NYMERIA 研究:系统性红斑狼疮患者与疾病和患者相关的负担及治疗策略的真实世界多中心当代评估。

Q4 Medicine
Mediterranean Journal of Rheumatology Pub Date : 2024-06-30 eCollection Date: 2024-06-01 DOI:10.31138/mjr.160524.tns
George Bertsias, Antonis Fanouriakis, Marina Bartsakoulia, Petros Galanakis, Dimitrios T Boumpas
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引用次数: 0

摘要

系统性红斑狼疮(SLE)有多种表型。其治疗目标应该是缓解或降低疾病活动性,预防复发和器官损伤,最大限度地减少药物相关的危害,以及优化与健康相关的生活质量。随着我们对疾病病理生理学认识的不断深入,靶向生物制剂扩大了治疗范围,它们在控制疾病活动、减少复发和糖皮质激素暴露以及改善患者相关预后方面均优于传统药物。有鉴于此,我们亟需真实世界的证据,以深入了解系统性红斑狼疮患者的活动范围、治疗情况和尚未满足的需求。这些信息可以为监管和报销决策提供支持。NYMERIA 多中心研究的主要目的是为在希腊接受常规治疗的系统性红斑狼疮患者的活动状态提供真实证据。总体目标是根据临床方面和患者角度来了解疾病负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The NYMERIA Study: A Real-World, Multicentre Contemporary Assessment of Disease- and Patient-Related Burden and Treatment Strategies in Patients with Systemic Lupus Erythematosus.

Systemic lupus erythematosus (SLE) has a spectrum of phenotypes. Its management should target remission or low disease activity, prevention of relapses and organ damage, minimisation of drug-related harms, and optimisation of health-related quality of life. Advances in our understanding of the disease pathophysiology have expanded the treatment armamentarium with targeted biologics that demonstrate superiority over conventional drugs in controlling activity, reducing flares and glucocorticoid exposure, and improving patient-related outcomes. In view of this, there is a critical need for real-world evidence providing insight into the spectrum of activity, the treatment landscape, and unmet needs among SLE patients. Such information can support regulatory and reimbursement decision-making. The primary objective of the NYMERIA multicentre study is to generate real-world evidence on the activity state of SLE patients treated in routine care settings in Greece. The overarching aim is to capture the disease burden based on both clinical aspects and the patient perspective.

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CiteScore
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