Department of Social Medicine and Public Health, Faculty of Public Health, Medical University of Plovdiv, Plovdiv, Bulgaria.
Institute for Rare Diseases, Plovdiv, Bulgaria.
Orphanet J Rare Dis. 2023 Jul 25;18(1):213. doi: 10.1186/s13023-023-02820-4.
BACKGROUND: Rare diseases (RDs) are life-threatening or chronically debilitating and offer a high level of complexity. The aim of this study is to assess medical students' knowledge and awareness of RDs as well as their perceptions of potential measures to boost training in RDs. The cross-sectional survey was conducted at the Medical University of Plovdiv, Bulgaria, in 2019. The questionnaire contained 12 questions, divided into three main categories: (1) sociodemographic profile; (2) knowledge and awareness of RDs; and (3) attitudes about potential measures to improve training in RDs. RESULTS: A total of 1189 medical students completed the survey with an overall response rate of 56.4%. Only 13% of participants knew the correct definition of RDs, and a low overall level of awareness was found with regard to orphan drugs (20.3%) and genetic counselling and testing (0.5%). Respondents believed that society as a whole was largely unaware of RDs as a major public health issue. Students suggested elective courses, and invited lectures by RDs experts, and participation in research projects as the most preferred measures to improve undergraduate training. CONCLUSIONS: It is crucial to address the gaps in medical students' knowledge and awareness of RDs. University curricula should consider incorporating different RDs training modalities. It is essential to encourage various stakeholders to play a more proactive role and to collaborate in these activities. Involvement of patient organisations and advocacy groups might enhance students' knowledge of the challenges faced by people with RDs. Not least, the media should be partners in this important endeavour as well.
背景:罕见病(RDs)具有危及生命或慢性衰弱的特点,且具有高度复杂性。本研究旨在评估医学生对罕见病的知识和认识,以及他们对潜在措施的看法,以提高罕见病培训。该横断面调查于 2019 年在保加利亚普罗夫迪夫医科大学进行。问卷包含 12 个问题,分为三个主要类别:(1)社会人口统计学概况;(2)对罕见病的认识和认识;(3)对改善罕见病培训的潜在措施的态度。
结果:共有 1189 名医学生完成了调查,总体回复率为 56.4%。只有 13%的参与者知道罕见病的正确定义,对孤儿药(20.3%)和遗传咨询和检测(0.5%)的总体认识水平较低。受访者认为,整个社会对罕见病作为一个主要的公共卫生问题基本上一无所知。学生们建议选修课程、邀请罕见病专家授课以及参与研究项目,作为改善本科培训的最受欢迎措施。
结论:必须解决医学生对罕见病知识和认识的差距。大学课程应考虑纳入不同的罕见病培训模式。必须鼓励各利益攸关方发挥更积极的作用,并在这些活动中进行合作。让患者组织和倡导团体参与,可能会提高学生对罕见病患者所面临挑战的认识。至关重要的是,媒体也应该成为这一重要努力的合作伙伴。
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