Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
Department of Health Research Methods, Evidence & Impact, McMaster University, Hamilton, Ontario, Canada.
JAMA Intern Med. 2022 Apr 1;182(4):376-385. doi: 10.1001/jamainternmed.2021.8515.
Vaccination against SARS-CoV-2 is a highly effective strategy to prevent infection and severe COVID-19 outcomes. The best strategy for a second dose of vaccine among persons who had an immediate allergic reaction to their first SARS CoV-2 vaccination is unclear.
To assess the risk of severe immediate allergic reactions (eg, anaphylaxis) to a second dose of SARS-CoV-2 mRNA vaccine among persons with immediate allergic reactions to their first vaccine dose.
MEDLINE, Embase, Web of Science, and the World Health Organization Global Coronavirus database were searched from inception through October 4, 2021.
Included studies addressed immediate allergic reactions of any severity to a second SARS-CoV-2 vaccine dose in persons with a known or suspected immediate allergic reaction (<4 hours after vaccination) after their first SARS-CoV-2 vaccine dose. Studies describing a second vaccine dose among persons reporting delayed reactions (>4 hours after vaccination) were excluded.
Paired reviewers independently selected studies, extracted data, and assessed risk of bias. Random-effects models were used for meta-analysis. The GRADE (Grading of Recommendation, Assessment, Development, and Evaluation) approach evaluated certainty of the evidence.
Risk of severe immediate allergic reaction and repeated severe immediate allergic reactions with a second vaccine dose. Reaction severity was defined by the reporting investigator, using Brighton Collaboration Criteria, Ring and Messmer criteria, World Allergy Organization criteria, or National Institute of Allergy and Infectious Diseases criteria.
Among 22 studies of SARS-CoV-2 mRNA vaccines, 1366 individuals (87.8% women; mean age, 46.1 years) had immediate allergic reactions to their first vaccination. Analysis using the pooled random-effects model found that 6 patients developed severe immediate allergic reactions after their second vaccination (absolute risk, 0.16% [95% CI, 0.01%-2.94%]), 232 developed mild symptoms (13.65% [95% CI, 7.76%-22.9%]), and, conversely, 1360 tolerated the dose (99.84% [95% CI, 97.09%-99.99%]). Among 78 persons with severe immediate allergic reactions to their first SARS-CoV-2 mRNA vaccination, 4 people (4.94% [95% CI, 0.93%-22.28%]) had a second severe immediate reaction, and 15 had nonsevere symptoms (9.54% [95% CI, 2.18%-33.34%]). There were no deaths. Graded vaccine dosing, skin testing, and premedication as risk-stratification strategies did not alter the findings. Certainty of evidence was moderate for those with any allergic reaction to the first dose and low for those with severe allergic reactions to the first dose.
In this systematic review and meta-analysis of case studies and case reports, the risk of immediate allergic reactions and severe immediate reactions or anaphylaxis associated with a second dose of an SARS-CoV-2 mRNA vaccine was low among persons who experienced an immediate allergic reaction to their first dose. These findings suggest that revaccination of individuals with an immediate allergic reaction to a first SARS-CoV-2 mRNA vaccine dose in a supervised setting equipped to manage severe allergic reactions can be safe.
重要性:接种 SARS-CoV-2 疫苗是预防感染和严重 COVID-19 结果的一种非常有效的策略。对于在首次 SARS CoV-2 疫苗接种后立即发生过敏反应的人,第二剂疫苗的最佳策略尚不清楚。
目的:评估在首次疫苗接种后立即发生过敏反应的人群中,接种第二剂 SARS-CoV-2 mRNA 疫苗后发生严重立即过敏反应(例如过敏反应)的风险。
数据来源:从研究开始到 2021 年 10 月 4 日,通过 MEDLINE、Embase、Web of Science 和世界卫生组织全球冠状病毒数据库进行了搜索。
研究选择:纳入的研究包括在已知或疑似首次 SARS-CoV-2 疫苗接种后 4 小时内发生任何严重程度的立即过敏反应(<4 小时)的人群中,第二次 SARS-CoV-2 疫苗接种的过敏反应。描述在报告延迟反应(>4 小时后接种疫苗)的人群中第二剂疫苗的研究被排除在外。
数据提取和综合:配对审查员独立选择研究、提取数据并评估偏倚风险。使用随机效应模型进行荟萃分析。使用 GRADE(推荐分级、评估、制定和评估)方法评估证据的确定性。
主要结果和措施:第二次疫苗接种后严重立即过敏反应和重复严重立即过敏反应的风险。反应严重程度由报告的研究者根据 Brighton 合作标准、Ring 和 Messmer 标准、世界过敏组织标准或国家过敏和传染病研究所标准定义。
结果:在 22 项 SARS-CoV-2 mRNA 疫苗研究中,1366 名(87.8%为女性;平均年龄 46.1 岁)对首次接种疫苗有立即过敏反应。使用汇总随机效应模型分析发现,6 名患者在第二次接种后出现严重立即过敏反应(绝对风险,0.16%[95%CI,0.01%-2.94%]),232 名患者出现轻度症状(13.65%[95%CI,7.76%-22.9%]),而 1360 名患者耐受剂量(99.84%[95%CI,97.09%-99.99%])。在 78 名对首次 SARS-CoV-2 mRNA 疫苗接种有严重立即过敏反应的患者中,4 人(4.94%[95%CI,0.93%-22.28%])有第二次严重立即反应,15 人有非严重症状(9.54%[95%CI,2.18%-33.34%])。没有死亡。分级疫苗接种、皮肤试验和预用药作为风险分层策略并没有改变这些发现。对于首次剂量有任何过敏反应的人,证据的确定性为中度,对于首次剂量有严重过敏反应的人,证据的确定性为低。
结论和相关性:在这项对病例研究和病例报告的系统评价和荟萃分析中,在首次接种 SARS-CoV-2 mRNA 疫苗后立即发生过敏反应的人群中,第二次接种 SARS-CoV-2 mRNA 疫苗与立即过敏反应和严重立即反应或过敏反应相关的风险较低。这些发现表明,在配备有管理严重过敏反应能力的监督环境中,对首次 SARS-CoV-2 mRNA 疫苗接种后立即发生过敏反应的个体进行疫苗复种可能是安全的。