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Errors in Genetic Testing: The Fourth Case Series

机译:遗传测试中的错误:第四个案例系列

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Purpose In this ongoing national case series, we document 25 new genetic testing cases in which tests were recommended, ordered, interpreted, or used incorrectly. Methods An invitation to submit cases of adverse events in genetic testing was issued to the general National Society of Genetic Counselors Listserv, the National Society of Genetic Counselors Cancer Special Interest Group members, private genetic counselor laboratory groups, and via social media platforms (i.e., Facebook, Twitter, LinkedIn). Examples highlighted in the invitation included errors in ordering, counseling, and/or interpretation of genetic testing and did not limit submissions to cases involving genetic testing for hereditary cancer predisposition. Clinical documentation, including pedigree, was requested. Twenty-six cases were accepted, and a thematic analysis was performed. Submitters were asked to approve the representation of their cases before manuscript submission. Results All submitted cases took place in the United States and were from cancer, pediatric, preconception, and general adult settings and involved both medical-grade and direct-to-consumer genetic testing with raw data analysis. In 8 cases, providers ordered the wrong genetic test. In 2 cases, multiple errors were made when genetic testing was ordered. In 3 cases, patients received incorrect information from providers because genetic test results were misinterpreted or because of limitations in the provider's knowledge of genetics. In 3 cases, pathogenic genetic variants identified were incorrectly assumed to completely explain the suspicious family histories of cancer. In 2 cases, patients received inadequate or no information with respect to genetic test results. In 2 cases, result interpretation/documentation by the testing laboratories was erroneous. In 2 cases, genetic counselors reinterpreted the results of people who had undergone direct-to-consumer genetic testing and/or clarifying medical-grade testing was ordered. Discussion As genetic testing continues to become more common and complex, it is clear that we must ensure that appropriate testing is ordered and that results are interpreted and used correctly. Access to certified genetic counselors continues to be an issue for some because of workforce limitations. Potential solutions involve action on multiple fronts: new genetic counseling delivery models, expanding the genetic counseling workforce, improving genetics and genomics education of nongenetics health care professionals, addressing health care policy barriers, and more. Genetic counselors have also positioned themselves in new roles to help patients and consumers as well as health care providers, systems, and payers adapt to new genetic testing technologies and models. The work to be done is significant, but so are the consequences of errors in genetic testing.
机译:目的在这个正在进行的国家案例系列中,我们记录了25个新的遗传测试案例,其中建议,订购,解释或使用不正确的测试。方法对遗传检测遗传咨询师的一般国家遗传咨询师学会提交遗传检测中不良事件案件的邀请,全国遗传咨询师癌症特殊兴趣小组成员,私人遗传辅导员实验室组,以及通过社交媒体平台(即, Facebook,Twitter,LinkedIn)。邀请突出显示的例子包括有序,咨询和/或遗传检测解释中的错误,并没有限制涉及遗传性癌症易感性遗传检测的病例的提交。请求临床文献,包括血统。接受了二十六种病例,并进行主题分析。提交者被要求在手稿提交之前批准其案件的代表。结果所有提交的案例发生在美国,并来自癌症,儿科,先入型和一般成人设置,并涉及医疗级和直接消费的遗传测试,并进行原始数据分析。在8例中,提供商命令错误的遗传测试。在2例中,在命令遗传测试时,进行了多种错误。在3例之前,患者从提供者接收了不正确的信息,因为遗传测试结果被误解或因提供者的遗传知识中的局限性而受到误解。在3例中,鉴定的致病性遗传变异被错误地假设彻底解释了可疑的癌症家族历史。在2例中,患者因遗传测试结果而接受不足或无信息。在2例中,测试实验室的结果解释/文件是错误的。在2例中,遗传辅导员重新解释了经过直接消费者遗传检测的人的结果和/或澄清医疗级测试。随着遗传测试的讨论仍然变得更加普遍和复杂,很明显,我们必须确保订购适当的测试,结果被解释并正确使用。获得认证的遗传辅导员因劳动力限制而导致一些问题是一个问题。潜在的解决方案涉及对多个阵线的动作:新的遗传咨询交付模式,扩大遗传咨询劳动力,改善整个遗传学卫生保健专业人员的遗传和基因组学教育,解决医疗保健政策障碍等等。遗传辅导员还将自己定位在新的作用中,以帮助患者和消费者以及医疗保健提供者,系统和应款者适应新的遗传测试技术和模型。要做的工作是显着的,但遗传测试中错误的后果是重要的。

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