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    Decreased placental and transcellular permeation of cefuroxime in pregnant women with diabetes

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    Authors
    Lalic-Popovic, M.
    Paunkovic, J.
    Grujic, Z.
    Golocorbin-Kon, S.
    Milasinovic, L.
    Al-Salami, Hani
    Mikov, M.
    Date
    2015
    Type
    Journal Article
    
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    Citation
    Lalic-Popovic, M. and Paunkovic, J. and Grujic, Z. and Golocorbin-Kon, S. and Milasinovic, L. and Al-Salami, H. and Mikov, M. 2015. Decreased placental and transcellular permeation of cefuroxime in pregnant women with diabetes. Journal of Diabetes. [In Press].
    Source Title
    Journal of Diabetes
    DOI
    10.1111/1753-0407.12288
    ISSN
    1753-0393
    School
    School of Pharmacy
    URI
    http://hdl.handle.net/20.500.11937/37305
    Collection
    • Curtin Research Publications
    Abstract

    Background: The present study investigated the transcellular and placental permeation of cefuroxime, an antibiotic used in cesarean sections, in pregnant women with diabetes and hypertension. Methods: Fifty-three women scheduled for cesarean section were divided into three groups: healthy women (n=18), women with arterial hypertension (n=21), and women with gestational diabetes (n=14). All women received 1.5g, i.v., cefuroxime. Cefuroxime concentrations were measured in maternal venous plasma before, during, and after delivery, as well as in fetal umbilical cord vein and artery plasma during delivery. The effects of diabetes and hypertension on cefuroxime placental-permeation were assessed by the fetomaternal plasma concentration ratios. Pharmacokinetic non-compartmental model analyses were performed and results were compared using anova. Results: Fetomaternal drug concentration ratios were lower in the diabetic group than in the hypertensive and control groups. There were no significant differences in umbilical arterial:venous plasma drug concentration ratios in the diabetic and hypertensive groups compared with the control group. Apparent volume of distribution and clearance were significantly lower in the diabetic group compared with the control and hypertensive groups. Conclusions: Diabetes led to decreased placental transfer of cefuroxime, as well as volume of distribution and clearance, but did not affect other pharmacokinetic parameters. Hypertension had no significant effect on the permeation of cefuroxime or on its pharmacokinetics. Prophylactic concentrations of cefuroxime were reached in all groups, but the dosing time of cefuroxime should not be less than 30min or greater than 2h prior to delivery.

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