Abstract
Objective: We sought to assess whether betamethasone (BETA) <34 weeks reduces adverse outcomes in late preterm infants. Study Design: We performed a retrospective cohort study of patients with spontaneous birth 34-36 6/7 weeks. We determined whether patients were exposed to preterm labor (PTL) <34 weeks and BETA and calculated the incidence of adverse respiratory and composite outcomes and neonatal intensive care unit admission. We used χ2 analyses to determine associations between PTL+BETA and adverse outcomes, and Poisson regression to model cumulative incidence and control for confounders. Results: We enrolled 700 mother-infant pairs. The 36-week PTL+BETA infants were at increased risk of respiratory outcome (incident risk ratio [IRR], 2.73; 95% confidence interval [CI], 1.37-5.45), neonatal intensive care unit admission (IRR, 2.01; 95% CI, 1.14-3.56), and composite outcome (IRR, 1.70; 95% CI, 1.08-2.68) compared to those without PTL+BETA. Chorioamnionitis was independently associated with all adverse outcomes. Conclusion: We hypothesize that early PTL is a surrogate for intrauterine inflammation and is responsible for the observed adverse outcomes in those with PTL+BETA.
Original language | English |
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Pages (from-to) | 140.e1-140.e7 |
Journal | American Journal of Obstetrics and Gynecology |
Volume | 203 |
Issue number | 2 |
DOIs | |
State | Published - 2010 |
Externally published | Yes |
Keywords
- adverse neonatal outcomes
- betamethasone
- late preterm infant
- prematurity
- preterm labor