3.8 Article

Apical surgery in cancer patients receiving high-dose antiresorptive medication-a retrospective clinical study with a mean follow-up of 13 months

Journal

ORAL AND MAXILLOFACIAL SURGERY-HEIDELBERG
Volume 25, Issue 2, Pages 237-246

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s10006-020-00909-9

Keywords

Antiresorptive medication; Denosumab; Bisphosphonate; Cancer; Apical surgery

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The study evaluated the results of apical surgery in patients receiving high-dose antiresorptive medication and found it to be a valid treatment option for apical periodontitis. None of the patients developed medication-related osteonecrosis of the jaw, indicating a positive outcome. Further research with larger study groups and longer follow-up periods is recommended.
Purpose The aim of the study is to evaluate the results of apical surgery (AS) in patients receiving high-dose antiresorptive medication (HDAR). Methods Retrospective descriptive quality control study conducted in an Oral and Maxillofacial Department at a University Hospital. Fourteen patients on HDAR met the inclusion criteria. Only descriptive statistics were applied. Results Fourteen patients had operation on seventeen teeth. Mean HDAR treatment period before apical surgery: 25 months (SD, +/- 24.27; range, 1-78 months). Drug holiday during surgery and initial healing: mean, 8 months (SD, +/- 5.96; range, 0.4-22 months). Sixteen out of seventeen teeth healed clinically and showed complete or ongoing radiographic healing. All patients except one became free of symptoms. Mean follow-up: 13 months (SD, +/- 9.05; range, 2-31 months). Radiographic healing according to Molven and Rud: 7, complete; 6, uncertain; 1, unsatisfactory. Three patients died during follow-up and were considered drop-outs. Conclusions The present case series suggest that apical surgery is a valid treatment option for apical periodontitis in patients on HDAR, where orthograde endodontic retreatment is not possible. None of the patients developed medication-related osteonecrosis of the jaw. Further studies in larger study groups and with longer follow-up periods are needed. The regional scientific ethical committee provided a document exemption, registration date 20 November 2013, and the local data protection agency approved handling of the recorded data (No. 2012-41-0045), registration date 11 January 2012.

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