Proportioned surgically implantable knee prosthesis

Abstract

A knee prosthesis for unicompartmental implantation into a knee joint is implantable without requiring bone resection and includes a body free of any means of fixation to a portion of knee joint, anatomy and having a substantially elliptical shape in plan and a pair of contoured opposed faces including a convex face and a concave face. A peripheral edge extends between the faces and includes a first side, a second side opposite the first side, a first end and a second end opposite the first end. A first dimension D is defined by the first end and the second end. A second dimension F is defined by the first side and the second side. The dimension F is from about 0.25 to about 1.5 of the dimension D.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation of U.S. application Ser. No. 10 / 232,608, filed Aug. 30, 2002, now U.S. Pat. No. 7,341,602, which is a continuation of U.S. application Ser. No. 09 / 934,364, filed Aug. 21, 2001, now abandoned, which is a continuation-in-part of U.S. application Ser. No. 09 / 664,939, filed Sep. 19, 2000, now U.S. Pat. No. 6,558,421, which is a continuation of U.S. application Ser. No. 09 / 297,943, filed May 10, 1999, now U.S. Pat. No. 6,206,927, which is the National Stage Entry of PCT / US99 / 07309 filed Apr. 2, 1999, each of which are each incorporated by reference herein.BACKGROUND OF THE INVENTION[0002]1. Field of the Invention[0003]The present invention pertains to prosthetic devices. More particularly, the invention pertains to knee joint prostheses which may be surgically implanted between the femoral condyle and tibial plateau of the knee joint.[0004]2. Background Art[0005]Articular cartilage and meniscal cartilage prov...

AI Technical Summary

Problems solved by technology

Damage to these surfaces is generally due to genetic predisposition, trauma, and / or aging.

The result is usually the development of chondromalacia, thinning and softening of the articular cartilage, and degenerative tearing of the meniscal cartilage.

In patients with osteoarthritis, degenerative process typically leads to an asymmetric wear pattern that leaves one compartment with significantly less articular cartilage covering the distal portions (or weight bearing area) of the tibia and femur than the other compartment.

As the disease progresses, large amounts of articular cartilage are worn away.

This increasing joint laxity is suspected of causing some of the pain one feels.

All of this shifting of the knee component geometry causes a misalignment of the mechanical axis of the joint.

The misalignment causes an increase in the rate of degenerative change to the diseased joint surfaces causing an ever-increasing amount of cartilage debris to build up in the joint, further causing joint inflammation and subsequent pain.

Currently, there is a void in options used to treat the relatively young patient with moderate to severe chondromalacia involving mainly one compartment of the knee.

Some patients cannot tolerate or do not want the risk of potential side effects of NSAIDs.

Repeated cortisone injections actually weaken articular cartilage after a long period of time.

HA has shown promising results but is only a short term solution for pain.

Arthroscopic debridement alone frequently does not provide long lasting relief of symptoms.

Unfortunately, the lack of long term success of these treatments leads to more invasive treatment methods.

These procedures are not suitable for addressing large areas of degeneration.

In addition, osteochondral allografts can only be used to address defects on the femoral condyle.

Tibial degeneration can not be addressed with this technique.

However, an HTO does leave a hard sclerotic region of bone which is difficult to penetrate making conversion to a total knee replacement (TKR) technically challenging.

Revision total knee replacement surgery is usually extensive and results in predictably diminished mechanical life expectancy.

Unfortunately, these natural articular materials and surgical technology required to accomplish this replacement task do not yet exist.

Currently, replacement of the existing surfaces, with materials other than articular cartilage, is only possible with a total or uni-condylar knee replacement, and these procedures require removal of significant amounts of the underlying bone structure.

Attaching a new bearing surface to the femoral condyle is technically challenging and was first attempted, with limited success, over 40 years ago with the MGH (Massachusetts General Hospital) knee.

Tibial covering devices such as the McKeever, Macintosh and Townley tibial tray, maintained the existing femoral surface as the bearing surface, but like the MGH knee, all required significant bone resection, thus making them less than ideal solutions as well.

These devices also made no particular attempt to match the patient's specific femoral or tibial geometry thus reducing their chances for optimal success.

Because these devices were made of CoCr, which has different visco-elastic and wear properties from the natural articular materials, any surface geometry which did not closely match the bearing surface of the tibia or femur, could cause premature wear of the remaining cartilage due to asymmetric loading.

All of these techniques are limited by one's ability to first of all fashion these materials in a conformal fashion to replicate the existing knee geometry, while at the same time, maintaining their location within the joint while further being able to survive the mechanical loading conditions of the knee.

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