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对唐氏综合征的认知:一项Q方法学调查

Understandings of Down's syndrome: a Q methodological investigation.

作者信息

Bryant Louise D, Green Josephine M, Hewison Jenny

机构信息

University of Leeds, Leeds, West Yorkshire UK.

出版信息

Soc Sci Med. 2006 Sep;63(5):1188-200. doi: 10.1016/j.socscimed.2006.03.004. Epub 2006 Apr 27.

Abstract

Down's syndrome has been, and continues to be, a central focus of prenatal testing technology. However, there has been surprisingly little examination of how parental understandings of the condition relate to prenatal testing choices. This study, carried out at the University of Leeds, uses Q methodology to identify 'competing equivalent stories' of Down's syndrome and to highlight the shared and distinct themes within these stories. Seventy-six people were selected as being likely to represent a diverse range of views about Down's syndrome, approximately half of whom had some known experience or expertise related either to the condition or to prenatal testing. The participants were asked to Q sort 50 propositions about Down's syndrome that were selected to reflect different views about the condition in terms of its impact on the affected person, on families with an affected child, and on society. Using Principal Components Analysis, five statistically independent factors were extracted that reflected a range of views towards, and experiences of, people with Down's syndrome. Despite a virtual consensus about the rights of existing people with Down's syndrome to healthcare, an education, and inclusion in their community, there were significant differences in how participants believed they personally would adjust to an affected child. Furthermore, whether or not people with Down's syndrome were seen to be within 'a continuum of normality' sheds light on how views about the condition may be linked to views about prenatal testing and termination of pregnancy. The study demonstrates that people hold complex and sometimes seemingly contradictory views about Down's syndrome, and that these are likely to influence their prenatal testing decisions. Antenatal settings currently provide little opportunity for people to discuss and explore their beliefs about disability. It is argued that this may affect the ability of some individuals to make decisions that are informed by their own views and values.

摘要

唐氏综合征一直是且仍然是产前检测技术的核心关注点。然而,令人惊讶的是,对于父母对该病症的理解如何与产前检测选择相关联,却很少有研究。这项在利兹大学开展的研究,运用Q方法来识别关于唐氏综合征的“相互竞争的等效观点”,并突出这些观点中共同和不同的主题。76人被挑选出来,他们可能代表了对唐氏综合征的各种不同观点,其中约一半人对该病症或产前检测有一定的已知经验或专业知识。参与者被要求对50条关于唐氏综合征的陈述进行Q分类,这些陈述被选出来以反映在该病症对患者本人、对有患病孩子的家庭以及对社会的影响方面的不同观点。通过主成分分析,提取出了五个统计上独立的因素,这些因素反映了对唐氏综合征患者的一系列看法和经历。尽管对于现有唐氏综合征患者获得医疗保健、接受教育以及融入社区的权利几乎达成了共识,但参与者认为自己个人会如何适应患病孩子,仍存在显著差异。此外,唐氏综合征患者是否被视为处于“正常范围之内”,揭示了对该病症的看法可能如何与对产前检测和终止妊娠的看法相关联。该研究表明,人们对唐氏综合征持有复杂且有时看似相互矛盾的观点,而这些观点可能会影响他们的产前检测决策。目前,产前检查环境几乎没有为人们提供讨论和探索其对残疾看法的机会。有人认为,这可能会影响一些人做出基于自身观点和价值观的明智决策的能力。

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