The Marquette Palliative Care System

R. Love, Sheikh Iqbal Ahamed
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引用次数: 2

Abstract

Worldwide, major clinical barriers to effective palliative care are the absence of a. current data on symptom type and intensity; b. immediately accessible information on practical, affordable, and effective interventions; and c. self-sustaining systems to facilitate physician engagement in continuing palliative care. Our adaptable system, developed for Bangladesh and Nepal, addresses these barriers. A tele-home palliative care program facilitates home care, minimizes expense, and encourages efficient professional practitioner involvement employing two information technology tools: a patient cell-phone “app” on the Android platform with a 15-item symptom questionnaire and an Internet website with health information sections for patients/families and for clinicians. The physician section contains a guide for patient symptom review, clinical practice palliative care guidelines, secured patient demographics, medical summaries, and current and past symptom reports along with prescription-writing capability. The system is managed by a local organization that registers patients and their physicians, instructs patients on the free download-able application and completes their demographic and medical summaries, and arranges collection of a modest fee. The organization also ensures regular physician/ clinic visits by the patient or by a family member with a patient phone check-in, at least every 2 weeks.
马奎特姑息治疗系统
在世界范围内,有效姑息治疗的主要临床障碍是缺乏a.症状类型和强度的当前数据;B.关于实用、负担得起和有效干预措施的可立即获得的信息;c.促进医生参与持续姑息治疗的自我维持系统。我们为孟加拉国和尼泊尔开发的适应性系统解决了这些障碍。远程家庭姑息治疗方案利用两种信息技术工具,促进家庭护理,最大限度地减少费用,并鼓励有效的专业医生参与:Android平台上的患者手机“应用程序”,包含15项症状问卷,以及为患者/家庭和临床医生提供健康信息部分的互联网网站。医生部分包含患者症状审查指南、临床实践姑息治疗指南、安全的患者人口统计数据、医学摘要、当前和过去的症状报告以及处方撰写能力。该系统由一个当地组织管理,该组织负责登记患者及其医生,指导患者使用可免费下载的应用程序,完成他们的人口统计和医疗摘要,并安排收取适当的费用。该组织还确保患者或家属至少每两周通过患者电话登记定期进行医生/诊所访问。
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来源期刊
自引率
0.00%
发文量
0
审稿时长
15 weeks
期刊介绍: Palliative Care and Social Practice is an international, peer-reviewed, open access journal that publishes articles on all aspects of palliative care. It welcomes articles from symptom science, clinical practice, and health services research. However, its aim is also to publish cutting-edge research from the realm of social practice - from public health theory and practice, social medicine, and social work, to social sciences related to dying and its care, as well as policy, criticism, and cultural studies. We encourage reports from work with under-represented groups, community development, and studies of civic engagement in end of life issues. Furthermore, we encourage scholarly articles that challenge current thinking about dying, its current care models and practices, and current understandings of grief and bereavement. We want to showcase the next generation of palliative care innovation research and practice - in clinics and in the wider society. Relaunched in July 2019. Partnered with Public Health Palliative Care International (PHPCI) (Title 2008-2018: - Palliative Care: Research and Treatment)
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