用于诊断罕见骨病的人工智能:对医疗保健专业人员的全球调查。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Behnam Javanmardi, Rebekah L Waikel, Tinatin Tkemaladze, Shahida Moosa, Alexander Küsshauer, Jean Tori Pantel, Minu Fardipour, Peter Krawitz, Benjamin D Solomon, Klaus Mohnike
{"title":"用于诊断罕见骨病的人工智能:对医疗保健专业人员的全球调查。","authors":"Behnam Javanmardi, Rebekah L Waikel, Tinatin Tkemaladze, Shahida Moosa, Alexander Küsshauer, Jean Tori Pantel, Minu Fardipour, Peter Krawitz, Benjamin D Solomon, Klaus Mohnike","doi":"10.1186/s13023-025-03875-1","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Rare bone diseases (RBDs) are an important group of conditions characterized by abnormalities in bone and cartilage. Their large number, individual rarity, and heterogeneity make accurate and timely diagnosis challenging. Establishing correlations between genotype and phenotype (mainly via imaging) is critical for diagnosing RBDs. Image recognition artificial intelligence (AI) has the potential to significantly improve the diagnostic process by assisting healthcare providers to identify and differentiate imaging patterns associated with various RBDs. This survey study sought to assess the interest of various healthcare providers worldwide in utilizing an AI-based assistant tool for the differential diagnosis of RBDs.</p><p><strong>Method: </strong>Survey data were collected from March to September 2024. The survey was performed online and the link was disseminated via direct email, newsletters, and flyers at scientific talks and conferences.</p><p><strong>Results: </strong>We received 103 completed surveys, representing respondents from 27 different countries covering most global regions, but mostly from Europe, the United States, and Canada. The majority of the participants are physicians (n = 92, 89%) and primarily work at academic medical centers (n = 84, 81%). While each participant could select multiple specialties, the most frequent clinician types were medical geneticists, pediatricians, and endocrinologists, accounting for 71 (69%) of the respondents. Ninety-four (91%) of the respondents find imaging to be very or extremely important, and the majority (n = 84, 81%) consider X-rays to be the most important imaging modality. Although around half of the participants (n = 45) have concerns about AI-related errors and consider the explainability of AI algorithms to be very (42/103) or extremely (9/103) important, 81% of the respondents report that they are somewhat (n = 39) or extremely (n = 45) likely to consider integrating image recognition AI into their current diagnostic workflow.</p><p><strong>Conclusions: </strong>Most survey participants are open to integrating image recognition AI into their RBD diagnostic workflow. However, concerns about AI-related errors, privacy, and model interpretability highlight the importance of transparent collaboration between developers and healthcare professionals throughout the development process to ensure that such technologies are clinically trustworthy and practically adoptable.</p>","PeriodicalId":19651,"journal":{"name":"Orphanet Journal of Rare Diseases","volume":"20 1","pages":"365"},"PeriodicalIF":3.4000,"publicationDate":"2025-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Artificial intelligence for diagnosing rare bone diseases: a global survey of healthcare professionals.\",\"authors\":\"Behnam Javanmardi, Rebekah L Waikel, Tinatin Tkemaladze, Shahida Moosa, Alexander Küsshauer, Jean Tori Pantel, Minu Fardipour, Peter Krawitz, Benjamin D Solomon, Klaus Mohnike\",\"doi\":\"10.1186/s13023-025-03875-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Rare bone diseases (RBDs) are an important group of conditions characterized by abnormalities in bone and cartilage. Their large number, individual rarity, and heterogeneity make accurate and timely diagnosis challenging. Establishing correlations between genotype and phenotype (mainly via imaging) is critical for diagnosing RBDs. Image recognition artificial intelligence (AI) has the potential to significantly improve the diagnostic process by assisting healthcare providers to identify and differentiate imaging patterns associated with various RBDs. This survey study sought to assess the interest of various healthcare providers worldwide in utilizing an AI-based assistant tool for the differential diagnosis of RBDs.</p><p><strong>Method: </strong>Survey data were collected from March to September 2024. The survey was performed online and the link was disseminated via direct email, newsletters, and flyers at scientific talks and conferences.</p><p><strong>Results: </strong>We received 103 completed surveys, representing respondents from 27 different countries covering most global regions, but mostly from Europe, the United States, and Canada. The majority of the participants are physicians (n = 92, 89%) and primarily work at academic medical centers (n = 84, 81%). While each participant could select multiple specialties, the most frequent clinician types were medical geneticists, pediatricians, and endocrinologists, accounting for 71 (69%) of the respondents. Ninety-four (91%) of the respondents find imaging to be very or extremely important, and the majority (n = 84, 81%) consider X-rays to be the most important imaging modality. Although around half of the participants (n = 45) have concerns about AI-related errors and consider the explainability of AI algorithms to be very (42/103) or extremely (9/103) important, 81% of the respondents report that they are somewhat (n = 39) or extremely (n = 45) likely to consider integrating image recognition AI into their current diagnostic workflow.</p><p><strong>Conclusions: </strong>Most survey participants are open to integrating image recognition AI into their RBD diagnostic workflow. However, concerns about AI-related errors, privacy, and model interpretability highlight the importance of transparent collaboration between developers and healthcare professionals throughout the development process to ensure that such technologies are clinically trustworthy and practically adoptable.</p>\",\"PeriodicalId\":19651,\"journal\":{\"name\":\"Orphanet Journal of Rare Diseases\",\"volume\":\"20 1\",\"pages\":\"365\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2025-07-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Orphanet Journal of Rare Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1186/s13023-025-03875-1\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Orphanet Journal of Rare Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1186/s13023-025-03875-1","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

摘要

背景:罕见骨病(rbd)是一类以骨和软骨异常为特征的重要疾病。其数量多、个体罕见和异质性使得准确和及时的诊断具有挑战性。建立基因型和表型之间的相关性(主要通过成像)对于诊断rbd至关重要。图像识别人工智能(AI)有可能通过帮助医疗保健提供者识别和区分与各种rbd相关的成像模式来显著改善诊断过程。本调查研究旨在评估全球各种医疗保健提供者对利用基于人工智能的辅助工具进行rbd鉴别诊断的兴趣。方法:于2024年3月~ 9月收集调查资料。该调查是在线进行的,链接通过直接电子邮件、新闻通讯和科学讲座和会议的传单传播。结果:我们收到了103份完整的调查,代表了来自27个不同国家的受访者,覆盖了全球大部分地区,但主要来自欧洲、美国和加拿大。大多数参与者是医生(n = 92,89%),主要在学术医疗中心工作(n = 84,81%)。虽然每个参与者可以选择多个专业,但最常见的临床医生类型是医学遗传学家、儿科医生和内分泌学家,占受访者的71人(69%)。94名(91%)受访者认为成像非常或极其重要,大多数(n = 84,81%)认为x射线是最重要的成像方式。尽管大约一半的参与者(n = 45)担心人工智能相关的错误,并认为人工智能算法的可解释性非常(42/103)或极其(9/103)重要,但81%的受访者报告说,他们有点(n = 39)或非常(n = 45)可能考虑将图像识别人工智能集成到他们当前的诊断工作流程中。结论:大多数调查参与者对将图像识别AI集成到他们的RBD诊断工作流程持开放态度。然而,对人工智能相关错误、隐私和模型可解释性的担忧突出了开发人员和医疗保健专业人员在整个开发过程中透明协作的重要性,以确保这些技术在临床上值得信赖和实际可采用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Artificial intelligence for diagnosing rare bone diseases: a global survey of healthcare professionals.

Background: Rare bone diseases (RBDs) are an important group of conditions characterized by abnormalities in bone and cartilage. Their large number, individual rarity, and heterogeneity make accurate and timely diagnosis challenging. Establishing correlations between genotype and phenotype (mainly via imaging) is critical for diagnosing RBDs. Image recognition artificial intelligence (AI) has the potential to significantly improve the diagnostic process by assisting healthcare providers to identify and differentiate imaging patterns associated with various RBDs. This survey study sought to assess the interest of various healthcare providers worldwide in utilizing an AI-based assistant tool for the differential diagnosis of RBDs.

Method: Survey data were collected from March to September 2024. The survey was performed online and the link was disseminated via direct email, newsletters, and flyers at scientific talks and conferences.

Results: We received 103 completed surveys, representing respondents from 27 different countries covering most global regions, but mostly from Europe, the United States, and Canada. The majority of the participants are physicians (n = 92, 89%) and primarily work at academic medical centers (n = 84, 81%). While each participant could select multiple specialties, the most frequent clinician types were medical geneticists, pediatricians, and endocrinologists, accounting for 71 (69%) of the respondents. Ninety-four (91%) of the respondents find imaging to be very or extremely important, and the majority (n = 84, 81%) consider X-rays to be the most important imaging modality. Although around half of the participants (n = 45) have concerns about AI-related errors and consider the explainability of AI algorithms to be very (42/103) or extremely (9/103) important, 81% of the respondents report that they are somewhat (n = 39) or extremely (n = 45) likely to consider integrating image recognition AI into their current diagnostic workflow.

Conclusions: Most survey participants are open to integrating image recognition AI into their RBD diagnostic workflow. However, concerns about AI-related errors, privacy, and model interpretability highlight the importance of transparent collaboration between developers and healthcare professionals throughout the development process to ensure that such technologies are clinically trustworthy and practically adoptable.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信