Concise report
Risk factors and prognostic influence of infection in a single
cohort of 87 adults with systemic lupus erythematosus
V Noël, O Lortholary, P Casassus, P Cohen, T Généreau, M-H André, L Mouthon, L Guillevin
Fédération
de Médecine Interne, Maladies Infectieuses et Tropicales, Hôpital
Avicenne, Université Paris-Nord, Bobigny, France
Correspondence to: Professor L Guillevin, Hôpital Avicenne, 125, route de Stalingrad, 93009 Bobigny, France loic.guillevin{at}avc.ap-hop-paris.fr
Accepted for publication 26 April 2001
OBJECTIVES
To describe
infectious complications and analyse their risk factors and prognostic
role in adults with systemic lupus erythematosus (SLE).
METHODS
A monocentric
cohort of 87 adults with SLE (1960-1997) was studied to determine the
risk factors for infection (disease activity evaluated by SLAM and
SLEDAI scores, type of organ(s) involved or any biological abnormality,
specific treatments) by comparing patients who had suffered at least
one infectious episode (n=35; 40%) with non-infected patients (n=52;
60%). Prognostic indicators were assessed by comparing survivors at 10 years with non-survivors.
RESULTS
Of the 57 infectious episodes, 47 (82%) were of bacterial origin, 16 (28%) were
pneumonia, and 46 (81%) were community acquired. According to
univariate analysis, significant risk factors for infection were:
severe flares, lupus glomerulonephritis, oral or intravenous
corticosteroids, pulse cyclophosphamide, and/or plasmapheresis. No
predictors were identified at the time of SLE diagnosis. Multivariate
analyses retained intravenous corticosteroids (p<0.001) and/or
immunosuppressants (p<0.01) as independent risk factors for infection,
which was the only factor for death after 10 years of evolution
(p<0.001).
CONCLUSION
In adults
with SLE, infections are common and most often caused by community
acquired bacteria. Intravenous corticosteroids and
immunosuppressants are independent risk factors for infection, which is
the only independent risk factor for death after 10 years of SLE evolution.
© 2001 by Annals of the Rheumatic Diseases
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