Moura C S, Rahme E, Maksymowych W P, Abrahamowicz M, Bessette L, 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.
Scand J Rheumatol. 2019 Mar;48(2):121-127. doi: 10.1080/03009742.2018.1470253. Epub 2018 Aug 16.
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.
评估强直性脊柱炎(AS)患者中使用改善病情抗风湿药物(DMARDs)和/或抗肿瘤坏死因子(抗TNF)药物引发住院感染的风险。
我们研究了2001年1月1日至2011年12月31日期间使用抗TNF药物和/或DMARDs的AS患者。队列进入定义为首次开具这些药物中任何一种的日期。我们使用Cox回归分析三种随时间变化的药物暴露情况:当前使用不含生物制剂的DMARDs、当前单独使用抗TNF药物或与DMARDs联合使用(抗TNF±DMARDs)以及当前未使用。模型根据患者基线社会人口统计学特征、合并症、门诊就诊和手术、既往感染、非甾体抗炎药以及皮质类固醇进行了调整。住院感染根据住院出院诊断(主要或非主要)中的感染编码来定义。
该队列包括747例AS患者,平均年龄51.1岁(标准差14.6),其中466例(62.4%)为男性。在中位随访1.98年期间,发生了57例住院感染,发病率为2.9/100人年。抗TNF±DMARDs组感染的调整后风险比(相对于未暴露组)为1.00 [95%置信区间(CI)0.47 - 2.11],单独使用DMARDs组为0.96(95%CI 0.45 - 2.04)。医疗保健的使用、皮质类固醇以及既往住院感染与感染相关。
我们没有发现明确证据表明住院感染风险与DMARDs和/或抗TNF药物的使用有关。由于关于AS患者感染风险的已发表文献稀少,我们的结果对临床医生具有重要意义。