Comparison of performance between Fast Track Diagnostics Respiratory Kit
and the CDC Global Reference Laboratory for Influenza rRT-PCR panel for
detection of influenza A and B
Abstract
Background Reliable diagnostics are key to identifying influenza
infections. Our objectives were to describe detection of influenza among
severe acute respiratory infection (SARI) cases, to compare test results
from the FTD-33 kit for influenza detection to the Centers for Disease
Control (CDC) human influenza virus detection and characterization
panel, and to assess seasonality of influenza in Burkina Faso. Methods:
Nasopharyngeal and oropharyngeal specimens from SARI cases (hospitalized
patients with fever, cough, and onset in the previous 10 days) were
tested using the FTD-33 kit and the CDC rRT-PCR influenza assays. We
assessed sensitivity and specificity of the FTD-33 kit for detecting
Influenza A, Influenza B, and the influenza A(H1N1)pdm09 strain using
the CDC human influenza rRT-PCR panel as the gold standard. Results:
From December 2016 to February 2019, 1706 SARI cases were identified,
1,511 specimens were tested, and 211 were positive for influenza A
(14.0%) and 100 for influenza B (6.6%) by either assay. Higher
influenza circulation occurred between November and April with varying
peaks of influenza A and B. Sensitivity of the FTD-33 assay was 91.9%
for influenza A, 95.7% for influenza B, and 93.8% for A(H1N1)pdm09
subtype. Specificity was over 99% for all three tests. Conclusions: Our
study indicates that Burkina Faso has one peak of influenza each year
which is similar to the Northern Hemisphere and differs from other
countries in West Africa. We found high concordance of influenza results
between the two assays indicating FTD-33 can be used to reliably detect
influenza among SARI cases.