A national education program for rapid genomics in pediatric acute care: Building workforce confidence, competence, and capability

IF 6.6 1区 医学 Q1 GENETICS & HEREDITY Genetics in Medicine Pub Date : 2024-07-30 DOI:10.1016/j.gim.2024.101224
Giulia McCorkell , Amy Nisselle , Donna Halton , Sophie E. Bouffler , Chirag Patel , John Christodoulou , Fran Maher , Belinda McClaren , Gemma R. Brett , Sarah Sandaradura , Kirsten Boggs , Michelle G. de Silva , Fiona Lynch , Ivan Macciocca , Elly Lynch , Melissa Martyn , Stephanie Best , Zornitza Stark , Clara L. Gaff
{"title":"A national education program for rapid genomics in pediatric acute care: Building workforce confidence, competence, and capability","authors":"Giulia McCorkell ,&nbsp;Amy Nisselle ,&nbsp;Donna Halton ,&nbsp;Sophie E. Bouffler ,&nbsp;Chirag Patel ,&nbsp;John Christodoulou ,&nbsp;Fran Maher ,&nbsp;Belinda McClaren ,&nbsp;Gemma R. Brett ,&nbsp;Sarah Sandaradura ,&nbsp;Kirsten Boggs ,&nbsp;Michelle G. de Silva ,&nbsp;Fiona Lynch ,&nbsp;Ivan Macciocca ,&nbsp;Elly Lynch ,&nbsp;Melissa Martyn ,&nbsp;Stephanie Best ,&nbsp;Zornitza Stark ,&nbsp;Clara L. Gaff","doi":"10.1016/j.gim.2024.101224","DOIUrl":null,"url":null,"abstract":"<div><h3>Purpose</h3><p>To develop and evaluate a scalable national program to build confidence, competence and capability in the use of rapid genomic testing (rGT) in the acute pediatric setting.</p></div><div><h3>Methods</h3><p>We used theory-informed approaches to design a modular, adaptive program of blended learning aimed at diverse professional groups involved in acute pediatric care. The program comprised 4 online learning modules and an online workshop and was centered on case-based learning. We evaluated the program using the Kirkpatrick 4-level model of training evaluation and report our findings using the Reporting Item Standards for Education and its Evaluation (RISE2) guidelines for genomics education and evaluation.</p></div><div><h3>Results</h3><p>Two hundred and two participants engaged with at least 1 component of the program. Participants self-reported increased confidence in using rGT, (<em>P</em> &lt; .001), and quiz responses objectively demonstrated increased competence (eg, correct responses to a question on pretest counseling increased from 30% to 64%; <em>P</em> &lt; .001). Additionally, their capability in applying genomic principles to simulated clinical cases increased (<em>P</em> &lt; .001), as did their desire to take on more responsibility for performing rGT. The clinical interpretation of more complex test results (such as negative results or variants of uncertain significance) appeared to be more challenging, indicating a need for targeted education in this area.</p></div><div><h3>Conclusion</h3><p>The program format was effective in delivering multidisciplinary and wide-scale genomics education in the acute care context. The modular approach we have developed now lends itself to application in other medical specialties or areas of health care.</p></div>","PeriodicalId":12717,"journal":{"name":"Genetics in Medicine","volume":"26 10","pages":"Article 101224"},"PeriodicalIF":6.6000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1098360024001588/pdfft?md5=3c682c51178587789cb8652060325281&pid=1-s2.0-S1098360024001588-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genetics in Medicine","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1098360024001588","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose

To develop and evaluate a scalable national program to build confidence, competence and capability in the use of rapid genomic testing (rGT) in the acute pediatric setting.

Methods

We used theory-informed approaches to design a modular, adaptive program of blended learning aimed at diverse professional groups involved in acute pediatric care. The program comprised 4 online learning modules and an online workshop and was centered on case-based learning. We evaluated the program using the Kirkpatrick 4-level model of training evaluation and report our findings using the Reporting Item Standards for Education and its Evaluation (RISE2) guidelines for genomics education and evaluation.

Results

Two hundred and two participants engaged with at least 1 component of the program. Participants self-reported increased confidence in using rGT, (P < .001), and quiz responses objectively demonstrated increased competence (eg, correct responses to a question on pretest counseling increased from 30% to 64%; P < .001). Additionally, their capability in applying genomic principles to simulated clinical cases increased (P < .001), as did their desire to take on more responsibility for performing rGT. The clinical interpretation of more complex test results (such as negative results or variants of uncertain significance) appeared to be more challenging, indicating a need for targeted education in this area.

Conclusion

The program format was effective in delivering multidisciplinary and wide-scale genomics education in the acute care context. The modular approach we have developed now lends itself to application in other medical specialties or areas of health care.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
儿科急症护理中的快速基因组学国家教育计划:培养工作人员的信心、能力和才干。
目的:制定并评估一项可扩展的全国性计划,以建立在急诊儿科环境中使用快速基因组检测的信心、能力和实力:方法:我们采用理论指导的方法,设计了一个模块化、适应性强的混合学习项目,面向参与急诊儿科护理的不同专业群体。该项目包括四个在线学习模块和一个在线研讨会,以案例学习为中心。我们使用柯克帕特里克四级培训评估模型对该项目进行了评估,并使用 RISE2 基因组学教育和评估指南报告了我们的评估结果:结果:22 名参与者至少参与了项目的一个部分。参加者自我报告说对使用 rGT 的信心增强了,(p 结论:该计划的形式有效地提供了多种基因组学知识:在急症护理领域开展多学科、大范围的基因组学教育,该项目形式非常有效。我们开发的模块化方法现在可以应用于其他医学专业或医疗保健领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Genetics in Medicine
Genetics in Medicine 医学-遗传学
CiteScore
15.20
自引率
6.80%
发文量
857
审稿时长
1.3 weeks
期刊介绍: Genetics in Medicine (GIM) is the official journal of the American College of Medical Genetics and Genomics. The journal''s mission is to enhance the knowledge, understanding, and practice of medical genetics and genomics through publications in clinical and laboratory genetics and genomics, including ethical, legal, and social issues as well as public health. GIM encourages research that combats racism, includes diverse populations and is written by authors from diverse and underrepresented backgrounds.
期刊最新文献
Pathogenicity assessment of genetic variants identified in patients with severe hypertriglyceridemia: novel cases of Familial Chylomicronemia Syndrome from the Dyslipidemia Registry of the Spanish Atherosclerosis Society. Genomic sequencing in diverse and underserved pediatric populations: parent perspectives on understanding, uncertainty, psychosocial impact, and personal utility of results. Newborn screening for common genetic variants associated with permanent hearing loss: Implementation in Ontario and a review of the first 3 years. Longitudinal Outcomes in Noonan Syndrome. The impact of genetic counselor involvement in genetic and genomic test order review: A scoping review.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1