Wang Jingyun, Hatt Sarah R, O'Connor Anna R, Drover James R, Adams Russell, Birch Eileen E, Holmes Jonathan M
Pediatric Eye Research Lab, Retina Foundation of the Southwest, Dallas, Texas 75231, USA.
J AAPOS. 2010 Apr;14(2):142-6. doi: 10.1016/j.jaapos.2009.12.159. Epub 2010 Mar 3.
Measurement of distance stereoacuity may be useful in assessing strabismic patients, especially those with intermittent exotropia. We developed the Distance Randot Stereotest as an easily administered quantitative test for distance stereoacuity in children. By using a prototype, we reported testability, validity, and normative data. Here we report normative and validity data for the final, commercially available version of the test.
We administered both the Prototype and the Final Version Distance Randot Stereotest to 156 normal volunteers (2-40 years of age) and 77 strabismic patients (4-62 years of age). Test-retest data were collected for the Final Version.
Normative Final Version scores were similar to those obtained with the Prototype; 96% were < or = 100 arcsec. Test-retests were identical in 82% and within one disparity level in 100%. Final Version scores were correlated with Prototype scores (rs = 0.64, p < 0.001). Among strabismic patients, 62.3% had abnormal stereoacuity; those with normal scores had incomitant or intermittent deviations. Nil stereoacuity was found in 27 patients, confirmed in 90.9% of retests; 17 had measurable stereoacuity, confirmed in 96.3% of retests. Patients with constant strabismus were more likely to have nil stereoacuity than patients who had intermittent strabismus (95% vs 12.2%).
Distance Randot scores from normal subjects have low variability within each age group and high test-retest reliability. There is little overlap between Distance Randot scores from normal control and strabismic patients. The Distance Randot Stereotest is a sensitive measurement of binocular sensory status that may be useful in monitoring progression of strabismus and/or recovery after strabismus surgery.
测量远距离立体视锐度可能有助于评估斜视患者,尤其是间歇性外斜视患者。我们开发了远距离兰多立体视测试,作为一种易于实施的儿童远距离立体视锐度定量测试。通过使用一个原型,我们报告了测试可行性、有效性和常模数据。在此,我们报告该测试最终商业可用版本的常模和有效性数据。
我们对156名正常志愿者(2至40岁)和77名斜视患者(4至62岁)进行了原型版和最终版远距离兰多立体视测试。收集了最终版的重测数据。
最终版的常模分数与原型版相似;96%的分数≤100角秒。82%的重测结果相同,100%在一个视差水平内。最终版分数与原型版分数相关(rs = 0.64,p < 0.001)。在斜视患者中,62.3%的人立体视锐度异常;分数正常的人有非共同性或间歇性斜视。27名患者立体视锐度为零,90.9%的重测结果得到证实;17名患者有可测量的立体视锐度,96.3%的重测结果得到证实。恒定斜视患者比间歇性斜视患者更有可能立体视锐度为零(95%对12.2%)。
正常受试者的远距离兰多分数在每个年龄组内变异性低,重测可靠性高。正常对照组和斜视患者的远距离兰多分数几乎没有重叠。远距离兰多立体视测试是一种对双眼感觉状态的敏感测量,可能有助于监测斜视的进展和/或斜视手术后的恢复情况。