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Effect of contraindicated drugs for heart failure on hospitalization among seniors with heart failure: A nested case-control study
Little is known about the effect of nonsteroidal anti-inflammatory drugs (NSAIDs), thiazolidinediones (TZDs), nifedipine and nondihydropyridine calcium channel blockers (CCBs) usage on the risk of all-cause hospitalization among seniors with heart failure (HF). We assessed the risk of all-cause hosp...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340463/ https://www.ncbi.nlm.nih.gov/pubmed/28248890 http://dx.doi.org/10.1097/MD.0000000000006239 |
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author | Girouard, Catherine Grégoire, Jean-Pierre Poirier, Paul Moisan, Jocelyne |
author_facet | Girouard, Catherine Grégoire, Jean-Pierre Poirier, Paul Moisan, Jocelyne |
author_sort | Girouard, Catherine |
collection | PubMed |
description | Little is known about the effect of nonsteroidal anti-inflammatory drugs (NSAIDs), thiazolidinediones (TZDs), nifedipine and nondihydropyridine calcium channel blockers (CCBs) usage on the risk of all-cause hospitalization among seniors with heart failure (HF). We assessed the risk of all-cause hospitalization associated with exposure to each of these drug classes, in a population of seniors with HF. Using the Quebec provincial databases, we conducted a nested case-control study in a population of individuals aged ≥65 with a first HF diagnosis between 2000 and 2009. Patients were considered users of a potentially inappropriate drug class if their date of hospital admission occurred in the interval between the date of the last drug claim and the end date of its days’ supply. The risks of hospitalization were estimated using multivariate conditional logistic regression. Of the 128,853 individuals included in the study population, 101,273 (78.6%) were hospitalized. When compared to nonusers, users of NSAIDs (adjusted odds ratio: 1.16; 95% confidence interval: 1.13–1.20), TZD (1.09; 1.04–1.14), and CCBs (1.03; 1.01–1.05) had an increased risk of all-cause hospitalization, but not the users of nifedipine (1.00; 0.97–1.03). Seniors with HF exposed to a potentially inappropriate drug class are at increased risk of worse health outcomes. Treatment alternatives should be considered, as they are available. |
format | Online Article Text |
id | pubmed-5340463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-53404632017-03-09 Effect of contraindicated drugs for heart failure on hospitalization among seniors with heart failure: A nested case-control study Girouard, Catherine Grégoire, Jean-Pierre Poirier, Paul Moisan, Jocelyne Medicine (Baltimore) 3400 Little is known about the effect of nonsteroidal anti-inflammatory drugs (NSAIDs), thiazolidinediones (TZDs), nifedipine and nondihydropyridine calcium channel blockers (CCBs) usage on the risk of all-cause hospitalization among seniors with heart failure (HF). We assessed the risk of all-cause hospitalization associated with exposure to each of these drug classes, in a population of seniors with HF. Using the Quebec provincial databases, we conducted a nested case-control study in a population of individuals aged ≥65 with a first HF diagnosis between 2000 and 2009. Patients were considered users of a potentially inappropriate drug class if their date of hospital admission occurred in the interval between the date of the last drug claim and the end date of its days’ supply. The risks of hospitalization were estimated using multivariate conditional logistic regression. Of the 128,853 individuals included in the study population, 101,273 (78.6%) were hospitalized. When compared to nonusers, users of NSAIDs (adjusted odds ratio: 1.16; 95% confidence interval: 1.13–1.20), TZD (1.09; 1.04–1.14), and CCBs (1.03; 1.01–1.05) had an increased risk of all-cause hospitalization, but not the users of nifedipine (1.00; 0.97–1.03). Seniors with HF exposed to a potentially inappropriate drug class are at increased risk of worse health outcomes. Treatment alternatives should be considered, as they are available. Wolters Kluwer Health 2017-03-03 /pmc/articles/PMC5340463/ /pubmed/28248890 http://dx.doi.org/10.1097/MD.0000000000006239 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | 3400 Girouard, Catherine Grégoire, Jean-Pierre Poirier, Paul Moisan, Jocelyne Effect of contraindicated drugs for heart failure on hospitalization among seniors with heart failure: A nested case-control study |
title | Effect of contraindicated drugs for heart failure on hospitalization among seniors with heart failure: A nested case-control study |
title_full | Effect of contraindicated drugs for heart failure on hospitalization among seniors with heart failure: A nested case-control study |
title_fullStr | Effect of contraindicated drugs for heart failure on hospitalization among seniors with heart failure: A nested case-control study |
title_full_unstemmed | Effect of contraindicated drugs for heart failure on hospitalization among seniors with heart failure: A nested case-control study |
title_short | Effect of contraindicated drugs for heart failure on hospitalization among seniors with heart failure: A nested case-control study |
title_sort | effect of contraindicated drugs for heart failure on hospitalization among seniors with heart failure: a nested case-control study |
topic | 3400 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5340463/ https://www.ncbi.nlm.nih.gov/pubmed/28248890 http://dx.doi.org/10.1097/MD.0000000000006239 |
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