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Mortality in Western Australian seniors with chronic respiratory diseases: a cohort study

BACKGROUND: Relatively few studies have examined survival by pharmacotherapy level and the effects of patient characteristics on mortality by pharmacotherapy level in older chronic respiratory disease (CRD) patients. This study aimed to investigate these issues in older (≥ 65) CRD patients in Wester...

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Autores principales: Einarsdóttir, Kristjana, Preen, David B, Sanfilippo, Frank M, Reeve, Raylene, Emery, Jon D, Holman, C D'Arcy J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2910678/
https://www.ncbi.nlm.nih.gov/pubmed/20591200
http://dx.doi.org/10.1186/1471-2458-10-385
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author Einarsdóttir, Kristjana
Preen, David B
Sanfilippo, Frank M
Reeve, Raylene
Emery, Jon D
Holman, C D'Arcy J
author_facet Einarsdóttir, Kristjana
Preen, David B
Sanfilippo, Frank M
Reeve, Raylene
Emery, Jon D
Holman, C D'Arcy J
author_sort Einarsdóttir, Kristjana
collection PubMed
description BACKGROUND: Relatively few studies have examined survival by pharmacotherapy level and the effects of patient characteristics on mortality by pharmacotherapy level in older chronic respiratory disease (CRD) patients. This study aimed to investigate these issues in older (≥ 65) CRD patients in Western Australia. METHODS: We identified 108,312 patients ≥ 65 years with CRD during 1992-2006 using linked medical, pharmaceutical, hospital and mortality databases held by the Commonwealth and State governments. Pharmacotherapy classification levels were designed by a clinical consensus panel. Cox regression was used to investigate the study aim. RESULTS: Patients using only short acting bronchodilators experienced similar, but slightly worse survival than patients in the highest pharmacotherapy level group using high dose inhaled corticosteroids (ICS) ± long acting bronchodilators (LABs) ± oral steroids. Patients using low to medium dose ICS ± LABs experienced relatively better survival. Also, male gender was associated with all-cause mortality in all patients (HR = 1.72, 95% CI 1.65-1.80) and especially in those in the highest pharmacotherapy level group (HR = 1.97, 95%CI = 1.84-2.10). The P-value of interaction between gender and pharmacotherapy level for the effect on all-cause death was significant (0.0003). CONCLUSIONS: Older patients with CRD not using ICS experienced the worst survival in this study and may benefit from an escalation in therapeutic regime. Males had a higher risk of death than females, which was more pronounced in the highest pharmacotherapy level group. Hence, primary health care should more actively direct disease management to mild-to-moderate disease patients.
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spelling pubmed-29106782010-07-28 Mortality in Western Australian seniors with chronic respiratory diseases: a cohort study Einarsdóttir, Kristjana Preen, David B Sanfilippo, Frank M Reeve, Raylene Emery, Jon D Holman, C D'Arcy J BMC Public Health Research Article BACKGROUND: Relatively few studies have examined survival by pharmacotherapy level and the effects of patient characteristics on mortality by pharmacotherapy level in older chronic respiratory disease (CRD) patients. This study aimed to investigate these issues in older (≥ 65) CRD patients in Western Australia. METHODS: We identified 108,312 patients ≥ 65 years with CRD during 1992-2006 using linked medical, pharmaceutical, hospital and mortality databases held by the Commonwealth and State governments. Pharmacotherapy classification levels were designed by a clinical consensus panel. Cox regression was used to investigate the study aim. RESULTS: Patients using only short acting bronchodilators experienced similar, but slightly worse survival than patients in the highest pharmacotherapy level group using high dose inhaled corticosteroids (ICS) ± long acting bronchodilators (LABs) ± oral steroids. Patients using low to medium dose ICS ± LABs experienced relatively better survival. Also, male gender was associated with all-cause mortality in all patients (HR = 1.72, 95% CI 1.65-1.80) and especially in those in the highest pharmacotherapy level group (HR = 1.97, 95%CI = 1.84-2.10). The P-value of interaction between gender and pharmacotherapy level for the effect on all-cause death was significant (0.0003). CONCLUSIONS: Older patients with CRD not using ICS experienced the worst survival in this study and may benefit from an escalation in therapeutic regime. Males had a higher risk of death than females, which was more pronounced in the highest pharmacotherapy level group. Hence, primary health care should more actively direct disease management to mild-to-moderate disease patients. BioMed Central 2010-07-01 /pmc/articles/PMC2910678/ /pubmed/20591200 http://dx.doi.org/10.1186/1471-2458-10-385 Text en Copyright ©2010 Einarsdóttir et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Einarsdóttir, Kristjana
Preen, David B
Sanfilippo, Frank M
Reeve, Raylene
Emery, Jon D
Holman, C D'Arcy J
Mortality in Western Australian seniors with chronic respiratory diseases: a cohort study
title Mortality in Western Australian seniors with chronic respiratory diseases: a cohort study
title_full Mortality in Western Australian seniors with chronic respiratory diseases: a cohort study
title_fullStr Mortality in Western Australian seniors with chronic respiratory diseases: a cohort study
title_full_unstemmed Mortality in Western Australian seniors with chronic respiratory diseases: a cohort study
title_short Mortality in Western Australian seniors with chronic respiratory diseases: a cohort study
title_sort mortality in western australian seniors with chronic respiratory diseases: a cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2910678/
https://www.ncbi.nlm.nih.gov/pubmed/20591200
http://dx.doi.org/10.1186/1471-2458-10-385
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