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Bone Scanning of Limited Value for Diagnosis of Symptomatic Oligofocal and Multifocal Osteonecrosis
MICHAEL A. MONT, SLIF D. ULRICH, THORSTEN M. SEYLER, JONATHAN M. SMITH, DAVID R. MARKER, MIKE S. McGRATH, DAVID S. HUNGERFORD, and LYNNE C. JONES
ABSTRACT. Methods. Forty-eight patients presented with suspected osteonecrosis of the shoulder, hip, knee, or ankle. All patients underwent simultaneous (< 3 months apart) bone scans and MRI studies as part of diagnostic investigations. Histological confirmation of osteonecrosis was obtained for all suspected lesions. The diagnostic result for each imaging modality was then assessed and compared. Results. All 163 (100%) histologically confirmed lesions were identified by MRI, while only 91 lesions (56%) were identified by bone scan. There was complete congruency of bone scans with MR images in only 38% of patients (18/48). Bone scanning identified 72% of lesions (47/65) in oligofocal patients (≤ 2 joints involved) compared with 45% of the lesions (44/98) in multifocal patients (≥ 3 joints involved). Sensitivity of lesions was highest for the knee and hip and lower for the shoulder and ankle. Larger and later-stage lesions had a higher bone scan sensitivity. Conclusion. Our results demonstrated the low sensitivity of bone scintigraphy for diagnosing symptomatic osteonecrosis. It is least sensitive for early-stage lesions where it might be most useful to diagnose the disease. Our study also confirms that this test is less sensitive for joints other than the hip and is also not useful as a screening tool. Our study does not support the use of bone scans as a diagnostic or screening tool for osteonecrosis. (First Release June 1 2008; J Rheumatol 2008; 35:1629–34) Key Indexing Terms:
OSTEONECROSIS
From the Rubin Institute for Advanced Orthopedics, Center for Joint Preservation and Reconstruction, Sinai Hospital of Baltimore; Good Samaritan Hospital, Orthopaedics Division, Johns Hopkins Medical Institution, Baltimore, Maryland, USA. M.A. Mont, MD, Director; J.M. Smith, BS, Graduate Student; D.R. Marker, BS, Graduate Student; M.S. McGrath, MD, Fellow; T.M. Seyler, MD, Fellow; S.D. Ulrich, MD, Fellow, Center for Joint Preservation and Reconstruction, Sinai Hospital of Baltimore; L.C. Jones, PhD, Professor; D.R. Hungerford, MD, Professor, Good Samaritan Hospital, Orthopaedics Division, Johns Hopkins Medical Institution. Dr. Mont and Dr. Ulrich contributed equally to this work. Address reprint requests to Dr. M.A. Mont, Rubin Institute of Advanced Orthopedics, Center for Joint Preservation and Reconstruction, Sinai Hospital of Baltimore, 2401 West Belvedere Avenue, Baltimore, MD 21215. E-mail: Sulrich@lifebridgehealth.org Accepted for publication March 12, 2008. |