Evidence map›Paper›PMID 42895544›Full record

ArticleClinical research in cardiology : official journal of the German Cardiac Society2026

Cardio-hepatic injury phenotypes and short-term outcomes in acute decompensated heart failure.

Gil Marcus, Shiri L Maymon, Ido Minha, Eran Kalmanovich, Gil Moravsky, Shmuel Fuchs, Sa'ar Minha, Avishay Grupper

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Article in Clinical research in cardiology : official journal of the German Cardiac Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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8 authors.

Gil MarcusDepartment of Cardiology, Shamir Medical Center, Be'er Ya'akov, Israel.
Shiri L MaymonDepartment of Otolaryngology, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.
Ido MinhaThe Rachel and Selim Benin School of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem, Israel.
Eran KalmanovichDepartment of Cardiology, Shamir Medical Center, Be'er Ya'akov, Israel.
Gil MoravskyDepartment of Cardiology, Shamir Medical Center, Be'er Ya'akov, Israel.
Shmuel FuchsDepartment of Cardiology, Shamir Medical Center, Be'er Ya'akov, Israel.
Sa'ar Minha *Department of Cardiology, Shamir Medical Center, Be'er Ya'akov, Israel.
Avishay Grupper *Department of Cardiology, Shamir Medical Center, Be'er Ya'akov, Israel. aagrupper@gmail.com.

Funding

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6 · The paper itself

Abstract

backgroundAbnormal liver biochemistry is common in acute decompensated heart failure (ADHF), yet most studies evaluate individual markers rather than clinically meaningful patterns of hepatic involvement. We examined whether cardiohepatic injury phenotypes derived from routine liver tests identify distinct short-term prognostic profiles in patients hospitalized with ADHF.

methodsIn this retrospective cohort study, we included consecutive adults hospitalized with ADHF between December 2006 and 2017. Using peak in-hospital values of aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, and total bilirubin, patients were classified into four phenotypes: no hepatic injury, hepatocellular injury, cholestatic injury, or combined injury. Associations with in-hospital mortality were evaluated using multivariable logistic regression. Post-discharge outcomes (30-day mortality, readmission, and their composite) were analyzed using Cox and Fine-Gray models.

resultsAmong 8332 ADHF admissions, 6792 (81.5%) had sufficient data for phenotype classification: 58.1% had no hepatic injury, 22.1% hepatocellular injury, 13.1% cholestatic injury, and 6.7% combined injury. In-hospital mortality differed markedly across phenotypes (3.5%, 16.3%, 9.0%, and 24.3%, respectively; p < 0.001). After adjustment, all injury phenotypes independently predicted in-hospital death compared with no injury. Among 6128 patients included in adjusted post-discharge analyses, hepatocellular and combined injury were independently associated with higher 30-day mortality and the composite outcome, whereas isolated cholestatic injury was not. Hepatocellular and combined injury independently predicted 30-day readmission.

conclusionsRoutine liver test patterns identify clinically meaningful cardiohepatic phenotypes in ADHF. While all hepatic injury phenotypes are associated with increased in-hospital mortality, only phenotypes with hepatocellular involvement predict adverse early post-discharge outcomes. Pattern-based interpretation of liver tests may improve early risk stratification in patients hospitalized with ADHF.

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Acute decompensated heart failureCardiohepaticHepatocellularPrognosis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.