School of Public Health and Social Work, Queensland University of Technology, Queensland, Australia.
Health Inf Manag. 2017 Sep;46(3):127-133. doi: 10.1177/1833358317699341. Epub 2017 Apr 27.
Differential uptake of, or access to, personal electronic health records (PEHRs) has the potential to impact on health disparities among certain social groups. In 2012, the Australian Government introduced the Personally Controlled Electronic Health Record (PCEHR), an opt-in system operated by the then National E-Health Transition Authority (NEHTA). In July 2016, the My Health Record (MyHR), an opt-out model, operated by the Australian Digital Health Agency replaced the PCEHR, providing additional support for consumers.
This research was carried out between 2012 and 2015, covering the opt-in PCEHR phase. The aim of the study was to explore demographic characteristics of Australian health consumers who were first to register for a PEHR, and to identify the age and gender populations less likely to register for a PEHR in the opt-in format. The study aimed to provide early data on registrants and potential methods to encourage individuals to register for a PEHR.
A cross-sectional study investigated differences in registrations for PEHRs from 2012 to 2015 by age and sex.
Results revealed that males were less likely to register than females, and adolescents of both sexes were the least likely to register when compared with any other age group. Similarly, middle-aged males had among the lowest reported registrations, as did older females.
While e-health has the potential to improve health outcomes and PEHRs the potential to empower consumers to better manage their health and improve their access health services, evidence from this study suggested that some population groups that experience health inequalities (e.g. older people) were underrepresented among registrants for PEHRs. As income, ethnicity and education are major drivers for health disparities in Australia, future research should focus on uptake and use of PEHRs (now the MyHR) from the perspective of these variables.
个人电子健康记录(PEHR)的获取或使用情况存在差异,这有可能对某些社会群体的健康差距产生影响。2012 年,澳大利亚政府推出了个人控制的电子健康记录(PCEHR),这是一个由当时的国家电子健康过渡管理局(NEHTA)运营的选择加入系统。2016 年 7 月,由澳大利亚数字健康局运营的、选择退出模式的“我的健康记录”(MyHR)取代了 PCEHR,为消费者提供了额外的支持。
本研究于 2012 年至 2015 年进行,涵盖了选择加入的 PCEHR 阶段。该研究的目的是探讨澳大利亚健康消费者中首先注册个人电子健康记录的人群的人口统计学特征,并确定在选择加入模式下不太可能注册个人电子健康记录的年龄和性别人群。该研究旨在提供有关注册者的早期数据,并为鼓励个人注册个人电子健康记录提供潜在方法。
一项横断面研究调查了 2012 年至 2015 年期间按年龄和性别划分的个人电子健康记录注册情况的差异。
结果表明,男性比女性更不可能注册,与其他任何年龄组相比,两性青少年的注册率最低。同样,中年男性的注册率最低,老年女性也是如此。
虽然电子健康有改善健康结果的潜力,个人电子健康记录有增强消费者管理自己健康和改善获得卫生服务能力的潜力,但本研究的证据表明,在经历健康不平等的一些人群中(例如老年人),个人电子健康记录的注册人数不足。由于收入、种族和教育是澳大利亚健康差距的主要驱动因素,未来的研究应侧重于从这些变量的角度来研究个人电子健康记录(现在是“我的健康记录”)的使用情况。