Red cell distribution in critically ill patients with chronic obstructive pulmonary disease

被引:14
|
作者
Lan, W. [1 ]
Liu, E. [2 ]
Sun, D. [1 ]
Li, W. [1 ]
Zhu, J. [3 ]
Zhou, J. [4 ]
Jin, M. [5 ]
Jiang, W. [6 ]
机构
[1] Lishui Municipal Cent Hosp, Dept Resp & Crit Care Med, Lishui 323000, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Dept Infect Dis, Zhejiang Prov Key Lab Accurate Diag & Treatment Ch, Affiliated Hosp 1, Wenzhou 325000, Zhejiang, Peoples R China
[3] Zhejiang Univ, Lishui Hosp, Dept Cardiol, Sch Med, Lishui 323000, Zhejiang, Peoples R China
[4] Zhejiang Univ, Lishui Hosp, Dept Pathol, Sch Med, Lishui 323000, Zhejiang, Peoples R China
[5] Yunhe Peoples Hosp, Dept Internal Med, Yunhe 323600, Zhejiang, Peoples R China
[6] Lishui Municipal Cent Hosp, Dept Gastroenterol, Lishui 323000, Zhejiang, Peoples R China
来源
PULMONOLOGY | 2024年 / 30卷 / 01期
关键词
Chronic obstructive pulmonary disease; Red blood cell distri-bution width; Mortality; Multiparameter intel-ligent monitoring in intensive care III; DISTRIBUTION WIDTH; MYOCARDIAL-INFARCTION; INDEPENDENT PREDICTOR; CLINICAL-OUTCOMES; MORTALITY; ELEVATION; RISK; EVENTS; SEPSIS; GENDER;
D O I
10.1016/j.pulmoe.2022.04.001
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Red blood cell distribution width (RDW) is associated with increased mortality risk in patients with chronic obstructive pulmonary disease (COPD). However, limited data are available for critically ill patients with COPD. Methods: Data from the Medical Information Mart for Intensive Care III V1.4 database were analyzed in this retrospective cohort research. The International Classification of Diseases codes were used to identify critically ill patients with COPD. The first value of RDW was extracted within the first 24 h after intensive care unit admission. The endpoint was 28-day all-cause mortality. Multivariable logistic regression analysis was performed to examine the relationship between RDW and 28-day mortality. Age, sex, ethnicity, anemia status, comorbidities, clinical therapy, and disease severity score were considered for subgroup analysis. Results: A total of 2,344 patients were included with mean (standard deviation) age of 72.3 (11.3) years, in which 1,739 (53.6%) patients were men. The increase in RDW was correlated with an increased risk of 28-day mortality in the multivariate logistic regression model (odds ratio [OR] 1.15; 95% confidence interval [CI] 1.09-1.21). In comparison with the low-RDW group, the middle and high-RDW groups tended to have higher risks of 28-day all-cause mortality (OR [95% CI] 1.03 [0.78-1.34]; OR [95% CI] 1.70 [1.29-2.22]; P trend < 0.0001). Subgroup analyses show no evidence of effect modifications on the correlation of RDW and 28-day all-cause mortality. Conclusion: An increase in RDW was associated with an increased risk of 28-day all-cause mortality in critically ill patients with COPD. Further studies are required to investigate this association.
引用
收藏
页码:34 / 42
页数:9
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