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Patients' experience with a diabetes support programme based on an interactive electronic medical record: qualitative study

机译:基于交互式电子病历的患者对糖尿病支持计划的经验:定性研究

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Objective To describe the experiences of patients with type 2 diabetes in a web based disease management programme based on an interactive electronic medical record. Design Qualitative analysis of semistructured interviews with patients enrolled in a diabetes care module that included access to their electronic medical record, secure email, ability to upload blood glucose readings, an education site with endorsed content, and an interactive online diary for entering exercise, diet, and medication. Setting Patients' homes in Washington state, United States. Participants Nine participants aged 45-65 completed interviews before and after they used the programme. Results Six themes emerged: feeling that non-acute concerns are uniquely valued; enhanced sense of security about health and health care; frustration with unmet expectations; feeling more able to manage; valuing feedback; and difficulty fitting the programme into activities of daily life. Three themes ― valuing non-acute concerns, feeling secure, and unmet expectations ― have particular relevance to the design and use of web based tools for care of patients with diabetes and chronic medical conditions. Conclusion Participants' experiences support further study of open access to the electronic medical record and online communication between patients and their care providers. The development of web based disease management programmes should take into account the specific needs and expectations of patients, and patients and providers should have candid discussions about what web based care can and cannot provide.
机译:目的在基于交互式电子病历的基于网络的疾病管理程序中描述2型糖尿病患者的经历。对参与糖尿病护理模块的患者进行的半结构式访谈的设计定性分析,包括访问其电子病历,安全的电子邮件,上传血糖读数的能力,带有认可内容的教育网站以及用于锻炼,饮食的交互式在线日记和药物。在美国华盛顿州设置患者家园。参与者九名45-65岁的参与者在使用该计划之前和之后均完成了访谈。结果出现了六个主题:感觉到非急性关注得到了独特重视;增强对健康和保健的安全感;未能满足期望而感到沮丧;感觉更有能力去管理;重视反馈;并且很难将程序融入到日常生活中。评估非急性问题,感到安全和未达到期望这三个主题与用于护理糖尿病和慢性病患者的基于Web的工具的设计和使用特别相关。结论参与者的经验支持进一步研究开放访问电子病历以及患者及其护理提供者之间的在线交流。基于网络的疾病管理计划的开发应考虑患者的具体需求和期望,患者和提供者应就基于网络的医疗可以提供和不能提供的内容进行坦率的讨论。

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