Bricker S R, Telford R J, Booker P D
Department of Anaesthetics, Royal Liverpool Hospital, United Kingdom.
Anesthesiology. 1989 Jun;70(6):942-7. doi: 10.1097/00000542-198906000-00010.
Pharmacokinetics and blood concentrations of bupivacaine were studied after intercostal nerve blocks were performed intraoperatively using 1.5 mg.kg-1 in 11 neonates (age 0-28 days) and 11 infants between age 1 and 6 months. The study aimed to provide pharmacokinetic data that are limited in these age groups, and to identify any adverse effects of intercostal nerve block in infancy. Arterial blood samples were taken at 0, 5, 10, 15, 20, 30, 60, 120, 240, and 360 min. Whole blood bupivacaine was assayed by high-performance liquid chromatography. Peak blood concentrations were attained within 10 min in 18 of 22 subjects, and were 087 micrograms.ml-1 [corrected] +/- 0.56 micrograms.ml-1 (mean and SD) and 0.91 +/- 0.27 micrograms.ml-1 in neonates and infants, respectively. Pharmacokinetic variables in the two groups included elimination half-life (t1/2 beta): 132 +/- 59 min and 102 +/- 39 min; steady-state volume of distribution (Vdss): 2.56 +/- 0.76 l.kg-1 and 2.17 +/- 0.17 l.kg-1; and total body clearance (Clt): 16.93 +/- 9.32 ml.min-1.kg-1 and 15.71 +/- 6.99 ml.min-1.kg-1. There was no statistically significant difference between neonates and infants with regard to any of these parameters. Patients were further divided into those with acyanotic and cyanotic disease. Cyanotic infants were significantly heavier than acyanotic infants (P less than 0.05), but no other differences were demonstrated. No adverse effects resulting from the technique were identified.(ABSTRACT TRUNCATED AT 250 WORDS)
对11名新生儿(年龄0 - 28天)和11名1至6个月大的婴儿在术中进行肋间神经阻滞,使用剂量为1.5mg/kg布比卡因后,研究了布比卡因的药代动力学和血药浓度。该研究旨在提供这些年龄组中有限的药代动力学数据,并确定婴儿期肋间神经阻滞的任何不良反应。在0、5、10、15、20、30、60、120、240和360分钟采集动脉血样。采用高效液相色谱法测定全血布比卡因含量。22名受试者中有18名在10分钟内达到血药浓度峰值,新生儿和婴儿的血药浓度峰值分别为0.87微克/毫升±0.56微克/毫升(均值和标准差)和0.91±0.27微克/毫升。两组的药代动力学变量包括消除半衰期(t1/2β):132±59分钟和102±39分钟;稳态分布容积(Vdss):2.56±0.76升/千克和2.17±0.17升/千克;以及全身清除率(Clt):16.93±9.32毫升/分钟·千克和15.71±6.99毫升/分钟·千克。在这些参数方面,新生儿和婴儿之间没有统计学上的显著差异。患者进一步分为无紫绀和有紫绀疾病的两组。有紫绀的婴儿明显比无紫绀的婴儿重(P<0.05),但未显示其他差异。未发现该技术导致的不良反应。(摘要截断于250字)