several slides are treated simultaneously in staining or
decolorization tanks. This can be avoided by processing
each slide separately, e.g. on a rack. Such racks are usually
made of wire and can be decontaminated easily by flaming.
Acid-fast bacilli may also be transferred accidentally
when the glass rod or dropper used for placing immersion
oil on the slide touches the surface of a positive slide
and rubs off some material. The same can happen when
blotting paper is used for drying several stained smear
consecutively. Therefore, the blotting paper should
not be used at all, or for no more than one slide. The oil
dropper should not touch the smear, and the oil should be
allowed to drip freely on to the slide. For the same reason,
the surface of the slide should not be rubbed with the
oil immersion objective. Before a new slide is examined,
the oil should be wiped off the lens with a piece of cotton
tissue or, even better, with special lens-cleaning paper.
When microscopy is used for the detection of acid-fast
bacilli, slides should never be used more than once.
False negative results are commonly due to deficiencies
in the preparation of the smear, in staining, and in
854 Concise Book of Medical Laboratory Technology: Methods and Interpretations
scanning. Adequate collection of the specimen and
subsequent “selection of sputum particles are essential
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