Pesudovs Konrad, Weisinger Harrison Scott
Department of Ophthalmology, Flinders Medical Centre, Flinders University, Bedford Park, South Australia, Australia.
Optom Vis Sci. 2004 Jul;81(7):554-8. doi: 10.1097/00006324-200407000-00018.
To compare the agreement between subjective refraction and autorefraction using two commercially available autorefractors.
Prospective data were collected for 190 subjects using either the Nidek ARK-700A (Fremont, CA) or the Topcon KR-8000 (Paramus, NJ) and subjective refraction (masked to autorefraction). Refractions were compared in terms of spherical equivalent using Bland-Altman limits of agreement and astigmatic vector difference using median and 95th percentile.
The two groups were similar for age, gender, spherical equivalent, and astigmatic power. The differences in spherical equivalent between subjective and autorefraction were significantly different (mean +/- SD; Nidek, -0.03 +/- 0.36 D; Topcon, +0.11 +/- 0.34 D; analysis of variance, F = 7.84; p < 0.01). However, the 95% limits of agreement were similar: Nidek, -0.74 to +0.68 D; Topcon, -0.55 to +0.77 D. The median differences in astigmatic vector difference were also similar: Nidek, 0.27 D and Topcon, 0.25 D. However, the 95th percentile was 0.67 D for Nidek and 1.09 D for Topcon. There was a low frequency of large (>1.00 D) differences in spherical equivalent, 1.1% with each autorefractor. There were five cases with astigmatic vector difference >1 D, all with the Topcon KR-8000 (5.3%).
Both autorefractors show excellent agreement with subjective refraction. Despite a statistically significant difference in mean spherical equivalent (0.14 D), near identical limits of agreement (0.10 D difference) suggest clinical equivalence. Conversely, for astigmatism, despite similar median scores, major outliers were more likely with the Topcon, reflected in a 0.42 D larger 95th percentile, which suggests a small advantage for the Nidek for avoiding large astigmatic errors.
使用两款市售自动验光仪比较主观验光与自动验光之间的一致性。
前瞻性收集了190名受试者的数据,使用尼德克ARK - 700A(加利福尼亚州弗里蒙特)或拓普康KR - 8000(新泽西州帕拉默斯)以及主观验光(对自动验光结果进行遮蔽)。使用布兰德 - 奥特曼一致性界限比较等效球镜度方面的验光结果,并使用中位数和第95百分位数比较散光矢量差。
两组在年龄、性别、等效球镜度和散光度数方面相似。主观验光与自动验光之间等效球镜度的差异具有显著统计学意义(均值±标准差;尼德克,-0.03±0.36 D;拓普康,+0.11±0.34 D;方差分析,F = 7.84;p < 0.01)。然而,95%一致性界限相似:尼德克,-0.74至+0.68 D;拓普康,-0.55至+0.77 D。散光矢量差的中位数差异也相似:尼德克为0.27 D,拓普康为0.25 D。然而,尼德克的第95百分位数为0.67 D,拓普康为1.09 D。等效球镜度差异大于1.00 D的情况频率较低,每种自动验光仪均为1.1%。有5例散光矢量差>1 D,均使用拓普康KR - 8000(5.3%)。
两款自动验光仪与主观验光均显示出良好的一致性。尽管等效球镜度均值存在显著统计学差异(0.14 D),但近乎相同的一致性界限(相差0.10 D)表明临床等效性。相反,对于散光,尽管中位数得分相似,但拓普康出现主要异常值的可能性更大,反映在第95百分位数大0.42 D,这表明尼德克在避免大散光误差方面有小优势。