Carroll J C, Brown J B, Reid A J, Pugh P
Family Medicine Centre, Mount Sinai Hospital.
Can Fam Physician. 2000 Mar;46:614-20.
To explore the ideas, opinions, feelings, and experiences of women regarding prenatal genetic screening, specifically maternal serum screening (MSS).
Qualitative technique of focus groups.
Northern, rural, inner-city, urban, and suburban communities in Ontario.
Women who had given birth to babies from January 1994 to May 1996, but who were not currently pregnant (n = 60).
Six focus groups composed of women living in various communities who had recently given birth to babies explored the experience of MSS.
Women want informed choice about prenatal genetic screening. Three factors influenced women's decisions to undergo or decline prenatal genetic screening: their personal values, including their philosophy of life, moral, and religious values, and attitudes regarding Down syndrome and disability; social support including their partners, families, and friends; and quality of information from health care providers. Women want their providers to give them information personally; they want to receive the information as early as possible in prenatal care to allow time for reflection; and they want unbiased, accurate information in order to make a decision that is in keeping with their personal values and beliefs.
Knowledge of women's ideas, opinions, feelings, and experiences regarding MSS suggests specific ways health care providers can facilitate informed decision making in prenatal screening. Providing information about genetic testing needs to be individualized, with women actively participating in the decision-making process. Information needs described by these women could apply to other prenatal genetic tests that might be available in the future.
探讨女性对于产前基因筛查,特别是母血清筛查(MSS)的想法、观点、感受和经历。
焦点小组定性研究方法。
安大略省北部、农村、市中心、城市和郊区社区。
在1994年1月至1996年5月间生育过婴儿但目前未怀孕的女性(n = 60)。
由居住在不同社区且近期生育过婴儿的女性组成六个焦点小组,探讨母血清筛查的经历。
女性希望在产前基因筛查方面能做出明智的选择。有三个因素影响女性决定接受或拒绝产前基因筛查:她们的个人价值观,包括生活理念、道德和宗教价值观,以及对唐氏综合征和残疾的态度;社会支持,包括伴侣、家人和朋友;以及医疗保健提供者提供信息的质量。女性希望医疗保健提供者亲自向她们提供信息;她们希望在产前护理早期就获得信息以便有时间思考;并且她们希望获得公正、准确的信息,以便做出符合其个人价值观和信仰的决定。
了解女性对于母血清筛查的想法、观点、感受和经历,提示了医疗保健提供者在产前筛查中促进明智决策的具体方法。提供有关基因检测的信息需要个性化,让女性积极参与决策过程。这些女性所描述的信息需求可能适用于未来可能出现的其他产前基因检测。