Abstract
BackgroundMethylmalonic acidemia (MMAemia) is a rare hereditary disease affecting organic acid metabolism. It causes recurrent metabolic acidosis and secondary mitochondrial dysfunction, resulting in a poor prognosis. Liver transplantation (LT) has been performed to facilitate the metabolism of organic acids and improve the prognosis of MMAemia. However, there have been few reports on perioperative management of LT.Case presentationA 22-month-old female with severe MMAemia was scheduled to receive LT to relieve recurrent metabolic acidosis despite dietary and pharmacological treatment. General anesthesia was maintained without propofol or nitrous oxide, which can worsen MMAemia-induced metabolic acidosis during anesthesia for LT. Strict metabolic and respiratory management enabled the operation to be successfully performed without metabolic acidosis.ConclusionPerioperative management of LT for MMAemia is challenging for anesthesiologists because of the possibility of serious metabolic acidosis. We succeeded in preventing metabolic decompensation by avoiding the use of propofol and nitrous oxide.
Highlights
Methylmalonic acidemia (MMAemia) is a rare hereditary disease affecting organic acid metabolism
Perioperative management of Liver transplantation (LT) for MMAemia is challenging for anesthesiologists because of the possibility of serious metabolic acidosis
We succeeded in preventing metabolic decompensation by avoiding the use of propofol and nitrous oxide
Summary
Perioperative management of LT for MMAemia is challenging for anesthesiologists because serious metabolic acidosis can occur.
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