Department of Neurosciences, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom; Department of Basic and Clinical Neuroscience, Division of Neuroscience, King's College London, London, United Kingdom; Parkinson's Foundation Centre of Excellence, King's College Hospital NHS Foundation Trust, London, United Kingdom.
Department of Neurosciences, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom; Department of Basic and Clinical Neuroscience, Division of Neuroscience, King's College London, London, United Kingdom; Parkinson's Foundation Centre of Excellence, King's College Hospital NHS Foundation Trust, London, United Kingdom; Department of Neurology, Centre of Expertise for Parkinson & Movement Disorders, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Int Rev Neurobiol. 2022;165:263-281. doi: 10.1016/bs.irn.2022.04.002. Epub 2022 Jul 14.
As a result of the Coronavirus Disease 2019 (Covid-19) pandemic the use of telemedicine and remote assessments for patients has increased exponentially, enabling healthcare professionals to reduce the need for in-person clinical visits and, consequently, reduce the exposure to the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2). This development has been aided by increased guidance on digital health technologies and cybersecurity measures, as well as reimbursement options within healthcare systems. Having been able to continue to connect with people with Parkinson's Disease (PwP, PD) has been crucial, since many saw their symptoms worsen over the pandemic. Inspite of the success of telemedicine, sometimes even enabling delivery of treatment and research, further validation and a unified framework are necessary to measure the true benefit to both clinical outcomes and health economics. Moreover, the use of telemedicine seems to have been biased towards people from a white background, those with higher education, and reliable internet connections. As such, efforts should be pursued by being inclusive of all PwP, regardless of geographical area and ethnic background. In this chapter, we describe the effect he Covid-19 pandemic has had on the use of telemedicine for care and research in people with PD, the limiting factors for further rollout, and how telemedicine might develop further.
由于 2019 年冠状病毒病(COVID-19)大流行,远程医疗和患者远程评估的使用呈指数级增长,使医疗保健专业人员能够减少对面对面临床就诊的需求,从而减少对严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)的暴露。这一发展得益于数字健康技术和网络安全措施的指导增加,以及医疗保健系统中的报销选择。能够继续与帕金森病患者(PwP,PD)保持联系至关重要,因为许多人在大流行期间看到自己的症状恶化。尽管远程医疗取得了成功,有时甚至能够提供治疗和研究,但仍有必要进一步验证和建立统一框架,以衡量其对临床结果和健康经济学的真正益处。此外,远程医疗的使用似乎偏向于白人背景、受过高等教育和有可靠互联网连接的人。因此,应该努力包容所有 PwP,无论其地理位置和种族背景如何。在本章中,我们描述了 COVID-19 大流行对 PD 患者护理和研究中使用远程医疗的影响、进一步推广的限制因素,以及远程医疗可能如何进一步发展。