Department of Ophthalmology, University of Lausanne, Jules-Gonin Eye Hospital, Fondation Asile des Aveugles, Lausanne, Switzerland.
Retina. 2018 Nov;38(11):2239-2246. doi: 10.1097/IAE.0000000000001866.
To determine the age distribution of children with Coats disease and the impact of age at diagnosis on the visual prognosis.
Consecutive Coats disease cases aged 18 years or younger at diagnosis were retrospectively included. Clinical and imaging parameters were analyzed by comparative, correlation, survival, univariate, and multivariate statistics.
Ninety-eight patients were included. At diagnosis, mean age was 5.4 years ± 4.3 years (1 month-18 years). Younger age at diagnosis was correlated with more severe disease stage (P < 0.0001, r = -0.52), which was confirmed by survival analysis (P < 0.0001). Comparative analysis was performed between patients younger and older than 4 years at diagnosis. Leukocoria or strabismus was more frequent at presentation in patients younger than 4 years (P < 0.0001). Areas of peripheral nonperfusion and peripheral telangiectasia were more extensive at presentation in younger than older patients (P = 0.0003 and P = 0.039). Foveal sparing at diagnosis was less frequent in younger than older patients (2% vs. 23%, P = 0.002). The incidence of structural complications or enucleation during follow-up (mean duration: 5.9 years ± 4.5 years) was higher, and last-recorded visual acuity was lower in younger than older patients (P = 0.001 and P = 0.0009). Final logarithm of the minimal angle of resolution visual acuity was negatively correlated with age at diagnosis (P = 0.001, Spearman r = -0.42). Multivariate analysis indicated that disease stage (P < 0.0001), but not age at diagnosis (P = 0.07), independently influenced the last-recorded visual acuity.
Onset of Coats disease in children of younger age is associated with more severe manifestations, more advanced stage, and worse visual outcome. Age, correlated with disease stage, should be considered a prognostic marker in Coats disease.
确定 Coats 病患儿的年龄分布以及诊断时的年龄对视觉预后的影响。
回顾性纳入了 18 岁以下诊断为 Coats 病的连续病例。通过比较、相关性、生存、单变量和多变量统计分析来分析临床和影像学参数。
共纳入 98 例患者。诊断时的平均年龄为 5.4 岁±4.3 岁(1 个月-18 岁)。诊断时年龄越小,疾病分期越严重(P<0.0001,r=-0.52),生存分析也证实了这一点(P<0.0001)。在诊断时年龄小于 4 岁和大于 4 岁的患者之间进行了比较分析。在年龄小于 4 岁的患者中,更常见的表现是白瞳或斜视(P<0.0001)。在年龄小于 4 岁的患者中,更常见的表现是周边无灌注区和周边毛细血管扩张(P=0.0003 和 P=0.039)。在诊断时保留中心凹的情况在年龄小于 4 岁的患者中较少见(2%比 23%,P=0.002)。在随访期间(平均随访时间:5.9 岁±4.5 岁),年龄较小的患者发生结构性并发症或眼球摘除的发生率更高,最后记录的视力也更低(P=0.001 和 P=0.0009)。最小分辨角对数视力的最终值与诊断时的年龄呈负相关(P=0.001,Spearman r=-0.42)。多变量分析表明,疾病分期(P<0.0001),而不是诊断时的年龄(P=0.07),独立影响最后记录的视力。
儿童 Coats 病的发病年龄越小,表现越严重,分期越晚,视力预后越差。年龄与疾病分期相关,应被视为 Coats 病的预后标志物。