AA Challenge: An interactive French-language educational program on the causes of AA amyloidosis - Analysis of 2,597 responses to 12 clinical quizzes

IF 0.7
Rim Bourguiba, Wafa Ammouri, Ciprian Jurcut, Elissar Dagher, Bertha-Maria Nassani, Ghalia Khellaf, Concetta Catalano, Jabber Laouni, Marion Delafosse, Lena Berchtold, Souhaibou Ndongo, Francine Katalay, Stéphanie Ducharme-Bénard, Fatma Said, Sophie Georgin-Lavialle
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引用次数: 0

Abstract

Introduction: AA amyloidosis (inflammatory amyloidosis) is a rare but serious complication of chronic inflammatory diseases. Its etiological spectrum is broad, potentially contributing to delayed diagnosis, particularly when the underlying cause is rare or poorly recognized. We developed the AA Challenge, an interactive French-language online educational program based on clinical cases, to improve the recognition of the causes of AA amyloidosis among French-speaking physicians.

Methods: The AA Challenge was an international, year-long educational program for French-speaking physicians. It consisted of monthly interactive clinical case quizzes, each illustrating a different cause of AA amyloidosis or a relevant differential diagnosis. Participants were asked to identify the underlying etiology based on the clinical, biological, and/or imaging data provided. The program was disseminated via email, social media, and the digital platforms of organizations involved in amyloidosis. An international steering committee comprising physicians from ten French-speaking countries contributed to the promotion of the program. Participants also received a monthly literature review on AA amyloidosis. Quiz responses, available participant characteristics, and the results of the final satisfaction survey were analyzed.

Results: Twelve clinical cases were released between 2022 and 2023. A total of 2,968 responses were recorded on the Eval&Go® platform. After exclusion of duplicate submissions, 2,597 responses were included in the performance analysis. Information on medical specialty was available for 2,536 responses. Participants were primarily specialists in internal medicine (n=1,534; 59.1%), nephrology (n=470; 18.1%), and rheumatology (n=199; 7.7%). The most represented countries were Morocco (n=646; 24.9%), France (n=537; 20.7%), Romania (n=420; 16.2%), and Tunisia (n=273; 10.5%). Correct response rates varied by etiology, ranging from 29.9% for the AL amyloidosis quiz to 89.0% for the Crohn's disease quiz. The most accurately recognized etiologies were Crohn's disease, rheumatoid arthritis, and spondyloarthritis, whereas AL amyloidosis, tuberculosis-associated bronchiectasis, mevalonate kinase deficiency, cryopyrin-associated autoinflammatory syndromes (CAPS), and primary hyperoxaluria were less frequently identified. The overall correct response rate was 62.1%. The monthly literature review covered 25 publications on AA amyloidosis. The final satisfaction survey received 124 responses and demonstrated a high level of overall satisfaction, with a mean score of 8.61 ± 1.36 out of 10.

Conclusion: The AA Challenge demonstrates the feasibility and value of an interactive French-language online educational program based on clinical cases designed to increase physicians' awareness of the diverse causes of AA amyloidosis. This initiative highlights the potential of digital educational tools to improve knowledge of rare diseases and could be adapted to other conditions in which earlier or more accurate diagnosis is needed.

AA挑战:一个关于AA淀粉样变原因的法语互动教育项目-对12项临床测试的2597份回复的分析
简介:AA型淀粉样变性是一种罕见但严重的慢性炎症性疾病并发症。其病因范围很广,可能导致诊断延误,特别是当根本原因罕见或认识不清时。我们开发了AA挑战,这是一个基于临床病例的交互式法语在线教育项目,以提高法语医生对AA淀粉样变病因的认识。方法:AA挑战是一项针对法语医师的为期一年的国际教育项目。它包括每月互动式临床病例测验,每个测验说明AA淀粉样变的不同原因或相关的鉴别诊断。参与者被要求根据所提供的临床、生物学和/或影像学资料确定潜在的病因。该计划通过电子邮件、社交媒体和淀粉样变相关组织的数字平台进行传播。一个由十个法语国家的医生组成的国际指导委员会为推广该方案作出了贡献。参与者还接受了AA淀粉样变的每月文献综述。对测验的回答、可用的参与者特征和最终满意度调查的结果进行了分析。结果:在2022 - 2023年间共发布临床病例12例。Eval&Go®平台共记录了2,968份回复。在排除重复提交后,2597份回复被纳入性能分析。2 536份答复提供了关于医学专业的信息。参与者主要是内科(n= 1534, 59.1%)、肾病学(n=470, 18.1%)和风湿病学(n=199, 7.7%)的专家。最具代表性的国家是摩洛哥(n=646, 24.9%)、法国(n=537, 20.7%)、罗马尼亚(n=420, 16.2%)和突尼斯(n=273, 10.5%)。正确反应率因病因而异,从AL淀粉样变测试的29.9%到克罗恩病测试的89.0%不等。最准确识别的病因是克罗恩病、类风湿性关节炎和脊椎关节炎,而AL淀粉样变性、肺结核相关的支气管扩张、甲羟戊酸激酶缺乏、低温蛋白相关的自身炎症综合征(CAPS)和原发性高草酸尿较少被识别。总体正确率为62.1%。每月的文献综述涵盖了25篇关于AA淀粉样变的出版物。最终的满意度调查收到124份回复,总体满意度很高,平均得分为8.61±1.36分(满分为10分)。结论:AA挑战展示了基于临床病例的交互式法语在线教育计划的可行性和价值,该计划旨在提高医生对AA淀粉样变性多种原因的认识。这一举措强调了数字教育工具在提高对罕见病的认识方面的潜力,并可适用于需要更早或更准确诊断的其他病症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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