Suppr超能文献

在新生儿重症监护病房环境中对非遗传学医疗服务提供者进行基因组测序结果反馈的教育与培训。

Education and Training of Non-Genetics Providers on the Return of Genome Sequencing Results in a NICU Setting.

作者信息

East Kelly M, Cochran Meagan E, Kelley Whitley V, Greve Veronica, Finnila Candice R, Coleman Tanner, Jennings Mikayla, Alexander Latonya, Rahn Elizabeth J, Danila Maria I, Barsh Greg, Korf Bruce, Cooper Greg

机构信息

HudsonAlpha Institute for Biotechnology, Huntsville, AL 35806, USA.

Division of Clinical Immunology/Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.

出版信息

J Pers Med. 2022 Mar 5;12(3):405. doi: 10.3390/jpm12030405.

Abstract

To meet current and expected future demand for genome sequencing in the neonatal intensive care unit (NICU), adjustments to traditional service delivery models are necessary. Effective programs for the training of non-genetics providers (NGPs) may address the known barriers to providing genetic services including limited genetics knowledge and lack of confidence. The SouthSeq project aims to use genome sequencing to make genomic diagnoses in the neonatal period and evaluate a scalable approach to delivering genome sequencing results to populations with limited access to genetics professionals. Thirty-three SouthSeq NGPs participated in a live, interactive training intervention and completed surveys before and after participation. Here, we describe the protocol for the provider training intervention utilized in the SouthSeq study and the associated impact on NGP knowledge and confidence in reviewing, interpreting, and using genome sequencing results. Participation in the live training intervention led to an increased level of confidence in critical skills needed for real-world implementation of genome sequencing. Providers reported a significant increase in confidence level in their ability to review, understand, and use genome sequencing result reports to guide patient care. Reported barriers to implementation of genome sequencing in a NICU setting included test cost, lack of insurance coverage, and turn around time. As implementation of genome sequencing in this setting progresses, effective education of NGPs is critical to provide access to high-quality and timely genomic medicine care.

摘要

为满足新生儿重症监护病房(NICU)当前及预期的未来基因组测序需求,有必要对传统服务提供模式进行调整。针对非遗传学专业人员(NGPs)的有效培训项目可能会解决提供遗传服务时已知的障碍,包括遗传学知识有限和缺乏信心等问题。SouthSeq项目旨在利用基因组测序在新生儿期进行基因组诊断,并评估一种可扩展的方法,将基因组测序结果提供给接触遗传学专业人员机会有限的人群。33名SouthSeq项目的非遗传学专业人员参与了一次现场互动培训干预,并在参与前后完成了调查。在此,我们描述了SouthSeq研究中使用的专业人员培训干预方案,以及对非遗传学专业人员在审查、解读和使用基因组测序结果方面的知识和信心的相关影响。参与现场培训干预使非遗传学专业人员在实际开展基因组测序所需的关键技能方面的信心水平有所提高。专业人员报告称,他们在审查、理解和使用基因组测序结果报告以指导患者护理方面的信心水平显著提高。在新生儿重症监护病房环境中实施基因组测序所报告的障碍包括检测成本、缺乏保险覆盖以及周转时间。随着在该环境中基因组测序的实施不断推进,对非遗传学专业人员进行有效的教育对于提供高质量和及时的基因组医学护理至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c19e/8949881/b97771c18d59/jpm-12-00405-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验