Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart and Chest Hospital, Liverpool, UK.
Eur Heart J Cardiovasc Pharmacother. 2023 Jul 29;9(5):403-412. doi: 10.1093/ehjcvp/pvad015.
Patients with atrial fibrillation (AF) have a higher risk of ischaemic stroke or systemic embolism, with a greater risk for female patients. This study aims to evaluate the risk of ischaemic stroke or systemic embolism and bleeding following COVID-19 vaccination in patients with AF and the sex differences.
Self-controlled case series (SCCS) analysis was conducted to evaluate the risk of ischaemic stroke or systemic embolism and bleeding following BNT162b2 or CoronaVac in patients with AF, using the territory-wide electronic medical records from the Hospital Authority and vaccination records from the Department of Health in Hong Kong. Patients with a primary diagnosis of ischaemic stroke, systemic embolism, or bleeding in the inpatient setting between 23 February 2021 and 31 March 2022 were included. A nested case-control analysis was also conducted with each case randomly matched with 10 controls according to sex, age, Charlson comorbidity index, and date of hospital admission. Conditional Poisson regression was used in the SCCS analysis, and conditional logistic regression was used in the nested case-control analysis to assess the risks, and all analyses were stratified by sex and type of vaccines. Among 51 158 patients with AF, we identified an increased risk of ischaemic stroke or systemic embolism after the first dose of BNT162b2 in SCCS analysis during 0-13 days [incidence rate ratio 6.60, 95% confidence interval (CI) 1.51-28.77] and 14-27 days (6.53, 95% CI 1.31-32.51), and nested case-control analysis during 0-13 days (adjusted odds ratio 6.21, 95% CI 1.14-33.91) and 14-27 days (5.52, 95% CI 1.12-27.26) only in female patients. The increased risk in female patients following the first dose of CoronaVac was only detected during 0-13 days (3.88, 95% CI 1.67-9.03) in the nested case-control analysis. No increased risk of ischaemic stroke or systemic embolism was identified in male patients, and no increased risk of bleeding was detected in all patients with AF for both vaccines. An increased risk of ischaemic stroke or systemic embolism after COVID-19 was also observed in both females (17.42, 95% CI 5.08-59.73) and males (6.63, 95% CI 2.02-21.79).
The risk of ischaemic stroke or systemic embolism after COVID-19 vaccination was only increased in female patients with AF. However, as the risk after COVID-19 was even higher, proactive uptake of COVID-19 vaccines is recommended to prevent the potential severe outcomes after infection.
患有心房颤动(AF)的患者发生缺血性卒中和全身性栓塞的风险更高,女性患者的风险更高。本研究旨在评估 AF 患者接种 COVID-19 疫苗后发生缺血性卒中和全身性栓塞以及出血的风险,以及性别差异。
使用香港医管局的全港电子病历和卫生署的疫苗接种记录,进行了自我对照病例系列(SCCS)分析,以评估 AF 患者接种 BNT162b2 或科兴疫苗后发生缺血性卒中和全身性栓塞以及出血的风险。2021 年 2 月 23 日至 2022 年 3 月 31 日期间,将因原发性缺血性卒中、全身性栓塞或出血而住院的患者纳入研究。还进行了嵌套病例对照分析,每个病例随机匹配 10 名按性别、年龄、Charlson 合并症指数和住院日期分层的对照。SCCS 分析中使用条件泊松回归,嵌套病例对照分析中使用条件逻辑回归评估风险,所有分析均按性别和疫苗类型分层。在 51158 例 AF 患者中,我们发现 SCCS 分析中 BNT162b2 第一剂后 0-13 天(发生率比 6.60,95%置信区间 [CI] 1.51-28.77)和 14-27 天(6.53,95% CI 1.31-32.51)缺血性卒中和全身性栓塞风险增加,嵌套病例对照分析中,0-13 天(调整后比值比 6.21,95% CI 1.14-33.91)和 14-27 天(5.52,95% CI 1.12-27.26)女性患者的风险增加。仅在嵌套病例对照分析中,女性患者接种科兴疫苗第一剂后 0-13 天(3.88,95% CI 1.67-9.03)观察到缺血性卒中和全身性栓塞风险增加。两种疫苗均未发现 AF 患者中男性缺血性卒中和全身性栓塞风险增加,也未发现所有患者出血风险增加。COVID-19 后还观察到女性(17.42,95% CI 5.08-59.73)和男性(6.63,95% CI 2.02-21.79)发生缺血性卒中和全身性栓塞的风险增加。
COVID-19 疫苗接种后发生缺血性卒中和全身性栓塞的风险仅在 AF 女性患者中增加。然而,由于 COVID-19 后发生的风险更高,建议积极接种 COVID-19 疫苗,以预防感染后的潜在严重后果。