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新型冠状病毒肺炎(COVID-19)疫苗接种后心肌炎和心包炎的发生率、危险因素、自然史和假设发病机制:基于实时证据的综合分析和综述。

Incidence, risk factors, natural history, and hypothesised mechanisms of myocarditis and pericarditis following covid-19 vaccination: living evidence syntheses and review.

机构信息

Alberta Research Centre for Health Evidence, Department of Pediatrics, University of Alberta, Edmonton, AB, Canada.

Department of Pediatrics, Division of Pediatric Cardiology, University of Alberta, Edmonton, AB, Canada.

出版信息

BMJ. 2022 Jul 13;378:e069445. doi: 10.1136/bmj-2021-069445.

Abstract

OBJECTIVES

To synthesise evidence on incidence rates and risk factors for myocarditis and pericarditis after use of mRNA vaccination against covid-19, clinical presentation, short term and longer term outcomes of cases, and proposed mechanisms.

DESIGN

Living evidence syntheses and review.

DATA SOURCES

Medline, Embase, and the Cochrane Library were searched from 6 October 2020 to 10 January 2022; reference lists and grey literature (to 13 January 2021). One reviewer completed screening and another verified 50% of exclusions, using a machine learning program to prioritise records. A second reviewer verified all exclusions at full text, extracted data, and (for incidence and risk factors) risk of bias assessments using modified Joanna Briggs Institute tools. Team consensus determined certainty of evidence ratings for incidence and risk factors using GRADE (Grading of Recommendations, Assessment, Development and Evaluation).

ELIGIBILITY CRITERIA FOR SELECTING STUDIES

Large (>10 000 participants) or population based or multisite observational studies and surveillance data (incidence and risk factors) reporting on confirmed myocarditis or pericarditis after covid-19 mRNA vaccination; case series (n≥5, presentation, short term clinical course and longer term outcomes); opinions, letters, reviews, and primary studies focused on describing or supporting hypothesised mechanisms.

RESULTS

46 studies were included (14 on incidence, seven on risk factors, 11 on characteristics and short term course, three on longer term outcomes, and 21 on mechanisms). Incidence of myocarditis after mRNA vaccines was highest in male adolescents and male young adults (age 12-17 years, range 50-139 cases per million (low certainty); 18-29 years, 28-147 per million (moderate certainty)). For girls and boys aged 5-11 years and women aged 18-29 years, incidence of myocarditis after vaccination with BNT162b2 (Pfizer/BioNTech) could be fewer than 20 cases per million (low certainty). Incidence after a third dose of an mRNA vaccine had very low certainty evidence. For individuals of 18-29 years, incidence of myocarditis is probably higher after vaccination with mRNA-1273 (Moderna) compared with Pfizer (moderate certainty). Among individuals aged 12-17, 18-29, or 18-39 years, incidence of myocarditis or pericarditis after dose two of an mRNA vaccine for covid-19 might be lower when administered ≥31 days compared with ≤30 days after dose one (low certainty). Data specific to men aged 18-29 years indicated that the dosing interval might need to increase to ≥56 days to substantially drop myocarditis or pericarditis incidence. For clinical course and short term outcomes, only one small case series (n=8) was found for 5-11 year olds. In adolescents and adults, most (>90%) myocarditis cases involved men of a median 20-30 years of age and with symptom onset two to four days after a second dose (71-100%). Most people were admitted to hospital (≥84%) for a short duration (two to four days). For pericarditis, data were limited but more variation than myocarditis has been reported in patient age, sex, onset timing, and rate of admission to hospital. Three case series with longer term (3 months; n=38) follow-up suggested persistent echocardiogram abnormalities, as well as ongoing symptoms or a need for drug treatments or restriction from activities in >50% of patients. Sixteen hypothesised mechanisms were described, with little direct supporting or refuting evidence.

CONCLUSIONS

These findings indicate that adolescent and young adult men are at the highest risk of myocarditis after mRNA vaccination. Use of a Pfizer vaccine over a Moderna vaccine and waiting for more than 30 days between doses might be preferred for this population. Incidence of myocarditis in children aged 5-11 years is very rare but certainty was low. Data for clinical risk factors were very limited. A clinical course of mRNA related myocarditis appeared to be benign, although longer term follow-up data were limited. Prospective studies with appropriate testing (eg, biopsy and tissue morphology) will enhance understanding of mechanism.

摘要

目的

综合评估 mRNA 疫苗接种后心肌炎和心包炎的发病率和风险因素、临床表现、短期和长期结局,以及提出的发病机制。

设计

活体证据综合和综述。

数据来源

2020 年 10 月 6 日至 2022 年 1 月 10 日检索 Medline、Embase 和 Cochrane 图书馆;参考列表和灰色文献(至 2021 年 1 月 13 日)。一位审稿人完成筛选,另一位审稿人使用机器学习程序对记录进行优先级排序,以验证 50%的排除结果。第二位审稿人在全文层面验证所有排除项,提取数据,并(对于发病率和风险因素)使用改良的 Joanna Briggs 研究所工具进行偏倚风险评估。使用 GRADE(推荐分级、评估、制定与评价)团队共识确定发病率和风险因素的证据质量等级。

纳入研究的选择标准

大型(>10000 名参与者)或基于人群或多地点观察性研究和监测数据(发病率和风险因素)报告新冠病毒 mRNA 疫苗接种后确诊心肌炎或心包炎;病例系列(n≥5,临床表现、短期临床病程和长期结局);关注描述或支持假设发病机制的意见、信件、综述和原始研究。

结果

纳入 46 项研究(14 项关于发病率,7 项关于风险因素,11 项关于特征和短期病程,3 项关于长期结局,21 项关于发病机制)。男性青少年和年轻男性(12-17 岁,每百万人中发病率 50-139 例;18-29 岁,每百万人中发病率 28-147 例,低确定性)接种 mRNA 疫苗后,心肌炎的发病率最高。5-11 岁的男孩和女孩以及 18-29 岁的女性接种 BNT162b2(辉瑞/生物技术)后,心肌炎的发病率可能低于每百万人 20 例(低确定性)。接种第三剂 mRNA 疫苗的发病率证据确定性非常低。对于 18-29 岁的人群,与接种 Pfizer(中度确定性)相比,接种 mRNA-1273(Moderna)后心肌炎的发病率可能更高。在 12-17 岁、18-29 岁或 18-39 岁的人群中,与首剂接种后≤30 天相比,第二剂接种后≥31 天接种新冠病毒 mRNA 疫苗后,心肌炎或心包炎的发病率可能更低(低确定性)。特定于 18-29 岁男性的数据表明,可能需要将给药间隔增加至≥56 天,以大幅降低心肌炎或心包炎的发病率。对于临床病程和短期结局,仅发现了一项针对 5-11 岁儿童的小型病例系列研究(n=8)。在青少年和成年人中,大多数(>90%)心肌炎病例涉及中位年龄为 20-30 岁的男性,且症状在第二剂接种后 2-4 天出现(71-100%)。大多数人因住院时间短(2-4 天)而住院(≥84%)。心包炎的数据有限,但与心肌炎相比,患者年龄、性别、发病时间和住院率的变化更大。三项随访时间为 3 个月(n=38)的病例系列研究表明,在>50%的患者中,超声心动图异常持续存在,以及持续存在症状或需要药物治疗或限制活动。描述了 16 种假设发病机制,但很少有直接的支持或反驳证据。

结论

这些发现表明,青少年和年轻男性接种 mRNA 疫苗后心肌炎的风险最高。对于该人群,可能更倾向于使用辉瑞疫苗而不是 Moderna 疫苗,且两次接种之间等待时间超过 30 天。5-11 岁儿童心肌炎的发病率非常低,但确定性较低。关于临床风险因素的数据非常有限。mRNA 相关心肌炎的临床病程似乎是良性的,尽管长期随访数据有限。进行适当检测(如活检和组织形态学)的前瞻性研究将有助于了解发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9511/9277081/bc58bbd4f3f6/pilj069445.f1.jpg

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