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toman's tuberculosis case detection, treatment and monitoring

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TOMAN’S TUBERCULOSIS<br />

pollen of certain pine trees is seen as short, coccoid rods occurring rarely in<br />

specimens.<br />

Scratches on the slide. Scratches may sometimes retain the red stain <strong>and</strong> confuse<br />

inexperienced microscopists. They are usually seen in parallel rows, are generally<br />

longer than AFB, <strong>and</strong> are undulated. They can be identified easily because they are<br />

found in a deeper layer on the slide, below the smear, <strong>and</strong> disappear when the microscopist<br />

focuses on the cells (e.g. leukocytes) in the smear.<br />

Contamination through the transfer of bacilli from one smear to another<br />

Acid-fast bacilli may be transferred accidentally from a positive slide to a negative one<br />

when several slides are treated simultaneously in staining or decolorization tanks. This<br />

can be avoided by processing each slide separately, e.g. on a rack. Contamination may<br />

also occur when the wire loop used for making the smear is not correctly flamed. Contamination<br />

from this source can be avoided by using disposable wooden sticks for<br />

making smears.<br />

Acid-fast bacilli may also be transferred accidentally when the glass rod or dropper<br />

used for placing immersion oil on the slide touches the surface of a positive slide <strong>and</strong><br />

rubs off some of the material onto the next slide. This can also happen if the oilimmersion<br />

lens touches the slide or when blotting paper is used for drying several<br />

stained smears consecutively. For these reasons, the oil dropper should not touch<br />

the smear – the oil should be allowed to drip freely onto the slide – <strong>and</strong> the oilimmersion<br />

objective should never touch the surface of the slide. Before a new smear<br />

is examined, the oil should be wiped off the lens with special lens-cleaning paper or<br />

a piece of clean cotton tissue. Blotting paper should not be used at all, or for no more<br />

than one slide. Slides should never be used more than once for the <strong>detection</strong> of AFB.<br />

False-negative results<br />

False-negative results (1–6) may be due to deficiencies in the preparation, staining, or<br />

examination of the smear. Proper collection of the specimen <strong>and</strong> subsequent selection<br />

of sputum particles are essential to the preparation of a smear <strong>and</strong> should receive<br />

special attention. Poor quality of the sputum sample is the most common reason for<br />

a negative sputum smear in a patient with smear-positive <strong>tuberculosis</strong>. The most<br />

common reasons for false-negative results are described below.<br />

Improper sputum collection<br />

Patients are sometimes not told clearly enough what constitutes a proper sputum<br />

specimen <strong>and</strong> how to produce one. It must be made clear that saliva <strong>and</strong> nasopharyngeal<br />

discharge are unsuitable for examination. Patients should be encouraged to<br />

st<strong>and</strong> <strong>and</strong> be given time to produce bronchial sputum from “deep in the chest”. They<br />

should be asked to take several deep breaths, coughing as hard <strong>and</strong> as deeply as they<br />

can. If repeated attempts fail, tickling of the inner surface of the epiglottis or trachea<br />

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