Oral Concurrent Session 2 - Clinical Obstetrics and Quality
Oral Concurrent Sessions
Linda M. Ernst, MD
Endeavor Health
Evanston, Illinois, United States
Alexa A. Freedman, PhD (she/her/hers)
Northwestern University
Chicago, Illinois, United States
Renee Odom-Konja, MPH
Research Coordinator, Department of Obstetrics and Gynecology
Endeavor Health
Evanston, Illinois, United States
Lauren Keenan-Devlin, MPH, PhD
Research Scientist, Research Assistant Professor
Endeavor Health, Evanston Hospital
Evanston, Illinois, United States
Greg E. Miller, PhD
Professor
Northwestern University
Chicago, Illinois, United States
Ann EB Borders, MD, MPH, MSc (she/her/hers)
Ian Bernard Horowitz Chair of Obstetrics, Clinical Professor
Endeavor Health, Evanston Hospital
Evanston, IL, United States
All placentas were prospectively collected from participants in the Stress, Pregnancy, and Health (SPAH) study, including those with and without CPE. In all cases, placental pathology was categorized and graded in 4 major groups: acute inflammation (AI), chronic inflammation (CI), fetal vascular malperfusion (FVM) and maternal vascular malperfusion (MVM). We compared the distribution of placental pathology in cases with and without CPE. Odds ratios (OR) for preterm birth (PTB) and small for gestational age (SGA) infant were calculated in the whole SPAH cohort and compared with the CPE sub-cohort. Relative odds ratios (ROR) were used to quantify selection bias. Models were adjusted for sociodemographic and pregnancy characteristics.
Results:
575 placentas were collected and examined, 287 with CPE and 288 without CPE. The prevalence of AI, CI and FVM was similar among the 2 groups. However, the prevalence of MVM was significantly higher in CPE placentas, particularly for high grade MVM (15% vs 8%, p< 0.001). In adjusted models, high grade MVM was significantly associated with increased odds of PTB and SGA in the whole SPAH cohort and the CPE sub-cohort (PTB: SPAH OR=5.62, CPE OR=7.56; SGA: SPAH OR=8.13, CPE OR=8.25). RORs show a 30% overestimation of the association between MVM and PTB, and only a 2% overestimation in SGA when using a CPE sample.
Conclusion: MVM was the only placental pathology seen more frequently in the CPE sample. Research using a CPE only sample may overestimate associations, particularly for MVM and PTB. Because we quantified the selection bias, the RORs from our data can be used to adjust estimates in studies using retrospective CPE samples.