Association between platelet-white cell ratio and all-cause mortality in critically ill patients with atrial fibrillation: a retrospective cohort study

Atrial fibrillation is common in intensive care units and portends poor prognosis. The platelet-to-white blood cell ratio is an emerging inflammatory-coagulatory biomarker with prognostic value in cardiovascular diseases. This study examines the association between platelet-white cell ratio (PWR) and all-cause mortality in this high-risk population. In this retrospective cohort study, clinical data were obtained from the MIMIC-IV database. We included adult intensive care unit (ICU) patients with a diagnosis of atrial fibrillation. The PWR was evaluated as the primary exposure, analysed both as a continuous measure and by quartiles. The primary endpoint was 28-day all-cause mortality, with secondary endpoints comprising mortality at 90 days, 180 days, and 1 year. Multivariable Cox models were used to evaluate the association between PWR and mortality, with adjustment for established confounders including demographics, comorbidity, and illness severity. Non-linearity was examined using restricted cubic splines, and subgroup analyses were conducted to evaluate the consistency of the association. The analysis included 2,401 patients. After full adjustment, a unit increase in PWR was independently associated with a 2% decrease in the hazard of 28-day mortality (HR 0.98, 95% CI 0.97–0.99, p < 0.001). When analysed by quartiles, a significant inverse dose-response relationship was observed (P for trend < 0.001). Compared to the lowest quartile (Q1), patients in the highest PWR quartile (Q4) exhibited a substantially reduced hazard of death at 28 days (adjusted HR 0.55, 95% CI 0.43–0.72, p < 0.001). This inverse association remained statistically significant for 90-day and 180-day mortality but was absent at 1 year. The relationship was linear across the range of PWR values for 28-day (P for non-linearity = 0.213), 90-day (P for non-linearity = 0.476), and 180-day mortality (P for non-linearity = 0.377). The results were robust across all predefined subgroups, with no evidence of significant effect modification. Among critically ill patients with atrial fibrillation, a higher platelet-to-white blood cell ratio at ICU admission is inversely and linearly associated with short- and intermediate-term mortality, demonstrating a clear dose-response relationship. As an easily derived biomarker, PWR has potential utility for enhancing risk assessment in this clinical setting.

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Journal
BMC Cardiovascular Disorders
Published
2026-03-16
DOI
https://doi.org/10.1186/s12872-026-05730-y
Primary Topic
Inflammatory Biomarkers in Disease Prognosis
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article
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article

Association between platelet-white cell ratio and all-cause mortality in critically ill patients with atrial fibrillation: a retrospective cohort study

Xiao-Jiao Cui, Jing Wang, Rong Zhou, Bo Xie et al.
BMC Cardiovascular Disorders
Inflammatory Biomarkers in Disease Prognosis
article

Association between platelet-white cell ratio and all-cause mortality in critically ill patients with atrial fibrillation: a retrospective cohort study

Xiao-Jiao Cui, Jing Wang, Rong Zhou, Bo Xie, Min Chen, Jin Xie
article en

Abstract

Atrial fibrillation is common in intensive care units and portends poor prognosis. The platelet-to-white blood cell ratio is an emerging inflammatory-coagulatory biomarker with prognostic value in cardiovascular diseases. This study examines the association between platelet-white cell ratio (PWR) and all-cause mortality in this high-risk population. In this retrospective cohort study, clinical data were obtained from the MIMIC-IV database. We included adult intensive care unit (ICU) patients with a diagnosis of atrial fibrillation. The PWR was evaluated as the primary exposure, analysed both as a continuous measure and by quartiles. The primary endpoint was 28-day all-cause mortality, with secondary endpoints comprising mortality at 90 days, 180 days, and 1 year. Multivariable Cox models were used to evaluate the association between PWR and mortality, with adjustment for established confounders including demographics, comorbidity, and illness severity. Non-linearity was examined using restricted cubic splines, and subgroup analyses were conducted to evaluate the consistency of the association. The analysis included 2,401 patients. After full adjustment, a unit increase in PWR was independently associated with a 2% decrease in the hazard of 28-day mortality (HR 0.98, 95% CI 0.97–0.99, p < 0.001). When analysed by quartiles, a significant inverse dose-response relationship was observed (P for trend < 0.001). Compared to the lowest quartile (Q1), patients in the highest PWR quartile (Q4) exhibited a substantially reduced hazard of death at 28 days (adjusted HR 0.55, 95% CI 0.43–0.72, p < 0.001). This inverse association remained statistically significant for 90-day and 180-day mortality but was absent at 1 year. The relationship was linear across the range of PWR values for 28-day (P for non-linearity = 0.213), 90-day (P for non-linearity = 0.476), and 180-day mortality (P for non-linearity = 0.377). The results were robust across all predefined subgroups, with no evidence of significant effect modification. Among critically ill patients with atrial fibrillation, a higher platelet-to-white blood cell ratio at ICU admission is inversely and linearly associated with short- and intermediate-term mortality, demonstrating a clear dose-response relationship. As an easily derived biomarker, PWR has potential utility for enhancing risk assessment in this clinical setting.

BMC Cardiovascular Disorders
Jiujiang University (CN), University of Electronic Science and Technology of China (CN), Integrated Chinese Medicine (China) (HK), Gansu Provincial Maternal and Child Health Hospital (CN), Chongqing Dazu District People's Hospital (CN)
Good health and well-being
Openalex Percentile: Top 20%
Inflammatory Biomarkers in Disease Prognosis
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