Reduced-fluence photodynamic therapy and anti-vascular endothelial growth factor for polypoidal choroidal vasculopathy in an Indian population

被引:3
作者
Sen, Parveen [1 ]
Bhende, Muna [1 ]
Sachidanandam, Ramya [2 ]
Bansal, Nishat [1 ]
Sharma, Tarun [1 ]
机构
[1] Sankara Nethralaya, Med Res Fdn, Shri Bhagwan Mahavir Vitreoretinal Serv, Dept Vitreoretinal Serv, Madras, Tamil Nadu, India
[2] Sankara Nethralaya, Med Res Fdn, Dept Optometry, Madras, Tamil Nadu, India
关键词
Anti-vascular endothelial growth factor; photodynamic therapy; polypoidal choroidal vasculopathy; reduced fluence; EPITHELIUM-DERIVED FACTOR; INTRAVITREAL BEVACIZUMAB; MACULAR DEGENERATION; CLINICAL CHARACTERISTICS; JAPANESE PATIENTS; RANIBIZUMAB; VERTEPORFIN; ANGIOGRAPHY; MANAGEMENT; EXPRESSION;
D O I
10.4103/0301-4738.198856
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Aims: The aim was to study the efficacy of combined therapy with reduced-fluence photodynamic therapy (RFPDT) and intravitreal bevacizumab/ranibizumab from the Indian subcontinent. Settings and Design: This was a single-center, retrospective interventional study. Methods: Thirty-five eyes of 34 patients diagnosed with polypoidal choroidal vasculopathy were included. All the patients underwent RFPDT, followed by intravitreal bevacizumab/ranibizumab. Statistical Analysis Used: SPSS software, version 17.0 (SPSS Inc., Chicago, IL, USA) was used to compare the logarithm of the minimal angle of resolution visual acuity at presentation and final follow-up. P < 0.05 was considered statistically significant. Results: Regression of polyps after a single session of RFPDT was seen in five eyes; multiple sessions of treatment were required in thirty eyes. An average number of intravitreal anti-vascular endothelial growth factor (anti-VEGF) injections given were 4 +/- 1.9 and average number of PDT sessions were 1.2 +/- 0.5. Visual acuity improvement was seen in 21 (60%) eyes (P < 0.001), decrease in visual acuity was seen in 7 (20%) eyes (P = 0.016), and in 7 eyes (20%), vision remained stable. Regression of polypoidal lesions was seen in 80% of cases. No complications of massive subretinal hemorrhage or breakthrough vitreous hemorrhage were noted in our patients. The mean follow-up period was 18 months (range, 12-24 months). Conclusions: RFPDT with anti-VEGF is safe and effective treatment with polyp regression and vision improvement in 80% of cases, without any complication of subretinal hemorrhage/vitreous hemorrhage.
引用
收藏
页码:908 / 913
页数:6
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