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利益相关者对跨卫生系统促进药物依从性技术发展和应用的跨学科术语达成共识:基于网络的实时德尔菲研究

Stakeholder Consensus on an Interdisciplinary Terminology to Enable the Development and Uptake of Medication Adherence Technologies Across Health Systems: Web-Based Real-Time Delphi Study.

作者信息

Dima Alexandra Lelia, Nabergoj Makovec Urska, Ribaut Janette, Haupenthal Frederik, Barnestein-Fonseca Pilar, Goetzinger Catherine, Grant Sean, Jácome Cristina, Smits Dins, Tadic Ivana, van Boven Job, Tsiligianni Ioanna, Herdeiro Maria Teresa, Roque Fátima

机构信息

Avedis Donabedian Research Institute (FAD), Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.

Avaluació de tecnologies sanitàries en atenció primària i salut mental (PRISMA), Institut de Recerca Sant Joan de Déu, Esplugues de Llobregat, Spain.

出版信息

J Med Internet Res. 2025 Mar 25;27:e59738. doi: 10.2196/59738.

DOI:10.2196/59738
PMID:40132192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11979531/
Abstract

BACKGROUND

Technology-mediated medication adherence interventions have proven useful, yet implementation in clinical practice is low. The European Network to Advance Best Practices and Technology on Medication Adherence (ENABLE) European Cooperation in Science and Technology Action (CA19132) online repository of medication adherence technologies (MATechs) aims to provide an open access, searchable knowledge management platform to facilitate innovation and support medication adherence management across health systems. To provide a solid foundation for optimal use and collaboration, the repository requires a shared interdisciplinary terminology.

OBJECTIVE

We consulted stakeholders on their views and level of agreement with the terminology proposed to inform the ENABLE repository structure.

METHODS

A real-time web-based Delphi study was conducted with stakeholders from 39 countries active in research, clinical practice, patient representation, policy making, and technology development. Participants rated terms and definitions of MATech and of 21 attribute clusters on product and provider information, medication adherence descriptors, and evaluation and implementation. Relevance, clarity, and completeness criteria were rated on 9-point scales, and free-text comments were provided interactively. Participants could reconsider their ratings based on real-time aggregated feedback and revisit the survey throughout the study period. We quantified agreement and process indicators for the complete sample and per stakeholder group and performed content analysis on comments. Consensus was considered reached for ratings with a disagreement index of <1. Median ratings guided decisions on whether attributes were considered mandatory, optional, or not relevant. We used the results to improve the terminology and repository structure.

RESULTS

Of 250 stakeholders invited, 117 (46.8%) rated the MATech definition, of whom 83 (70.9%) rated all attributes. Consensus was reached for all items. The definition was considered appropriate and clear (median ratings 7.02, IPR 6.10-7.69, and 7.26, IPR 6.73-7.90, respectively). Most attributes were considered relevant, mandatory, and sufficiently clear to remain unchanged except for ISO certification (considered optional; median relevance rating 6.34, IPR 5.50-7.24) and medication adherence phase, medication adherence measurement, and medication adherence intervention (candidates for optional changes; median clarity ratings 6.07, IPR 4.86-7.17; 6.37, IPR 4.80-6.67; and 5.67, IPR 4.66-6.61, respectively). Subgroup analyses found several attribute clusters considered moderately clear by some stakeholder groups. Results were consistent across stakeholder groups and time, yet response variation was found within some stakeholder groups for selected clusters, suggesting targets for further discussion. Comments highlighted issues for further debate and provided suggestions informing modifications to improve comprehensiveness, relevance, and clarity.

CONCLUSIONS

By reaching agreement on a comprehensive MATech terminology developed following state-of-the-art methodology, this study represents a key step in the ENABLE initiative to develop an information architecture capable of structuring and facilitating the development and implementation of MATech across Europe. The debates and challenges highlighted in stakeholders' comments outline a potential road map for further development of the terminology and the ENABLE repository.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): RR2-10.1136/bmjopen-2021-059674.

摘要

背景

技术介导的药物依从性干预已被证明是有用的,但在临床实践中的实施率较低。欧洲提高药物依从性最佳实践与技术网络(ENABLE)欧洲科技合作行动(CA19132)的药物依从性技术在线知识库(MATechs)旨在提供一个开放获取、可搜索的知识管理平台,以促进创新并支持跨卫生系统的药物依从性管理。为了为最佳使用和协作提供坚实基础,该知识库需要一个共享的跨学科术语。

目的

我们就利益相关者对为ENABLE知识库结构提供信息而提出的术语的看法和认同程度进行了咨询。

方法

对来自39个国家的活跃于研究、临床实践、患者代表、政策制定和技术开发领域的利益相关者进行了一项基于网络的实时德尔菲研究。参与者对MATech以及关于产品和提供者信息、药物依从性描述符、评估和实施的21个属性集群的术语和定义进行了评分。相关性、清晰度和完整性标准采用9分制进行评分,并交互式提供自由文本评论。参与者可以根据实时汇总反馈重新考虑他们的评分,并在整个研究期间重新访问该调查。我们对整个样本和每个利益相关者群体的一致性和过程指标进行了量化,并对评论进行了内容分析。对于分歧指数<1的评分,认为达成了共识。中位数评分指导关于属性是被视为强制性、可选性还是不相关的决策。我们利用结果改进术语和知识库结构。

结果

在邀请的250名利益相关者中,117名(46.8%)对MATech定义进行了评分,其中83名(70.9%)对所有属性进行了评分。所有项目均达成了共识。该定义被认为是适当且清晰的(中位数评分分别为7.02,四分位间距6.10 - 7.69,以及7.26,四分位间距6.73 - 7.90)。除ISO认证(被视为可选;中位数相关性评分为6.34,四分位间距5.50 - 7.24)以及药物依从性阶段、药物依从性测量和药物依从性干预(可选更改的候选项目;中位数清晰度评分分别为6.07,四分位间距4.86 - 7.17;6.37,四分位间距4.80 - 6.67;以及5.67四分位间距4.66 - 6.61)外,大多数属性被认为是相关的、强制性的且足够清晰无需更改。亚组分析发现一些利益相关者群体认为几个属性集群的清晰度一般。结果在利益相关者群体和时间上是一致的,但在一些利益相关者群体中,对于选定的集群发现了回答差异,这表明需要进一步讨论的目标。评论突出了需要进一步辩论的问题,并提供了建议以指导修改,以提高全面性、相关性和清晰度。

结论

通过就遵循最新方法学开发的全面MATech术语达成一致,本研究是ENABLE计划中关键的一步,该计划旨在开发一种信息架构,能够构建并促进MATech在欧洲的开发和实施。利益相关者评论中突出的辩论和挑战勾勒出了术语和ENABLE知识库进一步发展的潜在路线图。

国际注册报告识别码(IRRID):RR2 - 10.1136/bmjopen - 2021 - 059674。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/11979531/634845b63ac4/jmir_v27i1e59738_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/11979531/2e7f9bc2acb4/jmir_v27i1e59738_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/11979531/4fcd640629e6/jmir_v27i1e59738_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/11979531/634845b63ac4/jmir_v27i1e59738_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/11979531/2e7f9bc2acb4/jmir_v27i1e59738_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/11979531/4fcd640629e6/jmir_v27i1e59738_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/11979531/634845b63ac4/jmir_v27i1e59738_fig3.jpg

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