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What do patients with hereditary deafness think of genetic studies?

机译:遗传性耳聋患者如何看待遗传学研究?

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OBJECTIVE: We conducted an attitude survey for patients with hearing loss (HL). The aim of this study was to investigate the opinions of patients or parents of deaf children regarding the deafness gene, genetic testing and a gene related HL. METHOD: A questionnaire was sent to 201 individuals who visited the Department of Otolaryngology, Tokyo Medical and Dental University and who received genetic testing for HL from September 2000 to January 2006. There were 14 questions in the questionnaire that were classified into four topics related to a deafness gene and hereditary HL, genetic testing, outpatient department of medical genetics/genetic counseling, and the results of genetic testing. The study consisted of 140 respondents (70%) of 201 administered surveys. RESULT: Before visiting our department, only 36% of the respondents were aware that a genetic factor was a cause of HL. Despite our explanation of a deafness gene and hereditary HL, 23% of 134 respondents answered that they had not received any such explanation. Furthermore, 14% of the 103 respondents who had answered that they receive the explanation, however, they did not fully understand it. Thirty-nine percent of the respondents made their own decision regarding the genetic testing, whereas 53.5% received the tests upon the advice of a physician or family member. In contrast, 91% of the respondents had a positive attitude towards other future genetic tests. The existence of the genetic outpatient department or genetic counseling has been seldom acknowledged, but upon learning of its availability, nearly one third of the respondents indicated that they would like to receive genetic counseling. Although no respondent had social and/or family problems after being informed that they had a deafness gene mutation, some respondents worried about the result. CONCLUSION: The results of the survey suggested that the vast majority of the respondents were satisfied with genetic testing for HL and that the barriers to take the genetic test were less than expected. However, some respondents have a negative attitude towards genetic testing and counseling. Furthermore, the issue of disclosure may be burdensome to patients.
机译:目的:我们对听力损失(HL)患者进行了态度调查。这项研究的目的是调查聋儿的患者或父母对聋基因,基因检测和与基因有关的HL的看法。方法:向2000年9月至2006年1月访问东京医科牙科大学耳鼻咽喉科并接受HL基因检测的201人发送了问卷。问卷中有14个问题,分为与以下内容相关的四个主题:耳聋基因和遗传性HL,基因测试,医学遗传学/遗传咨询的门诊以及基因测试的结果。该研究由201项管理的调查中的140名受访者(占70%)组成。结果:在拜访我们部门之前,只有36%的受访者知道遗传因素是导致HL的原因。尽管我们解释了耳聋基因和遗传性HL,但134名受访者中有23%回答说他们没有收到任何此类解释。此外,在回答他们收到解释的103位受访者中,有14%的人对此没有完全理解。 39%的受访者对基因测试做出了自己的决定,而53.5%的受访者是在医师或家庭成员的建议下接受测试的。相反,91%的受访者对未来的其他基因检测持积极态度。很少承认遗传门诊或遗传咨询的存在,但是在得知遗传门诊或遗传咨询的可用性后,将近三分之一的受访者表示愿意接受遗传咨询。尽管没有受访者在被告知他们患有耳聋基因突变后出现了社交和/或家庭问题,但一些受访者仍对结果感到担忧。结论:调查结果表明,绝大多数受访者对HL的基因检测感到满意,并且进行基因检测的障碍比预期的要少。但是,一些受访者对基因检测和咨询持否定态度。此外,公开的问题可能给患者带来负担。

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