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他克莫司致类风湿关节炎患者肺损伤。

Tacrolimus-induced pulmonary injury in rheumatoid arthritis patients.

机构信息

Tokyo Medical and Dental University, Tokyo, Japan.

出版信息

Pulm Pharmacol Ther. 2011 Aug;24(4):401-6. doi: 10.1016/j.pupt.2011.01.016. Epub 2011 Feb 21.

Abstract

BACKGROUND

Tacrolimus (TAC) was approved in Japan in 2005 for rheumatoid arthritis (RA) patients having inadequate response to other disease-modifying anti-rheumatic drugs. As of May 2007, spontaneous reports identified twenty-seven cases of exacerbation or new development of interstitial pneumonia among RA patients given TAC in Japan.

OBJECTIVE

To describe the clinical and radiological characteristics of TAC-induced pulmonary injury (TIPI).

PATIENTS AND METHODS

Eleven RA patients diagnosed with de novo pulmonary injury or exacerbation of IP during treatment with TAC were identified. Clinical, radiological, and laboratory data of ten of these cases were retrospectively analyzed.

RESULTS

Baseline data for the ten patients were a mean age of 69.7 years; gender, 70% female; mean RA disease duration, 9.1 years; and pulmonary comorbidities, 90%. Six cases were classified as presumptive TAC-induced pulmonary injury (TIPI) and four as probable TIPI. Among the six presumptive cases, TIPI developed at an average of 84 days after initiation of treatment (n = 5) or four days after reinstitution of TAC (n = 1). Five cases were an exacerbation of pre-existing interstitial pneumonia and one was a de novo pulmonary injury. Radiological patterns of thoracic computed tomography (CT) scans of patients in the presumptive TIPI cases were hypersensitivity pneumonia like-pattern (n = 3), ground-glass opacity (n = 2), and organizing pneumonia-pattern (n = 1). All patients with presumptive TIPI were treated with high dosage glucocorticosteroids and one received concomitant immunosuppressants. Two of the six presumptive TIPI patients died.

CONCLUSION

Rheumatologists should be aware of this rare but potentially life-threatening adverse event in RA patients receiving TAC.

摘要

背景

他克莫司(TAC)于 2005 年在日本被批准用于治疗对其他疾病修饰抗风湿药物反应不足的类风湿关节炎(RA)患者。截至 2007 年 5 月,在日本使用 TAC 的 RA 患者中自发报告了 27 例间质性肺炎恶化或新发病例。

目的

描述他克莫司诱导的肺损伤(TIPI)的临床和影像学特征。

患者和方法

在使用 TAC 治疗期间,确定了 11 例新诊断为肺损伤或间质性肺炎恶化的 RA 患者。回顾性分析了其中 10 例患者的临床、影像学和实验室数据。

结果

10 例患者的基线数据为:平均年龄 69.7 岁;性别,70%为女性;平均 RA 病程为 9.1 年;肺部合并症为 90%。6 例被归类为疑似他克莫司诱导的肺损伤(TIPI),4 例为可能 TIPI。在 6 例疑似病例中,TIPI 在开始治疗后平均 84 天(n=5)或重新开始 TAC 治疗后 4 天(n=1)发生。5 例为原有间质性肺炎恶化,1 例为新发肺损伤。疑似 TIPI 患者的胸部计算机断层扫描(CT)扫描的影像学模式为:过敏性肺炎样模式(n=3)、磨玻璃影(n=2)和机化性肺炎样模式(n=1)。所有疑似 TIPI 患者均接受大剂量糖皮质激素治疗,1 例同时接受免疫抑制剂治疗。6 例疑似 TIPI 患者中有 2 例死亡。

结论

风湿科医生应意识到接受 TAC 治疗的 RA 患者中存在这种罕见但可能危及生命的不良事件。

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