Department of Ophthalmology, University of Cologne, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.
Department of Biometry and Epidemiology, University of Erlangen, Erlangen, Germany.
Am J Ophthalmol. 2020 May;213:69-75. doi: 10.1016/j.ajo.2020.01.011. Epub 2020 Jan 16.
Impaired subjective morning visual acuity with improvement of symptoms during the day is pathognomonic for corneal endothelial dysfunction in advanced Fuchs endothelial corneal dystrophy (FECD). This study aimed to analyze the daily fluctuations of corneal thickness, refraction, and (glare) visual acuity in advanced FECD.
Prospective cohort study.
Patients with advanced FECD (FECD group) and patients with normal cornea (control group) were enrolled. Routine clinical examination was performed using slit-lamp biomicroscopy, funduscopy, and macular optical coherence tomography. In addition, assessment using corneal Scheimpflug tomography (Pentacam), refraction, corrected distance visual acuity (CDVA), and glare CDVA was performed at 4 PM (afternoon) and the following day at 8 AM (morning).
A total of 29 FECD eyes and 22 control eyes were included. Diurnal variations from afternoon to morning were Δ corneal thickness (apex) ± standard deviation (SD) 41.45 ± 34.1 μm (P < .001, FECD group) and 5.5 ± 6.72 μm (P = .001, control group); Δ spherical equivalent ± SD -0.64 ± 0.6 diopters (D) (P < .001, FECD group) and -0.01 ± 0.50 D (P = .461, control group); Δ total corneal refractive power ± SD 0.60 ± 0.83 D (P = .001, FECD group) and -0.01 ± 0.49 D (P = .602, control group), Δ CDVA ± SD 0.15 ± 0.18 logarithm of minimal angle of resolution (logMAR) (P < .001, FECD group) and 0.02 ± 0.04 logMAR (P = .174, control group), Δ CDVA glare ± SD 0.34 ± 0.25 logMAR (P < .001, FECD group) and 0.05 ± 0.11 logMAR (P = .106, control group).
A morning myopic shift and increased glare paralleling increased corneal thickness may particularly contribute to subjective visual impairment in advanced FECD in the first hours after awaking. This should be taken into account during assessment and surgical decision-making in patients with FECD.
在晚期 Fuchs 角膜内皮营养不良(FECD)中,白天症状改善时出现的主观早晨视力下降,伴有角膜内皮功能障碍,这是其特征性表现。本研究旨在分析晚期 FECD 患者角膜厚度、屈光度和(眩光)视力的日常波动情况。
前瞻性队列研究。
纳入晚期 FECD 患者(FECD 组)和正常角膜患者(对照组)。使用裂隙灯生物显微镜、眼底镜和黄斑光学相干断层扫描进行常规临床检查。此外,在下午 4 点(下午)和次日上午 8 点(早晨)使用角膜 Scheimpflug 断层扫描(Pentacam)、屈光度、矫正远视力(CDVA)和眩光 CDVA 进行评估。
共纳入 29 只 FECD 眼和 22 只对照眼。从下午到上午的日间变化为:角膜厚度(顶点)的 Δ ± 标准差(SD)为 41.45 ± 34.1μm(P<0.001,FECD 组)和 5.5 ± 6.72μm(P=0.001,对照组);Δ 球镜当量 ± SD 为-0.64 ± 0.6 屈光度(D)(P<0.001,FECD 组)和-0.01 ± 0.50 D(P=0.461,对照组);Δ 总角膜屈光力 ± SD 为 0.60 ± 0.83 D(P=0.001,FECD 组)和-0.01 ± 0.49 D(P=0.602,对照组);Δ CDVA ± SD 为 0.15 ± 0.18 最小分辨角对数(logMAR)(P<0.001,FECD 组)和 0.02 ± 0.04 logMAR(P=0.174,对照组);Δ CDVA 眩光 ± SD 为 0.34 ± 0.25 logMAR(P<0.001,FECD 组)和 0.05 ± 0.11 logMAR(P=0.106,对照组)。
早晨近视漂移和眩光增加,同时角膜厚度增加,这可能是导致晚期 FECD 患者醒来后最初几小时出现主观视力障碍的主要原因。在 FECD 患者的评估和手术决策中应考虑到这一点。