Reconstruction of highly and extremely aberrated wavefront for ocular Shack-Hartmann sensor using multi-task Attention-UNet

IF 3 2区 医学 Q1 OPHTHALMOLOGY
Yibin Tian , Zipei Luo , Dajiang Lu , Cheng Liu , Christine Wildsoet
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引用次数: 0

Abstract

In certain ocular conditions, such as in eyes with keratoconus or after corneal laser surgery, Higher Order Aberrations (HOAs) may be dramatically elevated. Accurately recording interpretable wavefronts in such highly aberrated eyes using Shack-Hartmann sensor is a challenging task. While there are studies that have applied deep neural networks to Shack-Hartmann wavefront reconstructions, they have been limited to low resolution and small dynamic range cases. In this study, we introduce a multi-task learning scheme for High-Resolution and High Dynamic Range Shack-Hartmann wavefront reconstruction using a modified attention-UNet (HR-HDR-SHUNet), which outputs a wavefront map along with Zernike coefficients simultaneously. The HR-HDR-SHUNet was evaluated on three large datasets with different levels of HOAs (regularly, highly, and extremely aberrated), with successful reconstruction of all aberrated wavefronts, at the same time achieving significantly higher accuracy than both traditional methods and other deep learning networks; it is also computationally more efficient than the latter.
基于多任务注意- unet的高像差和极像差眼传感器波前重建
在某些情况下,如圆锥角膜或角膜激光手术后,高阶像差(HOAs)可能会显著升高。在这种高度像差的眼睛中,使用沙克-哈特曼传感器准确记录可解释的波前是一项具有挑战性的任务。虽然有研究将深度神经网络应用于Shack-Hartmann波前重建,但它们仅限于低分辨率和小动态范围的情况。在这项研究中,我们引入了一种多任务学习方案,用于使用改进的注意力- unet (HR-HDR-SHUNet)进行高分辨率和高动态范围的Shack-Hartmann波前重建,该方案同时输出波前图和Zernike系数。HR-HDR-SHUNet在三个具有不同hoa水平(不规则、高度和极度像差)的大型数据集上进行了评估,成功重建了所有像差波前,同时获得了比传统方法和其他深度学习网络更高的精度;它在计算上也比后者更有效率。
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
Experimental eye research
Experimental eye research 医学-眼科学
CiteScore
6.80
自引率
5.90%
发文量
323
审稿时长
66 days
期刊介绍: The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.
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