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Background: Postpartum hemorrhage is a major cause of maternal mortality and morbidity. It
has been identified that active management of third stage of labor is an
effective way in preventing postpartum hemorrhage. This randomized controlled
trial was conducted to compare sublingual misoprostol versus intravenous
oxytocin in the management of postpartum hemorrhage in nulliparous women.
Methods: In this randomized controlled trial conducted in Arash hospital from 2006
to 2009, Five hundred forty
two nulliparous pregnant women were enrolled. They were randomized to receive
either 400 microgram sublingual
misoprostol or 20 IU oxytocin
intravenously, immediately after the birth of newborn.
Results: Post partum Hemorrhage was significantly lower in women who received sublingual
misoprostol (p<0.0001). Patients who
received misoprostol had shorter length of third stage of labor (6.45
minute in misoprostol Vs 6.9
minute in oxytocin group, p=0.003). Comparison
of hemoglobin levels in two groups before and after delivery showed that there
is a significant lesser hemoglobin drop in misoprostol group p=0.046.
Side effects were more common in misoprostol group (p<0.0001).
However, they were not serious shivering (35.66%)
in misoprostol group and headache (9.63%)
in oxytocin group were the most common adverse effects.
Conclusions: Sublingual misoprostol is more effective than intravenous oxytocin in
preventing postpartum hemorrhage and is recommended for prevention of
postpartum hemorrhage.
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