Changes in branched‐chain amino acids in an infant with maple syrup urine disease during perioperative pediatric liver transplant: A case report

Author:

Saeyup Pipat1ORCID,Tubjaroen Chomchanat23ORCID,Kamolvisit Wuttichart45,Chongsrisawat Voranush23ORCID,Thaveepunsan Winnie1

Affiliation:

1. Department of Anesthesiology, King Chulalongkorn Memorial Hospital, Faculty of Medicine Chulalongkorn University Bangkok Thailand

2. Division of Gastroenterology and Hepatology, Department of Pediatrics, King Chulalongkorn Memorial Hospital, Faculty of Medicine Chulalongkorn University Bangkok Thailand

3. Excellence Center for Organ Transplantation King Chulalongkorn Memorial Hospital Bangkok Thailand

4. Center of Excellence for Medical Genomics, Medical Genomics Cluster, Department of Pediatrics, Faculty of Medicine Chulalongkorn University Bangkok Thailand

5. Excellence Center of Genomics and Precision Medicine King Chulalongkorn Memorial Hospital, The Thai Red Cross Society Bangkok Thailand

Abstract

AbstractAn 11‐month‐old female infant diagnosed with classic subtype IB maple syrup urine disease underwent living donor liver transplantation. Blood samples for plasma amino acid analysis were collected during the three phases of the operation. Despite the perioperative prophylactic administration of 12.5% hypertonic dextrose solution with insulin and a 20% intralipid emulsion, the blood levels of the branched‐chain amino acids increased dramatically during surgery, consistent with an acute intraoperative metabolic decompensation. However, these blood levels normalized soon after liver transplantation with an excellent outcome. We suggest that the occurrence of an intraoperative metabolic crisis during liver transplantation is not necessarily a sign of graft failure.

Publisher

Wiley

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