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The Impact of Disease and Drugs on Hip Fracture Risk

We report the risks of a comprehensive range of disease and drug categories on hip fracture occurrence using a strict population-based cohort design. Participants included the source population of a Swedish county, aged ≥50 years (n = 117,494) including all incident hip fractures during 1 year (n = ...

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Autores principales: Leavy, Breiffni, Michaëlsson, Karl, Åberg, Anna Cristina, Melhus, Håkan, Byberg, Liisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214955/
https://www.ncbi.nlm.nih.gov/pubmed/27671989
http://dx.doi.org/10.1007/s00223-016-0194-7
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author Leavy, Breiffni
Michaëlsson, Karl
Åberg, Anna Cristina
Melhus, Håkan
Byberg, Liisa
author_facet Leavy, Breiffni
Michaëlsson, Karl
Åberg, Anna Cristina
Melhus, Håkan
Byberg, Liisa
author_sort Leavy, Breiffni
collection PubMed
description We report the risks of a comprehensive range of disease and drug categories on hip fracture occurrence using a strict population-based cohort design. Participants included the source population of a Swedish county, aged ≥50 years (n = 117,494) including all incident hip fractures during 1 year (n = 477). The outcome was hospitalization for hip fracture (ICD-10 codes S72.0–S72.2) during 1 year (2009–2010). Exposures included: prevalence of (1) inpatient diseases [International Classification of Diseases (ICD) codes A00–T98 in the National Patient Register 1987–2010] and (2) prescribed drugs dispensed in 2010 or the year prior to fracture. We present age- and sex-standardized risk ratios (RRs), risk differences (RDs) and population attributable risks (PARs) of disease and drug categories in relation to hip fracture risk. All disease categories were associated with increased risk of hip fracture. Largest risk ratios and differences were for mental and behavioral disorders, diseases of the blood and previous fracture (RRs between 2.44 and 3.00; RDs (per 1000 person-years) between 5.0 and 6.9). For specific drugs, strongest associations were seen for antiparkinson (RR 2.32 [95 % CI 1.48–1.65]; RD 5.2 [1.1–9.4]) and antidepressive drugs (RR 1.90 [1.55–2.32]; RD 3.1 [2.0–4.3]). Being prescribed ≥10 drugs during 1 year incurred an increased risk of hip fracture, whereas prescription of cardiovascular drugs or ≤5 drugs did not appear to increase risk. Diseases inferring the greatest PARs included: cardiovascular diseases PAR 22 % (95 % CI 14–29) and previous injuries (PAR 21 % [95 % CI 16–25]; for specific drugs, antidepressants posed the greatest risk (PAR 16 % [95 % CI 12.0–19.3]). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00223-016-0194-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-52149552017-01-24 The Impact of Disease and Drugs on Hip Fracture Risk Leavy, Breiffni Michaëlsson, Karl Åberg, Anna Cristina Melhus, Håkan Byberg, Liisa Calcif Tissue Int Original Research We report the risks of a comprehensive range of disease and drug categories on hip fracture occurrence using a strict population-based cohort design. Participants included the source population of a Swedish county, aged ≥50 years (n = 117,494) including all incident hip fractures during 1 year (n = 477). The outcome was hospitalization for hip fracture (ICD-10 codes S72.0–S72.2) during 1 year (2009–2010). Exposures included: prevalence of (1) inpatient diseases [International Classification of Diseases (ICD) codes A00–T98 in the National Patient Register 1987–2010] and (2) prescribed drugs dispensed in 2010 or the year prior to fracture. We present age- and sex-standardized risk ratios (RRs), risk differences (RDs) and population attributable risks (PARs) of disease and drug categories in relation to hip fracture risk. All disease categories were associated with increased risk of hip fracture. Largest risk ratios and differences were for mental and behavioral disorders, diseases of the blood and previous fracture (RRs between 2.44 and 3.00; RDs (per 1000 person-years) between 5.0 and 6.9). For specific drugs, strongest associations were seen for antiparkinson (RR 2.32 [95 % CI 1.48–1.65]; RD 5.2 [1.1–9.4]) and antidepressive drugs (RR 1.90 [1.55–2.32]; RD 3.1 [2.0–4.3]). Being prescribed ≥10 drugs during 1 year incurred an increased risk of hip fracture, whereas prescription of cardiovascular drugs or ≤5 drugs did not appear to increase risk. Diseases inferring the greatest PARs included: cardiovascular diseases PAR 22 % (95 % CI 14–29) and previous injuries (PAR 21 % [95 % CI 16–25]; for specific drugs, antidepressants posed the greatest risk (PAR 16 % [95 % CI 12.0–19.3]). ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00223-016-0194-7) contains supplementary material, which is available to authorized users. Springer US 2016-09-26 2017 /pmc/articles/PMC5214955/ /pubmed/27671989 http://dx.doi.org/10.1007/s00223-016-0194-7 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Leavy, Breiffni
Michaëlsson, Karl
Åberg, Anna Cristina
Melhus, Håkan
Byberg, Liisa
The Impact of Disease and Drugs on Hip Fracture Risk
title The Impact of Disease and Drugs on Hip Fracture Risk
title_full The Impact of Disease and Drugs on Hip Fracture Risk
title_fullStr The Impact of Disease and Drugs on Hip Fracture Risk
title_full_unstemmed The Impact of Disease and Drugs on Hip Fracture Risk
title_short The Impact of Disease and Drugs on Hip Fracture Risk
title_sort impact of disease and drugs on hip fracture risk
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214955/
https://www.ncbi.nlm.nih.gov/pubmed/27671989
http://dx.doi.org/10.1007/s00223-016-0194-7
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