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医院管理人员作为罕见病护理中被遗忘的合作伙伴:国际医院联合会全球罕见儿科疾病网络的行动呼吁

Hospital administrators as forgotten partners in rare disease care: a call to action by the international hospital federation's global rare pediatric disease network.

作者信息

Stoesz Andrea, Joers Barbara, Gaviglio Amy

机构信息

Gillette Children's Specialty Healthcare, 200 University Avenue E., St. Paul, MN, 55101, USA.

Connetics Consulting, 5737 Standish Avenue, Minneapolis, MN, 55417, USA.

出版信息

Orphanet J Rare Dis. 2024 Dec 4;19(1):456. doi: 10.1186/s13023-024-03459-5.

Abstract

BACKGROUND

The global public health burden of rare diseases has become an increasingly discussed topic, and its societal impact cannot be overstated. While it may seem counterintuitive to discuss broad healthcare and public health impact in the context of rarity, taken together, over 400 million people worldwide are estimated to live with a rare disease. Over half of people living with a rare disease are children. Providing robust and comprehensive services to the rare disease community requires coordinated efforts of numerous experts and partners. Globally, there are many initiatives focused on improving the lives of people living with a rare disease. Most of these networks and organizations are region or country based and have historically centered on three focal areas: research; provision of education, support, and/or information; and direct clinical care. While all these efforts recognize the importance of a coordinated system of partners across a spectrum of disciplines to improve care for the rare disease community, one group has been largely untapped: hospital administrators and leadership. To address this gap, the International Hospital Federation (IHF) convened the Global Rare Pediatric Disease Network (GRPDN), composed of hospital leaders from around the world. To assess how hospital leadership can assist in providing the infrastructure for improving care for patients and families living with a rare disease, the GRPDN created a survey to gather feedback on hospital administrators' perspectives on needed efforts to improve global rare disease care.

RESULTS

The survey identified five themes: increased public awareness of rare diseases and support for families, diagnostic management and treatment guidelines, lifelong, multidisciplinary care, data and research, and funding.

CONCLUSIONS

Until recently, hospital leadership has been an untapped partner in addressing challenges faced by rare disease patients, and they are uniquely positioned to bridge existing gaps. The GRPDN will continue to focus on identifying practical strategies that hospital leaders-regardless of resource level-can implement to improve care for children living with a rare disease.

摘要

背景

罕见病的全球公共卫生负担已成为一个日益受到讨论的话题,其对社会的影响再怎么强调也不为过。虽然在罕见病的背景下讨论广泛的医疗保健和公共卫生影响可能看似有违直觉,但据估计,全球共有超过4亿人患有罕见病。超过半数的罕见病患者为儿童。为罕见病群体提供强大而全面的服务需要众多专家和合作伙伴的协同努力。在全球范围内,有许多旨在改善罕见病患者生活的倡议。这些网络和组织大多以地区或国家为基础,并且历来集中在三个重点领域:研究;提供教育、支持和/或信息;以及直接的临床护理。虽然所有这些努力都认识到跨学科的合作伙伴协调系统对于改善罕见病群体护理的重要性,但有一个群体在很大程度上尚未得到充分利用:医院管理人员和领导层。为了填补这一空白,国际医院联合会(IHF)召集了全球罕见儿科疾病网络(GRPDN),其成员包括来自世界各地的医院领导。为了评估医院领导层如何协助提供基础设施以改善对患有罕见病的患者及其家庭的护理,GRPDN开展了一项调查,以收集医院管理人员对改善全球罕见病护理所需努力的看法的反馈。

结果

该调查确定了五个主题:提高公众对罕见病的认识和对家庭的支持、诊断管理和治疗指南、终身多学科护理、数据与研究以及资金。

结论

直到最近,医院领导层在应对罕见病患者所面临的挑战方面一直是未被充分利用的合作伙伴,而且他们处于独特的地位来弥合现有差距。GRPDN将继续专注于确定医院领导(无论资源水平如何)可以实施的切实可行的策略,以改善对患有罕见病儿童的护理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c109/11616372/ecabbe531359/13023_2024_3459_Fig1_HTML.jpg

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