AI-based assessment of Clinical Activity Score and detection of active thyroid eye disease using facial images: validation of Glandy CAS.

IF 2.2 Q2 OPHTHALMOLOGY
Kyubo Shin, Jin-Sook Yoon, Jongchan Kim, Jaemin Park, Hyun Young Park, Namju Kim, Min Joung Lee, Ho-Kyung Choung, JaeSang Ko, Jae Hoon Moon
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引用次数: 0

Abstract

Purpose: The Clinical Activity Score (CAS) is widely used to assess thyroid eye disease (TED) activity but can vary based on the evaluator's expertise. We developed and externally validated Glandy CAS, a machine learning (ML)-assisted system for detecting active TED (CAS ≥3) using digital facial images. This clinical trial aimed to gain approval from the Korea Ministry of Food and Drug Safety (KMFDS) for this Software as a Medical Device (SaMD).

Methods: This is a clinical trial based on the retrospective cohort. Glandy CAS analysed 756 photos of patients with TED, classifying them as having active or inactive TED. Its diagnostic performance was compared with that of three general ophthalmologists (less than 5 years of experience), using the F1 score. The reference CAS was determined by an oculoplastic specialist.

Results: Active TED was detected in 207 of 756 patients. Glandy CAS achieved a sensitivity of 87.9%, specificity of 95.8% and an F1 score of 0.88. In comparison, general ophthalmologists had a sensitivity of 60.4%, specificity of 83.0% and an F1 score of 0.57. Glandy CAS predicted CAS within 1 point of the reference score in 82.3% of cases, with a mean absolute error of 0.83.

Conclusions: Glandy CAS, an ML-assisted system for detecting active TED using facial images, showed high accuracy and outperformed general ophthalmologists. This system can consistently and accurately assess disease activity, facilitating early detection and timely treatment of active TED. Based on this clinical trial, the SaMD received KMFDS approval (Product Licence No., 24-93).

基于人工智能的临床活动评分评估和面部图像检测活动性甲状腺眼病:Glandy CAS的验证。
目的:临床活动评分(CAS)被广泛用于评估甲状腺眼病(TED)活动,但可能因评估者的专业知识而异。我们开发并外部验证了Glandy CAS,这是一种机器学习(ML)辅助系统,用于使用数字面部图像检测活动TED (CAS≥3)。该临床试验旨在获得韩国食品药品安全部(KMFDS)对该软件作为医疗器械(SaMD)的批准。方法:这是一个基于回顾性队列的临床试验。Glandy CAS分析了756张TED患者的照片,将他们分为活跃TED和不活跃TED。使用F1评分将其诊断效果与3名普通眼科医生(少于5年经验)的诊断效果进行比较。参考CAS由眼科整形专家确定。结果:756例患者中有207例检测到活性TED。Glandy CAS的敏感性为87.9%,特异性为95.8%,F1评分为0.88。相比之下,普通眼科医生的敏感性为60.4%,特异性为83.0%,F1评分为0.57。在82.3%的病例中,Glandy CAS预测的CAS与参考评分误差在1分以内,平均绝对误差为0.83。结论:Glandy CAS是一种基于人脸图像的机器学习辅助TED检测系统,具有较高的准确率,优于普通眼科医生。该系统能够持续准确地评估疾病活动性,有助于早期发现和及时治疗活动性TED。基于该临床试验,SaMD获得了KMFDS批准(产品许可证号:, 24 - 93)。
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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来源期刊
BMJ Open Ophthalmology
BMJ Open Ophthalmology OPHTHALMOLOGY-
CiteScore
3.40
自引率
4.20%
发文量
104
审稿时长
20 weeks
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