Ca. Saceanu et al., EVALUATION OF SPUTUM SMEARS CONCENTRATED BY CYTOCENTRIFUGATION FOR DETECTION OF ACID-FAST BACILLI, Journal of clinical microbiology, 31(9), 1993, pp. 2371-2374
Early identification and isolation of tuberculosis patients is of utmo
st importance to minimize the risk of further epidemic spread of the d
isease. The traditional concentrated acid-fast smears are not very rel
iable tools for the presumptive diagnosis of tuberculosis. Acid-fast b
acillus (AFB) smears from 120 patient specimens and 80 simulated AFB s
amples were processed according to standard laboratory procedures and
by cytocentrifugation (Cyto-Tek, Ames Division, Miles Laboratories, In
c., Elkhart, Ind.). Prior to dispensing of samples into the Cyto-Tek c
hambers, specimens were liquefied and decontaminated by mixture with a
n equal volume of 5% sodium hypochlorite (household bleach). Culture a
nd smear results were correlated. Of 120 patient specimens, 43 were cu
lture and smear negative by both methods. Ten specimens were overgrown
with mold and bacteria, but 2 of them had positive AFB smears by cyto
centrifugation only. There were 67 positive AFB cultures, with 67 posi
tive cytocentrifuge smears and 34 positive smears by the conventional
technique. Of the 80 simulated positive AFB samples, all grew mycobact
eria on culture. Smears from the 10(5)- to 10(3)-CFU/ml specimens were
positive by both methods. The simulated samples with 10(2) CFU/ml yie
lded smears positive only by cytocentrifugation. The Cyto-Tek AFB smea
rs had a greater correlation with positive culture than did the smears
from concentrated specimens. The sensitivity, efficiency, and rapidit
y of the Cyto-Tek AFB smear technique resulted in increased detection
of mycobacteria in clinical specimens. The simplicity and safety of th
is method will enable qualified mycobacteriology technologists to rapi
dly and accurately perform sputum smears for AFB at clinics, emergency
rooms, and field sites, as well as in the traditional laboratory sett
ing.