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绘制新生儿筛查研究中的伦理前沿:来自新生儿筛查转化研究网络(NBSTRN)伦理、法律与社会问题(ELSI)研究者需求调查的见解

Charting the Ethical Frontier in Newborn Screening Research: Insights from the NBSTRN ELSI Researcher Needs Survey.

作者信息

Unnikumaran Yekaterina, Lietsch Mei, Brower Amy

机构信息

American College of Medical Genetics and Genomics (ACMG), Bethesda, MD 20814, USA.

Carver College of Medicine, University of Iowa, Iowa City, IA 52242, USA.

出版信息

Int J Neonatal Screen. 2024 Sep 19;10(3):64. doi: 10.3390/ijns10030064.

Abstract

From 2008 to 2024, the Newborn Screening Translational Research Network (NBSTRN), part of the National Institute of Child Health and Human Development (NICHD) Hunter Kelly Newborn Screening Program, served as a robust infrastructure to facilitate groundbreaking research in newborn screening (NBS), public health, rare disease, and genomics. Over its sixteen years, NBSTRN developed into a significant international network, supporting innovative research on novel technologies to screen, diagnose, treat, manage, and understand the natural history of more than 280 rare diseases. The NBSTRN tools and resources were used by a variety of stakeholders including researchers, clinicians, state NBS programs, parents, families, and policy makers. Resources and expertise for the newborn screening community in ethical, legal, and social issues (ELSI) has been an important area of focus for the NBSTRN and this includes efforts across the NBS system from pilot studies of candidate conditions to public health implementation of screening for new conditions, and the longitudinal follow-up of NBS-identified individuals to inform health outcomes and disease understanding. In 2023, the NBSTRN conducted a survey to explore ELSI issues in NBS research, specifically those encountered by the NBS community. Since NBS research involves collaboration among researchers, state NBS programs, clinicians, and families, the survey was broadly designed and disseminated to engage all key stakeholders. With responses from 88 members of the NBS community, including researchers and state NBS programs, the survey found that individuals rely most on institutional and collegial resources when they encounter ELSI questions. Most survey responses ranked privacy as extremely or very important in NBS research and identified the need for policies that address informed consent in NBS research. The survey results highlight the need for improved collaborative resources and educational programs focused on ELSI for the NBS community. The survey results inform future efforts in ELSI and NBS research in the United States (U.S.) and the rest of the world, including the development of policies and expanded ELSI initiatives and tools that address the needs of all NBS stakeholders.

摘要

2008年至2024年期间,新生儿筛查转化研究网络(NBSTRN)作为美国国立儿童健康与人类发展研究所(NICHD)亨特·凯利新生儿筛查项目的一部分,为促进新生儿筛查(NBS)、公共卫生、罕见病和基因组学领域的开创性研究提供了强大的基础设施。在其成立的十六年里,NBSTRN发展成为一个重要的国际网络,支持对新技术的创新性研究,以筛查、诊断、治疗、管理并了解280多种罕见病的自然病史。NBSTRN的工具和资源被包括研究人员、临床医生、州新生儿筛查项目、家长、家庭和政策制定者在内的各种利益相关者所使用。新生儿筛查领域在伦理、法律和社会问题(ELSI)方面的资源和专业知识一直是NBSTRN的一个重要关注领域,这包括整个新生儿筛查系统的各项工作,从候选病症的试点研究到新病症筛查的公共卫生实施,以及对通过新生儿筛查确定的个体进行纵向随访,以了解健康结果和疾病情况。2023年,NBSTRN开展了一项调查,以探讨新生儿筛查研究中的ELSI问题,特别是新生儿筛查领域所遇到的问题。由于新生儿筛查研究涉及研究人员、州新生儿筛查项目、临床医生和家庭之间的合作,该调查进行了广泛设计并分发,以吸引所有关键利益相关者参与。在收到来自88名新生儿筛查领域成员(包括研究人员和州新生儿筛查项目)的回复后,调查发现,当遇到ELSI问题时,个人最依赖机构和同行资源。大多数调查回复将隐私在新生儿筛查研究中列为极其重要或非常重要,并确定需要制定解决新生儿筛查研究中知情同意问题的政策。调查结果凸显了为新生儿筛查领域改进专注于ELSI的协作资源和教育项目的必要性。调查结果为美国及世界其他地区未来在ELSI和新生儿筛查研究方面的工作提供了参考,包括制定政策以及扩大ELSI举措和工具,以满足所有新生儿筛查利益相关者的需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0357/11417897/3c8af902095e/IJNS-10-00064-g001.jpg

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