How well are biologic and conventional DMARDs tolerated in psoriatic arthritis: A real world study.

IF 1.3 Q4 RHEUMATOLOGY
Issrah I Jawad, Muhammed K Nisar
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引用次数: 2

Abstract

Objective: Even though disease-modifying antirheumatic drugs (DMARDs) are well established in rou- tine clinical practice, longitudinal real-world data for their retention and tolerability are sparse, espe- cially in psoriatic arthritis (PsA) patients. Our objective was to describe the characteristics of our large PsA cohort including the comorbidities and evaluate real-world DMARD tolerability and discontinua- tion rates with reasons for stopping treatment.

Methods: We retrospectively interrogated the electronic, multipurpose, live setting database at our uni- versity hospital to identify 335 patients diagnosed with PsA who had received conventional DMARDs (cDMARDs) and/or biologic DMARDs (bDMARDs) between 1994 up to and including April 2019.

Results: In total, 170 (50.7%) patients had discontinued one or more cDMARDs prior with a mean dura- tion before discontinuation of 9.9 months. In contrast, only 28 (24.8%) patients had stopped a course of bDMARDs at some point. The mean duration before biologic therapy was discontinued was 18.2 months.

Conclusion: To our knowledge, this is the first dedicated retrospective review of a large real-world PsA cohort addressing drug survival and tolerability of DMARDs over a 20-year period. Our study shows that in reality, cDMARDs are not well tolerated. This should encourage review of international guid- ance allowing earlier employment of biologics in the treatment paradigm.

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银屑病关节炎患者对生物和传统DMARDs的耐受性如何:一项真实世界的研究。
目的:尽管改善疾病的抗风湿药物(DMARDs)在常规临床实践中得到了很好的建立,但其保留和耐受性的纵向真实世界数据很少,特别是在银屑病关节炎(PsA)患者中。我们的目的是描述我们的大型PsA队列的特征,包括合并症,评估现实世界的DMARD耐受性和停药率以及停药的原因。方法:我们回顾性地查询了我们大学医院的电子、多用途、实时设置数据库,以确定335名诊断为PsA的患者,这些患者在1994年至2019年4月期间接受了常规DMARDs (cDMARDs)和/或生物DMARDs (bDMARDs)。结果:总共有170例(50.7%)患者先前停药一种或多种cdmard,平均停药时间为9.9个月。相比之下,只有28例(24.8%)患者在某种程度上停止了bDMARDs疗程。停止生物治疗前的平均持续时间为18.2个月。结论:据我们所知,这是第一个针对20年期间DMARDs药物生存和耐受性的大型真实PsA队列的专门回顾性审查。我们的研究表明,在现实中,cDMARDs的耐受性并不好。这应该鼓励对国际指导方针的审查,允许在治疗范例中更早地使用生物制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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发文量
56
审稿时长
7 weeks
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