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Updated: Aug 9, 2026

Measurement of Chitinase Activity in Biological Samples
Published on: August 22, 2019
[Butyrylcholinesterase deficiency: how to analyse the cholinesterase activity in small children?]
C Lejus1, O Delaroche, E Trille
1Service d'Anesthésie et de Réanimation Chirurgicale, Hôtel-Dieu-Hôpital Mère-Enfant, CHU de Nantes, 44093 Nantes Cedex 01, France. corinne.lejus@chu-nantes.fr
Insights
Prolonged neuromuscular blockade occurred in an infant after succinylcholine. This was due to an atypical cholinesterase variant, highlighting age-specific normal values for children.
Area of Science:
- Anesthesiology
- Biochemistry
- Pediatrics
Background:
- Succinylcholine is a common muscle relaxant used in anesthesia.
- Genetic variations in pseudocholinesterase can affect drug metabolism.
- Pediatric patients may exhibit different physiological responses compared to adults.
Observation:
- An 18-month-old girl experienced prolonged neuromuscular blockade after a standard dose of succinylcholine.
- Cholinesterase activity in the patient was within adult normal ranges but lower than in a cohort of children.
- Familial analysis revealed an atypical pseudocholinesterase variant (AA phenotype).
Findings:
- The patient's low cholinesterase activity indicated a genetic predisposition to prolonged blockade.
- The AA phenotype of pseudocholinesterase is associated with reduced drug hydrolysis.
- Age-specific reference ranges for cholinesterase activity are crucial for pediatric diagnosis.
Implications:
- This case underscores the importance of considering genetic factors in anesthetic drug response.
- Accurate diagnosis of pseudocholinesterase variants is vital for patient safety.
- Establishing age-adjusted normal values for cholinesterase activity is necessary for pediatric care.
Abstract:
We report the case of a prolonged neuromuscular blockade in an 18-month-old age girl following administration of a usual dose of succinylcholine. The diagnosis was highly suggested by the clinical history while cholinesterase activity was included in adult normal values but below values of a personal series of 41 small children. The familial analysis of dibucaine and fluoride number confirmed the hypothesis of an atypical variant (AA phenotype). The cholinesterase activity is higher in small children than in adult and has to be analysed according to the age.
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