CBC Final
CBC Final
CBC Final
Dr. Saifeldein M. A. E.
MBBS, MMSC-PATH, MMSC-HEMA
Consultant of Hematopathology
Laboratory & Blood Bank Department
MCH-Najran
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OBJECTIVES
- To have an idea about the hematology analyzers.
- To know the different types of CBC data presentation.
- To be able to interpret CBC reports.
- To recognize common blood disorders.
- To be updated about the new CBC parameters.
- To know when to request hematology consultation.
- To know what is the next step or test to be requested.
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Introduction
Complete blood count is the most useful and informative single
test; which consists of RBC, WBC, and Platelets indices.
Hematology analyzers lay out these indices in form of crude numeric data,
intensity graphs and histograms.
CBC is used for:
• Screening.
• Diagnosis of hematological and systemic disorders.
• Follow up.
• Disease monitoring and effect of treatment.
• Routine
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base-line investigation. 3
Crude Data
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Flagging System
Parameters Validation
• Abnormalities of cells are signaled by certain ‘asterisk’ on CBC report.
• Every instrument has its own flagging system.
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Interpretive Messages (IP)
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HISTOGRAMS
• These are the graphical representation of numerical data of different cell
population on cell counter.
• Y axis represents the number of cells and X axis represents the cell size.
• Platelets volume is b/w 8 – 12 fl and counted b/w 2 – 25 fl.
• RBC volume is b/w 80 – 100 fl and counted b/w 25 – 250 fl.
• WBC Lower discriminator fluctuates between 30 -60 fl and upper discriminator
is fixed at 300 fl.
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Thrombocyte histogram
• The histogram curve should lie within the lower and upper platelet
discriminator (PL & PU) and start and end on the base line.
• 1 flexible Discriminator PL 2 to 6 fl.
• 1 flexible Discriminator PU 12-30 fl.
• 1 fixed Discriminator at 12 fl.
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• PL flag:
• When lower discriminator exceeds preset height by 10%, Platelet count, P-
LCR and MPV will show PL flag.
• Possible causes:
• High blank value.
• Cell fragments.
• High numbers of bacteria.
• Contaminated reagent.
• Platelet aggregation.
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PU flag:
• This occurs when UD exceeds the preset height by more than 40%.
Possible causes
• PLT clumps.
• EDTA-incompatibility.
• Clotted sample.
• Giant Platelets.
• Micro-erythrocytes.
• Fragmented or dysplastic RBC.
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Multiple peaks (MP)
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Platelets Parameters
Parameter Description
MPV Mean platelets volume.
• PLT 20 to 50000 - rarely have increased risk of spontaneous bleeding but there will be
an increased risk of bleeding from procedures.
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Possible causes of RL flag
• Giant platelets.
• Micro-erythrocytes.
• Fragmented RBCs.
• Platelet clumps.
• Due to high numbers of small RBCs the
platelet result might be false high.
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RU flag
• Flag is seen when UD exceeds the preset height by greater than 5 %.
Possible causes of RU flag:
• Cold agglutination.
• RBC agglutination.
• Rouleaux formation.
• Leucocytosis.
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Multiple peaks (MP)
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Diagnostic features of common hematological conditions
Iron deficiency Low Low Low Normal or low High Microcytic hypochromic
anemia zone
Beta Normal or low Low Low Normal or low Normal or near Normal Clustering in hypochromic
thalassemia microcytic zone
minor
Beta Very low Low Low Low Very high Similar to iron deficiency
thalassemia
major
Megaloblastic Low High Normal Normal High Wide spread microcytic zone
anemia
Dual deficiency Low Variable Variable Variable High Histogram extends in macrocytic and
anemia microcytic zones
Blood Normal or low Variable Variable Variable High Double plot of patients and
transfusion transfused cells
Cold agglutinin Normal or low Bizzare Bizzare Bizzare Bizzare Incubate blood at 37degree
centigrade
Spherocytosis Low Normal Normal High Normal Variable population in the hype-
rchromic zone
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Reticulocyte Indices
• RETIC. Count = 0.5% – 1.5%.
• RET-He.(30 – 36pg) Is a direct measurement of iron in the erythrocyte HGB.
• RMI Is the retics maturation index. This is determined according to the relative
amount of cellular RNA and hence it is divided into:
• 1- LFR – low fluorescence – intensity ratio. Mature retics. (85.8 _ 97.8%).
• 2- MFR – Middle fluorescence – intensity ratio. Immature cells. (1.91 _ 12.41%).
• 3- HFR – High fluorescence – intensity ratio. Most immature cells. (0.00 _ 1.9%).
• IRF – Immature reticulocytes fraction; is the sum of MFR and HFR(2.11 _ 14.14).
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Shift Correction Factor
Normal reticulocyte survive 3.5 days in marrow and 1 day in peripheral
circulation at normal PCV.
Maturation days depends on the PCV as follows:
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WBC histogram
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Complete Blood Count (CBC)
Interpretation
Dr. Saifeldein Mohammed A.E
MBBS
MSC-PATHOLOGY
MSC-HEMATOLOGY
Hematopathology Consultant
Laboratory Department
MCH – NAJRAN
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WL flag:
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WU flag:
• The histogram curve does not match the base line at upper discriminator
due to high numbers of large particles (WBC aggregation) or if the linearity
of the white blood cell count exceeds the limit. (WBC > 100 x 10³/μl).
• Pre-dilution (e.g. 1:5) of the sample might help to obtain correct results.
• Possible cause:
• Extreme Leucocytosis.
• Rare: WBC aggregation.
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T1 and T2 flags:
When discrimination between various cell population cannot be done due to
presence of abnormal leucocytes.
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Left Shift of Granulocytes
- The granulocytic “shift to left” reflects marrow response to bacterial
infection, and this is quantified as band count or immature granulocyte
count (IGC).
- IGC offers sensitivity of about 92.2%, and may be used for screening for
bacteremia.
- When IG cells are released from bone marrow , the peripheral neutrophil
count will still be in the normal or decreased range; this is called pseudo-
leucopenia which can develop upon the onset of infection.
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New WBC Indices
MNV Mean neutrophil volume
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Differentiation between SIRS and Sepsis
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Thank you
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