Soliman Mohamed Kamel, Zarranz-Ventura Javier, Chakravarthy Usha, McKibbin Martin, Brand Christopher, Menon Geeta, Cilliers Helena, Natha Salim, Ross Adam, Sarhan Mahmoud, Lobo Aires, Chong Victor, Mahmood Sajjad, Islam Niaz, Akerele Toks, Shakarchi Ahmed, Sallam Ahmed
Department of Ophthalmology, Faculty of Medicine, Assiut University, Assiut, Egypt.
Department of Ophthalmology and Visual Sciences, University Hospitals Eye Institute, Case Western Reserve University, Cleveland, Ohio.
Retina. 2023 Apr 1;43(4):679-687. doi: 10.1097/IAE.0000000000003698.
To study the treatment patterns, visual outcomes and safety profile of intravitreal dexamethasone implant (IDI) used for the treatment of macular edema secondary to retinal vein occlusion.
Up to 2 years of routinely collected anonymized data within electronic medical record systems were remotely extracted from 16 centers. The outcome measures include visual outcome, number of injections, and safety measures, including the rate of intraocular pressure (IOP) rise, frequency of IOP-lowering medication usage, and cataract surgery rates.
The study included 688 eyes (44.4%) with central retinal vein occlusion and 862 eyes (55.6%) with branch retinal vein occlusion; 1,250 eyes (80.6%) were treatment naive and 28% (275/989) had high IOP or were on IOP-lowering medications before IDI use. It was found that 31% (476) of eyes received two injections, and 11.7% (182) and 3.7% (58) of eyes received three and four injections, respectively. The mean baseline Snellen visual acuity improved from 20/125 to 20/40 after the first injection. The probability of cataract surgery was 15% at 24 months. The proportion of eyes with ≥10 mmHg change from baseline was higher in phakic (14.2%) compared with pseudophakic eyes (5.4%, P = 0.004). Three eyes required IOP filtering surgery (0.2%).
The visual results of IDI in eyes with macular edema secondary to retinal vein occlusion in the real world are comparable to those of clinical trial setting. Increased IOP in eyes with preexisting ocular hypertension or glaucoma can be controlled with additional medical treatment. Intraocular pressure rise with IDI may be more frequent in phakic than in pseudophakic eyes.
研究玻璃体内地塞米松植入物(IDI)用于治疗视网膜静脉阻塞继发黄斑水肿的治疗模式、视力结果和安全性。
从16个中心远程提取电子病历系统中长达2年的常规收集的匿名数据。结果指标包括视力结果、注射次数以及安全性指标,包括眼压(IOP)升高率、降低眼压药物使用频率和白内障手术率。
该研究纳入了688只(44.4%)中央视网膜静脉阻塞眼和862只(55.6%)分支视网膜静脉阻塞眼;1250只(80.6%)眼为初治眼,28%(275/989)的眼在使用IDI前眼压高或正在使用降低眼压药物。发现31%(476只)眼接受了两次注射,11.7%(182只)和3.7%(58只)眼分别接受了三次和四次注射。首次注射后,平均基线Snellen视力从20/125提高到20/40。24个月时白内障手术概率为15%。有晶状体眼(14.2%)中眼压较基线变化≥10 mmHg的眼的比例高于人工晶状体眼(5.4%,P = 0.004)。三只眼需要进行眼压滤过手术(0.2%)。
在现实世界中,IDI治疗视网膜静脉阻塞继发黄斑水肿的视力结果与临床试验结果相当。既往有高眼压或青光眼的眼中眼压升高可通过额外的药物治疗得到控制。IDI导致的眼压升高在有晶状体眼中可能比在人工晶状体眼中更频繁。