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. 2025 Aug 19:keaf438.
doi: 10.1093/rheumatology/keaf438. Online ahead of print.

High risk of bloodstream infections, diverse causal pathogens, and association with haemodialysis and plasma exchange in ANCA-associated vasculitis

Nanna Thuesen Bruun  1 , Dea H Kofod  1 , Nicholas Carlson  1 , Mads Hornum  1   2 , Emil L Fosbøl  3   2 , Lauge Østergaard  3 , Marianne Volstedlund  4 , Stine H Finsen  5 , Claus Moser  6   7 , Casper Rydahl  8 , Per Ivarsen  9   10 , Jon Waarst Gregersen  11 , Martin Egfjord  1   2 , Wladimir M Szpirt  1 , Karl Emil Nelveg-Kristensen  1 ; Danish Vasculitis Association (DANVAS)
Collaborators, Affiliations

High risk of bloodstream infections, diverse causal pathogens, and association with haemodialysis and plasma exchange in ANCA-associated vasculitis

Nanna Thuesen Bruun et al. Rheumatology (Oxford). .

Abstract

Objectives: Infections from immunosuppressive treatment are a major cause of hospitalisation and mortality in ANCA-associated vasculitis (AAV). This study examines bloodstream infections (BSIs) in incident AAV patients, comparing incidence, bacterial distribution, and risk to the general population, with emphasis on central venous catheters (CVCs).

Methods: Using Danish nationwide registries, we studied patients diagnosed from 2010 to 2018, followed until first BSI, death, or a maximum of five years. Controls were matched 1:4 by age and sex. Cumulative incidence was estimated using Aalen-Johansen, and adjusted Cox regression modelled survival time.

Results: A total of 111 BSIs were identified in 80 (8.5%) of 937 AAV patients, compared with 65 BSIs in 58 (1.7%) of 3476 controls. The incidence of BSIs was significantly higher in AAV patients (34.5/1000 person-years against 4.8/1000 person-years). One-year hazard ratio (HR) for first-time BSIs was significantly elevated in AAV patients (HR 10.5, [95% CI 5.58-11.9]), and those receiving haemodialysis (HR 34.8, 95% CI 3.35-360.8) or plasma exchange (HR 14.6, 95% CI 3.79-56.6) faced even higher infection rates. Following first-time BSI, one-year mortality rates were equally high in AAV patients (36.3%) and controls (34.5%). Most common microbial agents-E. coli, S. aureus, enterococci, and streptococci-were similar between the two groups. However, AAV patients exhibited higher microbial diversity, with 48.6% attributed to other pathogens like coagulase-negative staphylococci, K. pneumoniae, P. aeruginosa, and fungi.

Conclusion: AAV patients face high BSI risk, diverse microbiology, and increased one-year mortality, with CVC-related interventions as solitary risk factors.

Keywords: ANCA-associated vasculitis; bloodstream infections; central venous catheters; haemodialysis; microbial aetiology; plasma exchange.

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