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Fracture Risk Following an Atypical Femoral Fracture

Atypical femoral fractures (AFFs) occurring during the course of osteoporosis treatment usually lead to discontinuation of anti‐resorptive (AR) drugs. However, the risk of fracture after an AFF is unknown. We conducted a follow‐up study of patients with AFF matched 1:3 for age and gender with patien...

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Autores principales: Bégin, Marie‐Josée, Audet, Marie‐Claude, Chevalley, Thierry, Portela, Marina, Padlina, Ivan, Hannouche, Didier, Ing Lorenzini, Kuntheavy, Meier, Raphaël, Peter, Robin, Uebelhart, Brigitte, Rizzoli, René, Ferrari, Serge, Biver, Emmanuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298806/
https://www.ncbi.nlm.nih.gov/pubmed/34668223
http://dx.doi.org/10.1002/jbmr.4461
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author Bégin, Marie‐Josée
Audet, Marie‐Claude
Chevalley, Thierry
Portela, Marina
Padlina, Ivan
Hannouche, Didier
Ing Lorenzini, Kuntheavy
Meier, Raphaël
Peter, Robin
Uebelhart, Brigitte
Rizzoli, René
Ferrari, Serge
Biver, Emmanuel
author_facet Bégin, Marie‐Josée
Audet, Marie‐Claude
Chevalley, Thierry
Portela, Marina
Padlina, Ivan
Hannouche, Didier
Ing Lorenzini, Kuntheavy
Meier, Raphaël
Peter, Robin
Uebelhart, Brigitte
Rizzoli, René
Ferrari, Serge
Biver, Emmanuel
author_sort Bégin, Marie‐Josée
collection PubMed
description Atypical femoral fractures (AFFs) occurring during the course of osteoporosis treatment usually lead to discontinuation of anti‐resorptive (AR) drugs. However, the risk of fracture after an AFF is unknown. We conducted a follow‐up study of patients with AFF matched 1:3 for age and gender with patients with a peripheral major osteoporotic fracture (pMOF), in the setting of a fracture liaison service, to investigate the incidence of subsequent low‐trauma fractures. Fifty‐five patients with AFF (95% women, age [mean ± standard deviation] 75 ± 10 years, 89% exposed to AR drugs), followed for 6.2 ± 3.7 years, were compared to 165 matched controls with a pMOF (hip 85%) followed for 4.3 ± 2.6 years. During the follow‐up, 38% of patients in the AFF group and 16% in the pMOF group received AR therapies. Continuation of AR drugs after an AFF was associated with contralateral AFF in 27% of subjects. The risks of new low‐trauma, major osteoporotic and imminent (within 2 years) fractures, were similar between the two groups: incidence rate ratio (95% confidence interval [CI]) of subsequent fracture following AFF relative to pMOF, 1.30 (95% CI, 0.82–2.04), 1.28 (95% CI, 0.74–2.15), and 1.11 (95% CI, 0.54–2.15), respectively. Moreover, the risk of sustaining multiple fractures per participant was significantly increased among patients with AFF compared to pMOF (hazard ratio 1.48 [95% CI, 1.00–2.19]; p = 0.049). When taking mortality into account, the risk of subsequent fractures tended to be higher in the AFF group (sub‐hazard ratio 1.42 [95% CI, 0.95–2.12]). In conclusion, patients who sustained an AFF are at high risk of subsequent fragility fractures, at least equal or even greater to the risk observed after a pMOF. However, continuation of AR drugs increases the risk of contralateral AFF. Therefore, optimal modalities for secondary fracture prevention after AFF require further evaluation. © 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).
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spelling pubmed-92988062022-07-21 Fracture Risk Following an Atypical Femoral Fracture Bégin, Marie‐Josée Audet, Marie‐Claude Chevalley, Thierry Portela, Marina Padlina, Ivan Hannouche, Didier Ing Lorenzini, Kuntheavy Meier, Raphaël Peter, Robin Uebelhart, Brigitte Rizzoli, René Ferrari, Serge Biver, Emmanuel J Bone Miner Res Original Articles Atypical femoral fractures (AFFs) occurring during the course of osteoporosis treatment usually lead to discontinuation of anti‐resorptive (AR) drugs. However, the risk of fracture after an AFF is unknown. We conducted a follow‐up study of patients with AFF matched 1:3 for age and gender with patients with a peripheral major osteoporotic fracture (pMOF), in the setting of a fracture liaison service, to investigate the incidence of subsequent low‐trauma fractures. Fifty‐five patients with AFF (95% women, age [mean ± standard deviation] 75 ± 10 years, 89% exposed to AR drugs), followed for 6.2 ± 3.7 years, were compared to 165 matched controls with a pMOF (hip 85%) followed for 4.3 ± 2.6 years. During the follow‐up, 38% of patients in the AFF group and 16% in the pMOF group received AR therapies. Continuation of AR drugs after an AFF was associated with contralateral AFF in 27% of subjects. The risks of new low‐trauma, major osteoporotic and imminent (within 2 years) fractures, were similar between the two groups: incidence rate ratio (95% confidence interval [CI]) of subsequent fracture following AFF relative to pMOF, 1.30 (95% CI, 0.82–2.04), 1.28 (95% CI, 0.74–2.15), and 1.11 (95% CI, 0.54–2.15), respectively. Moreover, the risk of sustaining multiple fractures per participant was significantly increased among patients with AFF compared to pMOF (hazard ratio 1.48 [95% CI, 1.00–2.19]; p = 0.049). When taking mortality into account, the risk of subsequent fractures tended to be higher in the AFF group (sub‐hazard ratio 1.42 [95% CI, 0.95–2.12]). In conclusion, patients who sustained an AFF are at high risk of subsequent fragility fractures, at least equal or even greater to the risk observed after a pMOF. However, continuation of AR drugs increases the risk of contralateral AFF. Therefore, optimal modalities for secondary fracture prevention after AFF require further evaluation. © 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR). John Wiley & Sons, Inc. 2021-11-09 2022-01 /pmc/articles/PMC9298806/ /pubmed/34668223 http://dx.doi.org/10.1002/jbmr.4461 Text en © 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Bégin, Marie‐Josée
Audet, Marie‐Claude
Chevalley, Thierry
Portela, Marina
Padlina, Ivan
Hannouche, Didier
Ing Lorenzini, Kuntheavy
Meier, Raphaël
Peter, Robin
Uebelhart, Brigitte
Rizzoli, René
Ferrari, Serge
Biver, Emmanuel
Fracture Risk Following an Atypical Femoral Fracture
title Fracture Risk Following an Atypical Femoral Fracture
title_full Fracture Risk Following an Atypical Femoral Fracture
title_fullStr Fracture Risk Following an Atypical Femoral Fracture
title_full_unstemmed Fracture Risk Following an Atypical Femoral Fracture
title_short Fracture Risk Following an Atypical Femoral Fracture
title_sort fracture risk following an atypical femoral fracture
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298806/
https://www.ncbi.nlm.nih.gov/pubmed/34668223
http://dx.doi.org/10.1002/jbmr.4461
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