconstructed to complete the surgery. Usually, there is a hospital stay of 3-5 days and an intensive rehabilitation period of up to 3 months follows. Most of this post-operative schedule is for regaining movement due to the trauma to the muscles, tendons and other soft tissue.
In some cases, only one compartment of the knee joint is affected by trauma or disease, e.g., a medial condyle of the femur and medial plateau of the tibia. In this situation, a partial knee replacement (uni-compartmental) is done in which only the affected portion of the joint is removed and replaced with a prosthesis, such as taught by Treace, U.S. Pat. No. 4,193,140 issued Mar. 18, 1980. The operation may be completed with a much smaller incision, e.g., 3-5 inches on one side of the knee, and only a portion of the cartilage need be removed. The surgical trauma is much less extensive and the recovery time is greatly shortened.
There are conventional surgical procedures for reconstruction of the patella or kneecap, in the event only the patella-femoral compartment is distressed. Colleran et al, U.S. Pat. No. 5,944,723, and Petersen, U.S. Pat. No. 4,633,862, both teach the use of a forceps-like instrument to grasp the patella for reshaping, as part of a uni-compartmental operation or a total knee replacement.
However, the common practice if more than one compartment is involved is to do a total knee replacement. The general theory being that if more than one compartment is affected, it indicates a broader deteriorating condition and a partial knee replacement would be merely postponing the inevitable total replacement. Whether or not this is true, the result of such a decision is to require the patient to endure pain, long term rehabilitation, and diminished quality of life that his immediate condition does not warrant. In the older patients, the degree of mobility may never reach the potential for a total knee replacement.
U.S. Pat. No. 4,034,418 to Jackson et al discloses the use of separate prostheses for a bi-compartmental, medial and lateral compartments.
What is needed in the art is a partial knee replacement that addresses two contiguous compartments of the knee without resorting to a total replacement thereby providing all the advantages of minimal surgical trauma and a short rehabilitation of conventional partial knee replacements.
Disclosed is a prosthesis for a bi-compartmental partial knee replacement. The prosthesis includes an integral trochlear extension adapted to encompass the trochlear of a femur in a contiguous compartment of the knee, and an arcuate femoral prosthesis for fitting about one condyle of the femur.
Therefore, it is an objective of this invention to teach the performance of the partial knee replacement including the prosthesis and surgical implements.
It is another objective of this invention to teach the performance of a partial knee replacement involving two compartments of the knee in which the patella-femoral is one.
It is a further objective of this invention to teach the use of a patella button with an extension of the unicondylar femoral component for partial knee replacement.
It is still another objective of this invention to use the femoral prosthesis and a tibial prosthesis to replace the diseased medial or lateral compartment, medial or lateral femoral condyle, and medial or lateral tibial plateau with the medial or lateral femoral prosthesis replacing the diseased patella-femoral (trochlea) compartment. Specifically, the femoral prosthesis replaces the medial or lateral femoral condyle and the diseased trochlea of the femur. The tibial prosthesis replaces the diseased medial or lateral tibial plateau. The patella prosthesis replaces the diseased surface of the patella.
Referring to the figures in general, a patient's leg is illustrated with the medial compartment and the contiguous patello-femoral compartment exposed to show the prostheses attached to the medial condyle of the femur F, the proximal end of the tibia Ti, and the kneecap P.
The tibial prosthesis 12 has a tray 15 including a tibial anchor 16 to attach the prosthesis to the tibia Ti. The tray 15 has a proximal surface with an attached pad 14 which serves to replace the cartilage normally existing between the femur and the tibia and provide a smooth bearing surface contacting the femoral prosthesis 11. The pad 14 may be removably attached to the tray 15 in the event that wear, over time, requires replacement.
During the operation, the patella P shown in
Once the posterior, ventral or articular surface of the patella P is reshaped, a drill guide is placed against the surface to establish the location of bores in the patella matching the location of pegs formed on the button 13. These bores may be angled or perpendicular to the dorsal surface of the patella. The angled bores permit insertion of the button 13 in less vertical space. The drill guide also serves as a stop for the drill bit to prevent undue penetration of the patella. The button is attached to the patella with the pegs placed in the bores using cement, if desired. The small incision on the side of the knee is then closed to complete the operation.
Again referring to the figures set forth is a perspective of the bi-compartmental prosthesis in the flexed position showing the medial compartment 21 and patella femoral (trochlear) compartment 11, the remaining normal knee is the lateral compartment LC. In this embodiment, the medial tibial prosthesis 12 is positioned in operation with the medial compartment and patella femoral compartment shown in general as numeral 23.
All patents and publications mentioned in this specification are indicative of the levels of those skilled in the art to which the invention pertains. All patents and publications are herein incorporated by reference to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference.
It is to be understood that while a certain form of the invention is illustrated, it is not to be limited to the specific form or arrangement herein described and shown. It will be apparent to those skilled in the art that various changes may be made without departing from the scope of the invention and the invention is not to be considered limited to what is shown and described in the specification.
One skilled in the art will readily appreciate that the present invention is well adapted to carry out the objectives and obtain the ends and advantages mentioned, as well as those inherent therein. The embodiments, methods, procedures and techniques described herein are presently representative of the preferred embodiments, are intended to be exemplary and are not intended as limitations on the scope. Changes therein and other uses will occur to those skilled in the art which are encompassed within the spirit of the invention and are defined by the scope of the appended claims. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the described modes for carrying out the invention which are obvious to those skilled in the art are intended to be within the scope of the following claims.