Pregnancy outcome after exposure to misoprostol in Brazil: a prospective, controlled study.

Abstract

BACKGROUND:

Misoprostol, a synthetic prostaglandin E1 analog is labeled for the treatment of gastric and duodenal ulcers. In Brazil, where abortion is not a legal procedure, there is a widespread popular misuse of this drug in abortion attempts. This misuse and the fact that, in many cases the desired pregnancy termination does not occur, raise concerns about fetal safety. Case reports of congenital anomalies after maternal use of misoprostol have been published. The objective of this work was to compare pregnancy outcome following misoprostol exposure with a matched control group. This is the first prospective controlled study on fetal safety after misoprostol use.

METHODS:

A prospective, observational cohort study with 86 exposed and 86 pair-matched, non-exposed controls.

RESULTS:

There was no significant difference in the rates of major or minor birth between exposed compared to non-exposed infants (2/67 vs 2/81, major defects; 7/67 vs. 3/81, minor anomalies) There were significantly more miscarriages in the exposed group (17.1% vs. 5.8%; relative risk, 2.97; 95% confidence interval, 1.12 to 7.88). There was no statistical difference in gestational age at delivery, birth weight, sex ratio, rate of prematurity, low birth weight, or rates of cesarean section between groups.

CONCLUSIONS:

Our study, despite its limited statistical power, does not suggest a potent teratogenic action of misoprostol exposure during pregnancy.

• Authors: L Schüler, A Pastuszak, T V Sanseverino, I M Orioli, D Brunoni, P Ashton-Prolla, F Silva da Costa, R Giugliani, A M Couto, S B Brandao, G Koren
• Journal: Reproductive toxicology (Elmsford, N.Y.) (Reprod Toxicol) 1999 Mar-Apr Vol. 13 Issue 2 Pg. 147-51 ISSN: 0890-6238 [Print] United States
• PMID: 10213522 (Publication Type: Clinical Trial, Controlled Clinical Trial, Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't)

Chemical References

• Abortifacient Agents, Nonsteroidal
• Anti-Ulcer Agents
• Misoprostol

Topics

• Abnormalities, Drug-Induced (etiology)
• Abortifacient Agents, Nonsteroidal (adverse effects)
• Abortion, Criminal
• Abortion, Induced
• Anti-Ulcer Agents (adverse effects, therapeutic use)
• Brazil
• Female
• Fetal Death (chemically induced)
• Follow-Up Studies
• Humans
• Infant, Newborn
• Male
• Misoprostol (adverse effects, therapeutic use)
• Peptic Ulcer (drug therapy)
• Pregnancy
• Pregnancy Outcome
• Prospective Studies