Zhong Yuqiong, Hao Tianchi, Liu Xing, Zhang Xin, Wu Ying, Wang Xiaomin, Luo Dan
School of Humanities, Central South University, Lushan South Road, Yuelu District, Changsha, 410012, People's Republic of China.
Xiangya Hospital, Central South University, 87 Xiangya Road, Kaifu District, Changsha, 410008, People's Republic of China.
J Bioeth Inq. 2024 Aug 20. doi: 10.1007/s11673-024-10376-6.
The international community has proposed a comprehensive strategy to prevent congenital abnormalities. And China, with a high incidence of congenital diseases, has implemented measures including prenatal screening and diagnosis to reduce the morbidity of congenital abnormalities. However, ethical challenges arise in the practice of prenatal screening and diagnosis among healthcare professionals. Five focus group discussions were conducted with twenty-four health professionals working in maternal and child health services in Hunan Province, China, to explore the ethical challenges they encountered in prenatal testing decision-making and information disclosure practices, as well as their views on these challenges. Participants were selected through purposive sampling, ensuring maximum demographic diversity. Three main themes were identified: 1) balancing between information disclosure and privacy protection; 2) patient-oriented decision-making and tensions within family-oriented decision-making; 3) the disparity between the limited help clinical ethics committees (CECs) can provide and professionals' need for CECs. Ethical norms for information disclosure and autonomous decision-making within prenatal screening and diagnostic institutions must be established. Utilizing CECs is crucial to guide professionals in delivering prenatal testing services while simultaneously focusing on targeted improvement of communication skills among these professionals.
国际社会已经提出了一项预防先天性异常的全面战略。在中国,先天性疾病发病率较高,已实施了包括产前筛查和诊断在内的措施,以降低先天性异常的发病率。然而,医疗保健专业人员在产前筛查和诊断实践中面临伦理挑战。在中国湖南省,对24名从事妇幼保健服务的卫生专业人员进行了五次焦点小组讨论,以探讨他们在产前检测决策和信息披露实践中遇到的伦理挑战,以及他们对这些挑战的看法。通过目的抽样选择参与者,以确保最大程度的人口统计学多样性。确定了三个主要主题:1)信息披露与隐私保护之间的平衡;2)以患者为导向的决策与以家庭为导向的决策中的紧张关系;3)临床伦理委员会(CEC)所能提供的有限帮助与专业人员对CEC的需求之间的差距。必须建立产前筛查和诊断机构内信息披露和自主决策的伦理规范。利用临床伦理委员会对于指导专业人员提供产前检测服务至关重要,同时要注重有针对性地提高这些专业人员的沟通技巧。