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类风湿关节炎药物暴露后的脱髓鞘事件。

Demyelinating events in rheumatoid arthritis after drug exposures.

机构信息

Centre for Clinical Epidemiology, Jewish General Hospital-Lady Davis Institute, 3755 Cote Ste-Catherine, Montreal, Quebec, Canada.

出版信息

Ann Rheum Dis. 2010 Sep;69(9):1691-3. doi: 10.1136/ard.2009.111500. Epub 2009 Jul 23.

Abstract

OBJECTIVE

To estimate the effects of biological drugs on the risk of demyelinating events in rheumatoid arthritis (RA).

METHODS

Case-control analyses nested in an administrative database cohort.

RESULTS

Initially the risk of demyelinating events appeared to be increased after exposure to anakinra and decreased after exposure to antitumour necrosis factor (anti-TNF) agents. However, this apparent differential risk was due to more anakinra use (and avoidance of anti-TNF agents) in persons at high risk for demyelinating events. In individuals not at high risk, the adjusted rate ratio was 1.31 (95% CI 0.68 to 2.50) after exposure to anti-TNF agents and 0.80 (95% CI 0.29 to 2.24) after exposure to anakinra.

CONCLUSIONS

When accounting for differential prescription patterns, there was a trend towards more events after exposure to anti-TNF agents. When studying rare but important potential drug associations, pharmacoepidemiological studies are valuable but must be carefully performed.

摘要

目的

评估生物药物对类风湿关节炎(RA)患者发生脱髓鞘事件风险的影响。

方法

基于行政数据库队列的巢式病例对照研究。

结果

最初,与抗肿瘤坏死因子(anti-TNF)药物相比,使用阿那白滞素后脱髓鞘事件的风险似乎增加,而使用 anti-TNF 药物后风险降低。然而,这种明显的差异风险归因于高风险脱髓鞘事件人群中阿那白滞素的使用(和避免使用 anti-TNF 药物)更多。在无高风险人群中,anti-TNF 药物组校正后的率比值为 1.31(95%CI 0.68 至 2.50),阿那白滞素组为 0.80(95%CI 0.29 至 2.24)。

结论

在考虑到不同的处方模式后,anti-TNF 药物组的事件发生趋势更多。在研究罕见但重要的潜在药物相关性时,药物流行病学研究具有价值,但必须仔细进行。

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