Sen Parveen, Bhende Muna, Sachidanandam Ramya, Bansal Nishat, Sharma Tarun
Department of Vitreoretinal Services, Shri Bhagwan Mahavir Vitreoretinal Services, Medical Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu, India.
Deaprtment of Optometry, Medical Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu, India.
Indian J Ophthalmol. 2016 Dec;64(12):908-913. doi: 10.4103/0301-4738.198856.
The aim was to study the efficacy of combined therapy with reduced-fluence photodynamic therapy (RFPDT) and intravitreal bevacizumab/ranibizumab from the Indian subcontinent.
This was a single-center, retrospective interventional study.
Thirty-five eyes of 34 patients diagnosed with polypoidal choroidal vasculopathy were included. All the patients underwent RFPDT, followed by intravitreal bevacizumab/ranibizumab.
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.
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).
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.
本研究旨在探讨低能量光动力疗法(RFPDT)联合玻璃体内注射贝伐单抗/雷珠单抗治疗来自印度次大陆的息肉样脉络膜血管病变的疗效。
这是一项单中心回顾性干预研究。
纳入34例诊断为息肉样脉络膜血管病变患者的35只眼,并对所有患者先进行RFPDT治疗,随后玻璃体内注射贝伐单抗/雷珠单抗。
使用SPSS 17.0软件(美国伊利诺伊州芝加哥市SPSS公司)比较就诊时及末次随访时最小分辨角视力的对数。P<0.05被认为具有统计学意义。
单次RFPDT治疗后,5只眼息肉消退;30只眼需要多次治疗。玻璃体内抗血管内皮生长因子(抗VEGF)注射的平均次数为4±1.9次,光动力治疗的平均次数为1.2±0.5次。21只眼(60%)视力提高(P<0.001),7只眼(20%)视力下降(P=0.016),7只眼(20%)视力保持稳定。80%的病例息肉样病变消退。在我们的患者中未观察到大量视网膜下出血或玻璃体出血突破等并发症。平均随访期为18个月(范围12 - 24个月)。
抗VEGF联合RFPDT是一种安全有效的治疗方法,80%的病例息肉消退且视力改善,无视网膜下出血/玻璃体出血并发症。