Mansour Ahmad M, Dedhia Chintan, Chhablani Jay
Department of Ophthalmology, American University of Beirut, Beirut, Lebanon.
Department of Ophthalmology, Rafik Hariri University Hospital, Beirut, Lebanon.
Br J Ophthalmol. 2017 Feb;101(2):166-169. doi: 10.1136/bjophthalmol-2016-308679. Epub 2016 May 17.
We report the 3-month efficacy of monthly intravitreal ziv-aflibercept in patients with diabetic macular oedema (DME).
Prospectively, consecutive patients with DME underwent intravitreal injection of 0.05 ml of compounded ziv-aflibercept (1.25 mg) from March 2015 to November 2015. Monitoring of best-corrected visual acuity (BCVA), intraocular inflammation, cataract progression and retinal structure by spectral domain optical coherence tomography was carried out at baseline, 1 week, 1 month, 2 months and 3 months after 3 monthly injections.
A total of 17 eyes (11 right eyes and 6 left eyes) were treated. The participants were divided into 10 Caucasians and 6 Indians, 11 men and 5 women, and had a mean age of 61.5 years. Five eyes were treatment-naïve cases and 12 eyes were treatment non- naïve with last treatment received at least more than 4-month interval. Mean BCVA in log MAR (equivalent Snellen visual acuity) improved from baseline 0.70 (20/100) to 0.49 (20/60) at 1 month, 0.43 (20/50) at 2 months and 0.42 (20/50) at 3 months (p ≤ 0.003). Central macular thickness decreased from mean baseline 517.5 to 388.1 μm at 1 week, 355.4 μm at 1 month, 351.4 μm at 2 months and 322.2 μm at 3 months (p ≤ 0.001).
Off-label use of intravitreal ziv-aflibercept improves visual acuity, without detectable ocular toxicity or systemic side effects in DME. It offers a less expensive alternative to the approved intravitreal aflibercept (Eylea), especially in the low/middle-income countries and in countries where Eylea is not available.
我们报告每月玻璃体内注射阿柏西普治疗糖尿病性黄斑水肿(DME)患者3个月的疗效。
前瞻性地,2015年3月至2015年11月,连续的DME患者接受玻璃体内注射0.05 ml复合阿柏西普(1.25 mg)。在基线、3个月每月注射后1周、1个月、2个月和3个月时,通过光谱域光学相干断层扫描监测最佳矫正视力(BCVA)、眼内炎症、白内障进展和视网膜结构。
共治疗17只眼(11只右眼和6只左眼)。参与者分为10名白种人和6名印度人,11名男性和5名女性,平均年龄61.5岁。5只眼为初治病例,12只眼为非初治病例,上次治疗间隔至少超过4个月。平均对数最小分辨角(log MAR,相当于斯内伦视力)的BCVA从基线时的0.70(20/100)在1个月时提高到0.49(20/60),2个月时为0.43(20/50),3个月时为0.42(20/50)(p≤0.003)。中心黄斑厚度从平均基线时的517.5μm在1周时降至388.1μm,1个月时为355.4μm, 2个月时为351.4μm,3个月时为322.2μm(p≤0.001)。
玻璃体内注射阿柏西普的非标签使用可提高视力,在DME患者中未检测到眼毒性或全身副作用。它为已获批的玻璃体内注射阿柏西普(阿瓦斯汀)提供了一种成本较低的替代方案,特别是在低收入/中等收入国家以及无法获得阿瓦斯汀 的国家。