Glare prediction and mechanism of adaptation following implantation of hydrophilic and hydrophobic intraocular lenses

Gurpreet K. Bhogal-Bhamra, Maana Aujla, Sai Kolli, Amy L Sheppard, J. Wolffsohn
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Abstract

Glare is a known side effect of intraocular lens (IOL) implantation, affected principally by IOL material and optics, although it is reported subjectively to decrease in impact with time. However, little objective data have been published on changes over time, how these relate to subjective reports, and whether those who will report greater glare symptoms can be predicted prior to IOL implantation.A total of 32 patients (aged 72.4 ± 8.0 years) with healthy eyes were implanted bilaterally with hydrophilic 600s (Rayner, Worthing, UK) or hydrophobic Acrysof (Alcon, Texas, USA) acrylic IOLs (n = 16 each, randomly assigned). Each patient reported their dysphotopsia symptoms subjectively using the validated forced choice photographic questionnaire for photic phenomena, and halo size resulting from a bright light in a dark environment was quantified objectively in eight orientations using the Aston Halometer. Assessment was performed binocularly pre-operatively and at 1, 2, 3, and 4 weeks after IOL implantation.The study was carried out at the National Health Service Ophthalmology Department, Queen Elizabeth Hospital, Birmingham, UK.Visual acuity (average 0.37 ± 0.26 logMAR) did not correlate with subjective glare (r = 0.184, p = 0.494) or objective glare (r = 0.294, p = 0.270) pre-surgery. Objective halo size (F = 112.781, p < 0.001) decreased with cataract removal and IOL implantation and continued to decreased over the month after surgery. Subjective dysphotopsia complaints (p < 0.001) were also greater pre-surgery, but did not change thereafter (p = 0.228). In neither case was there a difference with IOL material (p > 0.05). It was not possible to predict post-surgery dysphotopsia from symptoms or a ratio of symptoms to halo size pre-surgery (p > 0.05).Subjective dysphotopsia and objective halos caused by cataracts are greatly reduced by implantation of IOL after cataract removal causing few perceivable symptoms. However, objective measures are able to quantify a further reduction in light scatter over the first month post-IOL implantation, suggesting that any subjective effects over this period are due to the healing process and not due to neuroadaptation.
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眩光预测和植入亲水性和疏水性眼内透镜后的适应机制
众所周知,眩光是眼内人工晶体(IOL)植入术的副作用之一,主要受人工晶体材料和光学器件的影响,不过据主观报告,眩光的影响会随着时间的推移而减弱。共有 32 名眼部健康的患者(年龄为 72.4 ± 8.0 岁)接受了双侧亲水性 600s(Rayner,英国沃辛)或疏水性 Acrysof(Alcon,美国德克萨斯州)丙烯酸人工晶体植入术(各 16 人,随机分配)。每位患者都使用经过验证的光现象强迫选择摄影问卷主观地报告了他们的视力障碍症状,并使用阿斯顿光晕计在八个方向上客观地量化了黑暗环境中的亮光所产生的光晕大小。视力(平均 0.37 ± 0.26 logMAR)与手术前的主观眩光(r = 0.184,p = 0.494)或客观眩光(r = 0.294,p = 0.270)无相关性。客观光晕大小(F = 112.781,p < 0.001)随着白内障摘除和人工晶体植入而减小,并在术后一个月内持续减小。主观视力障碍投诉(p < 0.001)在手术前也较大,但手术后没有变化(p = 0.228)。人工晶体材料也没有差异(p > 0.05)。白内障摘除术后植入人工晶体后,由白内障引起的主观视力障碍和客观光晕会大大减少,几乎不会出现可感知的症状。然而,客观测量能够量化人工晶体植入后第一个月内光散射的进一步减少,这表明这一时期内的任何主观影响都是由于愈合过程而非神经适应所致。
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