Department of Epidemiology, Children's Hospital Colorado, Aurora, Colorado, USA.
Department of Pediatrics (Center for Cancer and Blood Disorders), University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, Colorado, USA.
Pediatr Blood Cancer. 2021 Dec;68(12):e29277. doi: 10.1002/pbc.29277. Epub 2021 Aug 28.
We evaluated the length of time immunocompromised children (ICC) remain positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), identified factors associated with viral persistence, and determined cycle threshold (C ) values of children with viral persistence as a surrogate of viral load.
We conducted a retrospective cohort study of ICC at a pediatric hospital from March 2020 to March 2021. Immunocompromised status was defined as primary, secondary, or acquired due to medical comorbidities/immunosuppressive treatment. The primary outcome was time to first of two consecutive negative SARS-CoV-2 polymerase chain reaction (PCR) tests at least 24 hours apart. Testing of sequential clinical specimens from the same subject was conducted using the Centers for Disease Control (CDC) 2019-nCoV real-time reverse transcriptase (RT)-PCR Diagnostic Panel assay. Descriptive statistics, Kaplan-Meier curve median event times and log-rank tests were used to compare outcomes between groups.
Ninety-one children met inclusion criteria. Median age was 15.5 years (interquartile range [IQR] 8-18), 64% were male, 58% were White, and 43% were Hispanic/Latinx. Most (67%) were tested in outpatient settings and 58% were asymptomatic. The median time to two negative tests was 42 days (IQR 25.0-55.0), with no differences in median time by illness presentation or level of immunosuppression. Seven children had more than one sample available for repeat testing, and five of seven (71%) children had initial C values of <30 (moderate to high viral load); four children had C values of <30, 3-4 weeks later, suggesting persistent moderate to high viral loads.
Most ICC with SARS-CoV-2 infection had mild disease, with prolonged viral persistence >6 weeks and moderate to high viral load.
我们评估免疫功能低下儿童(ICC)持续感染严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的时间,确定与病毒持续存在相关的因素,并确定病毒持续存在儿童的循环阈值(C)值作为病毒载量的替代指标。
我们对 2020 年 3 月至 2021 年 3 月期间一家儿童医院的 ICC 进行了回顾性队列研究。免疫功能低下状态定义为原发性、继发性或由医疗合并症/免疫抑制治疗引起的获得性。主要结局是首次两次连续 SARS-CoV-2 聚合酶链反应(PCR)检测均为阴性的时间,两次检测至少相隔 24 小时。使用疾病控制与预防中心(CDC)2019-nCoV 实时逆转录(RT)-PCR 诊断试剂盒对同一受试者的连续临床标本进行检测。采用描述性统计、Kaplan-Meier 曲线中位数事件时间和对数秩检验比较组间结局。
91 名儿童符合纳入标准。中位年龄为 15.5 岁(四分位距 [IQR] 8-18),64%为男性,58%为白人,43%为西班牙裔/拉丁裔。大多数(67%)在门诊接受检测,58%为无症状。两次阴性检测的中位时间为 42 天(IQR 25.0-55.0),按疾病表现或免疫抑制程度不同,中位时间无差异。7 名儿童有 1 个以上样本可用于重复检测,7 名儿童中有 5 名(71%)初始 C 值<30(中至高病毒载量);4 名儿童在 3-4 周后 C 值<30,提示持续存在中至高病毒载量。
大多数 SARS-CoV-2 感染的 ICC 疾病较轻,病毒持续时间超过 6 周,病毒载量中至高。