Obstetrics/GynecologyORIGINAL ARTICLE

Associations in fetal outcomes from cesarean sections with maternal comorbidities: a cross-sectional study of the Pregnancy Risk Assessment Monitoring System

Mackenzie Enmeier, DO; Elise Stephenson, DO; Jordyn Prince, DO; Caroline Markey, MD; Binh Phung, DO; and Micah Hartwell, PhD
Notes and Affiliations
Notes and Affiliations

Received: March 27, 2024

Accepted: April 15, 2025

Published: May 22, 2025

  • Mackenzie Enmeier, DO, 

    Department of Obstetrics and Gynecology,
    8586
    University of Kansas School of Medicine-Wichita
    , Wichita, KS, USA

  • Elise Stephenson, DO, 

    Department of Pediatrics, University of Oklahoma School of Community Medicine, Tulsa, OK, USA

  • Jordyn Prince, DO, 

    Department of Obstetrics and Gynecology, SSM Health St. Anthony Hospital, Oklahoma City, OK, USA

  • Caroline Markey, MD, 

    Department of Obstetrics and Gynecology, University of Oklahoma School of Community Medicine, Tulsa, OK, USA

  • Binh Phung, DO, 

    Department of Pediatrics, Oklahoma State University Center for Health Sciences, Tulsa, OK, USA

  • Micah Hartwell, PhD, 

    Department of Psychiatry and Behavioral Sciences, Oklahoma State University Center for Health Sciences, Tulsa, OK, USA

Abstract

Context: Cesarean sections (CSs) can reduce maternal and fetal risk in medically necessary cases. However, studies show that CSs are associated with negative fetal outcomes, including birth defects, low birth weight, delayed fetal resuscitation, neonatal acidosis, and even infant mortality. Maternal comorbidities play a role in determining if a CS is necessary and may contribute to negative fetal outcomes following a CS.

Objectives: The primary objective of this study was to determine the prevalence of negative fetal outcomes such as low birth weight, birth defects, prolonged hospital stay, and infant mortality in CS deliveries and their increased risk of occurrence among mothers with comorbidities.

Methods: We conducted a cross-sectional study of the Phase 8 (2016–2019) Pregnancy Risk Assessment Monitoring System (PRAMS) to assess the associations of the aforementioned birth outcomes with pre-existing conditions such as high blood pressure (HBP), depression, and type II diabetes mellitus, as well as demographic factors in the United States (US).

Results: Our findings showed that mothers who delivered via CS with pre-existing or gestational HBP, or gestational diabetes, were less likely to experience infant mortality (adjusted odds ratio [AOR]: 0.4; confidence interval [CI]: 0.17–0.92, AOR: 0.2; CI: 0.09–0.44, and AOR: 0.09; CI: 0.03–0.33, respectively). However, mothers who delivered via CS with pre-existing or gestational diabetes, pre-existing or gestational HBP, or pre-existing or gestational depression had higher rates of prolonged infant hospital stay (AOR: 1.73; CI: 1.41–2.11, AOR: 1.21; CI: 1.05–1.39, AOR: 1.77; CI: 1.5–2.09, AOR: 2.58; CI: 2.31–2.88, AOR: 1.25; CI: 1.09–1.43 and AOR: 1.33; CI: 1.16–1.52, respectively). Likewise, mothers who delivered via CS with pre-existing or gestational HBP, or pre-existing or gestational depression, were more likely to deliver an infant with low birth weight (AOR: 1.88; CI: 1.62–2.19, AOR: 2.7; CI: 2.45–2.98, AOR: 1.24; CI: 1.09–1.41, and OR: 1.28; CI: 1.14–1.42, respectively).

Conclusions: Our study revealed a lower incidence of infant mortality following CS deliveries among mothers with pre-existing or gestational HBP, or gestational diabetes. This suggests a potential benefit in antenatal testing in mothers experiencing depression or those with no comorbidities. Additionally, infants born to mothers with these comorbidities experienced longer hospital stays, and infants of mothers with pre-existing or gestational HBP and depression had a higher incidence of low birth weight. Given the increasing rates of diabetes, HBP, and depression in the US, it is crucial to provide healthcare professionals with the necessary guidance to prevent and manage these comorbidities and improve fetal outcomes following CS deliveries.

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