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Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network

机译:了解基因组测序结果的返回过程:Emerge Research网络中参与者摘要信件的内容审查

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摘要

A challenge in returning genomic test results to research participants is how best to communicate complex and clinically nuanced findings to participants in a manner that is scalable to the large numbers of participants enrolled. The purpose of this study was to examine the features of genetic results letters produced at each Electronic Medical Records and Genomics (eMERGE3) Network site to assess their readability and content. Letters were collected from each site, and a qualitative analysis of letter content and a quantitative analysis of readability statistics were performed. Because letters were produced independently at each eMERGE site, significant heterogeneity in readability and content was found. The content of letters varied widely from a baseline of notifying participants that results existed to more detailed information about positive or negative results, as well as materials for sharing with family members. Most letters were significantly above the Centers for Disease Control-suggested reading level for health communication. While continued effort should be applied to make letters easier to understand, the ongoing challenge of explaining complex genomic information, the implications of negative test results, and the uncertainty that comes with some types of test and result makes simplifying letter text challenging.
机译:回归研究参与者的基因组测试结果的挑战是如何最好地以可扩展为大量参与者的参与者对参与者沟通复杂和临床细分的调查结果。本研究的目的是检查每个电子医疗记录和基因组学(EMERGE3)网站生产的遗传结果字母的特征,以评估其可读性和内容。从每个站点收集信件,并进行了对字母内容的定性分析和可读性统计数据的定量分析。因为在每个出现的网站上独立生产字母,发现了可读性和内容的显着异质性。信件内容从通知参与者的结果存在约正或负的成绩,以及为家庭成员共享材料的更多详细信息的基线相差很大。大多数信件明显高于疾病控制建议的健康沟通的阅读水平的中心。虽然继续努力,使信件更容易理解,持续的挑战,解释复杂的基因组信息,负面测试结果的影响以及某些类型的测试和结果具有的不确定性使得简化信文本挑战。

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