Department of Ophthalmology and Visual Sciences, College of Medicine, University of Iowa, Iowa City, Iowa, USA.
Ophthalmology. 2011 Jan;118(1):119-133.e1-2. doi: 10.1016/j.ophtha.2010.04.019. Epub 2010 Aug 17.
To investigate systematically the natural history of visual outcome in central retinal vein occlusion (CRVO).
Cohort study.
Six hundred sixty-seven consecutive patients (30 patients had both eyes involved resulting in 697 eyes) with CRVO first seen in the authors' clinic from 1973 through 2000.
At the first visit, all patients underwent a detailed ophthalmic and medical history and a comprehensive ophthalmic evaluation. Visual evaluation was carried out by recording visual acuity, using the Snellen visual acuity chart, and assessing visual fields with a Goldmann perimeter. The same ophthalmic evaluation was performed at each follow-up visit. Central retinal vein occlusion was classified into nonischemic (588 eyes) and ischemic (109 eyes) types at the initial visit based on functional and morphologic criteria.
Visual acuity and visual fields.
Of the eyes first seen within 3 months, visual acuity was 20/100 or better in 78% with nonischemic CRVO and in only 1% with ischemic CRVO (P < 0.0001), and visual field defects were minimal or mild in 91% and 8%, respectively (P < 0.0001). Final visual acuity, on resolution of macular edema, was 20/100 or better in 83% with nonischemic CRVO and in only 12% with ischemic CRVO (P < 0.0001), and visual field defects were minimal or mild in 95% and 18%, respectively (P < 0.0001). On resolution of macular edema, in eyes with initial visual acuity of 20/70 or worse, visual acuity improved in 59% with nonischemic CRVO, with no significant (P = 0.55) improvement in ischemic CRVO. Similarly, on resolution of macular edema, in eyes with moderate to severe initial visual field defect, improvement was seen in 86% of nonischemic CRVO eyes, but no significant (P = 0.83) improvement was seen in eyes with ischemic CRVO. In nonischemic CRVO, development of foveal pigmentary degeneration, epiretinal membrane, or both, was the main cause of poor final visual acuity. This shows that initial presentation and the final visual outcome in the 2 types of CRVO are entirely different.
A clear differentiation of CRVO into nonischemic and ischemic types, based primarily on functional criteria, is crucial and fundamental in determining visual outcome. Visual outcome is good in nonischemic CRVO and poor in ischemic CRVO.
系统研究视网膜中央静脉阻塞(CRVO)的视力结果自然史。
队列研究。
1973 年至 2000 年期间,作者诊所首次就诊的连续 667 例(30 例双眼受累,共 697 只眼)CRVO 患者。
首次就诊时,所有患者均接受详细的眼科和病史以及全面的眼科评估。视力评估通过记录视力(使用 Snellen 视力表)和使用 Goldmann 视野计评估视野来进行。每次随访时均进行相同的眼科评估。根据功能和形态标准,在初次就诊时将视网膜中央静脉阻塞分为非缺血型(588 只眼)和缺血型(109 只眼)。
视力和视野。
在 3 个月内首次就诊的眼中,非缺血性 CRVO 的视力为 20/100 或更好的占 78%,而缺血性 CRVO 的仅占 1%(P<0.0001),视野缺损分别为轻度或中度的占 91%和 8%(P<0.0001)。非缺血性 CRVO 黄斑水肿消退后的最终视力为 20/100 或更好的占 83%,而缺血性 CRVO 的仅占 12%(P<0.0001),视野缺损分别为轻度或中度的占 95%和 18%(P<0.0001)。在黄斑水肿消退后,初始视力为 20/70 或更差的眼中,非缺血性 CRVO 的视力改善了 59%,而缺血性 CRVO 的视力无显著改善(P=0.55)。同样,在黄斑水肿消退后,非缺血性 CRVO 中度至重度初始视野缺损的眼中有 86%得到改善,而缺血性 CRVO 中无显著改善(P=0.83)。在非缺血性 CRVO 中,黄斑部色素变性、视网膜内膜或两者的发展是导致最终视力不佳的主要原因。这表明,这两种类型的 CRVO 的初始表现和最终视力结果完全不同。
主要基于功能标准将 CRVO 明确分为非缺血型和缺血型,对于确定视力结果至关重要。非缺血性 CRVO 的视力结果良好,而缺血性 CRVO 的视力结果不佳。