Risk of Severed COVID-19 |
Panel's Recommendations |
Aged 12-17 years |
Aged <12 years |
Symptomatic, Regardless of Risk Factors |
Provide supportive care (AIII). |
Provide supportive care (AIII). |
High Riska,b |
Use 1 of the following options (listed in order of preference):c
- Nirmatrelvir co-packaged with ritonavir (Paxlovid) within 5 days of symptom onset (BIII)
- Remdesivir within 7 days of symptom onset (CIII)
|
Nirmatrelvir co-packaged with ritonavir is not authorized by the FDA for use in children aged <12 years.
There is insufficient evidence to recommend either for or against the routine use of remdesivir. Consider treatment based on age and other risk factors. |
Intermediate Riskb,d |
There is insufficient evidence to recommend either for or against the use of any antiviral therapy. Consider treatment based on age and other risk factors. |
There is insufficient evidence to recommend either for or against the routine use of remdesivir |
Low Riskb,e |
Manage with supportive care alone (BIII). |
Manage with supportive care alone (BIII). |
a. Molnupiravir is not authorized by the FDA for use in children aged <18 years and should not be used.
b. See Table 3b for the Panel's framework for assessing the risk of progression to severe COVID-19 based on patient conditions and COVID-19 vaccination status.
c. Initiate treatment as soon as possible after symptom onset.
d. The relative risk of severe COVID-19 for intermediate-risk patients is lower than the risk for high-risk patients but higher than the risk for low-risk patients.
e. Low-risk patients include those with comorbid conditions that have a weak or unknown association with severe COVID-19. Patients with no comorbidities are included in this group.
For more information, refer to Therapeutic Management of Nonhospitalized Children With COVID-19