阿尼单抗治疗可改善系统性红斑狼疮患者的生活质量,减少疾病活动和皮质类固醇的使用:丹麦的一项定性研究。

IF 1.9 4区 医学 Q3 RHEUMATOLOGY
Lupus Pub Date : 2024-08-01 Epub Date: 2024-06-20 DOI:10.1177/09612033241261746
Anne Troldborg, Lauren Remkus, Daniel Eek, Bent Deleuran
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引用次数: 0

摘要

Anifrolumab 是针对系统性红斑狼疮(SLE)患者的一种新疗法,旨在阻断 1 型干扰素通路。尽管有关阿尼洛单抗的文献越来越多,但仍缺少一个重要方面:患者对治疗效果的主观感受以及对患者健康相关生活质量(HRQoL)的影响。本研究旨在通过进行定性深入访谈(IDIs),阐明接受安非鲁单抗治疗的系统性红斑狼疮患者的细微观点,从而填补这一空白。奥胡斯大学医院的系统性红斑狼疮患者至少接受过三次安非鲁单抗输液治疗,他们都被纳入了这项研究:(1) 定性 IDI 和 (2) 从电子病历 (EMR) 中收集患者数据。IDI 采用半结构式,以讨论指南为基础,包括开放式和封闭式问题。使用定性软件对逐字记录誊本进行编码和分析,以了解对患者重要的概念,并了解患者在阿尼单抗治疗前后的自身经历。使用 EMR 数据对阿尼单抗开始治疗后的基线、3 个月和 6 个月进行了临床病历审查。14 名患者完成了 IDI,16 名患者收集了 EMR 数据(治疗天数范围:62-474 天)。在阿尼单抗治疗前患者自发报告的 23 种症状中,疲劳、关节疼痛、日光敏感、关节僵硬、皮疹和脱发最为常见。大多数症状在治疗期间得到了改善,没有任何症状恶化。治疗前,患者报告疾病对日常生活造成了重大影响:日常活动、社交生活、情绪方面、体力活动、注意力/记忆力、工作/就业以及家庭/情感关系。治疗后,患者表示各方面都有所改善,但仍受到影响。从 EMR 数据中,我们观察到治疗开始后疾病活动有所减少,同时皮质类固醇的使用也有所减少。这项研究为了解接受阿尼单抗治疗的系统性红斑狼疮患者的主观感受提供了宝贵的资料,研究结果有助于从患者的角度全面了解该疗法的疗效及其对系统性红斑狼疮患者主观和客观指标的实际影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anifrolumab treatment improves patient-reported quality of life and decreases disease activity and corticosteroid use in patients with systemic lupus erythematosus: A qualitative study in Denmark.

Anifrolumab is a new therapeutic approach for individuals with systemic lupus erythematosus (SLE) directed at blocking the type 1 interferon pathway. Despite the expanding body of literature on Anifrolumab, an essential aspect remains absent: the subjective patient experience of treatment effects and implications on patients' health-related quality of life (HRQoL). The present study aimed to fill this void by elucidating the nuanced perspectives of SLE patients receiving Anifrolumab treatment by conducting qualitative in-depth interviews (IDIs). SLE patients at Aarhus University Hospital who had received at least three infusions of Anifrolumab were approached for inclusion in the study, which comprised two main elements: (1) qualitative IDIs and (2) collection of patient data from electronic medical records (EMRs). The IDIs were semi-structured and based on a discussion guide that included open-ended and close-ended questions. Verbatim transcripts were coded and analysed using qualitative software to understand concepts important to patients and to understand patients' own experiences before and after Anifrolumab therapy. A clinical chart review was conducted using EMR data at baseline, 3 months, and 6 months after Anifrolumab initiation. IDIs were completed with 14 patients, and EMR data was collected from 16 patients (treatment days range: 62-474). Of the 23 symptoms spontaneously reported by patients prior to Anifrolumab treatment, fatigue, joint pain, sun sensitivity, joint stiffness, skin rashes, and hair loss were the most common. Most symptoms improved, and none worsened during treatment. Patients reported significant impacts of disease on daily life before treatment: day-to-day activities, social life, emotional aspects, physical activity, concentration/memory, work/employment, and family/romantic relationships. Patients reported improvements in all aspects after treatment but were still impacted. From the EMR data, we observed a fall in disease activity after treatment initiation with a concomitant reduction in the use of corticosteroids. This study provides valuable insights into the subjective experiences of SLE patients treated with Anifrolumab, and the findings collectively contribute to a comprehensive understanding of the treatment's efficacy from the patients' perspective and its tangible effects on both subjective and objective parameters in SLE patients.

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来源期刊
Lupus
Lupus 医学-风湿病学
CiteScore
4.20
自引率
11.50%
发文量
225
审稿时长
1 months
期刊介绍: The only fully peer reviewed international journal devoted exclusively to lupus (and related disease) research. Lupus includes the most promising new clinical and laboratory-based studies from leading specialists in all lupus-related disciplines. Invaluable reading, with extended coverage, lupus-related disciplines include: Rheumatology, Dermatology, Immunology, Obstetrics, Psychiatry and Cardiovascular Research…
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