Reconstruction of a cruciate ligament
First Claim
1. Process for surgically reconstructing the anterior cruciate ligament of the knee joint comprising the steps of forming aligned holes through both the tibia and the femur towards the points of origin of the damaged ligament, removing the damaged ligament and substituting a composite graft therefor by severing a strip of the patellar tendon, then fitting the same into an open-ended sleeve of synthetic biocompatible material, fitting the two-ply composite structure within the aligned holes formed in the tibia and femur and using a fastening means to secure the free end of the composite structure in place within the femur.
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Abstract
In a process for surgically reconstructing the anterior cruciate ligament of the knee to restore its normal stability, the damaged ligament is removed and holes are formed in both the tibia and the femur. The holes extend through the knee joint with their adjacent ends terminating approximately at the points of origin of the removed ligament. A strip is partially severed from the patellar tendon, except at its lower end where it remains attached to the tibia. The tendon strip is shaped and sutured into a tubular configuration and fitted into an open-ended, tubular sleeve of Dacron open mesh fabric. The composite Dacron fabric and the tendon segment is inserted into the hole provided in the tibia, fitted through the knee joint and then advanced upwardly through the hole in the femur. The upper end of the composite insert is fastened in place by means of a bone member fitted into the upper end of the hole in the femur to wedge the upper end of the insert in fixed position.
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Citations
5 Claims
- 1. Process for surgically reconstructing the anterior cruciate ligament of the knee joint comprising the steps of forming aligned holes through both the tibia and the femur towards the points of origin of the damaged ligament, removing the damaged ligament and substituting a composite graft therefor by severing a strip of the patellar tendon, then fitting the same into an open-ended sleeve of synthetic biocompatible material, fitting the two-ply composite structure within the aligned holes formed in the tibia and femur and using a fastening means to secure the free end of the composite structure in place within the femur.
Specification