Midtrimester pregnancy termination: a randomized trial of prostaglandin E2 versus concentrated oxytocin

Am J Obstet Gynecol. 1992 Oct;167(4 Pt 1):1112-6. doi: 10.1016/s0002-9378(12)80049-4.

Abstract

Objectives: The purpose of this study was to determine whether a concentrated oxytocin infusion can reliably effect uterine evacuation in the midtrimester and whether such an infusion is associated with fewer side effects than prostaglandin E2 vaginal suppositories.

Study design: Patients received either prostaglandin E2 (n = 42) or oxytocin (n = 45) for indicated midtrimester abortions in a prospective, randomized trial. Treatment consisted of either prostaglandin E2 vaginal suppositories (one every 4 hours) or infusions of an escalating concentration of oxytocin (one every 4 hours). Unless delivery had occurred or was imminent after 24 hours, the agent was considered to have failed, and patients were crossed to the alternative method.

Results: Delivery indications were similar between the two groups. There were 6 (14%) first-agent failures with prostaglandin E2 and 9 (20%) with oxytocin (p = 0.48). Considering the failures and subsequent crossovers, 103 patient trial regimens were completed. Fever, nausea, vomiting, and diarrhea were more frequent with prostaglandin E2 (p < 0.005).

Conclusions: Concentrated oxytocin is a satisfactory alternative to prostaglandin E2 for midtrimester abortion.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Abortifacient Agents*
  • Abortion, Induced / methods*
  • Delivery, Obstetric
  • Dinoprostone / adverse effects
  • Dinoprostone / pharmacology*
  • Female
  • Humans
  • Osmolar Concentration
  • Oxytocin / adverse effects
  • Oxytocin / pharmacology*
  • Palliative Care
  • Pessaries
  • Pregnancy
  • Pregnancy Trimester, Second*
  • Prospective Studies
  • Treatment Failure

Substances

  • Abortifacient Agents
  • Oxytocin
  • Dinoprostone