Skip to main content
. Author manuscript; available in PMC: 2024 Jun 21.
Published in final edited form as: J Clin Virol Plus. 2023 Nov;3(4):100168. doi: 10.1016/j.jcvp.2023.100168

Table 3. Summary of Sensitivities of the commercial tests across the years of infection and at different time points.

SENSITIVITY (95% Confidence Interval)
PANBIO RLF LABNOVATION RLF PLATELIA ELISA
TIMEPOINTS Y2020
N = 130
Y2021
N = 88
Y2022
N = 17
Y2020
N = 130
Y2021
N = 88
Y2022
N = 17
Y2020
N = 130
Y2021
N = 88
Y2022
N = 17
Day of diagnostic (DoD) N = 127
46%
(37.3%–54.3%)
N = 83
23%
(15.1%–33%)
N = 17
70%
(47%–87%)
N = 127
41%
(33%–50%)
N = 83
19%
(12.2%–29%)
N = 17
67%
(41.3%–83%)
N = 123
47%
(38%–55.1%)
N = 80
39%
(29%–49.3%)
N = 17
71%
(47%–87%)
14 days Post-DoD N = 62
87%
(77%–93.3%)
N = 45
76%
(61.3%–86%)
N = 17
88%
(66%–98%)
N = 62
65%
(52.1%–54.3%)
N = 45
69%
(54.3%–81%)
N = 17
82%
(59%–94%)
N = 60
89%
(78.4%–94.4%)
N = 44
84%
(71.2%–92.2%)
N = 16
94%
(73%–100%)
44 days Post-DoD N = 45
89%
(76%–95.1%)
N = 39
77%
(62%–87.4%)
- N = 45
89%
(76%–95.1%)
N = 39
62%
(50%–75.1%)
N = 42
93%
(82%–98%)
N = 39
72%
(56.2%–84%)
74 days Post-DoD N = 31
81%
(64.2%–91.1%)
N = 31
60%
(42.3%–75.4%)
N = 31
81%
(64.2%–91.1%)
N = 31
67%
(49%–81%)
N = 30
90%
(75.1%–97%)
N = 30
73%
(56%–86%)
104 days Post-DoD N = 18
83%
(61%–94.2%)
N = 28
54%
(365–70.4%)
N = 18
50%
(29%–71%)
N = 28
46%
(30%–64.2%)
N = 18
89%
(67.2%–985)
N = 25
71%
(53%–85%)
134 days Post-DoD N = 17
77%
(53%–90.4%)
N = 26
23%
(11%-42%)
N = 17
52%
(31%–74%)
N = 26
35%
(19.4%–54%)
N = 17
88%
(66%–98%)
N = 26
69%
(50%–84%)
164 days Post-DoD N = 14
64%
(39%–84%)
N = 24
25%
(12%–45%)
N = 14
71%
(45.4%–88.3%)
N = 24
29%
(15%–49.1%)
N = 14
86%
(60.1–98%)
N = 24
88%
(69%–96%)
194 days Post-DoD N = 9
56%
(27%–81.1%)
N = 17
29%
(13.2%–53.1%)
N = 9
44%
(19%–733.3%)
N = 17
29%
(13.2%–53.1%)
N = 9
89%
(57%–99.4%)
N = 17
77%
(53%–90.4%)