Pregnancy outcomes in women with rheumatoid arthritis: an 11-year French nationwide study

Author:

Pina Vegas LauraORCID,Drouin Jérôme,Weill Alain,Dray-Spira Rosemary

Abstract

BackgroundRheumatoid arthritis (RA) can affect women of childbearing age. The management of patients with RA during pregnancy has evolved over the past decades, especially with the availability of new therapeutic molecules.ObjectivesTo describe pregnancy in women with RA, to compare pregnancy outcomes with those of women in the general population and to compare pregnancy outcomes in women with active and inactive RA.MethodsUsing the French National Health Data System, we identified all pregnancies ending between 2010 and 2020 in patients with and without RA. Characteristics were described. Active RA was defined by conventional synthetic/biological/targeted synthetic disease-modifying antirheumatic drug initiation, systemic or intra-articular corticosteroid administration and/or RA-related hospitalisation. Pregnancy outcomes were compared computing multivariable logistic marginal regression model using generalised estimating equation (GEE).ResultsWe included 11 792 RA and 10 413 681 non-RA pregnancies. Among RA pregnancies, 74.5% ended in live births and 0.4% in stillbirths. RA pregnancies resulted more frequently in preterm births (adjusted OR (ORa) 1.84; 95% CI 1.69 to 2.00) and very preterm births (ORa1.43; 95% CI 1.20 to 1.71), low birth weight (ORa1.65; 95% CI: 1.52 to 1.90), caesarean section (ORa1.46; 95% CI 1.38 to 1.55) and pregnancy-related hospitalisation (ORa1.30; 95% CI 1.22 to 1.39). Disease activity decreased during pregnancy. Active RA had higher rates of prematurity (ORa2.02; 95% CI 1.71 to 2.38), small for gestational age (ORa1.53; 95% CI 1.28 to 1.83) and caesarean section (ORa1.25; 95% CI 1.11 to 1.40) than non-active RA.ConclusionPregnancies in women with RA were associated with more adverse outcomes, especially if the disease was active. These findings should encourage physicians to closely monitor RA during this crucial period.

Publisher

BMJ

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