Zhang Bingyu, Wu Qiong, Jhaveri Ravi, Zhou Ting, Becich Michael J, Bisyuk Yuriy, Blanceró Frank, Chrischilles Elizabeth A, Chuang Cynthia H, Cowell Linday G, Fort Daniel, Horowitz Carol R, Kim Susan, Ladino Nathalia, Liebovitz David M, Liu Mei, Mosa Abu S M, Schwenk Hayden T, Suresh Srinivasan, Taylor Bradley W, Williams David A, Morris Jeffrey S, Forrest Christopher B, Chen Yong
The Center for Health AI and Synthesis of Evidence (CHASE), University of Pennsylvania, Philadelphia, PA, USA.
The Graduate Group in Applied Mathematics and Computational Science, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA, USA.
medRxiv. 2025 Mar 30:2025.03.28.25324858. doi: 10.1101/2025.03.28.25324858.
Post-acute sequelae of SARS-CoV-2 infection (PASC) remains a major public health challenge. While previous studies have focused on characterizing PASC and identifying its subphenotypes in children and adolescents following an initial SARS-CoV-2 infection, the risks of PASC with Omicron-variant reinfections remain unclear. Using a real-world data approach, this study investigates the risks of PASC following reinfections during the Omicron phase in the pediatric population.
To investigate the risks of PASC diagnosis and 24 PASC symptoms and conditions after reinfection of SARS-CoV-2 during Omicron period in the pediatric population.
This retrospective cohort study used data from the RECOVER consortium comprising 40 children's hospitals and health institutions in U.S. between January 2022 and October 2023.
A second SARS-CoV-2 infection, confirmed by a positive polymerase-chain-reaction (PCR) or antigen tests, or a diagnose of COVID-19, occurring at least 60 days after the initial infection, compared to the initial infection.
PASC was identified using two approaches: (1) the ICD-10-CM diagnosis code U09.9 and (2) a symptom-based definition including 24 physician-identified symptoms and conditions. Absolute risks of incident PASC were reported, and relative risks (RRs) were calculated by comparing the second infection episode with the first infection episode groups using a modified Poisson regression model, adjusting for demographic, clinical, and healthcare utilization factors through exact matching and propensity scoring matching.
A total of 465,717 individuals under 21 years old (mean [SD] age 8.17 [6.58] years; 52% male) were included. Compared to the first infection, a second infection was associated with significantly increased risk of an overall PASC diagnosis (RR, 2.08; 95% confidence interval [CI], 1.68-2.59), and with many specific conditions including: myocarditis (RR, 3.60; 95% CI, 1.46-8.86); changes in taste and smell (RR, 2.83; 95% CI, 1.41-5.67); thrombophlebitis and thromboembolism (RR, 2.28; 95% CI, 1.71-3.04); heart disease (RR, 1.96; 95% CI, 1.69 to 2.28); acute kidney injury (RR, 1.90; 95% CI, 1.38 to 2.61); fluid and electrolyte (RR, 1.89; 95% CI, 1.62 to 2.20); generalized pain (RR, 1.70; 95% CI, 1.48 to ; arrhythmias (RR, 1.59; 95% CI, 1.45-1.74); abnormal liver enzyme (RR, 1.56; 95% CI, 1.24 to ; fatigue and malaise (RR, 1.50; 95% CI, 1.38 to 1.64); musculoskeletal pain (RR, 1.45; 95% CI, 1.37 to 1.54); abdominal pain (RR, 1.42; 95% CI, 1.34 to 1.50); postural orthostatic tachycardia syndromes (POTS)/dysautonomia (RR, 1.35; 95% CI, 1.20 to 1.51); cognitive functions (RR, 1.32; 95% CI, 1.15 to 1.50); and respiratory signs and symptoms (RR, 1.29; 95% CI, 1.25 to 1.33). The risks were consistent across various organ systems, including cardiovascular, respiratory, gastrointestinal, neurological, and musculoskeletal systems.
Children and adolescents face significantly higher risk of various PASC outcomes after reinfection with SARS-CoV-2. These findings suggest a cumulative risk of PASC and highlight the urgent need for targeted prevention strategies to reduce reinfections, which includes an increased emphasis on initial or re-vaccination of children.
新型冠状病毒2感染的急性后遗症(PASC)仍然是一项重大的公共卫生挑战。虽然先前的研究集中于描述PASC的特征并在初次感染新型冠状病毒2后识别儿童和青少年中的PASC亚表型,但奥密克戎变异株再次感染后的PASC风险仍不明确。本研究采用真实世界数据方法,调查儿科人群在奥密克戎阶段再次感染后的PASC风险。
调查儿科人群在奥密克戎时期再次感染新型冠状病毒2后PASC诊断以及24种PASC症状和病症的风险。
设计、设置和参与者:这项回顾性队列研究使用了来自RECOVER联盟的数据,该联盟包括2022年1月至2023年10月期间美国的40家儿童医院和卫生机构。
与初次感染相比,在初次感染至少60天后,通过聚合酶链反应(PCR)或抗原检测呈阳性确诊的第二次新型冠状病毒2感染,或确诊为新冠肺炎。
使用两种方法识别PASC:(1)国际疾病分类第十次修订本临床修订版(ICD-10-CM)诊断代码U09.9;(2)基于症状的定义,包括24种医生识别的症状和病症。报告了PASC发病的绝对风险,并通过使用修正泊松回归模型将第二次感染发作与第一次感染发作组进行比较来计算相对风险(RR),通过精确匹配和倾向评分匹配对人口统计学、临床和医疗保健利用因素进行调整。
共纳入465717名21岁以下个体(平均[标准差]年龄8.17[6.58]岁;52%为男性)。与初次感染相比,第二次感染与总体PASC诊断风险显著增加相关(RR,2.08;95%置信区间[CI],1.68-2.59),并与许多特定病症相关,包括:心肌炎(RR,3.60;95%CI,1.46-8.86);味觉和嗅觉改变(RR,2.83;95%CI,1.41-5.67);血栓性静脉炎和血栓栓塞(RR,2.28;95%CI,1.71-3.04);心脏病(RR,1.96;95%CI,1.69至2.28);急性肾损伤(RR,1.90;95%CI,1.38至2.61);体液和电解质(RR,1.89;95%CI,1.62至2.20);全身疼痛(RR,1.70;95%CI,1.48至 ;心律失常(RR,1.59;95%CI,1.45-1.74);肝酶异常(RR,1.56;95%CI,1.24至 ;疲劳和不适(RR,1.50;95%CI,1.38至1.64);肌肉骨骼疼痛(RR,1.45;95%CI,1.37至1.54);腹痛(RR,1.42;95%CI,1.34至1.50);体位性直立性心动过速综合征(POTS)/自主神经功能障碍(RR,1.35;95%CI,1.20至1.51);认知功能(RR,1.32;95%CI,1.15至1.50);以及呼吸道体征和症状(RR,1.29;95%CI,1.25至1.33)。这些风险在各个器官系统中是一致的,包括心血管、呼吸、胃肠、神经和肌肉骨骼系统。
儿童和青少年在再次感染新型冠状病毒2后面临各种PASC结局的显著更高风险。这些发现表明PASC存在累积风险,并突出了采取针对性预防策略以减少再次感染的迫切需求,这包括更加强调对儿童进行初次或再次接种疫苗。