巴西姑息治疗网络

J. Munis, Juliana Dias Reis Pessalacia, Jacqueline Resende Boaventura, Ana Paula Da Silva, Luciana Ferreira Da Silva, Aires Garcia dos Santos Júnior, A. M. Ferreira
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引用次数: 0

摘要

巴西是一个具有巨大多样性和独特现实的国家,因此,在提供一个方便、高质量和有效的统一和综合系统方面存在着相称的挑战和复杂性。人口老龄化和慢性退行性非传染性疾病(NCDs)发病率的增加增加了对姑息治疗(PC)的需求;然而,仍然需要实施公共政策,使这种护理包括充足的资金、专业培训和有保障的药物治疗。最近提出了第一个国家个人护理政策,为个人护理的组织提供了指导方针,强调了巴西卫生系统(SUS)中不同层次的护理和服务之间整合的重要性。然而,这项政策面临的挑战包括专业人员的培训、网络中的沟通、缺乏综合卫生信息系统以及为这种新的护理方式提供资金的有效机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Palliative Care Network in Brazil
Brazil is a country with great diversity and distinct realities, so there is a proportional challenge and complexity in offering a unified and integrated system which is accessible, of quality, and effective. Population aging and the increased incidence of chronic-degenerative noncommunicable diseases (NCDs) increase the need for palliative care (PC); however, public policies still need to be implemented so that this care encompasses adequate funding, professional training, and guaranteed medication. The first national policy for PC was recently proposed, providing guidelines for the organization of PC, emphasizing the importance of integration between the different levels of care and services in the Brazilian health system (SUS). Nevertheless, the challenges of this policy include the training of professionals, communication in the network, the absence of integrated health information systems, and effective mechanisms to finance this new modality of care.
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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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