Knowledge and attitudes towards genomic medicine and pharmacogenomics of medical undergraduate students in Sri Lanka: a cross-sectional study.

IF 1.5 Q4 GENETICS & HEREDITY Journal of Community Genetics Pub Date : 2024-11-26 DOI:10.1007/s12687-024-00754-3
Dilini N Kekulandara, M S Wickramarachchi
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Abstract

Genomic medicine and pharmacogenomics (PGX) are emerging practices in medicine that play a vital role in providing personalized and efficient treatments for patients. While many countries have integrated these novel concepts into their undergraduate medical curricula to enhance the quality of healthcare, Sri Lanka remains relatively new to these advancements. Herein, we accessed the knowledge and attitude of Sri Lankan medical undergraduates on genomic medicine and PGX and explored the readiness of introducing genomic insights to Sri Lankan undergraduate medical education. The study sample was the undergraduate students of Medical Faculty of Wayamba University in Sri Lanka, being a newly developed and diverse institution seeking research findings to enhance the curriculum and teaching-learning activities aiming to produce competent graduates. A descriptive cross-sectional study was conducted by distributing a questionnaire to all five student batches at Faculty of Medicine, Wayamba University of Sri Lanka. The data of 232 respondents (55% response rate), demonstrated a good level of knowledge on genomic medicine and PGX, with no significant variation of the level of knowledge across the five academic years. A nuanced range of attitudes, encompassing both negative and positive perspectives towards genomic medicine and PGX was observed varying according to the specific questions posed. However, heavy concerns regarding data privacy, insurance implications, and the timing of implementation appeared. The results of the study highlight a need for curriculum enhancement, acknowledging the level of knowledge while emphasizing areas for improvement in students' perspectives on genomic medicine and PGX for better advancements in future healthcare of Sri Lanka.

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斯里兰卡医学本科生对基因组医学和药物基因组学的认识和态度:一项横断面研究。
基因组医学和药物基因组学(PGX)是新兴的医学实践,在为患者提供个性化和高效治疗方面发挥着至关重要的作用。虽然许多国家已将这些新概念纳入医学本科课程,以提高医疗保健质量,但斯里兰卡对这些进步仍相对陌生。在此,我们了解了斯里兰卡医学本科生对基因组医学和 PGX 的认识和态度,并探讨了在斯里兰卡本科医学教育中引入基因组见解的准备情况。研究样本为斯里兰卡瓦扬巴大学医学系的本科生,这是一所新兴的多元化院校,旨在寻求研究成果,以加强课程和教学活动,培养合格的毕业生。通过向斯里兰卡瓦扬巴大学医学院所有五个批次的学生发放调查问卷,进行了一项描述性横断面研究。232名受访者(回复率为55%)的数据显示,他们对基因组医学和PGX的了解程度良好,五个学年的了解程度无明显差异。根据所提具体问题的不同,受访者对基因组医学和 PGX 的态度也不尽相同,既有消极态度,也有积极态度。不过,对数据隐私、保险影响和实施时机的担忧也很严重。研究结果凸显了加强课程设置的必要性,在承认知识水平的同时,强调了学生对基因组医学和 PGX 的看法中需要改进的地方,以便更好地推进斯里兰卡未来的医疗保健事业。
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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.
期刊最新文献
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