Jaruratanasirikul Sutep, Sriwiriyajan Somchai
Department of Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkla 90110, Thailand.
J Antimicrob Chemother. 2003 Sep;52(3):518-21. doi: 10.1093/jac/dkg378. Epub 2003 Aug 13.
The aim of this study was to compare the pharmacokinetics and pharmacodynamics of meropenem when administered by 3 h infusion or bolus injection regimens.
The study was a randomized three-way crossover study with a 1 week wash-out period in 12 healthy volunteers. Each subject received a single dose of meropenem in three regimens: (i) bolus injection of 1 g meropenem; (ii) 3 h infusion of 1 g meropenem; and (iii) 3 h infusion of 0.5 g meropenem.
Following bolus injection of 1 g meropenem, the mean +/- s.d. percentages of the t > MIC of 4, 2 and 1 mg/L were 42.50 +/- 6.20%, 54.38 +/- 7.64% and 67.04 +/- 8.47% of an 8 h dosing interval, respectively. For the 3 h infusion of 1 g meropenem, the percentages of the t > MIC of 4, 2 and 1 mg/L were 59.27 +/- 7.34%, 71.97 +/- 8.63% and 86.07 +/- 9.41% of an 8 h dosing interval, respectively. For the 3 h infusion of 0.5 g meropenem, the percentages of the t > MIC of 4, 2 and 1 mg/L were 47.27 +/- 5.34%, 59.36 +/- 6.60% and 71.44 +/- 8.45% of an 8 h dosing interval, respectively.
We conclude that a 3 h infusion of 0.5 g or 1 g of meropenem both give greater values for t > MIC than a 1 g bolus and that intermittent infusion may be a useful mode of administration in tropical countries where drug instability may prevent the use of continuous infusion.
本研究旨在比较美罗培南采用3小时输注或静脉推注给药方案时的药代动力学和药效学。
本研究为随机三交叉研究,12名健康志愿者中有1周的洗脱期。每位受试者接受三种给药方案的单剂量美罗培南:(i) 静脉推注1g美罗培南;(ii) 3小时输注1g美罗培南;(iii) 3小时输注0.5g美罗培南。
静脉推注1g美罗培南后,在8小时给药间隔内,4、2和1mg/L的t>MIC平均±标准差百分比分别为42.50±6.20%、54.38±7.64%和67.04±8.47%。对于3小时输注1g美罗培南,在8小时给药间隔内,4、2和1mg/L的t>MIC百分比分别为59.27±7.34%、71.97±8.63%和86.07±9.41%。对于3小时输注0.5g美罗培南,在8小时给药间隔内,4、2和1mg/L的t>MIC百分比分别为47.27±5.34%、59.36±6.60%和71.44±8.45%。
我们得出结论,0.5g或1g美罗培南3小时输注的t>MIC值均高于1g静脉推注,并且在药物不稳定可能妨碍持续输注使用的热带国家,间歇输注可能是一种有用的给药方式。