Literature DB >> 17803714

Misoprostol for treatment of incomplete abortion at the regional hospital level: results from Tanzania.

B Shwekerela1, R Kalumuna, R Kipingili, N Mashaka, E Westheimer, W Clark, B Winikoff.   

Abstract

OBJECTIVE: To investigate the safety, efficacy, and acceptability of misoprostol versus manual vacuum aspiration (MVA) for treatment of incomplete abortion.
DESIGN: A prospective open-label randomised trial.
SETTING: Kagera Regional Hospital, Bukoba, Tanzania. SAMPLE: Three hundred women with a clinical diagnosis of incomplete abortion and a uterine size <12 weeks.
METHODS: A total of 150 women were randomised to either a single dose of 600 micrograms of oral misoprostol or MVA. If abortion was clinically complete at 7-day follow up, the woman was released from the study. If it was still incomplete, the woman was offered the choice of an additional 1-week follow up or immediate MVA. Cases still incomplete after a further week were offered MVA. MAIN OUTCOME MEASURES: Incidence of successful abortion (success defined as no secondary surgical intervention provided), incidence of adverse effects, patient satisfaction.
RESULTS: Success was very high in both arms (misoprostol: 99%; MVA: 100%; difference not significant). Most adverse effects were higher in the misoprostol arm, although the mean pain score was higher in the MVA arm (3.0 versus 3.5; P < 0.001). More women were very satisfied with misoprostol (75%) than with MVA (55%, P = 0.001), and a higher proportion of women in the misoprostol arm said that they would recommend the treatment to a friend (95% versus 75%, P < 0.001).
CONCLUSION: Misoprostol is as effective as MVA at treating incomplete abortion at uterine size of <12 weeks. The acceptability of misoprostol appears higher. Given the many practical advantages of misoprostol over MVA in low-resource settings, misoprostol should be more widely available for treatment of incomplete abortion in the developing world.

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Year:  2007        PMID: 17803714     DOI: 10.1111/j.1471-0528.2007.01469.x

Source DB:  PubMed          Journal:  BJOG        ISSN: 1470-0328            Impact factor:   6.531


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