Comparison of mifepristone combination with misoprostol and misoprostol alone in the management of intrauterine death

Objectives: To compare the efficacy and safety of misoprostol and mifepristone combination with misoprostol alone in management of intrauterine death. Materials and Methods: It is a prospective study carried out in 40 pregnant women admitted with intrauterine death after 28 weeks of gestation at a t...

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Main Authors: Damyanti Sharma (Author), Savita Rani Singhal (Author), Poonam (Author), Anshu Paul (Author), Kunika (Author)
Format: Book
Published: Elsevier, 2011-09-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Damyanti Sharma  |e author 
700 1 0 |a Savita Rani Singhal  |e author 
700 1 0 |a Poonam  |e author 
700 1 0 |a Anshu Paul  |e author 
700 1 0 |a Kunika  |e author 
245 0 0 |a Comparison of mifepristone combination with misoprostol and misoprostol alone in the management of intrauterine death 
260 |b Elsevier,   |c 2011-09-01T00:00:00Z. 
500 |a 1028-4559 
500 |a 10.1016/j.tjog.2011.07.007 
520 |a Objectives: To compare the efficacy and safety of misoprostol and mifepristone combination with misoprostol alone in management of intrauterine death. Materials and Methods: It is a prospective study carried out in 40 pregnant women admitted with intrauterine death after 28 weeks of gestation at a tertiary care referral centre divided into two groups of 20 each. Every alternate patient was assigned Group I and Group II. Group I (combination group) - the women received 200 mg of mifepristone; and after 36 hours, misoprostol was administered orally (100 μg if pregnancy was <37 weeks and 50 μg if pregnancy was >37 weeks) for every 3 hour till they went into active labor for a maximum of four doses. Group II (misoprostol group) - Women received oral misoprostol (100 μg if pregnancy was <37 weeks and 50 μg if pregnancy was >37 weeks) for every three hours till she went into active labor for maximum of four doses. Primary outcome measures were achievement of successful induction and induction delivery interval (IDI). Women who did not deliver after four doses of misoprostol were considered as failure. In all the women, bishop score before the start of mifepristone and misoprostol, induction delivery interval, and adverse effect of the drug were noted. Data were analyzed by using Student t test and Chi-square test. Results: In the Group I, 60% of women, delivered with mifepristone alone. The rest of the patients [8 (40%)] had significant improvement of the bishop score after 36 hour. Parity, gestation, and bishop score did not affect the success of induction in the Group I. IDI was significantly less in the Group I (6.72 ± 3.34) as compared with that of the Group II (11.81 ± 6.33). Parity, gestation, and bishop score did not affect the IDI in the two groups. Number of doses of misoprostol required were significantly less in patients who were pretreated with mifepristone. Conclusion: Combination of mifepristone and misoprostol is more effective than the misoprostol alone for induction of labor in women with intrauterine death. 
546 |a EN 
690 |a Intrauterine death 
690 |a Mifepristone 
690 |a Misoprostol 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
655 7 |a article  |2 local 
786 0 |n Taiwanese Journal of Obstetrics & Gynecology, Vol 50, Iss 3, Pp 322-325 (2011) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S1028455911001288 
787 0 |n https://doaj.org/toc/1028-4559 
856 4 1 |u https://doaj.org/article/9afacba23f6048f08f051622f0a15ca9  |z Connect to this object online.