罕见病教育中的帕累托原则:评估常见罕见病在医学教育和编码系统中的代表性

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Alexandra Berger, Kai Lars Grimm, Richard Noll, Thomas OF Wagner
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引用次数: 0

摘要

帕累托原则(Pareto Principle)认为,只需付出很小的努力,就能取得很大一部分成果。Wakap 等人发现,约 80% 的罕见病 (RD) 患者患有 149 种特定罕见病中的一种。罕见病领域的一个重大挑战是信息匮乏,再加上大多数罕见病在 ICD-10 中无法具体编码,导致缺乏可靠的流行病学数据。此外,医学教育中的时间限制也阻碍了对所有 RD 的全面教学,从而导致无法识别疾病,造成诊断难题。我们从 Orphanet 流行病学档案中找出了发病率最高和第二高的 RD(发病率分别为 1-5/10,000 和 1-9/100,000),共计 454 种疾病。我们调查了使用 ICD-10-GM 进行特定编码的可行性,以及这些疾病是否明确列入了德国第二次国家人类医学考试的科目目录 (GK)。我们采用了双侧卡方检验来确定流行率组间的显著统计学差异。在 454 种疾病中,共有 34% 的疾病可在 ICD-10-GM 中进行具体编码,其中 49% 的疾病在 1-5/10,000 发病率范围内(153 例),26% 的疾病在 1-9/100,000 发病率范围内(301 例)有具体编码。在所有被调查的疾病中,约有 15%属于 GK,其中最流行的 RD 组和第二流行的 RD 组分别占 25%和 10%。在是否存在特定的 ICD-10-GM 代码和是否被纳入 GK 方面,各流行组之间存在明显的统计学差异。在发病率最高的 RD 患者中,只有 49% 的人可以进行具体编码,这凸显了 RD 流行病学数据有限所带来的挑战。在德国,除了在住院环境中使用 ICD-10 外,还引入了 Alpha-ID,以获得更多有效的 RD 流行病学数据。认识到帕累托原则的适用性,该研究强调了将最常见的罕见病纳入医学教育的重要性。在认识到局限性(尤其是在涵盖超罕见疾病方面)的同时,该研究强调了加强医学课程以提高对罕见病的认识和诊断准确性的潜在益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pareto-principle in rare disease education: assessing the representation of common rare diseases in medical education and coding systems
The Pareto Principle asserts that a large portion of results can be achieved with a small amount of effort. Wakap et al. found that around 80% of individuals with rare diseases (RD) suffer from one of 149 specific rare diseases. A significant challenge in the RD domain is the lack of information, compounded by the fact that most RD are not specifically codifiable in the ICD-10, leading to a deficit in reliable epidemiological data. Additionally, time constraints in medical education hinder the comprehensive teaching of all RD, contributing to the diagnostic odyssey problem through failure of recognizing diseases. We identified the most and second most prevalent RD (prevalences of 1–5/10,000 and 1–9/100,000, respectively) from the Orphanet Epidemiology File, totaling 454 diseases. We investigated the feasibility of specific coding using ICD-10-GM and whether these diseases were explicitly listed in the subject catalog (GK) of the second state examination in human medicine in Germany. A two-sided chi-square test was employed to identify statistically significant differences between prevalence groups. Out of 454 diseases, a total of 34% could be specifically coded in ICD-10-GM, with 49% of diseases in the 1–5/10,000 prevalence range (153 RD) and 26% in the 1–9/100,000 range (301 RD) having specific codes. Approximately 15% of all investigated diseases were part of the GK, with 25% of the most prevalent and 10% of the second most prevalent RD group, respectively. Statistically significant differences were observed between prevalence groups concerning the presence of a specific ICD-10-GM code and inclusion in the GK. Only 49% of the most prevalent RD can be specifically coded, highlighting the challenge of limited epidemiological data on RD. In Germany, the Alpha-ID was introduced in addition to ICD-10 in the inpatient setting to obtain more valid epidemiological data on RD. Recognizing the Pareto Principle’s applicability, the study emphasizes the importance of including the most common rare diseases in medical education. While recognizing the limitations, especially in covering ultra-rare diseases, the study underscores the potential benefits of enhancing medical curricula to improve rare disease awareness and diagnostic accuracy.
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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