Poster Session 2
Emily N. Adams, MD (she/her/hers)
Resident Physician
Johns Hopkins University
Baltimore, Maryland, United States
George U. Eleje, MBBS
Nnamdi Azikiwe University Teaching Hospital
Nnewi, Anambra, Nigeria
Ifeanyichukwu Ezebialu, MBBS
Chukwuemeka Odumegwu Ojukwu University Teaching Hospital
Amaku, Anambra, Nigeria
Ernie Shippey, MA
Vizient Center for Advanced Analytics
Chicago, Illinois, United States
Muktar Aliyu, DrPH, MBBS, MPH
Vanderbilt University
Nashville, Tennessee, United States
Ahizechukwu C. Eke, MD, MPH, PhD
Associate Professor of Gynecology & Obstetrics
Johns Hopkins University School of Medicine
Baltimore, Maryland, United States
This multi-center observational cohort study used data from 192 hospitals in 38 US states, sourced from the Vizient Clinical Database. We included pregnant patients with HIV on Atazanavir or Darunavir-based ART, who delivered between January 2021- April 2024. The primary outcome was intrahepatic cholestasis of pregnancy (ICP), with secondary outcomes including hypertensive disorders, preterm birth, and neonatal outcomes. We computed adjusted odds ratios (aOR) using multivariable logistic regression to adjust for potential confounders (maternal age, gestational age, diabetes mellitus, hypertension, baseline viral load and CD4 cell count).
Results: There were 251 patients in the Atazanavir and 218 patients in the Darunavir group. In the overall cohort at study entry, the median (interquartile range, IQR) maternal age was 31 (IQR 27-36) years with most patients identifying as Black (63.4%) . The frequency of ICP was similar in both groups (2.0% vs 2.8%; P=.59) - Table 1. The adjusted odds ratios (aOR) of ICP (aOR 1.83; 95% CI 0.51, 6.58), preterm birth (aOR 0.93; 95% CI 0.41, 2.12), gestational hypertension (aOR 0.82; 95% CI 0.44, 1.54), pre-eclampsia (aOR 1.07, 95% CI 0.58, 1.96), placental abruption (aOR 2.71; 95% CI 0.25, 28.93) and stillbirth (aOR 0.66; 95% CI 0.18, 2.25) were similar between both groups (Table 2).
Conclusion:
Atazanavir and Darunavir-based ART were safe for use during pregnancy and had similar pregnancy and neonatal outcomes.