Differences in Factors Associated With Preterm and Term Stillbirth: A Secondary Cohort Analysis of the DESiGN Trial
- PMID: 39291344
- PMCID: PMC11612614
- DOI: 10.1111/1471-0528.17951
Differences in Factors Associated With Preterm and Term Stillbirth: A Secondary Cohort Analysis of the DESiGN Trial
Abstract
Objective: To identify whether maternal and pregnancy characteristics associated with stillbirth differ between preterm and term stillbirth.
Design: Secondary cohort analysis of the DESiGN RCT.
Setting: Thirteen UK maternity units.
Population: Singleton pregnant women and their babies.
Methods: Multiple logistic regression was used to assess whether the 12 factors explored were associated with stillbirth. Interaction tests assessed for a difference in these associations between the preterm and term periods.
Main outcome measure: Stillbirth stratified by preterm (<37+0 weeks') and term (37+0-42+6 weeks') births.
Results: A total of 195 344 pregnancies were included. Six hundred and sixty-seven were stillborn (3.4 per 1000 births), of which 431 (65%) were preterm. Significant interactions were observed for maternal age, ethnicity, IMD, BMI, parity, smoking, PAPP-A, gestational hypertension, pre-eclampsia and gestational diabetes but not for chronic hypertension and pre-existing diabetes. Stronger associations with term stillbirth were observed in women with obesity compared to BMI 18.5-24.9 kg/m2 (BMI 30.0-34.9 kg/m2 term adjusted OR 2.1 [95% CI 1.4-3.0] vs. preterm aOR 1.1 [0.8-1.7]; BMI ≥ 35.0 kg/m2 term aOR 2.2 [1.4-3.4] vs. preterm aOR 1.5 [1.2-1.8]; p-interaction < 0.01), nulliparity compared to parity 1 (term aOR 1.7 [1.1-2.7] vs. preterm aOR 1.2 [0.9-1.6]; p-interaction < 0.01) and Asian ethnicity compared with White (p-interaction < 0.01). A weaker or lack of association with term, compared to preterm, stillbirth was observed for older maternal age, smoking and pre-eclampsia.
Conclusion: Differences in association exist between mothers experiencing preterm and term stillbirth. These differences could contribute to design of timely surveillance and interventions to further mitigate the risk of stillbirth.
Keywords: SGA; fetal growth restriction; perinatal death; premature birth; stillbirth; term birth.
© 2024 The Author(s). BJOG: An International Journal of Obstetrics and Gynaecology published by John Wiley & Sons Ltd.
Conflict of interest statement
M.C.V. was supported by CAPES (BEX 9571/13‐2). S.R., K.C., A.H. and J.S. were supported by the National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research and Care South London at King's College Hospital NHS Foundation Trust. D.A.L.'s contributions were supported by the Bristol NIHR Biomedical Research Centre and her NIHR Senior Investigator Award (NF‐0616‐10102). D.A.L. has received support from Medtronic Ltd. and Roche Diagnostics for research unrelated to that presented here and that ended 5 years or more ago. D.A.L.'s contribution is supported by the UK Medical Research Council (MC_UU_00032/05) and the British Heart Foundation (CH/F/20/90003). J.S. is supported by an NIHR Senior Investigator Award. N.M. reports personal fees from Takeda, personal fees from RSM Consulting, personal fees from Novartis, outside the submitted work. N.M. receives a proportion of funding from the Department of Health's NIHR Biomedical Research Centres funding scheme at UCLH/UCL. B.T. is the Clinical Director and J.S. is a programme lead of the Tommy's National Centre for Maternity Improvement based at the Royal College of Obstetrics and Gynaecology; the Centre's objective is to translate the latest evidence into clinical practice in the United Kingdom. J.S. is Head of Maternity and Midwifery Research at NHS England. The funders had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.
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