Primary ACL reconstruction using the LARS device is associated with a high failure rate at minimum of 6-year follow-up.

Purpose: The Ligament Augmentation and Reconstruction System (LARS) is a synthetic ligament consisting of fibres made of polyethylene terephthalate. Despite the LARS being used as an anterior cruciate ligament (ACL) device for nearly 30 years and the well-documented complications from earlier synthetic ligament designs, there is a paucity of published medium- to long-term results. The aim of this study is to report the clinical and functional outcomes after ACL reconstruction using the LARS at a minimum follow-up of 6 years.

Synovitis following anterior cruciate ligament reconstruction using the LARS device.

Purpose: The Ligament Augmentation and Reconstruction System (LARS) has been at the forefront of a recent revival in the use of synthetic ligaments for ACL reconstruction. However, despite promising short-to-mid-term results its role has been approached with caution due to a high number of major complications in previous synthetic graft designs including mechanical failures, synovitis and osteoarthritis. This study aims to report on the incidence of synovitis in a series of patients undergoing second-look surgery following LARS ACL reconstruction.