Inducing labor at 41 weeks’ gestation for women with low-risk pregnancies was associated with a 1.4% lower risk of adverse perinatal outcomes, compared with expectant management until 42 weeks, according to results from a randomized, controlled noninferiority trial.
“As with every intervention in the natural birth process, the decision to induce labour must be made with caution, as the expected benefits should outweigh possible adverse effects for both mother and child,” wrote Judit K.J. Keulen, of the department of obstetrics and gynecology at Amsterdam University Medical Center, and her colleagues. “The results of our study should be used to inform women approaching a gestational age of 41 weeks, so they can weigh the respective outcomes and decide whether to be induced at 41 weeks or to continue pregnancy until 42 weeks.”
Ms. Keulen and her colleagues randomized 1,801 women from 123 primary care midwifery practices and 45 hospitals across the Netherlands to receive induction (n = 900) at 41 weeks or expectant management (n = 901) at 42 weeks between 2012 and 2016. The investigators used a composite of perinatal mortality measures, which included Apgar score less than 7 at 5 minutes, arterial pH less than 7.05, meconium aspiration syndrome, neonatal ICU admission, intracranial hemorrhage, and/or brachial plexus injury.
Overall, there were 15 adverse perinatal outcomes in the induction group (1.7%) and 28 adverse outcomes in the expectant management group (3.1%; absolute risk difference, −1.4%). A lower number of infants (n = 11; 1.2%) in the induction group had an Apgar score less than 7 at 5 minutes, compared with infants (n = 23; 2.6%) in the expectant management group (relative risk, 0.48), and there were zero infants and 3 infants (RR, 0.3%) in the induction and expectant management groups, respectively, who had an Apgar score less than 4 at 5 minutes.
Three (0.3%) infants in the induction group and 8 (0.9%) infants in the expectant management group were admitted to the NICU (RR, 0.38). There was one (0.1%) case of fetal death in the induction group and two (0.2%) cases in the expectant management group, but there were no neonatal deaths in either group. With regard to composite adverse maternal outcomes, there were no significant differences between the induction group (n = 122; 14%) and the expectant management group (n = 102; 11%) and both groups had the same number of cesarean sections (n = 97; 11%).