Lactate to albumin ratio and 30-day mortality in ICU patients with influenza: a single-center retrospective cohort.

IF 4 3区 医学 Q2 VIROLOGY
Weichang Luan, Hongyi Chen, Chunhua Liu, Jingjing Liu, Yanan Qin
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引用次数: 0

Abstract

Background: The influenza virus exerts a substantial impact on morbidity, mortality, and overall disease burden among the population, particularly among intensive care unit (ICU) patients. Although multiple biomarkers have been studied for mortality risk stratification in this population, the prognostic relationship of the lactate-to-albumin ratio (LAR) remains incompletely defined in critically ill patients with influenza. This study aims to investigate whether baseline ICU admission LAR levels are independently associated with mortality in critically ill patients with influenza cases and assess its incremental predictive value beyond established scoring systems.

Methods: Utilizing data from the Medical Information Mart for Intensive Care IV database (MIMIC-IV, version 3.1), this retrospective cohort study enrolled adult patients diagnosed with influenza who required ICU admission. LAR was calculated based on lactate and albumin levels measured within 24 h of ICU admission. The primary outcome was 30-day mortality, with secondary outcomes including in-hospital, 60-day, 90-day, and 1-year mortality. The association between LAR and mortality risk was assessed using univariate and multivariate Cox proportional hazards regression models, with robustness evaluated through subgroup analyses and sensitivity analyses. Survival differences across LAR levels were compared via Kaplan-Meier curves and log-rank tests. Discriminative performance was assessed using receiver operating characteristic (ROC) curves and the C-index.

Results: A total of 142 critically ill patients with influenza were included, with an overall 30-day mortality of 22.53%. Univariate Cox regression analysis demonstrated that a higher LAR was associated with an increased risk of 30-day mortality in ICU patients with influenza (HR 2.43, 95% CI 1.80-3.29; P < 0.001). After adjusting for confounding factors, multivariable Cox proportional hazards analysis confirmed this association, showing a similarly elevated risk (HR 2.93, 95% CI 1.95-4.39; P < 0.001). Kaplan-Meier analysis indicated a substantially lower 30-day survival for the high-LAR group (Log-rank P < 0.0001). The AUC of LAR for predicting mortality was 0.783, comparable to APS III (AUC 0.785, 95% CI 0.696-0.874; P = 0.140), SAPS II (AUC 0.717, 95% CI 0.617-0.817; P = 0.157), OASIS (AUC 0.643, 95% CI 0.531-0.756; P = 0.168), and SOFA (AUC 0.687, 95% CI 0.580-0.794; P = 0.160). Notably, the AUC for albumin alone was 0.791, compared with 0.783 for LAR.

Conclusion: This study found that early LAR upon ICU admission is independently associated with the 30-day mortality rate in critically ill patients with influenza. Its predictive ability seems to be comparable to established clinical scoring systems. However, LAR did not outperform albumin alone, and its added prognostic value beyond albumin remains uncertain, and further validation in prospective studies is still needed.

ICU流感患者乳酸白蛋白比和30天死亡率:单中心回顾性队列研究
背景:流感病毒对人群,特别是重症监护病房(ICU)患者的发病率、死亡率和总体疾病负担有重大影响。尽管在这一人群中已经研究了多种生物标志物的死亡风险分层,但乳酸-白蛋白比(LAR)在流感危重患者中的预后关系仍未完全确定。本研究旨在探讨ICU入院时基线LAR水平是否与流感重症患者的死亡率独立相关,并评估其在现有评分系统之外的增量预测价值。方法:利用重症监护医学信息市场IV数据库(MIMIC-IV,版本3.1)的数据,本回顾性队列研究纳入诊断为流感并需要ICU住院的成年患者。LAR是根据ICU入院24小时内乳酸和白蛋白水平计算的。主要结局是30天死亡率,次要结局包括住院、60天、90天和1年死亡率。使用单变量和多变量Cox比例风险回归模型评估LAR与死亡风险之间的相关性,并通过亚组分析和敏感性分析评估稳健性。通过Kaplan-Meier曲线和log-rank检验比较不同LAR水平的生存差异。采用受试者工作特征(ROC)曲线和c -指数评估鉴别效果。结果:共纳入142例流感重症患者,总30天死亡率为22.53%。单因素Cox回归分析显示,较高的LAR与ICU流感患者30天死亡率增加相关(HR 2.43, 95% CI 1.80-3.29; P)结论:本研究发现,ICU入院时早期LAR与危重流感患者30天死亡率独立相关。它的预测能力似乎可以与现有的临床评分系统相媲美。然而,LAR并没有优于单独的白蛋白,其在白蛋白之外的附加预后价值仍不确定,仍需要在前瞻性研究中进一步验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Virology Journal
Virology Journal 医学-病毒学
CiteScore
7.40
自引率
2.10%
发文量
186
审稿时长
1 months
期刊介绍: Virology Journal is an open access, peer reviewed journal that considers articles on all aspects of virology, including research on the viruses of animals, plants and microbes. The journal welcomes basic research as well as pre-clinical and clinical studies of novel diagnostic tools, vaccines and anti-viral therapies. The Editorial policy of Virology Journal is to publish all research which is assessed by peer reviewers to be a coherent and sound addition to the scientific literature, and puts less emphasis on interest levels or perceived impact.
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