소아에서 Sevoflurane과 Propofol 마취 시 Rocuronium의 근이완 회복에 관한 비교
Background: Potent inhalation anesthetics potentiate the neuromuscular blocking effects of non-depolarizing muscle relaxants. Therefore, sevoflurane may increase the safety margin at the end of anesthesia by reducing the muscle relaxant dose requirements. We studied the recovery from rocuronium-indu...
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Veröffentlicht in: | Korean journal of anesthesiology 2005, 48(3), , pp.282-287 |
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Zusammenfassung: | Background: Potent inhalation anesthetics potentiate the neuromuscular blocking effects of non-depolarizing muscle relaxants. Therefore, sevoflurane may increase the safety margin at the end of anesthesia by reducing the muscle relaxant dose requirements. We studied the recovery from rocuronium-induced neuromuscular blockade during sevoflurane- versus propofol-based anesthesia in children.
Methods: Fifty pediatric patients were randomly allocated to maintenance of anesthesia with sevoflurane (n = 25) or propofol (n = 25). Neuromuscular block was maintained with rocuronium and monitored by acceleromyography (TOF-WatchⓇ) using train-of-four (TOF) stimulation every 12 seconds. Anesthetic agent administration was gradually reduced and then stopped toward the end of procedure. At the end of surgery, neostigmine 0.04 mg/kg was administered. Time of tracheal extubation, time of arrival in PACU, amount of rocuronium given were recorded.
Results: TOF ratio at the end of surgery was greater in sevoflurane group (73.0 ± 30.0) than in propofol group (50.0 ± 37.1)(P < 0.05). The dose of rocuronium administered as supplemental increments in sevoflurane group was significantly smaller than that in propofol group (0.9 ± 1.6 vs 2.8 ± 2.4μg/kg/min)(P < 0.05). Time to extubation (7.3 ± 2.0 vs 9.0 ± 2.6 min), and time to arrival in PACU (11.5 ± 2.9 vs 13.9 ± 2.6 min) from end of surgery were shorter in sevoflurane group than in propofol group (P < 0.05).
Conclusions: These results support the postulate that the potentiation of neuromuscular block by sevoflurane may provide additional safety for pediatric patients by reducing the muscle relaxant dose requirements. KCI Citation Count: 0 |
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ISSN: | 2005-6419 2005-7563 |