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Association between aspirin therapy and the outcome in critically ill patients: a nested cohort study

BACKGROUND: Antiplatelet therapy may attenuate the undesirable effects of platelets on the inflammatory cascades in critical illness. The objective of this study was to evaluate the association between aspirin therapy during intensive care unit (ICU) stay and all-cause mortality. METHODS: This was a...

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Autores principales: Al Harbi, Shmeylan A., Tamim, Hani M., Al-Dorzi, Hasan M., Sadat, Musharaf, Arabi, Yaseen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743206/
https://www.ncbi.nlm.nih.gov/pubmed/26850706
http://dx.doi.org/10.1186/s40360-016-0047-z
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author Al Harbi, Shmeylan A.
Tamim, Hani M.
Al-Dorzi, Hasan M.
Sadat, Musharaf
Arabi, Yaseen M.
author_facet Al Harbi, Shmeylan A.
Tamim, Hani M.
Al-Dorzi, Hasan M.
Sadat, Musharaf
Arabi, Yaseen M.
author_sort Al Harbi, Shmeylan A.
collection PubMed
description BACKGROUND: Antiplatelet therapy may attenuate the undesirable effects of platelets on the inflammatory cascades in critical illness. The objective of this study was to evaluate the association between aspirin therapy during intensive care unit (ICU) stay and all-cause mortality. METHODS: This was a nested cohort study within two randomized controlled trials in which all enrolled patients (N = 763) were grouped according to aspirin intake during ICU stay. The primary endpoints were all-cause ICU mortality and hospital mortality. Secondary endpoints included the development of severe sepsis during the ICU stay, ICU and hospital length of stay and the duration of mechanical ventilation. Propensity score was used to adjust for clinically and statistically relevant variables. RESULTS: Of the 763 patients, 154 patients (20 %) received aspirin. Aspirin therapy was not associated with a reduction in ICU mortality (adjusted OR 1.18, 95 % CI 0.69–2.02, P = 0.55) nor with hospital mortality (adjusted OR 0.95, 95 % CI 0.61–1.50, P = 0.82). Aspirin use had no preferential association with mortality among any of the study subgroups. Additionally, aspirin therapy was associated with higher risk of ICU-acquired severe sepsis, and increased mechanical ventilation duration and ICU length of stay. CONCLUSION: Our study showed that the use of aspirin in critically ill patients was not associated with lower mortality, but rather with an increased morbidity. TRIAL REGISTRATION NUMBER: ISRCTN07413772 and ISRCTN96294863.
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spelling pubmed-47432062016-02-06 Association between aspirin therapy and the outcome in critically ill patients: a nested cohort study Al Harbi, Shmeylan A. Tamim, Hani M. Al-Dorzi, Hasan M. Sadat, Musharaf Arabi, Yaseen M. BMC Pharmacol Toxicol Research Article BACKGROUND: Antiplatelet therapy may attenuate the undesirable effects of platelets on the inflammatory cascades in critical illness. The objective of this study was to evaluate the association between aspirin therapy during intensive care unit (ICU) stay and all-cause mortality. METHODS: This was a nested cohort study within two randomized controlled trials in which all enrolled patients (N = 763) were grouped according to aspirin intake during ICU stay. The primary endpoints were all-cause ICU mortality and hospital mortality. Secondary endpoints included the development of severe sepsis during the ICU stay, ICU and hospital length of stay and the duration of mechanical ventilation. Propensity score was used to adjust for clinically and statistically relevant variables. RESULTS: Of the 763 patients, 154 patients (20 %) received aspirin. Aspirin therapy was not associated with a reduction in ICU mortality (adjusted OR 1.18, 95 % CI 0.69–2.02, P = 0.55) nor with hospital mortality (adjusted OR 0.95, 95 % CI 0.61–1.50, P = 0.82). Aspirin use had no preferential association with mortality among any of the study subgroups. Additionally, aspirin therapy was associated with higher risk of ICU-acquired severe sepsis, and increased mechanical ventilation duration and ICU length of stay. CONCLUSION: Our study showed that the use of aspirin in critically ill patients was not associated with lower mortality, but rather with an increased morbidity. TRIAL REGISTRATION NUMBER: ISRCTN07413772 and ISRCTN96294863. BioMed Central 2016-02-05 /pmc/articles/PMC4743206/ /pubmed/26850706 http://dx.doi.org/10.1186/s40360-016-0047-z Text en © Al Harbi et al. 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Al Harbi, Shmeylan A.
Tamim, Hani M.
Al-Dorzi, Hasan M.
Sadat, Musharaf
Arabi, Yaseen M.
Association between aspirin therapy and the outcome in critically ill patients: a nested cohort study
title Association between aspirin therapy and the outcome in critically ill patients: a nested cohort study
title_full Association between aspirin therapy and the outcome in critically ill patients: a nested cohort study
title_fullStr Association between aspirin therapy and the outcome in critically ill patients: a nested cohort study
title_full_unstemmed Association between aspirin therapy and the outcome in critically ill patients: a nested cohort study
title_short Association between aspirin therapy and the outcome in critically ill patients: a nested cohort study
title_sort association between aspirin therapy and the outcome in critically ill patients: a nested cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743206/
https://www.ncbi.nlm.nih.gov/pubmed/26850706
http://dx.doi.org/10.1186/s40360-016-0047-z
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