帕金森病和认知障碍患者的远程会诊:对患者、护理人员和卫生保健专业人员的访谈研究

JMIR neurotechnology Pub Date : 2022-12-02 DOI:10.2196/39974
Jennifer S Pigott, Megan Armstrong, Elizabeth Chesterman, J. Read, D. Nimmons, K. Walters, N. Davies, A. Schrag
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引用次数: 2

摘要

COVID-19大流行导致许多咨询都是远程进行的。认知障碍被认为是远程医疗互动的潜在障碍,在帕金森病中是常见的和异质性的。研究表明,帕金森病的远程咨询是可行的,但对现实生活中的经验知之甚少,尤其是对那些有认知障碍的人。我们探讨了帕金森病和认知障碍患者远程会诊的经验和看法。本研究旨在从服务使用者和专业人员的角度探讨帕金森病和认知障碍患者远程会诊的体验,并调查未来服务提供的考虑因素。在2020年至2021年期间,对11名帕金森病和认知障碍患者、10名家庭护理人员和24名卫生保健专业人员(HCPs)进行了半结构化的远程访谈。采用有目的抽样。访谈录音,转录,并使用反身性主题分析进行分析。总的来说,确定了四个主题:“远程交互的本质”、“远程加剧的挑战”、“期望与现实”以及“面向未来的优化”。远程协商被认为是“事务性的”,不太个人化,在建立融洽关系方面有困难,并被认为发挥与面对面协商不同的作用。非语言沟通的丧失和医务人员感知能力的丧失导致所有群体都认为远程咨询风险更大。沟通和认知障碍引起的问题,平衡帕金森病患者和护理者的声音,以及对未来的讨论,特别影响到这一人群。据报告,所有3组的远程会诊都比预期的更成功。障碍并不总是如预期的那样;例如,年龄并没有像预期的那样成为障碍。许多参与者认为视频咨询比电话咨询更好,但并非所有帕金森病患者都能获得视频咨询。由于对正在进行的远程会诊的广泛期望,确定了对这3个群体和卫生保健服务的潜在改进,包括实践、准备、提高对问题的认识、hcp的期望管理以及更多的会诊时间和灵活性。确定了远程咨询对这一人群的优势和挑战。可以通过增加支助、实践、准备、对问题的认识以及在服务内增加时间和灵活性来改进协商。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Remote Consultations for People With Parkinson Disease and Cognitive Impairment: Interview Study With Patients, Caregivers, and Health Care Professionals
The COVID-19 pandemic led to many consultations being conducted remotely. Cognitive impairment is recognized as a potential barrier to remote health care interactions and is common and heterogeneous in Parkinson disease. Studies have shown remote consultations in Parkinson disease to be feasible, but little is known about real-life experience, especially for those with cognitive impairment. We explored the experiences and perceptions of remote consultations for people with Parkinson disease and cognitive impairment. This study aimed to explore the experiences of remote consultations for people with Parkinson disease and cognitive impairment from the perspective of service users and professionals and investigate considerations for future service delivery. Semistructured interviews were conducted remotely with 11 people with Parkinson disease and cognitive impairment, 10 family caregivers, and 24 health care professionals (HCPs) between 2020 and 2021. Purposive sampling was used. Interviews were audio-recorded, transcribed, and analyzed using reflexive thematic analysis. Overall, four themes were identified: “the nature of remote interactions,” “challenges exacerbated by being remote,” “expectation versus reality,” and “optimizing for the future.” Remote consultations were considered as “transactional” and less personal, with difficulties in building rapport, and considered to play a different role from that of in-person consultations. The loss of nonverbal communication and ability of HCPs to sense led to remote consultations being perceived as riskier by all groups. Issues arising from communication and cognitive impairment, balancing the voices of the person with Parkinson disease and the caregiver, and discussions of the future affect this population specifically. Remote consultations were reported to have been more successful than anticipated in all 3 groups. Obstacles were not always as expected; for example, age was less of a barrier than predicted. Video consultations were perceived as being preferable to telephone consultations by many participants, but not accessible to all people with Parkinson disease. With widespread expectation of ongoing remote consultations, potential improvements for these 3 groups and health care services were identified, including practice, preparation, increased awareness of issues, expectation management by HCPs, and more time and flexibility for consultations. Advantages and challenges of remote consultations for this population are identified. Consultations could be improved with increased support, practice, preparation, awareness of issues, and more time and flexibility within services.
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