Mensah-Osman Edith, Mukai Yuki, Wang Aobo, Matuszczak Maria, Saldien Vera, Leibensperger Heather, Speek Marcel, Locco Amy, Wrishko Rebecca, Gee Angela, Herring W Joseph
Merck & Co., Inc., Rahway, New Jersey.
UTHealth, Houston, Texas.
Anesthesiology. 2025 Aug 1;143(2):300-312. doi: 10.1097/ALN.0000000000005535. Epub 2025 May 5.
Sugammadex is well tolerated and effective for reversing neuromuscular blockade (NMB) in adults and children as young as 2 yr old. There is little information on its use in younger children. The aim of this study was to evaluate the efficacy and tolerability of sugammadex in children under 2 yr of age.
This was a phase IV, randomized, parallel-group, multicenter clinical trial of sugammadex in participants aged birth to less than 2 yr (NCT03909165). Part A was open label and included pharmacokinetic assessments to determine whether sugammadex dose adjustment for part B was necessary based on age. Part B was double-blind and evaluated doses of 2 and 4 mg/kg sugammadex. Participants were randomized to (1) moderate NMB and reversal with 2 mg/kg sugammadex; (2) moderate NMB and reversal with neostigmine + glycopyrrolate or atropine (hereafter, called neostigmine); or (3) deep NMB and reversal with 4 mg/kg sugammadex. The primary efficacy endpoint was time to neuromuscular recovery (TTNMR). The primary efficacy hypothesis was that 2 mg/kg sugammadex would be superior to neostigmine for the reversal of moderate NMB as measured by TTNMR in part B.
A total of 138 participants aged 1 to 720 days were treated in parts A and B (2 mg/kg sugammadex, n = 44; 4 mg/kg sugammadex, n = 63; and neostigmine, n = 31). Based on pharmacokinetic assessments in part A, no dose adjustments for age were needed. In part B, TTNMR for reversal of moderate NMB was faster with 2 mg/kg sugammadex than neostigmine (median of 1.4 min vs. 4.4 min; hazard ratio, 2.40; 95% CI, 1.37 to 4.18; P = 0.0002). A 4-mg/kg dose of sugammadex achieved rapid TTNMR for reversal of deep NMB with a median of 1.1 min (parts A and B). The percentage of participants with one or more adverse events (parts A and B) was similar for sugammadex and neostigmine. No deaths, drug-related serious adverse events, or hypersensitivity or anaphylaxis events were reported.
In children less than 2 yr old, 2 mg/kg sugammadex reversed moderate NMB faster than neostigmine, and 4 mg/kg sugammadex rapidly reversed deep NMB. Sugammadex doses of 2 and 4 mg/kg were well tolerated.
舒更葡糖钠耐受性良好,对成人及2岁儿童的神经肌肉阻滞(NMB)逆转有效。关于其在更小儿童中的应用信息较少。本研究的目的是评估舒更葡糖钠在2岁以下儿童中的疗效和耐受性。
这是一项舒更葡糖钠用于出生至未满2岁参与者的IV期、随机、平行组、多中心临床试验(NCT03909165)。A部分为开放标签,包括药代动力学评估,以确定是否需要根据年龄对B部分的舒更葡糖钠剂量进行调整。B部分为双盲,评估2mg/kg和4mg/kg舒更葡糖钠剂量。参与者被随机分为:(1)中度NMB并用2mg/kg舒更葡糖钠逆转;(2)中度NMB并用新斯的明+格隆溴铵或阿托品(以下简称新斯的明)逆转;或(3)深度NMB并用4mg/kg舒更葡糖钠逆转。主要疗效终点是神经肌肉恢复时间(TTNMR)。主要疗效假设是,在B部分中,以TTNMR衡量,2mg/kg舒更葡糖钠在逆转中度NMB方面优于新斯的明。
A部分和B部分共治疗了138名年龄在1至720天的参与者(2mg/kg舒更葡糖钠组,n = 44;4mg/kg舒更葡糖钠组,n = 63;新斯的明组,n = 31)。基于A部分的药代动力学评估,无需根据年龄调整剂量。在B部分,2mg/kg舒更葡糖钠逆转中度NMB的TTNMR比新斯的明快(中位数为1.4分钟对4.4分钟;风险比,2.40;95%CI,1.37至4.18;P = 0.0002)。4mg/kg剂量的舒更葡糖钠逆转深度NMB的TTNMR迅速,中位数为1.1分钟(A部分和B部分)。舒更葡糖钠组和新斯的明组发生一项或多项不良事件的参与者百分比相似。未报告死亡、药物相关严重不良事件或超敏反应或过敏反应事件。
在2岁以下儿童中,2mg/kg舒更葡糖钠逆转中度NMB比新斯的明快,4mg/kg舒更葡糖钠迅速逆转深度NMB。2mg/kg和4mg/kg的舒更葡糖钠剂量耐受性良好。