在初级医疗机构中对老年黄斑变性和糖尿病视网膜病变进行联合自动筛查。

Annals of Eye Science Pub Date : 2021-06-01 Epub Date: 2021-06-15 DOI:10.21037/aes-20-114
Alauddin Bhuiyan, Arun Govindaiah, Sharmina Alauddin, Oscar Otero-Marquez, R Theodore Smith
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引用次数: 0

摘要

背景:在美国和其他发达国家,老年性黄斑变性(AMD)和糖尿病视网膜病变(DR)是导致失明的主要原因之一。早期检测是预防和有效治疗的关键。方法:iHealthScreen 公司是一家独立的医疗软件公司,它利用基于深度机器学习技术的远程医疗平台开发了自动 AMD 和 DR 筛查系统。针对这两种疾病,我们对 340 名 50 岁以上未经选择的非散光受试者的双眼进行了前瞻性成像。具体到糖尿病,我们在纽约市的纽约眼耳学院视网膜诊所、眼科诊所和初级保健诊所为 152 名糖尿病患者拍摄了彩色眼底照相机。在对图像进行初步审查后,排除了 308 张存在高度近视和血管闭塞等其他混杂情况以及质量较差的图像,剩下 676 张符合 AMD 和 DR 评估条件的图像。三位眼科医生对每张图像进行了评估,经过裁定,患者被确定为可转诊或不可转诊为 AMD DR。在 AMD 方面,172 名患者被认定为可转诊(中期或晚期),504 名患者被认定为不可转诊(无或早期)。与此同时,关于 DR,33 例可转诊(中度或更严重),643 例不可转诊(无或轻度)。所有图像都上传到 iHealthScreen 的远程医疗平台,并由自动系统对这两种疾病进行分析。系统性能以每只眼睛为单位进行测试,测试结果包括敏感性、特异性、准确性以及与专业分级人员的 kappa 分数:在识别可转诊的 DR 方面,该系统的灵敏度为 97.0%,特异度为 96.3%,在前瞻性数据集上的 kappa 得分为 0.70。对于老年性黄斑变性,灵敏度为 86.6%,特异度为 92.1%,卡帕评分为 0.76:AMD和DR筛查工具在混合数据集中共同操作以前瞻性地识别两种视网膜疾病方面表现出色,证明了此类工具在眼病早期诊断中的可行性。这些早期筛查工具将有助于创建一个更全面的系统,能够对其他视网膜病变进行训练,这是公共卫生领域可以实现的目标。
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Combined automated screening for age-related macular degeneration and diabetic retinopathy in primary care settings.

Background: Age-related macular degeneration (AMD) and diabetic retinopathy (DR) are among the leading causes of blindness in the United States and other developed countries. Early detection is the key to prevention and effective treatment. We have built an artificial intelligence-based screening system which utilizes a cloud-based platform for combined large scale screening through primary care settings for early diagnosis of these diseases.

Methods: iHealthScreen Inc., an independent medical software company, has developed automated AMD and DR screening systems utilizing a telemedicine platform based on deep machine learning techniques. For both diseases, we prospectively imaged both eyes of 340 unselected non-dilated subjects over 50 years of age. For DR specifically, 152 diabetic patients at New York Eye and Ear faculty retina practices, ophthalmic and primary care clinics in New York city with color fundus cameras. Following the initial review of the images, 308 images with other confounding conditions like high myopia and vascular occlusion, and poor quality were excluded, leaving 676 eligible images for AMD and DR evaluation. Three ophthalmologists evaluated each of the images, and after adjudication, the patients were determined referrable or non-referable for AMD DR. Concerning AMD, 172 were labeled referable (intermediate or late), and 504 were non-referable (no or early). Concurrently, regarding DR, 33 were referable (moderate or worse), and 643 were non-referable (none or mild). All images were uploaded to iHealthScreen's telemedicine platform and analyzed by the automated systems for both diseases. The system performances are tested on per eye basis with sensitivity, specificity, accuracy, and kappa scores with respect to the professional graders.

Results: In identifying referable DR, the system achieved a sensitivity of 97.0% and a specificity of 96.3%, and a kappa score of 0.70 on this prospective dataset. For AMD, the sensitivity was 86.6%, the specificity of 92.1%, and a kappa score of 0.76.

Conclusions: The AMD and DR screening tools achieved excellent performance operating together to identify two retinal diseases prospectively in mixed datasets, demonstrating the feasibility of such tools in the early diagnosis of eye diseases. These early screening tools will help create an even more comprehensive system capable of being trained on other retinal pathologies, a goal within reach for public health deployment.

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