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Short- and long-term vitamin A treatment in children with cholestasis

O Amédée-Manesme1, M S Mourey, J Therasse

  • 1Département de Pédiatrie, Hôpital de Bicêtre, Le Kremlin, France.

Insights

Vitamin A deficiency is common in infants with chronic cholestasis. Intramuscular injections of vitamin A (retinyl palmitate) effectively correct this deficiency and are well-tolerated in children with extrahepatic biliary atresia.

Area of Science:

  • Nutritional Science
  • Pediatric Gastroenterology
  • Hepatology

Background:

  • Infants, especially newborns, have limited vitamin A reserves.
  • Chronic cholestasis impairs the ability of infants to build vitamin A stores, despite dietary intake.
  • Extrahepatic biliary atresia is a condition that can lead to vitamin A deficiency in pediatric patients.

Purpose of the Study:

  • To investigate liver vitamin A concentrations in children with extrahepatic biliary atresia.
  • To evaluate the efficacy and tolerance of vitamin A (retinyl palmitate) injections in infants with chronic cholestasis.

Main Methods:

  • Measurement of liver vitamin A concentrations in 30 children with extrahepatic biliary atresia.
  • Intramuscular administration of a water-miscible solution of retinyl palmitate (100,000 IU or 30 mg retinol equivalent).
  • Monitoring of liver and blood vitamin A concentrations over a 1-year period in nine children with chronic cholestasis.

Main Results:

  • Correction of vitamin A deficiency was observed following intramuscular retinyl palmitate administration.
  • The treatment demonstrated efficiency in improving vitamin A levels.
  • The vitamin A injections were well-tolerated by the pediatric patients.

Conclusions:

  • Intramuscular administration of vitamin A (retinyl palmitate) is an effective treatment for vitamin A deficiency in children with extrahepatic biliary atresia.
  • This therapeutic approach is safe and well-tolerated in infants suffering from chronic cholestasis.
  • Addressing vitamin A deficiency is crucial for improving the nutritional status of infants with chronic cholestasis.

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