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Towards Patient Empowerment - Can the Patient Really Decide?

机译:增强患者能力-患者能否真正决定?

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摘要

Throughout the modern world, healthcare is in a crisis. In response, health information systems are going through major changes: focusing more on the patient and what the patient can do to help to improve his own health care. A lot has been said about what the patient's role should be in the 21s' century. However, in a way, the patient is still being left out, without the ability to decide about his role and impotent to exercise his rights as the owner of his own EHR. Moreover, there exists a general lack of awareness among the general public about the major risks involved in the unbounded disclosure of personal health related data. The continuous growth of privacy incidents, resulting from target profiling and mining off individual health histories, by human resource departments or insurance companies, demonstrates the fragile perception the general public has for these matters. To help us in assessing this situation we have conducted several interviews with patients older than 18 years in order to determine their opinion on matters regarding 'patient empowerment' and their associated EHRs: particularly who should have access and what were the real reasons behind those answers. In this paper we analyze the results of our questionnaire and present and discuss in detail the answers provided by 100 patients: 70 female and 30 male from diverse strata of the Portuguese population.
机译:在整个现代世界中,医疗保健处于危机之中。作为响应,健康信息系统正在发生重大变化:更加关注患者以及患者可以采取哪些措施来改善自己的健康状况。关于患者在21世纪应该扮演的角色已有很多论述。但是,从某种意义上说,病人仍然被排除在外,无法决定自己的角色,也无力行使自己作为电子病历所有人的权利。此外,公众普遍缺乏对无限制公开个人健康相关数据所涉及的主要风险的认识。人力资源部门或保险公司对目标进行概要分析并挖掘出个人健康史的结果导致隐私事件的持续增长,表明了公众对于这些问题的脆弱认识。为了帮助我们评估这种情况,我们对18岁以上的患者进行了几次访谈,以确定他们对“患者赋权”及其相关的EHR的看法:特别是谁应该有机会以及这些答案背后的真正原因是什么? 。在本文中,我们分析了调查问卷的结果,并提出并详细讨论了来自葡萄牙人口不同阶层的100名患者提供的答案:70名女性和30名男性。

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