Pharmacokinetics of meperidine in spinal anaesthesia.

M. Naguib, C. E. Famewo, A. Absood
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引用次数: 12

Abstract

Five male patients undergoing haemorrhoidectomy received intrathecal meperidine 1 mg X kg-1 as the sole anaesthetic agent. Plasma concentration-time profiles were investigated. The peak plasma concentration of meperidine was 175 +/- 78.8 ng X ml-1 (mean +/- SD) and this occurred 90 minutes after intrathecal injection. The plasma concentrations generally were lower than those necessary for systemic analgesic effects. The terminal elimination half life of meperidine (t 1/2 beta) in the plasma was 198 minutes. Intrathecal meperidine produced good surgical anaesthesia in all patients studied. The mean duration of sensory and motor block was 77 +/- 18.8 and 47 +/- 7.4 minutes respectively. Four patients did not require any analgesic supplement during the postoperative period. No patient developed clinically evident respiratory depression or neurological sequelae. The pharmacokinetic data suggests that intrathecal meperidine provides prolonged postoperative analgesia through a regional effect on opioid receptors in the spinal cord.
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哌替啶在脊柱麻醉中的药代动力学。
5例男性痔疮切除术患者以鞘内哌哌啶1 mg X kg-1作为唯一麻醉剂。研究了血浆浓度-时间分布。甲哌啶的血药浓度峰值为175 +/- 78.8 ng X ml-1(平均+/- SD),发生在鞘内注射90分钟后。血浆浓度一般低于全身性镇痛作用所需的浓度。哌替啶在血浆中的终末消除半衰期(t1 /2 β)为198分钟。鞘内哌哌啶对所有患者均产生良好的手术麻醉效果。感觉阻滞和运动阻滞的平均持续时间分别为77 +/- 18.8和47 +/- 7.4分钟。4例患者术后不需要任何镇痛剂。没有患者出现临床明显的呼吸抑制或神经系统后遗症。药代动力学数据表明鞘内哌替啶通过对脊髓阿片受体的局部作用延长了术后镇痛时间。
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