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Volume 24, Issue 1, Pages 62-68 (January 2008)


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Outcomes of Osteochondral Lesions of the Knee Repaired With a Bioabsorbable Device

Joshua S. Dines, M.D.Corresponding Author Informationemail address, Stephen Fealy, M.D., Hollis G. Potter, M.D., Russell F. Warren, M.D.1

published online 05 November 2007.

Purpose: We sought to evaluate the functional and radiographic outcome of osteochondral lesions involving the femoral condyle that were arthroscopically repaired via a bioabsorbable fixation device made of self-reinforced poly-L-lactic acid. Methods: A retrospective clinical and radiographic evaluation of 9 patients (8 male and 1 female) with a mean age of 18 years at the time of surgery was carried out. Of these patients, 8 were diagnosed with osteochondritis dissecans and 1 had a traumatic chondral fracture. All patients underwent arthroscopic repair of a discrete osteochondral lesion involving the femoral condyle with a bioabsorbable fixation implant. All patients were evaluated at a mean of 33 months postoperatively. All patients had preoperative magnetic resonance imaging (MRI) documenting the integrity and location of the fragment. Patients were evaluated at follow-up with a physical examination, Lysholm questionnaire, and repeated MRI with specific cartilage pulse sequencing. Results: At surgery, the mean size of the fragment was 2 × 2 cm. A mean of 4 nails was used in each case (range, 2 to 10). All patients were treated with a postoperative rehabilitation protocol of non–weight-bearing for a minimum of 6 weeks. The mean postoperative Lysholm score was 94 (range, 78 to 100). The outcomes were excellent in 7 patients, good in 1, and fair in 1. After surgery, MRI evaluation of the osteochondral lesion and overlying cartilage was graded as healed in 7 patients and of questionable integrity in 2. Conclusions: This report documents the efficacy of a bioabsorbable nail to internally fix osteochondral lesions. It supports the use of MRI for both preoperative planning and postoperative assessment of fragment healing. Level of Evidence: Level IV, therapeutic case series.

Sports Medicine Service, Hospital for Special Surgery, New York, New York, U.S.A.

Corresponding Author InformationAddress correspondence and reprints requests to Joshua S. Dines, M.D., Kerlan-Jobe Orthopaedic Clinic, 6801 Park Terrace, Los Angeles, CA 90045, U.S.A.

1 R.F.W. received support exceeding $500 from ConMed Linvatec, Largo, Florida, related to this research.

PII: S0749-8063(07)00745-1

doi:10.1016/j.arthro.2007.07.025


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