Use of disease-modifying anti-rheumatic or anti-tumour necrosis factor drugs and risk of hospitalized infection in ankylosing spondylitis.


Journal

Scandinavian journal of rheumatology
ISSN: 1502-7732
Titre abrégé: Scand J Rheumatol
Pays: England
ID NLM: 0321213

Informations de publication

Date de publication:
Mar 2019
Historique:
pubmed: 17 8 2018
medline: 11 4 2019
entrez: 17 8 2018
Statut: ppublish

Résumé

To assess the risk of hospitalized infection among initiators of disease-modifying anti-rheumatic drugs (DMARDs) and/or anti-tumour necrosis factor (anti-TNF) agents in ankylosing spondylitis (AS). We studied AS patients, new users of anti-TNF drugs and/or DMARDs between 1 January 2001 and 31 December 2011. Cohort entry was defined as the date of first prescription of any of these drugs. We used Cox regression with three time-varying drug exposures: current use of DMARDs without biologics, current use of anti-TNF agents alone or in combination with DMARDs (anti-TNF ± DMARDs), and current non-use. Models were adjusted for baseline patient sociodemographic characteristics, comorbidity, outpatient visits and procedures, previous infection, non-steroidal anti-inflammatory drugs, and corticosteroids. Hospitalized infection was defined on the basis of hospitalization discharge diagnoses (primary or non-primary) coding for infection. The cohort included 747 AS patients, with a mean age of 51.1 years (sd 14.6), and 466 (62.4%) were men. During the median follow-up of 1.98 years, 57 hospitalized infections occurred, for an incidence rate of 2.9/100 person-years. The adjusted hazard ratio of infection (relative to unexposed) was 1.00 [95% confidence interval (CI) 0.47-2.11] for the anti-TNF ± DMARDs group and 0.96 (95% CI 0.45-2.04) for DMARDs alone. Use of healthcare, corticosteroids, and previous hospitalized infections were associated with infection. We found no clear evidence that the risk of hospitalized infection was linked to DMARD and/or anti-TNF drug use. Because of scarce published literature on infection risk in AS patients, our results have important implications for clinicians.

Identifiants

pubmed: 30112959
doi: 10.1080/03009742.2018.1470253
doi:

Substances chimiques

Antirheumatic Agents 0
Tumor Necrosis Factor-alpha 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

121-127

Auteurs

C S Moura (CS)

a Centre for Outcome Research and Evaluation (CORE) , McGill University , Montreal , Canada.
b Department of Medicine, Division of Rheumatology , McGill University , Montreal , Canada.

E Rahme (E)

b Department of Medicine, Division of Rheumatology , McGill University , Montreal , Canada.
c Department of Medicine, Division of Clinical Epidemiology , McGill University , Montreal , Canada.

W P Maksymowych (WP)

d Department of Medicine , University of Alberta , Edmonton , Canada.

M Abrahamowicz (M)

e Department of Epidemiology, Biostatistics and Occupational Health , McGill University , Montreal , Canada.

L Bessette (L)

f Division of Rheumatology, Department of Medicine , Laval University , Quebec City , Canada.

S Bernatsky (S)

a Centre for Outcome Research and Evaluation (CORE) , McGill University , Montreal , Canada.
b Department of Medicine, Division of Rheumatology , McGill University , Montreal , Canada.

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Classifications MeSH