Am J Perinatol 2015; 32(14): 1311-1317
DOI: 10.1055/s-0035-1563718
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Does Induction with Misoprostol Impact the Small for Gestational Age Neonate?

Megan E. Foeller
1   Department of Obstetrics and Gynecology, Medical College of Wisconsin, Milwaukee, Wisconsin
,
Meredith O. Cruz
1   Department of Obstetrics and Gynecology, Medical College of Wisconsin, Milwaukee, Wisconsin
,
Michelle A. Kominiarek
2   Department of Obstetrics and Gynecology, University of Illinois, Chicago, Illinois
3   Department of Obstetrics and Gynecology, Northwestern University, Chicago, Illinois
,
Judith U. Hibbard
1   Department of Obstetrics and Gynecology, Medical College of Wisconsin, Milwaukee, Wisconsin
› Author Affiliations
Further Information

Publication History

19 July 2015

21 July 2015

Publication Date:
09 September 2015 (online)

Abstract

Objective To compare outcomes in small for gestational age neonates induced with misoprostol to other cervical ripening agents. We hypothesized that misoprostol use will demonstrate no significant difference in outcomes compared with alternative agents.

Study Design Small for gestational age neonates (<10th percentile for gestational age) from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) sponsored Consortium on Safe Labor database were analyzed. Neonates induced with misoprostol ± oxytocin (n = 451) were compared with neonates induced with prostaglandin E2 ± oxytocin and/or mechanical dilation ± oxytocin (n = 663). Primary outcomes included intrapartum fetal distress, cesarean section for fetal distress, cesarean section for any reason, neonatal intensive care unit admission, low 5-minute Apgar, and composite neonatal morbidity. Multiple logistic regression was used to calculate adjusted odds ratios (aORs). Data were analyzed using SAS.

Results Small for gestational age neonates induced with misoprostol ± oxytocin compared with alternative agents had decreased low 5-minute Apgar scores (aOR 0.27 [0.10–0.71]). No significant differences were demonstrated among very small for gestational age neonates (<5th percentile for gestational age).

Conclusion Our results suggest that misoprostol does not increase risk of adverse outcomes in small for gestational age neonates; however, prospective studies are warranted to further assess optimal cervical ripening agents in this population.

Note

This study was conducted at the Medical College of Wisconsin (Milwaukee, WI) and University of Illinois, Chicago (Chicago, IL).


This study was presented in a poster format at the Society of Maternal-Fetal Medicine 35th Annual Meeting (February 2–7, 2015), San Diego, CA, February 5, 2015, #199.


 
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