Department of Adolescent Rheumatology, University College London Hospital (UCLH), London, United Kingdom.
Medical School, University College London (UCL), London, United Kingdom.
Front Immunol. 2023 Aug 25;14:1159269. doi: 10.3389/fimmu.2023.1159269. eCollection 2023.
Despite children and young people (CYP) having a low risk for severe coronavirus disease 2019 (COVID-19) outcomes, there is still a degree of uncertainty related to their risk in the context of immunodeficiency or immunosuppression, primarily due to significant reporting bias in most studies, as CYP characteristically experience milder or asymptomatic COVID-19 infection and the severe outcomes tend to be overestimated.
A comprehensive systematic review to identify globally relevant studies in immunosuppressed CYP and CYP in general population (defined as younger than 25 years of age) up to 31 October 2021 (to exclude vaccinated populations) was performed. Studies were included if they reported the two primary outcomes of our study, admission to intensive therapy unit (ITU) and mortality, while data on other outcomes, such as hospitalization and need for mechanical ventilation were also collected. A meta-analysis estimated the pooled proportion for each severe COVID-19 outcome, using the inverse variance method. Random effects models were used to account for interstudy heterogeneity.
The systematic review identified 30 eligible studies for each of the two populations investigated: immunosuppressed CYP ( = 793) and CYP in general population ( = 102,022). Our meta-analysis found higher estimated prevalence for hospitalization (46% vs. 16%), ITU admission (12% vs. 2%), mechanical ventilation (8% vs. 1%), and increased mortality due to severe COVID-19 infection (6.5% vs. 0.2%) in immunocompromised CYP compared with CYP in general population. This shows an overall trend for more severe outcomes of COVID-19 infection in immunocompromised CYP, similar to adult studies.
This is the only up-to-date meta-analysis in immunocompromised CYP with high global relevance, which excluded reports from hospitalized cohorts alone and included 35% studies from low- and middle-income countries. Future research is required to characterize individual subgroups of immunocompromised patients, as well as impact of vaccination on severe COVID-19 outcomes.
PROSPERO identifier, CRD42021278598.
尽管儿童和青少年(CYP)患严重 2019 冠状病毒病(COVID-19)的风险较低,但在免疫功能低下或免疫抑制的情况下,他们的风险仍存在一定程度的不确定性,主要是因为大多数研究中存在显著的报告偏倚,因为 CYP 典型地经历较轻或无症状的 COVID-19 感染,而严重结果往往被高估。
对截至 2021 年 10 月 31 日(排除接种人群)全球范围内与免疫抑制 CYP 和一般人群(定义为年龄小于 25 岁)中的 CYP 相关的研究进行了全面的系统评价。如果研究报告了我们研究的两个主要结果,即入住重症监护治疗病房(ITU)和死亡,同时还收集了其他结果(如住院和需要机械通气)的数据,则纳入研究。使用逆方差法对每个严重 COVID-19 结果的汇总比例进行荟萃分析。使用随机效应模型来解释研究间的异质性。
该系统评价为研究的两个人群各确定了 30 项符合条件的研究:免疫抑制 CYP(n=793)和一般人群中的 CYP(n=102022)。我们的荟萃分析发现,免疫功能低下 CYP 中因 COVID-19 感染而住院(46% vs. 16%)、入住 ICU(12% vs. 2%)、机械通气(8% vs. 1%)和因 COVID-19 感染而导致的死亡率增加(6.5% vs. 0.2%)的估计患病率较高。这表明,与一般人群中的 CYP 相比,免疫功能低下 CYP 的 COVID-19 感染的严重后果呈总体趋势。
这是唯一一项具有高度全球相关性的免疫抑制 CYP 的最新荟萃分析,它排除了仅来自住院队列的报告,并纳入了来自低收入和中等收入国家的 35%的研究。需要进一步研究以确定免疫抑制患者的各个亚组以及疫苗接种对严重 COVID-19 结局的影响。
PROSPERO 标识符,CRD42021278598。