Oral Corticosteroids and Risk of Preterm Birth in the California Medicaid Program

Kristin Palmsten1, Gretchen Bandoli2, Jim Watkins3

  • 1Research Division, HealthPartners Institute, Minneapolis, Minn; Department of Pediatrics, University of California, San Diego, Calif.

Insights

Higher doses of oral corticosteroids (OCS) early in pregnancy are linked to increased preterm birth (PTB) risk in women with asthma. For systemic lupus erythematosus (SLE), both early and late OCS use increased PTB risk.

Area of Science:

  • Obstetrics and Gynecology
  • Pharmacology
  • Maternal-Fetal Medicine

Background:

  • Limited data exists on oral corticosteroid (OCS) dose and timing effects on preterm birth (PTB).
  • This is particularly true for pregnant women with asthma.

Purpose of the Study:

  • To investigate the association between OCS dose and gestational timing and PTB risk.
  • To compare these risks in women with asthma versus systemic lupus erythematosus (SLE).

Main Methods:

  • Utilized California Medicaid data (2007-2013) linked to birth certificates.
  • Analyzed OCS cumulative dose trajectories and timing in women with asthma (n=22,084) and SLE (n=1,174).
  • Estimated risk ratios (RR) for exposures before gestational day 140 and hazard ratios (HR) for exposures after day 139.

Main Results:

  • For asthma, higher cumulative OCS doses early in pregnancy (first 139 days) correlated with increased PTB risk (aRR: 1.46 for high-dose group).
  • OCS use after day 139 was not clearly associated with PTB in asthma patients.
  • For SLE, higher OCS doses both early and late in pregnancy were associated with increased PTB risk (aRR: 1.80 for high-dose early; aHR: 2.54 for >20 mg/day late).

Conclusions:

  • Higher OCS doses early in pregnancy are associated with increased PTB risk in women with asthma.
  • For SLE patients, OCS use, both early and late in pregnancy, is linked to higher PTB risk.
  • Gestational timing and OCS dose significantly influence PTB risk differently based on the underlying maternal condition.
Abstract

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