Table 2.

Test Performance in Three Hypothetical Clinical Scenarios*

Panel a: Scenario 1 – Low Pretest Probability (LFA)
DxNo DxPPVNPV
Prevalence 0.1%, Sn 90, Sp 95
(+)95001.8%99.9%
(-)19490
Prevalence 0.2%, Sn 90, Sp 95
(+)184993.5%100.0%
(-)29481
Panel b: Scenario 2 – Intermediate Pretest Probability (RT-PCR Initially Negative)
DxNo DxPPVNPV
Prevalence 40%, Sn 85%, Sp 95%
(+)34391.9%90.5%
(-)657
Prevalence 60%, Sn 85%, Sp 95%
(+)51296.2%80.9%
(-)938
Panel c: Scenario 3 – High Pretest Probability (RT-PCR)
DxNo DxPPVNPV
Prevalence 80%, Sn 90%, Sp 95%
(+)72198.6%70.4%
(-)819
Prevalence 80%, Sn 80%, Sp 95%
(+)64198.4%54.3%
(-)1619
  • LFA, lateral flow assay; RT-PCR, real-time polymerase chain reaction.

  • *These tables describe the distribution of 10,000 (panel a) or 100 patients (panels b and c) with and without the disease (COVID-19) compared to with positive and negative test results.

  • Sensitivity (Sn), the proportion of infected individuals who test positive.

  • specificity (Sp), the proportion of uninfected individuals who test negative.

  • §Dx, patient has disease; no Dx, patient does not have disease.

  • ||(+), test result is positive; (-), test result is negative.

  • Positive predictive value (PPV), the probability that a positive test result actually means one has COVID-19.

  • ¶¶Negative predictive value (NPV), the probability that a negative test result actually means one does not have COVID-19.