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EULAR recommendations for the management of psoriatic arthritis with pharmacological therapies: 2019 update

  • Laure Gossec
  • , Xenofon Baraliakos
  • , Andreas Kerschbaumer
  • , Maarten de Wit
  • , Iain McInnes
  • , Maxime Dougados
  • , Jette Primdahl
  • , Dennis G. McGonagle
  • , Daniel Aletaha
  • , Andra Balanescu
  • , Peter V. Balint
  • , Heidi Bertheussen
  • , Wolf-Henning Boehncke
  • , Gerd R. Burmester
  • , Juan D. Canete
  • , Nemanja S. Damjanov
  • , Tue Wenzel Kragstrup
  • , Tore K. Kvien
  • , Robert B. M. Landewé
  • , Rik Jozef Urbain Lories
  • Helena Marzo-Ortega, Denis Poddubnyy, Santiago Andres Rodrigues Manica, Georg Schett, Douglas J. Veale, Filip E. van den Bosch, D. sirée van der Heijde, Josef S. Smolen

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

OBJECTIVE: To update the European League Against Rheumatism (EULAR) recommendations for the pharmacological treatment of psoriatic arthritis (PsA). METHODS: According to the EULAR standardised operating procedures, a systematic literature review was followed by a consensus meeting to develop this update involving 28 international taskforce members in May 2019. Levels of evidence and strengths of recommendations were determined. RESULTS: The updated recommendations comprise 6 overarching principles and 12 recommendations. The overarching principles address the nature of PsA and diversity of both musculoskeletal and non-musculoskeletal manifestations; the need for collaborative management and shared decision-making is highlighted. The recommendations provide a treatment strategy for pharmacological therapies. Non-steroidal anti-inflammatory drugs and local glucocorticoid injections are proposed as initial therapy; for patients with arthritis and poor prognostic factors, such as polyarthritis or monoarthritis/oligoarthritis accompanied by factors such as dactylitis or joint damage, rapid initiation of conventional synthetic disease-modifying antirheumatic drugs is recommended. If the treatment target is not achieved with this strategy, a biological disease-modifying antirheumatic drugs (bDMARDs) targeting tumour necrosis factor (TNF), interleukin (IL)-17A or IL-12/23 should be initiated, taking into account skin involvement if relevant. If axial disease predominates, a TNF inhibitor or IL-17A inhibitor should be started as first-line disease-modifying antirheumatic drug. Use of Janus kinase inhibitors is addressed primarily after bDMARD failure. Phosphodiesterase-4 inhibition is proposed for patients in whom these other drugs are inappropriate, generally in the context of mild disease. Drug switches and tapering in sustained remission are addressed. CONCLUSION: These recommendations provide stakeholders with an updated consensus on the pharmacological management of PsA, based on a combination of evidence and expert opinion.
Original languageEnglish
Pages (from-to)S700-S712
Number of pages13
JournalAnnals of the rheumatic diseases
Volume79
Issue number6
DOIs
Publication statusPublished - 1 Jun 2020

Keywords

  • DMARDs (biologic)
  • psoriatic arthritis
  • treatment

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