TY - JOUR
T1 - EULAR recommendations for the management of ANCA-associated vasculitis: 2022 update
AU - Hellmich, Bernhard
AU - Sanchez-Alamo, Beatriz
AU - Schirmer, Jan H.
AU - Berti, Alvise
AU - Blockmans, Daniel
AU - Cid, Maria C.
AU - Holle, Julia U.
AU - Hollinger, Nicole
AU - Karadag, Omer
AU - Kronbichler, Andreas
AU - Little, Mark A.
AU - Luqmani, Raashid A.
AU - Mahr, Alfred
AU - Merkel, Peter A.
AU - Mohammad, Aladdin J.
AU - Monti, Sara
AU - Mukhtyar, Chetan B.
AU - Musial, Jacek
AU - Price-Kuehne, Fiona
AU - Segelmark, Mårten
AU - Teng, Y. K. Onno
AU - Terrier, Benjamin
AU - Tomasson, Gunnar
AU - Vaglio, Augusto
AU - Vassilopoulos, Dimitrios
AU - Verhoeven, Peter
AU - Jayne, David
N1 - Acknowledgements: The authors wish to thank the librarian Oliver Weiner (Medical Department of the Kiel University Library, Kiel, Germany) for advice and assistance during the SLR. DJ was supported by the NIHR Cambridge Biomedical Research Centre.
PY - 2024/1
Y1 - 2024/1
N2 - Background: Since the publication of the EULAR recommendations for the management of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) in 2016, several randomised clinical trials have been published that have the potential to change clinical care and support the need for an update. Methods: Using EULAR standardised operating procedures, the EULAR task force undertook a systematic literature review and sought opinion from 20 experts from 16 countries. We modified existing recommendations and created new recommendations. Results: Four overarching principles and 17 recommendations were formulated. We recommend biopsies and ANCA testing to assist in establishing a diagnosis of AAV. For remission induction in life-threatening or organ-threatening AAV, we recommend a combination of high-dose glucocorticoids (GCs) in combination with either rituximab or cyclophosphamide. We recommend tapering of the GC dose to a target of 5 mg prednisolone equivalent/day within 4-5 months. Avacopan may be considered as part of a strategy to reduce exposure to GC in granulomatosis with polyangiitis (GPA) or microscopic polyangiitis (MPA). Plasma exchange may be considered in patients with rapidly progressive glomerulonephritis. For remission maintenance of GPA/MPA, we recommend rituximab. In patients with relapsing or refractory eosinophilic GPA, we recommend the use of mepolizumab. Azathioprine and methotrexate are alternatives to biologics for remission maintenance in AAV. Conclusions: In the light of recent advancements, these recommendations provide updated guidance on AAV management. As substantial data gaps still exist, informed decision-making between physicians and patients remains of key relevance.
AB - Background: Since the publication of the EULAR recommendations for the management of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) in 2016, several randomised clinical trials have been published that have the potential to change clinical care and support the need for an update. Methods: Using EULAR standardised operating procedures, the EULAR task force undertook a systematic literature review and sought opinion from 20 experts from 16 countries. We modified existing recommendations and created new recommendations. Results: Four overarching principles and 17 recommendations were formulated. We recommend biopsies and ANCA testing to assist in establishing a diagnosis of AAV. For remission induction in life-threatening or organ-threatening AAV, we recommend a combination of high-dose glucocorticoids (GCs) in combination with either rituximab or cyclophosphamide. We recommend tapering of the GC dose to a target of 5 mg prednisolone equivalent/day within 4-5 months. Avacopan may be considered as part of a strategy to reduce exposure to GC in granulomatosis with polyangiitis (GPA) or microscopic polyangiitis (MPA). Plasma exchange may be considered in patients with rapidly progressive glomerulonephritis. For remission maintenance of GPA/MPA, we recommend rituximab. In patients with relapsing or refractory eosinophilic GPA, we recommend the use of mepolizumab. Azathioprine and methotrexate are alternatives to biologics for remission maintenance in AAV. Conclusions: In the light of recent advancements, these recommendations provide updated guidance on AAV management. As substantial data gaps still exist, informed decision-making between physicians and patients remains of key relevance.
KW - cyclophosphamide
KW - granulomatosis with polyangiitis
KW - rituximab
KW - systemic vasculitis
UR - http://www.scopus.com/inward/record.url?scp=85152667500&partnerID=8YFLogxK
U2 - 10.1136/ard-2022-223764
DO - 10.1136/ard-2022-223764
M3 - Article
C2 - 36927642
AN - SCOPUS:85152667500
VL - 83
SP - 30
EP - 47
JO - Annals of the Rheumatic Diseases
JF - Annals of the Rheumatic Diseases
SN - 0003-4967
IS - 1
ER -