Patient perceptions of genetic counselors' role and emotional support needs in adults with Parkinson's disease

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY Journal of Genetic Counseling Pub Date : 2024-09-13 DOI:10.1002/jgc4.1971
Myka Radecki, Colin Halverson, Leah Wetherill, Mandy Miller
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Abstract

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.
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帕金森病成人患者对遗传咨询师作用和情感支持需求的看法
在返回帕金森病(PD)基因检测结果时,遗传咨询师的职责之一是为患者提供情感支持。然而,这些需求在遗传咨询过程中是否得到了满足还不得而知。在这项横断面定性研究中,我们对 15 名帕金森病研究参与者进行了半结构式访谈,以评估他们在整个遗传咨询过程中的情感需求和期望。访谈问题评估了参与者对遗传咨询的背景了解、遗传咨询前的信息和情感期望,以及在整个遗传咨询过程中获得情感支持的经历。通过反思性主题分析,我们确定了四大主题:(1)了解遗传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)不寻求遗传咨询师的情感支持;(4)对遗传咨询师的情感支持持矛盾态度。本研究最重要的发现之一是,无论参与者以前是否听说过遗传咨询,都不知道提供情感支持是遗传咨询师的职责之一。尽管大多数参与者并不期望从遗传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很重要或可能很重要。总之,这些发现突出表明,有必要加强与遗传咨询师受训提供的信息和情感支持有关的患者教育。我们建议,向患者阐明情感支持的作用可提高他们向遗传咨询师透露情感需求的舒适度,从而全面改善以患者为中心的医疗服务。
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来源期刊
Journal of Genetic Counseling
Journal of Genetic Counseling GENETICS & HEREDITY-
CiteScore
3.80
自引率
26.30%
发文量
113
审稿时长
6 months
期刊介绍: The Journal of Genetic Counseling (JOGC), published for the National Society of Genetic Counselors, is a timely, international forum addressing all aspects of the discipline and practice of genetic counseling. The journal focuses on the critical questions and problems that arise at the interface between rapidly advancing technological developments and the concerns of individuals and communities at genetic risk. The publication provides genetic counselors, other clinicians and health educators, laboratory geneticists, bioethicists, legal scholars, social scientists, and other researchers with a premier resource on genetic counseling topics in national, international, and cross-national contexts.
期刊最新文献
The current landscape of clinical exome and genome reanalysis in the U.S. A cross-sectional survey-based exploration of diversity in the admissions committees and student cohorts of genetic counseling programs over time. An analysis of direct-to-consumer genetic testing portals and their communication of health risk and test limitations. Patient perceptions of genetic counselors' role and emotional support needs in adults with Parkinson's disease Clinical genetic counselors' use of people‐ and identity‐first language in regard to patients' identification with disability
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