| Literature DB >> 26888948 |
Carina Götestam Skorpen1, Maria Hoeltzenbein2, Angela Tincani3, Rebecca Fischer-Betz4, Elisabeth Elefant5, Christina Chambers6, Josè da Silva7, Catherine Nelson-Piercy8, Irene Cetin9, Nathalie Costedoat-Chalumeau10, Radboud Dolhain11, Frauke Förger12, Munther Khamashta13, Guillermo Ruiz-Irastorza14, Angela Zink15, Jiri Vencovsky16, Maurizio Cutolo17, Nele Caeyers18, Claudia Zumbühl19, Monika Østensen20.
Abstract
A European League Against Rheumatism (EULAR) task force was established to define points to consider on use of antirheumatic drugs before pregnancy, and during pregnancy and lactation. Based on a systematic literature review and pregnancy exposure data from several registries, statements on the compatibility of antirheumatic drugs during pregnancy and lactation were developed. The level of agreement among experts in regard to statements and propositions of use in clinical practice was established by Delphi voting. The task force defined 4 overarching principles and 11 points to consider for use of antirheumatic drugs during pregnancy and lactation. Compatibility with pregnancy and lactation was found for antimalarials, sulfasalazine, azathioprine, ciclosporin, tacrolimus, colchicine, intravenous immunoglobulin and glucocorticoids. Methotrexate, mycophenolate mofetil and cyclophosphamide require discontinuation before conception due to proven teratogenicity. Insufficient documentation in regard to fetal safety implies the discontinuation of leflunomide, tofacitinib as well as abatacept, rituximab, belimumab, tocilizumab, ustekinumab and anakinra before a planned pregnancy. Among biologics tumour necrosis factor inhibitors are best studied and appear reasonably safe with first and second trimester use. Restrictions in use apply for the few proven teratogenic drugs and the large proportion of medications for which insufficient safety data for the fetus/child are available. Effective drug treatment of active inflammatory rheumatic disease is possible with reasonable safety for the fetus/child during pregnancy and lactation. The dissemination of the data to health professionals and patients as well as their implementation into clinical practice may help to improve the management of pregnant and lactating patients with rheumatic disease. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/Entities:
Keywords: DMARDs (biologic); DMARDs (synthetic); Nursing; Treatment
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Year: 2016 PMID: 26888948 DOI: 10.1136/annrheumdis-2015-208840
Source DB: PubMed Journal: Ann Rheum Dis ISSN: 0003-4967 Impact factor: 19.103