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Randomized Controlled Trial Clinical Trial
A randomised controlled trial of antibiotic prophylaxis in elective caesarean delivery.
- J S Bagratee, J Moodley, I Kleinschmidt, and W Zawilski.
- Department of Obstetrics and Gynaecology, Nelson R Mandela School of Medicine, University of Natal, South Africa.
- BJOG. 2001 Feb 1;108(2):143-8.
ObjectiveTo determine whether prophylactic antibiotic administration using cefoxitin at the time of elective caesarean section significantly reduces infectious morbidity.SettingA tertiary teaching hospital in a large urban city in South Africa.ParticipantsWomen undergoing elective caesarean section.DesignA prospective, double-blind randomised placebo-controlled trial.MethodsFour hundred and eighty women undergoing elective caesarean section had cefoxitin or placebo administration after umbilical cord clamping. Postpartum complications including febrile morbidity, wound infection, endometritis, urinary tract infection, pneumonia and transient postpartum fever were recorded, as were the duration of hospital stay and the need for therapeutic antibiotics.ResultsWound infection was the most common complication occurring in 13.3% and 12.5% of women in the placebo and cefoxitin groups, respectively. Prophylactic antibiotics did not decrease febrile morbidity, wound infection, endometritis, urinary tract infection and pneumonia. Women who received cefoxitin stayed on average a day less in hospital than those who received placebo (6.9 vs 7.8 days, risk difference 0.94 CI 1.57 - 0.31 days). Eleven women (4.6%) in the placebo group and eight (3.4%) in the cefoxitin group had microbiological evidence of wound infection. Staphylococcus aureus was the most common pathogen (43%) isolated. Similar proportions in both groups (6.3% placebo and 5.1% cefoxitin) required a course of therapeutic antibiotics.ConclusionAntibiotic prophylaxis with cefoxitin in elective caesarean section did not reduce post-operative infectious morbidity in this double-blind randomised placebo controlled trial.
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