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小儿患者中泰勒视力卡检查法的观察者间可靠性

Interobserver reliability of the Teller Acuity Card procedure in pediatric patients.

作者信息

Getz L M, Dobson V, Luna B, Mash C

机构信息

Department of Psychiatry, University of Pittsburgh, Pennsylvania, USA.

出版信息

Invest Ophthalmol Vis Sci. 1996 Jan;37(1):180-7.

PMID:8550321
Abstract

PURPOSE

To compare interobserver agreement for Teller Acuity Card estimates of grating acuity between children with ocular or neurologic abnormalities, or both, and age-matched healthy preterm children.

METHODS

Subjects were 57 children, 3 to 38 months of age, who were referred for visual assessment because of diagnosed or suspected visual impairment (clinical group), and 57 healthy preterm children with no known visual or neurologic abnormalities (control group), each of whom was matched to a clinical subject, based on corrected age at the time of testing, and type of testing (monocular or binocular). Each child's grating acuity was tested by two independent observers.

RESULTS

Interobserver agreement of 1 octave or better was found in 91% of the monocular and 96% of the binocular clinical test-retest comparisons and in 95% of the monocular and 96% of the binocular control comparisons. For estimates of interocular acuity difference, interobserver agreement of 1 octave or better was found in 88% of clinical subjects and 88% of control subjects. Average test time was significantly longer in the clinical group (4.1 minutes [SD = 1.9] for monocular and 3.6 minutes [SD = 1.9] for binocular tests) than in the control group (2.5 minutes [SD = 0.9] for monocular and 2.4 minutes [SD = 0.6] for binocular tests), suggesting that children in the clinical group were more difficult to test.

CONCLUSIONS

Teller Acuity Card testing conducted by experienced testers is as reliable in children with mild to severe ocular or neurologic abnormalities as it is in healthy children, even though children with abnormalities may be more difficult to test.

摘要

目的

比较患有眼部或神经异常或两者皆有的儿童与年龄匹配的健康早产儿童在使用泰勒视力卡评估光栅视力时观察者间的一致性。

方法

研究对象为57名3至38个月大的儿童,他们因已确诊或疑似视力障碍而被转诊进行视力评估(临床组),以及57名无已知视力或神经异常的健康早产儿童(对照组),每组中的每个儿童均根据测试时的矫正年龄和测试类型(单眼或双眼)与一名临床组儿童进行匹配。每个孩子的光栅视力由两名独立的观察者进行测试。

结果

在单眼临床测试 - 重测比较中,91%、双眼临床测试 - 重测比较中96%、单眼对照比较中95%以及双眼对照比较中96%的观察者间一致性达到1个倍频程或更好。对于双眼视力差异的评估,88%的临床组受试者和88%的对照组受试者的观察者间一致性达到1个倍频程或更好。临床组的平均测试时间显著长于对照组(单眼测试临床组为4.1分钟[标准差 = 1.9],双眼测试为3.6分钟[标准差 = 1.9];对照组单眼测试为2.5分钟[标准差 = 0.9],双眼测试为2.4分钟[标准差 = 0.6]),这表明临床组的儿童更难进行测试。

结论

由经验丰富的测试人员进行的泰勒视力卡测试,对于患有轻至重度眼部或神经异常的儿童与健康儿童一样可靠,尽管患有异常的儿童可能更难进行测试。

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