Department of Ophthalmology and Visual Sciences, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.
Bahamas Vision Center and Princess Margaret Hospital, Nassau, Bahamas.
Eur J Ophthalmol. 2024 May;34(3):683-690. doi: 10.1177/11206721231204383. Epub 2023 Oct 3.
To report the emergence and progress of four late-stage characteristics: incomplete retinal pigment epithelium and outer retinal atrophy (iRORA) and complete RPE and outer retinal atrophy (cRORA), drusen ooze and drusen collapse in eyes with dry age-related macular degeneration (AMD) using Spectral Domain Optical Coherence Tomography (SD-OCT).
This was a retrospective analysis of eyes with non-exudative AMD. Multimodal imaging was done at follow up visits ≤ 12 months. OCT volume scan was used to assess and identify the 4 characteristics. Univariate analysis was done for the various demographic and clinical characteristics.Patients with a mean age of 76.7 ± 10 years were followed up for 69.9 ± 20.6 months. iRORA, cRORA, drusen ooze was present in 15.6%, 15.6% and 15.6% of patients at baseline, respectively, and 25.0%, 40.6% and 53.1% of patients at the final follow-up, respectively. At baseline 9.1%, 0% and 9.1% of patients had bilateral drusen ooze, iRORA and cRORA, respectively. By the final follow-up, drusen collapse occurred in 46.9% and 18.8% patients in unilateral and bilateral eyes, respectively.For bilateral cases, the mean interval of time between emergence inthe two eyes for drusen ooze, drusen collapse, iRORA, and cRORA was 5 ± 1.4 years, 2.2 ± 2.2 years, 3.5 ± 0.7 and 1.7 ± 0.6 years, respectively.
Late-stage OCT biomarkers are seen bilaterally at 21.9% at baseline and at 56.3% at 5.8 years follow-up. Once present in one eye, cRORA had the shortest mean interval before appearance in the other eye.
报告在干性年龄相关性黄斑变性(AMD)患者中使用谱域光相干断层扫描(SD-OCT)出现和进展的四个晚期特征:不完全性视网膜色素上皮和外层视网膜萎缩(iRORA)以及完全性 RPE 和外层视网膜萎缩(cRORA)、渗出性硬性渗出和硬性渗出塌陷。
这是一项对非渗出性 AMD 患者的回顾性分析。在随访≤12 个月时进行多模态成像。使用 OCT 容积扫描来评估和识别这 4 种特征。对各种人口统计学和临床特征进行单变量分析。患者平均年龄为 76.7±10 岁,随访时间为 69.9±20.6 个月。在基线时,分别有 15.6%、15.6%和 15.6%的患者存在 iRORA、cRORA 和硬性渗出塌陷,在最终随访时,分别有 25.0%、40.6%和 53.1%的患者存在这些特征。在基线时,分别有 9.1%、0%和 9.1%的患者双眼存在硬性渗出塌陷、iRORA 和 cRORA。在最终随访时,分别有 46.9%和 18.8%的单侧和双侧患者出现硬性渗出塌陷。对于双侧病例,硬性渗出、硬性渗出塌陷、iRORA 和 cRORA 分别出现在双眼的平均时间间隔为 5±1.4 年、2.2±2.2 年、3.5±0.7 年和 1.7±0.6 年。
在基线时有 21.9%的患者存在晚期 OCT 生物标志物,在 5.8 年随访时有 56.3%的患者存在晚期 OCT 生物标志物。一旦出现在一眼,cRORA 出现在另一眼的平均时间间隔最短。