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临床实践中遗传性色觉缺陷的评估。

Assessment of inherited colour vision defects in clinical practice.

作者信息

Cole Barry L

机构信息

Department of Optometry and Vision Sciences, The University of Melbourne, Australia.

出版信息

Clin Exp Optom. 2007 May;90(3):157-75. doi: 10.1111/j.1444-0938.2007.00135.x.

DOI:10.1111/j.1444-0938.2007.00135.x
PMID:17425762
Abstract

BACKGROUND

Colour vision deficiency (CVD) has a high prevalence and is often a handicap in everyday life. Those who have CVD will be better able to adapt and make more informed career choices, if they know about their deficiency. The fact that from 20 to 30 per cent of adults with abnormal colour vision do not know they have CVD suggests that colour vision is not tested as often as it should be. This may be because of practitioner uncertainty about which tests to use, how to interpret them and the advice that should be given to patients on the basis of the results. The purpose of this paper is to recommend tests for primary care assessment of colour vision and provide guidance on the advice that can be given to patients with CVD.

METHODS

The literature on colour vision tests and the relationship between the results of the tests and performance at practical colour tasks was reviewed.

RESULTS

The colour vision tests that are most suitable for primary care clinical practice are the Ishihara test, the Richmond HRR 4th edition 2002 test, the Medmont C-100 test and the Farnsworth D15 test. These tests are quick to administer, give clear results and are easy to interpret. Tables are provided summarising how these tests should be interpreted, the advice that can be given to CVD patients on basis of the test results, and the occupations in which CVD is a handicap.

CONCLUSION

Optometrists should test the colour vision of all new patients with the Ishihara and Richmond HRR (2002) tests. Those shown to have CVD should be assessed with the Medmont C-100 test and the Farnsworth D15 test and given appropriate advice based on the test results.

摘要

背景

色觉缺陷(CVD)患病率很高,且在日常生活中常常造成不便。患有CVD的人如果了解自己的缺陷,将能更好地适应并做出更明智的职业选择。事实上,20%至30%的色觉异常成年人并不知道自己患有CVD,这表明色觉测试的频率未达到应有的水平。这可能是因为从业者对于使用哪些测试、如何解读测试结果以及应根据结果向患者提供何种建议存在不确定性。本文旨在推荐用于初级保健中色觉评估的测试,并为患有CVD的患者提供相关建议指导。

方法

回顾了有关色觉测试以及测试结果与实际颜色任务表现之间关系的文献。

结果

最适合初级保健临床实践的色觉测试有石原氏测试、2002年版里士满HRR第4版测试、Medmont C - 100测试和 Farnsworth D15测试。这些测试实施快速,结果清晰,易于解读。文中提供了表格,总结了这些测试应如何解读、根据测试结果可向CVD患者提供的建议以及CVD会造成不便的职业。

结论

验光师应对所有新患者使用石原氏测试和里士满HRR(2002)测试来检测色觉。那些被证明患有CVD的患者应使用Medmont C - 100测试和 Farnsworth D15测试进行评估,并根据测试结果给予适当建议。

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1
Assessment of inherited colour vision defects in clinical practice.临床实践中遗传性色觉缺陷的评估。
Clin Exp Optom. 2007 May;90(3):157-75. doi: 10.1111/j.1444-0938.2007.00135.x.
2
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Clin Exp Optom. 2006 Mar;89(2):73-80. doi: 10.1111/j.1444-0938.2006.00015.x.
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Search for coloured objects in natural surroundings by people with abnormal colour vision.色觉异常者在自然环境中寻找有色物体。
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Using clinical tests of colour vision to predict the ability of colour vision deficient patients to name surface colours.利用色觉临床测试来预测色觉缺陷患者命名表面颜色的能力。
Ophthalmic Physiol Opt. 2007 Jul;27(4):381-8. doi: 10.1111/j.1475-1313.2007.00493.x.
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Abnormal colour vision is a handicap to playing cricket but not an insurmountable one.色觉异常对打板球来说是个障碍,但并非无法克服。
Clin Exp Optom. 2007 Nov;90(6):451-6. doi: 10.1111/j.1444-0938.2006.00180.x.
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Impact of congenital colour vision defects on occupation.先天性色觉缺陷对职业的影响。
Arch Dis Child. 2005 Sep;90(9):906-8. doi: 10.1136/adc.2004.062067. Epub 2005 May 24.
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Does the Farnsworth D15 test predict the ability to name colours?法恩斯沃思 D15 测试能否预测颜色命名能力?
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