Factors influencing pregnant women's decision to accept or decline prenatal screening and diagnosis - a qualitative study.

IF 1.5 Q4 GENETICS & HEREDITY
Ellen Ternby, Ove Axelsson, Charlotta Ingvoldstad Malmgren, Susanne Georgsson
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Abstract

Background and objective:  Prenatal diagnosis for chromosomal anomalies is frequently used worldwide. It is important that pregnant women receive adequate counselling to make informed decisions regarding prenatal diagnosis. The aim of this study was to explore what factors influence pregnant women's decision-making process when accepting or declining prenatal screening and diagnosis.  Methods: A qualitative study using inductive qualitative content analysis. Individual, semi-structured phone interviews were carried out during a five-month period in 2016-2017 with 24 pregnant women in the first trimester, living in a medium-sized Swedish city.

Findings:  Two main themes emerged: (1)"Individual factors - The women's experiences, perceptions and values" with three categories "Attitude towards anomalies", "Worry and need for reassurance", "Self-perceived risk" and (2)"External factors - The women's perception of the test and others' views" with two categories "Test characteristics" and "Influence from others".  Conclusions: Pregnant women's decision-making process regarding prenatal tests is multidimensional, affected by both individual factors such as experiences, perceptions and values, and external factors such as test characteristics and influence from others. Information about both test characteristics and the conditions tested is of help pregnant women in the decision-making process since it provides a better understanding of how having a child with the condition in question can affect them and their family. It is important that healthcare professionals giving information about and offering prenatal tests for chromosomal anomalies are aware of how their attitudes can influence women's decisions.

影响孕妇决定接受或拒绝产前筛查和诊断的因素 - 一项定性研究。
背景和目的: 染色体异常的产前诊断在全球范围内被频繁使用。重要的是,孕妇应接受充分的咨询,以便就产前诊断做出明智的决定。本研究旨在探讨影响孕妇接受或拒绝产前筛查和诊断决策过程的因素。 研究方法采用归纳定性内容分析法进行定性研究。在2016-2017年的5个月期间,对居住在瑞典一个中等城市的24名怀孕前三个月的孕妇进行了个人半结构化电话访谈: 出现了两大主题:(1)"个体因素 - 孕妇的经历、认知和价值观",包括三个类别 "对异常的态度"、"担心和需要保证"、"自我认知的风险";(2)"外部因素 - 孕妇对检查的认知和他人的观点",包括两个类别 "检查特征 "和 "他人的影响"。 结论孕妇对产前检测的决策过程是多维的,既受到经验、认知和价值观等个体因素的影响,也受到检测特征和他人影响等外部因素的影响。有关检测特征和检测条件的信息有助于孕妇在决策过程中更好地了解如果孩子患有相关疾病会对她们及其家庭产生怎样的影响。重要的是,提供染色体异常产前检测信息和服务的医疗保健专业人员应意识到他们的态度会如何影响孕妇的决定。
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来源期刊
Journal of Community Genetics
Journal of Community Genetics GENETICS & HEREDITY-
CiteScore
3.30
自引率
5.30%
发文量
54
期刊介绍: The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities which identify persons at increased genetic risk and has an interest in assessing this risk, in order to enable those at risk to make informed decisions. Community genetics services thus encompass such activities as genetic screening, registration of genetic conditions in the population, routine preconceptional and prenatal genetic consultations, public education on genetic issues, and public debate on related ethical issues. The Journal of Community Genetics has a multidisciplinary scope. It covers medical genetics, epidemiology, genetics in primary care, public health aspects of genetics, and ethical, legal, social and economic issues. Its intention is to serve as a forum for community genetics worldwide, with a focus on low- and middle-income countries. The journal features original research papers, reviews, short communications, program reports, news, and correspondence. Program reports describe illustrative projects in the field of community genetics, e.g., design and progress of an educational program or the protocol and achievement of a gene bank. Case reports describing individual patients are not accepted.
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