Department of Ophthalmology, Leiden University Medical Center, Leiden, the Netherlands.
Department of Ophthalmology, University Hospital of Cologne, Cologne, Germany; F. Hoffmann-La Roche, Basel, Switzerland.
Ophthalmology. 2018 Oct;125(10):1547-1555. doi: 10.1016/j.ophtha.2018.04.021. Epub 2018 Jun 14.
To compare the anatomic and functional efficacy and safety of half-dose photodynamic therapy (PDT) versus high-density subthreshold micropulse laser (HSML) treatment in patients with chronic central serous chorioretinopathy (cCSC).
Open-label, multicenter, randomized controlled clinical trial.
Patients with cCSC whose disease had to be confirmed by both clinical characteristics and findings on multimodal imaging.
Eligible patients were randomized in a 1:1 allocation ratio. Treatment was evaluated during a follow-up visit, and the same treatment was repeated in patients who still demonstrated subretinal fluid (SRF).
The primary end point was the complete disappearance of SRF at the first evaluation visit at 6 to 8 weeks after treatment. As a secondary outcome measure, we assessed this anatomic result at the final evaluation visit at 7 to 8 months after treatment. Other secondary outcomes covered functional improvement and included change in best-corrected visual acuity (BCVA; measured in Early Treatment Diabetic Retinopathy Study [ETDRS] letters), retinal sensitivity (measured using microperimetry), and vision-related quality of life using a validated questionnaire.
Between November 2013 and September 2016, 179 patients were included: 89 patients were assigned randomly to half-dose PDT, and 90 were assigned randomly to HSML treatment. At their first evaluation visit, SRF had resolved in 51.2% and 13.8% of patients, respectively (P < 0.001). At their final evaluation visit, a significantly higher percentage of PDT-treated patients demonstrated no SRF (67.2% vs. 28.8%; P < 0.001). Moreover, at the first evaluation visit, the PDT-treated patients showed a significantly higher increase in BCVA (+4.60±6.62 ETDRS letters vs. +1.39±8.99 ETDRS letters; P = 0.011), and a significantly higher increase in retinal sensitivity on microperimetry (+2.01±3.04 dB vs. +0.92±3.65 dB; P = 0.046); however, the improvement in vision-related quality of life was similar (score of +2.87±8.35 vs. +2.56±7.36, respectively; P = 0.800).
Half-dose PDT is superior to HSML for treating cCSC, leading to a significantly higher proportion of patients with complete resolution of SRF and functional improvement.
比较半剂量光动力疗法(PDT)与高密度亚阈值微脉冲激光(HSML)治疗慢性中心性浆液性脉络膜视网膜病变(cCSC)的解剖和功能疗效及安全性。
开放性、多中心、随机对照临床试验。
符合以下条件的 cCSC 患者:疾病的临床特征和多模态成像结果均需得到确认。
将符合条件的患者按 1:1 比例随机分组。在 6 至 8 周的随访中进行治疗评估,对仍有视网膜下液(SRF)的患者重复相同的治疗。
主要终点是治疗后 6 至 8 周的首次评估访视中 SRF 完全消失。次要终点是治疗后 7 至 8 个月的最终评估访视中评估该解剖学结果。其他次要终点包括功能改善,包括最佳矫正视力(BCVA;用早期糖尿病视网膜病变研究[ETDRS]字母表示)、视网膜敏感度(用微视野计测量)和用经过验证的问卷评估视力相关生活质量的变化。
2013 年 11 月至 2016 年 9 月期间,共纳入 179 例患者:89 例患者被随机分配至半剂量 PDT 组,90 例患者被随机分配至 HSML 治疗组。首次评估访视时,分别有 51.2%和 13.8%的患者 SRF 得到缓解(P<0.001)。最终评估访视时,PDT 治疗组无 SRF 的患者比例显著更高(67.2%比 28.8%;P<0.001)。此外,首次评估访视时,PDT 治疗组患者的 BCVA 明显提高(增加 4.60±6.62 ETDRS 字母数比增加 1.39±8.99 ETDRS 字母数;P=0.011),微视野计测量的视网膜敏感度也明显提高(增加 2.01±3.04 dB 比增加 0.92±3.65 dB;P=0.046);然而,视力相关生活质量的改善相似(评分分别增加 2.87±8.35 比增加 2.56±7.36;P=0.800)。
半剂量 PDT 治疗 cCSC 优于 HSML,可显著提高 SRF 完全缓解率和功能改善率。