Spontaneous abortion: a randomized, controlled trial comparing surgical evacuation with conservative management using misoprostol

Fertil Steril. 1999 Jun;71(6):1054-9. doi: 10.1016/s0015-0282(99)00128-4.

Abstract

Objective: To compare the efficacy of surgical evacuation of the uterus with medical evacuation using misoprostol in cases of spontaneous abortion.

Design: A prospective, randomized, controlled trial.

Setting: A university teaching hospital.

Patient(s): Six hundred thirty-five women who aborted spontaneously and who consented to pretreatment randomization.

Intervention(s): Routine surgical evacuation or medical evacuation of the uterus using misoprostol.

Main outcome measure(s): Immediate, short-term (2-3 weeks), and medium-term (6 months) medical complications.

Result(s): There was a significantly lower incidence of immediate and short-term complications in the group treated with misoprostol compared with the surgically treated group. There were also fewer major complications in the 6 months after treatment in the medically treated group. Approximately 50% of the medically treated group subsequently required surgical evacuation, and these subjects required significantly more analgesia.

Conclusion(s): Treatment with misoprostol can reduce the demand for surgical evacuation in cases of spontaneous abortion, and its use is associated with fewer medical complications.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abortifacient Agents, Nonsteroidal / adverse effects
  • Abortifacient Agents, Nonsteroidal / therapeutic use
  • Abortion, Incomplete / drug therapy
  • Abortion, Incomplete / surgery
  • Abortion, Spontaneous / drug therapy*
  • Abortion, Spontaneous / surgery*
  • Adult
  • Analgesia
  • Female
  • Humans
  • Misoprostol / adverse effects
  • Misoprostol / therapeutic use*
  • Postoperative Complications
  • Pregnancy

Substances

  • Abortifacient Agents, Nonsteroidal
  • Misoprostol