Management of antineutrophil cytoplasmic antibody–associated vasculitis with glomerulonephritis as proposed by the ACR 2021, EULAR 2022 and KDIGO 2021 guidelines/recommendations
ERA (IWG) · 2023 · Europe
Source and licence
- Authors
- Marta Casal Moura, Philipp Gauckler, Hans-Joachim Anders et al.
- Title
- Management of antineutrophil cytoplasmic antibody–associated vasculitis with glomerulonephritis as proposed by the ACR 2021, EULAR 2022 and KDIGO 2021 guidelines/recommendations
- Journal
- Nephrology Dialysis Transplantation, 2023
- Licence
- CC BY 4.0
- Changes
- Verbatim excerpts; formatting adapted
Full text retrieved 2026-10-27 from Europe PMC · PMC10615627
Licence statement of the original publication
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
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Recommendations
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Abstract
Updated guidelines on the management of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) were released in 2021 by the American College of Rheumatology jointly with the Vasculitis Foundation and, subsequently, in 2022 by the European Alliance of Associations for Rheumatology. In addition, in 2021, the Kidney Disease: Improving Global Outcomes had released updated recommendations on the treatment of AAV with glomerulonephritis (AAV-GN). Kidney involvement is particularly relevant in microscopic polyangiitis and granulomatosis with polyangiitis, but is less frequent in eosinophilic granulomatosis with polyangiitis. The management of AAV-GN has been a focus for drug development and change over the past 10 years. Avoidance of progression to end-stage kidney disease (ESKD) or kidney failure is one of the main unmet needs in the management of AAV, with ESKD having a major impact on morbidity, health costs and mortality risk. Relevant changes in AAV-GN management are related to remission-induction treatment of patients with severe kidney disease, the use of glucocorticoids and avacopan, and remission-maintenance treatment. All the documents provide guidance in accordance with the evidence-based standard of care available at the time of their release. With our work we aim to (i) show the progress made and identify the differences between guidelines and recommendations, (ii) discuss the supporting rationale for those, and (iii) identify gaps in knowledge that could benefit from additional research and should be revised in subsequent updates.
Contents of the original publication
The section headings of the original.
- INTRODUCTION
- GENERAL PRINCIPLES OF AAV MANAGEMENT
- AAV-GN MANAGEMENT
- REMISSION-INDUCTION TREATMENT IN PATIENTS WITH ORGAN-/LIFE-THREATENING KIDNEY DISEASE
- RTX vs CYC
- RTX and CYC
- PLEX vs no-PLEX
- REMISSION-INDUCTION TREATMENT IN PATIENTS WITH NON-ORGAN-/LIFE-THREATENING KIDNEY INVOLVEMENT
- MMF
- GLUCOCORTICOIDS USE, GLUCOCORTICOID SPARING AND AVACOPAN
- Glucocorticoids
- Avacopan
- REMISSION-MAINTENANCE TREATMENT
- RTX vs AZA
- RTX use guided by fixed intervals vs CD19+ B-cell reconstitution
- Optimal length of non-GC immunosuppressive remission-maintenance treatment
- No start or withdrawal
- MONITORING DISEASE ACTIVITY
- Summary
- FUTURE RESEARCH AND GAPS IN KNOWLEDGE
- CONCLUSIONS
- Contributor Information
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