Testing and Treatment Protocol for SARS-CoV-2 (COVID-19)
For optimal patient outcomes, standard nucleic acid amplification testing (NAAT) is recommended as the first-line diagnostic test for symptomatic individuals suspected of having COVID-19, followed by appropriate treatment based on risk factors and disease severity.
Diagnostic Testing Algorithm
For Symptomatic Individuals:
Initial Testing Approach:
Specimen Collection Options:
- Acceptable specimens for NAAT (in order of preference):
- Nasopharyngeal (NP) swab (highest sensitivity)
- Midturbinate (MT) swab
- Combined anterior nasal (AN) plus oropharyngeal (OP) swab
- Saliva or mouth gargle specimens 1
- Note: OP swabs alone have a much lower detection rate (73.1% of NP positive cases were negative by OP swab) 1
- Acceptable specimens for NAAT (in order of preference):
Self-Collection Options:
Interpretation of Results:
- Positive NAAT: Confirms infection, no need for confirmatory testing
- Negative NAAT with high clinical suspicion: Consider repeat testing
- Positive antigen test: High specificity allows for treatment decisions without confirmation 1
- Negative antigen test with moderate/high clinical suspicion: Confirm with standard NAAT 1
For Asymptomatic Individuals with Known Exposure:
Testing Timing:
- Test at least 5 days after exposure
- If symptoms develop before 5 days, test immediately 1
Testing Approach:
Treatment Protocol for Confirmed COVID-19
For Non-Hospitalized Patients with Mild-to-Moderate COVID-19:
Risk Assessment:
- Identify patients at high risk for progression to severe disease
Treatment Options for High-Risk Patients:
- Remdesivir (Veklury): FDA-approved for non-hospitalized patients with mild-to-moderate COVID-19 at high risk for progression 2
- Adult and pediatric patients ≥40kg: 200mg IV on Day 1, followed by 100mg IV once daily from Day 2
- Pediatric patients <40kg: Weight-based dosing (see table below)
- Treatment should be initiated as soon as possible after diagnosis 2
Weight-Based Dosing for Pediatric Patients:
Patient Population Loading Dose Maintenance Dose <28 days old, ≥1.5kg 2.5 mg/kg 1.25 mg/kg once daily ≥28 days, 1.5kg to <3kg 5 mg/kg 2.5 mg/kg once daily ≥28 days, 3kg to <40kg 5 mg/kg 2.5 mg/kg once daily - Remdesivir (Veklury): FDA-approved for non-hospitalized patients with mild-to-moderate COVID-19 at high risk for progression 2
For Hospitalized Patients:
Treatment Options:
- Remdesivir (Veklury):
- For patients not requiring mechanical ventilation/ECMO: 5-day course
- For patients requiring mechanical ventilation/ECMO: 10-day course
- If no clinical improvement after 5 days, may extend treatment for up to 5 additional days 2
- Remdesivir (Veklury):
Monitoring During Treatment:
Important Considerations and Caveats
Testing Limitations:
- False negatives with RT-PCR: During the 4 days of asymptomatic infection, false-negative rates range from 100% on Day 1 to 68% on Day 4 1
- Optimal testing time: 3 days after symptom onset (minimizes false-negative rate to 20%) 1
- Antigen tests have lower sensitivity than NAAT, especially in asymptomatic individuals or late in infection 1, 3
Treatment Considerations:
Follow-up Testing:
By following this evidence-based algorithm for testing and treatment, clinicians can optimize diagnosis and management of COVID-19 to reduce morbidity and mortality while efficiently utilizing healthcare resources.