Poster Session 1
Category: Epidemiology
Poster Session 1
Jameaka L. Hamilton, MD (she/her/hers)
Fellow
The Ohio State University
Columbus, Ohio, United States
William A. Grobman, MBA, MD
Professor
Warren Alpert Medical School of Brown University
Providence, Rhode Island, United States
Jiqiang Wu, MSc
The Ohio State University Wexner Medical Center
Columbus, Ohio, United States
Sadiya S. Khan, MD, MSc
Associate Professor, Medicine (Cardiology)
Northwestern University
Chicago, Illinois, United States
Lynn M. Yee, MD, MPH (she/her/hers)
Associate Professor
Northwestern University Feinberg School of Medicine
Chicago, Illinois, United States
David M. Haas, MD
Attending Physician
Indiana University School of Medicine
Indianapolis, Indiana, United States
Rebecca B. McNeil, PhD
Senior Research Statistician
RTI International
Triangle Park, North Carolina, United States
Jessica Pippen, MD
MetroHealth Medical Center
Cleveland, Ohio, United States
Hyagriv Simhan, MD, MS
Professor
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, United States
Uma M. Reddy, MD, MPH
Professor
Columbia University Irving Medical Center
New York, New York, United States
Robert M. Silver, MD
Department of Obstetrics and Gynecology, University of Utah Health
Salt Lake City, Utah, United States
Lisa D. Levine, MD, MSCE (she/her/hers)
Associate Professor, Chair, Division of MFM.
Perelman School of Medicine, University of Pennsylvania
Philadelphia, Pennsylvania, United States
George R. Saade, MD
Department of Obstetrics and Gynecology, Eastern Virginia Medical School at Old Dominion University
Norfolk, Virginia, United States
Jun Wu, PhD
University of California, Irvine
Orange, California, United States
Courtney C. Lynch, MPH, PhD
Associate Professor
Ohio State University Wexner Medical Center
COLUMBUS, Ohio, United States
Eric Jelovsek, MD
Duke University
Raleigh, North Carolina, United States
Kartik K. Venkatesh, MD, PhD (he/him/his)
Associate Professor
The Ohio State University Wexner Medical Center
The Ohio State University Wexner Medical Center, Ohio, United States
A secondary analysis of data from the prospective Nulliparous Pregnancy Outcomes Study: Monitoring Mothers-To-Be observational cohort. A total of 19 individual and neighborhood-level SDOH factors conceptualized per 2030 Healthy People Domains were measured in early pregnancy. The outcome was CD. Sparse Principal Components Analysis was used to develop a polysocial risk score. Modified Poisson regression was used to determine the association between this polysocial risk score and CD as both a continuous measure and categorized into tertiles after adjustment for age, body mass index, chronic hypertension, and pregestational diabetes. Model discrimination per the c-statistic was done to assess the capability of the polysocial risk score to predict CD.
Results:
Among 9,012 eligible individuals, 24% experienced a CD. Those who had a CD were generally more likely to experience adverse SDOH factors. Among 19 candidate SDOH factors (6 neighborhood- and 13 individual-level), the polysocial risk score included a total of 11 variables using Sparse Principal Components Analysis for variable selection (Figure). In adjusted analyses, a higher polysocial risk score, whether evaluated as a continuous measure (aOR: 1.63; 95% CI: 1.35, 1.98) or after categorization in tertiles (T2 vs. T1: 40.9% vs. 26.1%; aRR: 1.35; 95% CI: 1.19, 1.53; and T3 vs. T1: 33.1% vs. 26.1%; aRR: 1.44; 95% CI: 1.25, 1.66) was associated with CD. The polysocial risk score provided satisfactory discrimination with a c-statistic of 0.68 (95% CI: 0.662, 0.688).
Conclusion:
A polysocial risk score was associated with an increased risk of CD among individuals who delivered term singletons in the vertex presentation.