4.6 Review

Frequency, risk factors and prophylaxis of infection in ANCA-associated vasculitis

Journal

EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
Volume 45, Issue 3, Pages 346-368

Publisher

WILEY
DOI: 10.1111/eci.12410

Keywords

ANCA-associated vasculitis; granulomatosis with polyangiitis; immunosuppression; infections; Pneumocystis jirovecii; trimethoprim-sulfamethoxazole

Funding

  1. ERA-EDTA
  2. Roche/Genentech
  3. GlaxoSmithKline
  4. Cambridge Biomedical Research Centre

Ask authors/readers for more resources

BackgroundAntineutrophil cytoplasm antibody (ANCA)-associated vasculitides are potentially life-threatening disorders. Materials and methodsEven though immunosuppressive therapy improves the prognosis, adverse events, either attributable to persistent disease activity or side effects of treatment remain a challenge. Infectious complications are the leading cause of death in the first year after diagnosis and a major cause of morbidity and mortality thereafter. ResultsTheir incidence in clinical trials varies considerably but opportunistic and life-threatening infections, such as Pneumocystis jirovecii pneumonia or systemic cytomegalovirus infections, are frequent and thus predisposing/risk factors need to be defined. Pneumocystis jirovecii pneumonia has been associated with a lymphocyte count below 300/mm(3). Additionally, besides the aggressiveness of the immunosuppressive regimen administered (especially the cumulative dose of steroids and cyclophosphamide), an elevated serum creatinine or dialysis dependency, older age and pulmonary involvement increase the rate of infectious complications. ConclusionsWe suggest to routinely prescribe trimethoprim-sulfamethoxazole or antimicrobial agents such as pentamidine in case of intolerance or contraindication in the early phase of induction therapy irrespective of the immunosuppressive strategy used and to continue therapy, together with other targeted measures (antiviral, antimycotic or antibiotic) in the presence of risk factors for a prolonged period of time. Finally, there is an urgent need to standardize the reporting of infectious complications in clinical trials to enable comparing the adverse event spectrum of distinct treatment approaches more appropriately.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available