New England Journal of Medicine · 2016 · 283 citations · 25 references
MedicineObstetricsPharmacotherapyAntimicrobial PharmacotherapyMaternal-fetal MedicineObstetric SurgeryAntibiotic ProphylaxisAntimicrobial ProphylaxisCesarean DeliveryInfection Prevention During LaborProphylactic Antimicrobial UseSurgical ProphylaxisAntibiotic Therapy In PregnancyCesarean Section ProphylaxisIntrapartum Antibiotic ProphylaxisMaternal Antibiotic ProphylaxisMaternal-intrapartum Antibiotic ProphylaxisObstetric Antimicrobial ProphylaxisObstetric ProphylaxisSystemic Antibiotic Prophylaxis
Azithromycin added to standard cesarean prophylaxis may further reduce postoperative infection rates. The study assessed the benefits and safety of adjunctive azithromycin prophylaxis in nonelective cesarean deliveries. In a multicenter randomized trial, 2013 women received either 500 mg IV azithromycin plus standard prophylaxis or placebo plus standard prophylaxis. Adjunctive azithromycin halved the composite infection rate (6.1% vs 12.0%) and reduced endometritis, wound infection, and serious maternal adverse events, with no neonatal benefit. The trial was funded by the Eunice Kennedy Shriver National Institute of Child Health and Human Development and registered at ClinicalTrials.gov (NCT01235546).
The addition of azithromycin to standard regimens for antibiotic prophylaxis before cesarean delivery may further reduce the rate of postoperative infection. We evaluated the benefits and safety of azithromycin-based extended-spectrum prophylaxis in women undergoing nonelective cesarean section.In this trial conducted at 14 centers in the United States, we studied 2013 women who had a singleton pregnancy with a gestation of 24 weeks or more and who were undergoing cesarean delivery during labor or after membrane rupture. We randomly assigned 1019 to receive 500 mg of intravenous azithromycin and 994 to receive placebo. All the women were also scheduled to receive standard antibiotic prophylaxis. The primary outcome was a composite of endometritis, wound infection, or other infection occurring within 6 weeks.The primary outcome occurred in 62 women (6.1%) who received azithromycin and in 119 (12.0%) who received placebo (relative risk, 0.51; 95% confidence interval [CI], 0.38 to 0.68; P<0.001). There were significant differences between the azithromycin group and the placebo group in rates of endometritis (3.8% vs. 6.1%, P=0.02), wound infection (2.4% vs. 6.6%, P<0.001), and serious maternal adverse events (1.5% vs. 2.9%, P=0.03). There was no significant between-group difference in a secondary neonatal composite outcome that included neonatal death and serious neonatal complications (14.3% vs. 13.6%, P=0.63).Among women undergoing nonelective cesarean delivery who were all receiving standard antibiotic prophylaxis, extended-spectrum prophylaxis with adjunctive azithromycin was more effective than placebo in reducing the risk of postoperative infection. (Funded by the Eunice Kennedy Shriver National Institute of Child Health and Human Development; C/SOAP ClinicalTrials.gov number, NCT01235546 . ).
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Guideline for Prevention of Surgical Site Infection, 1999
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