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Physiology Lab 2, Manual RBCs Count

Apr 07, 2015

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Physiology Lab 2, Manual RBCs Count
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Page 1: Physiology Lab 2, Manual RBCs Count

manual RBCs count

Page 2: Physiology Lab 2, Manual RBCs Count

Introduction

Erythrocyte (RBCs) are biconcave in appearance Have no nucleus

The interior of the cell contain red pigment called Hemoglobin which is responsible for red color of blood.

Life span 120 days

Page 3: Physiology Lab 2, Manual RBCs Count

Introduction

The function of erythrocytes to combine with O2 & to lesser extent CO2 & transport them through blood vessels.

Page 4: Physiology Lab 2, Manual RBCs Count
Page 5: Physiology Lab 2, Manual RBCs Count

Introduction

Normal range in healthy adult male has about 4.5-6 million RBCs/mm³

healthy adult female has about 4-5.5 million RBCs/mm³

Page 6: Physiology Lab 2, Manual RBCs Count

Principle of the test

In this experiment you are going to determine the # of RBCs in mm³, and because this # is very large, dilute a sample with an Isotonic Solution (Hayem’s solution), then multiply the counted # by correction factor.

Page 7: Physiology Lab 2, Manual RBCs Count

Material

1. Blood sample (EDTA anticoagulated blood or capillary blood)

2. RBCs diluting pipette3. Diluting solution (Hayemes solution)4. Hemocytometer5. microscope

Page 8: Physiology Lab 2, Manual RBCs Count

RBCs diluting pipette

Page 9: Physiology Lab 2, Manual RBCs Count

The Hemacytometer

]0.25mm

]0.20mm

Page 10: Physiology Lab 2, Manual RBCs Count

Methodology

With a safety bulb draw blood up to 0.5 marks on RBCs pipette and complete to 101 with RBCs diluting solution.

Mix for 2-3 minute.

Page 11: Physiology Lab 2, Manual RBCs Count

Charge hemacytometer

Discard the first 4-5 drops

Place tip of the pipette at the edge central platform

Then let the hemacytometer to stand on the bench for 3-5 minute.

Page 12: Physiology Lab 2, Manual RBCs Count

Count and calculate:

Page 13: Physiology Lab 2, Manual RBCs Count

Calculation

Number of RBCs/mm³=counted cells in 5 squares(80 small squares)

x diluting factor x volume correction factor.

Page 14: Physiology Lab 2, Manual RBCs Count

Calculation

The dilution factor= total volume/sample volume = 101-1/0.5 =200 Volume correction factor= Desired volume/counted volume in 5 squares 1 mm³/ counted volume

Page 15: Physiology Lab 2, Manual RBCs Count

Calculation

counted volume =The total volume of the 5 Medium

squares== Volume x number squares= (width x length x depth )x 5= (1/5mm x 1/5mm x 1/10 mm) x 5

=1/4000mm³

Page 16: Physiology Lab 2, Manual RBCs Count

Calculation

Total # of small squares= 5 x 16=80 Then The total volume of the 5

Medium squares=1/4000 x 80=1/50 Volume correction factor=

1/(1/50)=50

Page 17: Physiology Lab 2, Manual RBCs Count

Calculation

Example: If total # of RBCs in 5 medium

squares is 423 Then the # of RBCs in 1mm³= 423 x

200 x 50 = 4,230,000

Page 18: Physiology Lab 2, Manual RBCs Count

Calculation

Number of RBCs/mm³= counted cells in 5 m square x diluting factor x volume correction factor.

Number of cells/mm³= n x200 x 50 = n x 1000

Page 19: Physiology Lab 2, Manual RBCs Count

Significance of the test

The purpose of a RBCs count is to determine the # of ciculating RBCs per mm³ of blood

RBCs carry O2 to all tissues; thus a drastic reduction in the RBCs count will cause immediate reduction in the available O2.

Page 20: Physiology Lab 2, Manual RBCs Count

Significance of the test

Anemia: a decrease in number of RBCs below normal range

Polycythemia: Increase in number of RBCs above normal range

Physiological Polycythemia: (up to 8 million cells/mm³) due to:

Age: at birth RBCs count is 8-10 million cells/mm³ High altitude

Page 21: Physiology Lab 2, Manual RBCs Count

Significance of the test

Pathological Polycythemia: due to Primary Polycythemia: RBCs over 14

million cells/ mm³, occur in bone marrow malignancy.

Secondary Polycythemia: RBCs over 8 million cells/ mm³,due to:

Respiratory disease Heart disease Chronic carbon dioxide poisoning

Page 22: Physiology Lab 2, Manual RBCs Count

Sources of error

1. Flooding of chamber with excess sample

2. Failing to count all the cells in the squares or conversely including artifacts in the count.