Skip to main content
. 2020 Apr 2;15(4):e0230610. doi: 10.1371/journal.pone.0230610

Table 9. Sensitivity (%) and 95% confidence intervals (95% CI) of Kalazar Detect performed at the point of care (POC) and IT-Leish and other tests performed at IMT, in serum samples collected from patients with VL/aids, according to the collection site.

Locality (n) Sensitivity % (n)
CI 95%
KD-POC KD-IMT IT-Leish IFA ELISA
Campo Grande (11) 81.8 (9) 63.6 (7) 72.7 (8) 72.7 (8) 81.8 (9)
79.2–97.3 35.4–84.8 43.4–90.3 43.4–90.3 79.2–97.3
Bauru (5) 80.0 (4) 80.0 (4) 80.0 (4) 80.0 (4) 80.0 (4)
37.6–96.4 37.6–96.4 37.6–96.4 37.6–96.4 37.6–96.4
Natal (4) 25.0 (1) 25.0 (1) 25.0 (1) 75.0 (3) 75.0 (3)
4.56–70.0 4.6–69.9 4.6–69.9 30.1–95.4 30.1–95.4
Total (20) 70.0 (14) 60.0 (12) 65.0 (13) 75.0 (15) 80.0 (16)
48.1–85.5 38.7–78.1 43.3–81.9 53.1–88.8 58.4–91.9

n–number of samples.

KD-POC–Kalazar Detect performed at the point of care.

KD-IMT–Kalazar Detect processed at IMT.

IT-Leish–rK39 –RDT.

IFA–L. major-like based Indirect immunofluorescence assay.

ELISA–L. major-like based Enzyme-linked immunosorbent assay.

No difference across localities (chi-square test, p>0.05) or tests (McNemar’s test, p>0.05).