Oral Misoprostol Solution for Induction of Labour
- PMID: 28405116
- PMCID: PMC5371524
- DOI: 10.1007/s13224-016-0937-4
Oral Misoprostol Solution for Induction of Labour
Abstract
Objective: To determine the effects of oral misoprostol solution for induction of labour.
Study design: This is a prospective observational study.
Setting: This study was conducted in Government Medical College, Aurangabad.
Method: Patients undergoing induction of labour after 36 weeks of pregnancy were allocated by randomization to induction of labour with oral misoprostol solution administered 2 h apart. Delivery within 24 h after induction with oral misoprostol solution was the primary outcome on which the sample size was based. The data were analysed by Statistical Software for Social Sciences software.
Result: Two hundred patients were randomly selected for induction with oral misoprostol solution. There were no significant differences in substantive outcomes. Vaginal delivery within 24 h was achieved in 80.5 % of patients. The caesarean section rate was 19.5 %. Uterine hyperactivity occurred in 4 % of patients. The response to induction of labour in women with unfavourable cervices (modified Bishop's score <2) was somewhat slower with misoprostol, induction to delivery interval was more, oxytocin requirement was more, and vaginal delivery rate was less.
Conclusion: This new approach to oral misoprostol solution administration was successful in achieving vaginal delivery rate in 24 h in 80.5 % of patients; rate of LSCS was less 19.5 %.
Keywords: Induction of labour; Induction-delivery interval; Oral misoprostol solution.
Conflict of interest statement
Conflict of interest
None.
Ethical Approval
Approval of ethical committee has been taken from Government Medical College, Aurangabad.
References
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- Hofmeyr GJ, Alfirevic Z, Matonhodze B, et al. Titrated oral misoprostol solution for induction of labour: a multi-centre, randomised trial. RCOG2001, Br J Obstet Gynaecol. 2001;P11:S0306-5456(01)00231-5. - PubMed
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