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Benzodiazepines, Z-drugs and the risk of hip fracture: A systematic review and meta-analysis
BACKGROUND: Hip fractures in the older person lead to an increased risk of mortality, poorer quality of life and increased morbidity. Benzodiazepine (BNZ) use is associated with increased hip fracture rate, consequently Z-drugs are fast becoming the physician’s hypnotic prescription of choice yet da...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407557/ https://www.ncbi.nlm.nih.gov/pubmed/28448593 http://dx.doi.org/10.1371/journal.pone.0174730 |
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author | Donnelly, Karen Bracchi, Robert Hewitt, Jonathan Routledge, Philip A. Carter, Ben |
author_facet | Donnelly, Karen Bracchi, Robert Hewitt, Jonathan Routledge, Philip A. Carter, Ben |
author_sort | Donnelly, Karen |
collection | PubMed |
description | BACKGROUND: Hip fractures in the older person lead to an increased risk of mortality, poorer quality of life and increased morbidity. Benzodiazepine (BNZ) use is associated with increased hip fracture rate, consequently Z-drugs are fast becoming the physician’s hypnotic prescription of choice yet data on their use is limited. We compared the risk of hip fracture associated with Z-drugs and BNZ medications, respectively, and examined if this risk varied with longer-term use. METHODS AND FINDINGS: We carried out a systematic review of the literature and meta-analysis. MEDLINE and SCOPUS were searched to identify studies involving BNZ or Z-drugs and the risk of hip fracture up to May 2015. Each included study was quality-assessed. A pooled relative risk of hip fracture was calculated using the generic inverse variance method, with a random effects model, with the length of hypnotic usage as a subgroup. Both BNZ, and Z-drug use respectively, were significantly associated with an increased risk of hip fracture (RR = 1.52, 95% CI 1.37–1.68; and RR = 1.90, 95% CI 1.68–2.13). Short-term use of BNZ and Z-drugs respectively, was also associated with the greatest risk of hip fracture (RR = 2.40, 95% CI 1.88–3.05 and RR = 2.39, 95% CI 1.74–3.29). CONCLUSIONS: There is strong evidence that both BNZ and Z-drugs are associated with an increased risk of hip fracture in the older person, and there is little difference between their respective risks. Patients newly prescribed these medicines are at the greatest risk of hip fracture. Clinicians and policy makers need to consider the increased risk of fallings and hip fracture particularly amongst new users of these medications. |
format | Online Article Text |
id | pubmed-5407557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54075572017-05-14 Benzodiazepines, Z-drugs and the risk of hip fracture: A systematic review and meta-analysis Donnelly, Karen Bracchi, Robert Hewitt, Jonathan Routledge, Philip A. Carter, Ben PLoS One Research Article BACKGROUND: Hip fractures in the older person lead to an increased risk of mortality, poorer quality of life and increased morbidity. Benzodiazepine (BNZ) use is associated with increased hip fracture rate, consequently Z-drugs are fast becoming the physician’s hypnotic prescription of choice yet data on their use is limited. We compared the risk of hip fracture associated with Z-drugs and BNZ medications, respectively, and examined if this risk varied with longer-term use. METHODS AND FINDINGS: We carried out a systematic review of the literature and meta-analysis. MEDLINE and SCOPUS were searched to identify studies involving BNZ or Z-drugs and the risk of hip fracture up to May 2015. Each included study was quality-assessed. A pooled relative risk of hip fracture was calculated using the generic inverse variance method, with a random effects model, with the length of hypnotic usage as a subgroup. Both BNZ, and Z-drug use respectively, were significantly associated with an increased risk of hip fracture (RR = 1.52, 95% CI 1.37–1.68; and RR = 1.90, 95% CI 1.68–2.13). Short-term use of BNZ and Z-drugs respectively, was also associated with the greatest risk of hip fracture (RR = 2.40, 95% CI 1.88–3.05 and RR = 2.39, 95% CI 1.74–3.29). CONCLUSIONS: There is strong evidence that both BNZ and Z-drugs are associated with an increased risk of hip fracture in the older person, and there is little difference between their respective risks. Patients newly prescribed these medicines are at the greatest risk of hip fracture. Clinicians and policy makers need to consider the increased risk of fallings and hip fracture particularly amongst new users of these medications. Public Library of Science 2017-04-27 /pmc/articles/PMC5407557/ /pubmed/28448593 http://dx.doi.org/10.1371/journal.pone.0174730 Text en © 2017 Donnelly et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Donnelly, Karen Bracchi, Robert Hewitt, Jonathan Routledge, Philip A. Carter, Ben Benzodiazepines, Z-drugs and the risk of hip fracture: A systematic review and meta-analysis |
title | Benzodiazepines, Z-drugs and the risk of hip fracture: A systematic review and meta-analysis |
title_full | Benzodiazepines, Z-drugs and the risk of hip fracture: A systematic review and meta-analysis |
title_fullStr | Benzodiazepines, Z-drugs and the risk of hip fracture: A systematic review and meta-analysis |
title_full_unstemmed | Benzodiazepines, Z-drugs and the risk of hip fracture: A systematic review and meta-analysis |
title_short | Benzodiazepines, Z-drugs and the risk of hip fracture: A systematic review and meta-analysis |
title_sort | benzodiazepines, z-drugs and the risk of hip fracture: a systematic review and meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5407557/ https://www.ncbi.nlm.nih.gov/pubmed/28448593 http://dx.doi.org/10.1371/journal.pone.0174730 |
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