Moorfields Eye Hospital, London, United Kingdom; Department of Ophthalmology, San Gerardo Hospital, Monza, Italy.
Moorfields Eye Hospital, London, United Kingdom; Institute of Ophthalmology, University College London, London, United Kingdom; Department of Ophthalmology, University of California, San Francisco, California.
Ophthalmology. 2015 Jun;122(6):1195-202. doi: 10.1016/j.ophtha.2015.02.002. Epub 2015 Mar 29.
To review the anatomic and visual outcomes of a series of children diagnosed with Coats' disease and treated on the basis of intraoperative fluorescein angiography (FA) findings.
Retrospective case series.
Twenty-five children 2 to 15 years of age diagnosed with early Coats' disease and treated after intraoperative FA.
Retrospective review of patients who underwent treatment for stage 2 Coats' disease in a tertiary center in the United Kingdom between 2007 and 2012. The children underwent treatment to the telangiectatic vessels and associated areas of retinal nonperfusion identified on intraoperative FA performed with a wide-angle retinal camera (RetCam II).
Anatomic and structural assessment of the retina after treatment, visual acuity (VA), and complications related to treatment.
Twenty children with Coats' disease who underwent intraoperative RetCam FA and retinal ablative treatment and who had more than 3 months of follow-up were identified from clinical records. All had unilateral disease. Six eyes were classified as stage 2a, and 14 eyes were classified as stage 2b. The median duration of follow-up was 21 months (mean, 26 months). Fifteen eyes needed 1 treatment to stabilize the disease, and 5 eyes needed a second treatment. None of the patients demonstrated progression of the disease to a more severe stage. Twelve eyes had a final VA of 0.4 logarithm of the minimum angle of resolution (logMAR) or better, 6 patients had VA between 0.4 and 1.0 logMAR, and 2 patients had VA worse than 1.0 logMAR.
The treatment of retinal telangiectasia and areas of retinal nonperfusion identified by wide-angle intraoperative FA in children with stage 2 Coats' disease led to good anatomic outcome, with preservation of VA in most cases.
回顾一系列根据术中荧光素血管造影(FA)检查结果诊断为 Coats 病并接受治疗的儿童的解剖学和视觉结果。
回顾性病例系列。
25 名 2 至 15 岁的儿童,被诊断为早期 Coats 病,并在术中 FA 后接受治疗。
回顾性分析 2007 年至 2012 年期间在英国一家三级中心接受治疗的 stage 2 Coats 病患者。在术中 FA 下,使用广角视网膜相机(RetCam II)对病变的毛细血管扩张血管和相关的视网膜无灌注区进行治疗。
治疗后的视网膜解剖结构和结构评估、视力(VA)和与治疗相关的并发症。
从临床记录中确定了 20 名接受术中 RetCam FA 和视网膜光凝治疗并随访超过 3 个月的 Coats 病儿童。所有患者均为单侧病变。6 只眼为 stage 2a,14 只眼为 stage 2b。中位随访时间为 21 个月(平均 26 个月)。15 只眼只需 1 次治疗即可稳定病情,5 只眼需要 2 次治疗。无一例患者的病情进展为更严重的阶段。12 只眼的最终 VA 为 0.4 对数最小角分辨率(logMAR)或更好,6 例患者的 VA 在 0.4 至 1.0 logMAR 之间,2 例患者的 VA 差于 1.0 logMAR。
对 stage 2 Coats 病儿童进行广角术中 FA 识别的视网膜毛细血管扩张和视网膜无灌注区的治疗可获得良好的解剖学结果,大多数病例可保留 VA。