A recent study investigated maternal and neonatal
outcomes associated with planned elective labor induction (eIOL) – between 39
weeks and 39 weeks and 6 days of gestation. The research focused on nulliparous
singleton pregnancies, with outcomes tracked throughout the hospital stay.
This was a prospective observational study. Here,
consecutive nulliparous women with singleton pregnancies undergoing eIOL were
recruited within the specified gestational age range. Cases with planned
cesarean section or contraindications for vaginal delivery were excluded. The
primary outcomes included cesarean section incidence and neonatal intensive
care requirements. In contrast, the secondary outcomes were induction-delivery
interval, chorioamnionitis, postpartum hemorrhage, meconium aspiration
syndrome, APGAR scores at 1 minute, and neonatal mortality.
Overall, 304 mothers were assessed, of which 26.3%
underwent cesarean section; 15.8% of the neonates required intensive care.
Additionally, 4.9% of neonates needed respiratory support at birth, and the
mean induction-delivery interval was 19 hours and 42 minutes. There were 3%
cases with postpartum hemorrhage, no instances of chorioamnionitis, and 3.6% of
babies with an APGAR score ≤7 at 1 minute. While the meconium aspiration
syndrome cases were 2.9%, no maternal or neonatal mortality was reported.
The findings suggested that inducing labor at 39 weeks in low-risk nulliparous women did not lead to a reduction in cesarean section frequency or an increase in adverse perinatal outcomes.
Source:
Shajan A, Menon B, Gilvaz S, Biju N, Abraham
SV. The Journal of Obstetrics and Gynecology of India. 2023 Oct 31:1-7.
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