TABLE 4.
Method | No. of positive or equivocal results (specificity, %) |
95% CI of specificity | |||||||
---|---|---|---|---|---|---|---|---|---|
Chikungunya (n = 4) | Dengue (n = 34) | Parvovirus B19 (n = 35) | Roseola (n = 38) | Rubella (n = 36) | Zika (n = 3) | Unknownb (n = 37) | Total (n = 187) | ||
Enzygnost | 0 (100) | 0 (100) | 7 (80.0) | 2 (94.7) | 0 (100) | 0 (100) | 0 (100) | 9 (95.2) | 90.8–97.6 |
Euroimmun | 1 (75) | 0 (100) | 6 (82.9) | 1 (97.4) | 0 (100) | 0 (100) | 0 (100) | 8 (95.7) | 91.4–98.0 |
Euroimmun Nucleoprotein | 0 (100) | 0 (100) | 1 (97.1) | 0 (100) | 0 (100) | 0 (100) | 1 (97.3) | 2 (98.9) | 95.8–99.8 |
IBL | 0 (100) | 2 (94.1) | 0 (100) | 0 (100) | 3 (91.7) | 1 (66.7) | 1 (97.3) | 7 (96.3) | 92.1–98.3 |
LIAISON XL | 0 (100) | 0 (100) | 1 (97.1) | 0 (100) | 0 (100) | 0 (100) | 0 (100) | 1 (99.5d) | 96.6–100 |
Microimmune | 0 (100) | 1 (97.1) | 0 (100) | 2 (94.7) | 0 (100) | 1 (66.7) | 1 (97.3) | 5 (97.3) | 93.5–99.0 |
NovaLisa | 0 (100) | 2 (94.1) | 15 (57.1) | 2 (94.7) | 0 (100) | 1 (66.7) | 1 (97.3) | 21 (88.8d) | 83.1–92.8 |
Serion (activity calculator)c | 0 (100) | 0 (100) | 16 (54.3) | 2 (94.7) | 0 (100) | 2 (33.3) | 1 (97.3) | 21 (88.8d) | 83.1–92.8 |
Serion (OD range)c | 0 (100) | 0 (100) | 15 (57.1) | 2 (94.7) | 0 (100) | 2 (33.3) | 1 (97.3) | 20 (89.3d) | 83.7–93.2 |
Serion (special case formula)c | 1 (75) | 0 (100) | 17 (51.4) | 3 (92.1) | 0 (100) | 2 (33.3) | 2 (94.6) | 25 (86.6d) | 80.7–91.0 |
Specimens with equivocal results were counted as positive.
This panel of sera included fever/rash illness of unknown etiology.
Three methods of sample result determination, using the single set of optical density data from the test plates, were provided in the manufacturer’s IFU. All three methods were evaluated.
Significant difference (P < 0.05) between the most specific (LIAISON XL) and the least specific methods (Serion, all three result determination methods, and NovaLisa) based on nonoverlapping 95% confidence intervals.