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Clinical research on one-third dose verteporfin photodynamic therapy in the treatment of chronic central serous chorioretinopathy

机译:三分之一剂量维替泊芬光动力疗法治疗慢性中央性浆液性脉络膜视网膜病变的临床研究

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OBJECTIVE: To observe the curative effect and safety of one-third dose Verteporfin photodynamic therapy (PDT) in the treatment of chronic central serous chorioretinopathy (CSC). PATIENTS AND METHODS: A total of 60 patients (68 eyes) treated in our hospital from January 2016 to December 2016 were selected in this study, and they were diagnosed with chronic CSC via fluorescein fundus angiography (FFA), indocyanine green angiography (ICGA) and optical coherence tomography (OCT). Besides, patients were treated with one-third conventional dose Verteporfin PDT. The subfoveal choroidal thickness (SFCT), superior, inferior, nasal and temporal choroidal thickness at 1.5 mm away from macula central fovea, central choroidal capillary layer thickness, photoreceptor layer thickness, best corrected visual acuity (BCVA), subretinal fluid absorption, FFA and ICGA manifestations and complications of patients were observed and recorded before treatment and at 1, 3 and 6 months after treatment. RESULTS: After PDT via one-third conventional dose of Verteporfin, patients were followed up for 1 month, 3 months, and 6 months. The SFCT of affected eyes was changed from (381.23 ± 83.29) μm before treatment to (385.31 ± 90.89) μm, (369.59 ± 75.60) μm and (374.08 ± 102.81) μm successively, and the differences were statistically significant (p 0.05). At 6 months after treatment, the subretinal fluid in 63 eyes (92.6%) completely subsided, and a little subretinal fluid was retained in 5 eyes (7.4%). FFA and ICGA showed the choroidal vessel dilatation in affected eyes after treatment and significantly improved moderate-advanced high fluorescein leakage compared with that before treatment. There were no obvious complications in the body and fundus during the follow-up period. CONCLUSIONS: One-third dose Verteporfin PDT can improve BCVA, stop or reduce the choroidal vasodilatation and leakage, accelerate the absorption of serous subretinal fluid, and help the recovery of photoreceptor layer of patients with chronic CSC, which is safe and reliable.
机译:目的:观察三分之一剂量的维替泊芬光动力疗法(PDT)治疗慢性中央性浆液性脉络膜视网膜病变(CSC)的疗效和安全性。患者与方法:选择2016年1月至2016年12月在我院接受治疗的60例患者(68眼),通过荧光素眼底血管造影(FFA),吲哚菁绿血管造影(ICGA)诊断为慢性CSC。和光学相干断层扫描(OCT)。此外,患者接受了常规剂量Verteporfin PDT的三分之一治疗。距黄斑中央凹1.5 mm处的中央凹脉络膜厚度(SFCT),上,下,鼻和颞脉络膜厚度,中央脉络膜毛细血管层厚度,感光层厚度,最佳矫正视力(BCVA),视网膜下液吸收,FFA和在治疗前以及治疗后1、3和6个月观察并记录患者的ICGA表现和并发症。结果:PDT通过常规剂量的Verteporfin的三分之一后,患者接受了1个月,3个月和6个月的随访。患眼的SFCT从治疗前的(381.23±83.29)μm依次变为(385.31±90.89)μm,(369.59±75.60)μm和(374.08±102.81)μm,差异具有统计学意义(p 0.05)。治疗6个月后,63只眼(92.6%)的视网膜下液完全消退,5只眼(7.4%)的视网膜下液被保留。 FFA和ICGA显示治疗后患眼的脉络膜血管扩张,与治疗前相比,中度晚期高荧光素渗漏明显改善。在随访期间,身体和眼底无明显并发症。结论:Verteporfin PDT的三分之一剂量可改善BCVA,阻止或减少脉络膜血管舒张和渗漏,加速浆液性视网膜下液的吸收,并有助于慢性CSC患者的感光层恢复,安全可靠。

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