TABLE 1.
IFA | Test groupb | n | Positive (n) | Negative (n) | Sensitivity (%) | Specificity (%) |
---|---|---|---|---|---|---|
IgG (test A) | PCR, H | 20 | 20 | 0 | 100 | |
Clinical | 22 | 22 | 0 | 100 | ||
Control (total) | 270 | 81 | 189 | 70 | ||
Controlc | 100 | 25 | 75 | 75 | ||
LA | 55 | 5 | 50 | 91 | ||
IgM (test A) | PCR, H | 20 | 16 | 4 | 80 | |
Clinical | 22 | 21 | 1 | 95 | ||
Controlc | 100 | 5 | 95 | 95 | ||
IgG (test B) | PCR, H | 20 | 17 | 3 | 85 | |
Clinical | 22 | 22 | 0 | 100 | ||
Controlc | 100 | 27 | 73 | 73 | ||
IgM (test B) | PCR, H | 20 | 10 | 10 | 50 | |
Clinical | 22 | 17 | 5 | 77 | ||
Controlc | 100 | 14 | 86 | 86 |
Sensitivity was determined by dividing the number of positive cases by the total number of cases and multiplying the quotient by 100; specificity was determined by dividing the number of negative controls by the total number of controls and multiplying the quotient by 100.
PCR, H, patients for whom PCR and histologic analysis results were consistent with CSD; clinical, patients clinically suspected of having CSD; LA, patients with lymphadenopathy caused by infectious agents other than Bartonella spp.
Sera from the first 100 healthy adults in group C.