Suppr超能文献

罗库溴铵的起效时间:与阿曲库铵和维库溴铵的比较。

Rocuronium onset of action: a comparison with atracurium and vecuronium.

作者信息

Bartkowski R R, Witkowski T A, Azad S, Lessin J, Marr A

机构信息

Department of Anesthesiology, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA 19107.

出版信息

Anesth Analg. 1993 Sep;77(3):574-8. doi: 10.1213/00000539-199309000-00025.

Abstract

The onset, maximal neuromuscular block, and duration of rocuronium were compared with atracurium and vecuronium during enflurane anesthesia. Sixty patients received rocuronium (80, 100, 120, or 160 micrograms/kg). Enflurane enhanced a rocuronium neuromuscular block in a dose-related manner; the ED50 was 104 +/- 11 and 83 +/- 7 micrograms/kg (SEM) during 1% and 2% enflurane anesthesia, respectively. Patients receiving atracurium (0.12 mg/kg) or vecuronium (0.02 mg/kg) were studied during 1% enflurane anesthesia until seven in each group qualified by achieving a maximal block between 85% and 97%. These patients were matched with each other and with patients who had received rocuronium. Seven groups of three patients (rocuronium, vecuronium, and atracurium) were obtained. The average difference in maximal block was less than 2% between matched patients. The ratio of dose used to achieve a similar final block suggests potency ratios of 1, 8.5, and 1.2 for rocuronium, vecuronium, and atracurium. Rocuronium's onset time (time from drug administration to 50%, 75%, and 90% of final block) was significantly faster than either of the other two muscle relaxants (P < 0.01). Time to 90% of final block was 1.35 min for rocuronium, 3.06 min for atracurium, and 3.71 min for vecuronium. Using these equipotent doses, atracurium also had a shorter time to develop neuromuscular block than vecuronium (P < 0.05). For these three intermediate duration neuromuscular blockers, speed of onset was inversely related to their potency, confirming a relationship that had been demonstrated for the long-acting drugs pancuronium, d-tubocuranine, and gallamine.

摘要

在安氟醚麻醉期间,比较了罗库溴铵与阿曲库铵和维库溴铵的起效时间、最大神经肌肉阻滞作用及持续时间。60例患者接受了罗库溴铵(80、100、120或160微克/千克)。安氟醚以剂量相关的方式增强罗库溴铵的神经肌肉阻滞作用;在1%和2%安氟醚麻醉期间,其半数有效剂量(ED50)分别为104±11和83±7微克/千克(标准误)。在1%安氟醚麻醉期间,对接受阿曲库铵(0.12毫克/千克)或维库溴铵(0.02毫克/千克)的患者进行研究,直至每组有7例患者达到85%至97%的最大阻滞程度。这些患者相互匹配,并与接受罗库溴铵的患者匹配。得到了七组每组三名患者(罗库溴铵组、维库溴铵组和阿曲库铵组)。匹配患者之间最大阻滞的平均差异小于2%。用于达到相似最终阻滞程度的剂量比表明,罗库溴铵、维库溴铵和阿曲库铵的效价比为1、8.5和1.2。罗库溴铵的起效时间(从给药到最终阻滞的50%、75%和90%的时间)明显快于其他两种肌肉松弛剂(P<0.01)。达到最终阻滞90%的时间,罗库溴铵为1.35分钟,阿曲库铵为3.06分钟,维库溴铵为3.71分钟。使用这些等效剂量时,阿曲库铵产生神经肌肉阻滞的时间也比维库溴铵短(P<0.05)。对于这三种中效神经肌肉阻滞剂,起效速度与其效价呈负相关,这证实了长效药物泮库溴铵、d-筒箭毒碱和加拉明所显示的一种关系。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验