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Diagnosis and Management of Osteonecrosis of the Jaw: A Systematic Review and International Consensus
Author(s) -
Khan Aliya A,
Morrison Archie,
Hanley David A,
Felsenberg Dieter,
McCauley Laurie K,
O'Ryan Felice,
Reid Ian R,
Ruggiero Salvatore L,
Taguchi Akira,
Tetradis Sotirios,
Watts Nelson B,
Brandi Maria Luisa,
Peters Edmund,
Guise Teresa,
Eastell Richard,
Cheung Angela M,
Morin Suzanne N,
Masri Basel,
Cooper Cyrus,
Morgan Sarah L,
ObermayerPietsch Barbara,
Langdahl Bente L,
Al Dabagh Rana,
Davison K. Shawn,
Kendler David L,
Sándor George K,
Josse Robert G,
Bhandari Mohit,
El Rabbany Mohamed,
Pierroz Dominique D,
Sulimani Riad,
Saunders Deborah P,
Brown Jacques P,
Compston Juliet
Publication year - 2015
Publication title -
journal of bone and mineral research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.882
H-Index - 241
eISSN - 1523-4681
pISSN - 0884-0431
DOI - 10.1002/jbmr.2405
Subject(s) - medicine , osteonecrosis of the jaw , denosumab , population , osteoporosis , surgery , bisphosphonate , environmental health
This work provides a systematic review of the literature from January 2003 to April 2014 pertaining to the incidence, pathophysiology, diagnosis, and treatment of osteonecrosis of the jaw (ONJ), and offers recommendations for its management based on multidisciplinary international consensus. ONJ is associated with oncology‐dose parenteral antiresorptive therapy of bisphosphonates (BP) and denosumab (Dmab). The incidence of ONJ is greatest in the oncology patient population (1% to 15%), where high doses of these medications are used at frequent intervals. In the osteoporosis patient population, the incidence of ONJ is estimated at 0.001% to 0.01%, marginally higher than the incidence in the general population (<0.001%). New insights into the pathophysiology of ONJ include antiresorptive effects of BPs and Dmab, effects of BPs on gamma delta T‐cells and on monocyte and macrophage function, as well as the role of local bacterial infection, inflammation, and necrosis. Advances in imaging include the use of cone beam computerized tomography assessing cortical and cancellous architecture with lower radiation exposure, magnetic resonance imaging, bone scanning, and positron emission tomography, although plain films often suffice. Other risk factors for ONJ include glucocorticoid use, maxillary or mandibular bone surgery, poor oral hygiene, chronic inflammation, diabetes mellitus, ill‐fitting dentures, as well as other drugs, including antiangiogenic agents. Prevention strategies for ONJ include elimination or stabilization of oral disease prior to initiation of antiresorptive agents, as well as maintenance of good oral hygiene. In those patients at high risk for the development of ONJ, including cancer patients receiving high‐dose BP or Dmab therapy, consideration should be given to withholding antiresorptive therapy following extensive oral surgery until the surgical site heals with mature mucosal coverage. Management of ONJ is based on the stage of the disease, size of the lesions, and the presence of contributing drug therapy and comorbidity. Conservative therapy includes topical antibiotic oral rinses and systemic antibiotic therapy. Localized surgical debridement is indicated in advanced nonresponsive disease and has been successful. Early data have suggested enhanced osseous wound healing with teriparatide in those without contraindications for its use. Experimental therapy includes bone marrow stem cell intralesional transplantation, low‐level laser therapy, local platelet‐derived growth factor application, hyperbaric oxygen, and tissue grafting. © 2014 American Society for Bone and Mineral Research © 2014 American Society for Bone and Mineral Research