Table 3.
Variability in recommendations of targeted covid-19 therapies across guidelines
Country | Antivirals | Level of support | Notes |
---|---|---|---|
Italy | If need for oxygen or clinical worsening: remdesivir ampoules 150 mg 1 day 200 mg IV in 30 min, then 100 mg IV OD for another 9 days in combination with chloroquine 500 mg BD or hydroxychloroquine 200 mg BD (duration of treatment 5-20 days) | Expert consensus following literature review | Methods for reaching conclusions unclear |
In severe disease: remdesivir 1 day 200 mg IV, then 100 mg/day IV (days 2-10) + chloroquine 500 mg BD or hydroxychloroquine 200 mg × 2 PO 5-20 days | |||
Russia | In moderate to severe infections: 400 mg lopinavir/100 mg ritonavir BD for 14 days PO; or 400 mg lopinavir/100 mg ritonavir) (5 mL) BD 14 days NGT; or recombinant interferon 1b 0.25 mg/mL (8 million IU) SC every second day for 14 days; or ribavarin 2 g loading dose, then 1200 mg TID for 4 days, then 4-6 days 600 mg TID | Results from literature review led to three drugs being chosen. No preference or order is recommended. Not clear how authors excluded other options | Advises antivirals can be prescribed off label after benefits v risk assessment. Oseltamivir not recommended |
France | Advised for all patients admitted to ICU on confirmation of diagnosis. First line: lopinavir/ritonavir 400 mg BD; second line: hydroxychloroquine 200 mg BD | If parenchymal involvement. Recommendations based on data in SARS and MERS. First line treatment chosen because readily available | Advises against ribavarin owing to inconclusive data |
Netherlands | In moderate disease: first line chloroquine 600 mg PO, then 300 mg for 5 days; second line lopinavir/ritonavir 400/100 mg BD for 14 days | Noting that very little information is available, makes no definitive recommendations. Acknowledges lack of phase I data for remdesivir | Advises against use of ribavirin alone owing to toxicity at required doses. Notes poor evidence for interferon in combination with ribavirin. Oseltamivir not recommended |
In severe disease: remdesivir + chloroquine or lopinavir/ritonavir + chloroquine | |||
Spain | First line: lopinavir/ritonavir 400/100 mg BD PO until disappearance of fever for maximum 14 days; second line: interferon β1b 0.25 mg SC every 48 h for 14 days or interferon α2b 5 million units in 2 mL of sterile serum, BD INH | Only for severe pneumonia, CURB >65, SpO2 <90% | Notes in-vitro studies and ongoing Chinese trials. Oseltamivir not recommended |
Remdesivir 200 mg IV, then 100 mg IV OD for 9 days | For compassionate use only in severe disease | ||
China | Alpha-interferon (5 million units or equivalent dose BD INH) or lopinavir/ritonavir (200/50 mg × 2 BD for ≤10 days); or ribavirin (used jointly with interferon or lopinavir/ritonavir, 500 mg IV TID for adults, for ≤10 days); or chloroquine phosphate (500 mg BD for ≤10 days); or arbidol (200 mg TID for adults, for ≤10 days) | Does not recommend using three or more antiviral drugs at same time | |
Germany | Numerous antiviral therapies are used in the context of SARS-CoV-2. Too little data are currently available to make a therapy recommendation in Germany. Even for severe forms of COVID-19 there is insufficient evidence to recommend therapy | ||
Japan | No specific therapy recommended. Lopinavir/ritonavir, anti-influenza drug favipiravir, remdesivir, and ciclesonide, an inhaled steroid used in asthma, are listed as potential therapeutic agents | Advises these agents may be future therapeutic agents pending trials | |
South Korea | Lopinavir/ritonavir 400/100 mg BD for 7-10 days; or hydroxychloroquine 400 mg OD; or interferon can be administered in combination with lopinavir/ritonavir | Remdesivir only to be used in clinical trials | Ribavirin not recommended owing to adverse reactions |
BD=twice daily; ICU=intensive care unit; INH=inhalation; IV=intravenous; MERS=Middle East respiratory syndrome; NGT=nasogastric tube; OD=once daily; PO=oral; SARS-CoV-2=severe acute respiratory disorder coronavirus 2; SC=subcutaneous; TID=three times daily;