https://pubmed.ncbi.nlm.nih.gov/40150672/ biliary atresia

Children (Basel). 2025 Mar 20;12(3):391.
doi: 10.3390/children12030391.

Nutritional Management for Pediatric Biliary Atresia Patients Preparing for Liver Transplantation

Uyory Choe 1
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PMID: 40150672

PMCID: PMC11941163

DOI: 10.3390/children12030391
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Abstract

Biliary atresia, a rare pediatric liver condition, results in blocked bile ducts, impeding bile secretion and causing significant nutritional challenges. This perspective emphasizes the critical role of nutrition in supporting children with biliary atresia awaiting liver transplantation. The liver's multifaceted functions in energy metabolism, vitamin storage, and waste excretion emphasize the importance of tailored dietary interventions. Medium-chain triglyceride (MCT) oil serves as a crucial energy source, addressing fat malabsorption, while specialized water-soluble formulations deliver essential fat-soluble vitamins. Additionally, weaning strategies and developmental food practices are discussed to ensure optimal growth and development despite dietary restrictions. Feeding assistance through nasogastric or gastrostomy tubes is explored as a means to combat malnutrition and support liver function. The collective efforts of caregivers and healthcare providers are pivotal in preparing these children for successful liver transplantation, aiming to secure their future health and quality of life.