| Literature DB >> 28087505 |
Désirée van der Heijde1, Sofia Ramiro1, Robert Landewé2,3, Xenofon Baraliakos4, Filip Van den Bosch5, Alexandre Sepriano1,6, Andrea Regel4, Adrian Ciurea7, Hanne Dagfinrud8, Maxime Dougados9,10, Floris van Gaalen1, Pál Géher11, Irene van der Horst-Bruinsma12, Robert D Inman13, Merryn Jongkees14, Uta Kiltz4, Tore K Kvien15, Pedro M Machado16, Helena Marzo-Ortega17,18, Anna Molto9,10, Victoria Navarro-Compàn19, Salih Ozgocmen20, Fernando M Pimentel-Santos21, John Reveille22, Martin Rudwaleit23,24,25, Jochen Sieper26, Percival Sampaio-Barros27, Dieter Wiek28, Jürgen Braun4.
Abstract
To update and integrate the recommendations for ankylosing spondylitis and the recommendations for the use of tumour necrosis factor inhibitors (TNFi) in axial spondyloarthritis (axSpA) into one set applicable to the full spectrum of patients with axSpA. Following the latest version of the European League Against Rheumatism (EULAR) Standardised Operating Procedures, two systematic literature reviews first collected the evidence regarding all treatment options (pharmacological and non-pharmacological) that were published since 2009. After a discussion of the results in the steering group and presentation to the task force, overarching principles and recommendations were formulated, and consensus was obtained by informal voting. A total of 5 overarching principles and 13 recommendations were agreed on. The first three recommendations deal with personalised medicine including treatment target and monitoring. Recommendation 4 covers non-pharmacological management. Recommendation 5 describes the central role of non-steroidal anti-inflammatory drugs (NSAIDs) as first-choice drug treatment. Recommendations 6-8 define the rather modest role of analgesics, and disprove glucocorticoids and conventional synthetic disease-modifying antirheumatic drugs (DMARDs) for axSpA patents with predominant axial involvement. Recommendation 9 refers to biological DMARDs (bDMARDs) including TNFi and IL-17 inhibitors (IL-17i) for patients with high disease activity despite the use (or intolerance/contraindication) of at least two NSAIDs. In addition, they should either have an elevated C reactive protein and/or definite inflammation on MRI and/or radiographic evidence of sacroiliitis. Current practice is to start with a TNFi. Switching to another TNFi or an IL-17i is recommended in case TNFi fails (recommendation 10). Tapering, but not stopping a bDMARD, can be considered in patients in sustained remission (recommendation 11). The final two recommendations (12, 13) deal with surgery and spinal fractures. The 2016 Assessment of SpondyloArthritis international Society-EULAR recommendations provide up-to-date guidance on the management of patients with axSpA. 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); NSAIDs; Physcial therapy; Spondyloarthritis; Treatment
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Year: 2017 PMID: 28087505 DOI: 10.1136/annrheumdis-2016-210770
Source DB: PubMed Journal: Ann Rheum Dis ISSN: 0003-4967 Impact factor: 19.103