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METAMORPHOPSIA AND ITS QUANTIFICATION

机译:代谢性贫血及其量化

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Purpose:To discuss and analyze the pathophysiologic mechanisms underlying metamorphopsia, the nature of adaptational mechanisms to this symptom, the development and clinical utility of tests of metamorphopsia, and to discuss the cost-effectiveness of screening populations at risk of exudative age-related macular degeneration using such tests.Methods:A primary literature search of PubMed and Web of Science was conducted for articles covering the mechanisms and/or tests of metamorphopsia.Results:A number of possible mechanisms of metamorphopsia were identified in addition to lateral photoreceptor displacement. These included disorders of image formation, changes in effective axial length, and pathology of the visual pathways and centers. The simplest tests of metamorphopsia rely on highly subjective assessments of regular patterns, as exemplified by Amsler grids. Such tests seem to offer poor sensitivity when used in real-life home-monitoring situations. Newer tests such as so-called preferential hyperacuity perimetry may offer more robust paradigms to assess the perception of distortion but suffer from an inherent disadvantage of being unable to precisely correlate function to structure. The recently published findings of the AREDS2-HOME trial suggest that formalized monitoring of visual function using a preferential hyperacuity perimetry task results in detection of exudative age-related macular degeneration when vision is better-preserved. A cost-benefit analysis using the data from the AREDS2-HOME trial suggests that the calculated cost of screening per letter gained/saved is $3,351 per year.Conclusion:Metamorphopsia is an important symptom in retinal disease and may occur through a variety of mechanisms. Although the human visual system is exquisitely sensitive to metamorphopsia, commonly used tests of this symptom may be unreliable in real-life conditions. Newer tests of metamorphopsia such as preferential hyperacuity perimetry may improve early detection rates of exudative age-related macular degeneration in at-risk populations.
机译:目的:探讨和分析变态的潜在病理生理机制,适应这种症状的机制的性质,变态试验的发展和临床实用性,并讨论筛查具有渗出性年龄相关性黄斑变性风险的人群的成本效益方法:对PubMed和Web of Science进行了初步的文献检索,搜索了涉及变态的机制和/或测试的文章。结果:除了侧向感光体移位以外,还鉴定了许多可能的变态机制。这些包括图像形成障碍,有效轴向长度变化以及视觉通路和中心的病理。最简单的变态测试取决于对规则模式的高度主观评估,如Amsler网格所示。在现实生活中的家庭监控情况下,此类测试的灵敏度似乎较差。诸如所谓的优先超敏锐视力测定法之类的较新测试可以提供更健壮的范例来评估失真的感知,但存在无法将功能与结构精确关联的固有缺点。 AREDS2-HOME试验的最新发表的发现表明,当保留更好的视力时,使用优先的超敏锐度视野检查任务对视功能进行正式监测可检测出渗出性年龄相关性黄斑变性。使用AREDS2-HOME试验的数据进行的成本效益分析表明,获得/保存的每封信的筛查成本为每年3,351美元。结论:变形视力是视网膜疾病的重要症状,可能通过多种机制发生。尽管人类视觉系统对变形症非常敏感,但在现实生活中对这种症状的常用测试可能并不可靠。较新的变态检查,例如优先超敏眼视光检查,可以提高高危人群中与年龄相关的渗出性黄斑变性的早期发现率。

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