ergometrine/fever

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A randomized controlled trial of prophylactic sublingual misoprostol versus intramuscular methyl-ergometrine versus intramuscular 15-methyl PGF2alpha in active management of third stage of labor.

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OBJECTIVE To compare the efficacy and side effects of 0.2 mg methyl-ergometrine IM, 400 microg misoprostol sublingual and 125 microg 15 methyl PGF2alpha IM in active management of third stage of labor. METHODS Two hundred low risk pregnant women with induced or spontaneous labor were randomized to

A Study to Compare the Efficacy of Misoprostol, Oxytocin, Methyl-ergometrine and Ergometrine-Oxytocin in Reducing Blood Loss in Active Management of 3rd Stage of Labor.

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OBJECTIVE The purpose of the study was to compare the efficacy of misoprostol 400 μg per rectally, injection oxytocin 10 IU intramuscular, injection methylergometrine 0.2 mg intravenously and injection (0.5 mg ergometrine + 5 IU oxytocin) intramuscular on reducing blood loss in third stage of labor,

Uterotonic agents for preventing postpartum haemorrhage: a network meta-analysis.

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Postpartum haemorrhage (PPH) is the leading cause of maternal mortality worldwide. Prophylactic uterotonic drugs can prevent PPH, and are routinely recommended. There are several uterotonic drugs for preventing PPH but it is still debatable which drug is best. To identify the most effective

The misoprostol third stage of labour study: a randomised controlled comparison between orally administered misoprostol and standard management.

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OBJECTIVE To compare misoprostol with standard oxytocic regimens in the prevention of postpartum haemorrhage. METHODS Randomised controlled trial. METHODS Obstetric unit in a large teaching hospital. METHODS One thousand women randomised to 500 microg misoprostol given orally or to standard oxytocic

Intraumbilical veinous injection oxytocin in the active management of third stage of labour.

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OBJECTIVE To determine the role of intraumbilical vein oxytocin reducing blood loss during and after one hour of delivery of placenta and its efficacy in reducing the frequency of retained placenta. METHODS Randomized controlled trial. METHODS Combined Military Hospital, Multan, from June 2002 to

Treatment for primary postpartum haemorrhage.

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BACKGROUND Primary postpartum haemorrhage (PPH) is one of the top five causes of maternal mortality in both developed and developing countries. OBJECTIVE To assess the effectiveness and safety of pharmacological, surgical and radiological interventions used for the treatment of primary

Uterotonic agents for preventing postpartum haemorrhage: a network meta-analysis.

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Postpartum haemorrhage (PPH) is the leading cause of maternal mortality worldwide. Prophylactic uterotonic agents can prevent PPH, and are routinely recommended. The current World Health Organization (WHO) recommendation for preventing PPH is 10 IU (international units) of

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