Radecki Myka, Halverson Colin, Wetherill Leah, Miller Mandy
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Cancer Center, Franciscan Health, Indianapolis, Indiana, USA.
J Genet Couns. 2025 Apr;34(2):e1971. doi: 10.1002/jgc4.1971. Epub 2024 Sep 13.
One of the roles of a genetic counselor, when returning genetic test results for Parkinson's disease (PD), is to provide emotional support to the patient. However, whether or not these needs are being met in the genetic counseling setting is unknown. In this cross-sectional qualitative study, semi-structured interviews with 15 PD research participants were conducted to evaluate their emotional needs and expectations throughout the genetic counseling process. Interview questions assessed participants' background understanding of genetic counseling, informational and emotional expectations prior to the genetic counseling session, and experience with emotional support throughout the genetic counseling process. Through reflexive thematic analysis, we defined four major themes: (1) knowledge of genetic counselors' role in education but not in emotional support, (2) limited expectations for emotional support, (3) emotional support is not sought from genetic counselors, and (4) emotional support from genetic counselors was viewed ambivalently. One of the most important findings from this study was that regardless of whether participants had previously heard of genetic counseling, none of the participants knew that the provision of emotional support was an aspect of the genetic counselor's role. Although the majority of participants did not expect emotional support from their genetic counselor, over 60% of participants recognized that receiving emotional support is or could be important to them. Collectively, these findings highlight the necessity for enhanced patient education pertaining to the informational and emotional support that genetic counselors are trained to provide. We suggest that clarifying the role of emotional support with patients may increase comfort in disclosing their emotional needs with genetic counselors, improving patient-centered care overall.
基因咨询师在反馈帕金森病(PD)基因检测结果时的其中一项职责,是为患者提供情感支持。然而,在基因咨询过程中这些需求是否得到满足尚不清楚。在这项横断面定性研究中,我们对15名PD研究参与者进行了半结构化访谈,以评估他们在整个基因咨询过程中的情感需求和期望。访谈问题评估了参与者对基因咨询的背景了解、基因咨询 session 之前的信息和情感期望,以及在整个基因咨询过程中获得情感支持的经历。通过反思性主题分析,我们确定了四个主要主题:(1)了解基因咨询师在教育方面的作用,但不了解在情感支持方面的作用;(2)对情感支持的期望有限;(3)不向基因咨询师寻求情感支持;(4)对基因咨询师的情感支持看法矛盾。这项研究最重要的发现之一是,无论参与者之前是否听说过基因咨询,没有一个参与者知道提供情感支持是基因咨询师职责的一个方面。虽然大多数参与者不期望从他们的基因咨询师那里获得情感支持,但超过60%的参与者认识到获得情感支持对他们来说是或可能是重要的。总体而言,这些发现凸显了加强患者教育的必要性,内容涉及基因咨询师接受培训后所提供的信息和情感支持。我们建议,向患者阐明情感支持的作用可能会增加他们向基因咨询师披露情感需求时的舒适度,从而总体上改善以患者为中心的护理。