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患者最了解情况:关于家庭如何使用患者自控个人健康记录的定性研究。

Patients Know Best: Qualitative Study on How Families Use Patient-Controlled Personal Health Records.

作者信息

Schneider Hanna, Hill Susan, Blandford Ann

机构信息

UCLIC, UCL, London, United Kingdom.

出版信息

J Med Internet Res. 2016 Feb 24;18(2):e43. doi: 10.2196/jmir.4652.

Abstract

BACKGROUND

Self-management technologies, such as patient-controlled electronic health records (PCEHRs), have the potential to help people manage and cope with disease.

OBJECTIVE

This study set out to investigate patient families' lived experiences of working with a PCEHR.

METHODS

We conducted a semistructured qualitative field study with patient families and clinicians at a children's hospital in the UK that uses a PCEHR (Patients Know Best). All families were managing the health of a child with a serious chronic condition, who was typically under the care of multiple clinicians. As data gathering and analysis progressed, it became clear that while much of the literature assumes that patients are willing and waiting to take more responsibility for and control over their health management (eg, with PCEHRs), only a minority of participants in our study responded in this way. Their experiences with the PCEHR were diverse and strongly shaped by their coping styles. Theory on coping identifies a continuum of coping styles, from approach to avoidance oriented, and proposes that patients' information needs depend on their style.

RESULTS

We identified 3 groups of patient families and an outlier, distinguished by their coping style and their PCEHR use. We refer to the outlier as controlling (approach oriented, highly motivated to use PCEHR), and the 3 groups as collaborating (approach oriented, motivated to use PCEHR), cooperating (avoidance oriented, less motivated to use PCEHR), and avoiding (very avoidance oriented, not motivated to use PCEHR).

CONCLUSIONS

The PCEHR met the needs of controller and collaborators better than the needs of cooperators and avoiders. We draw on the Self-Determination Theory to propose ways in which a PCEHR design might better meet the needs of avoidance-oriented users. Further, we highlight the need for families to also relinquish control at times, and propose ways in which PCEHR design might support a better distribution of control, based on effective training, ease of use, comprehensibility of data security mechanisms, timely information provision (recognizing people's different needs), personalization of use, and easy engagement with clinicians through the PCEHR.

摘要

背景

自我管理技术,如患者控制的电子健康记录(PCEHRs),有潜力帮助人们管理和应对疾病。

目的

本研究旨在调查患者家庭使用PCEHR的实际体验。

方法

我们在英国一家使用PCEHR(患者了解最佳情况)的儿童医院,对患者家庭和临床医生进行了半结构化定性实地研究。所有家庭都在管理患有严重慢性病儿童的健康,该儿童通常由多名临床医生护理。随着数据收集和分析的进行,很明显,虽然许多文献假设患者愿意并等待对其健康管理承担更多责任并进行控制(例如使用PCEHRs),但我们研究中的参与者只有少数是这样的。他们使用PCEHR的经历各不相同,并受到他们应对方式的强烈影响。应对理论确定了从积极应对到回避应对的一系列应对方式,并提出患者的信息需求取决于他们的应对方式。

结果

我们确定了3组患者家庭和一个异常组,它们的区别在于应对方式和PCEHR的使用情况。我们将异常组称为控制型(积极应对型,使用PCEHR的积极性很高),3组分别为协作型(积极应对型,有使用PCEHR的积极性)、合作型(回避应对型,使用PCEHR的积极性较低)和回避型(非常回避应对型,没有使用PCEHR的积极性)。

结论

PCEHR更好地满足了控制型和协作型患者的需求,而不是合作型和回避型患者的需求。我们借鉴自我决定理论,提出PCEHR设计可以更好地满足回避型用户需求的方法。此外,我们强调家庭有时也需要放弃控制权,并提出PCEHR设计可以如何基于有效的培训、易用性、数据安全机制的可理解性、及时的信息提供(认识到人们的不同需求)、使用的个性化以及通过PCEHR与临床医生轻松互动来支持更好地分配控制权。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d83a/4785240/f494dad9cf6d/jmir_v18i2e43_fig1.jpg

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