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Back Manual Sahli Pipette Method | Up Hospital Corpsman 3 & 2 - Intro Navy Nursing manual for hospital training purposes | Next Figure 6-8.—Counting chambers. |
Figure 6-6.Hemacytometer counting chamber.
2.
3.
4.
to immerse in the drop of blood to avoid
air bubbles. If the blood level exceeds the
0.5 mark, withdraw excess blood by
touching the tip to the skin surface. Do not
touch it to gauze or cotton since these
material absorb the fluid portion of the
blood, leaving behind a much higher con-
centration of cells.
Wipe the blood from the outside of the
pipette, taking care not to touch the very
tip. Immerse the tip in the RBC diluting
fluid and aspirate fluid exactly to the 101
mark, slightly rotate the pipette while do-
ing so. It is best to hold the pipette in an
almost vertical position to avoid formation
of air bubbles in the bulb. DO NOT
DELAY BETWEEN STEPS 1 AND 2. IF
T H E B L O O D I S N O T D I L U T ED
PROMPTLY, IT WILL DRY IN THE PI-
PETTE. Start to draw diluting fluid into
the pipette as soon an the tip of the pipette
is immersed in fluid to avoid loss of blood
cells. Wipe the excess diluting fluid from
the pipette, taking care not to touch the
very tip. Filter the diluting fluid regularly
to remove accidentally introduced blood
cells.
Remove the suction tube and shake the
pipette vigorously for 3 minutes. DO NOT
SHAKE IN THE DIRECTION OF THE
LONG AXIS. (See figure 6-5.)
Discard the clear fluid (about three drops)
from the stem of the pipette. The counting
6-7
Figure 6-7.Loading the counting chamber.
5.
chamber (figure 6-6) must be loaded with
fluid from the pipettes bulb.
Place the coverglass on the counting
chamber, making sure both are clean and
grease-free. (Fingerprints must be com-
pletely removed.) Load the counting
chamber by touching the tip of the pipette
against the edge of the coverglass and the
surface of the counting chamber (figure
6-7). A properly loaded counting chamber
should have a thin, even film of fluid under
the coverglass. Allow 3 minutes for cells
to settle. If fluid flows into the grooves
(moats) at the edges of the chamber or if
air bubbles are seen in the field, the cham-
ber is flooded and must be cleaned with
distilled water, dried with lens tissue, and
reloaded. If the chamber is underloaded,
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