Hayashi Ken, Hayashi Hideyuki
Hayashi Eye Hospital, 4-7-13 Hakataekimae, Hakata-ku, Fukuoka 812-0011, Japan.
J Cataract Refract Surg. 2004 Jul;30(7):1466-70. doi: 10.1016/j.jcrs.2003.12.030.
To investigate the stereoacuity in patients who have had implantation of a monofocal intraocular lens (IOL) in each eye and to identify the principal risk factors for impaired stereoacuity.
Hayashi Eye Hospital, Fukuoka, Japan.
One hundred patients scheduled for bilateral phacoemulsification and monofocal IOL implantation were recruited. Near stereoacuity was measured approximately 2 weeks after surgery using the Titmus test. Various parameters that may be associated with stereoacuity in pseudophakic patients were measured using the New Aniseikonia Test (Handaya Corp.). Parameters included age, visual acuity, spherical equivalent, astigmatism, axial length, pupil diameters, IOL decentration and tilt, and aniseikonia. Stepwise multiple regression analysis was performed to identify independent predictors of impaired stereoacuity.
The mean stereoacuity was 57.1 seconds of arc +/- 36.9 (SD); 90 patients (90%) had a good stereoacuity (ie, 100 seconds of arc or better). Simple regression analysis showed that a larger difference in spherical equivalent between fellow eyes and older age was significantly associated with poor stereoacuity. The best final model (R(2) = 0.375) in the multiple regression analysis identified a greater difference in spherical equivalent to be the most significant predictor of impaired stereoacuity, followed by older age and a larger pupil diameter.
Ninety percent of patients with bilateral pseudophakia had useful stereoacuity. The main risk factor for poor stereoacuity was a greater difference in the spherical equivalent between the eyes, followed by older age and a larger pupil diameter. These results indicate the need for an accurate preoperative IOL power calculation.
研究双眼植入单焦点人工晶状体(IOL)患者的立体视锐度,并确定立体视锐度受损的主要危险因素。
日本福冈市林眼科医院。
招募100例计划行双眼超声乳化白内障吸除术并植入单焦点IOL的患者。术后约2周使用Titmus测试测量近立体视锐度。使用新型不等像视测试(Handaya公司)测量可能与假晶状体患者立体视锐度相关的各种参数。参数包括年龄、视力、等效球镜度、散光、眼轴长度、瞳孔直径、IOL偏心和倾斜以及不等像。进行逐步多元回归分析以确定立体视锐度受损的独立预测因素。
平均立体视锐度为57.1角秒±36.9(标准差);90例患者(90%)具有良好的立体视锐度(即100角秒或更好)。简单回归分析显示,双眼等效球镜度差异较大和年龄较大与立体视锐度差显著相关。多元回归分析中最佳的最终模型(R² = 0.375)确定等效球镜度差异较大是立体视锐度受损的最显著预测因素,其次是年龄较大和瞳孔直径较大。
90%的双眼假晶状体患者具有有用的立体视锐度。立体视锐度差的主要危险因素是双眼等效球镜度差异较大,其次是年龄较大和瞳孔直径较大。这些结果表明术前准确计算IOL度数的必要性。