Paneque Milena, Sequeiros Jorge, Skirton Heather
Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Centre for Predictive and Preventive Genetics, IBMC-Instituto de Biologia Molecular e Celular, UnIGENe, University of Porto, Porto, Portugal.
Eur J Hum Genet. 2015 Nov;23(11):1468-72. doi: 10.1038/ejhg.2015.23. Epub 2015 Feb 18.
Genetic counselling for presymptomatic testing is complex, bringing both ethical and practical questions. There are protocols for counselling but a scarcity of literature regarding quality assessment of such counselling practice. Generic quality assessment tools for genetic services are not specific to presymptomatic testing (PST). Therefore, the aim of this study was to identify aspects of effective counselling practice in PST for late-onset neurological disorders. We used the Delphi method to ascertain the views of relevant European experts in genetic counselling practice, ascertained via published literature and nomination by practitioners. Ethical approval was obtained. Questionnaires were sent electronically to a list of 45 experts, (Medical Doctors, Geneticists, Genetic Counsellors and Genetic Nurses), who each contributed to one to three rounds. In the first round, we provided a list of relevant indicators of quality of practice from a literature review. Experts were requested to evaluate topics in four domains: (a) professional standards; (b) service standards; (c) the consultant's perspective; and (d) protocol standards. We then removed items receiving less than 65% approval and added new issues suggested by experts. The second round was performed for the refinement of issues and the last round was aimed at achieving final consensus on high-standard indicators of quality, for inclusion in the assessment tool. The most relevant indicators were related to (1) consultant-centred practice and (2) advanced counselling and interpersonal skills of professionals. Defined high-standard indicators can be used for the development of a new tool for quality assessment of PST counselling practice.
针对症状前检测的遗传咨询很复杂,会带来伦理和实际问题。虽然有咨询方案,但关于此类咨询实践质量评估的文献却很匮乏。遗传服务的通用质量评估工具并不适用于症状前检测(PST)。因此,本研究的目的是确定针对迟发性神经系统疾病的PST有效咨询实践的各个方面。我们采用德尔菲法来确定遗传咨询实践方面相关欧洲专家的观点,这些专家是通过已发表的文献和从业者提名确定的。研究获得了伦理批准。通过电子邮件向45位专家(医生、遗传学家、遗传咨询师和遗传护士)发送了问卷,每位专家参与了一到三轮调查。在第一轮中,我们从文献综述中提供了一份相关实践质量指标清单。要求专家们对四个领域的主题进行评估:(a)专业标准;(b)服务标准;(c)咨询师的视角;(d)方案标准。然后我们删除了认可度低于65%的项目,并添加了专家提出的新问题。第二轮是为了完善问题,最后一轮旨在就高质量标准指标达成最终共识,以便纳入评估工具。最相关的指标与(1)以咨询师为中心的实践和(2)专业人员的高级咨询及人际沟通技巧有关。明确的高标准指标可用于开发一种新的PST咨询实践质量评估工具。