Suy Koen, Morias Karl, Cammu Guy, Hans Pol, van Duijnhoven Wilbert G F, Heeringa Marten, Demeyer Ignace
Department of Anesthesiology and Critical Care Medicine, Onze Lieve Vrouw Ziekenhuis, Belgium.
Anesthesiology. 2007 Feb;106(2):283-8. doi: 10.1097/00000542-200702000-00016.
Sugammadex rapidly reverses rocuronium-induced neuromuscular block. This study explored the dose-response relation of sugammadex given as a reversal agent at reappearance of the second muscle twitch after rocuronium- and vecuronium-induced block. A secondary objective was to investigate the safety of single doses of sugammadex.
In this two-center, phase II, dose-finding study, 80 patients (age >or= 18 yr, American Society of Anesthesiologists physical status I or II, surgery >or= 60 min requiring muscle relaxation for intubation) were randomly assigned to receive rocuronium (0.60 mg/kg) or vecuronium (0.10 mg/kg). Sugammadex or placebo was administered at reappearance of the second muscle twitch. The primary efficacy endpoint was time from starting sugammadex administration until recovery of the train-of-four ratio to 0.9.
Compared with placebo, sugammadex produced dose-dependent decreases in mean time to recovery for all train-of-four ratios in the rocuronium and vecuronium groups. The mean time for recovery of the train-of-four ratio to 0.9 in the rocuronium group was 31.8 min after placebo compared with 3.7 and 1.1 min after 0.5 and 4.0 mg/kg sugammadex, respectively. The mean time for recovery of the train-of-four ratio to 0.9 in the vecuronium group was 48.8 min after placebo, compared with 2.5 and 1.4 min after 1.0 and 8.0 mg/kg sugammadex, respectively. Sugammadex was well tolerated.
Sugammadex rapidly reversed rocuronium- or vecuronium-induced neuromuscular block at reappearance of the second muscle twitch and was well tolerated. A dose-response relation was observed with sugammadex for reversal of both rocuronium- and vecuronium-induced neuromuscular block.
舒更葡糖钠可迅速逆转罗库溴铵诱导的神经肌肉阻滞。本研究探讨了在罗库溴铵和维库溴铵诱导的阻滞出现第二次肌颤搐后,给予舒更葡糖钠作为逆转剂时的剂量-反应关系。次要目的是研究单次剂量舒更葡糖钠的安全性。
在这项双中心、II期、剂量探索研究中,80例患者(年龄≥18岁,美国麻醉医师协会身体状况I或II级,手术时间≥60分钟,插管需要肌肉松弛)被随机分配接受罗库溴铵(0.60mg/kg)或维库溴铵(0.10mg/kg)。在出现第二次肌颤搐时给予舒更葡糖钠或安慰剂。主要疗效终点是从开始给予舒更葡糖钠到四个成串刺激比值恢复至0.9的时间。
与安慰剂相比,舒更葡糖钠使罗库溴铵组和维库溴铵组所有四个成串刺激比值的平均恢复时间呈剂量依赖性缩短。罗库溴铵组在给予安慰剂后四个成串刺激比值恢复至0.9的平均时间为31.8分钟,而给予0.5mg/kg和4.0mg/kg舒更葡糖钠后分别为3.7分钟和1.1分钟。维库溴铵组在给予安慰剂后四个成串刺激比值恢复至0.9的平均时间为48.8分钟,而给予1.0mg/kg和8.0mg/kg舒更葡糖钠后分别为2.5分钟和1.4分钟。舒更葡糖钠耐受性良好。
在出现第二次肌颤搐时,舒更葡糖钠可迅速逆转罗库溴铵或维库溴铵诱导的神经肌肉阻滞,且耐受性良好。观察到舒更葡糖钠对罗库溴铵和维库溴铵诱导的神经肌肉阻滞的逆转存在剂量-反应关系。