Crosson Jason N, Swain Thomas A, Clark Mark E, Huisingh Carrie E, McGwin Gerald, Owsley Cynthia, Curcio Christine A
Retina Consultants of Alabama, Birmingham, Alabama; Department of Ophthalmology, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Department of Ophthalmology, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama; Department of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham, Alabama.
Ophthalmol Retina. 2019 Aug;3(8):670-680. doi: 10.1016/j.oret.2019.03.019. Epub 2019 Mar 30.
OCT has revealed many details of retinal disease that were not available with older imaging technologies. In eyes of adults older than 60 years with healthy maculas as determined by color fundus photography (CFP) and a validated grading system, we screened for pathologic features using OCT. We also tested visual function to assess potential impact of the observed pathologic features on patients.
Cross-sectional study.
Persons recruited from primary ophthalmology care clinics.
Color fundus photographs were assessed by the 9-step Age-Related Eye Disease Study scale. OCT macular volumes of participants at step 1 on the Age-Related Eye Disease Study scale, considered healthy, were reviewed by a retina specialist masked to other participant characteristics. Participants were tested for 6 different cone- and rod-mediated visual functions.
Percentage of participants with disorders detected on OCT review and visual function measures.
In 138 of 984 eyes (14%) considered healthy by CFP, pathologic features were detectable by OCT, with 8.4% having vitreomacular interface disorders. Among the low-prevalence disorders found, 5 eyes (0.5%) showed macular telangiectasia type 2. Relative to eyes lacking detectable chorioretinal pathologic features, eyes with any pathologic features were associated with poorer low-luminance visual acuity and rod-mediated dark adaptation. In eyes with epiretinal membranes, the largest single entity identified (n = 61 [6.2%]), significantly worse visual functions were best-corrected visual acuity (P = 0.0444), low-luminance visual acuity (P = 0.0151), and light sensitivity (central 3° and 9°; P = 0.0035 and P = 0.0097, respectively).
Macular pathologic features with functional visual implications not identified by clinical examination or CFP are detectable with OCT. Vitreomacular interface disorders often are visually significant and treatable conditions that are visible on OCT, but are easily missed on CFP and clinical examination. Another such condition best seen on OCT is macular telangiectasia type 2, an untreatable disorder for which a clinical trial is in progress. OCT has a potential role in primary eye care clinics to screen for retinal pathologic features, especially in eyes with decreased visual acuity and otherwise normal examination results.
光学相干断层扫描(OCT)揭示了许多视网膜疾病的细节,而这些细节是早期成像技术无法提供的。在年龄大于60岁、经彩色眼底照相(CFP)及有效分级系统判定黄斑健康的成年人眼中,我们使用OCT筛查病理特征。我们还测试了视觉功能,以评估所观察到的病理特征对患者的潜在影响。
横断面研究。
从眼科初级保健诊所招募的人员。
采用9步年龄相关性眼病研究量表评估彩色眼底照片。由一位对其他参与者特征不知情的视网膜专科医生复查年龄相关性眼病研究量表第1步中被认为健康的参与者的OCT黄斑体积。对参与者进行6种不同的视锥和视杆介导的视觉功能测试。
OCT复查及视觉功能测量中检测到疾病的参与者百分比。
在CFP认为健康的984只眼中,有138只(14%)通过OCT可检测到病理特征,其中8.4%有玻璃体黄斑界面疾病。在发现的低患病率疾病中,5只眼(0.5%)显示2型黄斑毛细血管扩张。与未检测到脉络膜视网膜病理特征的眼相比,有任何病理特征的眼与较差的低亮度视力和视杆介导的暗适应相关。在有视网膜前膜的眼中,这是识别出的最大单一病种(n = 61 [6.2%]),视觉功能明显更差的是最佳矫正视力(P = 0.0444)、低亮度视力(P = 0.0151)和光敏感度(中央3°和9°;分别为P = 0.0035和P = 0.0097)。
OCT可检测到临床检查或CFP未发现的具有功能性视觉影响的黄斑病理特征。玻璃体黄斑界面疾病通常具有视觉意义且可治疗,在OCT上可见,但在CFP和临床检查中容易漏诊。另一种在OCT上最易观察到的此类疾病是2型黄斑毛细血管扩张,这是一种正在进行临床试验的不可治疗疾病。OCT在眼科初级保健诊所有筛查视网膜病理特征的潜在作用,尤其是在视力下降但其他检查结果正常的眼中。