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受检者在接受扩展性携带者筛查结果为阴性后的反应及行为。

Patient actions and reactions after receiving negative results from expanded carrier screening.

机构信息

Treuman Katz Center for Pediatric Bioethics, Seattle Children's Hospital and Research Institute, Seattle, Washington.

Division of Bioethics, Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington.

出版信息

Clin Genet. 2018 May;93(5):962-971. doi: 10.1111/cge.13206. Epub 2018 Mar 13.

Abstract

With the expansion of carrier screening to general preconception and prenatal patient populations, most patients will receive negative results, which we define as indicating <25% risk of having a child with a genetic condition. Because there is limited experience with expanded carrier screening, it is important to understand how receiving negative results affects patients, especially as providers, payers, and policymakers consider whether to offer it. In this mixed-methods study, we asked preconception patients enrolled in the NextGen study about their expectations and experiences receiving negative expanded carrier screening results. Participants completed surveys at study enrollment (n = 110 women, 51 male partners), after receiving carrier results (n = 100 women, 38 male partners), after receiving secondary findings (n = 98 women, 36 male partners), and 6 months after receiving results (n = 95 women, 28 male partners). We also interviewed a subset of participants 12 to 24 months after receiving results (n = 24 women, 12 male partners). We found minimal negative emotional impact and privacy concerns, increased confidence in reproductive plans, and few changes to health behaviors, although some patients made health decisions based on misunderstandings of their results. These findings suggest that expanded carrier screening causes minimal psychosocial harms, but systems are needed to reduce the risk of misinterpreting results.

摘要

随着携带者筛查向一般孕前和产前患者人群的扩展,大多数患者将得到阴性结果,我们将其定义为表明生育携带遗传疾病孩子的风险<25%。由于对扩展携带者筛查的经验有限,了解接受阴性结果如何影响患者,特别是在提供者、支付者和政策制定者考虑是否提供它时,这一点很重要。在这项混合方法研究中,我们询问了参加 NextGen 研究的孕前患者对他们接受阴性扩展携带者筛查结果的期望和经验。参与者在研究入组时(n=110 名女性,51 名男性伴侣)、收到携带者结果后(n=100 名女性,38 名男性伴侣)、收到次要发现结果后(n=98 名女性,36 名男性伴侣)以及收到结果后 6 个月时(n=95 名女性,28 名男性伴侣)完成了调查。我们还在收到结果后 12 至 24 个月对部分参与者进行了访谈(n=24 名女性,12 名男性伴侣)。我们发现,负面情绪影响和隐私问题极小,对生殖计划的信心增强,尽管一些患者基于对结果的误解做出了健康决定,但健康行为几乎没有改变。这些发现表明,扩展携带者筛查几乎不会造成心理社会伤害,但需要建立系统来降低误解结果的风险。

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