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医疗保健实习生对遗传学和残疾的态度:获取医疗服务、医疗沟通及决策方面的问题

Attitudes of health care trainees about genetics and disability: issues of access, health care communication, and decision making.

作者信息

Ormond Kelly E, Gill Carol J, Semik Patrick, Kirschner Kristi L

机构信息

Center for Genetic Medicine, Northwestern University, 676 N. St. Clair #1271, Chicago, Illinois 60611, USA.

出版信息

J Genet Couns. 2003 Aug;12(4):333-49. doi: 10.1023/a:1023953022290.

Abstract

Prior studies suggest that knowledge and attitudes of health care professionals influence patient communication and medical decision-making. To study this dynamic in the context of genetic disability, we developed a survey on health professionals' attitudes regarding disability and genetic screening and pilot-tested it on a sample of medical students, residents, and genetic counseling students (N=85). Despite minimal experience with disability or genetics, most respondents reported feeling comfortable dealing with genetics (59%) and disability (75%). The majority felt that disability caused significant suffering for both the person (51%) and family (64%), and that research should be directed toward preventing genetic disability (62%). Similar to prior literature, perceived "Quality of Life" was most often based on degrees of physical and cognitive functioning, pain, and social support. However, differences were found between genetic counseling trainees and other medical trainees in their relative emphasis of social versus medical issues in questions of disability and genetic testing, and these response patterns were associated with differences in the groups' priorities for offering information about social resources. Respondents agreed that access to genetic testing and information is personal and that testing should be available upon request for oneself (68%) and to a lesser degree for one's fetus (55%) or child (41%). However, the same individuals frequently stated that society should regulate access to such technologies. Although most felt that the patient and professional should jointly make such decisions on a case-by-case basis, it was also seen as appropriate for the health care professional to occasionally decline genetic testing. It seems appropriate that training and experience influence knowledge and attitudes. Therefore, it is critical to document knowledge and attitudes of various health care providers and trainees, including differences between various specialties, to improve educational interventions geared to this area.

摘要

先前的研究表明,医疗保健专业人员的知识和态度会影响医患沟通及医疗决策。为了在基因残疾的背景下研究这种动态关系,我们针对医疗专业人员对残疾和基因筛查的态度开展了一项调查,并在医学生、住院医师和基因咨询专业学生样本(N = 85)中进行了预测试。尽管受访者在残疾或遗传学方面的经验很少,但大多数人表示在处理遗传学问题(59%)和残疾问题(75%)时感到自在。大多数人认为残疾会给患者本人(51%)和家庭(64%)带来巨大痛苦,并且研究应致力于预防基因残疾(62%)。与先前的文献相似,人们通常根据身体和认知功能、疼痛程度以及社会支持来感知“生活质量”。然而,在残疾和基因检测问题上,基因咨询学员与其他医学学员在对社会问题与医学问题的相对重视程度上存在差异,并且这些回答模式与两组在提供社会资源信息方面的优先事项差异相关。受访者一致认为,基因检测和信息获取是个人事务,检测应根据个人要求提供(68%),对胎儿(55%)或儿童(41%)的检测需求程度相对较低。然而,同样是这些人经常表示社会应该对这类技术的获取进行监管。尽管大多数人认为患者和专业人员应逐案共同做出此类决定,但医疗保健专业人员偶尔拒绝基因检测也被视为合适。培训和经验影响知识和态度似乎是合理的。因此,记录各类医疗保健提供者和学员的知识和态度,包括不同专业之间的差异,对于改进针对该领域的教育干预措施至关重要。

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