Remdesivir for COVID-19: Clinical Guidance
Indication: For hospitalized adults with severe COVID-19 requiring supplemental oxygen, but not mechanical ventilation.
Patient Selection: Initiate treatment if any of the following are present:
- Oxygen saturation ≤94% on room air
- Requiring supplemental oxygen (low-flow or high-flow)
- Respiratory rate >30 breaths/minute
- Respiratory distress with pulmonary infiltrates
Contraindications: Do not initiate in patients:
- Already on mechanical ventilation or ECMO.
- With eGFR ≥10 times upper limit of normal.
- With ALT elevation accompanied by signs/symptoms of liver inflammation.
- Who are pregnant.
- With severe hepatic dysfunction.
- With severe renal impairment (eGFR <30 mL/min/1.73m²).
Dosing (Adults ≥40 kg):
- Day 1: 200 mg IV loading dose
- Days 2-5: 100 mg IV daily
- Infusion Time: 30-120 minutes
Duration:
- 5 days: For patients not requiring mechanical ventilation/ECMO.
- 10 days: For patients requiring mechanical ventilation/ECMO.
- Extension to 10 days: Consider extending beyond 5 days based on clinical judgment if the patient worsens and requires supplemental oxygen (but not mechanical ventilation).
Timing: Initiate as soon as possible after diagnosis. Early treatment (within 2 days of admission) may reduce 30-day in-hospital mortality, particularly in patients needing high-flow oxygen.
Monitoring: Monitor for potential adverse events:
- Metabolic: Hyperglycemia, hypokalemia, hyponatremia
- Hepatic: Increased ALT/AST, increased bilirubin
- Renal: Acute kidney injury, increased blood urea nitrogen
- Gastrointestinal: Nausea, vomiting, constipation
- Hematologic: Anemia, thrombocytopenia
Important Note: Reassess renal function if clinical deterioration occurs due to risk of COVID-19 associated acute kidney injury.
References: 1, 2, 3, 5, 6 (original document references retained)
