Perioperative management of a child with very-long-chain acyl-coenzyme A dehydrogenase deficiency

L A Steiner1, W Studer, E R Baumgartner

  • 1Department of Anaesthesia, Universitätskinderspital beider Basel (UKBB), Basel, Switzerland. las30@cam.ac.uk

Insights

Very-long-chain acyl-coenzyme A dehydrogenase deficiency (VLCAD) management requires perioperative glucose infusion and stress reduction. Avoiding propofol is crucial to prevent fatty acid oxidation interference in affected children.

Area of Science:

  • Biochemistry
  • Genetics
  • Pediatrics

Background:

  • Very-long-chain acyl-coenzyme A dehydrogenase deficiency (VLCAD) is an inherited metabolic disorder affecting fatty acid oxidation.
  • VLCAD presents in severe infantile forms with cardiomyopathy and high mortality, or milder forms with hypoglycemia.

Observation:

  • Perioperative fasting and stress can precipitate metabolic decompensation in VLCAD patients.
  • This includes hypoglycemia, cardiac/hepatic dysfunction, and rhabdomyolysis.

Findings:

  • Successful perioperative management of a 9-year-old VLCAD patient undergoing circumcision.
  • Stable metabolism maintained via glucose-electrolyte infusion and a benzodiazepine-opioid/regional anesthesia technique.
  • Propofol use was avoided due to potential interference with fatty acid oxidation.

Implications:

  • Glucose infusion and stress minimization are key for perioperative VLCAD care.
  • Propofol should be avoided in VLCAD patients to prevent adverse metabolic effects.
  • This case highlights safe anesthetic strategies for children with inherited metabolic disorders.

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