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toman's tuberculosis case detection, treatment and monitoring

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5. How reliable is smear microscopy?<br />

K. Toman 1<br />

To assess the reliability of smear microscopy quantitatively, answers are needed to the<br />

following questions:<br />

1. What is the probability of finding acid-fast bacilli (AFB) in smears prepared from<br />

specimens containing few, some, or many bacilli?<br />

2. What is the probability of reporting a (false-)positive result for smears from specimens<br />

without tubercle bacilli?<br />

3. What is the frequency of agreement between microscopists or laboratories reporting<br />

the results for smears prepared from the same specimens?<br />

Table 1 under “How many bacilli are present in a sputum specimen found positive by<br />

smear microscopy?” (page 11) supplies part of the answer to the first question. The<br />

figures in that table are derived from experimental findings <strong>and</strong> have been extrapolated<br />

on the assumption that bacilli are evenly distributed throughout specimens.<br />

Since the bacillary content varies from one sample to another, however, such measurements<br />

must be performed on a large number of specimens, taking the results of<br />

culture as a yardstick (1). In several studies (2, 3), the bacillary counts of smears were<br />

compared with the number of colonies grown on cultures prepared from the same<br />

specimen.<br />

In a cooperative study by eight laboratories, it was confirmed that colony counts<br />

for samples taken from the same specimen varied from one sample to the next,<br />

although these variations were minimal. 2 The disparity of colony counts between<br />

samples from different specimens was due mainly to the variation in the concentration<br />

of bacilli in these specimens. It was concluded, therefore, that there is a positive<br />

correlation between the concentration of culturable bacilli in the specimens, the<br />

number of AFB in the corresponding smears, <strong>and</strong> the probability of their being identified<br />

by microscopy. The results (Table 2) show that the chance of finding AFB in a<br />

1 Deceased.<br />

2 David HL et al. Sensitivity <strong>and</strong> specificity of acid-fast microscopy. Atlanta, GA, United States Department<br />

of Health, Education <strong>and</strong> Welfare, Centers for Disease Control (unpublished document prepared for the<br />

WHO Expert Committee on Tuberculosis, Geneva, 1973).<br />

14

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