2000
DOI: 10.1007/bf03018850
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Neuromuscular effects of rapacuronium in pediatric patients during nitrous oxide-halothane anesthesia: comparison with mivacurium

Abstract: Purpose: To describe neuromuscular effects of rapacuronium in pediatric patients during N 2 O-halothane anesthesia and compare them with mivacurium in children.Methods: 103 pediatric patients, seven days -12 yr, received rapacuronium or mivacurium during N 2 O-halothane anesthesia. Onset and recovery of block were measured using EMG (Datex). Block was compared between groups based on drug treatment and age. Children < two years received 1 or 2 mg·kg Results: There were no differences in onset (1.7 ± 1.8 min) o… Show more

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Cited by 19 publications
(10 citation statements)
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“…Following anaesthesia with thiopental and fentanyl, the minimum doses of rapacuronium for satisfactory intubation conditions at 60 s were 1.5 and 2.0 mg kg À1 , respectively (%2-3 Â ED 95 ) in infants and children [33,34]. A dose of 2 mg kg À1 produces maximum block in 1.5-2.0 min followed by recovery of T 1 to 25% and 90% in 14-19 and 23-41 min, respectively, in infants and children (Table 2) [30]. Recovery from rapacuronium-induced block is age dependent and slower than that produced by mivacurium [30,33].…”
Section: Rapacuroniummentioning
confidence: 98%
See 1 more Smart Citation
“…Following anaesthesia with thiopental and fentanyl, the minimum doses of rapacuronium for satisfactory intubation conditions at 60 s were 1.5 and 2.0 mg kg À1 , respectively (%2-3 Â ED 95 ) in infants and children [33,34]. A dose of 2 mg kg À1 produces maximum block in 1.5-2.0 min followed by recovery of T 1 to 25% and 90% in 14-19 and 23-41 min, respectively, in infants and children (Table 2) [30]. Recovery from rapacuronium-induced block is age dependent and slower than that produced by mivacurium [30,33].…”
Section: Rapacuroniummentioning
confidence: 98%
“…Rapacuronium, is a monoquaternary aminosteroidal muscle relaxant characterized by a rapid onset and a short duration of action, suggesting a possible use in paediatric day case surgery [30]. It is metabolized in the liver primarily to a 3-hydroxy metabolite (Org 9488), which itself is a neuromuscular blocking drug, having twice the potency of rapacuronium (biophase EC 50 0.4 Â rapacuronium) and an intermediate to long duration of action [31].…”
Section: Rapacuroniummentioning
confidence: 99%
“…Rapacuronium is the first non-depolarizing relaxant combining both, rapid onset and short duration of action [6,[19][20][21][22]. Maximum block was achieved in 86 AE 7 s at the vocal cords and in 97 AE 4 s at the adductor pollicis, respectively, after administering a dose of 1.5 mg kg À1 [23].…”
Section: Rapacuroniummentioning
confidence: 99%
“…Rapacuronium is the first non-depolarizing relaxant combining both, rapid onset and short duration of action [6,[19][20][21][22]. Maximum block was achieved in 86 AE 7 s at the vocal cords and in 97 AE 4 s at the adductor pollicis, respectively, after administering a dose of 1.5 mg kg À1 [23].…”
Section: Rapacuroniummentioning
confidence: 99%