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WHO multinational study of three misoprostol regimens after mifepristone for early medical abortionHonkanen, Henry ...OBJECTIVES: To compare the side effect profiles of regimens of oral and vaginal administration of misoprostol after a single oral dose of 200 mg of mifepristone and to investigate patients' ... perceptions of medical abortion. DESIGN: Double-blind, randomised controlled trial. SETTING: Fifteen gynaecological clinics in 11 countries. POPULATION: A total of 2219 healthy pregnant women requesting medical abortion with < or =63 days of amenorrhoea. Two thousand women were asked about their perceptions of the method. METHODS: Mifepristone 200 mg orally on day one, followed by 0.8 mg misoprostol either orally or vaginally on day three. The oral group (O/O group) and one of the vaginal groups (V/O group) continued with 0.4 mg of oral misoprostol, and the vaginal-only group (V-only group) with oral placebo, twice daily for seven days. Side effects were recorded daily by women and reported at each visit. After misoprostol administration at the clinic, side effects were recorded at 1-hour interval up to 3 hours. Patients' perceptions were asked at the second follow up visit, six weeks after treatment. MAIN OUTCOME MEASURES: The outcomemeasures were the following: pregnancy-related symptoms (nausea, vomiting, breast tenderness, fatigue, dizziness, headache), drug-related side effects (diarrhoea, fever, rash and blood pressure change), side effects related to the abortion process (lower abdominal pain) and women's perceptionsof the method. RESULTS: The pregnancy-related symptoms decreased inall groups after misoprostol, and breast tenderness decreased already after mifepristone. Oral administration of misoprostol was associated with a higher frequency of nausea and vomiting than vaginal administration at 1 hour after administration. With oral misoprostol, diarrhoea was more frequent at 1, 2 andat 3 hours after administration than with vaginal administration. (Abstract truncated at 2000 characters)Vir: BJOG. - ISSN 1470-0328 (Letn. 111, št. 7, 2004, str. 715-725)Vrsta gradiva - članek, sestavni delLeto - 2004Jezik - angleškiCOBISS.SI-ID - 21805529
Avtor
Honkanen, Henry |
Pretnar-Darovec, Alenka
Teme
Patient Satisfaction |
Abdominal Pain |
Chemically Induced |
Abortifacient Agents, Steroidal |
Administration & Dosage |
Adverse Effects |
Abortion, Induced |
Methods |
Amenorrhea |
Etiology |
Analgesics |
Therapeutic Use |
Dizziness |
Chemically Induced |
Double-Blind Method |
Fatigue |
Chemically Induced |
Headache |
Chemically Induced |
Mifepristone |
Administration & Dosage |
Adverse Effects |
Misoprostol |
Adverse Effects |
Administration & Dosage |
Nausea |
Chemically Induced |
Parity |
Perception |
Treatment Outcome |
Vomiting |
Chemically Induced |
Bolnik, zadovoljstvo |
Abortivi steroidni |
Abortus inducirani |
Amenoreja |
Analgetiki |
Bruhanje |
Dvojnoslepa metoda |
Glavobol |
Mifepriston |
Mizoprostol |
Omotica |
Rodnost |
Slabost |
Trebušna bolečina |
Utrujenost |
Zaznava |
Zdravljenje, izid
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