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来氟米特相关的类风湿关节炎感染

Leflunomide-associated infections in rheumatoid arthritis.

作者信息

Jenks Katey A, Stamp Lisa K, O'Donnell John L, Savage Ruth L, Chapman Peter T

机构信息

Department of Rheumatology, Immunology and Allergy, Christchurch Hospital, Christchurch, New Zealand.

出版信息

J Rheumatol. 2007 Nov;34(11):2201-3. Epub 2007 Oct 15.

Abstract

OBJECTIVE

To determine the prevalence of severe infections in patients with rheumatoid arthritis (RA) prescribed leflunomide in North Canterbury, New Zealand.

METHODS

A case-note audit of all Christchurch Hospital patients with RA prescribed leflunomide between 2002 and 2006 was performed. The criterion for severe infection was inpatient hospitalization. Relevant reports to the national Pharmacovigilance Centre were also examined.

RESULTS

Since January 2002, 171 patients with RA have commenced taking leflunomide. Ninety-nine of 171 (57.9%) patients were also prescribed prednisone. Combination disease modifying antirheumatic drug therapy was common, with 82/171 (48.0%) taking methotrexate (MTX), 15/171 (8.8%) hydroxy-chloroquine, 11/171 (6.4%) sulfasalazine, and 8/171 (4.7%) anti-tumor necrosis factor therapy. Eleven patients developed infection requiring hospitalization while taking leflunomide including: lower respiratory tract infections (3), cellulitis (2), disseminated herpes zoster (2), probable TB liver (1), abdominal sepsis (1), mycotic aneurysm (1) and gastroenteritis (1). Nine of the 11 patients were also taking corticosteroids or corticosteroids with MTX. The 171 patients were treated for a total of 4005 months, giving an incidence for severe infection of 3.30/100 patient-years (95% CI 1.65-5.90). Patients at increased risk were those with severe disease and taking concomitant MTX and corticosteroids. The NZ Pharmacovigilance Centre has received 7 additional reports of severe infections in patients with RA taking leflunomide. Reported cases include probable pulmonary TB (1), pneumocystis pneumonia (1), other pulmonary infection (2), and septicemia (3) including a case of infective endocarditis. Four occurred in combination with MTX, one with adalimumab. All 5 patients were also taking -corticosteroids.

CONCLUSION

We believe this observed rate of serious infection is acceptable in the context of optimally treating active RA. Patients with severe disease and taking combination MTX and corticosteroids are at greatest risk. In our experience, once established, infections may rapidly progress in patients with RA taking leflunomide, and early cholestyramine washout is strongly recommended.

摘要

目的

确定在新西兰北坎特伯雷地区接受来氟米特治疗的类风湿关节炎(RA)患者中严重感染的患病率。

方法

对2002年至2006年间所有在克赖斯特彻奇医院接受来氟米特治疗的RA患者进行病历审查。严重感染的标准为住院治疗。同时也检查了向国家药物警戒中心提交的相关报告。

结果

自2002年1月以来,171例RA患者开始服用来氟米特。171例患者中有99例(57.9%)还同时服用泼尼松。联合使用改善病情抗风湿药物治疗很常见,82/171例(48.0%)服用甲氨蝶呤(MTX),15/171例(8.8%)服用羟氯喹,11/171例(6.4%)服用柳氮磺胺吡啶,8/171例(4.7%)接受抗肿瘤坏死因子治疗。11例患者在服用来氟米特期间发生了需要住院治疗的感染,包括:下呼吸道感染(3例)、蜂窝织炎(2例)、播散性带状疱疹(2例)、可能的肝结核(1例)、腹部脓毒症(1例)、霉菌性动脉瘤(1例)和胃肠炎(1例)。11例患者中有9例还同时服用皮质类固醇或皮质类固醇与MTX。171例患者总共接受了4005个月的治疗,严重感染的发生率为3.30/100患者年(95%可信区间1.65 - 5.90)。风险增加的患者是那些患有严重疾病且同时服用MTX和皮质类固醇的患者。新西兰药物警戒中心又收到了7例接受来氟米特治疗的RA患者发生严重感染的报告。报告的病例包括可能的肺结核(1例)、肺孢子菌肺炎(1例)、其他肺部感染(2例)和败血症(3例),包括1例感染性心内膜炎。4例与MTX联合发生,1例与阿达木单抗联合发生。所有5例患者也都同时服用皮质类固醇。

结论

我们认为在积极治疗活动性RA的背景下,观察到的严重感染率是可以接受的。患有严重疾病且同时服用MTX和皮质类固醇的患者风险最大。根据我们的经验,一旦感染发生,接受来氟米特治疗的RA患者感染可能迅速进展,强烈建议尽早使用考来烯胺进行洗脱。

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