Department of Infectious Diseases, Tan Tock Seng Hospital, Singapore, Singapore.
National Centre for Infectious Diseases, Singapore, Singapore.
BMC Infect Dis. 2023 Feb 14;23(1):93. doi: 10.1186/s12879-023-08056-8.
The objectives of this study were to describe the coronavirus disease caused by SARS-CoV-2 (COVID-19) reinfection evaluation algorithm used in the early phase of the pandemic in Singapore and analyze the clinical and laboratory characteristics of the cases evaluated.
We performed a retrospective case-control analysis including all COVID-19 cases evaluated for possible reinfection under the local COVID-19 reinfection evaluation programme between 1 June 2020-30 June 2021. Whole genome sequencing (WGS) was used as confirmatory testing. We compared all reinfection ("RI") cases against those who were evaluated but eventually assessed not to be reinfection ("non-RI").
There were 74 possible reinfection cases evaluated through the programme, of which 32 were subsequently classified as RI. There was strong statistical evidence that RI cases had a longer interval between 1st and 2nd episode (mean 297 days; 95%-confidence interval (CI) 267-327) compared to non-RI cases (mean 186 days; 95%-CI 144-228). The cycle threshold (Ct) value of initial polymerase chain rection (PCR) at 2nd episode was also found to be significantly lower in RI cases (mean 23; 95%-CI 20-26) compared to non-RI cases (mean 34; 95%-CI 32-36). There was no significant difference in the proportion of individuals who had fever, acute respiratory symptoms or asymptomatic in both groups. Delta and beta variants were most commonly identified from WGS and provide indication of re-infection as these were not 'wild-type' and were not circulating during the time period of the index infection.
Using a combination of serologic, microbiologic and genomic criteria to evaluate possible reinfection cases is useful and can provide a framework for evaluation that may be modified for future similar situations.
本研究的目的是描述 SARS-CoV-2(COVID-19)再感染评估算法在新加坡大流行早期的使用情况,并分析评估病例的临床和实验室特征。
我们对 2020 年 6 月 1 日至 2021 年 6 月 30 日期间通过当地 COVID-19 再感染评估计划评估的所有可能再感染 COVID-19 的病例进行了回顾性病例对照分析。全基因组测序(WGS)用于确证性检测。我们将所有再感染(“RI”)病例与那些经过评估但最终未被判定为再感染的病例(“非 RI”)进行比较。
通过该计划评估了 74 例可能的再感染病例,其中 32 例随后被归类为 RI。有强有力的统计证据表明,RI 病例的第 1 次和第 2 次发作之间的间隔时间更长(平均 297 天;95%置信区间(CI)267-327),而非 RI 病例(平均 186 天;95%CI 144-228)。RI 病例的第 2 次发作初始聚合酶链反应(PCR)的循环阈值(Ct)值也明显低于非 RI 病例(平均 23;95%-CI 20-26)。两组人群中发热、急性呼吸道症状或无症状的比例无显著差异。最常见的 WGS 检测到的 Delta 和 Beta 变体表明存在再感染,因为这些变体不是“野生型”,并且在索引感染期间未传播。
使用血清学、微生物学和基因组标准相结合来评估可能的再感染病例是有用的,并为评估提供了一个框架,该框架可能会根据未来类似情况进行修改。