Table 5.

Adjusted associations between disease severity measures in pregnant women with RA with pregnancy outcomes in the OTIS cohort (n = 440), 2005–2013.

Disease Severity MeasuresPreterm Delivery*, n = 66/439SGA**, n = 39/432Cesarean Delivery, n = 182/437
Crude RR (95% CI)aRR (95% CI)Crude RR (95% CI)aRR (95% CI)Crude RR (95% CI)aRR (95% CI)
HAQ-DI, 0–31.75 (1.37–2.34)1.58 (1.17–2.15)1.23 (1.08–1.89)1.31 (0.85–2.03)1.17 (0.99–1.38)1.15 (0.97–1.36)
HAQ-DI > 0.51.66 (1.06–2.58)1.48 (0.95–2.23)1.82 (1.01–3.29)1.81 (1.01–3.33)1.18 (0.94–1.48)1.04 (0.91–1.42)
PS, /20 units1.19 (1.03–1.39)1.18 (1.20–1.38)1.19 (0.98–1.44)1.21 (1.00–1.47)1.05 (0.98–1.14)1.05 (0.98–1.13)
PGS, /20 units1.27 (1.09–1.48)1.23 (1.05–1.45)1.22 (0.99–1.51)1.22 (0.99–1.51)1.03 (0.95–1.12)1.03 (0.95–1.12)
  • * Adjusted for previous preterm delivery, maternal age at delivery, prednisone (≥ 10 mg anytime during pregnancy), maternal education, and gestational age at enrollment.

  • ** Adjusted for Crohn disease, in vitro fertilization, and gestational age at enrollment.

  • Adjusted for maternal age, periconceptional use of vitamins containing folic acid, and gestational age at enrollment.

  • Using modified Poisson regression models. RA: rheumatoid arthritis; OTIS: Organization of Teratology Information Specialists Autoimmune Diseases in Pregnancy Project; SGA: small for gestational age; crude RR: crude relative risk; aRR: adjusted relative risk; HAQ-DI: Health Assessment Questionnaire–Disability Index measured in early pregnancy — for the continuous HAQ-DI, for every unit (0–1) increase, functional disability was configured using HAQ-DI > 0.5; PS: pain score; PGS: patient global score. Prednisone (≥ 10 mg anytime during pregnancy) was an independent predictor of preterm delivery (p = 0.009), but not for SGA.