J Knee Surg 2007; 20(3): 228-234
DOI: 10.1055/s-0030-1248048
Original Article

© 2007 Thieme Medical Publishers

Magnetic Resonance Imaging to Assess Knee Cartilage Repair Tissue After Microfracture of Chondral Defects

Arun J. Ramappa1 , Thomas J. Gill2 , Catharine H. Bradford3 , Charles P. Ho4 , J. Richard Steadman3
  • 1Beth Israel Deaconess Medical Center, Boston, Mass
  • 2Massachusetts General Hospital, Boston, Mass
  • 3Steadman-Hawkins Research Foundation, Vail, Colo
  • 4California Advanced Imaging of Atherton, Atherton, Calif
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Publikationsverlauf

Publikationsdatum:
20. Januar 2010 (online)

ABSTRACT

A noninvasive method to assess the repair tissue produced by chondral defect treatment techniques has not been established. The purpose of this study was to evaluate the ability of magnetic resonance imaging (MRI) specialized sequences to predict the presence and quality of repair tissue of knee articular cartilage defects treated by microfracture. Nineteen recreational or high-level athletes underwent standard microfracture technique for 22 traumatic full-thickness chondral defects. Patients subsequently underwent repeat arthroscopy for unrelated knee pathology. Magnetic resonance imaging studies were obtained prior to the second-look arthroscopies and evaluated for the presence of full-thickness articular cartilage defects and for the quality of repair tissue. At arthroscopy, the quality and quantity of the repair tissue was assessed. Twenty-one defects had 100% coverage with repair tissue, whereas 1 defect continued to have areas with full-thickness cartilage loss. Magnetic resonance imaging had sensitivity and specificity of 100% in predicting the presence of a full-thickness lesion after microfracture. In determining whether the repair tissue was of good or poor quality, MRI had a sensitivity of 80% and specificity of 82% using arthroscopy as the standard. Magnetic resonance imaging using specialized sequences proved to be a satisfactory technique for evaluating repair tissue in full-thickness traumatic defects treated by microfracture.