Premium
Perioperative management of a child with very‐long‐chain acyl‐coenzyme A dehydrogenase deficiency
Author(s) -
STEINER L.A.,
STUDER W.,
BAUMGARTNER E.R.,
FREI F.J.
Publication year - 2002
Publication title -
pediatric anesthesia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.704
H-Index - 82
eISSN - 1460-9592
pISSN - 1155-5645
DOI - 10.1046/j.1460-9592.2002.00809.x
Subject(s) - medicine , perioperative , metabolic acidosis , hypotonia , rhabdomyolysis , propofol , anesthesia , endocrinology
Very‐long‐chain acyl‐coenzyme A dehydrogenase deficiency is an inborn error of fatty acid metabolism. The clinical presentation of this disease in children is either a severe form with onset of symptoms in the first months of life, cardiomyopathy, metabolic acidosis, myopathy and a high mortality, or a less severe form manifesting mainly with hypoglycaemia. Perioperative fasting and (even emotional) stress can trigger metabolic decompensation through the altered metabolism of endogenous fatty acids resulting in hypoglycaemia, acute cardiac and hepatic dysfunction and rhabdomyolysis. We report the perioperative management of a 9‐year‐old boy suffering from the severe form of this disease who underwent circumcision. Metabolism was kept stable in this child by using a glucose–electrolyte infusion throughout the perioperative period to avoid the biochemical consequences of fasting and a benzodiazepine–opioid technique combined with regional anaesthesia to minimize the stress response. Considering reports about a possible interference of propofol with fatty acid oxidation and to avoid the unnecessary administration of fatty acids, propofol should not be used in these patients.