Abstract: SA-PO762
Clinical Frailty as a Proxy Measure for Infection Risk in ANCA-Associated Glomerulonephritis
Session Information
- ANCA-Associated Vasculitis, Anti-GBM Disease, and Other RPGN
October 26, 2024 | Location: Exhibit Hall, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: Glomerular Diseases
- 1402 Glomerular Diseases: Clinical, Outcomes, and Therapeutics
Authors
- Durailingam, Joshendra, The University of Manchester, Manchester, United Kingdom
- Gulati, Kavita, Imperial College London, London, United Kingdom
- Chapman, Gavin, University of Edinburgh, Edinburgh, United Kingdom
- Dhaun, Neeraj, University of Edinburgh, Edinburgh, United Kingdom
- McAdoo, Stephen Paul, Imperial College London, London, United Kingdom
- Brix, Silke R., The University of Manchester, Manchester, United Kingdom
Background
Frailty is a functional term referring to a decline in physiological function that leads to dependency, vulnerability and a high risk for poor health-related outcomes. Anti-neutrophil cytoplasmic antibody (ANCA) vasculitis affects the elderly and often results in a rapid decline in the general health. We aim to better understand the interaction between the rapid evolving ANCA associated inflammation and the impression of frailty to improve prediction modelling for adverse outcomes. Here, we investigated clinical frailty scale (CFS) at time of diagnosis for its association with clinical outcomes.
Methods
We performed a three-centre, retrospective analysis of newly diagnosed ANCA glomerulonephritis (GN) patients in the UK. Wilcoxon-Rank-Sum, Kruskal-Wallis and Fisher-Exact testing were used to analyse the relationships of age, CFS and infections, end stage kidney disease (ESKD) and death.
Results
A total of 275 patients were included, median follow-up 3.8 years (interquartile range, IQR, 2.1 – 5.3 years). The median age at presentation was 66.3 years (IQR, 54.7 – 74.5 years) and 145 were of male gender (52.3%). A total of 86 patients developed ESKD (31.3%), and 77 patients died (28%) during follow-up. Data on infection during the first year was available on 158 patients.
Age and CFS did not influence the development of ESKD (p=0.4 and p=0.21). Higher age and CFS were both associated with deaths during follow up (p=0.004 and p=0.002). The frequency and severity of infections did not differ across age (p=0.4 and p=0.2). CFS however associated with infections in frequency and severity (p=0.01 and p<0.001, Figure 1).
Conclusion
An initial frailty assessment at the time of diagnosis might assist in predicting infections in patients with newly diagnosed ANCA GN.
Funding
- Government Support – Non-U.S.