%0 Journal Article %T Vaginal misoprostol versus vaginal dinoprostone for cervical ripening and induction of labour: An individual participant data meta-analysis of randomised controlled trials. %A Patabendige M %A Chan F %A Vayssiere C %A Ehlinger V %A Van Gemund N %A le Cessie S %A Prager M %A Marions L %A Rozenberg P %A Chevret S %A Young DC %A Le Roux PA %A Gregson S %A Waterstone M %A Rolnik DL %A Mol BW %A Li W %J BJOG %V 131 %N 9 %D 2024 Aug 29 %M 38425020 %F 7.331 %R 10.1111/1471-0528.17794 %X BACKGROUND: Induction of labour (IOL) is common practice and different methods carry different effectiveness and safety profiles.
OBJECTIVE: To compare the effectiveness, and maternal and perinatal safety outcomes of IOL with vaginal misoprostol versus vaginal dinoprostone using individual participant data from randomised clinical trials.
METHODS: The following databases were searched from inception to March 2023: CINAHL Plus, ClinicalTrials.gov, Cochrane Pregnancy and Childbirth Group Trial Register, Ovid Embase, Ovid Emcare, Ovid MEDLINE, Scopus and the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP).
METHODS: Randomised controlled trials (RCTs), with viable singleton gestation, no language restrictions, and all published and unpublished data.
METHODS: An individual participant data meta-analysis was carried out.
RESULTS: Ten of 52 eligible trials provided individual participant data, of which two were excluded after checking data integrity. The remaining eight trials compared low-dose vaginal misoprostol versus dinoprostone, including 4180 women undergoing IOL, which represents 32.8% of all participants in the published RCTs. Of these, 2077 were assigned to low-dose vaginal misoprostol and 2103 were assigned to vaginal dinoprostone. Compared with vaginal dinoprostone, low-dose vaginal misoprostol had a comparable rate of vaginal birth. Composite adverse perinatal outcomes did not differ between the groups. Compared with vaginal dinoprostone, composite adverse maternal outcomes were significantly lower with low-dose vaginal misoprostol (aOR 0.80, 95% CI 0.65-0.98, P = 0.03, I2 = 0%).
CONCLUSIONS: Low-dose vaginal misoprostol and vaginal dinoprostone for IOL are comparable in terms of effectiveness and perinatal safety. However, low-dose vaginal misoprostol is likely to lead to a lower rate of composite adverse maternal outcomes than vaginal dinoprostone.