Department of Ophthalmology, Taichung Veterans General Hospital, Taichung, 407, Taiwan.
School of Medicine, National Yang-Ming University, Taipei, 112, Taiwan.
Eye (Lond). 2022 Jan;36(1):153-159. doi: 10.1038/s41433-021-01416-1. Epub 2021 Mar 2.
To evaluate whether intravitreal injections (IVI) of anti-vascular endothelial growth factor (anti-VEGF) in neovascular age-related macular degeneration (nAMD) patients with prior stroke or acute myocardial infarction (AMI) are associated with increased mortality.
From 2005 to 2013, nAMD patients in the Taiwan National Health Insurance Research Database who received IVI of anti-VEGF and had a diagnosis of stroke/AMI prior to their first injections were defined as the IVI group. The mortality of the IVI group during the study period was compared to that of the non-IVI group, which consisted of nAMD patients who had prior stroke/AMI but were never exposed to anti-VEGF. The IVI group and the non-IVI group were 1-4 matched according to propensity score (PS), which was derived from age, sex, date of stroke/AMI and comorbidities. PS-adjusted Cox regression analyses were used to estimate the hazard ratio (HR) for mortality associated with IVI of anti-VEGF. Subgroup analyses were also performed according to the interval between stroke/AMI and IVI (≤6 months, 6 months to 1 year, 1-2 years, >2 years).
There were 3384 individuals in the IVI group and 13,536 individuals in the non-IVI group. The IVI group had a significantly higher mortality risk (adjusted HR = 2.37; 95% confidence interval (CI), 2.14-2.62) than the non-IVI group. Subgroup analyses revealed that elevated mortality was significant when anti-VEGF was injected within 1 year after stroke/AMI.
We found an increased mortality risk associated with IVI of anti-VEGF in nAMD patients with prior stroke/AMI compared to the mortality risk of nAMD patients with prior stroke/AMD but without exposure to anti-VEGF.
评估在既往有卒中或急性心肌梗死(AMI)病史的新生血管性年龄相关性黄斑变性(nAMD)患者中,玻璃体内注射抗血管内皮生长因子(抗-VEGF)是否与死亡率增加相关。
从 2005 年至 2013 年,在台湾全民健康保险研究数据库中,接受抗-VEGF 玻璃体内注射且在首次注射前有卒中/AMI 诊断的 nAMD 患者被定义为抗-VEGF 玻璃体内注射组。在研究期间,将该组的死亡率与既往有卒中/AMI 但从未使用过抗-VEGF 的 nAMD 患者的非抗-VEGF 玻璃体内注射组的死亡率进行比较。通过年龄、性别、卒中/AMI 日期和合并症等因素,根据倾向评分(PS)对两组进行 1:4 匹配。采用 PS 调整的 Cox 回归分析来估计与抗-VEGF 玻璃体内注射相关的死亡率的危险比(HR)。还根据卒中/AMI 与抗-VEGF 玻璃体内注射之间的时间间隔(≤6 个月、6 个月至 1 年、1-2 年、>2 年)进行亚组分析。
抗-VEGF 玻璃体内注射组有 3384 例患者,非抗-VEGF 玻璃体内注射组有 13536 例患者。抗-VEGF 玻璃体内注射组的死亡率风险明显高于非抗-VEGF 玻璃体内注射组(调整后的 HR=2.37;95%置信区间[CI],2.14-2.62)。亚组分析显示,在卒中/AMI 后 1 年内注射抗-VEGF 时,死亡率升高具有显著意义。
与既往有卒中/AMD 但未接受抗-VEGF 治疗的 nAMD 患者的死亡率风险相比,我们发现既往有卒中/AMI 病史的 nAMD 患者接受抗-VEGF 玻璃体内注射后死亡率风险增加。