Clinical Obstetrics
Poster Session 4
Lauren M. Murphy, MD
Women & Infants Hospital of Rhode Island, Warren Alpert Medical School of Brown University
Providence, RI, United States
Melissa L. Russo, MD (she/her/hers)
Assistant Professor, Obstetrics and Gynecology
Women and Infants Hospital
Providence, RI, United States
Lauren Schlichting, PhD
Hassenfeld Child Health and Innovation Institute of Brown University
Providence, RI, United States
Lorraine Dugoff, MD (she/her/hers)
Professor, Chief of Reproductive Genetics
University of Pennsylvania
Philadelphia, PA, United States
Of the 1335 included subjects twin gestations, 320 took ASA and 1015 did not take ASA. Demographic and medical differences existed between the groups (Table 1). There was no difference in preeclampsia < 34 weeks, preeclampsia with severe features, preterm birth, fetal death, and gestational diabetes with respect to ASA exposure. There was a higher risk of preeclampsia in those who took ASA, however after adjustment for BMI, race, pre-gestational diabetes, cHTN and preeclampsia in a prior pregnancy, this association was no longer significant (RR 1.36 95% CI 1.04-1.77; aRR 1.11 95% CI 0.81-1.54).
Conclusion: In this cohort, prophylactic ASA did not significantly decrease risk for preeclampsia or spontaneous preterm birth. This information may prove to be helpful in counseling; additional prospective studies are indicated regarding ASA indications and benefits.