Prolonged curarisation following succinylcholine injection on butyrylcholinesterase deficiency and potentiated by a lithium treatment: a case report

Succinylcholine is a short-term curare which degradation depends on its quick hydrolysis by butyrylcholinesterase (or pseudocholinesterase). Thus, a butyrycholinesterase deficiency, congenital or acquired, is a cause of a prolonged neuromuscular block. From an autosomal recessive inheritance, geneti...

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Published in:Annales de biologie clinique (Paris) Vol. 71; no. 4; p. 485
Main Authors: Huynh-Moynot, Sophie, Moynot, Jean-Clair, Thill, Chloé, Commandeur, Diane, Ould-Ahmed, Mehdi, Drouillard, Isabelle
Format: Journal Article
Language:French
Published: France 01-07-2013
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Summary:Succinylcholine is a short-term curare which degradation depends on its quick hydrolysis by butyrylcholinesterase (or pseudocholinesterase). Thus, a butyrycholinesterase deficiency, congenital or acquired, is a cause of a prolonged neuromuscular block. From an autosomal recessive inheritance, genetic deficiency remains the first etiology. The most frequently discussed variant is the atypical variant which caused a 2 hours prolonged curarisation after administration of succinylcholine. We report a patient who had a prolonged curarisation after succinylcholine's injection, due to a congenital butyrylcholinestérase deficiency and contributed by a lithium treatment. Extubation was only possible 7 hours after administration of curare.
ISSN:1950-6112
DOI:10.1684/abc.2013.0865