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Loss of treatment benefit due to low compliance with bisphosphonate therapy
SUMMARY: Among 8,822 new female bisphosphonate users, non-compliant bisphosphonate use was associated with a 45% increased risk of osteoporotic fracture compared to compliant use (MPR ≥80%). Classifying compliance into five categories, fracture risk gradually increased with poorer compliance. These...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267483/ https://www.ncbi.nlm.nih.gov/pubmed/17874028 http://dx.doi.org/10.1007/s00198-007-0466-1 |
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author | Penning-van Beest, F. J. A. Erkens, J. A. Olson, M. Herings, R. M. C. |
author_facet | Penning-van Beest, F. J. A. Erkens, J. A. Olson, M. Herings, R. M. C. |
author_sort | Penning-van Beest, F. J. A. |
collection | PubMed |
description | SUMMARY: Among 8,822 new female bisphosphonate users, non-compliant bisphosphonate use was associated with a 45% increased risk of osteoporotic fracture compared to compliant use (MPR ≥80%). Classifying compliance into five categories, fracture risk gradually increased with poorer compliance. These results emphasize the importance of treatment compliance in obtaining maximal treatment benefit. INTRODUCTION: Bisphosphonates are widely used to treat osteoporosis and reduce fracture risk. Low compliance is frequent and will limit treatment benefit. METHODS: New female users of alendronate or risedronate between 1999–2004, aged ≥45 years were identified from PHARMO-RLS, including drug-dispensing and hospitalization data of ≥2 million residents of the Netherlands. Patients were followed until first hospitalisation for an osteoporotic fracture, death, or end of study period. Compliance with bisphosphonates during follow-up was measured over 90-day intervals using Medication Possession Ratio (MPR). The association between compliance and fracture risk was analyzed using time-dependent Cox-regression. RESULTS: The study cohort included 8,822 new female bisphosphonate users, contributing in total 22,484 person-years of follow-up. During follow-up, 176 osteoporotic fractures occurred (excluding the first six months). Non-compliant bisphosphonate use was associated with a 45% increased fracture risk compared to compliant use (MPR ≥80%). Classifying compliance into five categories, fracture risk gradually increased with poorer compliance (p-value <0.05 for trend). A MPR <20% was associated with an 80% increased fracture risk compared to a MPR ≥90%. CONCLUSIONS: These results show a statistically significant association between level of compliance with bisphosphonates and level of fracture risk, emphasizing the importance of treatment compliance in obtaining maximal treatment benefit. |
format | Text |
id | pubmed-2267483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-22674832008-03-14 Loss of treatment benefit due to low compliance with bisphosphonate therapy Penning-van Beest, F. J. A. Erkens, J. A. Olson, M. Herings, R. M. C. Osteoporos Int Original Article SUMMARY: Among 8,822 new female bisphosphonate users, non-compliant bisphosphonate use was associated with a 45% increased risk of osteoporotic fracture compared to compliant use (MPR ≥80%). Classifying compliance into five categories, fracture risk gradually increased with poorer compliance. These results emphasize the importance of treatment compliance in obtaining maximal treatment benefit. INTRODUCTION: Bisphosphonates are widely used to treat osteoporosis and reduce fracture risk. Low compliance is frequent and will limit treatment benefit. METHODS: New female users of alendronate or risedronate between 1999–2004, aged ≥45 years were identified from PHARMO-RLS, including drug-dispensing and hospitalization data of ≥2 million residents of the Netherlands. Patients were followed until first hospitalisation for an osteoporotic fracture, death, or end of study period. Compliance with bisphosphonates during follow-up was measured over 90-day intervals using Medication Possession Ratio (MPR). The association between compliance and fracture risk was analyzed using time-dependent Cox-regression. RESULTS: The study cohort included 8,822 new female bisphosphonate users, contributing in total 22,484 person-years of follow-up. During follow-up, 176 osteoporotic fractures occurred (excluding the first six months). Non-compliant bisphosphonate use was associated with a 45% increased fracture risk compared to compliant use (MPR ≥80%). Classifying compliance into five categories, fracture risk gradually increased with poorer compliance (p-value <0.05 for trend). A MPR <20% was associated with an 80% increased fracture risk compared to a MPR ≥90%. CONCLUSIONS: These results show a statistically significant association between level of compliance with bisphosphonates and level of fracture risk, emphasizing the importance of treatment compliance in obtaining maximal treatment benefit. Springer-Verlag 2007-09-14 2008-04 /pmc/articles/PMC2267483/ /pubmed/17874028 http://dx.doi.org/10.1007/s00198-007-0466-1 Text en © International Osteoporosis Foundation and National Osteoporosis Foundation 2007 |
spellingShingle | Original Article Penning-van Beest, F. J. A. Erkens, J. A. Olson, M. Herings, R. M. C. Loss of treatment benefit due to low compliance with bisphosphonate therapy |
title | Loss of treatment benefit due to low compliance with bisphosphonate therapy |
title_full | Loss of treatment benefit due to low compliance with bisphosphonate therapy |
title_fullStr | Loss of treatment benefit due to low compliance with bisphosphonate therapy |
title_full_unstemmed | Loss of treatment benefit due to low compliance with bisphosphonate therapy |
title_short | Loss of treatment benefit due to low compliance with bisphosphonate therapy |
title_sort | loss of treatment benefit due to low compliance with bisphosphonate therapy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267483/ https://www.ncbi.nlm.nih.gov/pubmed/17874028 http://dx.doi.org/10.1007/s00198-007-0466-1 |
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