首页> 外文期刊>BMC Medical Informatics and Decision Making >Caregivers' role in using a personal electronic health record: a qualitative study of cancer patients and caregivers in Germany
【24h】

Caregivers' role in using a personal electronic health record: a qualitative study of cancer patients and caregivers in Germany

机译:看护人员在利用个人电子健康记录中的作用:德国癌症患者和护理人员的定性研究

获取原文
           

摘要

Particularly in the context of severe diseases like cancer, many patients wish to include caregivers in the planning of treatment and care. Many caregivers like to be involved but feel insufficiently enabled. This study aimed at providing insight into patients’ and caregivers’ perspectives on caregivers’ roles in managing the patient portal of an electronic personal health record (PHR). A descriptive qualitative study was conducted comprising two study phases: (1) Usability tests and interviews with patients with cancer and caregivers (2) additional patient interviews after a 3-month-pilot-testing of the PHR. For both study parts, a convenience sample was selected, focusing on current state of health and therapy process and basic willingness to participate and ending up with a mixed sample as well as saturation of data. All interviews were audio-recorded, pseudonymized, transcribed verbatim and qualitatively analyzed. Two main categories emerged from qualitative data: ‘Caregivers’ role’ and ‘Graduation of access rights’ – consisting of four subcategories each. The interviewed patients (n?=?22) and caregivers (n?=?9) felt that the involvement of caregivers is central to foster the acceptance of a PHR for cancer patients. However, their role varied from providing technical support to representing patients, e.g. if the patient’s state of health made this necessary. Heterogeneous opinions emerged regarding the question whether caregivers should receive full or graduated access on a patient’s PHR. In order to support the patient and to participate in the care process, caregivers need up-to-date information on the patient’s health and treatment. Nevertheless, some patients do not want to share all medical data with caregivers, which might strain the patient-caregiver relationship. This needs to be considered in development and implementation of personal health records. Generally, in the debate on patient portals of a personal health record, paying attention to the role of caregivers is essential. By appreciating the important relationship between patients and caregivers right from the beginning, implementation, of a PHR would be enhanced. ISRCTN85224823 . Date of registration: 23/12/2015 (retrospectively registered).
机译:特别是在癌症等重症疾病的背景下,许多患者希望在治疗和护理计划中包括护理人员。许多照顾者喜欢参与其中,但感到不够。本研究旨在向患者和护理人员的角度提供洞察力,在管理电子个人健康记录(PHR)的患者门户网站方面的角色。进行了描述性定性研究,包括两项研究阶段:(1)可用性测试和对癌症和护理人员患者的访谈(2)在3个月的试验测试后额外的患者访谈。对于这两个研究零件来说,选择了一种方便样品,重点关注当前的健康和治疗过程状态以及与混合样品以及数据饱和度的基本意愿和基本意愿。所有访谈都是音频录制的,假义的,翻译逐字和定性分析。从定性数据中出现的两种主要类别:“看护人的角色”和“访问权毕业” - 由四个子类别组成。受访者(n?= 22)和护理人员(n?=?9)认为,护理人员的参与是培养癌症患者的接受的核心。但是,它们的作用因提供技术支持而变化,例如代表患者,例如,如果患者的健康状况做出了这一必要。有关护理人员是否应在患者的PHR上获得全面或毕业访问的问题出现了异质意见。为了支持患者并参与护理过程,护理人员需要关于患者的健康和治疗的最新信息。尽管如此,一些患者不想与护理人员分享所有医疗数据,这可能会留下患者护理人员的关系。这需要考虑在制定和实施个人健康记录中。一般来说,在对个人健康记录的患者门户网站的辩论中,关注护理人员的作用至关重要。通过欣赏从一开始,实施的患者和护理人员之间的重要关系将得到加强。 ISRCTN85224823。注册日期:2015年23日(回顾性注册)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号