Key result
Cardiogenic shock in acute heart failure is linked to ~122% higher 1-year mortality versus ADHF.
Why the study?
Differences in clinical characteristics and long-term outcomes among the four 2021 ESC-defined acute heart failure phenotypes in the emergency department remain unclear.
Do different ESC-defined acute heart failure phenotypes (ADHF, APO, IRVF, CS) predict 1-year all-cause and cardiovascular mortality in patients presenting to the emergency department?
Observational (n=2,960)
No
Do different ESC-defined acute heart failure phenotypes (ADHF, APO, IRVF, CS) predict 1-year all-cause and cardiovascular mortality in patients presenting to the emergency department?
In patients presenting to the emergency department with acute heart failure, the ESC-defined phenotypes of isolated right ventricular failure and cardiogenic shock are independently associated with significantly higher 1-year mortality compared to acute decompensated heart failure.
Answers are grounded in this paper and cite their sources.
CS phenotype flags high 1-year mortality in ED acute HF; supports ESC phenotypes for prognostication but leaves targeted interventions open.
The 2021 European Society of Cardiology (ESC) guidelines classify acute heart failure (AHF) into four phenotypes: acute decompensated heart failure (ADHF), acute pulmonary oedema (APO), isolated right ventricular failure (IRVF), and cardiogenic shock (CS). However, differences in clinical characteristics and long-term outcomes among these phenotypes in the emergency department (ED) remain unclear. This study aimed to evaluate their characteristics and prognostic implications in the ED setting. In this prospective–retrospective observational real-world study, adults presenting with AHF in the ED were consecutively enrolled and categorized according to ESC-defined phenotypes. The study endpoints were 1-year all-cause and cardiovascular mortality. Associations between phenotypes and mortality were assessed using Cox regression models with progressive adjustment. A total of 2,960 patients were included. Clinical characteristics and treatment patterns differed substantially across phenotypes. The 1-year all-cause mortality rates were 10.3% in ADHF, 11.0% in APO, 24.5% in IRVF, and 58.7% in CS ( P < 0.001). In multivariable Cox analyses adjusting for clinical variables and treatments, IRVF remained independently associated with increased risks of all-cause mortality (HR 1.92, 95% CI 1.02–3.63; P = 0.044) and cardiovascular mortality (HR 2.22, 95% CI 1.10–4.48; P = 0.027). CS was also independently associated with higher risks of all-cause mortality (HR 2.22, 95% CI 1.34–3.67; P = 0.002) and cardiovascular mortality (HR 2.71, 95% CI 1.57–4.66; P < 0.001). In this ED-based AHF cohort, IRVF and CS were independently associated with worse 1-year outcomes, supporting phenotype-based risk stratification in the ED.
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Liang et al. (2026) conducted an observational in Acute heart failure (n=2,960). Cardiogenic shock (CS) phenotype vs. Acute decompensated heart failure (ADHF) phenotype was evaluated on 1-year all-cause mortality (HR 2.22, 95% CI 1.34-3.67, p=0.002). In adults presenting to the emergency department with acute heart failure, the cardiogenic shock phenotype was independently associated with a higher risk of 1-year all-cause mortality (HR 2.22) compared to acute decompensated heart failure.
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