Ophthalmology. 1998 Jan;105(1):11-23.
This study aimed to describe the short-term effects of low-intensity laser treatment in eyes with drusen at risk of having choroidal neovascularization (CNV) develop secondary to age-related macular degeneration.
The study design was a multicentered, randomized clinical trial of laser treatment versus observation.
One hundred fifty-six patients without exudative age-related macular degeneration and with more than 10 large (> 63 microns) drusen in each eye were enrolled in the Bilateral Drusen Study. One hundred twenty patients with exudative age-related macular degeneration in 1 eye and more than 10 large drusen in the other eye were enrolled in the Fellow Eye Study.
The treatment protocol for most (85%) of the eyes consisted of 20 laser burns, 100 microns in diameter, in a pattern of 3 rows placed between the 12- and 6-o'clock positions beyond the temporal perimeter of the foveal avascular zone. The desired intensity of the burns was a gray-white lesion. Whenever the area of drusen had not been reduced by 50% or more at 6 months, a second treatment was applied nasal to the fovea in a mirror image of the first treatment. During the last 6 months of enrollment, a second laser treatment protocol was adopted that specified 24 laser burns, 100 microns in diameter, in a circular pattern of 2 rows surrounding the macular drusen.
Change in visual acuity is the primary outcome measure. Incidence of CNV, change in contrast threshold, and change in critical print size are secondary outcome measures.
In the Bilateral Drusen Study, CNV developed in 4 of 156 treated eyes and in 2 of 156 observed eyes (P = 0.62); in the Fellow Eye Study, the proportions are 10/59 treated eyes and 2/61 observed eyes (P = 0.02). Changes in visual acuity are similar in treated and observed eyes in the Bilateral Drusen Study through 18 months. However, by 18 months, observed eyes in the Fellow Eye Study have lost more visual acuity than treated eyes (P = 0.02). Changes in contrast threshold are similar in treated and observed eyes in each study.
Laser treatment to high-risk fellow eyes may increase the short-term incidence of CNV. Long-term effects in fellow eyes and effects in patients with bilateral drusen require additional observation.
本研究旨在描述低强度激光治疗对存在脉络膜新生血管(CNV)风险的玻璃膜疣眼的短期影响,这些玻璃膜疣眼继发于年龄相关性黄斑变性。
本研究设计为激光治疗与观察的多中心随机临床试验。
156例无渗出性年龄相关性黄斑变性且每只眼有超过10个大(>63微米)玻璃膜疣的患者纳入双侧玻璃膜疣研究。120例一只眼有渗出性年龄相关性黄斑变性且另一只眼有超过10个大玻璃膜疣的患者纳入对侧眼研究。
大多数(85%)眼睛的治疗方案包括在黄斑无血管区颞侧边缘以外12点至6点位置以3排模式进行20次直径100微米的激光烧灼。烧灼所需强度为灰白色病变。如果6个月时玻璃膜疣面积未减少50%或更多,则在黄斑中心凹鼻侧以第一次治疗的镜像方式进行第二次治疗。在入组的最后6个月,采用了第二种激光治疗方案,即围绕黄斑玻璃膜疣以2排圆形模式进行24次直径100微米的激光烧灼。
视力变化是主要观察指标。CNV发病率、对比阈值变化和临界印刷字体大小变化是次要观察指标。
在双侧玻璃膜疣研究中,156只接受治疗的眼中有4只发生CNV,156只观察眼中有2只发生CNV(P = 0.62);在对侧眼研究中,相应比例为治疗的59只眼中有10只,观察的61只眼中有2只(P = 0.02)。在双侧玻璃膜疣研究中,治疗眼和观察眼的视力变化在18个月内相似。然而,到18个月时,对侧眼研究中的观察眼比治疗眼丧失了更多视力(P = 0.02)。每项研究中治疗眼和观察眼的对比阈值变化相似。
对高危对侧眼进行激光治疗可能会增加CNV的短期发病率。对侧眼的长期影响以及双侧玻璃膜疣患者的影响需要进一步观察。