Ophthalmology. 2003 May;110(5):971-8. doi: 10.1016/S0161-6420(03)00098-8.
To update the findings from the Choroidal Neovascularization Prevention Trial (CNVPT) with respect to resolution of drusen, incidence of choroidal neovascularization, and visual function.
A multicenter, randomized, controlled, pilot clinical trial.
The 120 patients enrolled in the CNVPT. Patients had signs of choroidal neovascularization or retinal pigment epithelial detachment in 1 eye and had >/=10 large (>63- micro m) drusen in the contralateral, or fellow, eye.
The fellow eye of 59 patients was assigned randomly to argon green laser treatment consisting of multiple 100- micro m spots at least 750 micro m from the center of the fovea. The fellow eye of the remaining 61 patients was assigned randomly to observation.
Change in visual acuity was the primary outcome measure. Incidence of choroidal neovascularization, resolution of drusen, change in contrast threshold, change in critical print size for reading, and incidence of geographic atrophy were secondary outcome measures.
Throughout 4 years of follow-up, there were no statistically significant differences in change in visual acuity, contrast threshold, critical print size, or incidence of geographic atrophy. With additional follow-up, the large increase in the incidence of choroidal neovascularization observed within 18 months of treatment was maintained; however, by 30 months, the incidence in the two treatment groups was the same. Most drusen resolution in treated eyes occurred within 24 months of the initial treatment. Treated eyes that received higher-intensity laser burns had an increased risk of choroidal neovascularization. Among eyes developing choroidal neovascularization in each treatment group, most lesions (two thirds or more) were composed of occult neovascularization only.
Laser treatment as applied in the CNVPT caused an excess risk of choroidal neovascularization in the first year or so after treatment. The increased early incidence of choroidal neovascularization was not associated with either a harmful or beneficial effect in this pilot study.
更新脉络膜新生血管预防试验(CNVPT)关于玻璃膜疣消退、脉络膜新生血管发生率及视功能的研究结果。
一项多中心、随机、对照的试点临床试验。
120名参与CNVPT的患者。患者一只眼睛有脉络膜新生血管或视网膜色素上皮脱离体征,对侧眼或另一只眼有≥10个大的(>63微米)玻璃膜疣。
59名患者的对侧眼被随机分配接受氩绿激光治疗,由多个距黄斑中心至少750微米的100微米光斑组成。其余61名患者的对侧眼被随机分配接受观察。
视力变化是主要观察指标。脉络膜新生血管发生率、玻璃膜疣消退情况、对比阈值变化、阅读临界印刷字体大小变化及地图样萎缩发生率为次要观察指标。
在4年的随访期间,视力变化、对比阈值、临界印刷字体大小或地图样萎缩发生率无统计学显著差异。随着随访时间延长,治疗后18个月内观察到的脉络膜新生血管发生率大幅增加的情况持续存在;然而,到30个月时,两个治疗组的发生率相同。治疗眼的大多数玻璃膜疣消退发生在初始治疗后的24个月内。接受高强度激光烧灼的治疗眼发生脉络膜新生血管的风险增加。在每个治疗组中发生脉络膜新生血管的眼中,大多数病变(三分之二或更多)仅由隐匿性新生血管组成。
CNVPT中应用的激光治疗在治疗后的第一年左右导致脉络膜新生血管风险增加。在这项试点研究中,脉络膜新生血管早期发生率增加与有害或有益影响均无关。