From The Eye Institute of Utah (Cionni), Salt Lake City, Utah, and Alcon Laboratories Inc. (Dimalanta, Breen, Hamilton), Fort Worth, Texas, USA.
From The Eye Institute of Utah (Cionni), Salt Lake City, Utah, and Alcon Laboratories Inc. (Dimalanta, Breen, Hamilton), Fort Worth, Texas, USA.
J Cataract Refract Surg. 2018 Oct;44(10):1230-1235. doi: 10.1016/j.jcrs.2018.07.016. Epub 2018 Aug 10.
To evaluate differences between the absolute prediction error using an intraoperative aberrometry (IA) device for intraocular lens (IOL) power determination versus the error that would have resulted if the surgeon's preoperative plan had been followed.
Multiple centers in the United States.
Retrospective analysis of data collected using an IA device.
The database information was limited according to predetermined inclusion/exclusion criteria. Primary endpoints included the difference between mean and median absolute prediction error with IA use versus preoperative calculation, and the percentage of cases were compared when the prediction error was 0.5 diopters (D) or less.
A total of 32 189 eyes were analyzed. The IA mean absolute prediction error was lower than the preoperative calculation, 0.30 D ± 0.26 (SD) versus 0.36 ± 0.32 D (P < .0001). The aberrometry absolute median prediction error was lower than the preoperative calculation, 0.24 D versus 0.29 D (P < .0001). There was a significantly greater percentage of eyes with an aberrometry absolute prediction error of 0.5 D or less than eyes with a preoperative absolute prediction error of 0.5 D or less (26 357 [81.9%] of 32 189 vs. 24 437 [75.9%] of 32 189, P < .0001). In addition, in those cases in which power of the IOL implanted was different than the preoperatively planned IOL power, significantly more eyes had an aberrometry absolute prediction error of 0.5 D or less (10 385 [81.3%] of 12 779 vs. 8794 [68.8%] of 12 779, P < .0001).
In a database of more than 30 000 eyes, calculations incorporating IA outperformed preoperative calculations. The difference was more pronounced in those cases in which the preoperatively planned IOL power was different than the power of the IOL implanted.
评估使用术中像差仪(IA)设备进行人工晶状体(IOL)屈光力计算的绝对预测误差与遵循术前医生计划的误差之间的差异。
美国多个中心。
对使用 IA 设备收集的数据进行回顾性分析。
根据预定的纳入/排除标准限制数据库信息。主要终点包括使用 IA 与术前计算相比,平均和中位数绝对预测误差的差异,以及当预测误差为 0.5 屈光度(D)或更小时的病例百分比。
共分析了 32189 只眼。IA 的平均绝对预测误差低于术前计算,分别为 0.30 D ± 0.26(SD)和 0.36 ± 0.32 D(P < 0.0001)。像差绝对中位数预测误差低于术前计算,分别为 0.24 D 和 0.29 D(P < 0.0001)。IA 绝对预测误差为 0.5 D 或更小的眼明显多于术前绝对预测误差为 0.5 D 或更小的眼(32189 只眼中的 26357 只[81.9%]与 32189 只眼中的 24437 只[75.9%],P < 0.0001)。此外,在植入的 IOL 屈光力与术前计划的 IOL 屈光力不同的情况下,IA 绝对预测误差为 0.5 D 或更小的眼明显更多(12779 只眼中的 10385 只[81.3%]与 12779 只眼中的 8794 只[68.8%],P < 0.0001)。
在超过 30000 只眼的数据库中,包含 IA 的计算优于术前计算。在术前计划的 IOL 屈光力与植入的 IOL 屈光力不同的情况下,差异更为明显。