Perinatal pharmacokinetics of azithromycin for cesarean prophylaxis

被引:56
作者
Sutton, Amelia L. [1 ]
Acosta, Edward P. [2 ]
Larson, Kajal B. [2 ]
Kerstner-Wood, Corenna D. [2 ]
Tita, Alan T. [1 ]
Biggio, Joseph R. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Obstet & Gynecol, Div Maternal Fetal Med, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Pharmacol & Toxicol, Div Clin Pharmacol, Birmingham, AL 35294 USA
基金
美国国家卫生研究院;
关键词
azithromycin; breast milk; cesarean delivery; endometritis; pharmacokinetics; Ureaplasma; wound infection; BRONCHOPULMONARY DYSPLASIA; ANTIBIOTIC-PROPHYLAXIS; UREAPLASMA; ENDOMETRITIS; MYCOPLASMAS;
D O I
10.1016/j.ajog.2015.01.015
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
OBJECTIVE: Postpartum infections are polymicrobial and typically include Ureaplasma, an intracellular microbe that is treated by macrolides such as azithromycin. The aim of this study was to evaluate the perinatal pharmacokinetics of azithromycin after a single preincision dose before cesarean delivery. STUDY DESIGN: Thirty women who underwent scheduled cesarean delivery were assigned randomly to receive 500 mg of intravenous azithromycin that was initiated 15, 30, or 60 minutes before incision and infused over 1 hour. Serial maternal plasma samples were drawn from the end of infusion up to 8 hours after the infusion. Samples of amniotic fluid, umbilical cord blood, placenta, myometrium, and adipose tissue were collected intraoperatively. Breast milk samples were collected 12-48 hours after the infusion in 8 women who were breastfeeding. Azithromycin was quantified with high performance liquid chromatography separation coupled with tandem mass spectrometry detection. Plasma pharmacokinetic parameters were estimated with the use of noncompartmental analysis and compartmental modeling and simulations. RESULTS: The maximum maternal plasma concentration was reached within 1 hour and exceeded the in vitro minimum inhibitory concentration (MIC50) of 250 ng/mL of Ureaplasma spp in all 30 patients. The concentrations were sustained with a half-life of 6.7 hours. The median concentration of azithromycin in adipose tissue was 102 ng/g, which was below the MIC50. The median concentration in myometrium was 402 ng/g, which exceeded the MIC50. Azithromycin was detectable in both the umbilical cord plasma and amniotic fluid after the single preoperative dose. Azithromycin concentrations in breast milk were high and were sustained up to 48 hours after the single dose. Simulations demonstrated accumulation in breast milk after multiple doses. CONCLUSION: A single dose of azithromycin achieves effective plasma and tissue concentrations and is transported rapidly across the placenta. The tissue concentrations that are achieved in the myometrium exceed the MIC50 for Ureaplasma spp.
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页数:6
相关论文
共 20 条
[1]   Transplacental Transfer of Azithromycin and Its Use for Eradicating Intra-amniotic Ureaplasma Infection in a Primate Model [J].
Acosta, Edward P. ;
Grigsby, Peta L. ;
Larson, Kajal B. ;
James, Amanda M. ;
Long, Mary C. ;
Duffy, Lynn B. ;
Waites, Ken B. ;
Novy, Miles J. .
JOURNAL OF INFECTIOUS DISEASES, 2014, 209 (06) :898-904
[2]   Randomized clinical trial of extended spectrum antibiotic prophylaxis with coverage for Ureaplasma urealyticum to reduce post-cesarean delivery endometritis [J].
Andrews, WW ;
Hauth, JC ;
Cliver, SP ;
Savage, K ;
Goldenberg, RL .
OBSTETRICS AND GYNECOLOGY, 2003, 101 (06) :1183-1189
[3]   ASSOCIATION OF POSTCESAREAN DELIVERY ENDOMETRITIS WITH COLONIZATION OF THE CHORIOAMNION BY UREAPLASMA-UREALYTICUM [J].
ANDREWS, WW ;
SHAH, SR ;
GOLDENBERG, RL ;
CLIVER, SP ;
HAUTH, JC ;
CASSELL, GH .
OBSTETRICS AND GYNECOLOGY, 1995, 85 (04) :509-514
[4]  
[Anonymous], AM J OBSTET GYNECOL
[5]  
[Anonymous], 2011, Obstet Gynecol
[6]   Timing of administration of prophylactic antibiotics for caesarean section: a systematic review and meta-analysis [J].
Baaqeel, H. ;
Baaqeel, R. .
BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 2013, 120 (06) :661-669
[7]   Use of Azithromycin for the Prevention of Bronchopulmonary Dysplasia in Preterm Infants: A Randomized, Double-Blind, Placebo Controlled Trial [J].
Ballard, Hubert O. ;
Shook, Lori A. ;
Bernard, Philip ;
Anstead, Michael I. ;
Kuhn, Robert ;
Whitehead, Vicki ;
Grider, Deb ;
Crawford, Timothy N. ;
Hayes, Don, Jr. .
PEDIATRIC PULMONOLOGY, 2011, 46 (02) :111-118
[8]  
D'Argenio DZ., 2009, ADAPT 5 User's Guide: Pharmacokinetic/Pharmacodynamic Systems Analysis Software
[9]   Maternal azithromycin therapy for Ureaplasma intraamniotic infection delays preterm delivery and reduces fetal lung injury in a primate model [J].
Grigsby, Peta L. ;
Novy, Miles J. ;
Sadowsky, Drew W. ;
Morgan, Terry K. ;
Long, Mary ;
Acosta, Ed ;
Duffy, Lynn B. ;
Waites, Ken B. .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2012, 207 (06) :475.e1-475.e14
[10]   Pharmacokinetics, Safety, and Biologic Effects of Azithromycin in Extremely Preterm Infants at Risk for Ureaplasma Colonization and Bronchopulmonary Dysplasia [J].
Hassan, Hazem E. ;
Othman, Ahmed A. ;
Eddington, Natalie D. ;
Duffy, Lynn ;
Xiao, Li ;
Waites, Ken B. ;
Kaufman, David A. ;
Fairchild, Karen D. ;
Terrin, Michael L. ;
Viscardi, Rose M. .
JOURNAL OF CLINICAL PHARMACOLOGY, 2011, 51 (09) :1264-1275