hemoglobin

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Page 1: Hemoglobin

بـسم الله الرحمن الرحيم

Page 2: Hemoglobin

Practical Clinical Pathology

I-Introduction

II-Clinical Hematology

III-Clinical Biochemistry

IV- Urinalysis

V-Clinical Parasitology

Page 3: Hemoglobin

Clinical Hematology

1. Introduction to Clinical Hematology

2. Hemoglobin

3. PCV

4. ESR

5. Blood film and staining

6. Bone marrow examination

7. Reticulocyte counting

8. RBCs (count, morphology and indices)

9. WBCs (count, morphology and differential count)

Page 4: Hemoglobin

Clinical Hematology

1. Hemoglobin estimation by Sahli’s method

2. Hemoglobin estimation by Drabkin’s method

3. RBCs count

4. WBCS count (Total Leukocytic count)

5. Differential Leukocytic Count (DLC)

Page 5: Hemoglobin

Hemoglobin estimation

Direct matching methods

1. Tallquist method

2. Dare hemoglobinometer

Indirect methods

1. Sahli method (Acid hematin)

2. Drabkin method (Cyanomethemoglobin)

(Photometric method)

Page 6: Hemoglobin

Direct matching methods1-Tallquist method

Page 7: Hemoglobin

Direct matching methods2-Dare hemoglobinometer

A drop of blood is placed in a capillary space

between two glass pieces

The red color is compared through an eye piece

with red graded glass standards

Page 8: Hemoglobin

Dare hemoglobinometer

Page 9: Hemoglobin

Direct matching methodsAdvantages and Disadvantages

Advantages Simple,

Rapid

Inexpensive

Disadvantages Error ranges from 10% to 40%

Comparison of red color is difficult

Page 10: Hemoglobin

Hemoglobin estimationIndirect methods

Sahli method(Acid hematin)

Page 11: Hemoglobin

Sahli apparatus

• Two lateral standard tubes

• One central bigraduated tube

• Sahli pipette (20 µl)

Page 12: Hemoglobin

Central bigraduated tube2 scales

Gram/dl scale Percent % scale

Page 13: Hemoglobin

Sahli pipette Single mark pipette

Page 14: Hemoglobin

Sahli method

9 items in most practical experiments

Principle

Sample

Reagents

Procedures

Wavelength

Reading

Calculation

Normal values

Interpretation

Page 15: Hemoglobin

Sahli methodPrinciple

Hemoglobin + 0.1 N HCl

The resulting brown colour is matched with brown glass standard

Globin

Acid hematin (brown colour)

Page 16: Hemoglobin

Sahli methodSample

Whole blood

=

Anticoagulated blood

Page 17: Hemoglobin

Sahli methodReagents

0.1 N HCl Prepared by diluting 0.8 ml conc. HCl with 99.2 ml D.W.

Distilled Water (D.W.)

Page 18: Hemoglobin

Sahli methodProcedures

1. Place 0.1 N HCl into the central bigraduated tube till the mark 2 on the gram scale

2. Draw the blood into Sahli pipette exactly to the mark 20 Wipe off excess blood adhering to the pipette

3. Rinse the pipette by drawing the acid in the tube several times

4. Mix, let stand for 10 minutes

5. Add distilled water (drop by drop with mixing) until it matches the color of the standard tubes

6. Take the reading in g/dl scale

Page 19: Hemoglobin

Sahli methodWavelength

-----

Page 20: Hemoglobin

Sahli methodReading

Hb conc. = ----- g/dl

Page 21: Hemoglobin

Sahli methodCalculation

-----

Page 22: Hemoglobin

Sahli methodNormal values

Hb conc. = 11 -18 g/dl

In Equines

Page 23: Hemoglobin

Sahli methodInterpretation

Increased values (>18 g/dl)Physiological

High attitude

Young age

PathologicalDehydration

Page 24: Hemoglobin

Sahli methodInterpretation

Decreased values (<11 g/dl)Physiological

Fluid therapy

Pathological Anemia

Hemorrhage

Blood parasites

Malignant tumors

Page 25: Hemoglobin

Sahli methodAdvantages and Disadvantages

AdvantagesError may be 5-10% by careful technique

DisadvantagesDifficult colour matching

Colour fading by time

Page 26: Hemoglobin

Hemoglobin estimationIndirect methods

Drabkin method(Cyanmethemoglobin)

Page 27: Hemoglobin

Drabkin method

9 items in most practical experiments

Principle

Sample

Reagents

Procedures

Wavelength

Reading

Calculation

Normal values

Interpretation

Page 28: Hemoglobin

DrabkinPrinciple

Hemoglobin + Ferricyanide Methemoglobin

Cyanide ions

Cyamethemoglobin

- Stable red compound- Measured colorimetrically-Its intensity is directly proportional to the amount of hemoglobin in the sample

Page 29: Hemoglobin

Drabkin methodSample

Whole blood

=

Anticoagulated blood

Page 30: Hemoglobin

DrabkinReagents

Drabkin reagent

Potassium ferricyanide

Potassium cyanide

Sodium Bicarbonate

Sterox (Detergent)

Page 31: Hemoglobin

DrabkinProcedures

1. Add 2.5 ml of the reagent into both the blank and (test) tubes

2. Add 10 µl of blood into the (test) tube

3. Rinse the pipette several times

4. Mix well and allow to stand for 5 minutes

5. Use the blank tube to adjust the colorimeter to zero optical density at 546 nm wavelength.

6. Read the optical density of the test

Page 32: Hemoglobin

Blank Test

0 -

1 –

2 –

3 –

4 –

5 –

0 -

1 –

2 –

3 –

4 –

5 –

0 -

1 –

2 –

3 –

4 –

5 –

0 -

1 –

2 –

3 –

4 –

5 –

Drabkin reagent

Page 33: Hemoglobin

Blank’ Test

0 -

0.01 –

0.02 –

0.03 –

0.04 –

0.05 –

0.06 –

0.07 –

0.08 –

0.09 -

0 -

0.01 –

0.02 –

0.03 –

0.04 –

0.05 –

0.06 –

0.07 –

0.08 –

0.09 -

Blood

0 -

0.01 –

0.02 –

0.03 –

0.04 –

0.05 –

0.06 –

0.07 –

0.08 –

0.09 -

Page 34: Hemoglobin

Blank’ Test

Page 35: Hemoglobin

Blank’ Test

Page 36: Hemoglobin

Blank’ Test

Page 37: Hemoglobin

DrabkinWavelength

546 nm

Page 38: Hemoglobin

DrabkinReading

OD = 0.xxx

Page 39: Hemoglobin

DrabkinCalculation

Page 40: Hemoglobin
Page 41: Hemoglobin

Drabkin methodNormal values

Hb conc. = 11 -18 g/dl

In Equines

Page 42: Hemoglobin

Drabkin methodInterpretation

Increased values (>18 g/dl)Physiological

High attitude

Young age

PathologicalDehydration

Page 43: Hemoglobin

Drabkin methodInterpretation

Decreased values (<11 g/dl)Physiological

Fluid therapy

Pathological Anemia

Hemorrhage

Blood parasites

Malignant tumors

Page 44: Hemoglobin

Drabkin methodAdvantages and Disadvantages

AdvantagesAccurateRapidInternationally adapted

DisadvantagesCyanide is toxic solution

Lipemia may falsely increase the Hb values

Page 45: Hemoglobin

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Page 46: Hemoglobin

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