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新型基因检测模式:遗传咨询师与肾病学的合作

Novel genetic testing model: A collaboration between genetic counselors and nephrology.

机构信息

Precision Medicine/Genetic Testing Stewardship Program, Nemours A.I. duPont Hospital for Children Precision Medicine/Genetic Testing Stewardship Program, Wilmington, Delaware, USA.

Division of Nephrology, Nemours A.I. duPont Hospital for Children, Wilmington, Delaware, USA.

出版信息

Am J Med Genet A. 2021 Apr;185(4):1142-1150. doi: 10.1002/ajmg.a.62088. Epub 2021 Jan 21.

Abstract

Many barriers to genetic testing currently exist which delay or prevent diagnosis. These barriers include wait times, staffing, education, and cost. Specialists are able to identify patients with disease that may need genetic testing, but lack the genetics support to facilitate that testing in the most cost, time, and medically effective manner. The Nephrology Division and the Genetic Testing Stewardship Program at Nemours A.I. duPont Hospital for Children created a novel service delivery model in which nephrologists and genetic counselors collaborate in order to highlight their complementary strengths (clinical expertise of nephrologists and genetics and counseling skills of genetic counselors). This collaboration has reduced many barriers to care for our patients. This workflow facilitated the offering of genetic testing to 76 patients, with 86 tests completed over a 20-month period. Thirty-two tests were deferred. Twenty-seven patients received a diagnosis, which lead to a change in their medical management, three of whom were diagnosed by cascade family testing. Forty-two patients had a negative result and 16 patients had one or more variants of uncertain significance on testing. The inclusion of genetic counselors in the workflow is integral toward choosing the most cost and time effective genetic testing strategy, as well as providing psychosocial support to families. The genetic counselors obtain informed consent, and review genetic test results and recommendations with the patient and their family. The availability of this program to our patients increased access to genetic testing and helps to provide diagnoses and supportive care.

摘要

目前存在许多阻碍基因检测的因素,这些因素会导致诊断延迟或无法进行。这些障碍包括等待时间、人员配备、教育和成本。专家能够识别可能需要基因检测的疾病患者,但缺乏基因支持,无法以最具成本效益、最节省时间和最有效的方式进行检测。Nemours A.I. duPont 儿童医院肾脏病科和基因检测管理计划创建了一种新颖的服务交付模式,其中肾脏病专家和遗传咨询师合作,以突出他们互补的优势(肾脏病专家的临床专业知识以及遗传咨询师的遗传和咨询技能)。这种合作减少了许多患者的护理障碍。该工作流程为 76 名患者提供了基因检测服务,在 20 个月的时间内完成了 86 次检测。其中 32 次被推迟。27 名患者得到了诊断,这导致他们的医疗管理发生了变化,其中 3 名患者通过级联家族检测得到了诊断。42 名患者的检测结果为阴性,16 名患者的检测结果有一个或多个意义未明的变异。遗传咨询师参与工作流程对于选择最具成本效益和时间效益的基因检测策略以及为家庭提供心理社会支持至关重要。遗传咨询师会获得知情同意,并与患者及其家属一起审查基因检测结果和建议。为我们的患者提供该计划增加了获得基因检测的机会,并有助于提供诊断和支持性护理。

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