首页> 外文期刊>Anesthesia and Analgesia: Journal of the International Anesthesia Research Society >A randomized, dose-response study of sugammadex given for the reversal of deep rocuronium- or vecuronium-induced neuromuscular blockade under sevoflurane anesthesia.
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A randomized, dose-response study of sugammadex given for the reversal of deep rocuronium- or vecuronium-induced neuromuscular blockade under sevoflurane anesthesia.

机译:sugammadex的一项随机剂量反应研究,用于逆转七氟醚麻醉下由罗库溴铵或维库溴铵引起的深部神经肌肉阻滞。

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BACKGROUND: Sugammadex is the first of a new class of selective muscle relaxant binding drugs developed for the rapid and complete reversal of neuromuscular blockade induced by rocuronium and vecuronium. Many studies have demonstrated a dose-response relationship with sugammadex for reversal of neuromuscular blockade in patients induced and maintained under propofol anesthesia. However, sevoflurane anesthesia, unlike propofol, can prolong the effect of neuromuscular blocking drugs (NMBDs) such as rocuronium and vecuronium. METHODS: We designed this randomized, open-label, dose-response trial to explore the dose-response relationship of sugammadex for the reversal of deep neuromuscular blockade induced by rocuronium or vecuronium under propofol-induced and sevoflurane-maintained anesthesia. As a secondary objective, the safety variables of sugammadex were evaluated. After anesthesia induction with propofol, 102 patients aged > or = 20 and < 65 yr were randomized to receive a single bolus dose of rocuronium 0.9 mg/kg (n = 50) or vecuronium 0.1 mg/kg (n = 52), followed by maintenance doses (rocuronium 0.1-0.2 mg/kg or vecuronium 0.02-0.03 mg/kg) as needed. Neuromuscular blockade was monitored using acceleromyography. After the last dose of NMBD, at 1-2 posttetanic counts, a single bolus dose of sugammadex 0.5, 1.0, 2.0, 4.0, or 8.0 mg/kg was administered. The primary efficacy variable was time from start of sugammadex administration to recovery of the T(4)/T(1) ratio to 0.9. RESULTS: The per-protocol population consisted of 48 patients in the rocuronium group and 47 in the vecuronium group. A dose-response effect was demonstrated for decreased mean time to recovery of the T(4)/T(1) ratio to 0.9 with increasing sugammadex dose in both NMBD groups (per-protocol population): rocuronium group, 79.8 (SD 33.0) min (sugammadex 0.5 mg/kg) to 1.7 (0.7) min (4.0 mg/kg) and 1.1 (0.3) min (8.0 mg/kg subgroup); vecuronium group, 68.4 (31.9) min (0.5 mg/kg) to 3.3 (3.5) min (4.0 mg/kg), and 1.7 (0.8) min (8.0 mg/kg subgroup). Neuromuscular monitoring showed recurrent neuromuscular blockade in 5 patients, all in the rocuronium group (2 given sugammadex 0.5 mg/kg and 3 given 1.0 mg/kg), but there were no clinical events attributable to recurrent or residual neuromuscular blockade. CONCLUSION: Sugammadex at doses of > or = 4 mg/kg provides rapid reversal of deep rocuronium- and vecuronium-induced neuromuscular blockade under sevoflurane maintenance anesthesia.
机译:背景:Sugammadex是为快速,完全逆转由罗库溴铵和维库溴铵诱导的神经肌肉阻滞而开发的新型选择性肌肉松弛剂结合药物中的第一种。许多研究表明,在丙泊酚麻醉下诱导和维持的患者中,舒马葡糖具有逆转神经肌肉阻滞的剂量反应关系。但是,与异丙酚不同,七氟醚麻醉可以延长罗库溴铵和维库溴铵等神经肌肉阻滞药(NMBD)的作用。方法:我们设计了这项随机,开放标签,剂量反应试验,以探讨舒丙酰胺在丙泊酚诱导和七氟醚维持麻醉下逆转由罗库溴铵或维库溴铵引起的深层神经肌肉阻滞的剂量反应关系。次要目标是评估sugammadex的安全性变量。异丙酚麻醉诱导后,年龄≥20岁或≤65岁且年龄≥20岁和<65岁的102名患者被随机分配接受单次推注剂量的罗库溴铵0.9 mg / kg(n = 50)或维库溴铵0.1 mg / kg(n = 52),然后是维持剂量(罗库溴铵0.1-0.2 mg / kg或维库溴铵0.02-0.03 mg / kg)。使用加速肌电图监测神经肌肉阻滞。在最后一次NMBD给药后,在1-2次强直计数下,单次推注剂量的sugammadex 0.5、1.0、2.0、4.0或8.0 mg / kg。主要功效变量是从开始添加舒马葡糖到恢复T(4)/ T(1)比率至0.9所需的时间。结果:按方案人群包括罗库溴铵组48例,维库溴铵组47例。在两个NMBD组(按协议人群)中,随着sugammadex剂量的增加,证明了剂量响应效应可将T(4)/ T(1)比恢复至0.9的平均时间缩短:罗库溴铵组,79.8(SD 33.0)分钟(Sugammadex 0.5 mg / kg)至1.7(0.7)分钟(4.0 mg / kg)和1.1(0.3)分钟(8.0 mg / kg亚组);维库溴铵组:68.4(31.9)分钟(0.5 mg / kg)至3.3(3.5)分钟(4.0 mg / kg)和1.7(0.8)分钟(8.0 mg / kg亚组)。在罗库溴铵组中,神经肌肉监测显示有5例患者出现复发性神经肌肉阻滞(2例给予舒马葡糖0.5 mg / kg,3例给予1.0 mg / kg),但没有因复发或残留神经肌肉阻滞而引起的临床事件。结论:Sugammadex剂量≥4 mg / kg可在七氟醚维持麻醉下快速逆转由罗库溴铵和维库溴铵引起的深层神经肌肉阻滞。

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