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Research Article| Volume 116, ISSUE 1, P34-38, September 10, 2004

Influence of misoprostol or prostaglandin E2 for induction of labor on the incidence of pathological CTG tracing: a randomized trial

      Abstract

      Objective: To compare the efficacy and safety of misoprostol (prostaglandin E1 (PGE1)) with dinoprostone (prostaglandin E2 (PGE2)) for third trimester cervical ripening and labor induction. Study design: Patients requiring induction of labor were randomly assigned to receive either 50 μg of intravaginal misoprostol every 4 h or 0.5 mg of intracervical dinoprostone gel every 6 h. Eligibility criteria included gestation = 36 weeks. Primary outcome was the time interval from induction to delivery; secondary outcomes were mode of delivery, perinatal outcome, and interpretation of cardiotocogram (CTG) records. Results: Two hundred women were randomly enrolled to receive either misoprostol (n=100) or dinoprostone (n=100). Time induction-to-delivery at 12, 24 and 48 h and the need for oxytocin were reduced with misoprostol (P<0.05). Pathological CTG tracing according to FIGO and Melchior scores were more frequent in the misoprostol-treated group (P<0.001). Conclusion: Misoprostol shortened the induction-to-delivery interval, but is associated with a higher incidence of abnormal CTG than prostaglandin E2.

      Keywords

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