{"title":"Optimal dose of mivacurium for laser-assisted laryngeal microsurgery: a pharmacokinetic study using closed-loop target-controlled infusion.","authors":"Yan Liu, Yong Wang, Meng Xie, Li Jia","doi":"10.5114/ait.2024.145249","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Mivacurium is a short-acting, non-depolarising neuromuscular blocking agent that provides adequate vocal cord myorelaxation during transoral laser microsurgery. This study aimed to determine the optimal dose of mivacurium by comparing the infusion rate delivered via a closed-loop target-controlled infusion system.</p><p><strong>Methods: </strong>A prospective, randomized clinical trial was conducted on 60 patients undergoing laser-assisted laryngeal microsurgery for vocal cord tumours. All patients received an induction mivacurium dose of 0.2 mg kg -1 and were randomized to 3 groups, namely C1, C2 and C3, each receiving infusion rates of 6 μg kg -1 min -1 , 7 μg kg -1 min -1 , 8 μg kg -1 min -1 , respectively. Neuromuscular monitoring and pharmacodynamic para-meters of mivacurium were recorded.</p><p><strong>Results: </strong>No cases of airway spasms, blood pressure or heart rate fluctuations were observed. Three patients had skin redness at the injection site. The onset time, no- response time, and recovery index (RI) of mivacurium did not differ significantly among the groups. However, additional mivacurium doses were needed for 15 patients in C1, 10 patients in C2, and 3 patients in C3 ( P 5.68 min was correlated with reduced mivacurium supplementation, and it was associated with no-response time and total mivacurium dose. The recovery index of all patients was also positively correlated with total mivacurium dosage ( p < 0.0001, r = 0.7838).</p><p><strong>Conclusions: </strong>A mivacurium infusion rate of 8 μg kg -1 min -1 offered the most favourable surgical field condition with no involuntary vocal cord movements, less need for supplementary doses, and fewer adverse reactions in laser-assisted laryngeal microsurgery.</p>","PeriodicalId":7750,"journal":{"name":"Anaesthesiology intensive therapy","volume":"56 4","pages":"231-240"},"PeriodicalIF":1.6000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11736911/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Anaesthesiology intensive therapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5114/ait.2024.145249","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ANESTHESIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: Mivacurium is a short-acting, non-depolarising neuromuscular blocking agent that provides adequate vocal cord myorelaxation during transoral laser microsurgery. This study aimed to determine the optimal dose of mivacurium by comparing the infusion rate delivered via a closed-loop target-controlled infusion system.
Methods: A prospective, randomized clinical trial was conducted on 60 patients undergoing laser-assisted laryngeal microsurgery for vocal cord tumours. All patients received an induction mivacurium dose of 0.2 mg kg -1 and were randomized to 3 groups, namely C1, C2 and C3, each receiving infusion rates of 6 μg kg -1 min -1 , 7 μg kg -1 min -1 , 8 μg kg -1 min -1 , respectively. Neuromuscular monitoring and pharmacodynamic para-meters of mivacurium were recorded.
Results: No cases of airway spasms, blood pressure or heart rate fluctuations were observed. Three patients had skin redness at the injection site. The onset time, no- response time, and recovery index (RI) of mivacurium did not differ significantly among the groups. However, additional mivacurium doses were needed for 15 patients in C1, 10 patients in C2, and 3 patients in C3 ( P 5.68 min was correlated with reduced mivacurium supplementation, and it was associated with no-response time and total mivacurium dose. The recovery index of all patients was also positively correlated with total mivacurium dosage ( p < 0.0001, r = 0.7838).
Conclusions: A mivacurium infusion rate of 8 μg kg -1 min -1 offered the most favourable surgical field condition with no involuntary vocal cord movements, less need for supplementary doses, and fewer adverse reactions in laser-assisted laryngeal microsurgery.
目的:Mivacurium是一种短效,非去极化神经肌肉阻断剂,在经口激光显微手术中提供足够的声带肌肉松弛。本研究旨在通过比较闭环靶控输注系统的输注速率来确定微真空的最佳剂量。方法:对60例接受激光辅助喉部显微手术治疗声带肿瘤的患者进行前瞻性随机临床试验。所有患者均给予诱导微量剂量0.2 mg kg -1,随机分为C1、C2、C3 3组,各组输注剂量分别为6 μg kg -1 min -1、7 μg kg -1 min -1、8 μg kg -1 min -1。记录神经肌肉监测和药效学参数。结果:无气道痉挛、血压、心率波动。3例患者注射部位皮肤发红。两组间的起效时间、无反应时间和恢复指数(RI)无显著差异。然而,15例C1患者、10例C2患者和3例C3患者需要额外的微量元素剂量(P 5.68 min与减少微量元素补充相关,并与无反应时间和总微量元素剂量相关)。所有患者的恢复指数也与总微量剂量呈正相关(p < 0.0001, r = 0.7838)。结论:8 μg kg -1 min -1的微量输注速度是激光辅助喉部显微手术最有利的手术野条件,无声带不自主运动,需要补充剂量少,不良反应少。