接种 BNT162b2、CoronaVac 和 ChAdOx1 疫苗以及感染 SARS-CoV-2 后发生重大脑心血管不良事件的风险:一项自我对照病例系列研究。

Vaccine Pub Date : 2024-12-02 Epub Date: 2024-10-23 DOI:10.1016/j.vaccine.2024.126465
Norazida Ab Rahman, Teck Long King, Kalaiarasu M Peariasamy, Sheamini Sivasampu
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引用次数: 0

摘要

目的评估与 COVID-19 疫苗接种和 SARS-CoV-2 感染相关的重大不良脑-心血管事件 (MACCE) 的潜在风险:这项自我对照病例系列研究使用了马来西亚全国健康数据库。研究对象包括 2021 年 2 月 24 日至 2022 年 6 月 30 日期间住院的年龄≥18 岁的人。研究结果是MACCE的综合结果:中风、急性缺血性心脏病和心血管死亡。暴露因素为 COVID-19 疫苗接种和 SARS-CoV-2 感染。风险期为暴露后的第 1 天至第 21 天。采用条件泊松回归模型估算了风险期和对照期结果的发病率比(IRR)和95%置信区间(CI):每 10 万剂疫苗接种后 21 天内发生 MACCE 的风险分别为 12.0(95% CI 11.9-12.1)(BNT162b2)、9.2(95% CI 9.1-9.3)(CoronaVac)和 6.8(95% CI 6.6-7.0)(ChAdOx1)。发病率比显示,对于未患心血管疾病 (CVD) 的人来说,接种第一、第二或第三剂 BNT162b2、CoronaVac 和 ChAdOx1 疫苗不会增加 MACCE 风险。对于患有心血管疾病的人来说,这一结果是一致的。无论是同源疫苗还是异源疫苗,疫苗加强剂量都不会增加 MACCE 风险。按种族群体进行的分析发现,印度人在首次接种 ChAdOx1 后发生 MACCE 的风险略有升高(IRR 为 1.64;95% CI 为 1.08-2.48)。在其他亚组分析中未观察到明显关联。在无心血管疾病(IRR为3.54;95% CI为3.32-3.76)和有心血管疾病(IRR为1.98;95% CI为1.61-2.34)的人群中,SARS-CoV-2感染与MACCE风险显著增加有关:我们的研究结果支持COVID-19疫苗良好的安全性,并表明COVID-19疫苗的总体效益风险比仍然是积极的。
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Risk of major adverse cerebro-cardiovascular events following BNT162b2, CoronaVac, and ChAdOx1 vaccination and SARS-CoV-2 infection: A self-controlled case-series study.

Objective: To assess the potential risk of major adverse cerebro-cardiovascular events (MACCE) associated with COVID-19 vaccination and SARS-CoV-2 infection.

Methods: This self-controlled case series study used nationwide health database from Malaysia. The study included individuals aged ≥18 years who were hospitalised between 24 February 2021 and 30 June 2022. Outcomes were composite of MACCE: stroke, acute ischaemic heart disease, and cardiovascular death. Exposures were COVID-19 vaccination and SARS-CoV-2 infection. The risk period was day 1 to day 21 following exposure. Conditional Poisson regression model was used to estimate the incidence rate ratios (IRRs) and 95 % confidence interval (CI) comparing the outcomes in the risk and control periods.

Results: The risk of MACCE within 21 days after vaccination per 100,000 doses administered were 12.0 (95% CI 11.9-12.1) (BNT162b2), 9.2 (95% CI 9.1-9.3) (CoronaVac), and 6.8 (95% CI 6.6-7.0) (ChAdOx1). The incidence rate ratios showed no increased risk of MACCE associated with the first, second, or third doses of BNT162b2, CoronaVac, and ChAdOx1 vaccines for individuals without prior cardiovascular disease (CVD). This finding was consistent for individuals with CVD. Vaccine booster dose, whether in a homologous or heterologous schedule, did not show increased risk of MACCE. Analysis by ethnic groups detected a slightly elevated risk of MACCE in Indian after the first dose of ChAdOx1 (IRR 1.64; 95% CI 1.08-2.48) in those without CVD. No significant association were observed in other subgroup analyses. SARS-CoV-2 infection was associated with significantly increased risk of MACCE in individuals without CVD (IRR 3.54; 95% CI 3.32-3.76) and with CVD (IRR 1.98; 95% CI 1.61-2.34).

Conclusions: Our findings support the favourable safety profile of these COVID-19 vaccines and indicate that the overall benefit-risk ratio of the COVID-19 vaccines remains positive.

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