The urgency for a change in genetics healthcare provision: views from Portuguese medical geneticists.

IF 1.5 Q4 GENETICS & HEREDITY
Journal of Community Genetics Pub Date : 2024-06-01 Epub Date: 2024-03-01 DOI:10.1007/s12687-024-00702-1
Catarina Costa, Lídia Guimarães, Ruxanda Lungu Baião, Marina Serra de Lemos, Luís Filipe Azevedo, Milena Paneque
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Abstract

In the last decades, genetics has experienced significant technological advancements worldwide. However, in Portugal, serious limitations persist, compromising the functioning of healthcare in medical genetics. This study aimed to promote sharing and discussion among genetic medical professionals, to outline concrete actions to address gaps in clinical practice. Three focus groups were conducted with 19 specialists in medical genetics. The data were analyzed using the thematic analysis method to extract the main themes from the discussions. From the analysis, four conceptual themes emerged: (i) framing Portuguese genetic services in light of the European context; (ii) improvement of medical genetics education and population literacy; (iii) transforming of medical genetics services; and (iv) operationalizing the change. The results demonstrated that increasing training resources and strengthening multiprofessional teams by hiring more genetic professionals, such as clinical geneticists, molecular geneticists, and other genetic specialists, is crucial to enhancing the responsiveness of genetic services. Integrating medical genetics into all specialties and primary care, as well as updating the national network of medical genetics, are critical points for increasing equity and enabling healthcare to be provided more fairly. Including other medical genetics professionals such as genetic counsellors, nurses and psychologists also plays a significant role in providing comprehensive and quality care. This collaborative approach aims to provide effective genetic assistance and enhance the adequacy of genetic healthcare. The findings are compiled as recommendations to support the profession moving forward that can be applied to other healthcare contexts worldwide.

遗传学医疗服务变革的紧迫性:葡萄牙医学遗传学家的观点。
在过去的几十年里,遗传学在全球范围内取得了显著的技术进步。然而,在葡萄牙,严重的局限性依然存在,损害了医学遗传学医疗保健的功能。这项研究旨在促进遗传学医疗专业人员之间的交流和讨论,概述解决临床实践差距的具体行动。与 19 名医学遗传学专家进行了三次焦点小组讨论。采用主题分析法对数据进行了分析,以提取讨论中的主要议题。通过分析,得出了四个概念性主题:(i) 根据欧洲背景构建葡萄牙遗传学服务框架;(ii) 改善医学遗传学教育和人口扫盲;(iii) 医学遗传学服务转型;(iv) 实施变革。研究结果表明,通过聘用更多遗传学专业人员(如临床遗传学家、分子遗传学家和其他遗传学专家)来增加培训资源和加强多专业团队,对于提高遗传学服务的响应能力至关重要。将医学遗传学纳入所有专科和初级保健,以及更新全国医学遗传学网络,是提高公平性和使医疗保健服务更加公平的关键点。将遗传咨询师、护士和心理学家等其他医学遗传学专业人员纳入其中,对于提供全面、优质的医疗服务也具有重要作用。这种合作方式旨在提供有效的遗传学援助,提高遗传学医疗保健的充分性。研究结果汇编成建议,以支持该行业向前发展,并可应用于全球其他医疗保健领域。
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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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