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Association of red blood cell distribution width to albumin ratio with the prognosis of acute severe pulmonary embolism: A cohort study

Red blood cell distribution width (RDW) to human serum albumin (ALB) ratio (RDW/ALB Ratio, RAR) is a prognostic factor for adverse outcomes in different disease populations. However, the relationship between RAR and pulmonary embolism outcomes remains unclear. Therefore, this study set out to invest...

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Autores principales: Ding, Chaowei, Zhang, Ziping, Qiu, Jiayong, Du, Dan, Liu, Zexin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10681614/
https://www.ncbi.nlm.nih.gov/pubmed/38013321
http://dx.doi.org/10.1097/MD.0000000000036141
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author Ding, Chaowei
Zhang, Ziping
Qiu, Jiayong
Du, Dan
Liu, Zexin
author_facet Ding, Chaowei
Zhang, Ziping
Qiu, Jiayong
Du, Dan
Liu, Zexin
author_sort Ding, Chaowei
collection PubMed
description Red blood cell distribution width (RDW) to human serum albumin (ALB) ratio (RDW/ALB Ratio, RAR) is a prognostic factor for adverse outcomes in different disease populations. However, the relationship between RAR and pulmonary embolism outcomes remains unclear. Therefore, this study set out to investigate the association between RAR and the risk of all-cause death in acute pulmonary embolism (APE) patients admitted to the intensive care unit (ICU). This is a retrospective study based on the MIMIC-IV database. The primary outcome was all-cause mortality among patients with APE (in-hospital and 1-year mortality). The relationship between RAR and all-cause mortality was assessed using Cox regression analysis. The survival curve was drawn to evaluate the predictive value of RAR for patient mortality. Correlations and threshold effects between RAR and all-cause mortality were analyzed using the generalized additive model (GAM). The study included 773 patients, and fully adjusted Cox regression models showed that RAR was associated with higher all-cause mortality in the hospital and one year later (all P < .05). In the GAM, the relationship between RAR and all-cause mortality was shown to be nonlinear, with a positive association between RAR and all-cause mortality in APE patients when RAR values were at low to moderate levels. This study revealed a significant association between RAR and the risk of all-cause day death in patients with pulmonary embolism. Higher RAR value was associated with increased in-hospital mortality and 1-year mortality.
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spelling pubmed-106816142023-11-24 Association of red blood cell distribution width to albumin ratio with the prognosis of acute severe pulmonary embolism: A cohort study Ding, Chaowei Zhang, Ziping Qiu, Jiayong Du, Dan Liu, Zexin Medicine (Baltimore) 3400 Red blood cell distribution width (RDW) to human serum albumin (ALB) ratio (RDW/ALB Ratio, RAR) is a prognostic factor for adverse outcomes in different disease populations. However, the relationship between RAR and pulmonary embolism outcomes remains unclear. Therefore, this study set out to investigate the association between RAR and the risk of all-cause death in acute pulmonary embolism (APE) patients admitted to the intensive care unit (ICU). This is a retrospective study based on the MIMIC-IV database. The primary outcome was all-cause mortality among patients with APE (in-hospital and 1-year mortality). The relationship between RAR and all-cause mortality was assessed using Cox regression analysis. The survival curve was drawn to evaluate the predictive value of RAR for patient mortality. Correlations and threshold effects between RAR and all-cause mortality were analyzed using the generalized additive model (GAM). The study included 773 patients, and fully adjusted Cox regression models showed that RAR was associated with higher all-cause mortality in the hospital and one year later (all P < .05). In the GAM, the relationship between RAR and all-cause mortality was shown to be nonlinear, with a positive association between RAR and all-cause mortality in APE patients when RAR values were at low to moderate levels. This study revealed a significant association between RAR and the risk of all-cause day death in patients with pulmonary embolism. Higher RAR value was associated with increased in-hospital mortality and 1-year mortality. Lippincott Williams & Wilkins 2023-11-24 /pmc/articles/PMC10681614/ /pubmed/38013321 http://dx.doi.org/10.1097/MD.0000000000036141 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal.
spellingShingle 3400
Ding, Chaowei
Zhang, Ziping
Qiu, Jiayong
Du, Dan
Liu, Zexin
Association of red blood cell distribution width to albumin ratio with the prognosis of acute severe pulmonary embolism: A cohort study
title Association of red blood cell distribution width to albumin ratio with the prognosis of acute severe pulmonary embolism: A cohort study
title_full Association of red blood cell distribution width to albumin ratio with the prognosis of acute severe pulmonary embolism: A cohort study
title_fullStr Association of red blood cell distribution width to albumin ratio with the prognosis of acute severe pulmonary embolism: A cohort study
title_full_unstemmed Association of red blood cell distribution width to albumin ratio with the prognosis of acute severe pulmonary embolism: A cohort study
title_short Association of red blood cell distribution width to albumin ratio with the prognosis of acute severe pulmonary embolism: A cohort study
title_sort association of red blood cell distribution width to albumin ratio with the prognosis of acute severe pulmonary embolism: a cohort study
topic 3400
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10681614/
https://www.ncbi.nlm.nih.gov/pubmed/38013321
http://dx.doi.org/10.1097/MD.0000000000036141
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