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2
Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of Results.电子病历和基因组学网络中的家族性高胆固醇血症:患病率、外显率、心血管风险以及结果回报后的结局。
Circ Genom Precis Med. 2023 Apr;16(2):e003816. doi: 10.1161/CIRCGEN.122.003816. Epub 2023 Feb 22.
3
Interpreting Incidentally Identified Variants in Genes Associated With Heritable Cardiovascular Disease: A Scientific Statement From the American Heart Association.偶然发现与遗传性心血管疾病相关基因中的变异的解读:美国心脏协会的科学声明。
Circ Genom Precis Med. 2023 Apr;16(2):e000092. doi: 10.1161/HCG.0000000000000092. Epub 2023 Mar 27.
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Returning integrated genomic risk and clinical recommendations: The eMERGE study.返回整合基因组风险和临床建议:eMERGE 研究。
Genet Med. 2023 Apr;25(4):100006. doi: 10.1016/j.gim.2023.100006. Epub 2023 Jan 6.
5
Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research.儿科研究中返回具有医学可操作性基因组结果的结局。
J Pers Med. 2022 Nov 16;12(11):1910. doi: 10.3390/jpm12111910.
6
The Research Program: Data quality, utility, and diversity.研究计划:数据质量、效用和多样性。
Patterns (N Y). 2022 Aug 12;3(8):100570. doi: 10.1016/j.patter.2022.100570.
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The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.核算:向 eMERGE3 网络的 1444 名参与者返还基因组学结果。
Genet Med. 2022 May;24(5):1130-1138. doi: 10.1016/j.gim.2022.01.015. Epub 2022 Feb 23.
9
Lessons learned from the eMERGE Network: balancing genomics in discovery and practice.从eMERGE网络中吸取的经验教训:在发现与实践中平衡基因组学。
HGG Adv. 2020 Dec 25;2(1):100018. doi: 10.1016/j.xhgg.2020.100018. eCollection 2021 Jan 14.
10
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.eMERGE-III 测序研究中的心律失常变异体关联和重新分类。
Circulation. 2022 Mar 22;145(12):877-891. doi: 10.1161/CIRCULATIONAHA.121.055562. Epub 2021 Dec 21.

从临床测序中获得有明确临床意义的单基因检测结果后的医疗保健利用的前瞻性、多中心研究。

Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.

机构信息

Vanderbilt University Medical Center, Nashville, TN 37203, USA.

Vanderbilt University Medical Center, Nashville, TN 37203, USA.

出版信息

Am J Hum Genet. 2023 Nov 2;110(11):1950-1958. doi: 10.1016/j.ajhg.2023.10.006. Epub 2023 Oct 25.

DOI:10.1016/j.ajhg.2023.10.006
PMID:37883979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10645563/
Abstract

As large-scale genomic screening becomes increasingly prevalent, understanding the influence of actionable results on healthcare utilization is key to estimating the potential long-term clinical impact. The eMERGE network sequenced individuals for actionable genes in multiple genetic conditions and returned results to individuals, providers, and the electronic health record. Differences in recommended health services (laboratory, imaging, and procedural testing) delivered within 12 months of return were compared among individuals with pathogenic or likely pathogenic (P/LP) findings to matched individuals with negative findings before and after return of results. Of 16,218 adults, 477 unselected individuals were found to have a monogenic risk for arrhythmia (n = 95), breast cancer (n = 96), cardiomyopathy (n = 95), colorectal cancer (n = 105), or familial hypercholesterolemia (n = 86). Individuals with P/LP results more frequently received services after return (43.8%) compared to before return (25.6%) of results and compared to individuals with negative findings (24.9%; p < 0.0001). The annual cost of qualifying healthcare services increased from an average of $162 before return to $343 after return of results among the P/LP group (p < 0.0001); differences in the negative group were non-significant. The mean difference-in-differences was $149 (p < 0.0001), which describes the increased cost within the P/LP group corrected for cost changes in the negative group. When stratified by individual conditions, significant cost differences were observed for arrhythmia, breast cancer, and cardiomyopathy. In conclusion, less than half of individuals received billed health services after monogenic return, which modestly increased healthcare costs for payors in the year following return.

摘要

随着大规模基因组筛查的日益普及,了解可操作结果对医疗保健利用的影响对于估计潜在的长期临床影响至关重要。eMERGE 网络对多个遗传条件下的可操作基因个体进行测序,并将结果返回给个体、提供者和电子健康记录。在返回结果前后,将具有致病性或可能致病性 (P/LP) 发现的个体与具有阴性发现的匹配个体之间,在返回结果后 12 个月内提供的推荐健康服务(实验室、影像和程序检测)的差异进行了比较。在 16218 名成年人中,有 477 名未选择的个体患有心律失常(n=95)、乳腺癌(n=96)、心肌病(n=95)、结直肠癌(n=105)或家族性高胆固醇血症(n=86)的单基因风险。与返回结果之前(25.6%)相比,具有 P/LP 结果的个体在返回结果后(43.8%)更频繁地接受服务,与具有阴性结果的个体相比(24.9%;p<0.0001)。在 P/LP 组中,从返回结果前的平均每年 162 美元增加到返回结果后的 343 美元(p<0.0001);阴性组的差异无统计学意义。差异的平均差异为 149 美元(p<0.0001),这描述了 P/LP 组内由于阴性组成本变化而校正的增加成本。按个体疾病分层时,心律失常、乳腺癌和心肌病的成本差异显著。总之,不到一半的个体在单基因检测后接受了计费的健康服务,这在返回后的一年中适度增加了支付者的医疗保健成本。