Service d'Ophtalmologie, Hôpital Pellegrin, Centre Hospitalier et Unversitaire de Bordeaux, France.
J Refract Surg. 2011 Dec;27(12):869-75. doi: 10.3928/1081597X-20110725-01. Epub 2011 Jul 29.
To assess glistenings in AcrySof (Alcon Laboratories Inc) intraocular lenses (IOLs), to quantify any effects of glistenings on the visual function of patients with healthy eyes, and to investigate whether glistenings were associated with demographic or lens characteristics.
Case files from a consecutive series of healthy eyes were retrospectively analyzed. Subjective glistening grades were investigated for associations with the following parameters: contrast sensitivity, corrected distance visual acuity (CDVA), intraocular light scattering (measured by C-Quant [Oculus Optikgeräte GmbH]), posterior capsule opacification, demographic characteristics, lens power, and duration of pseudophakia. The subjective grading method was compared to objective software-based quantitation of glistenings.
The study cohort included 97 eyes from 65 patients with a mean age of 65 ± 11 years. Mean follow-up was 18 ± 17 months. Glistening grades did not vary by duration of pseudophakia (P=.19), although study design limited confidence in this result. Glistening grades had no associations with lens power (P=.41), intraocular light scattering (P=.31), logMAR CDVA (P=.64), contrast sensitivity at any spatial frequency (all P ≥.22), or with any other parameter under investigation. The software-based assessment confirmed the validity of the subjective grading method: glistening grades correlated with vacuoles/mm(2) (P<.0001) and mean values for vacuoles/mm(2) were statistically significant for each glistening grade (all P ≤.004).
In healthy eyes, glistening grade was not associated with contrast sensitivity, CDVA, intraocular light scatter, or any lens or demographic characteristics that were investigated.
评估 AcrySof(爱尔康实验室公司)人工晶状体(IOL)中的闪光现象,量化闪光对健康人眼视觉功能的任何影响,并研究闪光是否与人口统计学或晶状体特征有关。
回顾性分析连续系列健康眼中的病例档案。研究了主观闪光等级与以下参数的相关性:对比敏感度、矫正远视力(用 C-Quant[Oculus Optikgeräte GmbH]测量)、眼内光散射、后囊混浊、人口统计学特征、晶状体度数和人工晶状体植入时间。将主观分级方法与闪光的基于客观软件的定量进行了比较。
该研究队列包括 65 名患者的 97 只眼,平均年龄为 65±11 岁。平均随访时间为 18±17 个月。闪光等级与人工晶状体植入时间无相关性(P=.19),尽管研究设计对此结果的可信度有限。闪光等级与晶状体度数(P=.41)、眼内光散射(P=.31)、logMAR 远视力(P=.64)、任何空间频率的对比敏感度(均 P≥.22)或任何其他研究参数均无相关性。基于软件的评估证实了主观分级方法的有效性:闪光等级与空泡/平方毫米(mm²)(P<.0001)相关,并且每个闪光等级的空泡/mm²平均值均具有统计学意义(均 P≤.004)。
在健康眼中,闪光等级与对比敏感度、远视力、眼内光散射或任何调查的晶状体或人口统计学特征均无相关性。