Journal
CLINICAL CHEMISTRY AND LABORATORY MEDICINE
Volume 58, Issue 7, Pages 1095-1099Publisher
WALTER DE GRUYTER GMBH
DOI: 10.1515/cclm-2020-0398
Keywords
aspartate aminotransferase; blood test; COVID-19; lactate dehydrogenase; RT-PCR; WBC
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Objectives: The outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to date, the epidemic has gradually spread to 209 countries worldwide with more than 1.5 million infected people and 100,000 deaths. Amplification of viral RNA by rRT-PCR serves as the gold standard for confirmation of infection, yet it needs a long turnaround time (3-4 h to generate results) and shows false-negative rates as large as 15%-20%. In addition, the need of certified laboratories, expensive equipment and trained personnel led many countries to limit the rRT-PCR tests only to individuals with pronounced respiratory syndrome symptoms. Thus, there is a need for alternative, less expensive and more accessible tests. Methods: We analyzed the plasma levels of white blood cells (WBCs), platelets, C-reactive protein (CRP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma-glutamyl transpeptidase (GGT), alkaline phosphatase and lactate dehydrogenase (LDH) of 207 patients who, after being admitted to the emergency room of the San Raffaele Hospital (Milan, Italy) with COVID-19 symptoms, were rRT-PCR tested. Of them, 105 tested positive, whereas 102 tested negative. Results: Statistically significant differences were observed for WBC, CRP, AST, ALT and LDH. Empirical thresholds for AST and LDH allowed the identification of 70% of either COVID-19-positive or -negative patients on the basis of routine blood test results. Conclusions: Combining appropriate cutoffs for certain hematological parameters could help in identifying falsepositive/negative rRT-PCR tests. Blood test analysis might be used as an alternative to rRT-PCR for identifying COVID19-positive patients in those countries which suffer from a large shortage of rRT-PCR reagents and/or specialized laboratory.
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