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COVID-19 疫苗在多发性硬化症中的安全性:系统评价和荟萃分析。

Safety of COVID-19 vaccines in multiple sclerosis: A systematic review and meta-analysis.

机构信息

Second Department of Neurology, "Attikon" University Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

First Department of Neurology, Eginition Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

出版信息

Mult Scler. 2023 Apr;29(4-5):585-594. doi: 10.1177/13524585221150881. Epub 2023 Feb 1.

DOI:10.1177/13524585221150881
PMID:36722184
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9895285/
Abstract

BACKGROUND

Data are sparse regarding the safety of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines in patients with multiple sclerosis (MS).

OBJECTIVE

To estimate (1) the pooled proportion of MS patients experiencing relapse among vaccine recipients; (2) the rate of transient neurological worsening, adverse events, and serious adverse events; (3) the previous outcomes of interest for different SARS-CoV-2 vaccine types.

METHODS

Systematic review and meta-analysis of pharmacovigilance registries and observational studies.

RESULTS

Nineteen observational studies comprising 14,755 MS patients who received 23,088 doses of COVID-19 vaccines were included. Mean age was 43.3 years (95% confidence interval (CI): 40-46.6); relapsing-remitting, secondary-progressive, primary-progressive MS and clinically isolated syndrome were diagnosed in 82.6% (95% CI: 73.9-89.8), 12.6% (95% CI: 6.3-20.8), 6.7% (95% CI: 4.2-9.9), and 2.9% (95% CI: 1-5.9) of cases, respectively. The pooled proportion of MS patients experiencing relapse at a mean time interval of 20 days (95% CI: 12-28.2) from vaccination was 1.9% (95% CI: 1.3%-2.6%;  = 78%), with the relapse risk being independent of the type of administered SARS-CoV-2-vaccine ( for subgroup differences = 0.7 for messenger RNA (mRNA), inactivated virus, and adenovector-based vaccines). After vaccination, transient neurological worsening was observed in 4.8% (95% CI: 2.3%-8.1%) of patients. Adverse events and serious adverse events were reported in 52.8% (95% CI: 46.7%-58.8%) and 0.1% (95% CI: 0%-0.2%) of vaccinations, respectively.

CONCLUSION

COVID-19 vaccination does not appear to increase the risk of relapse and serious adverse events in MS. Weighted against the risks of SARS-CoV-2-related complications and MS exacerbations, these safety data provide compelling pro-vaccination arguments for MS patients.

摘要

背景

关于多发性硬化症(MS)患者接种严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)疫苗的安全性数据有限。

目的

估计(1)疫苗接种者中出现 MS 患者复发的比例;(2)短暂性神经恶化、不良事件和严重不良事件的发生率;(3)不同 SARS-CoV-2 疫苗类型的先前关注结局。

方法

对药物警戒登记处和观察性研究进行系统评价和荟萃分析。

结果

纳入了 19 项包含 14755 名 MS 患者的观察性研究,他们接受了 23088 剂 COVID-19 疫苗。患者的平均年龄为 43.3 岁(95%置信区间[CI]:40-46.6);82.6%(95%CI:73.9-89.8)的患者被诊断为复发缓解型、继发进展型、原发进展型 MS 和临床孤立综合征,12.6%(95%CI:6.3-20.8)、6.7%(95%CI:4.2-9.9)和 2.9%(95%CI:1-5.9)的患者被诊断为其他类型的 MS。在接种疫苗后 20 天(95%CI:12-28.2)的平均时间间隔内,MS 患者复发的比例为 1.9%(95%CI:1.3%-2.6%; = 78%),接种的 SARS-CoV-2 疫苗类型与复发风险无关(对于亚组差异 = 0.7 信使 RNA(mRNA)、灭活病毒和腺病毒载体疫苗)。接种疫苗后,有 4.8%(95%CI:2.3%-8.1%)的患者出现短暂性神经恶化。分别有 52.8%(95%CI:46.7%-58.8%)和 0.1%(95%CI:0%-0.2%)的患者报告了不良事件和严重不良事件。

结论

COVID-19 疫苗接种似乎不会增加 MS 患者的复发和严重不良事件的风险。权衡 SARS-CoV-2 相关并发症和 MS 恶化的风险,这些安全性数据为 MS 患者提供了有力的疫苗接种理由。