Genomic findings with familial implications: agenda setting in light of mainstreaming.

Open research Europe Pub Date : 2025-01-10 eCollection Date: 2025-01-01 DOI:10.12688/openreseurope.19128.1
Amicia Phillips, Eva Van Steijvoort, Maria Siermann, Janneke M L Kuiper, Álvaro Mendes, Sandrine de Montgolfier, Helle Vendel Petersen, Anna Rosén, Hilde Van Esch, Laurent Pasquier, Danya F Vears, Christine Patch, Wannes Van Hoof, Ainsley J Newson, Saskia Bulk, Carla van El, Eline Dancet, Emmanuelle Rial-Sebbag, Colin Mitchell, Pascal Borry
{"title":"Genomic findings with familial implications: agenda setting in light of mainstreaming.","authors":"Amicia Phillips, Eva Van Steijvoort, Maria Siermann, Janneke M L Kuiper, Álvaro Mendes, Sandrine de Montgolfier, Helle Vendel Petersen, Anna Rosén, Hilde Van Esch, Laurent Pasquier, Danya F Vears, Christine Patch, Wannes Van Hoof, Ainsley J Newson, Saskia Bulk, Carla van El, Eline Dancet, Emmanuelle Rial-Sebbag, Colin Mitchell, Pascal Borry","doi":"10.12688/openreseurope.19128.1","DOIUrl":null,"url":null,"abstract":"<p><p>An international workshop was held in Leuven, Belgium, on June 19-20, 2023, to discuss the communication of genetic risk information within families in the context of personalized prevention. Organized as part of the Horizon Europe project PROPHET (PeRsOnalised Prevention roadmap for the future HEalThcare in Europe), the event gathered interdisciplinary stakeholders to explore the benefits and challenges of various policy approaches for returning genetic test results with implications for family members. Five key themes emerged from the discussions: (1) recognizing family communication as an ongoing process, (2) adopting a family-centered approach rather than an individual one, (3) clarifying roles and responsibilities in the communication process, (4) addressing the lack of clear guidelines and policies, and (5) ensuring sufficient resources. To enhance family communication of genetic risk information, participants emphasized the importance of improving pre-test counseling and follow-up procedures, implementing policies to clarify roles and responsibilities, and providing training for healthcare professionals both within and outside genetic services.</p>","PeriodicalId":74359,"journal":{"name":"Open research Europe","volume":"5 ","pages":"4"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11982804/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Open research Europe","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12688/openreseurope.19128.1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

An international workshop was held in Leuven, Belgium, on June 19-20, 2023, to discuss the communication of genetic risk information within families in the context of personalized prevention. Organized as part of the Horizon Europe project PROPHET (PeRsOnalised Prevention roadmap for the future HEalThcare in Europe), the event gathered interdisciplinary stakeholders to explore the benefits and challenges of various policy approaches for returning genetic test results with implications for family members. Five key themes emerged from the discussions: (1) recognizing family communication as an ongoing process, (2) adopting a family-centered approach rather than an individual one, (3) clarifying roles and responsibilities in the communication process, (4) addressing the lack of clear guidelines and policies, and (5) ensuring sufficient resources. To enhance family communication of genetic risk information, participants emphasized the importance of improving pre-test counseling and follow-up procedures, implementing policies to clarify roles and responsibilities, and providing training for healthcare professionals both within and outside genetic services.

具有家族意义的基因组研究结果:主流化的议程设置。
2023年6月19日至20日在比利时鲁汶举行了一次国际研讨会,讨论了在个性化预防背景下家庭内遗传风险信息的交流。作为Horizon Europe项目PROPHET(欧洲未来医疗保健个性化预防路线图)的一部分,该活动聚集了跨学科的利益相关者,探讨各种政策方法的好处和挑战,以返回对家庭成员的影响的基因检测结果。讨论中出现了五个关键主题:(1)认识到家庭沟通是一个持续的过程;(2)采用以家庭为中心而不是以个人为中心的方法;(3)澄清沟通过程中的角色和责任;(4)解决缺乏明确指导方针和政策的问题;(5)确保足够的资源。为了加强遗传风险信息的家庭沟通,与会者强调了改进检测前咨询和后续程序、实施明确角色和责任的政策以及为遗传服务机构内外的卫生保健专业人员提供培训的重要性。
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 求助全文
来源期刊
CiteScore
1.50
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信