Enhancing the delivery of comprehensive care for people living with HIV in Canada: insights from citizen panels and a national stakeholder dialogue.

IF 3.6 2区 医学 Q1 HEALTH POLICY & SERVICES Health Research Policy and Systems Pub Date : 2024-05-27 DOI:10.1186/s12961-024-01147-1
Michael G Wilson, Cristina Mattison, Kerry Waddell, Jean Bacon, Marissa Becker, Christine Bibeau, John N Lavis, Ron Rosenes, Claire E Kendall
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Abstract

Background: People living with human immunodeficiency virus (HIV) are living longer with health-related disability associated with ageing, including complex conditions. However, health systems in Canada have not adapted to meet these comprehensive care needs.

Methods: We convened three citizen panels and a national stakeholder dialogue. The panels were informed by a plain-language citizen brief that outlined data and evidence about the challenge/problem, elements of an approach for addressing it and implementation considerations. The national dialogue was informed by a more detailed version of the same brief that included a thematic analysis of the findings from the panels.

Results: The 31 citizen panel participants emphasized the need for more prevention, testing and social supports, increased public education to address stigma and access to more timely data to inform system changes. The 21 system leaders emphasized the need to enhance person-centred care and for implementing learning and improvement across provinces, territories and Indigenous communities. Citizens and system leaders highlighted that policy actions need to acknowledge that HIV remains unique among conditions faced by Canadians.

Conclusions: Action will require a national learning collaborative to support spread and scale of successful prevention, care and support initiatives. Such a collaborative should be grounded in a rapid-learning and improvement approach that is anchored on the needs, perspectives and aspirations of people living with HIV; driven by timely data and evidence; supported by appropriate decision supports and aligned governance, financial and delivery arrangements; and enabled with a culture of and competencies for rapid learning and improvement.

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加强为加拿大艾滋病毒感染者提供全面护理:公民小组和全国利益相关者对话的见解。
背景:人类免疫缺陷病毒(HIV)感染者的寿命越来越长,他们的健康因年龄增长而出现残疾,其中包括复杂的病症。然而,加拿大的医疗系统尚未进行调整,以满足这些综合护理需求:我们召集了三个公民小组和一次全国利益相关者对话。公民小组会议参考了一份通俗易懂的公民简报,该简报概述了有关挑战/问题的数据和证据、解决方法的要素以及实施方面的考虑因素。全国对话则参考了同一简报的更详细版本,其中包括对小组讨论结果的专题分析:31 位公民小组参与者强调,需要更多的预防、检测和社会支持,加强公众教育以解决耻辱化问题,并获得更及时的数据,为系统变革提供信息。21 位系统领导人强调,需要加强以人为本的护理,并在各省、地区和土著社区开展学习和改进工作。公民和系统领导人强调,政策行动需要承认艾滋病毒在加拿大人所面临的状况中仍然是独一无二的:行动将需要一个全国性的学习合作组织,以支持成功的预防、护理和支持举措的推广和规模化。这种合作应立足于快速学习和改进的方法,以艾滋病毒感染者的需求、观点和愿望为基础;以及时的数据和证据为驱动力;以适当的决策支持和统一的治理、财务和交付安排为后盾;以快速学习和改进的文化和能力为支撑。
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来源期刊
Health Research Policy and Systems
Health Research Policy and Systems HEALTH POLICY & SERVICES-
CiteScore
7.50
自引率
7.50%
发文量
124
审稿时长
27 weeks
期刊介绍: Health Research Policy and Systems is an Open Access, peer-reviewed, online journal that aims to provide a platform for the global research community to share their views, findings, insights and successes. Health Research Policy and Systems considers manuscripts that investigate the role of evidence-based health policy and health research systems in ensuring the efficient utilization and application of knowledge to improve health and health equity, especially in developing countries. Research is the foundation for improvements in public health. The problem is that people involved in different areas of research, together with managers and administrators in charge of research entities, do not communicate sufficiently with each other.
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