Estimation of Hemoglobin
Dr.Shah Shabnam N
• Hemoglobinometry --Measurement of the concentration (amount) of Hb in
the blood.
• PRINCIPLE --The Hb present in a measured amount of blood is converted by
dilute hydrochloric acid into acid hematin, which in dilution is golden brown
in color. The intensity of color depends on the concentration of acid hematin
which, in turn, depends on the concentration of Hb. The color of the solution
(i.e. its hue and depth), after dilution with water, is matched against
goldenbrown tinted glass rods by direct vision. The readings are obtained in
g%.
APPARATUS AND MATERIALS
• A. Sahli (Sahli-Adams) Hemoglobinometer (Hemometer)
Estimation of Hemoglobin.pptx sahib khan
Comparator
It is a rectangular plastic box with
a slot in the middle which
accommodates the calibrated Hb
tube.
Non-fading, standardized, golden-
brown glass rods are fitted on
each side of the slot for matching
the color.
An opaque white glass (or plastic)
is fitted behind the slot to provide
uniform illumination during direct
visual color matching.
Hemoglobin tube
The square or round glass tube is
calibrated in g Hb % (2–24 g%) in
yellow color on one side, and in
percentage Hb (20–160%) in red
color on the other side. There is a
brush to clean the tube.
Hemoglobin pipette
It is a glass capillary pipette with
only a single calibration mark-0.02
ml (20 cmm, cubic millimeters; or
20 micro liters). There is no bulb in
this pipette (as compared to cell
pipettes) as no dilution of blood is
done
Stirrer & Distilled water
It is a thin glass rod with a flattened end which is used for stirring and
mixing the blood and dilute acid.
B. N/10 hydrochloric acid (0.1 N HCl) solution.
Mixing 36 g HCl in distilled water to 1 liter gives ‘Normal’ HCl; and
diluting it 10 times will give N/10 HCl solution.
C. Materials for skin prick.
• Sterile lancet/needle • Sterile gauze and cotton swabs • spirit
PROCEDURE
• Using a dropper, place 8–10 drops of N/10 HCl in the Hb tube, or up to the
mark 20% or 3 g.
• Get a finger prick under aseptic conditions, wipe away the first 2 drops of
blood. When a large drop of free-flowing blood has formed again, draw blood
up to the 20 cmm mark (0.02 ml).
• Without any waiting, immerse the tip of the pipette to the bottom of the acid
solution and expel the blood gently. Rinse the pipette 3–4 times by drawing up
and blowing out the clear upper part of the acid solution till all the blood has
been washed out from it. Avoid frothing of the mixture. Note the time.
• Withdraw the pipette from the tube, touching it to the side of the tube, thus
ensuring that no mixture is carried out of the tube. Mix the blood with the
acid solution with the flat end of the stirrer by rotating and gently moving it
up and down.
• Put the Hb tube back in the comparator and let it stand for 6–8 minutes (or
as advised by the manufacturer). During this time, the acid ruptures the red
cells, releasing their Hb into the solution (hemolysis). The acid acts on the Hb
and converts it into acid hematin which is deep golden brown in color.
• Diluting and matching the color. The next step is to dilute the acid
hematin solution with distilled water (preferably buffered water, if
available) till its color matches the color of the standard tinted glass
rods in the comparator.
OBSERVATIONS AND RESULTS
• 1st reading, when the color is slightly darker than the standard:………….
…..g/dl.
• 2nd reading, when, after adding a few drops of distilled water, the color
exactly matches the standard: ………..……… g/dl.
• 3rd reading, when, after adding some more drops, the color becomes a
little lighter than the standard:………..…….. g/dl.
Normal Values
•Males: 14.5 g/dl (13.5–18 g/dl).
•Females: 12.5 g/dl (11.5–16 g/dl).
Def.
• Anemia – Decreased oxygen carrying capacity of blood due
to decreased RBC count and/or Hb in blood.
CLASSIFICATION
Etiological classification
Main
etiology Increased blood
loss
Increased breakdown of RBC Decreased production
of RBC
Various
causes
Acute blood
loss
Chronic
blood loss
Red cell
membrane
Enzyme
defect
Abnorma
l Hb
Immune
mediated
hemolysis
Deficiency of
nutrients
Bone
marrow
disorders
Eg. Acute
hemorrhage
due to road
traffic
accidents,major
surgeries,etc.
Piles,
hookworm
infestation,
DUB in
females,etc
Hereditory
spherocytos
-is,
ovalocytosis
Glucose – 6-
phosphate
dehydrogen
ase(G6PD)
deficiency
Sickle cell
anemia
Incompatibl-
-e
ABO blood
transfusion
Iron
deficiency,folic
acid/Vit B12
deficiency,prot
ein deficiency
Aplastic
anemia
Morphological classification
Hypochromic
(MCHC<31g/dL)
Normochromic
(MCHC =31-33g/dL)
Size of
RBC<7microm(microcytic,
MCV <80femtoL)
Iron deficiency
anemia,thalassemia,lead
poisoning
Chronic infection
Size of
RBC=7microm(normocytic,
MCV =80-100fL)
Chronic hemorrhage Acute blood
loss,hemolysis,Aplastic anemia
Size of
RBC>7microm(macrocytic,
MCV >100fL)
Liver disease Vit.B12 deficiency,Folic acid
deficiency
Clinical classification
Conc. of Hb Grades of anemia
> 10g/dL No anemia
8-10g/dL Mild anemia
5-8g/dL Moderate anemia
< 5g/dL Severe anemia

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Estimation of Hemoglobin.pptx sahib khan

  • 2. • Hemoglobinometry --Measurement of the concentration (amount) of Hb in the blood. • PRINCIPLE --The Hb present in a measured amount of blood is converted by dilute hydrochloric acid into acid hematin, which in dilution is golden brown in color. The intensity of color depends on the concentration of acid hematin which, in turn, depends on the concentration of Hb. The color of the solution (i.e. its hue and depth), after dilution with water, is matched against goldenbrown tinted glass rods by direct vision. The readings are obtained in g%.
  • 3. APPARATUS AND MATERIALS • A. Sahli (Sahli-Adams) Hemoglobinometer (Hemometer)
  • 5. Comparator It is a rectangular plastic box with a slot in the middle which accommodates the calibrated Hb tube. Non-fading, standardized, golden- brown glass rods are fitted on each side of the slot for matching the color. An opaque white glass (or plastic) is fitted behind the slot to provide uniform illumination during direct visual color matching.
  • 6. Hemoglobin tube The square or round glass tube is calibrated in g Hb % (2–24 g%) in yellow color on one side, and in percentage Hb (20–160%) in red color on the other side. There is a brush to clean the tube.
  • 7. Hemoglobin pipette It is a glass capillary pipette with only a single calibration mark-0.02 ml (20 cmm, cubic millimeters; or 20 micro liters). There is no bulb in this pipette (as compared to cell pipettes) as no dilution of blood is done
  • 8. Stirrer & Distilled water It is a thin glass rod with a flattened end which is used for stirring and mixing the blood and dilute acid.
  • 9. B. N/10 hydrochloric acid (0.1 N HCl) solution. Mixing 36 g HCl in distilled water to 1 liter gives ‘Normal’ HCl; and diluting it 10 times will give N/10 HCl solution. C. Materials for skin prick. • Sterile lancet/needle • Sterile gauze and cotton swabs • spirit
  • 10. PROCEDURE • Using a dropper, place 8–10 drops of N/10 HCl in the Hb tube, or up to the mark 20% or 3 g. • Get a finger prick under aseptic conditions, wipe away the first 2 drops of blood. When a large drop of free-flowing blood has formed again, draw blood up to the 20 cmm mark (0.02 ml). • Without any waiting, immerse the tip of the pipette to the bottom of the acid solution and expel the blood gently. Rinse the pipette 3–4 times by drawing up and blowing out the clear upper part of the acid solution till all the blood has been washed out from it. Avoid frothing of the mixture. Note the time.
  • 11. • Withdraw the pipette from the tube, touching it to the side of the tube, thus ensuring that no mixture is carried out of the tube. Mix the blood with the acid solution with the flat end of the stirrer by rotating and gently moving it up and down. • Put the Hb tube back in the comparator and let it stand for 6–8 minutes (or as advised by the manufacturer). During this time, the acid ruptures the red cells, releasing their Hb into the solution (hemolysis). The acid acts on the Hb and converts it into acid hematin which is deep golden brown in color.
  • 12. • Diluting and matching the color. The next step is to dilute the acid hematin solution with distilled water (preferably buffered water, if available) till its color matches the color of the standard tinted glass rods in the comparator.
  • 13. OBSERVATIONS AND RESULTS • 1st reading, when the color is slightly darker than the standard:…………. …..g/dl. • 2nd reading, when, after adding a few drops of distilled water, the color exactly matches the standard: ………..……… g/dl. • 3rd reading, when, after adding some more drops, the color becomes a little lighter than the standard:………..…….. g/dl.
  • 14. Normal Values •Males: 14.5 g/dl (13.5–18 g/dl). •Females: 12.5 g/dl (11.5–16 g/dl).
  • 15. Def. • Anemia – Decreased oxygen carrying capacity of blood due to decreased RBC count and/or Hb in blood.
  • 17. Main etiology Increased blood loss Increased breakdown of RBC Decreased production of RBC Various causes Acute blood loss Chronic blood loss Red cell membrane Enzyme defect Abnorma l Hb Immune mediated hemolysis Deficiency of nutrients Bone marrow disorders Eg. Acute hemorrhage due to road traffic accidents,major surgeries,etc. Piles, hookworm infestation, DUB in females,etc Hereditory spherocytos -is, ovalocytosis Glucose – 6- phosphate dehydrogen ase(G6PD) deficiency Sickle cell anemia Incompatibl- -e ABO blood transfusion Iron deficiency,folic acid/Vit B12 deficiency,prot ein deficiency Aplastic anemia
  • 18. Morphological classification Hypochromic (MCHC<31g/dL) Normochromic (MCHC =31-33g/dL) Size of RBC<7microm(microcytic, MCV <80femtoL) Iron deficiency anemia,thalassemia,lead poisoning Chronic infection Size of RBC=7microm(normocytic, MCV =80-100fL) Chronic hemorrhage Acute blood loss,hemolysis,Aplastic anemia Size of RBC>7microm(macrocytic, MCV >100fL) Liver disease Vit.B12 deficiency,Folic acid deficiency
  • 19. Clinical classification Conc. of Hb Grades of anemia > 10g/dL No anemia 8-10g/dL Mild anemia 5-8g/dL Moderate anemia < 5g/dL Severe anemia