• 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

利益相关者参与患者报告结局(PRO)指标的实施:来自SAFTINet基于实践的研究网络(PBRN)的报告。

Stakeholder Engagement in a Patient-Reported Outcomes (PRO) Measure Implementation: A Report from the SAFTINet Practice-based Research Network (PBRN).

作者信息

Kwan Bethany M, Sills Marion R, Graham Deborah, Hamer Mika K, Fairclough Diane L, Hammermeister K E, Kaiser Alicyn, de Jesus Diaz-Perez Maria, Schilling Lisa M

机构信息

From the Departments of Family Medicine (BMK), Pediatrics (MRS), and Emergency Medicine (MRS), and Divisions of Cardiology (KEH) and General Internal Medicine (LMS), Department of Medicine, and Adult and Child Consortium for Health Outcomes Research and Delivery Science (ACCORDS) (BMK, MRS, MKH, DLF, KEH, LMS), University of Colorado School of Medicine, Aurora, CO; Children's Hospital Colorado, Aurora, CO (MRS); The DARTNet Institute, Aurora, CO (DG); Department of Biostatistics and Informatics, Colorado School of Public Health, Aurora, CO (DLF); Metro Community Provider Network, Englewood, CO (AK); Salud Family Health Centers, Fort Lupton, CO (MdJD-P).

出版信息

J Am Board Fam Med. 2016 Jan-Feb;29(1):102-15. doi: 10.3122/jabfm.2016.01.150141.

DOI:10.3122/jabfm.2016.01.150141
PMID:26769882
Abstract

PURPOSE

Patient-reported outcome (PRO) measures offer value for clinicians and researchers, although priorities and value propositions can conflict. PRO implementation in clinical practice may benefit from stakeholder engagement methods to align research and clinical practice stakeholder perspectives. The objective is to demonstrate the use of stakeholder engagement in PRO implementation.

METHOD

Engaged stakeholders represented researchers and clinical practice representatives from the SAFTINet practice-based research network (PBRN). A stakeholder engagement process involving iterative analysis, deliberation, and decision making guided implementation of a medication adherence PRO measure (the Medication Adherence Survey [MAS]) for patients with hypertension and/or hyperlipidemia.

RESULTS

Over 9 months, 40 of 45 practices (89%) implemented the MAS, collecting 3,247 surveys (mean = 72, median = 30, range: 0 - 416). Facilitators included: an electronic health record (EHR) with readily modifiable templates; existing staff, tools and workflows in which the MAS could be integrated (e.g., health risk appraisals, hypertension-specific visits, care coordinators); and engaged leadership and quality improvement teams.

CONCLUSION

Stakeholder engagement appeared useful for promoting PRO measure implementation in clinical practice, in a way that met the needs of both researchers and clinical practice stakeholders. Limitations of this approach and opportunities for improving the PRO data collection infrastructure in PBRNs are discussed.

摘要

目的

患者报告结局(PRO)测量为临床医生和研究人员提供了价值,尽管优先级和价值主张可能存在冲突。临床实践中PRO的实施可能受益于利益相关者参与方法,以使研究和临床实践利益相关者的观点保持一致。目的是展示利益相关者参与在PRO实施中的应用。

方法

参与的利益相关者代表了来自SAFTINet基于实践的研究网络(PBRN)的研究人员和临床实践代表。一个涉及迭代分析、审议和决策的利益相关者参与过程指导了针对高血压和/或高脂血症患者的药物依从性PRO测量(药物依从性调查[MAS])的实施。

结果

在9个月的时间里,45家诊所中的40家(89%)实施了MAS,收集了3247份调查问卷(平均 = 72份,中位数 = 30份,范围:0 - 416份)。促进因素包括:具有易于修改模板的电子健康记录(EHR);可以整合MAS的现有工作人员、工具和工作流程(例如,健康风险评估、高血压专项就诊、护理协调员);以及积极参与的领导和质量改进团队。

结论

利益相关者参与似乎有助于在临床实践中促进PRO测量的实施,其方式满足了研究人员和临床实践利益相关者的需求。讨论了这种方法的局限性以及改善PBRN中PRO数据收集基础设施的机会。

相似文献

1
Stakeholder Engagement in a Patient-Reported Outcomes (PRO) Measure Implementation: A Report from the SAFTINet Practice-based Research Network (PBRN).利益相关者参与患者报告结局(PRO)指标的实施:来自SAFTINet基于实践的研究网络(PBRN)的报告。
J Am Board Fam Med. 2016 Jan-Feb;29(1):102-15. doi: 10.3122/jabfm.2016.01.150141.
2
Patient and Stakeholder Engagement in the PCORI Pilot Projects: Description and Lessons Learned.患者及利益相关者参与患者为中心的结果研究所试点项目:描述与经验教训
J Gen Intern Med. 2016 Jan;31(1):13-21. doi: 10.1007/s11606-015-3450-z. Epub 2015 Jul 10.
3
A Multilevel Approach to Stakeholder Engagement in the Formulation of a Clinical Data Research Network.多层次方法在临床数据研究网络制定中的利益相关者参与。
Med Care. 2018 Oct;56 Suppl 10 Suppl 1(10 Suppl 1):S22-S26. doi: 10.1097/MLR.0000000000000778.
4
Engaging Stakeholders to Develop a Patient-centered Research Agenda: Lessons Learned From the Research Action for Health Network (REACHnet).让利益相关者参与制定以患者为中心的研究议程:从健康网络研究行动(REACHnet)中吸取的经验教训。
Med Care. 2018 Oct;56 Suppl 10 Suppl 1(10 Suppl 1):S27-S32. doi: 10.1097/MLR.0000000000000785.
5
Assessing Patient and Provider Perceptions of Factors Associated with Patient Engagement in Asthma Care.评估患者和提供者对与哮喘护理中患者参与相关的因素的看法。
Ann Am Thorac Soc. 2017 May;14(5):659-666. doi: 10.1513/AnnalsATS.201608-602OC.
6
A Novel Stakeholder Engagement Approach for Patient-centered Outcomes Research.一种以患者为中心的结局研究的新型利益相关者参与方法。
Med Care. 2018 Oct;56 Suppl 10 Suppl 1(10 Suppl 1):S41-S47. doi: 10.1097/MLR.0000000000000790.
7
Integrating the use of patient-reported outcomes for both clinical practice and performance measurement: views of experts from 3 countries.整合患者报告结局在临床实践和绩效评估中的应用:来自三个国家的专家观点
Milbank Q. 2014 Dec;92(4):754-75. doi: 10.1111/1468-0009.12091.
8
A systematic review of stakeholder engagement in comparative effectiveness and patient-centered outcomes research.利益相关者参与比较效果研究和以患者为中心的结局研究的系统评价。
J Gen Intern Med. 2014 Dec;29(12):1692-701. doi: 10.1007/s11606-014-2878-x. Epub 2014 Jun 4.
9
A tall order on a tight timeframe: stakeholder perspectives on comparative effectiveness research using electronic clinical data.在紧迫的时间内完成艰巨的任务:利益相关者对使用电子临床数据进行的比较有效性研究的看法。
J Comp Eff Res. 2012 Sep;1(5):441-51. doi: 10.2217/cer.12.47.
10
Building Meaningful Patient Engagement in Research: Case Study From ADVANCE Clinical Data Research Network.建立有意义的患者参与研究:来自 ADVANCE 临床数据研究网络的案例研究。
Med Care. 2018 Oct;56 Suppl 10 Suppl 1(10 Suppl 1):S58-S63. doi: 10.1097/MLR.0000000000000791.

引用本文的文献

1
Leveraging stories of cardiac amyloidosis patients of African ancestry or descent to support patient-derived data elements for efficient diagnosis and treatment.利用非洲裔心脏淀粉样变性患者的故事来支持源自患者的数据元素,以实现高效诊断和治疗。
Front Pharmacol. 2023 Nov 24;14:1276396. doi: 10.3389/fphar.2023.1276396. eCollection 2023.
2
Attitudes of primary healthcare chief physicians towards research in Finland - a national study.初级保健首席医师对芬兰研究的态度-一项全国性研究。
Scand J Prim Health Care. 2023 Jun;41(2):140-151. doi: 10.1080/02813432.2023.2196537. Epub 2023 Apr 18.
3
Patient engagement in a national research network: barriers, facilitators, and impacts.
患者参与国家研究网络:障碍、促进因素及影响
Res Involv Engagem. 2023 Mar 8;9(1):7. doi: 10.1186/s40900-023-00418-5.
4
Facilitators and barriers to implementing electronic patient-reported outcome and experience measures in a health care setting: a systematic review.在医疗保健环境中实施电子患者报告的结果和体验测量的促进因素和障碍:系统评价。
J Patient Rep Outcomes. 2023 Feb 14;7(1):13. doi: 10.1186/s41687-023-00554-2.
5
Reaching Consensus on Principles of Stakeholder Engagement in Research.达成利益相关者参与研究原则的共识。
Prog Community Health Partnersh. 2020;14(1):117-127. doi: 10.1353/cpr.2020.0014.
6
Applying a Commercialization-Readiness Framework to Optimize Value for Achieving Sustainability of an Electronic Health Data Research Network and Its Data Capabilities: The SAFTINet Experience.应用商业化准备框架以优化价值,实现电子健康数据研究网络及其数据能力的可持续性:SAFTINet经验
EGEMS (Wash DC). 2019 Aug 29;7(1):48. doi: 10.5334/egems.295.
7
Implementing eScreening technology in four VA clinics: a mixed-method study.在四家退伍军人事务部诊所实施电子筛查技术:一项混合方法研究。
BMC Health Serv Res. 2019 Aug 28;19(1):604. doi: 10.1186/s12913-019-4436-z.
8
Variation and Change Over Time in PROMIS-29 Survey Results Among Primary Care Patients With Type 2 Diabetes.2型糖尿病初级保健患者中PROMIS-29调查结果随时间的变化与差异
J Patient Cent Res Rev. 2019 Apr 29;6(2):135-147. doi: 10.17294/2330-0698.1694. eCollection 2019 Spring.
9
Assessing the Content Validity of a New Patient-Reported Measure of Barriers to Antiretroviral Therapy Adherence for Electronic Administration in Routine HIV Care: Proposal for a Web-Based Delphi Study.评估一种新的患者报告的抗逆转录病毒治疗依从性障碍测量方法在常规HIV护理中电子管理的内容效度:基于网络的德尔菲研究提案。
JMIR Res Protoc. 2019 Aug 2;8(8):e12836. doi: 10.2196/12836.
10
Developing a patient-reported outcome measure for HIV care on perceived barriers to antiretroviral adherence: assessing the needs of HIV clinicians through qualitative analysis.开发一种针对 HIV 护理的患者报告结局测量工具,以了解患者对抗逆转录病毒药物依从性的障碍:通过定性分析评估 HIV 临床医生的需求。
Qual Life Res. 2018 Feb;27(2):379-388. doi: 10.1007/s11136-017-1711-5. Epub 2017 Oct 13.