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一种针对普拉德-威利综合征临床管理的多学科方法。

A multidisciplinary approach to the clinical management of Prader-Willi syndrome.

作者信息

Duis Jessica, van Wattum Pieter J, Scheimann Ann, Salehi Parisa, Brokamp Elly, Fairbrother Laura, Childers Anna, Shelton Althea Robinson, Bingham Nathan C, Shoemaker Ashley H, Miller Jennifer L

机构信息

Division of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.

Department of Psychiatry, Child Study Center, Yale School of Medicine, New Haven, Connecticut.

出版信息

Mol Genet Genomic Med. 2019 Mar;7(3):e514. doi: 10.1002/mgg3.514. Epub 2019 Jan 29.

Abstract

BACKGROUND

Prader-Willi syndrome (PWS) is a complex neuroendocrine disorder affecting approximately 1/15,000-1/30,000 people. Unmet medical needs of individuals with PWS make it a rare disease that models the importance of multidisciplinary approaches to care with collaboration between academic centers, medical homes, industry, and parent organizations. Multidisciplinary clinics support comprehensive, patient-centered care for individuals with complex genetic disorders and their families. Value comes from improved communication and focuses on quality family-centered care.

METHODS

Interviews with medical professionals, scientists, managed care experts, parents, and individuals with PWS were conducted from July 1 to December 1, 2016. Review of the literature was used to provide support.

RESULTS

Data are presented based on consensus from these interviews by specialty focusing on unique aspects of care, research, and management. We have also defined the Center of Excellence beyond the multidisciplinary clinic.

CONCLUSION

Establishment of clinics motivates collaboration to provide evidence-based new standards of care, increases the knowledge base including through randomized controlled trials, and offers an additional resource for the community. They have a role in global telemedicine, including to rural areas with few resources, and create opportunities for clinical work to inform basic and translational research. As a care team, we are currently charged with understanding the molecular basis of PWS beyond the known genetic cause; developing appropriate clinical outcome measures and biomarkers; bringing new therapies to change the natural history of disease; improving daily patient struggles, access to care, and caregiver burden; and decreasing healthcare load. Based on experience to date with a PWS multidisciplinary clinic, we propose a design for this approach and emphasize the development of "Centers of Excellence." We highlight the dearth of evidence for management approaches creating huge gaps in care practices as a means to illustrate the importance of the collaborative environment and translational approaches.

摘要

背景

普拉德-威利综合征(PWS)是一种复杂的神经内分泌疾病,影响约1/15000 - 1/30000的人群。PWS患者未得到满足的医疗需求使其成为一种罕见病,它体现了学术中心、医疗之家、行业和家长组织之间合作的多学科护理方法的重要性。多学科诊所为患有复杂遗传疾病的个体及其家庭提供全面的、以患者为中心的护理。其价值源于改善沟通,并专注于高质量的以家庭为中心的护理。

方法

2016年7月1日至12月1日,对医学专业人员、科学家、管理式医疗专家、家长以及PWS患者进行了访谈。通过文献回顾提供支持。

结果

根据这些访谈的专业共识,按专业呈现数据,重点关注护理、研究和管理的独特方面。我们还定义了多学科诊所之外的卓越中心。

结论

诊所的建立促进了合作,以提供基于证据的新护理标准,增加了知识库,包括通过随机对照试验,并为社区提供了额外资源。它们在全球远程医疗中发挥作用,包括对资源匮乏的农村地区,为临床工作创造机会以指导基础研究和转化研究。作为一个护理团队,我们目前的任务是了解PWS已知遗传病因之外的分子基础;制定适当的临床结局指标和生物标志物;带来新疗法以改变疾病的自然病程;改善患者日常困境、获得护理的机会以及照顾者负担;并减轻医疗负担。基于目前PWS多学科诊所的经验,我们提出了这种方法的设计,并强调“卓越中心”的发展。我们强调管理方法缺乏证据,这在护理实践中造成了巨大差距,以此说明合作环境和转化方法的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73a0/6418440/ec83cb7dbe92/MGG3-7-na-g001.jpg

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