Not hospitalized, mild-to-moderate |
NIH: Bamlanivimab + etesevimabb or casirivimab + imdevimabb or sotrovimab; 3-day course of remdesivir in settings where omicron is the dominant variant; ritonavir-boosted nirmatrelvir, molnupiravir
ERS: N/A
WHO: Among patients at high risk of progression to severe disease casirivimab + imdevimab (conditional recommendation)
IDSA: Among ambulatory patients with mild-to-moderate COVID-19 at high risk of progression to severe disease; bamlanivimab/etesevimab, casirivimab/imdevimab or sotrovimab, remdesivir, ritonavir-boosted nirmatrelvir, molnupiravir (conditional recommendation)
|
Hospitalized and not requiring supplemental oxygen |
|
Hospitalized and requiring supplemental oxygen |
NIH: Remdesivir; dexamethasone + remdesivir; dexamethasone (when combination with remdesivir is not possible)
ERS: Corticosteroids + tocilizumab (conditional recommendation)
WHO: Systemic corticosteroids + tocilizumab or sarilumab; casirivimab + imdevimab (conditional recommendation)
IDSA: Dexamethasone or alternative corticosteroids; tocilizumabc + corticosteroids; sarilumab; remdesivir (5 days vs.10 days; conditional recommendation); baricitinib + remdesivird or baricitinib + remdesivir + corticosteroids (conditional recommendation); tofacitinib
|
Hospitalized and requiring oxygen delivery through high-flow device or noninvasive ventilation |
NIH: Dexamethasone; dexamethasone + remdesivir; add baricitinib or tocilizumab for recently hospitalized with increasing oxygen needs and systemic inflammation. If neither are available or feasible to use, use tofacitinib instead of baricitinib or sarilumab instead of tocilizumab
ERS: Corticosteroids + tocilizumab (conditional recommendation)
WHO: Systemic corticosteroids + tocilizumab or sarilumab; casirivimab + imdevimab (conditional recommendation in seronegative patients)
IDSA: Dexamethasone or alternative corticosteroids; tocilizumabc + corticosteroids; sarilumab; remdesivir (5 days vs.10 days; conditional recommendation); baricitinib + remdesivir or baricitinib + remdesivir + corticosteroids (conditional recommendation); tofacitinib
|
Hospitalized and requiring mechanical ventilation |
NIH: Dexamethasone; add tocilizumab for patients who are within 24 hours of ICU admission or sarilumab if tocilizumab is not available or feasible to use
ERS: Corticosteroids + tocilizumab
WHO: Systemic corticosteroids + tocilizumab or sarilumab; casirivimab + imdevimab (conditional recommendation in seronegative patients)
IDSA: Dexamethasone or alternative corticosteroids; tocilizumabc; sarilumab
|
Not recommended |
NIH: Dexamethasone or other systemic glucocorticoids in non-hospitalized patients; continuation of remdesivir or baricitinib in patients discharged from hospital not requiring supplemental oxygen; chloroquine or hydroxychloroquine and/or azithromycin, lopinavir/ritonavir and other HIV protease inhibitors for outpatient treatment; antibacterial therapy in outpatients; dexamethasone in hospitalized patients not requiring supplemental oxygen; baricitinib + tocilizumab in combination; interferons; acalabrutinib, ibrutinib, zanubrutinib; ruxolitinib, tofacitinib; non-SARS-CoV-2-specific intravenous immunoglobulin; sarilumab in patients not requiring ICU care or admitted to ICU but not requiring ventilation or high-flow oxygen; siltuximab; colchicine in hospitalized patients; convalescent plasma (low titer; any titer in mechanically ventilated patients; high titer in hospitalized patients who are not mechanically ventilated)
ERS: Hydroxychloroquine; azithromycin; hydroxychloroquine + azithromycin; lopinavir/ritonavir; interferon beta; remdesivir in patients who require invasive mechanical ventilation
WHO: Chloroquine or hydroxychloroquine; lopinavir/ritonavir; remdesivir (conditional); ivermectin (research use only)
IDSA: Corticosteroids (hospitalized patients not needing supplemental oxygen); remdesivir (hospitalized patients not needing supplemental oxygen; patients on invasive ventilation, with septic shock or on ECMO); hydroxychloroquine or chloroquine; hydroxychloroquine ± azithromycin; lopinavir/ritonavir; convalescent plasma (hospitalized patients); famotidine; ivermectin; bamlanivimab monotherapy
|
Insufficient data to support a recommendation, or no recommendation |
NIH: Continued remdesivir or baricitinib after hospital discharge in patients requiring supplemental oxygen; ivermectin; convalescent plasma (high titer in hospitalized patients with impaired immunity or non-hospitalized patients); colchicine (for non-hospitalized patients); fluvoxamine; granulocyte-macrophage colony-stimulating factor inhibitors for hospitalized patients; inhaled budesonide; interleukin-1 inhibitors (e.g. anakinra); interferon beta for early mild-to-moderate disease; sarilumab (for patients within 24 hours of ICU admission who require ventilation or high-flow oxygen)
ERS: Remdesivir in hospitalized patients not requiring invasive mechanical ventilation
WHO: N/A
IDSA: Convalescent plasma (ambulatory patients with mild-moderate disease – research use only); ivermectin (research use only)
|