Authors
Kadir Bıyıklı, Tezel Kovancı, Barkın Kültürsay, Hasan Karaot, Ömer Doğukan Ertan, Cemalettin Yılmaz, Doğancan Çeneli, Neşri Danışman, Mustafa Ferhat Keten
Published in
Acta cardiologica. Pages 1-11. Jul 08, 2026. Epub Jul 08, 2026.
Abstract
Infective endocarditis (IE), involving both native and prosthetic valves, remains a severe multisystem disease associated with high early and long-term mortality despite advances in antimicrobial therapy and cardiac surgery. Early risk stratification is important for clinical decision-making; however, existing prognostic models are often complex and may include subjective variables. The albumin-bilirubin (ALBI) score, derived from routinely available laboratory parameters, reflects hepatic dysfunction and systemic inflammatory burden and may represent a prognostic tool in IE.
This retrospective cohort study included 130 patients with native or prosthetic valve IE evaluated at a tertiary cardiovascular referral centre. The ALBI score was calculated at admission. The primary endpoint was 30-day all-cause mortality, while long-term mortality was assessed as a secondary outcome. Associations between ALBI score and outcomes were evaluated using multivariable logistic regression, generalised additive models, and Cox proportional hazards regression.
Higher ALBI scores were associated with increased inflammatory burden and impaired renal function. The admission ALBI score independently predicted 30-day mortality (odds ratio per 1-SD increase: 2.22, p = 0.014). A non-linear relationship between ALBI score and early mortality was observed (p = 0.0002). During follow-up, ALBI remained independently associated with mortality (hazard ratio per 1-SD increase: 1.92, p < 0.001). Incremental analyses demonstrated improved discrimination and risk reclassification after the addition of ALBI to a baseline clinical model.
The admission ALBI score may serve as a simple and objective marker for risk stratification in infective endocarditis and may provide incremental prognostic information beyond established clinical risk domains. These findings require external validation in larger multicentre cohorts.
PMID:
42418519
Bibliographic data and abstract were imported from PubMed on 09 Jul 2026.
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