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Fracture risk after deprescription of bisphosphonates: Application of real-world data in primary care

PURPOSE: To compare the effect of discontinuing bisphosphonate treatment on fracture risk in postmenopausal women at high versus low risk of fracture. DESIGN: Retrospective, longitudinal and population-based cohort study. SETTING: Barcelona City Primary Care. Catalan Health Institute. PARTICIPANTS:...

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Autores principales: Troncoso-Mariño, Amelia, Lestón Vázquez, Marta, Gallardo Borge, Sara, Del Val Garcia, José Luís, Amado Guirado, Ester, Violán, Concepción
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196911/
https://www.ncbi.nlm.nih.gov/pubmed/37187104
http://dx.doi.org/10.1016/j.aprim.2023.102651
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author Troncoso-Mariño, Amelia
Lestón Vázquez, Marta
Gallardo Borge, Sara
Del Val Garcia, José Luís
Amado Guirado, Ester
Violán, Concepción
author_facet Troncoso-Mariño, Amelia
Lestón Vázquez, Marta
Gallardo Borge, Sara
Del Val Garcia, José Luís
Amado Guirado, Ester
Violán, Concepción
author_sort Troncoso-Mariño, Amelia
collection PubMed
description PURPOSE: To compare the effect of discontinuing bisphosphonate treatment on fracture risk in postmenopausal women at high versus low risk of fracture. DESIGN: Retrospective, longitudinal and population-based cohort study. SETTING: Barcelona City Primary Care. Catalan Health Institute. PARTICIPANTS: All women attended by primary care teams who in January 2014 had received bisphosphonate treatment for at least five years were included and followed for another five years. INTERVENTION: Patients were classified according to their risk of new fractures, defined as those who had a history of osteoporotic fracture and/or who received treatment with an aromatase inhibitor, and the continuity or deprescription of the bisphosphonate treatment was analyzed over fiver year follow-up. MAIN MEASUREMENTS: The cumulative incidence of fractures and the incidence density were calculated and analyzed using logistic regression and Cox models. RESULTS: We included 3680 women. There were no significant differences in fracture risk in high-risk women who discontinued versus continued bisphosphonate treatment (hazard ratio [HR] 1.17, 95% confidence interval [CI] 0.87–1.58 for total osteoporotic fractures). However, discontinuers at low risk had a lower incidence of fracture than continuers. This difference was significant for vertebral fractures (HR 0.64, 95% CI 0.47–0.88) and total fractures (HR 0.77, 95% CI 0.64–0.92). CONCLUSION: Our results suggest that deprescribing bisphosphonates in women who have already received five years of treatment does not increase fracture risk. In low-risk women, continuing this treatment might could even favor the appearance of new osteoporotic fractures.
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spelling pubmed-101969112023-05-20 Fracture risk after deprescription of bisphosphonates: Application of real-world data in primary care Troncoso-Mariño, Amelia Lestón Vázquez, Marta Gallardo Borge, Sara Del Val Garcia, José Luís Amado Guirado, Ester Violán, Concepción Aten Primaria Original Article PURPOSE: To compare the effect of discontinuing bisphosphonate treatment on fracture risk in postmenopausal women at high versus low risk of fracture. DESIGN: Retrospective, longitudinal and population-based cohort study. SETTING: Barcelona City Primary Care. Catalan Health Institute. PARTICIPANTS: All women attended by primary care teams who in January 2014 had received bisphosphonate treatment for at least five years were included and followed for another five years. INTERVENTION: Patients were classified according to their risk of new fractures, defined as those who had a history of osteoporotic fracture and/or who received treatment with an aromatase inhibitor, and the continuity or deprescription of the bisphosphonate treatment was analyzed over fiver year follow-up. MAIN MEASUREMENTS: The cumulative incidence of fractures and the incidence density were calculated and analyzed using logistic regression and Cox models. RESULTS: We included 3680 women. There were no significant differences in fracture risk in high-risk women who discontinued versus continued bisphosphonate treatment (hazard ratio [HR] 1.17, 95% confidence interval [CI] 0.87–1.58 for total osteoporotic fractures). However, discontinuers at low risk had a lower incidence of fracture than continuers. This difference was significant for vertebral fractures (HR 0.64, 95% CI 0.47–0.88) and total fractures (HR 0.77, 95% CI 0.64–0.92). CONCLUSION: Our results suggest that deprescribing bisphosphonates in women who have already received five years of treatment does not increase fracture risk. In low-risk women, continuing this treatment might could even favor the appearance of new osteoporotic fractures. Elsevier 2023-07 2023-05-13 /pmc/articles/PMC10196911/ /pubmed/37187104 http://dx.doi.org/10.1016/j.aprim.2023.102651 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Troncoso-Mariño, Amelia
Lestón Vázquez, Marta
Gallardo Borge, Sara
Del Val Garcia, José Luís
Amado Guirado, Ester
Violán, Concepción
Fracture risk after deprescription of bisphosphonates: Application of real-world data in primary care
title Fracture risk after deprescription of bisphosphonates: Application of real-world data in primary care
title_full Fracture risk after deprescription of bisphosphonates: Application of real-world data in primary care
title_fullStr Fracture risk after deprescription of bisphosphonates: Application of real-world data in primary care
title_full_unstemmed Fracture risk after deprescription of bisphosphonates: Application of real-world data in primary care
title_short Fracture risk after deprescription of bisphosphonates: Application of real-world data in primary care
title_sort fracture risk after deprescription of bisphosphonates: application of real-world data in primary care
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196911/
https://www.ncbi.nlm.nih.gov/pubmed/37187104
http://dx.doi.org/10.1016/j.aprim.2023.102651
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