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Onset and duration of mivacurium‐induced neuromuscular blockade in children with Charcot–Marie–Tooth disease. A case series with five children
Author(s) -
SCHMITT HUBERT J.,
WICK STEFANIE,
MÜNSTER TINO
Publication year - 2006
Publication title -
pediatric anesthesia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.704
H-Index - 82
eISSN - 1460-9592
pISSN - 1155-5645
DOI - 10.1111/j.1460-9592.2005.01627.x
Subject(s) - medicine , anesthesia , neuromuscular transmission , neuromuscular blockade , neuromuscular disease , propofol , adductor pollicis muscle , fentanyl , neuromuscular monitoring , surgery , disease , ulnar nerve , elbow
Summary Background: The Charcot–Marie–Tooth (CMT) disorders are a group of hereditary motor and sensory neuropathies characterized clinically by peripheral muscle wasting and weakness. We hypothesized that unknown involvement of the muscle used for monitoring neuromuscular block may account for the conflicting reports about the effect of nondepolarizing neuromuscular agents in these patients. The aim of this study was to compare onset and recovery from mivacurium‐induced neuromuscular block on the adductor pollicis and orbicularis oculi muscles. Methods: We used mivacurium 0.2 mg·kg −1 in five children (aged 7–12 years) with CMT type I undergoing propofol–fentanyl–oxygen–air anesthesia for orthopedic surgery. Using acceleromyography, neuromuscular transmission was monitored in parallel in the eye and thumb muscles, and onset and duration times were recorded. Results: Following bolus administration of 0.2 mg·kg −1 of mivacurium the onset time ranged between 135 and 240 s and 75 and 165 s in the eye and in the thumb, respectively. The recovery time varied between 5.3 and 16 min and 6 and 31.3 min in the eye and in the thumb, respectively. Conclusions: In our small series of patients with CMT the clinical duration of mivacurium‐induced neuromuscular block was similar to data known from children without neuromuscular disease.