Influence of Body Weight, Ethnicity, Oral Contraceptives, and Pregnancy on the Pharmacokinetics of Azithromycin in Women of Childbearing Age

被引:18
|
作者
Fischer, James H. [1 ]
Sarto, Gloria E. [2 ,3 ]
Habibi, Mitra [1 ]
Kilpatrick, Sarah J. [4 ]
Tuomala, Ruth E. [5 ]
Shier, Janice M. [6 ]
Wollett, Lori [7 ]
Fischer, Patricia A. [1 ]
Khorana, Kinnari S. [1 ]
Rodvold, Keith A. [1 ]
机构
[1] Univ Illinois, Coll Pharm, Dept Pharm Practice, Chicago, IL 60680 USA
[2] Univ Wisconsin, Dept Obstet & Gynecol, Sch Med & Publ Hlth, Madison, WI 53706 USA
[3] Univ Wisconsin Obstet Serv, Meriter Hosp, Madison, WI USA
[4] Univ Illinois, Coll Med, Dept Obstet & Gynecol, Chicago, IL 60612 USA
[5] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Obstet & Gynecol, Boston, MA 02115 USA
[6] Univ Michigan, Dept Obstet & Gynecol, Coll Med, Ann Arbor, MI 48109 USA
[7] Univ Wisconsin, Off Clin Trials, Madison, WI USA
关键词
IMMEDIATE-RELEASE FORMULATIONS; ORGANIC ANION TRANSPORTERS; EXTENDED-RELEASE; LUNG-TISSUE; SERUM; DISPOSITION; AMOXICILLIN; RESISTANCE; DESIGN; CLARITHROMYCIN;
D O I
10.1128/AAC.00717-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Women of childbearing age commonly receive azithromycin for the treatment of community-acquired infections, including during pregnancy. This study determined azithromycin pharmacokinetics in pregnant and nonpregnant women and identified covariates contributing to pharmacokinetic variability. Plasma samples were collected by using a sparse-sampling strategy from pregnant women at a gestational age of 12 to 40 weeks and from nonpregnant women of childbearing age receiving oral azithromycin for the treatment of an infection. Pharmacokinetic data from extensive sampling conducted on 12 healthy women were also included. Plasma samples were assayed for azithromycin by high-performance liquid chromatography. Population data were analyzed by nonlinear mixed-effects modeling. The population analysis included 53 pregnant and 25 nonpregnant women. A three-compartment model with first-order absorption and a lag time provided the best fit of the data. Lean body weight, pregnancy, ethnicity, and the coadministration of oral contraceptives were covariates identified as significantly influencing the oral clearance of azithromycin and, except for oral contraceptive use, intercompartmental clearance between the central and second peripheral compartments. No other covariate relationships were identified. Compared to nonpregnant women not receiving oral contraceptives, a 21% to 42% higher dose-adjusted azithromycin area under the plasma concentration-time curve (AUC) occurred in non-African American women who were pregnant or receiving oral contraceptives. Conversely, azithromycin AUCs were similar between pregnant African American women and nonpregnant women not receiving oral contraceptives. Although higher levels of maternal and fetal azithromycin exposure suggest that lower doses be administered to non-African American women during pregnancy, the consideration of azithromycin pharmacodynamics during pregnancy should guide any dose adjustments.
引用
收藏
页码:715 / 724
页数:10
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