青光眼视野的计算机辅助判读。

Acta ophthalmologica. Supplement Pub Date : 1992-01-01
P Asman
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引用次数: 0

摘要

视野异常是青光眼的重要诊断征象。因此,视野丧失的存在与否通常会强烈影响青光眼的诊断和治疗决策。然而,解释视野结果通常是困难的。生理变化的周边灵敏度值有助于这些困难。我们的目标是开发改进的计算机辅助方法来识别早期青光眼视野丧失。因此,我们的方法是设计对微小但显著偏离常态高度敏感的技术。我们已经研究了正常的生理变异性的周边测量结果,并将所获得的知识与病理生理模型相结合,该模型对青光眼中常见的视野丧失的空间模式敏感。因此,我们设计了概率评分,以考虑复杂的生理变异性,并基于视网膜神经纤维层的正常解剖结构开发了半场分析和弓形聚类分析。在本项目中,收集规范数据和选择青光眼病例的基本方法是使用非视界标准选择受试者(除去大视场缺陷)。我们的目标是减少对视野的先入为主的偏见。该方法用于(1)生理变异的实证研究,(2)分析方法的开发,以及(3)对这些方法的评估。青光眼患者的选择基于视盘外观的评估。正常受试者从未仅根据周边测量结果排除。与以前可用的技术相比,在这些研究中开发的新方法显着改善了正常和青光眼视野结果的区分。我们的研究结果表明,概率分数的使用是这种改进的主要来源,而观测到的异常场的位置和空间建模是其他重要因素。没有正确结合空间分析和规范分析的候选方法导致中外周假阳性缺陷和/或低估了中央旁青光眼野缺陷。基于视野结果的意义分类和视野丧失的特定空间模式识别的类似方法可用于将视野异常作为重要诊断标志的其他疾病组。(摘要删节为400字)
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Computer-assisted interpretation of visual fields in glaucoma.

Visual field abnormality is an important diagnostic sign in glaucoma. Therefore, the presence or absence of visual field loss most often strongly influences diagnostic and therapeutic decisions in glaucoma management. Interpretation of visual field results is often difficult, however. Physiological variability of perimetric sensitivity values contributes to these difficulties. It has been our aim to develop improved computer-assisted methods for the recognition of early glaucomatous field loss. Our approach has therefore been to design techniques that are highly sensitive to small but significant departures from normality. We have investigated normal physiological variability in perimetric results and combined the obtained knowledge with pathophysiological models which are sensitive to the spatial patterns of field loss commonly seen in glaucoma. Thus, we have devised probability scores in order to take the complex physiological variability into account, and developed a hemifield analysis and an arcuate cluster analysis based on the normal anatomy of the retinal nerve fibre layer. A fundamental approach in the collection of normative data and the selection of glaucoma cases used in this project has been to select subjects using non-perimetric criteria (except for the removal of large field defects). Our objective here was to reduce bias from pre-conceived ideas of visual fields. This approach was used for (1) empirical studies on physiological variability, (2) development of analysis methods, and (3) evaluation of such methods. Glaucoma patients were selected based on evaluations of optic disc appearance. Normal subjects were never eliminated on the basis of perimetric results alone. The new methods developed in these studies have significantly improved discrimination between normal and glaucomatous field results, as compared with previously available techniques. Our results indicated that the usage of probability scores was the main source of this improvement, and that the location of observed field abnormalities and spatial modelling were other important factors. Candidate methods which did not properly combine spatial and normative analyses resulted in false positive defects in the mid-periphery and/or underestimated paracentral glaucomatous field defects. Similar approaches based on classification of visual field results in terms of significances, and on recognition of specific spatial patterns of field loss could be used for other groups of diseases having visual field abnormality as an important diagnostic sign.(ABSTRACT TRUNCATED AT 400 WORDS)

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