Associations of periconceptional oral contraceptive use with pregnancy complications and adverse birth outcomes

Author:

Schreuder Anton1,Mokadem Ibtissam2,Smeets Nori J L3,Spaanderman Marc E A45,Roeleveld Nel2,Lupattelli Angela6ORCID,van Gelder Marleen M H J2ORCID

Affiliation:

1. Department of Medical Imaging, Radboud University Medical Center , Nijmegen, The Netherlands

2. Department for Health Evidence, Radboud University Medical Center , Nijmegen, The Netherlands

3. Department of Pharmacology and Toxicology, Radboud University Medical Center , Nijmegen, The Netherlands

4. Department of Obstetrics and Gynaecology, Radboud University Medical Center , Nijmegen, The Netherlands

5. Department of Obstetrics and Gynaecology, School for Oncology and Developmental Biology (GROW), Maastricht University Medical Center , Maastricht, The Netherlands

6. PharmacoEpidemiology and Drug Safety Research Group, School of Pharmacy, and PharmaTox Strategic Research Initiative, Faculty of Mathematics and Natural Sciences, University of Oslo , Oslo, Norway

Abstract

Abstract Background Periconceptional use of oral contraceptives (OCs) has been reported to increase risks of pregnancy complications and adverse birth outcomes, but risks are suggested to differ depending on the timing of discontinuation, amount of oestrogen and progestin content. Methods Prospective cohort study among 6470 pregnancies included in the PRegnancy and Infant DEvelopment (PRIDE) Study in 2012–19. Exposure was defined as any reported use of OCs within 12 months pre-pregnancy or after conception. Outcomes of interest were gestational diabetes, gestational hypertension, pre-eclampsia, pre-term birth, low birthweight and small for gestational age (SGA). Multivariable Poisson regression using stabilized inverse probability weighting estimated relative risks (RRs) with 95% CIs. Results Any periconceptional OC use was associated with increased risks of pre-eclampsia (RR 1.38, 95% CI 0.99–1.93), pre-term birth (RR 1.38, 95% CI 1.09–1.75) and low birthweight (RR 1.45, 95% CI 1.10–1.92), but not with gestational hypertension (RR 1.09, 95% CI 0.91–1.31), gestational diabetes (RR 1.02, 95% CI 0.77–1.36) and SGA (RR 0.96, 95% CI 0.75–1.21). Associations with pre-eclampsia were strongest for discontinuation 0–3 months pre-pregnancy, for OCs containing ≥30 µg oestrogen and for first- or second-generation OCs. Pre-term birth and low birthweight were more likely to occur when OCs were discontinued 0–3 months pre-pregnancy, when using OCs containing <30 µg oestrogen and when using third-generation OCs. Associations with SGA were observed for OCs containing <30 µg oestrogen and for third- or fourth-generation OCs. Conclusions Periconceptional OC use, particularly those containing oestrogen, was associated with increased risks of pre-eclampsia, pre-term birth, low birthweight and SGA.

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Epidemiology

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