Rachman Maria Jessica, Kalanjati Viskasari P, Rimbun Rimbun, Khadijah Fira
Master Program of Basic Medical Science, Faculty of Medicine, Universitas Airlangga, Surabaya, East Java, Indonesia.
Faculty of Medicine, Universitas Ciputra, Surabaya, East Java, Indonesia.
Clin Ophthalmol. 2023 Sep 28;17:2825-2842. doi: 10.2147/OPTH.S426428. eCollection 2023.
Vaccines are highly effective in lowering the mortality due to COVID-19. Although several suspected adverse events or side effects after vaccination including retinal vein occlusion (RVO) have been reported. We conducted a systematic review using PRISMA methods to analyze the occurrence of RVO among people vaccinated by COVID-19 mRNA- vs viral vector- vaccines on 4 databases from 1-1-2021 to 31-12-2022 using specified MeSH terms. All included studies were assessed using JBI critical appraisal tools for eligibility. The final included studies are 31 studies (n=78 cases from 75 patients; 3 of these patients suffered twice). The median age of the patients was 61 years (28 to 96 years old) and most of them were female (52.00%). Thirty-nine patients received the mRNA vaccine (52.00%), while 36 patients received the viral vector vaccine (48.00%) before the event. The RVO diagnoses are based on physical examination confirmed by Fluorescein Angiography (FA), and/or Optical Coherence Tomography (OCT). The median time interval between vaccination and RVO was 6 days in the mRNA vaccine group and 4 days in the viral vector vaccine group. Central retinal vein occlusion (CRVO) and Branch Retinal Vein Occlusion (BRVO) were tied as the most common diagnosis in the mRNA vaccine group (20.51% and 20.51%), whilst in the viral vector vaccine group CRVO was the most common diagnosis (17.94%). Most of these cases had good outcomes with improved visual impairment in one or both eyes. From this review, we could not ascertain that the RVO occurs due to the type of COVID-19 vaccines because of the detailed data on the dosage and the history of illness of each patient. However, the awareness that the RVO could develop after COVID-19 vaccination must be taken into consideration, even though it is rare.
疫苗在降低新冠病毒所致死亡率方面非常有效。尽管已有报告称接种疫苗后出现了包括视网膜静脉阻塞(RVO)在内的多种疑似不良事件或副作用。我们采用PRISMA方法进行了一项系统评价,以分析在2021年1月1日至2022年12月31日期间,使用特定医学主题词在4个数据库中接种新冠病毒mRNA疫苗与病毒载体疫苗的人群中RVO的发生情况。所有纳入研究均使用JBI批判性评价工具进行合格性评估。最终纳入31项研究(75例患者中的78例;其中3例患者出现两次)。患者的中位年龄为61岁(28至96岁),大多数为女性(52.00%)。事件发生前,39例患者接种了mRNA疫苗(52.00%),36例患者接种了病毒载体疫苗(48.00%)。RVO诊断基于荧光素血管造影(FA)和/或光学相干断层扫描(OCT)确认的体格检查。mRNA疫苗组接种疫苗至RVO的中位时间间隔为6天,病毒载体疫苗组为4天。中央视网膜静脉阻塞(CRVO)和分支视网膜静脉阻塞(BRVO)在mRNA疫苗组中并列最常见诊断(均为20.51%),而在病毒载体疫苗组中CRVO是最常见诊断(17.94%)。这些病例大多预后良好,一只或两只眼睛的视力障碍得到改善。通过本次评价,由于缺乏每位患者的详细剂量和病史数据,我们无法确定RVO的发生是否因新冠病毒疫苗类型所致。然而,尽管RVO在新冠病毒疫苗接种后很少见,但仍必须考虑到其可能发生。