Abstract | OBJECTIVE: To assess the efficacy and maternal side-effects of oral misoprostol for second trimester termination of pregnancies with intrauterine fetal death. METHODS: A prospective descriptive study was conducted on 63 pregnant women who had intrauterine fetal death with unfavorable cervix (Bishop scores </=4). All received 400 micro g of misoprostol orally every 4 h until favorable cervix was achieved. Main outcome measures included success rate of termination within 12, 24, 36 and 48 h, mean induction to delivery time and maternal side-effects. RESULTS: The success rates of termination within 12, 24, 36, 48 h were 50.8%, 84.1%, 88.9% and 92.1%, respectively. Mean induction to delivery time in cases of delivery within 48 h was 13.2 +/- 8.4 h, range 2.25-22.9 h. The most common maternal side-effect was chill (33.3%). No serious maternal complication was detected. CONCLUSION: 400 micro g oral misoprostol every 4 h is effective for pregnancy termination in cases of intrauterine fetal death and may be an alternative regimen because of its ease and convenience.
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Authors | Saipin Pongsatha, Theera Tongsong |
Journal | The journal of obstetrics and gynaecology research
(J Obstet Gynaecol Res)
Vol. 30
Issue 3
Pg. 217-20
(Jun 2004)
ISSN: 1341-8076 [Print] Australia |
PMID | 15210046
(Publication Type: Evaluation Study, Journal Article)
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Chemical References |
- Abortifacient Agents, Nonsteroidal
- Misoprostol
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Topics |
- Abortifacient Agents, Nonsteroidal
(administration & dosage)
- Abortion, Therapeutic
(methods)
- Administration, Oral
- Adolescent
- Adult
- Female
- Fetal Death
- Humans
- Misoprostol
(administration & dosage)
- Pregnancy
- Pregnancy Trimester, Second
- Prospective Studies
- Treatment Outcome
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