Impact of quality of life on overall work productivity impairment and activity impairment of patients with systemic lupus erythematosus: the PEONY study.

IF 3.7 2区 医学 Q1 RHEUMATOLOGY
Yoshiya Tanaka, Yusuke Miyazaki, Shintaro Hirata, Katsuhide Kusaka, Shunpei Kosaka, Keisuke Nakatsuka, Kazuyoshi Saito, Shigeru Iwata, Yoshiyuki Yamaguchi, Toshiki Yabe-Wada, Masakazu Fujiwara, Yoshifumi Arita, Mitsuru Hoshino, Naoko Ozaki, Kunihiro Yamaoka, Shingo Nakayamada
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Abstract

Objectives: Even in a lupus low disease activity state (LLDAS), many patients with SLE continue to face residual symptoms and disease burden. We aimed to evaluate the quality of life, activity impairment and overall work productivity impairment among patients in LLDAS. Residual disease burden was also evaluated for patients in LLDAS.

Methods: This prospective, cross-sectional study enrolled Japanese outpatients with SLE. Patients completed patient-reported outcome (PRO) questionnaires, including LupusPRO, Work Productivity and Activity Impairment-Lupus, EQ-5D-5L and Health Assessment Questionnaire-Disability Index. Disease activity and organ damage were investigator-assessed. The primary objective was to assess the residual burden in patients in LLDAS and to investigate the association of LupusPRO domains with activity impairment using multivariate regression analysis. Other objectives were to investigate the relationship between overall work productivity impairment or activity impairment and other PRO or disease activity measures.

Results: The analysis set included 205 patients; 93.2% were female, mean (SD) age at index date was 52.5 (14.7) years, mean (SD) duration of morbidity was 167.2 (125.2) months and 164 were in LLDAS. The mean per cent overall work productivity impairment was 22.8% and mean per cent activity impairment was 30.0% for the LLDAS group. Among patients in LLDAS, overall work productivity impairment was significantly associated with the LupusPRO domains Desires-Goals, Body Image and Pain Vitality, and activity impairment was significantly associated with the LupusPRO domains Pain Vitality, Physical Health and Lupus Symptoms.

Conclusions: Patients with SLE in LLDAS still experience symptoms associated with activity impairment. Work productivity also showed impairments. Improving their quality of life and achieving social remission will require ongoing monitoring of PROs and tailoring treatments to optimise these outcomes.

Trial registration number: jRCT1030210647.

生活质量对系统性红斑狼疮患者整体工作效率障碍和活动障碍的影响:牡丹研究
目的:即使处于狼疮低疾病活动性状态(LLDAS),许多SLE患者仍然面临残留症状和疾病负担。我们旨在评估LLDAS患者的生活质量、活动障碍和整体工作效率障碍。对LLDAS患者的残留疾病负担也进行了评估。方法:这项前瞻性横断面研究纳入了日本SLE门诊患者。患者完成患者报告结果(PRO)问卷,包括LupusPRO、工作效率和活动障碍-狼疮、EQ-5D-5L和健康评估问卷-残疾指数。疾病活动性和器官损害由研究者评估。主要目的是评估LLDAS患者的剩余负担,并使用多变量回归分析调查LupusPRO结构域与活动障碍的关联。其他目的是调查总体工作效率损害或活动损害与其他PRO或疾病活动测量之间的关系。结果:分析集纳入205例患者;93.2%为女性,指数日平均(SD)年龄为52.5(14.7)岁,平均(SD)发病时间为167.2(125.2)个月,LLDAS为164例。LLDAS组整体工作效率平均下降22.8%,活动效率平均下降30.0%。在LLDAS患者中,整体工作效率障碍与LupusPRO域的欲望-目标、身体形象和疼痛活力显著相关,活动障碍与LupusPRO域的疼痛活力、身体健康和狼疮症状显著相关。结论:LLDAS的SLE患者仍然会出现与活动障碍相关的症状。工作效率也受到影响。改善他们的生活质量和实现社会缓解需要持续监测PROs和定制治疗以优化这些结果。试验注册号:jRCT1030210647。
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来源期刊
Lupus Science & Medicine
Lupus Science & Medicine RHEUMATOLOGY-
CiteScore
5.30
自引率
7.70%
发文量
88
审稿时长
15 weeks
期刊介绍: Lupus Science & Medicine is a global, peer reviewed, open access online journal that provides a central point for publication of basic, clinical, translational, and epidemiological studies of all aspects of lupus and related diseases. It is the first lupus-specific open access journal in the world and was developed in response to the need for a barrier-free forum for publication of groundbreaking studies in lupus. The journal publishes research on lupus from fields including, but not limited to: rheumatology, dermatology, nephrology, immunology, pediatrics, cardiology, hepatology, pulmonology, obstetrics and gynecology, and psychiatry.
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