Poster Session 4
Stephanie L. Pierce, MD, MS
Associate Professor
University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, United States
Jennifer Peck, PhD
University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, United States
Erin Schone, MS
University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, United States
Dean Myers, PhD
University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, United States
Rodney Edwards, MD, MS
University of Florida College of Medicine
Gainesville, Florida, United States
This prospective cohort study enrolled women age 18-45 years, term, and undergoing labor induction (IOL) with cervical Foley and oxytocin. Exclusion criteria were known fetal demise and multiple gestation. We drew blood samples prior to IOL and 6-12 and 18-24 hours (h) after IOL start and compared pro-inflammatory cytokine levels (IL-1α, IL-1β, IL-6, IL-8, GM-CSF, IFN-g, MCP-1, and TNF-α) in those who received IAP versus those who did not. We used linear mixed models to evaluate differences in labor cytokines between IAP groups over time, controlling for obesity, parity, race/ethnicity, chronic hypertension, preeclampsia and diabetes.
Results:
113 women (n=59 did not receive IAP and n=54 received IAP) were recruited. Cytokine concentrations significantly increased between pre-labor and 12-24h post-IOL measures with the exception of IFN-g, IL-1α and TNF-α (Figure). Overall, patients who received IAP had higher mean concentrations of IFN-g (unadjusted geometric mean ratio [GMR] 1.27 [95% CI 1.05, 1.55]) and lower levels of TNF- α (unadjusted GMR 0.87 [95% CI 0.76, 0.99]; Table). IL-1α levels did not differ by IAP status pre-labor but were 80% greater for those with IAP at 6-12h post-IOL. TNF-α concentrations at 6-12h were significantly lower in those who received IAP compared with those who did not (GMR 0.84 [95% CI 0.71, 0.99]).
Conclusion:
Intrapartum TNF-α concentration was lower in those who received IAP for GBS compared with those who did not, while IFN-g, IL-1α concentrations were higher. Given the known effects of these cytokines on uterine contractility and labor, this could suggest a mechanism by which prophylactic antibiotics during labor induction may influence uterine activity and the risk of abnormal labor.