TABLE 1

Key points for laboratory and imaging findings

Co-infection and secondary bacterial infection
• Viral co-infection incidence varies based on case series (0% to 15%)27
• Combine bacterial and viral infection is rare in COVID-19 patients3,810
• Secondary bacterial infection is not uncommon and leads to significant morbidity and mortality, especially in the elderly4,9,16
Procalcitonin
• Detectable in 2 to 4 hours, peaks at 12 to 24 hours, and has a half-life of 25 to 30 hours
• Levels are normal (< 0.5 μg/L) in COVID-19 patients with mild disease and may be elevated (≥ 0.50 μg/L) in patients with severe disease10,14
• Elevated levels are correlated to a nearly 5-fold higher risk for severe SARS- CoV-2 infection17
• Elevated levels are not specific to bacterial infection because they can also be raised in patients with acute respiratory distress syndrome, end-stage renal disease, cardiogenic shock, and multi-organ failure18
• A normal level makes bacterial infection less likely and can guide antibiotic discontinuation19,20
• In bacterial infection, levels may be less affected by IL-6 inhibitors than C-reactive protein (CRP)2123
CRP, Erythrocyte sedimentation rate (ESR)
• CRP and ESR are non-specific inflammatory markers. Both are generally elevated in COVID-19 and are therefore not helpful in differentiating this from bacterial infection
• Tocilizumab rapidly reduces CRP and leukocytosis and may suppress fever2426
Typical radiographic features
COVID-19
• Chest radiography: Bilateral, peripheral, lower-zone predominant air-space disease27
• Computed tomography: Bilateral, predominantly peripheral ground glass opacities, crazy-paving and consolidation28; findings vary based on stage/phase of the disease
Bacterial pneumonia
• Chest radiography: Lobar or segmental air-space opacification ± air bronchograms
• Computed tomography: Segmental or lobar focal dense consolidation ± ground-glass opacities