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Long-term persistence with anti-osteoporosis drugs after fracture
SUMMARY: Long-term persistence with anti-osteoporosis drugs and determinants for discontinuation among fracture patients were examined. Persistence was 75.0 and 45.3 % after 1 and 5 years, respectively. Those aged ≥80 years were at increased risk of early discontinuation. Within 1 year after discont...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer London
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469296/ https://www.ncbi.nlm.nih.gov/pubmed/25822104 http://dx.doi.org/10.1007/s00198-015-3084-3 |
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author | Klop, C. Welsing, P. M. J. Elders, P. J. M. Overbeek, J. A. Souverein, P. C. Burden, A. M. van Onzenoort, H. A. W. Leufkens, H. G. M. Bijlsma, J. W. J. de Vries, F. |
author_facet | Klop, C. Welsing, P. M. J. Elders, P. J. M. Overbeek, J. A. Souverein, P. C. Burden, A. M. van Onzenoort, H. A. W. Leufkens, H. G. M. Bijlsma, J. W. J. de Vries, F. |
author_sort | Klop, C. |
collection | PubMed |
description | SUMMARY: Long-term persistence with anti-osteoporosis drugs and determinants for discontinuation among fracture patients were examined. Persistence was 75.0 and 45.3 % after 1 and 5 years, respectively. Those aged ≥80 years were at increased risk of early discontinuation. Within 1 year after discontinuation, 24.3 % restarted therapy, yet 47.0 % persisted for 1 year. INTRODUCTION: The risk of osteoporotic fracture can effectively be reduced with use of anti-osteoporosis drugs. However, little is known about persistence with these drugs after fracture where subsequent fracture risk is high. The aims were to determine long-term persistence with anti-osteoporosis drugs among fracture patients, including its determinants, and to describe restart and subsequent persistence. METHODS: A cohort study was conducted within the Dutch PHARMO Database Network. Patients aged ≥50 years (n = 961) who received anti-osteoporosis drugs within 1 year after fracture, but not in the preceding year, were included (2002–2011). Persistence (defined as the proportion on treatment) and the proportion restarting after discontinuation were estimated using Kaplan-Meier analyses. Time-dependent Cox regression was used to identify determinants of non-persistence including age, sex, initial dosage regime, fracture type, comorbidities, and drug use. RESULTS: Persistence with anti-osteoporosis drugs was 75.0 % (95 % confidence interval (CI) 72.0–77.7) and 45.3 % (95 % CI 40.4–50.0) after 1 and 5 years, respectively. A significant determinant of non-persistence was age ≥80 years (reference 50–59 years: adjusted hazard ratio [adj. HR] 1.65; 95 % CI 1.15–2.38). This effect was not constant over time (≤360 days following initiation: adj. HR 2.07; 95 % CI 1.27–3.37; >360 days: adj. HR 1.08; 95 % CI 0.62–1.88). Within 1 year after discontinuation, 24.3 % (95 % CI 20.1–29.2) restarted therapy, yet 47.0 % persisted for 1 year. CONCLUSIONS: This study identified suboptimal persistence with anti-osteoporosis drugs among fracture patients. Major target groups for measures aimed to improve persistence may be those aged >80 years and those restarting therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00198-015-3084-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4469296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer London |
record_format | MEDLINE/PubMed |
spelling | pubmed-44692962015-06-17 Long-term persistence with anti-osteoporosis drugs after fracture Klop, C. Welsing, P. M. J. Elders, P. J. M. Overbeek, J. A. Souverein, P. C. Burden, A. M. van Onzenoort, H. A. W. Leufkens, H. G. M. Bijlsma, J. W. J. de Vries, F. Osteoporos Int Original Article SUMMARY: Long-term persistence with anti-osteoporosis drugs and determinants for discontinuation among fracture patients were examined. Persistence was 75.0 and 45.3 % after 1 and 5 years, respectively. Those aged ≥80 years were at increased risk of early discontinuation. Within 1 year after discontinuation, 24.3 % restarted therapy, yet 47.0 % persisted for 1 year. INTRODUCTION: The risk of osteoporotic fracture can effectively be reduced with use of anti-osteoporosis drugs. However, little is known about persistence with these drugs after fracture where subsequent fracture risk is high. The aims were to determine long-term persistence with anti-osteoporosis drugs among fracture patients, including its determinants, and to describe restart and subsequent persistence. METHODS: A cohort study was conducted within the Dutch PHARMO Database Network. Patients aged ≥50 years (n = 961) who received anti-osteoporosis drugs within 1 year after fracture, but not in the preceding year, were included (2002–2011). Persistence (defined as the proportion on treatment) and the proportion restarting after discontinuation were estimated using Kaplan-Meier analyses. Time-dependent Cox regression was used to identify determinants of non-persistence including age, sex, initial dosage regime, fracture type, comorbidities, and drug use. RESULTS: Persistence with anti-osteoporosis drugs was 75.0 % (95 % confidence interval (CI) 72.0–77.7) and 45.3 % (95 % CI 40.4–50.0) after 1 and 5 years, respectively. A significant determinant of non-persistence was age ≥80 years (reference 50–59 years: adjusted hazard ratio [adj. HR] 1.65; 95 % CI 1.15–2.38). This effect was not constant over time (≤360 days following initiation: adj. HR 2.07; 95 % CI 1.27–3.37; >360 days: adj. HR 1.08; 95 % CI 0.62–1.88). Within 1 year after discontinuation, 24.3 % (95 % CI 20.1–29.2) restarted therapy, yet 47.0 % persisted for 1 year. CONCLUSIONS: This study identified suboptimal persistence with anti-osteoporosis drugs among fracture patients. Major target groups for measures aimed to improve persistence may be those aged >80 years and those restarting therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00198-015-3084-3) contains supplementary material, which is available to authorized users. Springer London 2015-03-31 2015 /pmc/articles/PMC4469296/ /pubmed/25822104 http://dx.doi.org/10.1007/s00198-015-3084-3 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by-nc/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Article Klop, C. Welsing, P. M. J. Elders, P. J. M. Overbeek, J. A. Souverein, P. C. Burden, A. M. van Onzenoort, H. A. W. Leufkens, H. G. M. Bijlsma, J. W. J. de Vries, F. Long-term persistence with anti-osteoporosis drugs after fracture |
title | Long-term persistence with anti-osteoporosis drugs after fracture |
title_full | Long-term persistence with anti-osteoporosis drugs after fracture |
title_fullStr | Long-term persistence with anti-osteoporosis drugs after fracture |
title_full_unstemmed | Long-term persistence with anti-osteoporosis drugs after fracture |
title_short | Long-term persistence with anti-osteoporosis drugs after fracture |
title_sort | long-term persistence with anti-osteoporosis drugs after fracture |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469296/ https://www.ncbi.nlm.nih.gov/pubmed/25822104 http://dx.doi.org/10.1007/s00198-015-3084-3 |
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