Bradshaw Steven E, Gala Smeet, Nanavaty Merena, Shah Anshul, Mwamburi Mkaya, Kefalas Panos
Valid Insight®, Kemp House, 152 City Road, London, EC1V 2NX, UK.
Market Access Solutions, 575 State Route 28, Raritan, NJ, 08869, USA.
BMC Ophthalmol. 2016 Jul 11;16:104. doi: 10.1186/s12886-016-0282-5.
To understand the clinical and economic outcomes of treatments for managing complications of ischemic central retinal vein occlusion (iCRVO).
We conducted a systematic literature review by searching multiple databases and ophthalmology conferences from 2004 to 2015. Studies published in English language and populations of age ≥45 years were included. For clinical endpoints, we defined eligibility criteria as randomized controlled trials, prospective before-and-after study designs, and non-randomized studies reporting on treatments in patients with iCRVO. For economic endpoints, all types of study design except cost-of-illness studies were included. We evaluated the definitions of ischemia, clinical and economic endpoints, and rate of development of complications. Risk of bias was assessed for clinical studies using the Cochrane risk-of-bias tool.
A total of 20 studies (1338 patients) were included. Treatments included anti-vascular endothelial growth factors (anti-VEGFs), steroids, and procedures primarily targeting macular edema and neovascularization. Ischemia was not defined consistently in the included studies. The level of evidence was mostly low. Most treatments did not improve visual acuity significantly. Development of treatment complications ranged from 11 to 57 %. Incremental cost-effectiveness ratios reported for anti-VEGFs and steroids were below the accepted threshold of GB£30,000, but considering such treatments only ameliorate disease symptoms they seem relatively expensive.
There is a lack of evidence for any intervention being effective in iCRVO, especially in the prevention of neovascularisation. iCRVO poses a significant clinical and economic burden. There is a need to standardize the definition of ischemia, and for innovative treatments which can significantly improve visual outcomes and prevent neovascular complications.
了解缺血性视网膜中央静脉阻塞(iCRVO)并发症治疗的临床和经济结果。
我们通过检索2004年至2015年的多个数据库和眼科会议进行了系统的文献综述。纳入以英文发表且年龄≥45岁人群的研究。对于临床终点,我们将纳入标准定义为随机对照试验、前瞻性前后对照研究设计以及报告iCRVO患者治疗情况的非随机研究。对于经济终点,纳入除疾病成本研究外的所有类型研究设计。我们评估了缺血、临床和经济终点的定义以及并发症的发生率。使用Cochrane偏倚风险工具评估临床研究的偏倚风险。
共纳入20项研究(1338例患者)。治疗方法包括抗血管内皮生长因子(抗VEGF)、类固醇以及主要针对黄斑水肿和新生血管形成的手术。纳入研究中对缺血的定义不一致。证据水平大多较低。大多数治疗方法并未显著提高视力。治疗并发症的发生率在11%至57%之间。抗VEGF和类固醇的增量成本效益比低于公认的30,000英镑阈值,但考虑到这些治疗仅能改善疾病症状,它们似乎相对昂贵。
缺乏证据表明任何干预措施对iCRVO有效,尤其是在预防新生血管形成方面。iCRVO带来了重大的临床和经济负担。需要规范缺血的定义,并需要创新治疗方法以显著改善视力结果并预防新生血管并发症。