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. 2023 May 8;38(22):e172. doi: 10.3346/jkms.2023.38.e172

Table 6. Effects of the biologics administration during pregnancy on adverse pregnancy outcomes.

Outcomes No. Univariate analysis Multivariate analysis
Unadjusted OR (95% CIs) Adjusted ORa (95% CIs)
Fetal loss
Biologics naïve group 940 Reference Reference
Biologics use during pregnancy 29 0.307 (0.208–0.453) 0.274 (0.183–0.411)
Preterm delivery
Biologics naïve group 405 Reference Reference
Biologics use during pregnancy 60 1.968 (1.458–2.656) 1.859 (1.353–2.554)
Preeclampsia/eclampsia
Biologics naïve group 141 Reference Reference
Biologics use during pregnancy 18 1.568 (0.947–2.598) 1.762 (1.033–3.006)
Gestational diabetes mellitus
Biologics naïve group 1,323 Reference Reference
Biologics use during pregnancy 101 0.879 (0.687–1.125) 0.903 (0.697–1.169)
Intrauterine growth retardation
Biologics naïve group 88 Reference Reference
Biologics use during pregnancy 24 3.471 (2.176–5.537) 3.487 (2.109–5.767)
Cesarean section
Biologics naïve group 1,118 Reference Reference
Biologics use during pregnancy 145 2.047 (1.621–2.584) 1.831 (1.430–2.344)b

CI = confidence interval, OR = odds ratio, FDA = Federal Drug Administration.

aAdjusted for recorded diagnosis, age, Charlson Comorbidity Index, previous long-term use of glucocorticoids, non-steroid anti-inflammatory drugs, and FDA category X drugs, previous history of infertility, and abortion.

bAdjusted for recorded diagnosis, age, Charlson Comorbidity Index, previous long-term glucocorticoids use, non-steroidal anti-inflammatory drugs, and FDA category X drugs, previous history of infertility, abortion, and cesarean section.