Shri Bhagwan Mahavir Vitreo Retinal Services, Sankara Nethralaya, 18 College Road, Chennai - 600 006, Tamil Nadu, India.
Indian J Ophthalmol. 2011 May-Jun;59(3):242-6. doi: 10.4103/0301-4738.81049.
This retrospective, interventional case series analyses treatment outcomes in eyes with choroidal neovascularization (CNV) secondary to pathological myopia, managed with photodynamic therapy, (PDT), (Group 1, N = 11), PDT and intravitreal triamcinolone acetonide (4 mg/0.1ml) (Group 2, N = 3), PDT and intravitreal anti-vascular endothelial growth factor (anti-VEGF) bevacizumab 1.25 mg/0.05 ml, ranibizumab 0.5 mg/0.05 ml and reduced-fluence PDT and intravitreal ranibizumab 0.5 mg/0.05 ml (Group 3, N=12). All the patients underwent PDT. Intravitreal injections were repeated as required. SPSS 14 software was used to evaluate the data. Wilcoxon signed ranks test was used to evaluate pre- and post-treatment vision. The Kruskal-Wallis test was used for comparison between the groups. All the groups were statistically comparable. All the eyes showed complete regression of CNV, with a minimum follow-up of six months. All groups had visual improvement; significantly in Group 3 ( p = 0.003). Combination PDT with anti-VEGF agents appeared to be efficacious in eyes with myopic CNV. However, a larger study with a longer follow-up is required to validate these results.
本回顾性、干预性病例系列分析了接受光动力疗法(PDT)治疗的病理性近视继发脉络膜新生血管(CNV)患者(第 1 组,N=11)、PDT 联合玻璃体腔内曲安奈德(4 mg/0.1ml)(第 2 组,N=3)、PDT 联合玻璃体腔内抗血管内皮生长因子(抗-VEGF)贝伐单抗 1.25 mg/0.05 ml、雷珠单抗 0.5 mg/0.05 ml 和低强度 PDT 联合玻璃体腔内雷珠单抗 0.5 mg/0.05 ml(第 3 组,N=12)的治疗结果。所有患者均接受 PDT 治疗。必要时重复进行玻璃体内注射。采用 SPSS 14 软件评估数据。Wilcoxon 符号秩检验用于评估治疗前后的视力。Kruskal-Wallis 检验用于组间比较。所有组在统计学上均具有可比性。所有眼均显示 CNV 完全消退,随访时间至少为 6 个月。所有组的视力均有改善;第 3 组的改善具有统计学意义(p=0.003)。PDT 联合抗 VEGF 药物似乎对近视性 CNV 有效。然而,需要更大规模的长期随访研究来验证这些结果。