Poster Session 1
Category: Genetics
Poster Session 1
Neel K. Rana, BA, MD (he/him/his)
Fellow, Maternal-Fetal Medicine
Oregon Health & Science University
Portland, Oregon, United States
Bharti Garg, MBBS, MPH (she/her/hers)
Biostatistician 3
Oregon Health & Science University
Oregon Health & Science University, Oregon, United States
Alyssa R. Hersh, MD, MPH (she/her/hers)
Fellow
Oregon Health & Science University
Portland, Oregon, United States
Marie J. Boller, MD
Fellow Physician, Maternal-Fetal Medicine
Oregon Health and Science University
Portland, Oregon, United States
Aaron B. Caughey, MD, PhD
Chair and Professor of Obstetrics and Gynecology
Oregon Health & Science University
Oregon Health & Science University, Oregon, United States
Since 2001, the American College of Obstetrics and Gynecology (ACOG) has recommended cystic fibrosis (CF) screening in pregnancy for individuals at elevated risk. In 2011 ACOG updated their recommendation to universal screening in pregnant individuals. Despite increasing numbers of pregnant individuals learning they are carriers for CF, data regarding the impact of this status on pregnancy outcomes remain limited. This study aimed to investigate the risk of adverse perinatal outcomes in CF carriers compared to those without CF.
Study Design:
This is a retrospective cohort study using linked vital statistics and hospital discharge data for births in California (2008-2020). We included pregnant individuals with singleton gestation who delivered between 23 and 42 weeks. We compared demographic characteristics and outcomes between pregnant individuals who are CF carriers to those without a CF mutation. ICD-9 and ICD-10 codes were used to identify CF carriers (V83.81/Z14.1). Chi-square tests and multivariable Poisson regression models were used to assess risk of outcomes.
Results:
A total of 5,395,388 births were included, with 11,851 (0.22%) identified as CF carriers. CF carriers were more likely be non-Hispanic White (60.0% vs 26.5%,), to have private insurance (75.4% vs 48.4%,), and be nulliparous (46.4% vs 39.4%,) than those without. After adjusting for confounders, CF carriers were more likely to develop hypertensive disease of pregnancy (aRR = 1.25, 95% CI 1.19-1.31), severe maternal morbidity (aRR = 1.30, 95% CI 1.12-1.51), non-transfusion severe maternal morbidity (aRR 1.30, 95% CI 1.04-1.63), PPROM (aRR = 1.29, 95% CI 1.15-1.44), and neonatal hypoglycemia (aRR = 1.39, 95% CI 1.25-1.54).
Conclusion:
We found that CF carriers are at increased risk of adverse perinatal outcomes. These findings can be used for patient counseling and delivery planning. Future studies should further investigate these findings and strategies to mitigate these risks.