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DR.ANINDITA SAHA
RBC COUNT
RED BLOOD CELLS
 Red blood cells, or erythrocytes, are
the most abundant cells in the
bloodstream and contains hemoglobin,
the compound that carries oxygen
through the body.
 . Any disruption of the red blood cells,
its quantity, shape, size, structure or life
cycle can therefore affect the oxygen-
carrying capacity of the blood.
Shape and size of RBCs
 A red blood cell is a biconcave disc. Simply it
is a round ball that is squeezed from two
opposite ends to appear, widest at the sides
and narrowest in the middle.
 A red blood cell measures about 6 to 8
micrometers in diameter (average = 7.8 um)
with an average thickness of 2 micrometers
(2.5 um at the thickest point and less than 1um
at the center). Although a red blood cell is
wider than some capillaries, its flexibility allows
it to become distorted as it squeezes through
narrow passages and then restores to its
METHODS OF RBC COUNT:
1) Visual haemocytometer( manual
method )
2) Automated method
MANUAL METHOD:
EQUIPMENTS REQUIRED:
1)Haemocytometer or improved
Neubauer’s chamber
2)RBC pipette
FLUIDS REQUIRED :
 RBC diluting fluid
 Blood sample (capillary blood or EDTA
anticoagulated blood can be used )
RBC DILUTING FLUID
 RBCs are around only 5 millions/cumm
of blood.
 Counting this much number is highly
imposible.
 Therefore the blood sample is diluted
with the help of RBC diluting fluid.
 It fixes and preserves RBCs.
 It is isotonic to RBCs.
NEUBAUER CHAMBER:
 The improved neubauer’s chamber has
a metalized surface and improved
neubauer rulings.
 The chamber has two ruled areas.
 Each ruled area:
dimension = 3mm x 3mm
consists of 9 large squares each
measuring
1mm x 1mm
Depth – 0.1 mm
 The central large square is divided into
25 squares.
 Each of this 25 square is further divided
into 16 small squares.
 Each group of 16 small squares is
separated by closely ruled triple lines.
 The 4 corner squares are further
divided into 16 small squares.
Coverslips used in neubauer’s
chamber:
 The coverslips used for the chamber are
special.
 They are thick and optically flat so that
the volume occupied by the diluted
blood in each large square is 0.1 ml
when covered by the coverslip.
RBC PIPETTE:
 The pippete has a bulb for dilution and
mixing and is caliberated to deliver 20ul
or 0.02 ml of blood.
 The bulb contains a red bead which
facilitates the mixing of blood with the
diluting fluid.
 Freely mobile bead indicates dry pipette.
 Markings on pipette are 0.5 , 1 , 101.
DILUTING FLUID
 Two types of diluting fluids are used for
RBC counting.
1) Hayem’s fluid
2) Dacie’s fluid
Composition of Hayem’s fluid:
a. Sodium chloride -0.5 gm
b. Sodium sulfate -2.5 gm
c. Mercuric chloride -0.25 gm
d. Distilled water – 100 ml.
Composition of Dacie’s fluid:
i. Trisodium citrate – 3 gm.
ii. Formalin – 1 ml.
iii. Distill water – 99 ml.
This diluting fluid is cheap and
commonly used.
PROCEDURE
 Assemble all the equipment; draw the blood
directly from finger or collected sample into
RBC pipette upto 0.5 mark.
 Wipe off the tip of pipette to remove extra
blood, if present. Then immediately draw up
the diluting fluid upto 101 mark.
 Now rotate the pipette gently for 2 – 3 mins
so that the diluting fluid gets mixed properly.
This will give dilution 1: 200.
 Place the cover slip in position over the
ruled area of chamber. Once again mix the
solution thoroughly by rotating the pipette.
 Discard first 1 – 2 drops of blood from
pipette.Now apply slight pressure on the
rubber tube of pipette, so that the third
drop of fluid is in hanging position.
 Touch the tip of pipette (hanging drop)
against the edge of cover slip. The angle
between pipette and cover slip is 45°. With
this process, chamber gets filled with the
fluid. This is known as charging of the
chamber.
 The care should be taken that, no air
bubble is present inside the chamber and
there is no over filling beyond the ruled
area.
 Leave the counting chamber as it,
without disturbing for about 3 min. This
will allow the settling down of RBCs.
 Place the chamber on stage of
microscope. Adjust the light and ruled
area. Make sure that, the distribution of
RBC over the chamber is uniform.
 Now count the RBC using 40x in Central
Square. The central square is subdivided
into 25 squares.
 Out of 25 squares, count four at each
corner and one at center. Each of these
five squares is subdivided into 16 small
squares. Thus, RBCs are counted in 16 x 5
= 80 small squares.
 In case of marginal cells, count the cells on
‘L’ line, i.e. either right and lower or left and
upper margin. Make the total of cells
counted in 5 squares.
 Let the no. of RBC counted in 80 small
squares = N
 Volume of area in which RBCs counted =
( 1/5 x 1/5 x 0.1 ) x 5=1/50
 No of RBCs in 1/50 mm3= N
No of RBCs in 1 mm3= Nx50
 Dilution factor = 200
 RBC count per mm3 = Nx50x200=N x 10000
No. of cells in neubeaur chamber=
N x dilution factor
Volume of chamber in which
cells counted
 For RBC
N x 10000
ERRORS OF RBC COUNT
 TECHNICAL ERRORS:
defective apparatus/defective
technique
Technical errors can be minimised by
the use of accurately caliberated
apparatus and by careful technique.
 INHERENT ERROR:
The distribution of RBCs is of an
irregular pattern in the counting
chamber.This affects the accuracy of
visual count which can be minimised by
counting a large no. of RBCs.
AUTOMATED METHOD
 Electronic counter is based on the
principle of aperture impendence
method .
 Anticoagulated blood is diluted with
particle free diluting fluid such as
physiological saline or phosphate buffer
saline.
 Particles passing through a chamber in
single file scatter the light and convert
by a detector into pulses proportional to
size of the cells which are then counted
electronically.
Advantages:
1) Easy and rapid method
2) Many thousand of cells are counted
compared to fewer cells counted in
manual method.
Disadvantages:
1)Costly equipment
2) Caliberation error
3) Altered composition of diluent causes
erroneous results.
4)Gaint platelets are counted as RBCs.
5)High WBC count alters results.
Reference range:
 Adult male – 4.5 to 5.5 million/cumm
 Adult female – 3.8 to 5.2 million /cumm
 At birth – 6 to 8 million/cumm
Conditions of decreased RBC count:
1)Anaemia
2)Pregnancy
Conditions of increased RBC count:
Physiological: 1)new borns and infants
Pathological : 1)
polycythemia(polycythemivera,kidney
tumours,high altitude)
2) dehydration
3 ) hypoxia(COPD,
congenital heart disease)
THANK
YOU

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Rbc count

  • 2. RED BLOOD CELLS  Red blood cells, or erythrocytes, are the most abundant cells in the bloodstream and contains hemoglobin, the compound that carries oxygen through the body.  . Any disruption of the red blood cells, its quantity, shape, size, structure or life cycle can therefore affect the oxygen- carrying capacity of the blood.
  • 3. Shape and size of RBCs  A red blood cell is a biconcave disc. Simply it is a round ball that is squeezed from two opposite ends to appear, widest at the sides and narrowest in the middle.  A red blood cell measures about 6 to 8 micrometers in diameter (average = 7.8 um) with an average thickness of 2 micrometers (2.5 um at the thickest point and less than 1um at the center). Although a red blood cell is wider than some capillaries, its flexibility allows it to become distorted as it squeezes through narrow passages and then restores to its
  • 4.
  • 5. METHODS OF RBC COUNT: 1) Visual haemocytometer( manual method ) 2) Automated method
  • 6. MANUAL METHOD: EQUIPMENTS REQUIRED: 1)Haemocytometer or improved Neubauer’s chamber 2)RBC pipette
  • 7. FLUIDS REQUIRED :  RBC diluting fluid  Blood sample (capillary blood or EDTA anticoagulated blood can be used )
  • 8. RBC DILUTING FLUID  RBCs are around only 5 millions/cumm of blood.  Counting this much number is highly imposible.  Therefore the blood sample is diluted with the help of RBC diluting fluid.  It fixes and preserves RBCs.  It is isotonic to RBCs.
  • 9. NEUBAUER CHAMBER:  The improved neubauer’s chamber has a metalized surface and improved neubauer rulings.  The chamber has two ruled areas.
  • 10.  Each ruled area: dimension = 3mm x 3mm consists of 9 large squares each measuring 1mm x 1mm Depth – 0.1 mm
  • 11.  The central large square is divided into 25 squares.  Each of this 25 square is further divided into 16 small squares.  Each group of 16 small squares is separated by closely ruled triple lines.  The 4 corner squares are further divided into 16 small squares.
  • 12. Coverslips used in neubauer’s chamber:  The coverslips used for the chamber are special.  They are thick and optically flat so that the volume occupied by the diluted blood in each large square is 0.1 ml when covered by the coverslip.
  • 13.
  • 14.
  • 15.
  • 16.
  • 17. RBC PIPETTE:  The pippete has a bulb for dilution and mixing and is caliberated to deliver 20ul or 0.02 ml of blood.  The bulb contains a red bead which facilitates the mixing of blood with the diluting fluid.  Freely mobile bead indicates dry pipette.  Markings on pipette are 0.5 , 1 , 101.
  • 18.
  • 19.
  • 20. DILUTING FLUID  Two types of diluting fluids are used for RBC counting. 1) Hayem’s fluid 2) Dacie’s fluid
  • 21. Composition of Hayem’s fluid: a. Sodium chloride -0.5 gm b. Sodium sulfate -2.5 gm c. Mercuric chloride -0.25 gm d. Distilled water – 100 ml.
  • 22. Composition of Dacie’s fluid: i. Trisodium citrate – 3 gm. ii. Formalin – 1 ml. iii. Distill water – 99 ml. This diluting fluid is cheap and commonly used.
  • 23. PROCEDURE  Assemble all the equipment; draw the blood directly from finger or collected sample into RBC pipette upto 0.5 mark.  Wipe off the tip of pipette to remove extra blood, if present. Then immediately draw up the diluting fluid upto 101 mark.  Now rotate the pipette gently for 2 – 3 mins so that the diluting fluid gets mixed properly. This will give dilution 1: 200.  Place the cover slip in position over the ruled area of chamber. Once again mix the solution thoroughly by rotating the pipette.
  • 24.  Discard first 1 – 2 drops of blood from pipette.Now apply slight pressure on the rubber tube of pipette, so that the third drop of fluid is in hanging position.  Touch the tip of pipette (hanging drop) against the edge of cover slip. The angle between pipette and cover slip is 45°. With this process, chamber gets filled with the fluid. This is known as charging of the chamber.  The care should be taken that, no air bubble is present inside the chamber and there is no over filling beyond the ruled area.
  • 25.  Leave the counting chamber as it, without disturbing for about 3 min. This will allow the settling down of RBCs.  Place the chamber on stage of microscope. Adjust the light and ruled area. Make sure that, the distribution of RBC over the chamber is uniform.
  • 26.  Now count the RBC using 40x in Central Square. The central square is subdivided into 25 squares.  Out of 25 squares, count four at each corner and one at center. Each of these five squares is subdivided into 16 small squares. Thus, RBCs are counted in 16 x 5 = 80 small squares.  In case of marginal cells, count the cells on ‘L’ line, i.e. either right and lower or left and upper margin. Make the total of cells counted in 5 squares.
  • 27.
  • 28.  Let the no. of RBC counted in 80 small squares = N  Volume of area in which RBCs counted = ( 1/5 x 1/5 x 0.1 ) x 5=1/50  No of RBCs in 1/50 mm3= N No of RBCs in 1 mm3= Nx50  Dilution factor = 200  RBC count per mm3 = Nx50x200=N x 10000
  • 29. No. of cells in neubeaur chamber= N x dilution factor Volume of chamber in which cells counted  For RBC N x 10000
  • 30. ERRORS OF RBC COUNT  TECHNICAL ERRORS: defective apparatus/defective technique Technical errors can be minimised by the use of accurately caliberated apparatus and by careful technique.  INHERENT ERROR: The distribution of RBCs is of an irregular pattern in the counting chamber.This affects the accuracy of visual count which can be minimised by counting a large no. of RBCs.
  • 31. AUTOMATED METHOD  Electronic counter is based on the principle of aperture impendence method .  Anticoagulated blood is diluted with particle free diluting fluid such as physiological saline or phosphate buffer saline.  Particles passing through a chamber in single file scatter the light and convert by a detector into pulses proportional to size of the cells which are then counted electronically.
  • 32. Advantages: 1) Easy and rapid method 2) Many thousand of cells are counted compared to fewer cells counted in manual method. Disadvantages: 1)Costly equipment 2) Caliberation error 3) Altered composition of diluent causes erroneous results. 4)Gaint platelets are counted as RBCs. 5)High WBC count alters results.
  • 33. Reference range:  Adult male – 4.5 to 5.5 million/cumm  Adult female – 3.8 to 5.2 million /cumm  At birth – 6 to 8 million/cumm
  • 34. Conditions of decreased RBC count: 1)Anaemia 2)Pregnancy Conditions of increased RBC count: Physiological: 1)new borns and infants Pathological : 1) polycythemia(polycythemivera,kidney tumours,high altitude) 2) dehydration 3 ) hypoxia(COPD, congenital heart disease)