利用多模态成像预测晚期老年性黄斑变性发展的临床表现。

IF 4.9 2区 医学 Q1 OPHTHALMOLOGY
Kai Lyn Goh BOptom, PhD, Carla J. Abbott BOptom, PhD, Thomas G. Campbell DPhil, FRANZCO, Amy C. Cohn MMed, FRANZCO, Dai Ni Ong BMedSc(Hons), FRANZCO, Sanjeewa S. Wickremasinghe DMSc, FRANZCO, Lauren A. B. Hodgson MPH, Robyn H. Guymer PhD, FRANZCO, Zhichao Wu BAppSc(Optom), PhD
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引用次数: 0

摘要

背景:目的:研究使用多模态成像(MMI)预测晚期老年性黄斑变性(AMD)发展的临床表现与仅使用彩色眼底照相(CFP)相比是否有所改善,以及这与使用已确立的AMD风险因素的基本预测模型相比有何不同:本研究中的 AMD 患者在基线时接受了包括光学相干断层扫描 (OCT)、眼底自动荧光、近红外反射和 CFP 在内的 MMI 检查,然后在 3 年内每 6 个月接受一次检查,以确定 MMI 定义的晚期 AMD 发展情况。四位视网膜专家分别用 CFP 和 MMI 评估了每只基线眼在 3 年内发展为 MMI 定义的晚期 AMD 的可能性。CFP和MMI的预测性能相互比较,并与使用年龄、是否存在色素异常和基于OCT的色素沉着量的基本预测模型进行比较:临床医生使用 CFP 的预测性能[AUC = 0.75;95% 置信区间 (CI) = 0.68-0.82]在使用 MMI 时有所提高(AUC = 0.79;95% CI = 0.72-0.85;p = 0.034)。然而,基本预测模型的表现优于使用 CFP 或 MMI 的临床医生(AUC = 0.85;95% CI = 0.78-91;p ≤ 0.002):结论:与CFP相比,使用MMI预测晚期AMD发展的临床效果更好。结论:与CFP相比,使用MMI预测AMD晚期发展的临床表现更好。然而,使用成熟的AMD风险因素的基本预测模型的表现优于视网膜专家,这表明这种模型可以进一步改善临床实践中对AMD早期患者的个性化咨询和监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical performance of predicting late age-related macular degeneration development using multimodal imaging

Clinical performance of predicting late age-related macular degeneration development using multimodal imaging

Background

To examine whether the clinical performance of predicting late age-related macular degeneration (AMD) development is improved through using multimodal imaging (MMI) compared to using colour fundus photography (CFP) alone, and how this compares with a basic prediction model using well-established AMD risk factors.

Methods

Individuals with AMD in this study underwent MMI, including optical coherence tomography (OCT), fundus autofluorescence, near-infrared reflectance and CFP at baseline, and then at 6-monthly intervals for 3-years to determine MMI-defined late AMD development. Four retinal specialists independently assessed the likelihood that each eye at baseline would progress to MMI-defined late AMD over 3-years with CFP, and then with MMI. Predictive performance with CFP and MMI were compared to each other, and to a basic prediction model using age, presence of pigmentary abnormalities, and OCT-based drusen volume.

Results

The predictive performance of the clinicians using CFP [AUC = 0.75; 95% confidence interval (CI) = 0.68–0.82] improved when using MMI (AUC = 0.79; 95% CI = 0.72–0.85; p = 0.034). However, a basic prediction model outperformed clinicians using either CFP or MMI (AUC = 0.85; 95% CI = 0.78–91; p ≤ 0.002).

Conclusions

Clinical performance for predicting late AMD development was improved by using MMI compared to CFP. However, a basic prediction model using well-established AMD risk factors outperformed retinal specialists, suggesting that such a model could further improve personalised counselling and monitoring of individuals with the early stages of AMD in clinical practice.

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来源期刊
CiteScore
7.60
自引率
12.50%
发文量
150
审稿时长
4-8 weeks
期刊介绍: Clinical & Experimental Ophthalmology is the official journal of The Royal Australian and New Zealand College of Ophthalmologists. The journal publishes peer-reviewed original research and reviews dealing with all aspects of clinical practice and research which are international in scope and application. CEO recognises the importance of collaborative research and welcomes papers that have a direct influence on ophthalmic practice but are not unique to ophthalmology.
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