Wu Yu-Cheng, Chen Hsin-Hua, Chao Wen-Cheng
Department of Critical Care Medicine, Taichung Veterans General Hospital, Taichung City, Taiwan.
Doctoral Program in Translational Medicine, National Chung Hsing University, Taichung City, Taiwan.
J Intensive Care. 2024 Sep 18;12(1):34. doi: 10.1186/s40560-024-00747-x.
Sepsis is the leading cause of death worldwide, and a number of biomarkers have been developed for early mortality risk stratification. Red blood cell distribution width (RDW) is a routinely available hematological data and has been found to be associated with mortality in a number of diseases; therefore, we aim to address the association between RDW and mortality in critically ill patients with sepsis.
We analyzed data of critically ill adult patients with sepsis on the TriNetX platform, excluding those with hematologic malignancies, thalassemia, and iron deficiency anemia. Propensity score-matching (PSM) (1:1) was used to mitigate confounding effects, and hazard ratio (HR) with 95% confidence (CI) was calculated to determine the association between RDW and 30-day mortality. We further conducted sensitivity analyses through using distinct cut-points of RDW and severities of sepsis.
A total of 256,387 critically ill septic patients were included in the analysis, and 40.0% of them had RDW equal to or higher than 16%. After PSM, we found that high RDW was associated with an increased 30-day mortality rate (HR: 1.887, 95% CI 1.847-1.928). The associations were consistent using distinct cut-points of RDW, with the strength of association using cut-points of 12%, 14%, 16%, 18% and 20% were 2.098, 2.204, 1.887, 1.809 and 1.932, respectively. Furthermore, we found consistent associations among critically ill septic patients with distinct severities, with the association among those with shock, receiving mechanical ventilation, bacteremia and requirement of hemodialysis being 1.731, 1.735, 2.380 and 1.979, respectively.
We found that RDW was associated with 30-day mortality in critically ill septic patients, underscoring the potential as a prognostic marker in sepsis. More studies are needed to explore the underlying mechanisms.
脓毒症是全球范围内主要的死亡原因,已经开发了多种生物标志物用于早期死亡风险分层。红细胞分布宽度(RDW)是一项常规可得的血液学数据,并且已发现在多种疾病中与死亡率相关;因此,我们旨在探讨RDW与重症脓毒症患者死亡率之间的关联。
我们分析了TriNetX平台上成年重症脓毒症患者的数据,排除了患有血液系统恶性肿瘤、地中海贫血和缺铁性贫血的患者。采用倾向得分匹配(PSM)(1:1)来减轻混杂效应,并计算95%置信区间(CI)的风险比(HR)以确定RDW与30天死亡率之间的关联。我们还通过使用不同的RDW切点和脓毒症严重程度进行了敏感性分析。
共有256,387例重症脓毒症患者纳入分析,其中40.0%的患者RDW等于或高于16%。PSM后,我们发现高RDW与30天死亡率增加相关(HR:1.887,95%CI 1.847 - 1.928)。使用不同的RDW切点时,这种关联是一致的,使用12%、14%、16%、18%和20%切点时的关联强度分别为2.098、2.204、1.887、1.809和1.932。此外,我们发现在不同严重程度的重症脓毒症患者中存在一致的关联,休克、接受机械通气、菌血症和需要血液透析患者中的关联分别为1.731、1.735、2.380和1.979。
我们发现RDW与重症脓毒症患者的30天死亡率相关,这突出了其作为脓毒症预后标志物的潜力。需要更多研究来探索其潜在机制。