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糖尿病眼部筛查的扫描共焦检眼镜检查(CONCORDIA)研究论文1。

The Scanning CONfoCal Ophthalmoscopy foR DIAbetic eye screening (CONCORDIA) study paper 1.

作者信息

Scanlon Peter H, Gruszka-Goh Marta, Javed Ushna, Vukic Anthony, Hapeshi Julie, Chave Steve, Galsworthy Paul, Vallance Scott, Aldington Stephen J

机构信息

Gloucestershire Retinal Research Group (GRRG), Cheltenham General Hospital, Cheltenham, UK.

Nuffield Department of Clinical Neuroscience, University of Oxford, Cheltenham, UK.

出版信息

Eye (Lond). 2024 Dec;38(18):3539-3546. doi: 10.1038/s41433-024-03360-2. Epub 2024 Oct 8.

Abstract

OBJECTIVE

This project was to determine the performance of the Zeiss Clarus 700 (Clarus) and the Optos California (Optos) with staged mydriasis in a Diabetic Eye Screening Programme (DESP).

METHODS

Trial participants were recruited from people attending appointments in DESP or Virtual Eye clinics for delayed hospital appointments. Non-mydriatic photographs from the Clarus and Optos cameras were compared to 2-field 45 degrees mydriatic digital photography (the reference standard) and mydriatic photographs compared if the non-mydriatic photos were unassessable (staged mydriasis).

RESULTS

1573 patients were recruited. 76 individuals were withdrawn, leaving 1497 individuals (2993 eyes). For the Clarus and the Optos, the sensitivity for any retinopathy were 94.2% (95% CI: 92.9-95.3%) and 91.9% (95% CI: 90.5-93.2%) with specificities of 87.3% (95% CI: 85.4-89.0%) and 78.1% (95% CI: 75.7-80.3%) respectively. For referable DR the sensitivities for the Clarus and Optos were 86.0% (95% CI: 82.9-88.8%) and 77.6% (95% CI: 73.9-80.9%) with specificities of 92.8% (95% CI: 91.7-93.8%) and 95.4% (95% CI: 94.5-96.2%) respectively. The Clarus and Optos without mydriasis produced 100 (3.3%) and 152 (5.1%) unassessable eyes respectively, and after staged mydriasis 51 (1.7%) and 102 (3.4%) respectively with 52 (1.7%) reference standard images unassessable.

CONCLUSIONS

This study reports the performance of the Clarus and the Optos using staged mydriasis in DR screening with wider fields detecting more referable retinopathy peripherally with some reduction in sensitivity centrally for macular lesions.

摘要

目的

本项目旨在确定蔡司Clarus 700(Clarus)和Optos California(Optos)在糖尿病眼病筛查项目(DESP)中进行分阶段散瞳检查时的性能。

方法

试验参与者从参加DESP预约或虚拟眼科诊所延迟医院预约的人群中招募。将Clarus和Optos相机拍摄的非散瞳照片与2视野45度散瞳数字摄影(参考标准)进行比较,如果非散瞳照片无法评估,则比较散瞳照片(分阶段散瞳)。

结果

共招募了1573名患者。76人退出,剩余1497人(2993只眼)。对于Clarus和Optos,任何视网膜病变的敏感度分别为94.2%(95%CI:92.9 - 95.3%)和91.9%(95%CI:90.5 - 93.2%),特异度分别为87.3%(95%CI:85.4 - 89.0%)和78.1%(95%CI:75.7 - 80.3%)。对于可转诊的糖尿病视网膜病变(DR),Clarus和Optos的敏感度分别为86.0%(95%CI:82.9 - 88.8%)和77.6%(95%CI:73.9 - 80.9%),特异度分别为92.8%(95%CI:91.7 - 93.8%)和95.4%(95%CI:94.5 - 96.2%)。未散瞳的Clarus和Optos分别产生了100只(3.3%)和152只(5.1%)无法评估的眼睛,分阶段散瞳后分别为51只(1.7%)和102只(3.4%),参考标准图像中有52只(1.7%)无法评估。

结论

本研究报告了Clarus和Optos在DR筛查中使用分阶段散瞳的性能,更宽的视野能检测到更多周边可转诊的视网膜病变,但黄斑病变的中央敏感度有所降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0d0/11621412/0ae9632b2691/41433_2024_3360_Fig1_HTML.jpg

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