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Use of the my health record by people with communication disability in Australia: A review to inform the design and direction of future research

机译:澳大利亚沟通障碍者对我的健康记录的使用:审查以告知未来研究的设计和方向

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Background: People with communication disability often struggle to convey their health information to multiple service providers and are at increased risk of adverse health outcomes related to the poor exchange of health information. Objective: The purpose of this article was to (a) review the literature informing future research on the Australian personally controlled electronic health record, ‘My Health Record’ (MyHR), specifically to include people with communication disability and their family members or service providers, and (b) to propose a range of suitable methodologies that might be applied in research to inform training, policy and practice in relation to supporting people with communication disability and their representatives to engage in using MyHR. Method: The authors reviewed the literature and, with a cross-disciplinary perspective, considered ways to apply sociotechnical, health informatics, and inclusive methodologies to research on MyHR use by adults with communication disability. Research outcomes: This article outlines a range of research methods suitable for investigating the use of MyHR by people who have communication disability associated with a range of acquired or lifelong health conditions, and their family members, and direct support workers. Conclusion: In planning the allocation of funds towards the health and well-being of adults with disabilities, both disability and health service providersmust consider the supports needed for people with communication disability to use MyHR.There is an urgent need to focus research efforts on MyHR in populations with communication disability, who struggle to communicate their health information acrossmultiple health and disability service providers. The design of studies and priorities for future research should be set in consultation with people with communication disability and their representatives.
机译:背景:沟通障碍者经常难以将他们的健康信息传递给多个服务提供商,并且由于不良健康信息交流而导致不良健康后果的风险增加。目的:本文的目的是(a)回顾文献,为将来有关澳大利亚个人控制的电子健康记录“我的健康记录”(MyHR)的研究提供信息,特别是将交流障碍者及其家人或服务提供者包括在内(b)提出一系列可能适用于研究的合适方法,以提供有关支持残疾人士及其代表参与使用MyHR的培训,政策和实践的信息。方法:作者回顾了文献,并从跨学科的角度,研究了将社会技术,健康信息学和包容性方法应用于研究交流障碍成年人使用MyHR的方法。研究成果:本文概述了一系列研究方法,这些方法适用于调查患有与一系列获得性或终生健康状况相关的沟通障碍的人及其家人和直接支持人员对MyHR的使用情况。结论:在规划用于残疾成人健康和福祉的资金分配时,残疾和医疗服务提供者都必须考虑交流障碍者使用MyHR所需的支持。迫切需要将研究重点放在MyHR上在有沟通障碍的人群中,他们难以在多个健康和残疾服务提供商之间交流其健康信息。研究的设计和未来研究的重点应与沟通障碍者及其代表协商。

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