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Published on: November 27, 2019
Pediatric acute liver failure: An experience of a pediatric intensive care unit from resource limited settings
Puja Amatya1, Sudeep Kumar Kapalavai1, Akash Deep2
1Department of Pediatric Critical Care, Kanchi Kamakoti CHILDS Trust Hospital, Chennai, India.
Insights
Infections are the most common cause of pediatric acute liver failure, but most children recover with medical management. Peak alanine transaminase and inotrope use predict poor outcomes, guiding potential liver transplantation decisions.
Area of Science:
- Hepatology
- Pediatric Critical Care
- Transplantation Medicine
Background:
- Pediatric acute liver failure (PALF) is a rare, severe condition with liver transplantation as a primary treatment for non-recoverable cases.
- Advancements in medical care have led to increased spontaneous liver regeneration, potentially obviating the need for transplantation in some children.
- Understanding etiologies, outcomes, and prognostic factors is crucial for managing PALF and evaluating transplantation criteria.
Purpose of the Study:
- To identify the causes, outcomes, and prognostic factors of acute liver failure in children.
- To assess the validity of existing liver transplantation criteria in predicting outcomes for pediatric acute liver failure.
- To analyze the rate of spontaneous liver regeneration in pediatric acute liver failure cases.
Main Methods:
- A retrospective study was conducted in a tertiary pediatric critical care unit in South India from January 2014 to December 2019.
- The study enrolled 125 children aged 1 month to 18 years diagnosed with acute liver failure.
- Data collected included etiologies, clinical scores, treatment interventions, and patient outcomes.
Main Results:
- Infections (32%) were the most common cause of PALF, with Dengue being the most frequent infection (55%).
- Spontaneous regeneration occurred in 63.2% of patients, notably higher in paracetamol-induced (92.3%) versus non-paracetamol-induced (55.5%) cases.
- Only two patients underwent liver transplantation; 35% of patients died. Peak alanine transaminase and inotrope use were significant predictors of outcome. The INR > 4 criteria showed higher sensitivity than King's College Hospital criteria for predicting transplantation need.
Conclusions:
- Infections are a primary cause of PALF, yet most children experience spontaneous liver regeneration with medical management.
- Inotropes, advanced hepatic encephalopathy, and peak alanine transaminase levels are key predictors of poor outcomes in pediatric acute liver failure.
- Developing improved prognostic predictors for PALF is essential, particularly in resource-limited settings, to guide timely liver transplantation decisions.
Introduction:
Pediatric acute liver failure is a rare and serious disease. Though liver transplantation is considered as the established treatment option for patients who are unlikely to recover with medical management, however, with the advancement of medical care there has been an increase in spontaneous regeneration of liver, obviating the need for liver transplantation. We identified the etiologies, outcome and prognostic factors of acute liver failure and the validity of the existing liver transplantation criteria to predict the outcome of pediatric acute liver failure.
Materials And Methods:
This was a retrospective study done from January 2014 to December 2019 in a tertiary pediatric critical care unit in South India. All children aged between 1 month to 18 years admitted with acute liver failure were enrolled.
Results:
Of 125 children with acute liver failure, the main etiologies were infections (32%), indeterminate (23%), paracetamol toxicity (21%), metabolic (13%) and others (11%). Dengue was the most common infection (55%). The median pediatric logistic organ dysfunction score at admission was 12 (4-27). Of 125 patients, 63.2% (n = 79) had spontaneous regeneration which was higher in paracetamol induced (92.3%) compared to non-paracetamol induced acute liver failure (55.5%). Only two patients underwent liver transplantation and 35% died. Peak alanine transaminase and use of inotropes significantly predicted the outcome of disease. Of 38 children meeting King's College Hospital criteria for liver transplantation, 57.9% had spontaneous regeneration and 36.8% died. Of 74 children meeting INR > 4 criteria, 54% (n = 40) had spontaneous regeneration and 43.2% died. INR >4 criteria was more sensitive than King's College Hospital criteria for predicting the need for liver transplantation.
Conclusion:
Pediatric acute liver failure is caused by varied etiologies and infections were the commonest cause. Despite having a seriously ill cohort of patients, medical management resulted in spontaneous regeneration in the majority of children with acute liver failure. The use of inotropes, advanced hepatic encephalopathy, and peak alanine transaminase were predictors of poor outcome in children with acute liver failure and these patients could be considered for liver transplantation as available. Therefore, we may need to develop better predictors of pediatric acute liver failure in resource limited settings.
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