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European League Against Rheumatism (EULAR) recommendations for the management of psoriatic arthritis with pharmacological therapies: 2015 update.

Authors :
Gossec L
Smolen JS
Ramiro S
de Wit M
Cutolo M
Dougados M
Emery P
Landewé R
Oliver S
Aletaha D
Betteridge N
Braun J
Burmester G
Cañete JD
Damjanov N
FitzGerald O
Haglund E
Helliwell P
Kvien TK
Lories R
Luger T
Maccarone M
Marzo-Ortega H
McGonagle D
McInnes IB
Olivieri I
Pavelka K
Schett G
Sieper J
van den Bosch F
Veale DJ
Wollenhaupt J
Zink A
van der Heijde D
Source :
Annals of the rheumatic diseases [Ann Rheum Dis] 2016 Mar; Vol. 75 (3), pp. 499-510. Date of Electronic Publication: 2015 Dec 07.
Publication Year :
2016

Abstract

Background: Since the publication of the European League Against Rheumatism recommendations for the pharmacological treatment of psoriatic arthritis (PsA) in 2012, new evidence and new therapeutic agents have emerged. The objective was to update these recommendations.<br />Methods: A systematic literature review was performed regarding pharmacological treatment in PsA. Subsequently, recommendations were formulated based on the evidence and the expert opinion of the 34 Task Force members. Levels of evidence and strengths of recommendations were allocated.<br />Results: The updated recommendations comprise 5 overarching principles and 10 recommendations, covering pharmacological therapies for PsA from non-steroidal anti-inflammatory drugs (NSAIDs), to conventional synthetic (csDMARD) and biological (bDMARD) disease-modifying antirheumatic drugs, whatever their mode of action, taking articular and extra-articular manifestations of PsA into account, but focusing on musculoskeletal involvement. The overarching principles address the need for shared decision-making and treatment objectives. The recommendations address csDMARDs as an initial therapy after failure of NSAIDs and local therapy for active disease, followed, if necessary, by a bDMARD or a targeted synthetic DMARD (tsDMARD). The first bDMARD would usually be a tumour necrosis factor (TNF) inhibitor. bDMARDs targeting interleukin (IL)12/23 (ustekinumab) or IL-17 pathways (secukinumab) may be used in patients for whom TNF inhibitors are inappropriate and a tsDMARD such as a phosphodiesterase 4-inhibitor (apremilast) if bDMARDs are inappropriate. If the first bDMARD strategy fails, any other bDMARD or tsDMARD may be used.<br />Conclusions: These recommendations provide stakeholders with an updated consensus on the pharmacological treatment of PsA and strategies to reach optimal outcomes in PsA, based on a combination of evidence and expert opinion.<br /> (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/)

Details

Language :
English
ISSN :
1468-2060
Volume :
75
Issue :
3
Database :
MEDLINE
Journal :
Annals of the rheumatic diseases
Publication Type :
Academic Journal
Accession number :
26644232
Full Text :
https://doi.org/10.1136/annrheumdis-2015-208337