• 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
Identifying clinically meaningful severity categories for PROMIS pediatric measures of anxiety, mobility, fatigue, and depressive symptoms in juvenile idiopathic arthritis and childhood-onset systemic lupus erythematosus.确定青少年特发性关节炎和儿童发病的系统性红斑狼疮中 PROMIS 儿童焦虑、移动性、疲劳和抑郁症状测量的有临床意义的严重程度类别。
Qual Life Res. 2020 Sep;29(9):2573-2584. doi: 10.1007/s11136-020-02513-6. Epub 2020 May 14.
2
Establishing clinical meaning and defining important differences for Patient-Reported Outcomes Measurement Information System (PROMIS) measures in juvenile idiopathic arthritis using standard setting with patients, parents, and providers.利用患者、家长和医疗服务提供者共同参与的标准设定,确定青少年特发性关节炎患者报告结局测量信息系统(PROMIS)指标的临床意义并界定重要差异。
Qual Life Res. 2017 Mar;26(3):565-586. doi: 10.1007/s11136-016-1468-2. Epub 2016 Dec 2.
3
Construct validity of Patient-Reported Outcomes Measurement Information System Paediatric measures in juvenile idiopathic arthritis and systemic lupus erythematosus: cross-sectional evaluation.患者报告结局测量信息系统儿科测量量表在青少年特发性关节炎和系统性红斑狼疮中的结构效度:横断面评估。
BMJ Open. 2023 Jan 27;13(1):e063675. doi: 10.1136/bmjopen-2022-063675.
4
Use of PROMIS® to screen for depression in children with arthritis.使用 PROMIS®量表筛查关节炎儿童的抑郁症状。
Pediatr Rheumatol Online J. 2020 Nov 23;18(1):92. doi: 10.1186/s12969-020-00482-1.
5
Psychometric Properties of the Pediatric Patient-Reported Outcomes Measurement Information System Item Banks in a Dutch Clinical Sample of Children With Juvenile Idiopathic Arthritis.儿童青少年特发性关节炎荷兰临床样本中儿童患者报告结局测量信息系统项目库的心理计量学特性。
Arthritis Care Res (Hoboken). 2020 Dec;72(12):1780-1789. doi: 10.1002/acr.24094.
6
Anxiety and Depressive Symptoms in Juvenile Idiopathic Arthritis Correlate With Pain and Stress Using PROMIS Measures.使用患者报告结果测量信息系统(PROMIS)评估,幼年特发性关节炎患者的焦虑和抑郁症状与疼痛及压力相关。
J Rheumatol. 2022 Jan;49(1):74-80. doi: 10.3899/jrheum.210101. Epub 2021 Aug 1.
7
Moderate Weightbearing Restrictions Are Associated with Worse Depressive Symptoms and Anxiety in Children Aged 5 to 7 Years with Perthes Disease.中重度负重限制与 5 至 7 岁儿童佩特氏病的抑郁症状和焦虑有关。
Clin Orthop Relat Res. 2022 Mar 1;480(3):587-599. doi: 10.1097/CORR.0000000000002010.
8
Establishing clinically-relevant terms and severity thresholds for Patient-Reported Outcomes Measurement Information System (PROMIS) measures of physical function, cognitive function, and sleep disturbance in people with cancer using standard setting.使用标准设定方法为癌症患者的患者报告结局测量信息系统(PROMIS)身体功能、认知功能和睡眠障碍测量制定具有临床相关性的术语和严重程度阈值。
Qual Life Res. 2019 Dec;28(12):3355-3362. doi: 10.1007/s11136-019-02261-2. Epub 2019 Aug 13.
9
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.
10
Multicenter Study of Utility and Acceptability of Depression and Anxiety Screening in Adolescents and Young Adults With Childhood-Onset Systemic Lupus.儿童期起病的系统性红斑狼疮青少年及年轻成人抑郁和焦虑筛查的效用和可接受性的多中心研究
Arthritis Care Res (Hoboken). 2023 Apr;75(4):724-733. doi: 10.1002/acr.24825. Epub 2022 Dec 23.

引用本文的文献

1
Psychosocial Outcomes in Parents of Children with Acute Lymphoblastic Leukaemia in Australia and New Zealand Through and Beyond Treatment.澳大利亚和新西兰急性淋巴细胞白血病患儿父母在治疗期间及之后的心理社会结局
Cancers (Basel). 2025 Apr 6;17(7):1238. doi: 10.3390/cancers17071238.
2
The quality of life assessment in children with juvenile idiopathic arthritis- comparison of PROMIS generic and disease-specific cut-off points: a pilot study.幼年特发性关节炎患儿的生活质量评估——PROMIS通用型与疾病特异性切点的比较:一项试点研究。
Rheumatol Int. 2025 Feb 24;45(3):61. doi: 10.1007/s00296-025-05797-4.
3
A Maximum-Use Trial of Ruxolitinib Cream in Children Aged 2-11 Years with Moderate to Severe Atopic Dermatitis.芦可替尼乳膏用于2至11岁中重度特应性皮炎儿童的最大用量试验。
Am J Clin Dermatol. 2025 Mar;26(2):275-289. doi: 10.1007/s40257-024-00909-5. Epub 2025 Jan 6.
4
Association between maternal stress and child sleep quality: a nationwide ECHO prospective cohort study.母亲压力与儿童睡眠质量之间的关联:一项全国性的ECHO前瞻性队列研究。
Pediatr Res. 2025 Feb;97(3):980-988. doi: 10.1038/s41390-024-03542-4. Epub 2024 Oct 11.
5
Patient-Reported Outcomes in Autosomal Dominant Osteopetrosis: Findings From the Osteopetrosis Registry Study.常染色体显性遗传性骨硬化症患者报告的结局:骨硬化症注册研究的结果
J Clin Endocrinol Metab. 2025 Feb 18;110(3):e607-e614. doi: 10.1210/clinem/dgae285.
6
Multi-omics analysis of the gut microbiome and metabolites associated with the psychoneurological symptom cluster in children with cancer receiving chemotherapy.癌症化疗患儿精神神经症状群相关肠道微生物组和代谢物的多组学分析。
J Transl Med. 2024 Mar 9;22(1):256. doi: 10.1186/s12967-024-05066-1.
7
Using bookmarking methods with orthopedic clinicians and patients with fractures produces score interpretation labels for patient-reported outcome measures.使用书签标记方法与骨科临床医生和骨折患者一起,为患者报告的结果测量产生评分解释标签。
Qual Life Res. 2023 Oct;32(10):2779-2787. doi: 10.1007/s11136-023-03439-5. Epub 2023 May 25.
8
Pediatric Lyme disease: systematic assessment of post-treatment symptoms and quality of life.儿童莱姆病:治疗后症状和生活质量的系统评估。
Pediatr Res. 2024 Jan;95(1):174-181. doi: 10.1038/s41390-023-02577-3. Epub 2023 Mar 30.
9
Patient-reported outcomes in children with sickle cell disease at presentation for an acute pain episode.镰状细胞病患儿急性疼痛发作就诊时的患者报告结局
Blood Adv. 2023 Sep 12;7(17):5103-5107. doi: 10.1182/bloodadvances.2021006794.
10
A Review of Patient-Reported Outcome Measures in Childhood Cancer.儿童癌症患者报告结局指标综述
Children (Basel). 2022 Sep 30;9(10):1497. doi: 10.3390/children9101497.

本文引用的文献

1
PRO-Bookmarking to Estimate Clinical Thresholds for Patient-reported Symptoms and Function.PRO 书签法预估患者报告症状和功能的临床阈值。
Med Care. 2019 May;57 Suppl 5 Suppl 1:S13-S17. doi: 10.1097/MLR.0000000000001087.
2
Making a picture worth a thousand numbers: recommendations for graphically displaying patient-reported outcomes data.用图像呈现千言万语:推荐用于图形化展示患者报告结局数据的方法。
Qual Life Res. 2019 Feb;28(2):345-356. doi: 10.1007/s11136-018-2020-3. Epub 2018 Oct 10.
3
Assessing responsiveness over time of the PROMIS pediatric symptom and function measures in cancer, nephrotic syndrome, and sickle cell disease.评估 PROMIS 儿童症状和功能测量在癌症、肾病综合征和镰状细胞病中的随时间变化的反应性。
Qual Life Res. 2018 Jan;27(1):249-257. doi: 10.1007/s11136-017-1697-z. Epub 2017 Sep 7.
4
What do these scores mean? Presenting patient-reported outcomes data to patients and clinicians to improve interpretability.这些分数是什么意思?向患者和临床医生展示患者报告的结局数据以提高可解释性。
Cancer. 2017 May 15;123(10):1848-1859. doi: 10.1002/cncr.30530. Epub 2017 Jan 13.
5
Establishing clinical meaning and defining important differences for Patient-Reported Outcomes Measurement Information System (PROMIS) measures in juvenile idiopathic arthritis using standard setting with patients, parents, and providers.利用患者、家长和医疗服务提供者共同参与的标准设定,确定青少年特发性关节炎患者报告结局测量信息系统(PROMIS)指标的临床意义并界定重要差异。
Qual Life Res. 2017 Mar;26(3):565-586. doi: 10.1007/s11136-016-1468-2. Epub 2016 Dec 2.
6
Estimating minimally important difference (MID) in PROMIS pediatric measures using the scale-judgment method.使用量表判断法估计患者报告结果测量信息系统(PROMIS)儿科测量指标的最小重要差异(MID)
Qual Life Res. 2016 Jan;25(1):13-23. doi: 10.1007/s11136-015-1058-8. Epub 2015 Jun 29.
7
Communicating patient-reported outcome scores using graphic formats: results from a mixed-methods evaluation.使用图形格式传达患者报告的结局评分:一项混合方法评估的结果
Qual Life Res. 2015 Oct;24(10):2457-72. doi: 10.1007/s11136-015-0974-y. Epub 2015 May 27.
8
PROMIS(®) pediatric self-report scales distinguish subgroups of children within and across six common pediatric chronic health conditions.患者报告结果测量信息系统(PROMIS)儿童自评量表可区分六种常见儿童慢性健康状况内及跨这些状况的儿童亚组。
Qual Life Res. 2015 Sep;24(9):2195-208. doi: 10.1007/s11136-015-0953-3. Epub 2015 Feb 26.
9
Using item response theory to enrich and expand the PROMIS® pediatric self report banks.运用项目反应理论丰富和扩展患者报告结果测量信息系统(PROMIS®)儿科自评库。
Health Qual Life Outcomes. 2014 Oct 25;12:160. doi: 10.1186/s12955-014-0160-x.
10
Creating meaningful cut-scores for Neuro-QOL measures of fatigue, physical functioning, and sleep disturbance using standard setting with patients and providers.通过与患者和医疗服务提供者进行标准设定,为疲劳、身体功能和睡眠障碍的神经生活质量量表创建有意义的划界分数。
Qual Life Res. 2015 Mar;24(3):575-89. doi: 10.1007/s11136-014-0790-9. Epub 2014 Aug 23.

确定青少年特发性关节炎和儿童发病的系统性红斑狼疮中 PROMIS 儿童焦虑、移动性、疲劳和抑郁症状测量的有临床意义的严重程度类别。

Identifying clinically meaningful severity categories for PROMIS pediatric measures of anxiety, mobility, fatigue, and depressive symptoms in juvenile idiopathic arthritis and childhood-onset systemic lupus erythematosus.

机构信息

Department of Population Health Sciences, Duke University School of Medicine, Durham, NC, USA.

Department of Pediatrics and Duke Clinical Research Institute, Duke Health, Durham, NC, USA.

出版信息

Qual Life Res. 2020 Sep;29(9):2573-2584. doi: 10.1007/s11136-020-02513-6. Epub 2020 May 14.

DOI:10.1007/s11136-020-02513-6
PMID:32410143
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10505945/
Abstract

PURPOSE

A key limitation to widespread adoption of patient-reported outcome (PRO) measures is the lack of interpretability of scores. We aim to identify clinical severity thresholds to distinguish categories of no problems, mild, moderate, and severe along the PROMIS® Pediatric T-score metric for measures of anxiety, mobility, fatigue, and depressive symptoms for use in populations with juvenile idiopathic arthritis (JIA) and childhood-onset systemic lupus erythematosus (cSLE).

METHODS

We used a modified standard setting methodology from educational testing to identify clinical severity thresholds (clinical cut scores). Using item response theory-based parameters from PROMIS item banks, we developed a series of clinical vignettes that represented different severity or ability levels along the PROMIS Pediatric T-score metric. In stakeholder workshops, participants worked individually and together to reach consensus on clinical cut scores. Median cut-score placements were taken when consensus was not reached. Focus groups were recorded and qualitative analysis was conducted to identify decision-making processes.

RESULTS

Nine adolescents (age 13-17 years) with JIA (33% female) and their caregivers, five adolescents (age 14-16 years) with cSLE (100% female) and their caregivers, and 12 pediatric rheumatologists (75% female) participated in bookmarking workshops. Placement of thresholds for bookmarks was highly similar across stakeholder groups (differences from 0 to 5 points on the PROMIS t-score metric) for all but one bookmark placement.

CONCLUSION

This study resulted in clinical thresholds for severity categories for PROMIS Pediatric measures of anxiety, mobility, fatigue, and depressive symptoms, providing greater interpretability of scores in JIA and cSLE populations.

摘要

目的

患者报告结局(PRO)测量的广泛采用的一个关键限制是缺乏对评分的可解释性。我们旨在确定临床严重程度阈值,以区分无问题、轻度、中度和重度类别,这些类别沿 PROMIS®儿科 T 评分量表衡量焦虑、移动性、疲劳和抑郁症状,用于青少年特发性关节炎(JIA)和儿童发病的系统性红斑狼疮(cSLE)人群。

方法

我们使用教育测试中的一种改良标准设定方法来确定临床严重程度阈值(临床切割分数)。使用 PROMIS 项目库中的基于项目反应理论的参数,我们开发了一系列临床情景,代表了 PROMIS 儿科 T 评分量表上不同的严重程度或能力水平。在利益相关者研讨会上,参与者单独和共同工作,就临床切割分数达成共识。在未达成共识时,采用中位数切割分数。记录焦点小组并进行定性分析以确定决策过程。

结果

9 名患有 JIA(33%女性)的青少年(13-17 岁)及其照顾者、5 名患有 cSLE(100%女性)的青少年及其照顾者,以及 12 名儿科风湿病学家(75%女性)参加了书签研讨班。除了一个书签放置外,书签放置的阈值在利益相关者群体之间非常相似(在 PROMIS t 评分量表上的差异为 0 到 5 分)。

结论

本研究为 PROMIS 儿科焦虑、移动性、疲劳和抑郁症状测量的严重程度类别确定了临床阈值,为 JIA 和 cSLE 人群的评分提供了更大的可解释性。