• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
A case-control study on health-related quality of life of systemic lupus erythematosus patients.一项关于系统性红斑狼疮患者健康相关生活质量的病例对照研究。
Sci Rep. 2024 Mar 4;14(1):5234. doi: 10.1038/s41598-024-55833-9.
2
EQ-5D and SF-36 quality of life measures in systemic lupus erythematosus: comparisons with rheumatoid arthritis, noninflammatory rheumatic disorders, and fibromyalgia.系统性红斑狼疮患者的 EQ-5D 和 SF-36 生活质量测量:与类风湿关节炎、非炎症性风湿性疾病和纤维肌痛的比较。
J Rheumatol. 2010 Feb;37(2):296-304. doi: 10.3899/jrheum.090778. Epub 2009 Dec 23.
3
Impact of disease activity on health-related quality of life in systemic lupus erythematosus - a cross-sectional analysis of the Swiss Systemic Lupus Erythematosus Cohort Study (SSCS).疾病活动对系统性红斑狼疮患者健康相关生活质量的影响——瑞士系统性红斑狼疮队列研究(SSCS)的横断面分析
BMC Immunol. 2017 Mar 28;18(1):17. doi: 10.1186/s12865-017-0200-5.
4
Functional disability and health-related quality of life in South Africans with rheumatoid arthritis and systemic lupus erythematosus.南非类风湿性关节炎和系统性红斑狼疮患者的功能残疾与健康相关生活质量
Clin Rheumatol. 2007 Jan;26(1):24-9. doi: 10.1007/s10067-006-0215-4. Epub 2006 Mar 15.
5
Influence of social support on health-related quality of life in patients with systemic lupus erythematosus.社会支持对系统性红斑狼疮患者健康相关生活质量的影响。
Clin Rheumatol. 2009 Mar;28(3):265-9. doi: 10.1007/s10067-008-1033-7. Epub 2008 Nov 11.
6
Health-related quality of life in systemic sclerosis compared with other rheumatic diseases: a cross-sectional study.系统性硬化症与其他风湿性疾病的健康相关生活质量比较:一项横断面研究。
Arthritis Res Ther. 2019 Feb 15;21(1):61. doi: 10.1186/s13075-019-1842-x.
7
Health-related quality of life and utility: comparison of ankylosing spondylitis, rheumatoid arthritis, and systemic lupus erythematosus patients in Taiwan.健康相关生活质量与效用:台湾强直性脊柱炎、类风湿性关节炎和系统性红斑狼疮患者的比较。
Clin Rheumatol. 2017 Jan;36(1):133-142. doi: 10.1007/s10067-016-3471-y. Epub 2016 Nov 12.
8
Fatigue in systemic lupus erythematosus : Association with disease activity, quality of life and psychosocial factors.系统性红斑狼疮中的疲劳:与疾病活动、生活质量及心理社会因素的关联
Z Rheumatol. 2017 Dec;76(10):913-919. doi: 10.1007/s00393-016-0185-0.
9
Quality of life among female patients with systemic lupus erythematosus in remission.红斑狼疮女性患者缓解期的生活质量。
Rheumatol Int. 2019 Aug;39(8):1351-1358. doi: 10.1007/s00296-019-04329-1. Epub 2019 May 25.
10
Reduced Aerobic Capacity and Quality of Life in Physically Inactive Patients With Systemic Lupus Erythematosus With Mild or Inactive Disease.身体活动不足的轻度或非活动性系统性红斑狼疮患者的有氧能力和生活质量降低
Arthritis Care Res (Hoboken). 2016 Dec;68(12):1780-1786. doi: 10.1002/acr.22905. Epub 2016 Oct 28.

引用本文的文献

1
Impact of Systemic Lupus Erythematosus on Health-Related Quality of Life in Colombian Patients: A Cross-Sectional Analytical Study.系统性红斑狼疮对哥伦比亚患者健康相关生活质量的影响:一项横断面分析研究。
Patient Prefer Adherence. 2025 May 2;19:1263-1272. doi: 10.2147/PPA.S498414. eCollection 2025.
2
Holistic approaches in systemic lupus erythematosus: do physicians avoid addressing difficult-to-treat but highly relevant symptoms?系统性红斑狼疮的整体治疗方法:医生是否会避免处理难以治疗但高度相关的症状?
RMD Open. 2025 Mar 7;11(1):e005400. doi: 10.1136/rmdopen-2024-005400.

本文引用的文献

1
Impact of demographic, clinical, and treatment compliance characteristics on quality of life of Venezuelan patients with systemic lupus erythematosus.人口统计学、临床及治疗依从性特征对委内瑞拉系统性红斑狼疮患者生活质量的影响
BMC Rheumatol. 2022 Jan 4;6(1):2. doi: 10.1186/s41927-021-00232-0.
2
Living with systemic lupus erythematosus in 2020: a European patient survey.2020 年系统性红斑狼疮患者的生活状况:一项欧洲患者调查。
Lupus Sci Med. 2021 Apr;8(1). doi: 10.1136/lupus-2020-000469.
3
Fatigue in patients with systemic lupus erythematosus and neuropsychiatric symptoms is associated with anxiety and depression rather than inflammatory disease activity.系统性红斑狼疮和神经精神症状患者的疲劳与焦虑和抑郁有关,而与炎症性疾病活动无关。
Lupus. 2021 Jun;30(7):1124-1132. doi: 10.1177/09612033211005014. Epub 2021 Mar 28.
4
Update οn the diagnosis and management of systemic lupus erythematosus.红斑狼疮诊断与治疗的最新进展。
Ann Rheum Dis. 2021 Jan;80(1):14-25. doi: 10.1136/annrheumdis-2020-218272. Epub 2020 Oct 13.
5
The diagnostic accuracies of the 2012 SLICC criteria and the proposed EULAR/ACR criteria for systemic lupus erythematosus classification are comparable.2012 年 SLICC 标准和建议的 EULAR/ACR 标准对系统性红斑狼疮分类的诊断准确性相当。
Lupus. 2019 May;28(6):778-782. doi: 10.1177/0961203319846388. Epub 2019 May 2.
6
Sex Differences in Pediatric Rheumatology.儿科风湿病学中的性别差异。
Clin Rev Allergy Immunol. 2019 Jun;56(3):293-307. doi: 10.1007/s12016-017-8642-3.
7
Assessment of disease activity, damage and quality of life in systemic lupus erythematosus: new aspects.评估系统性红斑狼疮的疾病活动、损害和生活质量:新的方面。
Best Pract Res Clin Rheumatol. 2013 Jun;27(3):309-18. doi: 10.1016/j.berh.2013.10.003. Epub 2013 Oct 5.
8
Drivers of cost and health-related quality of life in patients with systemic lupus erythematosus (SLE): a Swedish nationwide study based on patient reports.系统性红斑狼疮(SLE)患者的成本和健康相关生活质量的驱动因素:基于患者报告的瑞典全国性研究。
Lupus. 2013 Jul;22(8):793-801. doi: 10.1177/0961203313491849. Epub 2013 Jun 11.
9
The impact of rural residency on the expression and outcome of systemic lupus erythematosus: data from a multiethnic Latin American cohort.农村居住对系统性红斑狼疮表达和结局的影响:来自多民族拉丁美洲队列的数据。
Lupus. 2012 Nov;21(13):1397-404. doi: 10.1177/0961203312458465. Epub 2012 Aug 31.
10
Quality of life in patients with systemic lupus erythematosus (SLE) compared with related controls within a unique African American population.系统性红斑狼疮(SLE)患者与独特的非裔美国人人群中的相关对照者的生活质量比较。
Lupus. 2012 Apr;21(5):563-9. doi: 10.1177/0961203311426154. Epub 2011 Oct 26.

一项关于系统性红斑狼疮患者健康相关生活质量的病例对照研究。

A case-control study on health-related quality of life of systemic lupus erythematosus patients.

作者信息

Refai Rania H, Hussein Mohammed F, Abdou Mamdouh H, Abou-Raya Anna N

机构信息

Department of Medicine Supply and Pharmacy, Alexandria University Hospitals, Alexandria University, Alexandria, Egypt.

High Institute of Public Health, Alexandria University, Alexandria, Egypt.

出版信息

Sci Rep. 2024 Mar 4;14(1):5234. doi: 10.1038/s41598-024-55833-9.

DOI:10.1038/s41598-024-55833-9
PMID:38433285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10909868/
Abstract

Systemic lupus erythematosus (SLE) is a chronic rheumatic autoimmune condition that can cause a wide range of symptoms and problems that may affect the health-related quality of life. The main objective of the study was to assess the SLE burden by exploring the effect of the disease on health-related quality of life. The study consisted of 29 female SLE patients and 27 healthy female controls; they were matched for age and parity. A 36-item Short Form health survey questionnaire (SF-36) was used to collect data from participants through face-to-face interviews and to assess their health-related quality of life. SF-36 summary scores for the physical and mental components were decreased in the studied patients compared with controls; PCS was 28.81 ± 16.63, 77.25 ± 15.75 for cases and controls, respectively; and MCS was 32.75 ± 18.69, and 78.75 ± 10.63 for cases and controls, respectively (p < 0.05). The high correlation between the two dimensions characterizes this decrease. SLE negatively affected the quality of life of the patients. Measures such as lifestyle modifications, physical activity, and a healthy diet should be taken to improve the health-related quality of life in SLE patients. In addition, raising the patient's awareness about the disease and its consequences could help to cope with the illness and engage in social and physical activities.

摘要

系统性红斑狼疮(SLE)是一种慢性风湿性自身免疫性疾病,可导致多种症状和问题,可能影响与健康相关的生活质量。该研究的主要目的是通过探讨疾病对与健康相关生活质量的影响来评估SLE负担。该研究包括29名女性SLE患者和27名健康女性对照;她们在年龄和生育情况上相匹配。采用一份包含36个条目的简短健康调查问卷(SF-36),通过面对面访谈从参与者那里收集数据,并评估她们与健康相关的生活质量。与对照组相比,研究患者的身体和心理成分的SF-36汇总得分降低;病例组和对照组的身体成分得分分别为28.81±16.63和77.25±15.75;心理成分得分分别为32.75±18.69和78.75±10.63(p<0.05)。两个维度之间的高度相关性说明了这种降低。SLE对患者的生活质量产生了负面影响。应采取诸如改变生活方式、进行体育活动和保持健康饮食等措施,以改善SLE患者与健康相关的生活质量。此外,提高患者对疾病及其后果的认识有助于应对疾病并参与社交和体育活动。