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老年患者同时口服环丙沙星和利福平治疗的多剂量药代动力学

Multiple-dose pharmacokinetics of concurrent oral ciprofloxacin and rifampin therapy in elderly patients.

作者信息

Chandler M H, Toler S M, Rapp R P, Muder R R, Korvick J A

机构信息

College of Pharmacy, University of Kentucky, Lexington 40536-0082.

出版信息

Antimicrob Agents Chemother. 1990 Mar;34(3):442-7. doi: 10.1128/AAC.34.3.442.

Abstract

The purpose of this clinical study was to investigate the influence of concomitant drug therapy with ciprofloxacin and rifampin on the individual pharmacokinetic profile of each agent in elderly patients. Twelve nursing home patients (age, 74 +/- 7 years), colonized with methicillin-resistant Staphylococcus aureus, were randomized to receive 14-day therapy with oral ciprofloxacin (750 mg every 12 h) (group A; n = 6) or ciprofloxacin (750 mg every 12 h) and oral rifampin (300 mg every 12 h) (group B; n = 6). Serial blood samples were obtained from 0 to 12 h following ciprofloxacin doses 1 and 13 and from 0 to 36 h after the last ciprofloxacin dose. No significant differences (P greater than 0.05) were found between or within groups in any pharmacokinetic parameter. The mean ciprofloxacin oral clearance values were 0.35 +/- 0.06, 0.41 +/- 0.15, and 0.38 +/- 0.11 liter/h per kg for doses 1, 13, and 28, respectively, in group A patients. The mean oral clearance values in group B patients for the respective doses were 0.53 +/- 0.36, 0.32 +/- 0.13, and 0.36 +/- 0.17 liter/h per kg. Likewise, no significant differences (P greater than 0.05) in rifampin pharmacokinetic parameters were found when compared with historical controls. These data suggest that ciprofloxacin and rifampin may be given concomitantly in standard clinical dosing regimens. The combination results in therapeutic levels of both drugs and appears to be safe for administration to elderly nursing home patients.

摘要

本临床研究的目的是调查环丙沙星和利福平联合药物治疗对老年患者中每种药物个体药代动力学特征的影响。12名耐甲氧西林金黄色葡萄球菌定植的养老院患者(年龄74±7岁)被随机分为两组,一组接受为期14天的口服环丙沙星治疗(每12小时750mg)(A组;n = 6),另一组接受环丙沙星(每12小时750mg)和口服利福平(每12小时300mg)治疗(B组;n = 6)。在环丙沙星第1剂和第13剂给药后0至12小时以及最后一剂环丙沙星给药后0至36小时采集系列血样。在任何药代动力学参数方面,组间或组内均未发现显著差异(P>0.05)。A组患者第1剂、第13剂和第28剂环丙沙星的平均口服清除率值分别为每千克体重0.35±0.06、0.41±0.15和0.38±0.11升/小时。B组患者各剂量的平均口服清除率值分别为每千克体重0.53±0.36、0.32±0.13和0.36±0.17升/小时。同样,与历史对照相比,利福平药代动力学参数也未发现显著差异(P>0.05)。这些数据表明,环丙沙星和利福平可以按照标准临床给药方案联合使用。联合用药可使两种药物达到治疗水平,且对老年养老院患者给药似乎是安全的。

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