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Manual RBC, WBC platelet count
sop
Pathofast CBC Peripheral Smear -
Normal Ranges
Manual RBC count
• Take 3.98 ml( 3980ul) of RBC diluting fluid in a
test tube
• Mix EDTA sample well. Take 20 ul of blood
into pipette. Wipe off excess blood from the
tip of the pipette
• Add into the test tube.
• Charging the Improved Neubar chamber.
• Take 10 ul of fluid into the pipette
• Place a coverslip over the chamber
• Discharge the fluid into the chamber
• Make sure it doesn’t overflow or is underfilled
Counting of cells
• Counting is done under high power
• The number of cells in the RBC counting chamber is
counted
• Calculations:
• No of cells/ul=no of cells counted
• dilution x depthx area
• RBCs /ul=no.of cellsx10000
Manual WBC count
• Take 0.38 ml( 380ul) of WBC diluting fluid
• Add 20 ul of whole blood
• Allow to stand for 10 min
• Load on Neubars chamber as described before
Wbc count
• calculate no. of cells in all 4 large
squares
(depth=1/10 mm
dilution=1:20)
No. of WBCs= no. of cells
counted in 4 chambersx50
Ex: no. of cells counted in 4 wbc
chambers is 150
then wbc count is 150x50=7500
Manual Platelet Count
• Take 1.98 ml of platelet diluting fluid
• Add 20 ul of blood
• Allow to stand for 5 min
• Charge the neubars chamber as described
before
• Count all platelets in 4 large wbc squares
• Platelet/ul
=no. of platelets in 4 WBC squaresx10x2.0x1/
4x1x0.02
Or count platelets in 25 small RBC squares
x1000
• Charging the Improved Neubar chamber.
• Take 10 ul of fluid into the pipette
• Place a coverslip over the chamber
• Discharge the fluid into the chamber
• Make sure it doesn’t overflow or is underfilled
depth=1/10
dilution= 1:10
• Reference
• Handbook of medical laboratory technology.
Robert Carman. Christian Medical Association
of India. Reprint 2013.

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Manual RBC, WBC platelet count sop (1).pptx

  • 1. Manual RBC, WBC platelet count sop Pathofast CBC Peripheral Smear - Normal Ranges
  • 2. Manual RBC count • Take 3.98 ml( 3980ul) of RBC diluting fluid in a test tube • Mix EDTA sample well. Take 20 ul of blood into pipette. Wipe off excess blood from the tip of the pipette • Add into the test tube.
  • 3. • Charging the Improved Neubar chamber. • Take 10 ul of fluid into the pipette • Place a coverslip over the chamber • Discharge the fluid into the chamber • Make sure it doesn’t overflow or is underfilled
  • 4. Counting of cells • Counting is done under high power • The number of cells in the RBC counting chamber is counted • Calculations: • No of cells/ul=no of cells counted • dilution x depthx area • RBCs /ul=no.of cellsx10000
  • 5. Manual WBC count • Take 0.38 ml( 380ul) of WBC diluting fluid • Add 20 ul of whole blood • Allow to stand for 10 min • Load on Neubars chamber as described before
  • 6. Wbc count • calculate no. of cells in all 4 large squares (depth=1/10 mm dilution=1:20) No. of WBCs= no. of cells counted in 4 chambersx50 Ex: no. of cells counted in 4 wbc chambers is 150 then wbc count is 150x50=7500
  • 7. Manual Platelet Count • Take 1.98 ml of platelet diluting fluid • Add 20 ul of blood • Allow to stand for 5 min • Charge the neubars chamber as described before
  • 8. • Count all platelets in 4 large wbc squares • Platelet/ul =no. of platelets in 4 WBC squaresx10x2.0x1/ 4x1x0.02 Or count platelets in 25 small RBC squares x1000
  • 9. • Charging the Improved Neubar chamber. • Take 10 ul of fluid into the pipette • Place a coverslip over the chamber • Discharge the fluid into the chamber • Make sure it doesn’t overflow or is underfilled
  • 11. • Reference • Handbook of medical laboratory technology. Robert Carman. Christian Medical Association of India. Reprint 2013.