Table 3.
Nucleic Acid Amplification Test (NAATs) | Antigen Tests | |
---|---|---|
Analyte Detected | Diagnose current infection | Diagnose current infection |
Specimen Type(s) | Nasal, Nasopharyngeal, Oropharyngeal, Sputum, Saliva | Nasal, Nasopharyngeal, Breath |
Sensitivity (for accuracy) | Laboratory tests: generally high Point-of-Care tests: moderate-to-high |
Generally moderate-to-high at peak viral load. More accurate if symptomatic |
Specificity | High | High |
Authorized for Use at the Point-of-Care | Most are not | Most are |
Turnaround Time | Most are 1–3 days Some rapid tests in 15 min |
Most are 15–30 min |
Cost per Test | Moderate (~$75–$100/test) | Low (~$5–$50/test) |
Advantages | Most sensitive test available Short turnaround time for NAAT Point-of-Care tests (rare) Usually does not need to be repeated to confirm results |
Short turnaround time (~15 min) Allows for rapid identification of infected people, thus preventing further virus transmission in the community, workplace, etc. Comparable performance to NAATs for diagnosis in symptomatic persons and whether a culturable virus is present or not |
Disadvantages | Longer turnaround time for lab-based tests (1–3 days) Higher cost per test A positive NAAT diagnostic test should not be repeated within 90 days in case detectable RNA is still present after risk of transmission has passed |
Less sensitive (more false negative results) compared to NAATs, especially among asymptomatic people and with some variants May need to be repeated to confirm results (any negative test on a symptomatic person should be confirmed with a PCR or NAAT test (CDC, 2022) |