Bulla Mario Cesar, Lavinsky Daniel
Clínica Bulla, São Leopoldo, RS, Brazil.
Departamento de Oftalmologia, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Arq Bras Oftalmol. 2025 Apr 28;88(4):e20240277. doi: 10.5935/0004-2749.2024-0277. eCollection 2025.
This retrospective study evaluated the safety and efficacy of real-world antiangiogenic therapy for ocular conditions in the private healthcare sector in southern Brazil.
Medical records from patients who underwent intravitreal anti-vascular endothelial growth factor injections over the past 12 years were reviewed retrospectively. Data collection included the primary diagnoses, drugs administered, injection techniques, adverse effects, and treatment efficacy. Efficacy was assessed by comparing preand posttreatment visual acuity and central subfield thickness in eyes with followup exceeding 2 years.
A total of 1,024 patients, 1,310 treated eyes, and 11,377 injections were analyzed. The injections included aflibercept (6,833), ranibizumab (3,692), bevacizumab (843), and brolucizumab (9), administered either bilaterally (3,696) or unilaterally (7,681). The most common diagnoses were diabetic macular edema, exudative age-related macular degeneration, retinal vein occlusion related macular edema, and proliferative diabetic retinopathy. No endophthalmitis cases were reported. Vitritis with transient visual acuity loss occurred in two cases following aflibercept injections. One retinal detachment case was successfully treated with vitrectomy. The median number of injections per patient was 6 (IQR [interquartile range], 3-13). Among 445 eyes from 328 patients with followup over 2 years (median, 4.05 years; IQR, 2.89-6.29), there was a significant improvement in best-corrected visual acuity from 0.3 to 0.4 (Snellen) (p<0.001) and a reduction in central subfield thickness from 361 to 267 microns (p<0.001). CST comparisons included patients with age-related macular degeneration, diabetic macular edema, and retinal vein occlusion related macular edema.
This real-world study, the largest of its kind in Brazil, confirms the safety and efficacy of antiangiogenic therapies in the southern Brazilian private healthcare system. The findings highlight a low incidence of severe adverse events and outcomes consistent with global studies, supporting the ongoing use of antiangiogenic agents as effective and well-tolerated treatments for various ocular conditions in developing countries.
本回顾性研究评估了巴西南部私立医疗保健部门中针对眼部疾病的实际抗血管生成疗法的安全性和有效性。
回顾性分析了过去12年中接受玻璃体内抗血管内皮生长因子注射患者的病历。数据收集包括主要诊断、所用药物、注射技术、不良反应和治疗效果。通过比较随访超过2年的眼睛治疗前后的视力和中心子野厚度来评估疗效。
共分析了1024例患者、1310只治疗眼和11377次注射。注射药物包括阿柏西普(6833次)、雷珠单抗(3692次)、贝伐单抗(843次)和布罗利尤单抗(9次),双侧注射(3696次)或单侧注射(7681次)。最常见的诊断为糖尿病性黄斑水肿、渗出性年龄相关性黄斑变性、视网膜静脉阻塞相关黄斑水肿和增殖性糖尿病视网膜病变。未报告眼内炎病例。阿柏西普注射后有2例发生伴有短暂视力丧失的玻璃体炎。1例视网膜脱离病例经玻璃体切除术成功治疗。每位患者的注射中位数为6次(四分位间距[IQR],3 - 13次)。在328例随访超过2年(中位数4.05年;IQR,2.89 - 6.29年)患者的445只眼中,最佳矫正视力从0.3显著提高至0.4(Snellen)(p<0.001),中心子野厚度从361微米降至267微米(p<0.001)。中心子野厚度比较包括年龄相关性黄斑变性、糖尿病性黄斑水肿和视网膜静脉阻塞相关黄斑水肿患者。
这项巴西同类研究中规模最大的实际研究证实了巴西南部私立医疗保健系统中抗血管生成疗法的安全性和有效性。研究结果突出了严重不良事件的低发生率以及与全球研究一致的结果,支持在发展中国家持续使用抗血管生成药物作为治疗各种眼部疾病的有效且耐受性良好的疗法。