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首页> 外文期刊>Journal of Ophthalmology >Eyes that Do Not Meet the Eligibility Criteria of Clinical Trials on Age-Related Macular Degeneration: Proportion of the Real-World Patient Population and Reasons for Exclusion
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Eyes that Do Not Meet the Eligibility Criteria of Clinical Trials on Age-Related Macular Degeneration: Proportion of the Real-World Patient Population and Reasons for Exclusion

机译:不符合年龄相关黄斑变性的临床试验资格标准的眼睛:现实世界患者人口的比例和排除的原因

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Background . To evaluate the proportion of eyes that do not meet the eligibility criteria of clinical trials on neovascular age-related macular degeneration (AMD) and the reasons for exclusion. Methods . This retrospective, observational study included 512 eyes of 463 patients diagnosed with treatment-na?ve neovascular AMD. The proportion of eyes that did not meet the eligibility criteria of the Vascular Endothelial Growth Factor Trap-Eye: Investigation of Efficacy and Safety in Wet AMD (VIEW) studies were evaluated. The two most common reasons for exclusion were also evaluated in each subtype of neovascular AMD (typical neovascular AMD, polypoidal choroidal vasculopathy (PCV), and type 3 neovascularization). Results . Among the 512 eyes, 229 (44.7%) did not meet the eligibility criteria. In all the included eyes, the most common reasons for exclusion were good or poor visual acuity (169 eyes, 33.0%), followed by the presence of subretinal hemorrhage (47 eyes, 9.5%). Moreover, good or poor visual acuity was the most common reason for exclusion in all three subtypes of neovascular AMD. The second most common reason was a fovea-involving scar or fibrosis in typical neovascular AMD, subretinal hemorrhage in PCV, and other vascular diseases affecting the retina in type 3 neovascularization. Conclusions . Among the included cases, 44.7% did not meet the eligibility criteria for VIEW study, suggesting that the conclusion derived from clinical trials may not directly reflect the real-world outcomes. Additionally, the reasons for ineligibility differed among the different subtypes of neovascular AMD.
机译:背景 。为了评估不符合新生血管结合相关黄斑变性(AMD)的临床试验资格标准的比例以及排除的原因。方法 。这种回顾性的观察研究包括诊断为治疗 - Na ve新生血管AMD的463名患者的512只眼睛。不符合血管内皮生长因子捕获者的资格标准的眼睛比例:评估湿AMD(观察)研究的疗效和安全性的研究。还在新生血管AMD(典型的新生血管AMD,息肉脉络膜血管病变(PCV)和3型新血管内化的每种亚型中排除的两个最常见原因。结果 。在512只眼中,229(44.7%)未达到资格标准。在所有包括的眼睛中,排除的最常见原因是良好或差的视力(169只眼,33.0%),然后存在沉积地出血(47只眼,9.5%)。此外,良好或差的视力是排除在新血管AMD的所有三个亚型中的最常见原因。第二种最常见的原因是涉及典型新生血管AMD,PCV的次震位出血的瘢痕或纤维化,以及影响3型新生血管中的视网膜的其他血管疾病。结论。在此案例中,44.7%不符合视图研究的资格标准,表明临床试验的结论可能不会直接反映现实世界的成果。另外,在新血管AMD的不同亚型中的缺陷差异的原因不同。

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