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顺式阿曲库铵和维库溴铵给药后的起效时间、气管插管条件及血浆组胺水平。

Onset time, endotracheal intubating conditions, and plasma histamine after cisatracurium and vecuronium administration.

作者信息

Doenicke A W, Czeslick E, Moss J, Hoernecke R

机构信息

Department of Anesthesia, Ludwig Maximilians University of Munich, Germany.

出版信息

Anesth Analg. 1998 Aug;87(2):434-8. doi: 10.1097/00000539-199808000-00038.

DOI:10.1097/00000539-199808000-00038
PMID:9706946
Abstract

UNLABELLED

Cisatracurium is a nondepolarizing muscle relaxant with a slow onset. We performed a prospective, randomized, double-blind clinical trial in 60 patients (ASA physical status I or II) to assess whether cisatracurium (0.15 or 0.25 mg/kg) or vecuronium (0.15 mg/kg), administered as a bolus immediately after induction of anesthesia with fentanyl and thiopental, would provide a faster onset time and better tracheal intubating conditions than previously reported. We sought to determine whether patients given muscle relaxants in this commonly used induction sequence would exhibit cutaneous, systemic, or chemical evidence of histamine release. Onset time of the relaxants was determined by using mechanomyography. Intubating conditions were scored on a defined interval scale by an anesthesiologist blinded to the relaxant administered. Heart rate and arterial blood pressure were measured noninvasively every minute from 10 min before to 5 min after the application of the muscle relaxant. Mean (+/- SD) onset times for 0.25 mg/kg cisatracurium (68.3 +/- 19.5 s) and for 0.15 mg/kg vecuronium (69.5 +/- 29.2 s) were significantly different from those in the 0.15 mg/kg cisatracurium group (105 +/- 41.2 s). The intubating conditions were better with the larger dose of cisatracurium or vecuronium (P < 0.03). Although plasma histamine levels were not statistically different among groups, levels >1 ng/mL were observed in 5 of 40 patients who received cisatracurium but in none of the 20 patients who received vecuronium. There were no significant hemodynamic differences among the groups. In a dose of 0.25 mg/kg, cisatracurium has as rapid an onset time as vecuronium 0.15 mg/kg, but the former shows evidence of histamine release.

IMPLICATIONS

Cisatracurium has been considered a drug with a relatively slow onset but that has the significant benefit of being devoid of chemically mediated histamine release. In this study, we describe an onset time faster than previously reported when cisatracurium was given immediately after thiopental. We also note that several patients had abnormal histamine levels after cisatracurium administration.

摘要

未标注

顺式阿曲库铵是一种起效缓慢的非去极化肌松药。我们对60例美国麻醉医师协会(ASA)身体状况分级为I或II级的患者进行了一项前瞻性、随机、双盲临床试验,以评估在使用芬太尼和硫喷妥钠诱导麻醉后立即静脉推注顺式阿曲库铵(0.15或0.25mg/kg)或维库溴铵(0.15mg/kg),是否会比先前报道的起效更快且气管插管条件更好。我们试图确定按照这种常用诱导顺序给予肌松药的患者是否会出现组胺释放的皮肤、全身或化学证据。通过使用肌动描记法测定肌松药的起效时间。由对所给予的肌松药不知情的麻醉医师按照定义的间隔量表对插管条件进行评分。在应用肌松药前10分钟至应用后5分钟期间,每分钟无创测量心率和动脉血压。0.25mg/kg顺式阿曲库铵组的平均(±标准差)起效时间为(68.3±19.5秒),0.15mg/kg维库溴铵组为(69.5±29.2秒),与0.15mg/kg顺式阿曲库铵组(105±41.2秒)有显著差异。给予较大剂量的顺式阿曲库铵或维库溴铵时,插管条件更好(P<0.03)。尽管各组间血浆组胺水平无统计学差异,但在接受顺式阿曲库铵的40例患者中有5例组胺水平>1ng/mL,而接受维库溴铵的20例患者中无一例出现这种情况。各组间血流动力学无显著差异。0.25mg/kg剂量的顺式阿曲库铵起效时间与0.15mg/kg维库溴铵一样快,但前者有组胺释放的证据。

启示

顺式阿曲库铵一直被认为是一种起效相对缓慢但具有无化学介导组胺释放这一显著优点的药物。在本研究中,我们描述了在硫喷妥钠后立即给予顺式阿曲库铵时起效时间比先前报道的更快。我们还注意到,给予顺式阿曲库铵后有几名患者组胺水平异常。

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