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对未确诊疾病的成年患者及其对外显子组测序产生的未解决不确定性的反应。

Adult patients with undiagnosed conditions and their responses to unresolved uncertainty from exome sequencing.

机构信息

Department of Health, Behavior, & Society, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.

Medical Genomics & Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.

出版信息

J Genet Couns. 2020 Dec;29(6):992-1003. doi: 10.1002/jgc4.1223. Epub 2020 Feb 6.

Abstract

Patients pursuing exome sequencing (ES) in their quest for diagnosis will most often experience unresolved uncertainty from their ES results because the majority of ES results are non-diagnostic. This study explored and compared the experiences of receiving two types of ES results that may result in diagnostic uncertainty. Semi-structured phone interviews were conducted with 23 adult patients with undiagnosed conditions who received either a negative result or a result with one or more variants of uncertain significance (VUSs) from ES. Interviews were transcribed and subjected to thematic and comparative analyses. Participants accurately understood their results and described various sources of genomic uncertainty including probability, complexity, and ambiguity. Their acclimation to illness uncertainty resulted in realistic expectations about and acceptance of their results. Participants still hoped that ES would end their diagnostic odyssey. Hope and optimism were used to cope with continued uncertainty. No thematic differences were found between the experiences of those who received negative results versus those who received VUSs. Our findings may inform clinical practices of informed consent and disclosure of negative results and VUSs through a greater consideration of patients' reactions, concerns, and challenges with adaptation to uncertainty.

摘要

患者在寻求诊断时进行外显子组测序(ES),他们的 ES 结果通常会带来无法解决的不确定性,因为大多数 ES 结果是无诊断意义的。本研究探讨并比较了两种可能导致诊断不确定性的 ES 结果的体验。对 23 名患有未确诊疾病的成年患者进行了半结构化电话访谈,他们的 ES 结果要么是阴性的,要么是有一个或多个意义不确定的变异(VUS)。对访谈进行了转录,并进行了主题和比较分析。参与者准确地理解了他们的结果,并描述了各种来源的基因组不确定性,包括概率、复杂性和模糊性。他们对疾病不确定性的适应导致他们对结果有了现实的期望和接受。参与者仍然希望 ES 能够结束他们的诊断之旅。希望和乐观被用来应对持续的不确定性。对于那些接受阴性结果和 VUS 的患者,其经历没有发现主题上的差异。我们的研究结果可能会通过更多地考虑患者对不确定性的反应、关注和适应挑战,为知情同意和阴性结果及 VUS 的披露提供临床实践依据。

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