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Volume 67, Issue 7, Pages 1363-1372 (July 2009)


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Intravenous Bisphosphonate-Related Osteonecrosis of the Jaw: Bone Scintigraphy as an Early Indicator

Felice S. O'Ryan, DDSCorresponding Author Informationemail address, Sam Khoury, DMD, Wendy Liao, DDS, Myo M. Han, MD§, Rita L. Hui, PharmD, MS, David Baer, MD, Daniel Martin, DDS#, Donald Liberty, DDS⁎⁎, Joan C. Lo, MD††

Purpose

Bisphosphonate-related osteonecrosis of the jaw (BRONJ) is recognized as a serious complication among patients receiving bisphosphonate therapy. However, methods for early detection and identification of patients at risk for osteonecrosis of the jaw (ONJ) need further investigation. The purpose of this study was to characterize BRONJ among patients receiving intravenous bisphosphonates and to examine bone scintigraphy findings that preceded manifestation of frank ONJ.

Materials and Methods

We identified all known cases of BRONJ (defined according to 2006 American Association of Oral and Maxillofacial Surgeons criteria) diagnosed between January 2004 and September 2008 among patients who received intravenous bisphosphonate therapy (IVBP). The medical records were abstracted, and the clinical and radiographic features of BRONJ and relevant comorbidities were characterized. Technetium Tc 99 bone scintigrams were systematically reviewed among the subset of patients who received these imaging studies for oncologic care and imaging findings were correlated with the temporal development of ONJ.

Results

We identified 59 cases of intravenous BRONJ (median age, 61.4 ± 10.7 years; 57.6% female), of whom 44.1% had breast cancer, 33.9% had multiple myeloma, and the remainder had metastatic prostate cancer (15.3%) or other cancers (6.8%). One third (32.2%) of the cohort was diabetic. In addition to IVBP, the vast majority (86.4%) had also received prior systemic glucocorticoid therapy. The median cumulative number of IVBP doses was 25 (interquartile range, 16-39) at the time of BRONJ diagnosis. Half of the patients had prior invasive dental procedures; ONJ developed spontaneously in 27.1%, and in the remainder ONJ developed in the setting of periodontal disease (10.1%) or local trauma (8.4%). Most patients presented with painful stage 2 disease involving the mandible (75%), and Actinomyces was present in more than 77% of available histologic specimens. During the median follow-up of 1.5 years, 15 patients (25.4%) regressed to a less severe stage, with healing in 6 patients; 16 (27.1%) worsened; and the remainder stayed within the same stage, but in almost half of these patients, the extent of involvement progressed. Of the 38 patients who had 99Tc bone scintigraphy, 35 had bone scans before development of BRONJ, and among these patients, 23 (67.5%) had positive tracer uptake in areas that subsequently developed BRONJ.

Conclusions

In this study bone scintigraphy showed positive tracer uptake before the development of BRONJ in almost 66% of patients who had these scans before clinical evidence of frank osteonecrosis. BRONJ subsequently developed in the areas identified on scintigraphy in these patients. Further studies should explore the role of bone scintigraphy in the detection of early subclinical BRONJ.

 Director, Division of Maxillofacial Surgery, Kaiser Permanente Oakland Medical Center, Oakland, CA

 Resident, Department of Oral and Maxillofacial Surgery, Highland General Hospital, and Division of Maxillofacial Surgery, Kaiser Permanente Oakland Medical Center, Oakland, CA

 Former Resident, Department of Oral and Maxillofacial Surgery, Highland General Hospital, Oakland, CA; and Currently, Private Practice, San Francisco, CA

§ Associate Physician, Department of Nuclear Medicine, Kaiser Permanente East Bay Medical Center, Oakland, CA

 Pharmacist, Pharmacy Outcomes Research Group, Drug Information Services, Kaiser Permanente Northern California, Oakland, CA

 Chief, Department of Oncology, Kaiser Permanente Medical Center Oakland/Richmond, Oakland, CA

# Resident, Division of Oral and Maxillofacial Surgery, Alameda County Medical Center/University of the Pacific School of Dentistry, Oakland, CA

⁎⁎ Chief, Division of Maxillofacial Surgery, Department of Head and Neck Surgery, Kaiser Permanente South Sacramento Medical Center, Sacramento, CA

†† Research Scientist, Division of Research, Kaiser Permanente Northern California, Oakland, CA

Corresponding Author InformationAddress correspondence and reprint requests to Dr O'Ryan: Division of Maxillofacial Surgery, Kaiser Permanente, 280 W MacArthur Blvd, Oakland, CA 94611

PII: S0278-2391(09)00292-4

doi:10.1016/j.joms.2009.03.005


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