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Published on: February 8, 2019
EULAR/ERA-EDTA recommendations for the management of ANCA-associated vasculitis
M Yates1, R A Watts2, I M Bajema3
1Department of Rheumatology, Norfolk and Norwich University Hospital, Norwich, UK Norwich Medical School, University of East Anglia, Norwich, UK.
Insights
Updated European League Against Rheumatism (EULAR) guidelines offer evidence-based management strategies for antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). These recommendations focus on remission induction, maintenance, and specific treatments for severe AAV cases.
Area of Science:
- Rheumatology
- Immunology
- Nephrology
Background:
- The 2009 European League Against Rheumatism (EULAR) recommendations for managing antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) required an update.
- ANCA-associated vasculitis encompasses primary small and medium vessel vasculitis, necessitating updated clinical guidance.
Purpose of the Study:
- To update the 2009 EULAR recommendations for the management of ANCA-associated vasculitis (AAV).
- To provide evidence-based guidance for healthcare professionals treating patients with AAV.
Main Methods:
- An international task force, including EULAR, European Renal Association, and European Vasculitis Society (EUVAS) representatives, developed the updated recommendations.
- Recommendations were based on systematic literature reviews and expert consensus, including consensus-finding, voting processes, and online surveys for relevance assessment.
- Levels of evidence, grades of recommendations, and strengths of recommendations were determined.
Main Results:
- Fifteen updated recommendations were developed, addressing general aspects like remission and shared decision-making.
- Specific recommendations include using immunosuppressive therapy with glucocorticoids for remission induction and maintenance.
- Cyclophosphamide and rituximab show similar efficacy for inducing remission in severe or life-threatening AAV; plasma exchange is recommended for severe renal or pulmonary involvement.
Conclusions:
- The updated 2015 EULAR recommendations provide comprehensive guidance for AAV management.
- Shared decision-making and tailored treatment strategies are emphasized for optimal patient outcomes.
- These guidelines are intended for a wide range of healthcare professionals and regulatory bodies.
Abstract:
In this article, the 2009 European League Against Rheumatism (EULAR) recommendations for the management of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) have been updated. The 2009 recommendations were on the management of primary small and medium vessel vasculitis. The 2015 update has been developed by an international task force representing EULAR, the European Renal Association and the European Vasculitis Society (EUVAS). The recommendations are based upon evidence from systematic literature reviews, as well as expert opinion where appropriate. The evidence presented was discussed and summarised by the experts in the course of a consensus-finding and voting process. Levels of evidence and grades of recommendations were derived and levels of agreement (strengths of recommendations) determined. In addition to the voting by the task force members, the relevance of the recommendations was assessed by an online voting survey among members of EUVAS. Fifteen recommendations were developed, covering general aspects, such as attaining remission and the need for shared decision making between clinicians and patients. More specific items relate to starting immunosuppressive therapy in combination with glucocorticoids to induce remission, followed by a period of remission maintenance; for remission induction in life-threatening or organ-threatening AAV, cyclophosphamide and rituximab are considered to have similar efficacy; plasma exchange which is recommended, where licensed, in the setting of rapidly progressive renal failure or severe diffuse pulmonary haemorrhage. These recommendations are intended for use by healthcare professionals, doctors in specialist training, medical students, pharmaceutical industries and drug regulatory organisations.
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