与患者社区共同创建癌症护理远程医疗的新框架。

IF 3.4 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Bonnie Addario, Violeta Astratinei, Louise Binder, Jan Geissler, Marcia K Horn, Linda U Krebs, Bryan Lewis, Kathy Oliver, Andrew Spiegel
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引用次数: 0

摘要

在2019年冠状病毒病大流行期间,远程医疗在癌症治疗中的使用有所增加,这增加了我们对这种模式的了解和经验,在疗效、成本以及患者和医疗保健专业经验方面都有好处。然而,也发现远程保健并非普遍适用于所有癌症患者,也不适用于每一次保健互动;此外,并非所有患者都喜欢它。既然对冠状病毒疾病的限制基本上已经结束,并且出现了重新评估癌症护理中的远程医疗服务的机会,我们提供了一个框架,旨在确保将患者群体的需求和偏好纳入远程医疗服务的发展。这一过程中的利益相关者包括患者、患者倡导者、医疗保健提供者、医疗保健服务专员、管理人员和政策制定者。该框架概述了患者权益倡导者如何在远程保健服务发展的所有阶段与其他利益攸关方作为平等伙伴开展合作。患者倡导者社区对患者的观点有独特的理解,并在医疗保健设计和交付方面拥有专业知识。这使倡导者能够从政策和指南的制定到患者导航,为制定远程保健服务做出贡献。可能需要为所有利益攸关方提供适当的资源、教育和培训,以支持建立有效的远程保健系统。与其他利益攸关方一起,患者倡导者可以为优化以患者为中心的适当癌症护理远程保健提供作出重要贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A New Framework for Co-Creating Telehealth for Cancer Care with the Patient Community.

A New Framework for Co-Creating Telehealth for Cancer Care with the Patient Community.

The increased use of telehealth in cancer care during the coronavirus disease 2019 pandemic has added to our knowledge and experience of the modality with benefits in terms of efficacy, cost, and patient and healthcare professional experience reported. However, telehealth has also been found not to be universally available to all patients with cancer, nor to be appropriate for every healthcare interaction; additionally, not all patients prefer it. Now that coronavirus disease restrictions have essentially ended and an opportunity to re-assess telehealth provision in cancer care presents, we offer a framework that aims to ensure that the needs and preferences of the patient community are included in the development of telehealth provision. Stakeholders in this process include patients, patient advocates, healthcare providers, healthcare services commissioners, managers, and policy makers. The framework outlines how patient advocates can work with other stakeholders as equal partners at all stages of telehealth service development. The patient advocate community has a unique understanding of the patient perspective as well as expertise in healthcare design and delivery. This enables advocates to contribute to shaping telehealth provision, from policy and guideline formulation to patient navigation. Appropriate resources, education and training may be needed for all stakeholders to support the development of an effective telehealth system. Together with other stakeholders, patient advocates can make an important contribution to optimizing appropriate patient-centred telehealth provision in cancer care.

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来源期刊
Patient-Patient Centered Outcomes Research
Patient-Patient Centered Outcomes Research HEALTH CARE SCIENCES & SERVICES-
CiteScore
6.60
自引率
8.30%
发文量
44
审稿时长
>12 weeks
期刊介绍: The Patient provides a venue for scientifically rigorous, timely, and relevant research to promote the development, evaluation and implementation of therapies, technologies, and innovations that will enhance the patient experience. It is an international forum for research that advances and/or applies qualitative or quantitative methods to promote the generation, synthesis, or interpretation of evidence. The journal has specific interest in receiving original research, reviews and commentaries related to qualitative and mixed methods research, stated-preference methods, patient reported outcomes, and shared decision making. Advances in regulatory science, patient-focused drug development, patient-centered benefit-risk and health technology assessment will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in The Patient may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances. All manuscripts are subject to peer review by international experts.
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