Abstract
Objective:
The objective of this study is to determine whether low-dose aspirin (LDA) reduced the rate of preterm birth (PTB) in a cohort of women at high risk for preeclampsia.
Study Design:
Secondary analysis of the Maternal-Fetal Medicine Units High-Risk Aspirin trial. Preterm births were categorized by phenotype: indicated, spontaneous or due to preterm premature rupture of membranes (PPROMs).
Results:
Of 1789 randomized women, 30.5% delivered before 37 weeks (18.5% indicated, 5.8% spontaneous and 6.2% following preterm PPROMs). Among women randomized to LDA, we observed a trend favoring fewer PTBs due to spontaneous preterm labor and preterm PPROMs, odds ratio (OR: 0.826 (0.620, 1.099)); the incidence of indicated PTBs appeared unchanged, OR: 0.999 (0.787, 1.268).
Conclusion:
Although not reaching significance, we observed an effect size similar to other studies of both low- and high-risk women. These results support findings from other studies assessing LDA as a PTB prevention strategy.
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Acknowledgements
We appreciate the assistance of the National Institute of Child Health and Human Development (NICHD) and the Maternal-Fetal Medicine Units Network in making the database from the Maternal-Fetal Medicine Units High-Risk Aspirin Trial available for secondary analysis. The contents of this report represent the views of the authors and do not represent the views of the Eunice Kennedy Shriver NICHD Maternal-Fetal Medicine Units Network or the National Institutes of Health.
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Allshouse, A., Jessel, R. & Heyborne, K. The impact of low-dose aspirin on preterm birth: secondary analysis of a randomized controlled trial. J Perinatol 36, 427–431 (2016). https://doi.org/10.1038/jp.2016.3
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DOI: https://doi.org/10.1038/jp.2016.3