Total bilirubin as a marker for hemolysis and outcome in patients with severe ARDS treated with veno-venous ECMO

被引:0
作者
Buenger, Victoria [1 ,2 ,3 ]
Menk, Mario [1 ,2 ,3 ,4 ]
Hunsicker, Oliver [1 ,2 ,3 ]
Krannich, Alexander [5 ,6 ]
Balzer, Felix [7 ]
Spies, Claudia D. [1 ,2 ,3 ]
Kuebler, Wolfgang M. [8 ]
Weber-Carstens, Steffen [1 ,2 ,3 ]
Graw, Jan A. [1 ,2 ,3 ,9 ]
机构
[1] Charite, Dept Anesthesiol & Intens Care Med, CCM CVK, Augustenburger Pl 1, D-13353 Berlin, Germany
[2] Humboldt Univ, Freie Univ Berlin, Augustenburger Pl 1, D-13353 Berlin, Germany
[3] Charite Univ Med Berlin, ARDS ECMO Ctr Charite, Berlin, Germany
[4] Tech Univ Dresden, Univ Hosp Carl Gustav Carus, Dept Anesthesiol & Intens Care Med, Dresden, Germany
[5] Charite Univ Med Berlin, ECRC, Berlin, Germany
[6] BioStats GmbH, Nauen, Germany
[7] Charite Univ Med Berlin, Inst Med Informat, Berlin, Germany
[8] Charite Univ Med Berlin, Inst Physiol, Berlin, Germany
[9] Ulm Univ, Univ Klinikum Ulm, Dept Anesthesiol & Intens Care Med, Ulm, Germany
来源
BMC ANESTHESIOLOGY | 2025年 / 25卷 / 01期
关键词
Total bilirubin; Hemolysis; Extracorporeal membrane oxygenation; Acute lung injury; Hyperbilirubinemia; RESPIRATORY-DISTRESS-SYNDROME; CELL-FREE HEMOGLOBIN; MORTALITY; CARE; SEPSIS; RISK;
D O I
10.1186/s12871-025-02988-1
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background Hemolysis is a common complication in critically ill patients with sepsis, acute respiratory distress syndrome (ARDS) or therapy with extracorporeal membrane oxygenation (ECMO). Heme degradation product bilirubin might accumulate in conditions of significant hemolysis. In patients with ARDS and therapy with veno-venous ECMO (vvECMO), the prognostic potential of elevated initial total bilirubin (tBili) was investigated. Methods Retrospective analysis of patients with ARDS and vvECMO-therapy (n = 327) admitted to a tertiary ARDS center. A tBili cut-off value was determined by binary recursive partitioning. Baseline characteristics were compared and relevant variables were included in a multivariate logistic regression model with backward variable selection. Primary endpoint was survival within 28 days analyzed with Kaplan-Meier-curves and cox regression. Secondary endpoints included failure free composites for organ dysfunction, renal replacement therapy (RRT), vasopressor therapy and ECMO within 28 days and were compared using competing risk regression analysis. Results A cut-off value of 3.6mg/dl divided the cohort for ICU mortality (tBili <= 3.6mg/dl: 46% (n = 273) vs. tBili > 3.6mg/dl: 78% (n = 54), p < 0.001). The group with tBili > 3.6mg/dl showed a higher 28-day mortality (HR 3.03 [95%CI 2.07-4.43], p < 0.001) and significantly lower chances of successful recovery from organ dysfunction (subdistribution hazard ratio (SHR) 0.29 [0.13-0.66], p < 0.001), RRT (SHR 0.34 [0.14-0.85], p = 0.02), and ECMO (SHR 0.46 [0.25-0.86], p = 0.015) compared to the group with tBili <= 3.6mg/dl. Recovery from vasopressor therapy did not differ between groups (SHR 0.63 [0.32-1.24], p = 0.18). Conclusion Patients with ARDS, vvECMO-therapy and tBili > 3.6mg/dl had a higher mortality and lower chances for recovery from organ dysfunction, RRT, and ECMO within 28 days. The tBili-cut-off value may be useful to identify patients at risk for unfavorable outcomes.
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页数:9
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