High anal swab viral load predisposes adverse clinical outcomes in severe COVID-19 patients.
Haibo LiLili RenLulu ZhangYeming WangLi GuoConghui WangYan XiaoYing WangJian RaoXinming WangYing LiuChaolin HuangXiaoying GuGuohui FanHui LiBinghuai LuBin CaoJianwei WangPublished in: Emerging microbes & infections (2021)
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.
Keyphrases
- sars cov
- mechanical ventilation
- young adults
- respiratory syndrome coronavirus
- coronavirus disease
- early onset
- intensive care unit
- acute respiratory distress syndrome
- high grade
- clinical trial
- emergency department
- nucleic acid
- study protocol
- mesenchymal stem cells
- bone marrow
- phase ii
- respiratory failure
- aqueous solution