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Association between maternal dupilumab exposure and pregnancy outcomes in patients with moderate‐to‐severe atopic dermatitis: A nationwide retrospective cohort study

杜皮鲁玛 医学 特应性皮炎 回顾性队列研究 队列 怀孕 队列研究 皮肤病科 内科学 生物 遗传学
作者
Gianluca Avallone,Francesco Cavallo,Annalisa Tancredi,Carlo Alberto Maronese,Martina Bertello,Alessandro Fraghì,Claudio Conforti,Giulia Calabrese,Matteo Riccardo Di Nicola,Giorgio Oddenino,Luigi Gargiulo,Niccolò Gori,Camilla Loi,Paolo Romita,Viviana Piras,Laura Bonzano,Ersilia Tolino,Giovanni Paolino,Maddalena Napolitano,Cataldo Patruno,Eustachio Nettis,Caterina Ferreli,Gabriele Roccuzzo,Luca Marozio,Martina Silvio,Filomena Russo,Luca Bettolini,Rosella Gallo,Santo Raffaele Mercuri,Luca Mastorino,Mariateresa Rossi,Iris Zalaudek,Giuseppe Argenziano,Ilaria Trave,Antonio Costanzo,Andrea Chiricozzi,Carlotta Gurioli,Caterina Foti,Concetta Potenza,Silvia Ferrucci,Anna Balato,Aurora Parodi,Angelo Valerio Marzano,Michela Ortoncelli,Simone Ribero,Pietro Quaglino
出处
标识
DOI:10.1111/jdv.19794
摘要

Abstract Background There is limited epidemiological evidence on outcomes associated with dupilumab exposure during pregnancy; monitoring pregnancy outcomes in large populations is required. Objective To investigate the potential association between exposure to dupilumab in pregnant women with atopic dermatitis and any adverse pregnancy, neonatal, congenital and post‐partum outcomes. Methods We performed a multicentre retrospective cohort study across 19 Italian tertiary referral hospital. Childbearing women were eligible if aged 18–49 years and carried out the pregnancy between 1 October 2018 and 1 September 2022. Results We retrospectively screened records of 5062 patients receiving dupilumab regardless of age and gender, identifying 951 female atopic dermatitis patients of childbearing age, 29 of whom had been exposed to the drug during pregnancy (3%). The median duration of dupilumab treatment prior to conception was 22.5 weeks (range: 3–118). The median time of exposure to the drug during pregnancy was 6 weeks (range: 2–24). All the documented pregnancies were unplanned, and the drug was discontinued in all cases once pregnancy status was reported. The comparison of the study cohort and the control group found no significant drug‐associated risk for adverse pregnancy, congenital, neonatal or post‐partum outcomes. The absence of a statistically significant effect of exposure on the event was confirmed by bivariate analysis and multivariate analysis adjusted for other confounding factors. Conclusions This cohort of pregnant patients exposed to dupilumab adds to the existing evidence concerning the safety of biologic agents in pregnancy. No safety issues were identified regarding the primary outcome assessed. In clinical practice, these data provide reassurance in case of dupilumab exposure during the first trimester. However, the continuous use of dupilumab throughout pregnancy warrants further research.
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