Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, Ohio; Center for Ophthalmic Bioinformatics, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio; Case Western Reserve University School of Medicine, Cleveland, Ohio.
Center for Ophthalmic Bioinformatics, Cole Eye Institute, Cleveland Clinic, Cleveland, Ohio; Case Western Reserve University School of Medicine, Cleveland, Ohio.
Ophthalmology. 2024 Sep;131(9):1076-1082. doi: 10.1016/j.ophtha.2024.02.024. Epub 2024 Feb 24.
To determine the risk of optic neuritis (ON) after mRNA Coronavirus Disease 2019 (COVID-19) vaccine administration.
U.S. National aggregate database retrospective cohort study.
Patients were placed into cohorts based on mRNA COVID-19 vaccination status (no vaccine and positive history of COVID-19 infection, 1 vaccine, or 2 vaccines received) from December 2020 to June 2022. Two control cohorts were created with patients vaccinated against influenza or tetanus, diphtheria, and pertussis (Tdap) from June 2018 to December 2019. Patients with any history of ON or significant risk factors for ON development including infectious, inflammatory, and neoplastic diseases were excluded.
A large deidentified database was queried for the Common Procedural Technology codes for immunization encounters specific to first dose and second dose of mRNA COVID-19 vaccine, influenza, or Tdap. Cohorts were 1:1 propensity score matched on age, sex, race, and ethnicity. The risk of ON development after vaccination was calculated and compared for all 5 cohorts with 95% confidence intervals (CIs) reported.
Risk ratio (RR) of ON 21 days after vaccination (or COVID-19 infection) and incidence of ON per 100 000 individuals.
After matching, the first dose COVID-19 and influenza vaccine cohorts (n = 1 678 598, mean age [standard deviation] at vaccination of 45.5 [23.3] years and 43.2 [25.5] years, 55% female) the RR of developing ON was 0.44 (95% CI, 0.28-0.80). The first dose of COVID-19 and Tdap vaccinations (n = 797 538, mean age 38.9 [20.0] years, 54.2% female) cohort had 10 and 16 patients develop ON (RR, 0.63; 95% CI, 0.28-1.38). Comparison of COVID-19-vaccinated patients (n = 3 698 848, 48.2 [21.5] years, 54.7% female) to unvaccinated and COVID-19-infected patients (n = 3 698 848, 49.6 [22.0] years, 55.2% female) showed 49 and 506 patients developing ON, respectively (RR, 0.09; 95% CI, 0.07-0.12). The incidence per 100 000 for ON was 1 in the first dose COVID-19 vaccine cohort, 2 in the influenza cohort, and 2 in the Tdap cohort, and 14 in the COVID-19-infected and unvaccinated cohorts.
Risk of ON after mRNA COVID-19 vaccination is rare and comparable to Tdap vaccination, decreased compared with influenza vaccination, and decreased compared with COVID-19 infection in the absence of vaccination.
FINANCIAL DISCLOSURE(S): Proprietary or commercial disclosure may be found after the references.
确定 mRNA 冠状病毒病 2019(COVID-19)疫苗接种后发生视神经炎(ON)的风险。
美国国家综合数据库回顾性队列研究。
根据 mRNA COVID-19 疫苗接种状况(无疫苗和 COVID-19 感染史阳性、1 剂或 2 剂疫苗),将患者分为队列,时间为 2020 年 12 月至 2022 年 6 月。从 2018 年 6 月至 2019 年 12 月创建了两个对照队列,其中患者接种了流感或破伤风、白喉和百日咳(Tdap)疫苗。排除任何 ON 病史或 ON 发展的显著危险因素,包括感染、炎症和肿瘤疾病。
使用大型匿名数据库查询特定于 mRNA COVID-19 疫苗、流感或 Tdap 首剂和第二剂免疫接种的常见程序技术代码。在年龄、性别、种族和民族方面对队列进行 1:1 倾向评分匹配。计算并比较了所有 5 个队列在疫苗接种后 21 天(或 COVID-19 感染后)发生 ON 的风险比(RR)和每 10 万人发生 ON 的发病率。
疫苗接种后(或 COVID-19 感染后)发生 ON 的 RR 和每 10 万人发生 ON 的发病率。
匹配后,第一剂 COVID-19 和流感疫苗队列(n=1678598,接种时的平均年龄[标准差]分别为 45.5[23.3]岁和 43.2[25.5]岁,55%为女性)发生 ON 的 RR 为 0.44(95%CI,0.28-0.80)。第一剂 COVID-19 和 Tdap 疫苗接种(n=797538,平均年龄 38.9[20.0]岁,54.2%为女性)队列中有 10 例和 16 例患者发生 ON(RR,0.63;95%CI,0.28-1.38)。与未接种疫苗和 COVID-19 感染的患者(n=3698848,49.6[22.0]岁,55.2%为女性)相比,比较 COVID-19 接种患者(n=3698848,48.2[21.5]岁,54.7%为女性)分别有 49 例和 506 例患者发生 ON(RR,0.09;95%CI,0.07-0.12)。ON 的发病率为每 100000 人中有 1 人在第一剂 COVID-19 疫苗接种队列中,2 人在流感队列中,2 人在 Tdap 队列中,14 人在 COVID-19 感染和未接种疫苗的队列中。
mRNA COVID-19 疫苗接种后发生 ON 的风险罕见且与 Tdap 疫苗接种相当,与流感疫苗接种相比风险降低,与 COVID-19 感染且无疫苗接种相比风险降低。
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