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Published on: November 27, 2019
Prognostic Markers in Pediatric Acute Liver Failure
Andreia Filipa Nogueira1, Catarina Teixeira1, Carla Fernandes1
1Pediatric Intensive Care Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal.
Insights
Lactate levels at admission can predict outcomes in pediatric acute liver failure (PALF), offering a simple yet effective prognostic tool. This finding aids in managing PALF patients and optimizing organ allocation decisions.
Area of Science:
- Pediatric critical care medicine
- Hepatology
- Biomarker research
Background:
- Pediatric acute liver failure (PALF) is a rare but severe condition with high mortality.
- Accurate prognostic markers are crucial for optimizing organ allocation and patient management.
- Existing prognostic scores require validation in diverse pediatric populations.
Purpose of the Study:
- To evaluate the accuracy of various biomarkers and prognostic scores in predicting outcomes for pediatric acute liver failure (PALF).
- To identify reliable predictors of spontaneous recovery versus the need for liver transplantation or death.
Main Methods:
- Retrospective observational study of PALF patients admitted to a pediatric intensive care unit (PICU) over 28 years.
- Patients were categorized into spontaneous recovery (SR) and non-spontaneous recovery (NSR) groups.
- Analysis included lactate, ammonia, INR levels, and prognostic scores (LIU, PRISM, PALF-ds) for predictive accuracy.
Main Results:
- Lactate at admission (AUC 0.72), peak ammonia (AUC 0.72), and peak INR (AUC 0.70) showed acceptable accuracy in predicting non-spontaneous recovery (NSR).
- Lactate at admission was identified as an independent predictor of NSR.
- The LIU (AUC 0.73) and PRISM (AUC 0.71) scores demonstrated acceptable discrimination, while the PALF delta score (PALF-ds) showed lower capacity (AUC 0.63).
Conclusions:
- Lactate levels upon admission are a valuable and easily obtainable biomarker for predicting outcomes in pediatric acute liver failure (PALF).
- The prognostic performance of admission lactate is comparable to more complex scores like LIU and PRISM.
- The dynamic PALF-ds score demonstrated lower predictive value in this cohort than anticipated.
Introduction:
Acute liver failure (ALF), although rare in children, is a complex progressive pathology, with multisystem involvement and high mortality. Isolated variables or those included in prognostic scores have been studied, to optimize organ allocation. However, its validation is challenging. This study aimed to assess the accuracy of several biomarkers and scores as predictors of prognosis in pediatric ALF (PALF).
Methods:
An observational study with retrospective data collection, including all cases of ALF, was defined according to the criteria of the Pediatric Acute Liver Failure Study Group, admitted to a pediatric intensive care unit (PICU) for 28 years. Two groups were defined: spontaneous recovery (SR) and non-SR (NSR) - submitted to liver transplantation (LT) or death at PICU discharge.
Results:
Fifty-nine patients were included, with a median age of 24 months, and 54% were female. The most frequent etiologies were metabolic (25.4%) and infectious (18.6%); 32.2% were undetermined. SR occurred in 21 patients (35.6%). In NSR group (N = 38, 64.4%), 25 required LT (42.4%) and 19 died (32.2%), 6 (15.7%) of whom after LT. The accuracy to predict NSR was acceptable for lactate at admission (AUC 0.72; 95% CI: 0.57-0.86; p = 0.006), ammonia peak (AUC 0.72; 95% CI: 0.58-0.86; p = 0.006), and INR peak (AUC 0.70; 95% CI: 0.56-0.85; p = 0.01). The cut-off value for lactate at admission was 1.95 mmol/L (sensitivity 78.4% and specificity 61.9%), ammonia peak was 64 μmol/L (sensitivity 100% and specificity 38.1%), and INR peak was 4.8 (sensitivity 61.1% and specificity 76.2%). Lactate on admission was shown to be an independent predictor of NSR on logistic regression model. Two prognostic scores had acceptable discrimination for NSR, LIU (AUC 0.73; 95% CI: 0.59-0.87; p = 0.004) and PRISM (AUC 0.71; 95% CI: 0.56-0.86; p = 0.03). In our study, the PALF delta score (PALF-ds) had lower discrimination capacity (AUC 0.63; 95% CI: 0.47-0.78; p = 0.11).
Conclusions:
The lactate at admission, an easily obtained parameter, had a similar capacity than the more complex scores, LIU and PRISM, to predict NSR. The prognostic value in our population of the promising dynamic score, PALF-ds, was lower than expected.
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