Simmons Zachary
Continuum (Minneap Minn). 2016 Dec;22(6, Muscle and Neuromuscular Junction Disorders):2006-2011. doi: 10.1212/01.CON.0000511073.81209.24.
Patients and their family members often ask about genetic testing for asymptomatic individuals who are at risk for developing a genetic disorder. Ordering a genetic test is a complex process involving consideration of many basic ethical principles including autonomy, beneficence, and nonmaleficence, as well as the physician's duty to act in the patient's best interest. Physicians have many choices regarding what tests to order, and they must develop the knowledge and skills to best discuss genetic testing with their patients. Integration of core ethical principles into these processes will permit physicians to best serve their patients when obtaining informed consent, considering advantages and harms of potential results, disclosing those results, and providing follow-up.
患者及其家属经常会询问,对于有患遗传性疾病风险的无症状个体,是否需要进行基因检测。安排基因检测是一个复杂的过程,需要考虑许多基本的伦理原则,包括自主性、有益性和无害性,以及医生为患者的最大利益行事的职责。医生在选择进行何种检测方面有多种选择,他们必须培养相关知识和技能,以便与患者就基因检测进行最佳的沟通。将核心伦理原则融入这些过程,将使医生在获取知情同意、考虑潜在结果的利弊、披露检测结果以及提供后续跟进时,能够更好地为患者服务。