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遗传咨询中的风险沟通:探索复发数量的接受度和感知,以及它们对患者结局的影响。

Risk communication in genetic counseling: Exploring uptake and perception of recurrence numbers, and their impact on patient outcomes.

机构信息

Department of Medical Genetics, University of British Columbia, Vancouver, Canada.

Department of Psychiatry, University of British Columbia, Vancouver, Canada.

出版信息

Clin Genet. 2018 Aug;94(2):239-245. doi: 10.1111/cge.13379. Epub 2018 Jun 12.

DOI:10.1111/cge.13379
PMID:29766486
Abstract

Providing recurrence numbers is often considered a fundamental component of genetic counseling. We sought to fill knowledge gaps regarding how often patients actively seek recurrence numbers, and how they impact patient outcomes. We conducted a retrospective chart review at a clinic where patients routinely complete the Genetic Counseling Outcomes Scale (GCOS, measuring empowerment) pre (T1)/post (T2) appointment. Using analysis of covariance, we evaluated the effect on T2 GCOS score of: (1) receiving recurrence numbers and (2) patient perception of recurrence numbers. Recurrence numbers were a primary indication for 134/300 patients (45%). After counseling about etiology and risk-reducing strategies, 116 patients (39%) opted to receive recurrence numbers, with most (n = 64, 55%) perceiving the number to be lower than expected. There was no difference in T2 GCOS scores between those who: (1) received recurrence numbers vs those who did not, or (2) perceived the number to be lower than expected vs those with other perceptions. However, a subset of patients who did not receive recurrence numbers had larger increases in GCOS scores. Our data provide impetus to question the assumption that recurrence numbers should be routinely provided in genetic counseling, and show that in naturalistic practice, optimal patient outcomes are not contingent on receipt of recurrence numbers.

摘要

提供复发率数据通常被认为是遗传咨询的一个基本组成部分。我们试图填补关于患者主动寻求复发率的频率以及它们如何影响患者结局的知识空白。我们在一家诊所进行了回顾性图表审查,在那里患者通常在预约前(T1)/后(T2)完成遗传咨询结局量表(GCOS,衡量赋权)。我们使用协方差分析,评估了以下因素对 T2 GCOS 评分的影响:(1)获得复发率数据,以及(2)患者对复发率数据的感知。复发率数据是 300 名患者中的 134 名(45%)的主要指征。在对病因和降低风险策略进行咨询后,116 名患者(39%)选择获得复发率数据,其中大多数(n=64,55%)认为该数字低于预期。那些:(1)获得复发率数据与未获得复发率数据的患者,或(2)认为数字低于预期与其他感知的患者,在 T2 GCOS 评分上没有差异。然而,一组未获得复发率数据的患者的 GCOS 评分增加幅度更大。我们的数据为质疑遗传咨询中应常规提供复发率数据的假设提供了动力,并表明在自然实践中,最佳患者结局并不取决于获得复发率数据。

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