Prolonged paralysis following mivacurium administration in a pediatric patient with previously undiagnosed pseudocholinesterase deficiency: a case report

Abstract Background Pseudocholinesterase, an enzyme produced by the liver and abundantly present in plasma, plays a role in the metabolism of neuromuscular blocking agents such as mivacurium. The administration of mivacurium to patients with pseudocholinesterase deficiency during general anesthesia...

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Bibliographic Details
Published in:BMC Pediatrics
Main Authors: Davut Deniz Uzun, Katharina Wildenberg, Fabian Ruping, Jens H. Westhoff, Felix C.F. Schmitt, Markus A. Weigand, Aleksandar R. Zivkovic
Format: Article
Language:English
Published: BMC 2025-08-01
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Online Access:https://doi.org/10.1186/s12887-025-05996-9