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植入前基因诊断决策中的挑战、困境及相关因素:提供者与患者的观点、经历及决策

Challenges, Dilemmas and Factors Involved in PGD Decision-Making: Providers' and Patients' Views, Experiences and Decisions.

作者信息

Klitzman Robert

机构信息

Columbia University, 1051 Riverside Drive, Mail Unit #15, New York, NY, 10032, USA.

出版信息

J Genet Couns. 2018 Aug;27(4):909-919. doi: 10.1007/s10897-017-0173-9. Epub 2017 Dec 16.

Abstract

Providers and patients are considering and pursuing PGD for ever-more conditions, but questions arise concerning how they make, view and experience these decisions, and what challenges they may face. Thirty-seven in-depth semi-structured interviews were conducted (with 27 IVF providers and 10 patients). Patients and providers struggled with challenges and dilemmas about whether to pursue PGD in specific cases, and how to decide. Respondents varied in how they viewed, experienced and made these choices, and for which conditions to pursue PGD (from lethal, childhood-onset conditions to milder, treatable, or adult-onset disorders). Several factors were involved, including differences in gene penetrance, predictability, and phenotypic expression, and disease severity, age of onset, treatability, stigma and degree of disability. Providers and patients face questions regarding possibilities of screening for more than one condition in one set of embryos, and limitations of PGD (e.g., inaccurate results). Characteristics of providers (e.g., amount of PGD experience, understandings of genetics, and use of genetic counselors), and of patients (e.g., related to broader moral and social attitudes) can also affect these decisions. These data, the first to examine several key questions concerning PGD, suggest that providers and patients confront several dilemmas. These findings have critical implications for future practice, guidelines, education and research.

摘要

医疗服务提供者和患者正在考虑并寻求针对越来越多的病症进行胚胎植入前基因诊断(PGD),但关于他们如何做出、看待和体验这些决策,以及可能面临哪些挑战的问题也随之出现。研究人员进行了37次深入的半结构化访谈(对象包括27位体外受精(IVF)医疗服务提供者和10位患者)。在特定病例中是否进行PGD以及如何做出决定的问题上,患者和医疗服务提供者都面临着挑战和困境。对于如何看待、体验和做出这些选择,以及针对哪些病症进行PGD(从致死性的儿童期发病病症到较轻的、可治疗的或成人期发病的疾病),受访者的看法各不相同。其中涉及几个因素,包括基因外显率、可预测性和表型表达的差异,以及疾病严重程度、发病年龄、可治疗性、污名化和残疾程度。医疗服务提供者和患者面临着关于在一组胚胎中筛查多种病症的可能性以及PGD局限性(例如结果不准确)的问题。医疗服务提供者的特征(例如PGD经验量、对遗传学的理解以及对遗传咨询师的使用情况)和患者的特征(例如与更广泛的道德和社会态度相关的特征)也会影响这些决策。这些数据首次审视了有关PGD的几个关键问题,表明医疗服务提供者和患者面临着一些困境。这些发现对未来的实践、指南制定、教育和研究具有至关重要的意义。

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