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Serious infections in patients with rheumatoid arthritis and other immune-mediated connective tissue diseases exposed to anti-TNF or rituximab: Data from the Spanish registry BIOBADASER 2.0

机译:暴露于抗TNF或利妥昔单抗的类风湿性关节炎和其他免疫介导的结缔组织病患者的严重感染:来自西班牙注册表BIOBADASER 2.0的数据

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Data on infections in patients exposed to biologic therapies are mainly focused on rheumatoid arthritis (RA). Little is known about the safety profile in other immune-mediated connective tissue diseases (ICTD). The purpose of this study was to describe and to compare the risk of serious infections (SI) in patients with RA and other ICTD on anti-TNF or rituximab and to identify predictors of SI. We analyzed RA or other ICTD patients on anti-TNF or rituximab included in the Spanish registry BIOBADASER 2.0 (2000-2011). For each disease group, incidence rate (IR), mortality rate (MR) and IR ratio (IRR) of SI with 95 % CI were estimated. Risks were then standardized by age and sex to the general population. Risk factors for SI were assessed by Poisson regression models. A total of 3,301 patients on anti-TNF (n = 3,166) or rituximab (n = 135), of which 176 (5 %) had ICTD other than RA, were analyzed. IR of SI was higher in non-RA ICTD than in RA, with an IRR of 3.15 (95 % CI 1.86, 5.31) before adjustment and 1.96 (95 % CI 1.06, 3.65) after adjustment for age, comorbidity and corticoid use. Mortality due to infections was higher in ICTD although it did not reach statistical significance. Age, disease duration, comorbidities, corticosteroids and ICTD different to RA were all independently associated with SI. Patients with ICTD other than RA are at a high risk of SI when prescribed anti-TNF or rituximab, partly due to the excess comorbidity and immunosuppressive co-treatment, but also to the inflammatory disease. When evaluating the risk/benefit ratio of off-label medications in ICTD patients, age, comorbidities and corticoid use should carefully be taken into account, applying adequate preventive measures.
机译:接受生物疗法的患者的感染数据主要集中在类风湿关节炎(RA)上。关于其他免疫介导的结缔组织病(ICTD)的安全性了解甚少。这项研究的目的是描述和比较RA和其他ICTD的抗TNF或利妥昔单抗治疗的严重感染(SI)的风险,并确定SI的预测因子。我们对西班牙登记册BIOBADASER 2.0(2000-2011)中包含的抗TNF或利妥昔单抗的RA或其他ICTD患者进行了分析。对于每个疾病组,估计具有95%CI的SI的发生率(IR),死亡率(MR)和IR比(IRR)。然后,按年龄和性别对普通人群进行风险标准化。 SI的危险因素通过泊松回归模型进行评估。分析了总共3,301例接受抗TNF(n = 3,166)或利妥昔单抗(n = 135)的患者,其中176名(5%)患有RA以外的ICTD。在非RA ICTD中,SI的IR高于RA,在调整年龄,合并症和使用皮质激素后,IRR为3.15(95%CI 1.86,5.31),调整后为1.96(95%CI 1.06,3.65)。尽管未达到统计学意义,但ICTD中因感染引起的死亡率较高。与RA不同的年龄,疾病持续时间,合并症,皮质类固醇和ICTD与SI均独立相关。除RA以外的ICTD患者在接受抗TNF或利妥昔单抗治疗时有SI的高风险,部分原因是由于合并症过多和免疫抑制联合治疗,还由于炎症性疾病。在评估ICTD患者中不合格药物的风险/获益比时,应谨慎考虑年龄,合并症和使用皮质类固醇,并采取适当的预防措施。

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