SAT0129 DISEASE FLARES DURING PREGNANCY IN RHEUMATOID ARTHRITIS: WHAT IS THE IMPACT OF STOPPING BDMARDS AT THE BEGINNING OF PREGNANCY?

医学 怀孕 类风湿性关节炎 产科 疾病 内科学 生物 遗传学
作者
Maria Chiara Gerardi,Antía García Fernández,Laura Andréoli,Francesca Crisafulli,Matteo Filippini,Micaela Fredi,Roberto Gorla,Maria Grazia Lazzaroni,Cecilia Nalli,Marco Taglietti,Andrea Lojacono,Sonia Zatti,Anǵela Tincani
标识
DOI:10.1136/annrheumdis-2019-eular.7614
摘要

Background:

During pregnancy, patients with rheumatoid arthritis (RA) can experience flares, which might influence pregnancy ouctomes.

Objectives:

To assess disease course during pregnancy and identify possible risk factors of disease flares in RA.

Methods:

Data on RA patients prospectively-followed in a pregnancy clinic were retrospectively analyzed before conception and during each trimester. Clinical characteristics, disease activity (DAS28-CRP3), medication use, and pregnancy outcomes were analyzed. Flare was defined by an increase of DAS28-CRP3 greater than 0.6.

Results:

Among 85 RA-pregnancies (mean age 34, SD 4,8; median disease duration 97 months, IQR 31-156) in 66 patients enrolled between 2010 and 2018, 8 pregnancies ended with early miscarriages, 1 with intrauterine fetal death and 2 were voluntary interrupted (1 for MTX exposure and 1 for encephalocele). The remaining seventy-four pregnancies in 62 patients were analyzed. Before conception, 52(71%) were in remission, 13(18%) in low disease activity and 8(11%) with moderate disease activity. Flares occurred in 29/74 (39%) patients during pregnancy (14/1° trimester,18 2° trimester,9 3° trimester). Flares occured more frequently in patients with a previous use of more than one conventional DMARDs (cDMARDs)(p 0,28) and a higher disease activity before conception (0,025) and in the 1°trimester (p 0,08). At conception, 30 (41%) patients were on biological DMARDs (bDMARDs) (16 ETA, 8 CTZ, 3 GOL, 2 ADA) and 16% with an active disease. 29 discontinued the treatment at positive pregnancy test and 8(27%) reintroduced bDMARDs because a flare during 1° (1 CTZ, 1 ETA), 2°(1 ADA, 2CTZ, 2 ETA) and 3° trimester (1 ETA) (Figure 1). 20/30(66%) experienced at least one flare during pregnancy.Forty-four (59%) patients were bDMARDs naive at conception (47% CCS, 41% HCQ, 16% SSZ, 2,3% MTX, 4,5% CyA), 6(7%) with an active disease. 16/44(36%) patients experienced at least one flare during pregnancy, 3 more than one flare (Figure 1). Seventeen live births were accompanied by complications (7 preterm deliveries, 2 very preterm deliveries, 6 premature rupture of membranes and 2 newborns small for gestational age). 60% of preterm births occurred in patients with a flare during pregnancy.

Conclusion:

In a cohort of prospectively-followed RA-pregnancies 39% of patients experienced at least one flare during pregnancy. A higher frequency was observed in patients on bDMARDs at conception after stopping the drug at positive pregnancy test. This suggests that patients with a more aggressive disease, as those on bDMARDs, require continuing treatment beyond conception. Counselling of patients on preconception treat-to-target management may help to achieve lower disease activity, especially in patients with a more severe disease (active disease or previous use of more than one cDMARDs). This may result in better pregnancy outcomes.

Acknowledgement:

None

Disclosure of Interests:

Maria Chiara Gerardi: None declared, Antía García Fernández: None declared, Laura Andreoli: None declared, Francesca Crisafulli: None declared, Matteo Filippini: None declared, Micaela Fredi: None declared, Roberto Gorla: None declared, Maria Grazia Lazzaroni: None declared, Cecilia Nalli: None declared, Marco Taglietti: None declared, Andrea Lojacono: None declared, Sonia Zatti: None declared, Angela Tincani Consultant for: UCB, Pfizer, Abbvie, BMS, Sanofi, Roche, GSK, AlphaSigma, Lillly, Jannsen, Cellgene, Novartis
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