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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。

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.

作者信息

Engler Kim, Ahmed Sara, Lessard David, Vicente Serge, Lebouché Bertrand

机构信息

Center for Outcomes Research and Evaluation, Research Institute of the McGill University Health Centre, Montreal, QC, Canada.

School of Physical & Occupational Therapy, McGill University, Montreal, QC, Canada.

出版信息

JMIR Res Protoc. 2019 Aug 2;8(8):e12836. doi: 10.2196/12836.

Abstract

BACKGROUND

Adherence to lifesaving antiretroviral therapy (ART) for HIV infection remains a challenge for many patients. Routine screening for barriers to ART adherence could help make HIV care more patient-centered and prevent virologic rebound or failure. Our team is currently developing a new HIV-specific patient-reported outcome measure (PROM) of these barriers for use in Canada and France along with a digital app for its electronic administration. In our previous work, we developed the PROM's multidimensional conceptual framework and generated 100 English items, which have been translated to French.

OBJECTIVE

This study aims to use a Web-based Delphi to help validate and select the content of this new HIV-specific PROM, based on the perspective of anglophone and francophone patients and providers in Canada and France. Here, we present the proposal for this Delphi.

METHODS

This modified Delphi will involve a diverse panel of patients (n=32) and providers (n=52) recruited especially from the 9 sites of the PROM development study (site locations in Canada: Montreal, Toronto, Vancouver; in France: Paris, Nantes, Clermont-Ferrand, Saint-Martin, Cayenne). Overall, 2 rounds of Web-based questionnaires will be conducted. The threshold for consensus is set at 60% and will determine which items are carried forward to the second round. Per item, 3 aspects will be rated: importance as a barrier to ART adherence, relevance for HIV care, and clarity. In both rounds, space will be available for free text comments. Overall comprehensiveness will be assessed in the second round.

RESULTS

This study has undergone a methodological review by experts in patient-oriented research. It has received approval from a research ethics board of the McGill University Health Centre. It is financially supported, in part, by the Canadian Institutes of Health Research's Strategy for Patient-Oriented Research-Quebec Support Unit (M006). As of May 21, 2019, 15 people living with HIV and 25 providers completed the first round of the Delphi (24 from Canada and 16 from France).

CONCLUSIONS

To our knowledge, this is the first Delphi to seek consensus on the most relevant and clinically actionable barriers to ART adherence, collecting opinions on an extensive list of barriers. Drawing on a relatively large and diverse panel of HIV patients and providers, it essentially engages key stakeholders in decision making about the PROM's final content, helping to ensure its utility and adoption.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): PRR1-10.2196/12836.

摘要

背景

坚持接受用于治疗HIV感染的挽救生命的抗逆转录病毒疗法(ART)对许多患者来说仍是一项挑战。对ART依从性障碍进行常规筛查有助于使HIV护理更以患者为中心,并预防病毒学反弹或治疗失败。我们的团队目前正在开发一种针对这些障碍的新型HIV特异性患者报告结局量表(PROM),供加拿大和法国使用,同时还开发了一款用于电子管理的数字应用程序。在我们之前的工作中,我们构建了该PROM的多维概念框架,并生成了100个英文条目,这些条目已被翻译成法语。

目的

本研究旨在基于加拿大和法国英语和法语患者及医疗服务提供者的视角,使用基于网络的德尔菲法来帮助验证和选择这种新型HIV特异性PROM的内容。在此,我们展示该德尔菲法的方案。

方法

这种改良的德尔菲法将涉及一个多元化的小组,包括特意从PROM开发研究的9个地点招募的患者(n = 32)和医疗服务提供者(n = 52)(加拿大的地点:蒙特利尔、多伦多、温哥华;法国的地点:巴黎、南特、克莱蒙费朗、圣马丁、卡宴)。总体而言,将进行两轮基于网络的问卷调查。共识阈值设定为60%,并将决定哪些条目进入第二轮。对于每个条目,将对三个方面进行评分:作为ART依从性障碍的重要性、与HIV护理的相关性以及清晰度。在两轮调查中,都将提供自由文本评论的空间。在第二轮中将评估总体全面性。

结果

本研究已接受以患者为导向研究领域专家的方法学审查。它已获得麦吉尔大学健康中心研究伦理委员会的批准。它部分得到了加拿大卫生研究院面向患者研究战略魁北克支持单位(M006)的资助。截至2019年5月21日,15名HIV感染者和25名医疗服务提供者完成了第一轮德尔菲调查(24名来自加拿大,16名来自法国)。

结论

据我们所知,这是首个就ART依从性最相关且具有临床可操作性的障碍达成共识的德尔菲法,就一系列广泛的障碍收集意见。借助一个规模相对较大且多元化的HIV患者和医疗服务提供者小组,它实质上让关键利益相关者参与到关于PROM最终内容的决策中,有助于确保其效用和采用率。

国际注册报告识别码(IRRID):PRR1 - 10.2196/12836。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90e5/6696859/adc8ec92f1b4/resprot_v8i8e12836_fig1.jpg

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