Comparison between Focal Laser Photocoagulation and Intravitreal Bevacizumab Injection for Treating Chronic Central Serous Chorioretinopathy

Young Bin Yoon, Woo Seok Choi, Kyoo Won Lee, Dong-Geun Park
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Abstract

Purpose: We compared the efficacy of focal laser photocoagulation and intravitreal bevacizumab injection in the treatment of chronic central serous chorioretinopathy.Methods: We conducted a retrospective analysis involving 46 eyes of 46 patients with chronic central serous chorioretinopathy who received focal laser photocoagulation (22 eyes) or intravitreal bevacizumab injection (24 eyes). Changes in best-corrected visual acuity (BVCA), central macular thickness, and rates of complete subretinal fluid (SRF) resolution and recurrence were compared over a 6-month period.Results: Although the focal laser photocoagulation and intravitreal bevacizumab injection groups demonstrated a significant reduction in central macular thickness at 6 months (p < 0.001), no statistically significant differences were observed between these groups at the end of the follow-up period. Notably, a gradual improvement in BVCA was observed in both groups following initial treatment, with significant improvement seen at 6 months (p = 0.049 and p = 0.048 for the laser and injection groups, respectively). However, no statistically significant difference in BVCA improvement was observed between the groups. Complete SRF resolution was achieved in 22 eyes in the laser group and 23 eyes in the injection group. Although recurrence of SRF was observed in 9 and 13 eyes in the laser and injection groups, respectively, there was no statistically significant difference between the groups (p = 0.229).Conclusions: Focal laser photocoagulation and intravitreal bevacizumab injection significantly improved anatomical and visual acuity outcomes in patients with chronic central serous chorioretinopathy. Although focal laser photocoagulation was associated with more rapid visual recovery and a lower recurrence rate compared to intravitreal bevacizumab injection, further studies are needed to evaluate its potential complications.
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治疗慢性中心性浆液性脉络膜视网膜病变的局部激光光凝与玻璃体内注射贝伐单抗的比较
目的:我们比较了局灶性激光光凝和玻璃体内注射贝伐单抗治疗慢性中心性浆液性脉络膜视网膜病变的疗效:我们对46名慢性中心性浆液性脉络膜视网膜病变患者的46只眼睛进行了回顾性分析,这些患者接受了局灶激光光凝(22只眼睛)或玻璃体内贝伐单抗注射(24只眼睛)。研究人员比较了6个月内最佳矫正视力(BVCA)、黄斑中心厚度以及视网膜下积液(SRF)完全消退率和复发率的变化:虽然病灶激光光凝组和玻璃体内贝伐单抗注射组在 6 个月时黄斑中心厚度显著降低(p < 0.001),但在随访期结束时,这两组之间并没有统计学意义上的显著差异。值得注意的是,在初始治疗后,两组的 BVCA 都有逐渐改善,6 个月时有明显改善(激光组和注射组分别为 p = 0.049 和 p = 0.048)。不过,两组之间的 BVCA 改善情况在统计学上没有明显差异。激光组中有 22 只眼睛实现了 SRF 完全消退,注射组中有 23 只眼睛实现了 SRF 完全消退。虽然激光组和注射组分别有 9 只和 13 只眼睛复发了 SRF,但两组之间的差异无统计学意义(P = 0.229):结论:局灶性激光光凝和玻璃体内注射贝伐单抗能显著改善慢性中心性浆液性脉络膜视网膜病变患者的解剖和视力。虽然与玻璃体内注射贝伐珠单抗相比,病灶激光光凝术的视力恢复更快,复发率更低,但仍需进一步研究以评估其潜在并发症。
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