Infectious Diseases
Poster Session 4
Advaita Punjala-Patel, MD
Atrium Health Wake Forest Baptist Medical Center
Winston-Salem, NC, United States
Sophia Alvarado, BS
Wake Forest University School of Medicine
Winston-Salem, NC, United States
Austin French, BS
Wake Forest University School of Medicine
Winston-Salem, NC, United States
Rebekah Lassiter, BS
Wake Forest University School of Medicine
Winston-Salem, NC, United States
David M. Stamilio, MD, MSCE
Professor, Maternal and Fetal Medicine
Wake Forest University School of Medicine
Winston-Salem, NC, United States
We aimed to estimate the association between antenatal maternal COVID-19 (C-19) infection and the risk for small-for-gestational-age (SGA) neonatal birthweight. We also sought to assess if gestational timing or severity of C-19 infection differentially impacts the risk of SGA.
Study Design:
This retrospective cohort study included all pregnant patients with C-19 infection and randomly selected unexposed controls who delivered at a tertiary care center from 10/1/2020 to 6/1/2022. We also assessed C-19 exposure by trimester of infection and disease severity. The primary outcome, SGA, was defined as neonatal birthweight < 10th percentile for gestational age based on a standard growth curve. Secondary outcomes included birth length and head circumference (HC) percentiles, APGAR scores and neonatal hospital length of stay (LOS). We used chi-squared and t-tests to estimate differences between C-19 exposed and unexposed groups, and multivariable logistic regression analysis to estimate the association between C-19 and SGA.
Results:
Among 1011 patients, 502 had C-19 infection and 509 did not. Baseline demographics between groups were similar. Overall C-19 was not associated with increased risk of SGA adjusting for confounding by maternal age, hypertension and race. Among patients with C-19, 15.2%, 31.1% and 53.7% had infection in the 1st, 2nd, and 3rd trimester and 68.4%, 25.4% and 6.2% had mild, moderate, or severe disease respectively. First trimester C-19 infection was associated with a 2-fold increase in SGA (aOR 2.3, 95% CI 1.1-5.1), compared to 2nd or 3rd trimester infection. Stratifying by C-19 disease severity, moderate-severe disease was associated with a 2-fold increase in SGA (aOR 2.1, 95% CI 1.1-3.5), but mild disease did not increase this risk. C-19 exposure was not associated with increased risk of any other secondary neonatal outcomes (Table 1).
Conclusion:
When stratifying by antenatal C-19 disease severity and timing of infection, we observed a two-fold increased risk of SGA in patients with severe C-19 disease and with infection in the 1st trimester.