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Int J Gynaecol Obstet · Apr 2001
Randomized Controlled Trial Clinical TrialMisoprostol for prevention of postpartum hemorrhage.
- A Bugalho, A Daniel, A Faúndes, and M Cunha.
- Maternity of the Hospital Central de Maputo, Maputo, Mozambique. abugalho@zebra.uem.mz
- Int J Gynaecol Obstet. 2001 Apr 1;73(1):1-6.
ObjectiveTo compare the effectiveness of 400 microg rectal misoprostol in 5 cm(3) of saline with oxytocin 10 IU, i.m., in reducing bleeding during the third stage of labor.DesignA double blind, randomized, clinical trial including 663 women with uncomplicated vaginal delivery who received misoprostol (n=324) or oxytocin (n=339).Main Outcome MeasuresChanges in hemoglobin and hematocrit from before to 72 h postpartum; blood loss during the third stage; duration of the third stage of labor; need for additional oxytocic drug; frequency of requisition and of administration of blood; changes in blood pressure; and occurrence of side effects.ResultsNo significant differences were observed between groups, before and 72 h postpartum, in mean hemoglobin and hematocrit, on volume of blood loss and duration of third stage of labor. The incidence of shivering and mean temperature (P<0.01) was significantly greater among women receiving misoprostol than oxytocin.ConclusionsMisoprostol administered as a micro-enema, 400 microg in 5 ml of saline during the third stage of labor, appears to be as effective as oxytocin 10 IU, i.m., but misoprostol produced more side effects than oxytocin.
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