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Incidence of hypoxic hepatitis in patients with cardiogenic shock and association with mortality

心源性休克 医学 入射(几何) 内科学 心脏病学 心肌梗塞 物理 光学
作者
Benedikt N. Beer,Lisa Besch,Jessica Weimann,Kishore Surendra,Kevin Roedl,Jörn Grensemann,Jonas Sundermeyer,Angela Dettling,Stefan Kluge,Paulus Kirchhof,Stefan Blankenberg,Clemens Scherer,Benedikt Schrage
出处
期刊:European heart journal. Acute cardiovascular care [Oxford University Press]
卷期号:12 (10): 663-670 被引量:11
标识
DOI:10.1093/ehjacc/zuad076
摘要

Abstract Aims Shock of any cause leads to end-organ damage due to ischaemia, especially in perfusion-sensitive organs such as the liver. In septic shock, hypoxic hepatitis (S-HH) is defined as the 20-fold increase of the upper normal limit of aspartate aminotransferase (ASAT) and alanine aminotransferase (ALAT) and is associated with a mortality of up to 60%. However, as pathophysiology, dynamics, and treatment differ between septic and cardiogenic shock (CS), the S-HH definition may not be suitable for CS. Therefore, we aim to evaluate if the S-HH definition is applicable in CS patients. Methods and results This analysis was based on a registry of all-comer CS patients treated between 2009 and 2019 at a tertiary care centre with exclusion of minors and patients without all necessary ASAT and ALAT values. N = 698. During in-hospital follow-up, 386 (55.3%) patients died. The S-HH was not significantly associated with in-hospital mortality in CS patients. To define HH among patients with CS (C-HH), optimal cut-off values were found to be ≥1.34-fold increase for ASAT and ≥1.51-fold increase for ALAT in serial measurements. The incidence of C-HH was 254/698 patients (36%) and C-HH showed a strong association with in-hospital mortality (odds ratio 2.36, 95% confidence interval: 1.61, 3.49). Conclusion The C-HH is a frequent and relevant comorbidity in patients with CS, although its definition varies from the established definition of HH in patients with septic shock. As C-HH contributed to excess mortality risk, these findings emphasize the need for further investigation of therapies reducing the occurrence of C-HH and also improving the associated outcome.
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