U. Niriain et al., TRANSPORT OF DIGESTED DECONTAMINATED SPUTUM SPECIMENS TO A CENTRAL LABORATORY FOR TESTING FOR MYCOBACTERIUM-TUBERCULOSIS BY AMPLICOR MTB TEST, Irish journal of medical science, 167(2), 1998, pp. 79-80
Rapid diagnosis of tuberculosis may improve management of infected pat
ients and facilitate infection control procedures The relatively slow
growth rate of M. tuberculosis and the limited sensitivity and specifi
city of microscopy make rapid diagnosis difficult.;Nucleic acid amplif
ication techniques have been extensively studied for the detection of
M. tuberculosis DNA and a number of commercial products for detection
of M. tuberculosis nucleic acid in clinical specimens are now availabl
e. As performance of diagnostic PCR at central reference laboratories
may be desirable, the impact of specimen transport on the performance
of the Amplicor MTB PCR assay is of practical importance. We have asse
ssed the performance of the Amplicor MTB PCR on specimens submitted an
d initially processed in laboratories in 3 cities and then transported
to a single laboratory for PCR assay. The overall sensitivity of the
PCR test was 97 per cent and the corrected specificity was 100 per cen
t. All of 23 culture positive specimens collected locally were PCR pos
itive compared with 10 of 11 culture positive specimens transported fr
om elsewhere. In this study transportation of digested decontaminated
specimens to a central laboratory either frozen at -20 degrees, or ove
rnight at room temperature had no apparent effect on the performance c
haracteristic of the Amplicor MTB PCR assay.