Jing Rui, Yu Baolong, Xu Chenchen, Zhao Ying, Cao Hongmei, He Wenhui, Wang Haili
Department of Pediatrics, Weifang People's Hospital, Weifang, Shandong, China.
Department of Pediatrics, Gaomi Maternal and Child Health Hospital, Weifang, Shandong, China.
Front Pediatr. 2024 Mar 6;12:1352195. doi: 10.3389/fped.2024.1352195. eCollection 2024.
This study aimed to assess the association between Red Cell Distribution Width-to-Albumin Ratio (RAR) and the clinical outcomes in Pediatric Intensive Care Unit (PICU) patients.
This is a retrospective cohort study.
We conducted a retrospective cohort study based on the Pediatric Intensive Care database. The primary outcome was the 28-day mortality rate. Secondary outcomes included the 90-day mortality rate, in-hospital mortality rate, and length of hospital stay. We explored the relationship between RAR and the prognosis of patients in the PICU using multivariate regression and subgroup analysis.
A total of 7,075 participants were included in this study. The mean age of the participants was 3.4 ± 3.8 years. Kaplan-Meier survival curves demonstrated that patients with a higher RAR had a higher mortality rate. After adjusting for potential confounding factors, we found that for each unit increase in RAR, the 28-day mortality rate increased by 6% (HR = 1.06, 95% CI: 1.01-1.11, = 0.015). The high-RAR group (RAR ≥ 4.0) had a significantly increased 28-day mortality rate compared to the low-RAR group (RAR ≤ 3.36) (HR = 1.7, 95% CI: 1.23-2.37, < 0.001). Similar results were observed for the 90-day and in-hospital mortality rate. No significant interactions were observed in the subgroup analysis.
Our study suggests a significant association between RAR and adverse outcomes in PICU patients. A higher RAR is associated with higher 28-day, 90-day, and in-hospital mortality rates.
本研究旨在评估红细胞分布宽度与白蛋白比值(RAR)与儿科重症监护病房(PICU)患者临床结局之间的关联。
这是一项回顾性队列研究。
我们基于儿科重症监护数据库进行了一项回顾性队列研究。主要结局是28天死亡率。次要结局包括90天死亡率、住院死亡率和住院时间。我们使用多变量回归和亚组分析探讨了RAR与PICU患者预后之间的关系。
本研究共纳入7075名参与者。参与者的平均年龄为3.4±3.8岁。Kaplan-Meier生存曲线表明,RAR较高的患者死亡率较高。在调整潜在混杂因素后,我们发现RAR每增加一个单位,28天死亡率增加6%(HR=1.06,95%CI:1.01-1.11,P=0.015)。与低RAR组(RAR≤3.36)相比,高RAR组(RAR≥4.0)的28天死亡率显著增加(HR=1.7,95%CI:1.23-2.37,P<0.001)。90天和住院死亡率也观察到类似结果。亚组分析未观察到显著的相互作用。
我们的研究表明RAR与PICU患者的不良结局之间存在显著关联。较高的RAR与较高的28天、90天和住院死亡率相关。