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Methotrexate and misoprostol for early abortion
1Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco.
Contraception
|October 1, 1993
Summary
Intramuscular methotrexate followed by vaginal misoprostol effectively terminates early intrauterine pregnancies. Vaginal misoprostol (800 mcg) proved more effective than oral misoprostol (600 mcg) for medical abortion.
Area of Science:
- Reproductive Endocrinology
- Pharmacology
- Gynecology
Background:
- Methotrexate is a cytotoxic agent used for gestational trophoblastic neoplasia and ectopic pregnancy.
- Its cytotoxic effects on intrauterine trophoblast suggest potential for early pregnancy termination.
- Minimal side effects are noted with low-dose methotrexate.
Purpose of the Study:
- To test the hypothesis that methotrexate's cytotoxic effects on intrauterine trophoblast can induce abortion.
- To compare the efficacy of oral versus vaginal misoprostol in conjunction with methotrexate for early pregnancy termination.
Main Methods:
- Ten pregnant women (< 8 weeks' gestation) received intramuscular methotrexate (50 mg/m2).
- Patients were subsequently administered either oral misoprostol (600 mcg, n=4) or vaginal misoprostol (800 mcg, n=6) three days later.
- Abortion rates, time to abortion, and complications were monitored.
Main Results:
- Vaginal misoprostol (800 mcg) resulted in significantly higher abortion rates (p = 0.005) compared to oral misoprostol (600 mcg).
- Abortion occurred within 3-8 hours with vaginal misoprostol, while oral administration showed delayed or no abortion.
- No methotrexate side effects were observed; vaginal bleeding averaged 29 days with vaginal misoprostol.
Conclusions:
- Intramuscular methotrexate combined with vaginal misoprostol is an effective method for early pregnancy termination.
- Vaginal administration of misoprostol is superior to oral administration in this regimen.
- This combination therapy offers a viable medical alternative for early intrauterine pregnancy.
Keywords:
Abortifacient Agents--administraction and dosageAbortifacient Agents--side effectsAbortion, Drug InducedAbortion, InducedAmericasBiologyCaliforniaComparative StudiesContraceptionContraceptive UsageDeveloped CountriesEndocrine SystemFamily PlanningFertility Control, PostconceptionGonadotropinsGonadotropins, ChorionicHormonesMethod AcceptabilityNorth AmericaNorthern AmericaPhysiologyPilot ProjectsProspective StudiesProstaglandins--administraction and dosageResearch MethodologyStudiesUltrasonicsUnited States