Beijing Tongren Eye Center, Beijing Tongren Hospital, Beijing Key Laboratory of Ophthalmology & Visual Sciences, Capital Medical University, No. 1 Dong Jiao Min Xiang Street, Dongcheng District, Beijing, 100730, People's Republic of China.
Graefes Arch Clin Exp Ophthalmol. 2024 Jan;262(1):305-312. doi: 10.1007/s00417-023-06162-6. Epub 2023 Jul 8.
To evaluate the long-term safety and efficacy of adjuvant intravitreal anti-VEGF therapy in juvenile Coats disease.
This retrospective, observational study included a total of 62 eyes in 62 pediatric patients with juvenile Coats disease treated with intravitreal anti-VEGF agents followed for a mean of 67.08 months (ranged from 60 to 93 months). All affected eyes were managed initially with one session of ablative treatment plus adjuvant intravitreal anti-VEGF agent (0.5 mg/0.05 ml ranibizumab or conbercept). Ablative treatment was repeated if telangiectatic retinal vessels were not completely regressed or recurred. Anti-VEGF therapy was repeated if subretinal fluid or macular edema still existed. Treatments above were repeated every 2 to 3 months. We reviewed clinical and photographic records of patients including the demographics, clinical characteristics and interventions.
At final visit, all 62 affected eyes had partially or completely disease resolution; none progressed to advanced stage namely neovascular glaucoma or phthisis bulbi, respectively. No ocular or systemic side effects related to intravitreal injections were observed during follow-up. In terms of 42 affected eyes that could cooperate with visual examination, best corrected visual acuity improved in 14 (14/42, 33.3%) eyes, stabled in 25 (25/42, 59.5%) eyes, and worsened in 3 (3/42, 7.1%) eyes. In the field of complications, 22 (22/62, 35.5%) eyes developed cataracts; 33 (33/62, 53.2%) eyes developed vitreoretinal fibrosis, of whom 14 (14/33, 42.4%) eyes in the subgroup of stage 3B developed progressive TRD; 40 (40/62, 64.5%) eyes developed subretinal fibrosis. Multivariate regression analysis showed increased clinical stage may be associated with the development of vitreo- and subretinal fibrosis (adjusted odds ratio:16.77,17.59; 95% CI:4.50-62.53, 3.98-77.86, respectively, all P < 0.001).
Adjuvant intravitreal ranibizumab or conbercept combined with ablative therapies may be a long-term safe and effective treatment for juvenile Coats disease.
评估辅助性玻璃体内抗血管内皮生长因子治疗青少年 Coats 病的长期安全性和疗效。
本回顾性观察性研究纳入了 62 例(62 只眼)接受玻璃体内抗血管内皮生长因子药物治疗的青少年 Coats 病患儿,平均随访 67.08 个月(范围为 60 至 93 个月)。所有受影响的眼睛最初均接受一次消融治疗加辅助性玻璃体内抗血管内皮生长因子药物治疗(0.5mg/0.05ml 雷珠单抗或康柏西普)。如果毛细血管扩张性视网膜血管未完全消退或复发,则重复消融治疗。如果仍存在视网膜下积液或黄斑水肿,则重复抗血管内皮生长因子治疗。上述治疗每 2 至 3 个月重复一次。我们回顾了患者的临床和照片记录,包括人口统计学、临床特征和干预措施。
在最终随访时,所有 62 只受影响的眼睛均部分或完全缓解疾病;无一例进展为晚期,即新生血管性青光眼或眼球萎缩。在随访期间,未观察到与玻璃体内注射相关的眼部或全身副作用。在可配合视力检查的 42 只受影响的眼睛中,14 只(14/42,33.3%)视力改善,25 只(25/42,59.5%)视力稳定,3 只(3/42,7.1%)视力恶化。在并发症方面,22 只(22/62,35.5%)眼睛发生白内障;33 只(33/62,53.2%)眼睛发生玻璃体积血和视网膜纤维化,其中 3B 期亚组的 14 只(14/33,42.4%)眼睛发生进行性 TRD;40 只(40/62,64.5%)眼睛发生视网膜下纤维化。多变量回归分析显示,临床分期增加可能与玻璃体内和视网膜下纤维化的发生有关(调整后的优势比:16.77,17.59;95%置信区间:4.50-62.53,3.98-77.86,均 P<0.001)。
辅助性玻璃体内雷珠单抗或康柏西普联合消融治疗可能是青少年 Coats 病的一种长期安全有效的治疗方法。