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Clinical Course among Cases of Acute Liver Failure of Indeterminate Diagnosis

Authors :
Ruosha Li
Steven H. Belle
Simon Horslen
Ling-wan Chen
Song Zhang
Robert H. Squires
Kathryn Bukauskas
Michael R. Narkewicz
Michelle Hite
Kathleen M. Loomes
Elizabeth B. Rand
David Piccoli
Deborah Kawchak
Rene Romero
Saul Karpen
Liezl de la Cruz-Tracy
Vicky Ng
Kelsey Hunt
Girish C. Subbarao
Ann Klipsch
Estella M. Alonso
Lisa Sorenson
Susan Kelly
Dhey Delute
Katie Neighbors
Philip J. Rosenthal
Shannon Fleck
Mike A. Leonis
John Bucuvalas
Tracie Horning
Norberto Rodriguez Baez
Shirley Montanye
Margaret Cowie
Karen Murray
Melissa Young
Heather Vendettuoli
David A. Rudnick
Ross W. Shepherd
Kathy Harris
Saul J. Karpen
Alejandro De La Torre
Dominic Dell Olio
Deirdre Kelly
Carla Lloyd
Steven J. Lobritto
Sumerah Bakhsh
Maureen Jonas
Scott A. Elifoson
Roshan Raza
Kathleen B. Schwarz
Wikrom W. Karnsakul
Mary Kay Alford
Anil Dhawan
Emer Fitzpatrick
Nanda N. Kerkar
Brandy Haydel
Sreevidya Narayanappa
M. James Lopez
Victoria Shieck
Source :
The Journal of pediatrics. 171
Publication Year :
2015

Abstract

To investigate the heterogeneity in clinical course among those with pediatric acute liver failure (PALF) of indeterminate disease etiology.We studied participants enrolled in the PALF registry study with indeterminate final diagnosis. Growth mixture modeling was used to analyze participants' international normalized ratio, total bilirubin, and hepatic encephalopathy trajectories in the first 7 days following enrollment. Participants with at least 3 values for 1 or more of the measurements were included. We examined the association between the resulting latent subgroup classification with participants' characteristics and disease outcomes. Data from participants with PALF of specified etiologies were used to investigate the potential diagnostic value of the latent subgroups.In this sample of 380 participants with indeterminate final diagnosis, 115 (30%) experienced mild and quickly improving disease trajectories and another 48 (13%) started with severe disease but improved by day 7. The majority of participants (216, 57%) had disease trajectories that worsened over time. The identified patterns of disease trajectories are predictive of outcome (P.001). The trajectory patterns are associated with the underlying disease etiology (P.001) for the 488 participants with PALF of specified etiologies.The clinical courses of participants with PALF of indeterminate disease etiology exhibit distinct trajectory patterns, which have important prognostic and potentially diagnostic value.

Details

ISSN :
10976833
Volume :
171
Database :
OpenAIRE
Journal :
The Journal of pediatrics
Accession number :
edsair.doi.dedup.....42e3a8b46b1575d9cbd240a6df8e1c0e