Pharmacokinetics of ertapenem in patients with varying degrees of renal insufficiency and in patients on hemodialysis

被引:42
|
作者
Mistry, Goutam C.
Majumdar, Anup K.
Swan, Suzanne
Sica, Domenic
Fisher, Alison
Xu, Yang
Hesney, Michael
Xi, Liwen
Wagner, John A.
Deutsch, Paul J.
机构
[1] Merck Res Labs, Dept Clin Pharmacol, Rahway, NJ 07065 USA
[2] Merck Sharp & Dohme Ltd, Dept Drug Metab, West Point, PA 19486 USA
[3] Dept Clin Biostat, Blue Bell, PA USA
[4] Merck Res Labs, Minneapolis, MN USA
[5] Virginia Commonwealth Univ, Med Coll Virginia, Dept Clin Pharmacol & Hypertens, Richmond, VA 23298 USA
来源
JOURNAL OF CLINICAL PHARMACOLOGY | 2006年 / 46卷 / 10期
关键词
ertapenem; pharmacokinetics; renal insufficiency;
D O I
10.1177/0091270006291839
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Eitapenem is a parenteral beta-lactam carbapenem antibiotic. This open-label study examined the pharmacokinetics of single 1-g intravenous doses of ertapenem, administered over 30 minutes, in patients with mild, moderate, and advanced renal insufficiency (RI) and in patients with end-stage renal disease (ESRD) requiring hemodialysis. Pharmacokinetics were compared with historical controls pooled across healthy young and elderly subjects. Area under the concentration-time curve from time zero to infinity increased 7% in mild, 53% in moderate, 158% in advanced RI, and 192% in ESRD,end of infusion concentration changed minimally, half-life was 4.5 hours in the historical control group and 4.4, 6.1, 10.6, and 14.1 hours in mild RI, moderate RI, advanced RI, and ESRD, respectively. Hemodialysis cleared similar to 30% of the dose. The recommended dose in mild to moderate RI and after hemodialysis is unchanged at 1 g daily; and in advanced RI and ESRD is reduced to 0.5 g daily. If the daily dose is given 6 hours prior to hemodialysis, a supplementary 150-mg dose (30% of the daily dose) is recommended postdialysis.
引用
收藏
页码:1128 / 1138
页数:11
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