Abstract | OBJECTIVE: The purpose of this study was to determine the effect of intrapartum prophylactic antibiotics in the prevention of postpartum sepsis in laboring women who were infected with HIV. STUDY DESIGN: In a double-blind, randomized trial that was conducted in Durban (South Africa), pregnant women who were infected with HIV in whom vaginal delivery was anticipated were randomized to receive either a single dose of cefoxitin (2 g) or placebo intrapartum. Signs of sepsis were evaluated within 72 hours and at 1 and 2 weeks postpartum. RESULTS: Of the 424 women who were enrolled, 213 women received cefoxitin, and 211 women received placebo. Both groups were comparable in all baseline parameters. The overall sepsis rate was 19% (40/211 women) in the placebo group and 16.9% (36/213 women) in the cefoxitin group (P = .581). There was a 53% reduction in risk of postpartum endometritis in the cefoxitin group (95% confidence interval, 0.24-0.9). CONCLUSION: The use of prophylactic intrapartum cefoxitin in HIV-infected women reduces the risk of postpartum endometritis.
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Authors | H M Sebitloane, J Moodley, T M Esterhuizen |
Journal | American journal of obstetrics and gynecology
(Am J Obstet Gynecol)
Vol. 198
Issue 2
Pg. 189.e1-6
(Feb 2008)
ISSN: 1097-6868 [Electronic] United States |
PMID | 17997391
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Anti-Bacterial Agents
- Cefoxitin
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Topics |
- Adult
- Anti-Bacterial Agents
(administration & dosage, therapeutic use)
- Antibiotic Prophylaxis
- Cefoxitin
(administration & dosage, therapeutic use)
- Double-Blind Method
- Drug Administration Schedule
- Endometritis
(mortality, pathology, prevention & control)
- Female
- HIV Infections
- Humans
- Incidence
- Pregnancy
- Pregnancy Complications, Infectious
- Puerperal Disorders
(mortality, pathology, prevention & control)
- South Africa
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