Key result
Higher FIB-4 index linked to ~9% higher 30-day mortality per point in acute HF.
Why the study?
Acute heart failure has high early mortality, but the predictive power of the FIB-4 index for short-term outcomes in developing countries is not well established.
Does the FIB-4 index predict 30-day all-cause mortality in adults hospitalized with acute heart failure?
Cohort (n=413)
No
Does the FIB-4 index predict 30-day all-cause mortality in adults hospitalized with acute heart failure?
Relative Risk: 1.09 (95% CI 1.01–1.17)
p-value: p=0.034
The FIB-4 index, measured at admission, independently predicts 30-day all-cause mortality in patients hospitalized with acute heart failure, suggesting its potential utility for early clinical risk stratification.
FIB-4 may support risk stratification in acute HF; leaves open prospective validation and impact on management.
Acute heart failure (AHF) has high early mortality. The FIB-4 index indicates hepatic dysfunction in AHF, but its predictive power for short-term outcomes in developing countries is not well established. We conducted a prospective cohort study at Can Tho Central General Hospital, Vietnam, from May to December 2024 including adults aged ≥18, hospitalized with AHF and NT-proBNP levels ≥300 pg/mL. Exclusions were for those who died before blood sample collection, transferred, declined consent, or had chronic liver disease, active cancer, or end-stage renal disease. Survivors were followed up via phone for 30 days post-discharge. The primary endpoint was 30-day all-cause mortality. The final analysis included 413 patients (mean age 70, 47.7% male). In-hospital mortality was 5.1% and did not associate to FIB-4. At 30 days post-discharge, 42(17%) of 247 patients with follow-up data died (37.3% loss to follow-up). Non-survivors had higher FIB-4 scores than survivors (3.3 vs. 2.3, p = 0.006). After adjusting for age, sex, comorbidities, LVEF, and NT-proBNP, each one-point increase in FIB-4 raised the 30-day mortality risk by 9% (RR 1.09; 95%CI: 1.01–1.17). A cut-off of 3.1 identified high-risk patients, with a RR of 1.82 (95%CI: 1.03–3.22). FIB-4 demonstrated an AUC of 0.634 (95%CI: 0.535–0.733) which was comparable to NT-proBNP (AUC 0.650; 95%CI: 0.559–0.742). In this exploratory single-center study of patients with AHF, FIB-4 demonstrated an independent association with 30-day mortality, with a threshold of 3.1 identifying high-risk individuals. These findings are hypothesis-generating, and external validation is warranted before FIB-4 can be recommended for risk stratification.
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Truyen et al. (2026) conducted a cohort in Acute heart failure (n=413). FIB-4 index vs. Lower FIB-4 index was evaluated on 30-day all-cause mortality (RR 1.09, 95% CI 1.01-1.17, p=0.034). After multivariable adjustment, each one-point increase in the FIB-4 index was independently associated with a 9% higher risk of 30-day all-cause mortality in acute heart failure patients (RR 1.09).
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