Improved mortality prediction for pediatric acute liver failure using dynamic prediction strategy

Author:

Li Ruosha1,Wang Jingyan1,Zhang Cuihong1,Squires James E.2,Belle Steven H.3,Ning Jing4,Cai Jianwen5,Squires Robert H.2

Affiliation:

1. Department of Biostatistics and Data Sciences The University of Texas Health Science Center at Houston Houston Texas USA

2. Division of Pediatric Gastroenterology and Hepatology, Department of Pediatrics University of Pittsburgh School of Medicine Pittsburgh Pennsylvania USA

3. Department of Epidemiology University of Pittsburgh School of Public Health Pittsburgh Pennsylvania USA

4. Department of Biostatistics The University of Texas MD Anderson Cancer Center Houston Texas USA

5. Department of Biostatistics The University of North Carolina at Chapel Hill Chapel Hill North Carolina USA

Abstract

AbstractObjectivesTo develop and validate a prediction tool for pediatric acute liver failure (PALF) mortality risks that captures the rapid and heterogeneous clinical course for accurate and updated prediction.MethodsData included 1144 participants with PALF enrolled during three phases of the PALF registry study over 15 years. Using joint modeling, we built a dynamic prediction tool for mortality by combining longitudinal trajectories of multiple laboratory and clinical variables. The predictive performance for 7‐day and 21‐day mortality was assessed using the area under curve (AUC) through cross‐validation and split‐by‐time validation.ResultsWe constructed a prognostic joint model that combines the temporal trajectories of international normalized ratio, total bilirubin, hepatic encephalopathy, platelet count, and serum creatinine. Dynamic prediction using updated information improved predictive performance over static prediction using the information at enrollment (Day 0) only. In cross‐validation, AUC increased from 0.784 to 0.887 when measurements obtained between Days 1 and 2 were incorporated. AUC remained similar when we used the earlier subset of the sample for training and the later subset for testing.ConclusionsSerial measurements of five variables in the first few days of PALF capture the dynamic clinical course of the disease and improve risk prediction for mortality. Continuous disease monitoring and updating risk prognosis are beneficial for timely and judicious medical decisions.

Publisher

Wiley

Subject

Gastroenterology,Pediatrics, Perinatology and Child Health

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