Amoxicillin pharmacokinetics in pregnant women with preterm premature rupture of the membranes

被引:19
作者
Muller, Anouk E. [1 ]
DeJongh, Joost [3 ]
Oostvogel, Paul M. [2 ]
Voskuyl, Rob A. [4 ]
Doerr, Joep [1 ]
Danhof, Meindert [4 ]
Mouton, Johan W. [5 ]
机构
[1] Med Ctr Haaglanden, Dept Obstet & Gynecol, The Hague, Netherlands
[2] Med Ctr Haaglanden, Dept Clin Microbiol, The Hague, Netherlands
[3] LAP&P Consultants BV, Leiden, Netherlands
[4] Leiden Univ, Leiden Amsterdam Ctr Drug Res, Div Pharmacol, Leiden, Netherlands
[5] Canisius Wilhelmina Hosp, Dept Clin Microbiol & Infect Dis, Nijmegen, Netherlands
关键词
clearance; interindividual variability; pregnancy; preterm premature rupture of the membranes; volume of distribution;
D O I
10.1016/j.ajog.2007.05.018
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: This study was undertaken to study the pharmacokinetics of intravenously administered amoxicillin in pregnant women with preterm premature rupture of the membranes (PPROM). STUDY DESIGN: Healthy women with PPROM were recruited and treated with amoxicillin (2 g initially and 1 g subsequently). Blood samples were obtained from the opposite arm and concentrations determined with the use of high-pressure liquid chromatography. Nonlinear mixed-effects modeling was performed in nonlinear mixed effect ( population) modeling. RESULTS: The pharmacokinetics of 17 patients was described by a 3-compartment model. Clearance and volume of distribution at steady state were 22.8 L/h and 21.4 L/h, respectively, similar to values in nonpregnant individuals. There was little variability between patients. No relationship was observed between values of individual pharmacokinetic parameters and various covariates. CONCLUSION: The pharmacokinetics of amoxicillin in pregnant patients with PPROM similar to nonpregnant individuals. Given the small interindividual variability in pharmacokinetics, no dose adjustments are required to account for differences between subjects under normal circumstances.
引用
收藏
页码:108.e1 / 108.e6
页数:6
相关论文
共 36 条
[1]   PHARMACOKINETICS OF AMOXICILLIN AND FLUCLOXACILLIN FOLLOWING THE SIMULTANEOUS INTRAVENOUS ADMINISTRATION OF 4-G AND 1-G, RESPECTIVELY [J].
ADAM, D ;
KOEPPE, P ;
HEILMANN, HD .
INFECTION, 1983, 11 (03) :150-154
[2]   Animal model pharmacokinetics and pharmacodynamics: a critical review [J].
Andes, D ;
Craig, WA .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2002, 19 (04) :261-268
[3]   ABSORPTION AND DISPOSITION KINETICS OF AMOXICILLIN IN NORMAL HUMAN-SUBJECTS [J].
ARANCIBIA, A ;
GUTTMANN, J ;
GONZALEZ, G ;
GONZALEZ, C .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1980, 17 (02) :199-202
[4]  
BASTERT G, 1973, Zeitschrift fuer Geburtshilfe und Perinatologie, V177, P330
[5]   Recommended reading in population pharmacokinetic pharmacodynamics [J].
Bonate P.L. .
The AAPS Journal, 7 (2) :E363-E373
[6]   THE INVITRO ACTIVITY OF AMPICILLIN, AMOXICILLIN, CEPHALEXIN, NITROFURANTOIN, SULFADIAZINE AND TRIMETHOPRIM AGAINST STREPTOCOCCUS AGALACTIAE ISOLATED FROM URINARY AND OTHER INFECTIONS [J].
BRANDER, P ;
JOKIPII, L ;
JOKIPII, AMM .
INFECTION, 1982, 10 (05) :299-302
[7]   TRANSFER OF AMPICILLIN INTO FETUS AND AMNIOTIC FLUID FROM MATERNAL PLASMA IN LATE PREGNANCY [J].
BRAY, RE ;
BOE, RW ;
JOHNSON, WL .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1966, 96 (07) :938-&
[8]  
Centers for Disease Control and Prevention (CDC), 2002, MMWR Morb Mortal Wkly Rep, V51, P1
[9]   PHARMACOKINETICS OF AMPICILLIN AND SULBACTAM IN PREGNANCY [J].
CHAMBERLAIN, A ;
WHITE, S ;
BAWDON, R ;
THOMAS, S ;
LARSEN, B .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1993, 168 (02) :667-673
[10]   COMPARATIVE PHARMACOKINETIC ANALYSIS OF AMOXYCILLIN USING OPEN 2-COMPARTMENT AND 3-COMPARTMENT MODELS [J].
DALHOFF, A ;
KOEPPE, P .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1982, 22 (03) :273-279