Author: Perkins, A.; Stephens, M.; Alvarez Barrios, W.; Cavany, S. M.; Rulli, L.; Pfrender, M. E.
                    Title: Performance of three molecular tests for SARS-CoV-2 on a university campus estimated jointly with Bayesian latent class modeling  Cord-id: ehu99xwn  Document date: 2021_8_2
                    ID: ehu99xwn
                    
                    Snippet: Accurate tests for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have been critical in efforts to control its spread. The accuracy of molecular tests for SARS-CoV-2 has been assessed numerous times, usually in reference to a gold standard diagnosis. One major disadvantage of that approach is the possibility of error due to inaccuracy of the gold standard, which is especially problematic for evaluating testing in a real-world surveillance context. We used an alternative approach kn
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: Accurate tests for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have been critical in efforts to control its spread. The accuracy of molecular tests for SARS-CoV-2 has been assessed numerous times, usually in reference to a gold standard diagnosis. One major disadvantage of that approach is the possibility of error due to inaccuracy of the gold standard, which is especially problematic for evaluating testing in a real-world surveillance context. We used an alternative approach known as Bayesian latent class modeling (BLCM), which circumvents the need to designate a gold standard by simultaneously estimating the accuracy of multiple tests. We applied this technique to a collection of 1,716 tests of three types applied to 853 individuals on a university campus during a one-week period in October 2020. We found that reverse transcriptase polymerase chain reaction (RT-PCR) testing of saliva samples performed at a campus facility had higher sensitivity (median: 0.923; 95% credible interval: 0.732-0.996) than RT-PCR testing of nasal samples performed at a commercial facility (median: 0.859; 95% CrI: 0.547-0.994). The reverse was true for specificity, although the specificity of saliva testing was still very high (median: 0.993; 95% CrI: 0.983-0.999). An antigen test was less sensitive and specific than both of the RT-PCR tests. These results suggest that RT-PCR testing of saliva samples at a campus facility can be an effective basis for surveillance screening to prevent SARS-CoV-2 transmission in a university setting.
 
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