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Andreas Kronbichler, Johannes Leierer, Gisela Leierer, Gert Mayer, Alina Casian, Peter Höglund, Kerstin Westman, David Jayne, TO039
RISK OF VENOUS THROMBOEMBOLIC EVENTS IN ANCA ASSOCIATED VASCULITIS, Nephrology Dialysis Transplantation, Volume 31, Issue suppl_1, May 2016, Pages i77–i78, https://doi.org/10.1093/ndt/gfw150.03 - Share Icon Share
Introduction and Aims: To assess potential risk factors for the development of venous thromboembolic events in patients with anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitides.
Methods: 417 patients with appropriate follow-up data enrolled in randomised controlled trials conducted by the European Vasculitis Society (EUVAS) were identified. Univariate and multivariate analyses were performed in order to validate previously proposed and identify novel risk factors.
Results: Venous thromboembolism (VTE) occurred in 41 of 417 (9.8%) patients. Multivariate analysis retained Birmingham Vasculitis Activity Score (BVAS, OR 1.05, P=0.013), subsequent malignancy (OR 2.47, P=0.027), cutaneous (OR (4.07, P=0.001), gastrointestinal (OR 5.6, P=0.002) and mucous membrane / eye involvement (OR 2.73, P=0.005) as significant predictors for the development of VTE.
Conclusions: Our results highlight a role of higher disease activity and cutaneous, gastrointestinal and mucous membrane / eye involvement as risk factors to predict thromboembolic events. Moreover, our analysis revealed the association of a classic risk factor (malignancy) with VTE risk in patients with ANCA-associated vasculitides.
Table 1. In multivariate analysis, potential risk factors.
6 models (each adjusted for age, gender, baseline creatinine) . | OR . | (95 % CI) . | p-value . |
---|---|---|---|
BVAS | 1.05 | (1.01-1.10) | 0.013 |
Cutaneous | 4.07 | (1.97-8.37) | 0.001 |
Diabetes during follow-up | 0.60 | (0.20-1.77) | 0.355 |
GI | 5.60 | (1.93-16.22) | 0.002 |
Mucous Membrane / Eyes | 2.73 | (1.35-5.50) | 0.005 |
Subsequent Cancer | 2.47 | (1.11-5.52) | 0.027 |
6 models (each adjusted for age, gender, baseline creatinine) . | OR . | (95 % CI) . | p-value . |
---|---|---|---|
BVAS | 1.05 | (1.01-1.10) | 0.013 |
Cutaneous | 4.07 | (1.97-8.37) | 0.001 |
Diabetes during follow-up | 0.60 | (0.20-1.77) | 0.355 |
GI | 5.60 | (1.93-16.22) | 0.002 |
Mucous Membrane / Eyes | 2.73 | (1.35-5.50) | 0.005 |
Subsequent Cancer | 2.47 | (1.11-5.52) | 0.027 |
Table 1. In multivariate analysis, potential risk factors.
6 models (each adjusted for age, gender, baseline creatinine) . | OR . | (95 % CI) . | p-value . |
---|---|---|---|
BVAS | 1.05 | (1.01-1.10) | 0.013 |
Cutaneous | 4.07 | (1.97-8.37) | 0.001 |
Diabetes during follow-up | 0.60 | (0.20-1.77) | 0.355 |
GI | 5.60 | (1.93-16.22) | 0.002 |
Mucous Membrane / Eyes | 2.73 | (1.35-5.50) | 0.005 |
Subsequent Cancer | 2.47 | (1.11-5.52) | 0.027 |
6 models (each adjusted for age, gender, baseline creatinine) . | OR . | (95 % CI) . | p-value . |
---|---|---|---|
BVAS | 1.05 | (1.01-1.10) | 0.013 |
Cutaneous | 4.07 | (1.97-8.37) | 0.001 |
Diabetes during follow-up | 0.60 | (0.20-1.77) | 0.355 |
GI | 5.60 | (1.93-16.22) | 0.002 |
Mucous Membrane / Eyes | 2.73 | (1.35-5.50) | 0.005 |
Subsequent Cancer | 2.47 | (1.11-5.52) | 0.027 |
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