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首页> 外文期刊>Journal of the Indian Medical Association. >A pharmacodynamic basis for the peak effect of vecuronium: peak twitch versus peak tetanic fade.
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A pharmacodynamic basis for the peak effect of vecuronium: peak twitch versus peak tetanic fade.

机译:维库溴铵峰值作用的药效学基础:峰值抽搐与峰值破伤风褪色。

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摘要

Double burst stimulation (DBS), a tetanic test, shows two types of changes during nondepolarising neuromuscular block (NMB) viz, amplitude (D1) suppression and fading of second response (D2), quantified as DBS ratio (D2/D1). During subclinical dose effect of vecuronium bromide both parameters show peak suppression at two distinct intervals. To evaluate, which of the two is the true peak effect of vecuronium, twenty-two ASA 1 patients were given im buprenorphine (5 micro/kg) premedication and iv diazepam (0.1 mg/kg). Vecuronium bromide (0.015 mg/kg) effect was monitored by stimulating ulnar nerve at the wrist. Adductor pollicis response of supramaximal DBS stimuli was recorded on myograph. DBS ratio was calculated with each DBS stimuli, using pocket calculator. In randomly allocated group 1 (n = 11) patients, repeat dose of vecuronium (0.08 mg/kg) was given at the peak D1 suppression and in group 2 (n = 11) at peak DBS ratio suppression. The onset time of repeat dose of vecuronium monitored by one Hz stimuli, to '0' response in group 2 (37.3 +/- 6.65 second) was significantly (p < 0.01) shorter than in group 1 patients (46.8 +/- 9.3 second). It was noteworthy that at the repeat dose of vecuronium while D1 showed recovery in group 2 patients, DBS ratio was concomitantly and significantly lower (0.37 +/- 0.10) (more intense NMB) than in group 1 (0.49 +/- 0.17) patients, with quicker onset of repeat dose. These findings suggest that as the NMB agents show two types of changes during clinical monitoring, DBS test seems to be a better clinical pharmacodynamics-monitoring test for NMB agents. In addition, the peak tetanic fade (peak DBS ratio suppression) correlated with peak effect of vecuronium than the usually measured peak twitch suppression.
机译:两次破发刺激(DBS)是一项强直性测试,显示了非去极化神经肌肉阻滞(NMB)期间的两种变化,即振幅(D1)抑制和第二反应(D2)的淡入,量化为DBS比(D2 / D1)。在亚临床剂量的溴化维库溴铵作用期间,两个参数在两个不同的时间间隔处均显示出峰抑制。为了评估维库溴铵的真正峰值效果,两者中的哪一个是真正的峰值疗效,对22名ASA 1患者给予了丁丙诺啡(5 micro / kg)的预防用药和静脉注射地西epa(0.1 mg / kg)。通过刺激腕尺神经来监测维库溴铵(0.015 mg / kg)的作用。在肌电描记器上记录了最大DBS刺激的收效者花粉病反应。使用袖珍计算器对每种DBS刺激计算DBS比率。在随机分配的第1组(n = 11)患者中,在D1抑制峰时重复给予维库溴铵(0.08 mg / kg),在第2组(n = 11)抑制DBS比峰时给予重复剂量的维库溴铵。在第2组(37.3 +/- 6.65秒)中,通过1 Hz刺激监测的维库溴铵重复剂量对“ 0”应答的开始时间比第1组患者(46.8 +/- 9.3秒)明显缩短(p <0.01) )。值得注意的是,在重复剂量维库溴铵的同时,D1在第2组患者中恢复,DBS比率相应地且显着低于第1组(0.49 +/- 0.17)(0.37 +/- 0.10)(更强的NMB)。 ,重复给药的发作更快。这些发现表明,由于NMB药物在临床监测期间显示出两种类型的变化,DBS测试似乎是NMB药物更好的临床药效学监测方法。另外,与通常测量的峰值抽搐抑制相比,峰值强直褪色(峰值DBS比抑制)与维库溴铵的峰值效应相关。

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