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氟氯西林和双氯芬酸不会导致舒更葡糖钠逆转神经肌肉阻滞后复发。

Flucloxacillin and diclofenac do not cause recurrence of neuromuscular blockade after reversal with sugammadex.

机构信息

Merck Sharp & Dohme Corp., Whitehouse Station, NJ 07065-0900, USA.

出版信息

Clin Drug Investig. 2012 Mar 1;32(3):203-12. doi: 10.2165/11598980-000000000-00000.

Abstract

BACKGROUND

Sugammadex, a modified γ-cyclodextrin, facilitates rapid reversal of rocuronium- and vecuronium-induced neuromuscular blockade (NMB). Cyclodextrins are known for their ability to form inclusion complexes with various drugs. Theoretically, molecules with a high affinity for sugammadex could interact and displace sugammadex from the sugammadex-rocuronium or sugammadex-vecuronium complex, potentially resulting in the recurrence of NMB due to recirculation of free rocuronium or vecuronium.

OBJECTIVE

This study aimed to evaluate whether the administration of high doses of flucloxacillin or diclofenac can result in recurrence of NMB through displacement of sugammadex from its complex with rocuronium or vecuronium, following successful reversal of NMB by a suboptimal dose of sugammadex 2 mg/kg. Flucloxacillin has previously been identified using a modelling approach as a drug with displacement potential, while diclofenac was assessed due to its common intravenous use in the peri-operative and post-surgery setting.

METHODS

This was a randomized, open-label, parallel, single-centre study conducted at SGS Life Services-CPU, Antwerp, Belgium. Twenty-four healthy, propofol-anaesthetized, adult volunteers were randomized to either rocuronium 0.6 mg/kg or vecuronium 0.1 mg/kg, followed by a suboptimal dose of sugammadex 2 mg/kg 15 minutes after induction of NMB. Five minutes after successful sugammadex reversal, subjects received either diclofenac 75 mg (15-minute infusion) or flucloxacillin 2 g (5-minute infusion) according to randomization. The suboptimal dose of sugammadex and relatively high doses of diclofenac and flucloxacillin were applied to create favourable conditions for the potential displacement of sugammadex from the sugammadex-rocuronium or sugammadex-vecuronium complex, and thus possible recurrence of NMB due to recirculation of free rocuronium or vecuronium. Possible recurrence of NMB was assessed by neuromuscular monitoring, performed with acceleromyography, and was continued until ∼90 minutes after the start of diclofenac or flucloxacillin administration. Recurrence of NMB was concluded if three consecutive train-of-four (TOF) ratios were <0.8.

RESULTS

Following successful reversal with a suboptimal dose of sugammadex 2 mg/kg administered 15 minutes after NMB induction, subsequent administration of diclofenac or flucloxacillin did not result in recurrence of NMB in any subject based on measurement of TOF ratios during anaesthesia and neuromuscular function tests upon awakening. There were no adverse events considered to be related to sugammadex.

CONCLUSION

Administration of flucloxacillin or diclofenac does not result in recurrence of NMB through displacement of sugammadex from the sugammadex-rocuronium or sugammadex-vecuronium complex.

摘要

背景

琥乙红霉素是一种改良的γ-环糊精,可促进罗库溴铵和维库溴铵引起的神经肌肉阻滞(NMB)的快速逆转。环糊精以能够与各种药物形成包合物而闻名。理论上,与琥乙红霉素亲和力高的分子可能会相互作用并将琥乙红霉素从琥乙红霉素-罗库溴铵或琥乙红霉素-维库溴铵复合物中置换出来,从而导致由于游离罗库溴铵或维库溴铵的再循环而重新出现 NMB。

目的

本研究旨在评估在使用亚最优剂量的琥乙红霉素 2mg/kg 成功逆转 NMB 后,高剂量氟氯西林或双氯芬酸是否会通过从琥乙红霉素-罗库溴铵或琥乙红霉素-维库溴铵复合物中置换琥乙红霉素而导致 NMB 复发,因为先前使用建模方法鉴定氟氯西林具有置换潜力,而选择双氯芬酸是因为它在围手术期和手术后环境中经常静脉使用。

方法

这是一项在比利时安特卫普 SGS Life Services-CPU 进行的随机、开放标签、平行、单中心研究。24 名健康、异丙酚麻醉的成年志愿者随机接受罗库溴铵 0.6mg/kg 或维库溴铵 0.1mg/kg,然后在 NMB 诱导后 15 分钟给予亚最优剂量的琥乙红霉素 2mg/kg。NMB 成功逆转后 5 分钟,根据随机分组接受双氯芬酸 75mg(15 分钟输注)或氟氯西林 2g(5 分钟输注)。应用亚最优剂量的琥乙红霉素和相对较高剂量的双氯芬酸和氟氯西林,为琥乙红霉素从琥乙红霉素-罗库溴铵或琥乙红霉素-维库溴铵复合物中置换创造有利条件,从而可能由于游离罗库溴铵或维库溴铵的再循环而导致 NMB 再次发生。通过肌动描记术进行神经肌肉监测来评估可能发生的 NMB 复发,并持续至双氯芬酸或氟氯西林给药开始后约 90 分钟。如果连续三个强直刺激(TOF)比值<0.8,则认为出现 NMB 复发。

结果

在 NMB 诱导后 15 分钟给予亚最优剂量的琥乙红霉素成功逆转后,随后给予双氯芬酸或氟氯西林在任何受试者中均未导致 NMB 复发,这是基于麻醉期间 TOF 比值的测量和在肌电图监测和神经肌肉功能测试中醒来时的功能。没有被认为与琥乙红霉素有关的不良事件。

结论

氟氯西林或双氯芬酸的给药不会通过从琥乙红霉素-罗库溴铵或琥乙红霉素-维库溴铵复合物中置换琥乙红霉素而导致 NMB 复发。

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