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具有不一致分类的基因变异:对遗传咨询师态度和实践的评估。

Genetic variants with discordant classifications: An assessment of genetic counselor attitudes and practices.

作者信息

Lahiri Sayoni, Reys Brian, Wunder Julia, Pirzadeh-Miller Sara

机构信息

Cancer Genetics Program, UT Southwestern Medical Center, Dallas, Texas, USA.

Oncology-Abstraction, Tempus Labs, Inc., Chicago, Illinois, USA.

出版信息

J Genet Couns. 2023 Feb;32(1):100-110. doi: 10.1002/jgc4.1626. Epub 2022 Aug 17.

Abstract

Discordant variant classifications (DVCs) can impact patient care and pose challenges for clinicians. A survey-based study was conducted to examine genetic counselor (GC) attitudes and practices related to DVCs. Most GCs (202/229, 88%) in the study provide direct patient care across clinical specialties; review patients' genetic test results to determine if reported genetic variants have DVCs (176/202, 88%); and inform patients of known DVCs that impact medical management (165/202, 82%). DVC review, which takes 41 min (range: 5-240) on average per week, is typically prompted by the identification of a variant of uncertain significance (VUS) (160/176, 90%) and is primarily conducted using public databases (176/176, 100%). While most GCs felt it would not be ethical to knowingly provide different medical management recommendations to patients with the same genetic variant (152/229, 66%), they also stated they would rely on the variant classification on the test report (141/229, 61%) and/or the patient's personal/family history (188/229, 82%) to determine which classification to follow if a DVC is identified. Both factors are patient-specific and, inherently, could lead to differing recommendations. When posed with a hypothetical scenario in which two patients have the same genetic variant, but test reports show a DVC (pathogenic vs VUS), most GCs (179/229, 78.2%) stated they would make the same recommendation for both patients regardless of management guidelines. One-third (52/179, 29.1%) cited patient-specific factors, such as personal/family history, would impact their recommendations. Disagreements about whether the pathogenic or VUS classification should be used to make medical management recommendations were noted. Differing practices and opinions on how to manage patients with DVCs, as well as the fact that most GCs (209/229, 91.3%) have consulted with colleagues on this matter, highlight the need for more professional guidance to ensure equitable patient care.

摘要

不一致的变异分类(DVCs)会影响患者护理,并给临床医生带来挑战。开展了一项基于调查的研究,以检查遗传咨询师(GC)与DVCs相关的态度和做法。该研究中的大多数遗传咨询师(229名中的202名,88%)跨临床专科直接为患者提供护理;审查患者的基因检测结果,以确定报告的基因变异是否存在DVCs(202名中的176名,88%);并告知患者影响医疗管理的已知DVCs(202名中的165名,82%)。DVC审查平均每周需要41分钟(范围:5 - 240分钟),通常是由发现意义不确定的变异(VUS)引发的(176名中的160名,90%),并且主要使用公共数据库进行(176名中的176名,100%)。虽然大多数遗传咨询师认为,明知为具有相同基因变异的患者提供不同的医疗管理建议是不符合伦理道德的(229名中的152名,66%),但他们也表示会依赖检测报告上的变异分类(229名中的141名,61%)和/或患者的个人/家族病史(229名中的188名,82%)来确定如果识别出DVC应遵循哪种分类。这两个因素都是针对患者的,本质上可能导致不同的建议。当面对一个假设情景,即两名患者具有相同的基因变异,但检测报告显示存在DVC(致病与VUS)时,大多数遗传咨询师(229名中的179名,78.2%)表示,无论管理指南如何,他们会对两名患者给出相同的建议。三分之一(179名中的52名,29.1%)提到患者特异性因素,如个人/家族病史,会影响他们的建议。关于应使用致病还是VUS分类来做出医疗管理建议存在分歧。对于如何管理患有DVC的患者存在不同的做法和意见,而且大多数遗传咨询师(229名中的209名,91.3%)就此事咨询过同事,这凸显了需要更多专业指导以确保公平的患者护理。

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