• 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
Responsiveness of the Patient-Reported Outcomes Measurement Information System Global Health Short Form in Outpatients With Systemic Lupus Erythematosus.患者报告结局测量信息系统全球健康简短量表在系统性红斑狼疮门诊患者中的反应性。
Arthritis Care Res (Hoboken). 2020 Sep;72(9):1282-1288. doi: 10.1002/acr.24026.
2
Feasibility, Validity, and Reliability of the 10-item Patient Reported Outcomes Measurement Information System Global Health Short Form in Outpatients with Systemic Lupus Erythematosus.10 项患者报告结局测量信息系统全球健康简短量表用于系统性红斑狼疮门诊患者的可行性、有效性和可靠性。
J Rheumatol. 2018 Mar;45(3):397-404. doi: 10.3899/jrheum.170590. Epub 2018 Feb 1.
3
Validity and Reliability of Patient Reported Outcomes Measurement Information System Computerized Adaptive Tests in Systemic Lupus Erythematosus.患者报告结局测量信息系统计算机自适应测试在系统性红斑狼疮中的效度和信度
J Rheumatol. 2017 Jul;44(7):1024-1031. doi: 10.3899/jrheum.161202. Epub 2017 Apr 15.
4
Validation of Patient-Reported Outcomes Measurement Information System Short Forms for Use in Childhood-Onset Systemic Lupus Erythematosus.用于儿童期起病的系统性红斑狼疮的患者报告结局测量信息系统简表的验证
Arthritis Care Res (Hoboken). 2017 Jan;69(1):133-142. doi: 10.1002/acr.22927. Epub 2016 Nov 28.
5
Responsiveness of the 36-item Short Form Health Survey and the Lupus Quality of Life questionnaire in SLE.36项简明健康调查问卷及狼疮生活质量问卷在系统性红斑狼疮中的反应性
Rheumatology (Oxford). 2015 May;54(5):940-9. doi: 10.1093/rheumatology/keu410. Epub 2014 Oct 30.
6
Feasibility of Patient-Reported Outcomes Measurement Information System (PROMIS®) computerized adaptive tests in systemic lupus erythematosus outpatients.患者报告结局测量信息系统(PROMIS®)计算机自适应测试在系统性红斑狼疮门诊患者中的可行性
Lupus. 2018 Sep;27(10):1591-1599. doi: 10.1177/0961203318778372. Epub 2018 May 24.
7
Comparison of performance of specific (SLEQOL) and generic (SF36) health-related quality of life questionnaires and their associations with disease status of systemic lupus erythematosus: a longitudinal study.比较特定(SLEQOL)和通用(SF36)健康相关生活质量问卷的表现及其与系统性红斑狼疮疾病状态的关联:一项纵向研究。
Arthritis Res Ther. 2020 Jan 10;22(1):8. doi: 10.1186/s13075-020-2095-4.
8
Sensitivity to Change and Minimal Important Differences of the LupusQoL in Patients With Systemic Lupus Erythematosus.系统性红斑狼疮患者对LupusQoL变化的敏感性及最小重要差异
Arthritis Care Res (Hoboken). 2016 Oct;68(10):1505-13. doi: 10.1002/acr.22850. Epub 2016 Sep 2.
9
Fatigue, patient reported outcomes, and objective measurement of physical activity in systemic lupus erythematosus.系统性红斑狼疮中的疲劳、患者报告结局以及身体活动的客观测量
Lupus. 2016 Oct;25(11):1190-9. doi: 10.1177/0961203316631632. Epub 2016 Feb 10.
10
Lupus Impact Tracker is responsive to physician and patient assessed changes in systemic lupus erythematosus.狼疮影响追踪器可反映医生和患者评估的系统性红斑狼疮的变化。
Lupus. 2015 Dec;24(14):1486-91. doi: 10.1177/0961203315593168. Epub 2015 Jul 9.

引用本文的文献

1
Impact of an Employee Health and Wellness Coaching Program on Self-Reported Stress, Physical Health, and Mental Health in Hospital and University Employees.员工健康与福祉辅导计划对医院和大学员工自我报告的压力、身体健康和心理健康的影响。
Glob Adv Integr Med Health. 2025 Jul 29;14:27536130251363933. doi: 10.1177/27536130251363933. eCollection 2025 Jan-Dec.
2
Quality of life in Saudi Arabia: a patient-reported outcome measurement information system (PROMIS) - 10 global health study.沙特阿拉伯的生活质量:一项患者报告结局测量信息系统(PROMIS)-10全球健康研究。
BMC Public Health. 2025 May 6;25(1):1662. doi: 10.1186/s12889-025-22674-8.
3
Clinical integration of patient-reported outcome measures to enhance the care of patients with SLE: a multi-centre prospective cohort study.患者报告结局测量在 SLE 患者治疗中的临床整合:一项多中心前瞻性队列研究。
Rheumatology (Oxford). 2022 Nov 28;61(12):4763-4774. doi: 10.1093/rheumatology/keac200.
4
Patient-Reported Outcomes for Quality of Life in SLE: Essential in Clinical Trials and Ready for Routine Care.系统性红斑狼疮患者报告的生活质量结局:在临床试验中至关重要且可用于常规护理
J Clin Med. 2021 Aug 23;10(16):3754. doi: 10.3390/jcm10163754.

本文引用的文献

1
Patient-reported outcome measures for use in clinical trials of SLE: a review.用于系统性红斑狼疮临床试验的患者报告结局指标:综述
Lupus Sci Med. 2018 Aug 21;5(1):e000279. doi: 10.1136/lupus-2018-000279. eCollection 2018.
2
Feasibility, Validity, and Reliability of the 10-item Patient Reported Outcomes Measurement Information System Global Health Short Form in Outpatients with Systemic Lupus Erythematosus.10 项患者报告结局测量信息系统全球健康简短量表用于系统性红斑狼疮门诊患者的可行性、有效性和可靠性。
J Rheumatol. 2018 Mar;45(3):397-404. doi: 10.3899/jrheum.170590. Epub 2018 Feb 1.
3
Validity and Reliability of Patient Reported Outcomes Measurement Information System Computerized Adaptive Tests in Systemic Lupus Erythematosus.患者报告结局测量信息系统计算机自适应测试在系统性红斑狼疮中的效度和信度
J Rheumatol. 2017 Jul;44(7):1024-1031. doi: 10.3899/jrheum.161202. Epub 2017 Apr 15.
4
Using a Self-Reported Global Health Measure to Identify Patients at High Risk for Future Healthcare Utilization.使用自我报告的全球健康指标来识别未来医疗保健利用高风险患者。
J Gen Intern Med. 2017 Aug;32(8):877-882. doi: 10.1007/s11606-017-4041-y. Epub 2017 Mar 24.
5
American College of Rheumatology White Paper on Performance Outcome Measures in Rheumatology.美国风湿病学会关于风湿病性能结局指标的白皮书。
Arthritis Care Res (Hoboken). 2016 Oct;68(10):1390-401. doi: 10.1002/acr.22936. Epub 2016 Sep 16.
6
Incorporating Patient-Reported Outcomes Into Health Care To Engage Patients And Enhance Care.将患者报告的结果纳入医疗保健,以促使患者参与并改善护理。
Health Aff (Millwood). 2016 Apr;35(4):575-82. doi: 10.1377/hlthaff.2015.1362.
7
Sensitivity to Change and Minimal Important Differences of the LupusQoL in Patients With Systemic Lupus Erythematosus.系统性红斑狼疮患者对LupusQoL变化的敏感性及最小重要差异
Arthritis Care Res (Hoboken). 2016 Oct;68(10):1505-13. doi: 10.1002/acr.22850. Epub 2016 Sep 2.
8
Responsiveness of the 36-item Short Form Health Survey and the Lupus Quality of Life questionnaire in SLE.36项简明健康调查问卷及狼疮生活质量问卷在系统性红斑狼疮中的反应性
Rheumatology (Oxford). 2015 May;54(5):940-9. doi: 10.1093/rheumatology/keu410. Epub 2014 Oct 30.
9
Harmonizing and consolidating the measurement of patient-reported information at health care institutions: a position statement of the Mayo Clinic.协调与整合医疗机构中患者报告信息的测量:梅奥诊所的立场声明。
Patient Relat Outcome Meas. 2014 Feb 10;5:7-15. doi: 10.2147/PROM.S55069. eCollection 2014.
10
Fatigue, health-related quality of life and other patient-reported outcomes in systemic lupus erythematosus.系统性红斑狼疮的疲劳、健康相关生活质量和其他患者报告结局。
Best Pract Res Clin Rheumatol. 2013 Jun;27(3):363-75. doi: 10.1016/j.berh.2013.07.009.

患者报告结局测量信息系统全球健康简短量表在系统性红斑狼疮门诊患者中的反应性。

Responsiveness of the Patient-Reported Outcomes Measurement Information System Global Health Short Form in Outpatients With Systemic Lupus Erythematosus.

机构信息

Tufts Medical Center, Boston, Massachusetts.

New York University Langone Health, New York.

出版信息

Arthritis Care Res (Hoboken). 2020 Sep;72(9):1282-1288. doi: 10.1002/acr.24026.

DOI:10.1002/acr.24026
PMID:31309733
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6960367/
Abstract

OBJECTIVE

To evaluate the longitudinal responsiveness (sensitivity to change) of the Patient-Reported Outcomes Measurement Information System (PROMIS) Global Health Short Form (PROMIS10) in outpatients with systemic lupus erythematosus (SLE).

METHODS

Outpatients with SLE who were receiving care at an academic medical center completed the PROMIS10 at 2 visits that were a minimum of 1 month apart. Responsiveness of the PROMIS10 global physical and mental health domains to Patient-Reported improvement or deterioration of health status was evaluated, as measured by standard validated instruments. Effect sizes of changes in PROMIS10 scores between visits were evaluated using Kruskal-Wallis testing.

RESULTS

A total of 223 SLE patients enrolled and completed baseline surveys, with 186 (83.4%) completing a second set of questionnaires. The PROMIS10 demonstrated mild-to-moderate responsiveness to Patient-Reported improvement (effect size 0.29) and worsening (effect sizes -0.27 and -0.54) of health status for both global physical health and global mental health. Changes in the PROMIS10 correlated poorly with changes in physician-reported measures of disease activity.

CONCLUSION

The PROMIS10 showed responsiveness over time to Patient-Reported changes in SLE health status, but not physician-assessed changes. These data suggest that the PROMIS10 can be used to efficiently measure and monitor important aspects of the SLE patient experience that are not captured by standard physician-derived metrics. Further studies are needed to evaluate the role of the PROMIS10 in optimizing longitudinal disease management in SLE and to determine its responsiveness in other chronic health conditions.

摘要

目的

评估患者报告结局测量信息系统(PROMIS)全球健康简短量表(PROMIS10)在系统性红斑狼疮(SLE)门诊患者中的纵向反应性(变化敏感性)。

方法

在学术医疗中心接受治疗的 SLE 门诊患者在至少相隔 1 个月的 2 次就诊时完成了 PROMIS10。通过标准验证工具评估 PROMIS10 全球身体和心理健康领域对患者报告的健康状况改善或恶化的反应性。使用 Kruskal-Wallis 检验评估两次就诊之间 PROMIS10 评分变化的效应大小。

结果

共有 223 名 SLE 患者入组并完成了基线调查,其中 186 名(83.4%)完成了第二套问卷。PROMIS10 对患者报告的健康状况改善(效应大小 0.29)和恶化(全球身体和全球心理健康的效应大小分别为-0.27 和-0.54)具有轻度至中度反应性。PROMIS10 的变化与医生报告的疾病活动度测量值的变化相关性较差。

结论

PROMIS10 随着时间的推移对 SLE 健康状况的患者报告变化具有反应性,但对医生评估的变化没有反应性。这些数据表明,PROMIS10 可用于有效地测量和监测 SLE 患者体验中未被标准医生衍生指标捕捉到的重要方面。需要进一步的研究来评估 PROMIS10 在 SLE 纵向疾病管理中的作用,并确定其在其他慢性健康状况中的反应性。