| Literature DB >> 33259268 |
Haibo Li1,2, Lili Ren3,4, Lulu Zhang3, Yeming Wang1,5, Li Guo3,4, Conghui Wang3, Yan Xiao3,4, Ying Wang3, Jian Rao3, Xinming Wang3, Ying Liu6, Chaolin Huang6, Xiaoying Gu7, Guohui Fan7, Hui Li1,2, Binghuai Lu1,2, Bin Cao1,2,5,8, Jianwei Wang3,4.
Abstract
To identify the association between the kinetics of viral load and clinical outcome in severe coronavirus disease 2019 (COVID-19) patients, a retrospective study was performed by involved 188 hospitalized severe COVID-19 patients in the LOTUS China trial. Among the collected 578 paired throat swab (TS) and anal swab (AS) samples, viral RNA was detected in 193 (33.4%) TS and 121 (20.9%) AS. A higher viral RNA load was found in TS than that of AS, with means of 1.0 × 106 and 2.3 × 105 copies/ml, respectively. In non-survivors, the viral RNA in AS was detected earlier than that in survivors (median of 14 days vs 19 days, P = 0.007). The positivity and viral load in AS were higher in non-survivors than that of survivors at week 2 post symptom onset (P = 0.006). A high initial viral load in AS was associated with death (OR 1.368, 95% CI 1.076-1.741, P = 0.011), admission to the intensive care unit (OR 1.237, 95% CI 1.001-1.528, P = 0.049) and need for invasive mechanical ventilation (OR 1.340, 95% CI 1.076-1.669, P = 0.009). Our findings indicated viral replication in extrapulmonary sites should be monitored intensively during antiviral therapy.Entities:
Keywords: COVID-19; SARS-CoV-2; anal swabs; clinical outcome; viral load
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Year: 2020 PMID: 33259268 PMCID: PMC7782020 DOI: 10.1080/22221751.2020.1858700
Source DB: PubMed Journal: Emerg Microbes Infect ISSN: 2222-1751 Impact factor: 7.163