罕见黑客马拉松:一项课外教育活动,旨在提高医学和生命科学专业学生对罕见疾病的认识

Rare Pub Date : 2025-01-01 DOI:10.1016/j.rare.2025.100106
Begum Utz , Emine Eylul Taskin , Ayca Yigit , Emre Ozzeybek , Kutay Bulut , Ece Sonmezler , Aykut Kuruoglu , Aliye Kubra Unal , Noor Fatima , Pinar Gencpinar , Duygu Sag , Yavuz Oktay , Nur Arslan , Ayse Semra Hiz , Nese Atabey , Ugur Ozbek
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引用次数: 0

摘要

在全球范围内,数以百万计的人受到罕见病的影响,但在罕见病的医学和生命科学教育方面仍然存在重大差距。这一差距经常导致患者在临床环境中的延误和挑战,并对研发研究产生负面影响。为了解决这个问题,欧盟资助的RareBoost项目团队组织了“罕见黑客马拉松”,作为2025年罕见病日活动的一部分。黑客马拉松是为本科生和研究生设计的教育活动,学生团队被要求“解决”两个复杂的罕见疾病场景。与类似的黑客马拉松不同,该活动不涉及患者队列再分析。这些团队开发了诊断解决方案,研究了基因型-表型相关性,并提出了研究基因-疾病关系的实验疾病模型。在公开环节,参赛队伍向评审团展示了他们的解决方案,并获得了奖励,以进一步促进他们的科学教育。一项事后调查显示,大多数学生之前对rd的接触有限。学生们报告说,黑客马拉松帮助他们更好地了解了研发研究、诊断和挑战。许多学生也表达了将来在研发领域工作的兴趣。此外,学生们提出了宝贵的建议,如延长活动时间,纳入培训课程,并包括治疗设计方面。Rare黑客马拉松成功地展示了课外活动如何提高医学和生命科学专业学生对rd的认识。在学生的学术培训中纳入类似的活动可以帮助缩小研发教育的差距,从而改善患有罕见疾病的个人的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Rare Hackathon: An extracurricular educational event to promote rare disease awareness among students in medicine and life sciences
Globally, millions of individuals are affected by rare diseases (RDs), yet there remains a significant gap in medical and life sciences education regarding RDs. This gap frequently leads to delays and challenges for patients in clinical settings and negatively impacts RD research. To address this, the EU-funded RareBoost project team organized the ‘Rare Hackathon’, as part of 2025 Rare Disease Day activities. The hackathon was designed as an educational event for undergraduate and graduate students, in which the student teams were asked to ‘solve’ two complex rare disease scenarios. Unlike similar hackathons, this event did not involve a patient cohort reanalysis. The teams developed diagnostic solutions, investigated genotype-phenotype correlations, and suggested experimental disease models to study gene-disease relationships. In a public session, the teams presented their solutions to a jury and received awards to further boost their scientific education. A post-event survey revealed that most students had limited prior exposure to RDs. The students reported that the hackathon helped them gain a better understanding of RD research, diagnosis, and challenges. Many students also expressed interest in working in the RD field in the future. Furthermore, students had valuable suggestions such as extending the event duration, incorporating training sessions, and including treatment design aspects. The Rare Hackathon successfully demonstrated how an extracurricular activity can raise awareness of RDs among medical and life sciences students. Incorporating similar events during students’ academic training can help close the gap in RD education, and as a result, improve outcomes for individuals living with rare conditions.
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