12-Utility of Testing for Respiratory Viral Co-Infections With SARS-CoV-2 at Time of Initial Diagnosis
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The Society of Critical Care Medicine's Critical Care Congress features internationally renowned faculty and content sessions highlighting the most up-to-date, evidence-based developments in critical care medicine. This is a presentation from the 2021 Critical Care Congress held virtually from January 31-February 12, 2021.
Matthew Norris, MD
Introduction/Hypothesis: Over 4.8 million cases of COVID-19 have been diagnosed in the United States as of 8/2/2020, with >50,000 new cases diagnosed per day since 6/24/2020. The question arises at the point of care of whether to test patients initially diagnosed with SARS-CoV-2 for a secondary respiratory co-infection. The CDC has endorsed testing for respiratory pathogens other than SARS-CoV-2 to date. However, there is little evidence to support, or recommend against, additional respiratory pathogen testing.
Methods: The following is a retrospective cohort study of all adult patients with nasal swabs positive for SARS-CoV-2 by PCR from 3/16/2020 to 4/20/2020 at a 500-bed community teaching hospital in Northern New Jersey. Decisions regarding test selection for secondary respiratory pathogens were performed by emergency department providers per individual clinical judgement. Both a 12-25 target respiratory PCR panel and 3-target PCR were available at our institution. Being unable to measure direct costs, 2020 Medicare clinical laboratory fee schedules were used to estimate cost. Approval to perform this study (IRB #1597737, decision 4/29/2020) was obtained through the Atlantic Health System Institutional Review Board.
Results: 1,676 adult patients without a prior SARS-CoV-2 diagnosis were identified as having the virus at time of emergency department presentation. 572 patients were tested with a 12-25 target respiratory PCR while 195 patients were tested with a 3-target viral PCR. Seven 12-25 target PCRs were positive for a co-infection (1 Influenza B, 1 Human Metapneumovirus, 2 Rhinovirus/enterovirus, 3 non-COVID coronaviruses) while all 3-target PCRs were negative. Positive viral testing changed management in one case (patient who tested positive for Influenza B received oseltamivir).
Conclusions: Data supports emerging literature showing respiratory viral co-infection during the initial outbreak was rare. Testing at our hospital cost an estimated $326,425.45 but had minimal impact on patient care. As most respiratory viral co-infections are unlikely to change management in patients with SARS-CoV-2 infection, minimizing use of high-target respiratory viral PCRs will free up laboratories to perform more targeted viral testing and allow better resource allocation during our current pandemic.