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Association of platelet count with all‐cause mortality from acute respiratory distress syndrome: A cohort study
BACKGROUND: The purpose of this study was to investigate whether platelet count was associated with mortality in acute respiratory distress syndrome (ARDS) patients. METHODS: We analyzed patients with ARDS from Multi‐parameter Intelligent Monitoring in Intensive Care Database III (MIMIC‐III). Platel...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102613/ https://www.ncbi.nlm.nih.gov/pubmed/35358347 http://dx.doi.org/10.1002/jcla.24378 |
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author | Wang, Rennv Dai, Haiwen |
author_facet | Wang, Rennv Dai, Haiwen |
author_sort | Wang, Rennv |
collection | PubMed |
description | BACKGROUND: The purpose of this study was to investigate whether platelet count was associated with mortality in acute respiratory distress syndrome (ARDS) patients. METHODS: We analyzed patients with ARDS from Multi‐parameter Intelligent Monitoring in Intensive Care Database III (MIMIC‐III). Platelet count was measured at the time of intensive care unit (ICU) admission. The cox proportional hazard model and subgroup analysis were used to determine the relationship between the platelet count and mortality of ARDS, as well as the consistency of its association. The primary outcome of this study was 365‐day mortality from the date of ICU admission. RESULT: This study enrolled a total of 395 critically ill patients with ARDS. After adjustment for age, gender and ethnicity, the multivariate cox regression model showed that the hazard ratios (HRs) (95% confidence intervals [CIs]) of platelet count <192 × 10(9)/L and >296 × 10(9)/L were 2.08 (1.43, 3.04) and 1.35 (0.91, 2.01), respectively, compared with the reference (192–296 ×10(9)/L). After adjusting for confounding factors, lower platelet count (<192 × 10(9)/L) was associated with increased mortality (adjusted HR, 1.71; 95% CI 1.06–2.76, p = 0.0284). However, there was no similar trend in the 30‐day (adjusted HR,1.02; 95% CI 0.54–1.94) or 90‐day (adjusted HR, 1.65; 95% CI 0.94–2.89) mortality. In the subgroup analysis, lower platelet count showed significant interactions with specific populations (p interaction = 0.0413), especially in patients with atrial fibrillation. CONCLUSION: Taken together, our analysis showed that platelet count is an independent predictor of mortality in critically ill patients with ARDS. |
format | Online Article Text |
id | pubmed-9102613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91026132022-05-18 Association of platelet count with all‐cause mortality from acute respiratory distress syndrome: A cohort study Wang, Rennv Dai, Haiwen J Clin Lab Anal Research Articles BACKGROUND: The purpose of this study was to investigate whether platelet count was associated with mortality in acute respiratory distress syndrome (ARDS) patients. METHODS: We analyzed patients with ARDS from Multi‐parameter Intelligent Monitoring in Intensive Care Database III (MIMIC‐III). Platelet count was measured at the time of intensive care unit (ICU) admission. The cox proportional hazard model and subgroup analysis were used to determine the relationship between the platelet count and mortality of ARDS, as well as the consistency of its association. The primary outcome of this study was 365‐day mortality from the date of ICU admission. RESULT: This study enrolled a total of 395 critically ill patients with ARDS. After adjustment for age, gender and ethnicity, the multivariate cox regression model showed that the hazard ratios (HRs) (95% confidence intervals [CIs]) of platelet count <192 × 10(9)/L and >296 × 10(9)/L were 2.08 (1.43, 3.04) and 1.35 (0.91, 2.01), respectively, compared with the reference (192–296 ×10(9)/L). After adjusting for confounding factors, lower platelet count (<192 × 10(9)/L) was associated with increased mortality (adjusted HR, 1.71; 95% CI 1.06–2.76, p = 0.0284). However, there was no similar trend in the 30‐day (adjusted HR,1.02; 95% CI 0.54–1.94) or 90‐day (adjusted HR, 1.65; 95% CI 0.94–2.89) mortality. In the subgroup analysis, lower platelet count showed significant interactions with specific populations (p interaction = 0.0413), especially in patients with atrial fibrillation. CONCLUSION: Taken together, our analysis showed that platelet count is an independent predictor of mortality in critically ill patients with ARDS. John Wiley and Sons Inc. 2022-03-31 /pmc/articles/PMC9102613/ /pubmed/35358347 http://dx.doi.org/10.1002/jcla.24378 Text en © 2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wang, Rennv Dai, Haiwen Association of platelet count with all‐cause mortality from acute respiratory distress syndrome: A cohort study |
title | Association of platelet count with all‐cause mortality from acute respiratory distress syndrome: A cohort study |
title_full | Association of platelet count with all‐cause mortality from acute respiratory distress syndrome: A cohort study |
title_fullStr | Association of platelet count with all‐cause mortality from acute respiratory distress syndrome: A cohort study |
title_full_unstemmed | Association of platelet count with all‐cause mortality from acute respiratory distress syndrome: A cohort study |
title_short | Association of platelet count with all‐cause mortality from acute respiratory distress syndrome: A cohort study |
title_sort | association of platelet count with all‐cause mortality from acute respiratory distress syndrome: a cohort study |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102613/ https://www.ncbi.nlm.nih.gov/pubmed/35358347 http://dx.doi.org/10.1002/jcla.24378 |
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