Oral corticosteroid use during pregnancy and risk of preterm birth

Author:

Palmsten Kristin12,Bandoli Gretchen23,Vazquez-Benitez Gabriela1,Xi Min1,Johnson Diana L2,Xu Ronghui34,Chambers Christina D23

Affiliation:

1. HealthPartners Institute, Minneapolis, MN

2. Department of Pediatrics, University of California, CA, USA

3. Department of Family Medicine and Public Health, University of California, CA, USA

4. Department of Mathematics, University of California, CA, USA

Abstract

Abstract Objective To evaluate the associations between oral corticosteroid (OCS) dose early and late in pregnancy and preterm birth (PTB) among women with RA. Methods Pregnant women in the MotherToBaby Pregnancy Studies (2003–2014) with RA (n = 528) were included in the primary analysis. Information was collected by phone interview and from medical records. We estimated risk ratios (RR) for OCS dose trajectories and other disease-related medications before gestational day 140 and hazard ratios (HR) for time-varying exposures after gestational day 139. Results PTB risk was 15.5% overall. Compared with no OCS, PTB risk was increased in high (adjusted (a)RR: 4.77 (95% CI: 2.76, 8.26)) and medium (aRR: 1.81 (95% CI: 1.10, 2.97)) cumulative OCS dose trajectories during the first 139 gestational days. The low cumulative trajectory group was associated with an increased risk of PTB that was not statistically significant (aRR: 1.38 (95% CI: 0.79, 2.38)), and DMARDs were not associated with PTB (biologic DMARDs aHR: 1.08 (95% CI: 0.70, 1.66); non-biologic DMARDs aHR: 0.87 (95% CI: 0.55, 1.38)). OCS exposure to ⩾10 mg of prednisone equivalent daily dose after gestational day 139 vs none was associated with increased PTB rate (aHR: 2.45 (95% CI: 1.32, 4.56)), whereas <10 mg was associated with a modestly increased rate of PTB that was not statistically significant (aHR: 1.18 (95% CI: 0.60, 2.30)). Conclusion Higher OCS doses vs no OCS use, both earlier and later in pregnancy, were associated with an increase in PTB among women with RA.

Funder

National Institutes of Health

Eunice Kennedy Shriver National Institute of Child Health & Human Development

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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