Service d'Anesthésie-Réanimation, Hôpital Henri Mondor, 94010 Créteil, France.
Anesth Analg. 2010 Jan 1;110(1):74-82. doi: 10.1213/ANE.0b013e3181c3be3c. Epub 2009 Nov 21.
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.
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.
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.
Sugammadex at doses of > or = 4 mg/kg provides rapid reversal of deep rocuronium- and vecuronium-induced neuromuscular blockade under sevoflurane maintenance anesthesia.
琥胆酸是一类新型的选择性肌肉松弛剂结合药物,用于快速和完全逆转罗库溴铵和维库溴铵引起的神经肌肉阻滞。许多研究表明,琥胆酸与罗库溴铵在异丙酚麻醉诱导和维持下,逆转神经肌肉阻滞存在剂量反应关系。然而,不同于异丙酚,七氟醚麻醉可延长罗库溴铵和维库溴铵等神经肌肉阻滞药物(NMBDs)的作用时间。
我们设计了这项随机、开放标签、剂量反应试验,以探讨琥胆酸在异丙酚诱导和七氟醚维持麻醉下,逆转罗库溴铵或维库溴铵引起的深度神经肌肉阻滞的剂量反应关系。作为次要目标,评估了琥胆酸的安全性变量。在异丙酚诱导麻醉后,102 名年龄大于或等于 20 岁且小于 65 岁的患者被随机分为两组,分别接受罗库溴铵 0.9mg/kg(n=50)或维库溴铵 0.1mg/kg(n=52)单次推注,然后按需给予维持剂量(罗库溴铵 0.1-0.2mg/kg 或维库溴铵 0.02-0.03mg/kg)。使用加速度肌电图监测神经肌肉阻滞。在最后一次 NMBD 剂量后,在强直刺激后 1-2 计数时,给予琥胆酸 0.5、1.0、2.0、4.0 或 8.0mg/kg 单次推注。主要疗效变量为琥胆酸开始给药至 T4/T1 比值恢复至 0.9 的时间。
在罗库溴铵组和维库溴铵组中,分别有 48 名和 47 名患者符合方案人群。在两组 NMBD 中,随着琥胆酸剂量的增加,T4/T1 比值恢复至 0.9 的平均时间均显示出剂量反应效应(符合方案人群):罗库溴铵组,79.8(SD 33.0)min(琥胆酸 0.5mg/kg)至 1.7(0.7)min(4.0mg/kg)和 1.1(0.3)min(8.0mg/kg 亚组);维库溴铵组,68.4(31.9)min(0.5mg/kg)至 3.3(3.5)min(4.0mg/kg)和 1.7(0.8)min(8.0mg/kg 亚组)。神经肌肉监测显示 5 名患者出现复发性神经肌肉阻滞,均发生在罗库溴铵组(2 名给予琥胆酸 0.5mg/kg,3 名给予 1.0mg/kg),但无临床事件归因于复发性或残留的神经肌肉阻滞。
琥胆酸剂量大于或等于 4mg/kg 可在七氟醚维持麻醉下快速逆转深度罗库溴铵和维库溴铵引起的神经肌肉阻滞。