# Childhood follow-up study of obesity and neurodevelopment after perinatal exposure to adjunctive azithromycin prophylaxis for cesarean delivery

> **NIH NIH R01** · UNIVERSITY OF ALABAMA AT BIRMINGHAM · 2021 · $646,325

## Abstract

PROJECT SUMMARY/ABSTRACT
We propose a large multi-center non-inferiority follow-up cohort study designed to evaluate long-term
obesity/growth and neurodevelopment after perinatal exposure to adjunctive azithromycin as compared with
placebo (plus standard cephalosporin) to prevent surgical site infections at cesarean delivery. The parent
C/SOAP randomized trial of adjunctive azithromycin (4/2011–11/2014) demonstrated a significant reduction in
maternal infections (endometritis and wound infection) without any significant effect on short-term neonatal
outcomes in the azithromycin group. This reduction in maternal infection (a major cause of death) was so
significant that azithromycin use was found to be cost-saving – saving ~$360/unscheduled cesarean and $270
million/year in US healthcare costs. However, enthusiasm for adjunctive azithromycin has been tempered
given reports of changes induced by azithromycin on the newborn gut microbiome that may be associated with
childhood weight gain/obesity and neurodevelopmental impairment. In September 2018, ACOG suggested
“consideration” of adjunctive azithromycin, but emphasized the need for studies of its effect on long-term
childhood outcomes. In response to these concerns, we proposed an R01 study evaluating pulmonary and
gastrointestinal (GI) health after perinatal azithromycin exposure (6th percentile score). Reviewers emphasized
the need to evaluate obesity/growth and neurodevelopment (NIH officers advised a separate application due to
cap limitations). Thus, in this proposal, we hypothesize that perinatal exposure to adjunctive azithromycin
compared to standard cesarean prophylaxis alone is not associated with increased risk of obesity/weight gain
or neurodevelopmental impairment (i.e. is non-inferior). We propose a follow-up study of the offspring of the
C/SOAP trial cohort at target age of 7 years (range 6-9) at the 14 sites in the parent trial. We expect at least
1410 of 2013 children (70% follow-up) whose mothers were enrolled in C/SOAP will undergo a single study
visit incorporating growth/biometry and neurodevelopment assessments to address the following specific aims:
 1) To compare the incidence of obese/overweight children (primary outcome), and other biophysical
 measurements, between cohort offspring aged 7 (range 6-9 years) after perinatal exposure to
 adjunctive azithromycin versus placebo (standard prophylaxis alone)
 2) To compare neurodevelopmental outcomes including cognitive ability (primary outcome), functional and
 behavioral impairment, and motor proficiency, between cohorts at age 7 (range 6-9 years) after
 perinatal exposure to adjunctive azithromycin versus placebo
This study, along with the companion study evaluating pulmonary and GI outcomes (award notice pending), is
the only opportunity to efficiently provide comprehensive long-term safety data from a large US trial to inform
and strengthen the newly recommended use of adjunctive azithromycin for cesarean delivery.

## Key facts

- **NIH application ID:** 10249196
- **Project number:** 5R01HD102962-02
- **Recipient organization:** UNIVERSITY OF ALABAMA AT BIRMINGHAM
- **Principal Investigator:** Akila Subramaniam
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $646,325
- **Award type:** 5
- **Project period:** 2020-07-20 → 2026-03-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10249196

## Citation

> US National Institutes of Health, RePORTER application 10249196, Childhood follow-up study of obesity and neurodevelopment after perinatal exposure to adjunctive azithromycin prophylaxis for cesarean delivery (5R01HD102962-02). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10249196. Licensed CC0.

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