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Improved mortality prediction for pediatric acute liver failure using dynamic prediction strategy.
Li, Ruosha; Wang, Jingyan; Zhang, Cuihong; Squires, James E; Belle, Steven H; Ning, Jing; Cai, Jianwen; Squires, Robert H.
Afiliação
  • Li R; Department of Biostatistics and Data Sciences, The University of Texas Health Science Center at Houston, Houston, Texas, USA.
  • Wang J; Department of Biostatistics and Data Sciences, The University of Texas Health Science Center at Houston, Houston, Texas, USA.
  • Zhang C; Department of Biostatistics and Data Sciences, The University of Texas Health Science Center at Houston, Houston, Texas, USA.
  • Squires JE; Division of Pediatric Gastroenterology and Hepatology, Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
  • Belle SH; Department of Epidemiology, University of Pittsburgh School of Public Health, Pittsburgh, Pennsylvania, USA.
  • Ning J; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Cai J; Department of Biostatistics, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Squires RH; Division of Pediatric Gastroenterology and Hepatology, Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
J Pediatr Gastroenterol Nutr ; 78(2): 320-327, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38374548
ABSTRACT

OBJECTIVES:

To 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.

METHODS:

Data 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.

RESULTS:

We 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.

CONCLUSIONS:

Serial 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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encefalopatia Hepática / Falência Hepática Aguda Limite: Child / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encefalopatia Hepática / Falência Hepática Aguda Limite: Child / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article