Current best evidence for clinical care (more info)
We conducted a multicenter clinical validity study of the Panbio coronavirus disease 2019 Antigen Rapid Test of nasopharyngeal samples in pediatric patients with coronavirus disease 2019-compatible symptoms of =5 days of evolution. Our study showed limited accuracy in nasopharyngeal antigen testing: overall sensitivity was 45.4%, and 99.8% of specificity, positive-predictive value was 92.5%.
Discipline / Specialty Area | Score |
---|---|
Pediatric Emergency Medicine | |
Pediatric Hospital Medicine | |
Pediatric Neonatology | |
Infectious Disease | |
Emergency Medicine | |
As most ED clinicians won't have much say in which rapid Covid-19 tests are being ordered by their hospitals, this is not particularly clinically relevant. It essentially reports poor sensitivity and accuracy of a rapid antigen test compared to a gold-standard reverse transcriptase test.
This rapid Ag test for COVID-19 had high specificity (99.8%), but low sensitivity (45.4%) when compared with RT-PCR. However several things to note: 1) the prevalence was only 4.8% in 1620 patients. If the prevalence were higher, the number of "missed" infections (when compared with RT-PCR) would increase (NPV goes down) 2) the +LR was 233.8 - if you had a positive test, it was positive; however the -LR was only 0.54, which is not very helpful; 3) it's unclear if the + RT-PCR was from a previous infection (prolong shedding state) and the symptoms were not related to COVID, although this is probably unlikely; 4) it's unclear how the sensitivity/specificity performs >5 days.
Rapid antigen tests for Covid-19 should be interpreted with caution, more so in children.
This test is not used widely, so results are of limited use.
Large well designed study comparing antigen test to gold standard PCR. The sensitivity of only 45% c/w 85% in adults underscores that children are not small adults. This is a poorly performing rule-out test in children.