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药物诱导的系统性红斑狼疮:使用世界卫生组织药物警戒数据库重新审视该疾病不断变化的谱。

Drug-induced systemic lupus: revisiting the ever-changing spectrum of the disease using the WHO pharmacovigilance database.

机构信息

Service de rhumatologie, Hôpitaux Universitaires de Strasbourg, Laboratoire d'Immuno Rhumatologie Moléculaire, INSERM UMR_S1109, Strasbourg, France

Centre National de Références des Maladies Systémiques et Autoimmunes Rares Est Sud-Ouest (RESO), Université de Strasbourg, Strasbourg, France.

出版信息

Ann Rheum Dis. 2019 Apr;78(4):504-508. doi: 10.1136/annrheumdis-2018-214598. Epub 2019 Feb 4.

Abstract

OBJECTIVE

Drug-induced lupus (DIL) is an idiosyncratic side effect of treatments in which symptoms overlap with those of systemic lupus erythematosus (SLE). The spectrum of DIL constantly evolves with that of the pharmacopoeia. Here, we used VigiBase, the WHO global individual case safety reports (ICSRs) database, to identify the main drugs associated with DIL.

METHODS

We analysed all ICSRs classified as 'systemic lupus erythematosus' according to the Medical Dictionary for Drug Regulatory Activities term (preferred term level) in VigiBase. The drugs considered in the analysis were those not used to treat SLE, with a positive lower end of the 95% credibility interval for the information component (IC) ≥0, an indicator value for disproportionate Bayesian reporting.

RESULTS

A total of 12 166 DIL ICSRs were identified using VigiBase. From those, 8163 ICSRs reporting on 118 suspected drugs with IC ≥0 were extracted. The median age at DIL onset was 49 years and the female to male sex ratio was 4.3. The median delay between start of suspected treatment and DIL occurrence was 172 days. DIL was reported as serious adverse event in 55.4%. Among the 118 suspected drugs, 42 had not been previously reported in association with DIL. The drugs associated with the highest number of DIL cases were infliximab, adalimumab, etanercept, procainamide and hydralazine.

CONCLUSION

This study enables the identification of 118 drugs associated with DIL. The list of suspected drugs may prove useful to physicians when confronted with potential DIL cases.

TRIAL REGISTRATION NUMBER

NCT03480529.

摘要

目的

药物性狼疮(DIL)是治疗过程中的一种特发性副作用,其症状与系统性红斑狼疮(SLE)重叠。DIL 的范围随着药物学的发展而不断变化。在这里,我们使用了世界卫生组织全球个体病例安全报告(ICSR)数据库 VigiBase,以确定与 DIL 相关的主要药物。

方法

我们分析了 VigiBase 中根据药物监管活动医学词典(首选术语级别)分类为“系统性红斑狼疮”的所有 ICSR。分析中考虑的药物是那些不用于治疗 SLE 的药物,其信息成分(IC)的 95%置信区间下限(IC)为正值,且不平衡贝叶斯报告指标值≥0。

结果

使用 VigiBase 共确定了 12166 例 DIL ICSR。从这些 ICSR 中提取了 8163 例报告了 118 种可疑药物的 ICSR,这些药物的 IC 值均≥0。DIL 发病的中位年龄为 49 岁,男女比例为 4.3。可疑药物治疗开始至 DIL 发生的中位时间为 172 天。55.4%的 DIL 报告为严重不良事件。在 118 种可疑药物中,有 42 种药物以前未报告与 DIL 有关。与 DIL 病例数量最多相关的药物是英夫利昔单抗、阿达木单抗、依那西普、普鲁卡因胺和肼屈嗪。

结论

本研究确定了 118 种与 DIL 相关的药物。可疑药物清单可能对医生在处理潜在的 DIL 病例时有所帮助。

试验注册编号

NCT03480529。

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