• Wien. Klin. Wochenschr. · Aug 2023

    [Diagnosis and therapy of granulomatosis with polyangiitis and microscopic polyangiitis-2023: consensus of the Austrian society of nephrology (ÖGN) and Austrian society of rheumatology (ÖGR)].

    • Balazs Odler, Martin Windpessl, Kathrin Eller, Marcus D Säemann, Karl Lhotta, Irmgard Neumann, Gregor Öberseder, Christina Duftner, Christian Dejaco, Michael Rudnicki, Philipp Gauckler, Rainer Hintenberger, Jochen Zwerina, Jens Thiel, and Andreas Kronbichler.
    • Klinische Abteilung für Nephrologie, Abteilung für Innere Medizin III (Nephrologie, Dialyse und Hypertensiologie), Medizinische Universität Graz, Graz, Österreich.
    • Wien. Klin. Wochenschr. 2023 Aug 1; 135 (Suppl 5): 656674656-674.

    AbstractANCA-associated vasculitides (AAV) are rare, complex systemic diseases that are often difficult to diagnose, because of unspecific clinical symptoms at presentation. However, the clinical course may be very dramatic and even life-threatening, necessitating prompt diagnosis and treatment.Therefore, it is important to increase disease awareness among physicians and support colleagues who are not confronted with these rare diseases on a regular basis. Here, the Austrian Society of Nephrology (ÖGN) and the Austrian Society of Rheumatology (ÖGR) provide a joint consensus on how to best diagnose and manage patients with granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA).© 2023. The Author(s).

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