首页> 外文期刊>European journal of human genetics: EJHG >Experiences, considerations and emotions relating to cardiogenetic evaluation in relatives of young sudden cardiac death victims
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Experiences, considerations and emotions relating to cardiogenetic evaluation in relatives of young sudden cardiac death victims

机译:年轻的突发性心脏病死亡受害者亲属中与心源性评估有关的经验,考虑和情感

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Relatives of young sudden cardiac death (SCD) victims are at increased risk of carrying a potentially fatal inherited cardiac disease. Hence, it is recommended to perform an autopsy on the victim and to refer his or her relatives to a cardiogenetics clinic for a full evaluation to identify those at risk and allow preventive measures to be taken. However, at present, the number of families attending a cardiogenetics clinic after the SCD of a young relative is low in the Netherlands. We performed a qualitative study and report on the experiences and attitudes of first-degree relatives who attended a cardiogenetics clinic for evaluation. In total, we interviewed nine first-degree relatives and one spouse of seven SCD victims about their experiences, considerations and emotions before attendance and at the first stage of the cardiogenetic evaluation before DNA results were available. Interviews were transcribed verbatim and analysed. Medical professionals did not have an important role in informing or referring relatives to a cardiogenetics clinic. Importantly, all participants indicated that they would have appreciated a more directive approach from medical professionals, because their mourning process hampered their own search for information and decision-making. A need to understand the cause of death and wanting to prevent another SCD event occurring in the family were the most important reasons for attending a clinic. There are possibilities to improve the information process and better support their decision-making. The multidisciplinary cardiogenetic evaluation was appreciated, but could be improved by minor changes in the way it is implemented.
机译:年轻的猝死性心脏病(SCD)受害者的亲属患上可能致命的遗传性心脏病的风险增加。因此,建议对受害者进行尸检,并将其亲属转介至心脏遗传学诊所进行全面评估,以识别有危险的人并采取预防措施。但是,目前,荷兰年轻亲属的SCD后到心脏遗传学诊所就诊的家庭数量很少。我们进行了定性研究,并报告了参加心脏遗传学诊所进行评估的一级亲属的经历和态度。我们总共采访了9名一级亲属和7名SCD受害者的配偶,询问他们出勤之前以及在获得DNA结果之前在心源性评估的第一阶段的经历,考虑和情感。采访被逐字记录和分析。医学专业人员在告知或转介亲属心脏遗传学诊所方面没有重要作用。重要的是,所有参与者都表示,他们本来希望医学专业人员采取更具指导性的方法,因为他们的哀悼过程阻碍了他们自己寻求信息和决策的努力。需要了解死亡原因并希望防止家庭中再次发生SCD事件是前往诊所就诊的最重要原因。有可能改善信息流程并更好地支持其决策。多学科的心源性评估受到赞赏,但可以通过实施方式的微小变化加以改进。

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