Lai Timothy Y Y, Wong Raymond L M, Chan Wai-Man
Department of Ophthalmology & Visual Sciences, The Chinese University of Hong Kong, Hong Kong 2010 Retina & Macula Centre, Kowloon, Hong Kong.
Department of Ophthalmology & Visual Sciences, The Chinese University of Hong Kong, Hong Kong.
Trans Am Ophthalmol Soc. 2015;113:T8.
To evaluate whether half-dose verteporfin photodynamic therapy (PDT) is better than natural history for the treatment of central serous chorioretinopathy (CSC).
Retrospective review of consecutive CSC patients treated with half-dose verteporfin PDT or untreated with observation and a minimum follow-up of 36 months. The main outcome measures included mean change in visual acuity and CSC recurrence. Survival analysis was performed to compare the CSC recurrence rates between the two groups.
A total of 192 eyes of 192 patients were included; 75 eyes were treated with half-dose verteporfin PDT and 117 were untreated. The mean follow-up duration was 74.1 months. At the last follow-up, the mean logMAR visual acuity was significantly better in the half-dose verteporfin PDT group compared with the untreated control group (P=.005). The mean visual improvement of the half-dose verteporfin PDT group at the last follow-up was 1.8 lines, compared with 0.0 line in the untreated control group (P<.001). Recurrence of CSC developed in 15 eyes (20%) in the half-dose verteporfin PDT group compared with 63 eyes (53.8%) in the untreated control group (P<.001). Survival analysis demonstrated that eyes treated with half-dose verteporfin PDT were significantly less likely to develop CSC recurrence compared with untreated controls (P<.001). Regression analysis showed that half-dose verteporfin PDT was the only significant factor in reducing the risk of CSC recurrence.
Half-dose verteporfin PDT for the treatment of CSC resulted in significantly better visual acuity outcomes and lower recurrence rate in the long term compared with untreated controls.
评估半剂量维替泊芬光动力疗法(PDT)治疗中心性浆液性脉络膜视网膜病变(CSC)是否优于自然病程。
回顾性分析连续接受半剂量维替泊芬PDT治疗或未治疗仅观察且随访至少36个月的CSC患者。主要观察指标包括视力的平均变化和CSC复发情况。进行生存分析以比较两组CSC的复发率。
共纳入192例患者的192只眼;75只眼接受半剂量维替泊芬PDT治疗,117只眼未治疗。平均随访时间为74.1个月。在最后一次随访时,半剂量维替泊芬PDT组的平均logMAR视力显著优于未治疗的对照组(P = 0.005)。半剂量维替泊芬PDT组在最后一次随访时的平均视力改善为1.8行,而未治疗对照组为0.0行(P < 0.001)。半剂量维替泊芬PDT组有15只眼(20%)发生CSC复发,未治疗对照组有63只眼(53.8%)发生复发(P < 0.001)。生存分析表明,与未治疗的对照组相比,接受半剂量维替泊芬PDT治疗的眼发生CSC复发的可能性显著降低(P < 0.001)。回归分析显示,半剂量维替泊芬PDT是降低CSC复发风险的唯一显著因素。
与未治疗的对照组相比,半剂量维替泊芬PDT治疗CSC在长期内可显著改善视力并降低复发率。