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Erschienen in: Archives of Gynecology and Obstetrics 1/2011

01.07.2011 | Materno-fetal Medicine

Randomized trial of oral versus sublingual misoprostol 24 h after mifepristone for medical abortion

verfasst von: Krishna Dahiya, Sonika Mann, Smiti Nanda

Erschienen in: Archives of Gynecology and Obstetrics | Ausgabe 1/2011

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Abstract

Objectives

To assess the efficacy, side effects, and acceptability of medical abortion using oral mifepristone (200 mg) followed 24 h later by oral or sublingual misoprostol (400 μg).

Materials and methods

A total of 93 women with pregnancies up to 56 days of gestational age were assigned to two groups according to the different misoprostol regimen (group I 400 μg orally and group II 400 μg sublingually). The principle outcome measure was complete abortion defined as a complete expulsion of intrauterine contents without a need for surgical intervention 7 days after the procedure.

Results

Successful abortion occurred in 87.5% of patients in group 1 and 95.5% patients in group 2 (p = 0.166, 95% CI −0.194, 0.033). The patient acceptability and satisfaction rates were similar in both the groups.

Conclusion

It is concluded that 400 μg of sublingual misoprostol is as effective as oral misoprostol 24 h after mifepristone for medical abortion of ≤56 days.
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Metadaten
Titel
Randomized trial of oral versus sublingual misoprostol 24 h after mifepristone for medical abortion
verfasst von
Krishna Dahiya
Sonika Mann
Smiti Nanda
Publikationsdatum
01.07.2011
Verlag
Springer-Verlag
Erschienen in
Archives of Gynecology and Obstetrics / Ausgabe 1/2011
Print ISSN: 0932-0067
Elektronische ISSN: 1432-0711
DOI
https://doi.org/10.1007/s00404-010-1590-2

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