UNIT 1 Flashcards
Manual Hematology Methods Microhematocrit ESR Slide Making and Staining Manual Differential Hemocytometer Cell Counts Understand the WBC Scatterplot Instrumentation Flags Correct WBC Count
Hematology
Study of cellular components of blood
- Cell identification
- Blood forming organs: BM, liver
- Blood related disorders
- Heme lab tests
Hemostasis
aka Coagulation System
A study of the mechanisms that the body employs to ensure balance & order in the circulatory system.
Hematocrit
Percentage of packed RBCs in a given volume of centrifuged blood.
Manual Differential
Count the first 100 WBCs seen on the slide & report the # of each types using 100x with oil.
Buffy Coat
Makes up < 1%
Made up of WBC & Platelets
EDTA
A Ca2+ chelating agent that is used as an anticoagulant
Na+ Citrate 3.2%
Blue tube that chelates Ca2+
Must fill tube 9:1 ratio.
Ideal for platelet clumper patients
Rouleaux
Penny stacking of RBCs
Zeta Potential
A negative charge that causes red cells to repel each other. (Aggregation inhibited by the electrical charge on RBCs).
Decreases when inflammatory proteins are increased.
Microhematocrit
Quick screening for Anemia, uses small volume of blood & spun at high speed.
Falsely Increased Microhematocrit
Excessive Trapped Plasma
Centrifuge Speed Too Low
Not Centrifuging Long Enough
Poikilocytosis
Poikilocytosis
Variation of RBCs shape. Thus, RBCs are stacked higher than normal, causing a falsely increased microhematocrit.
Falsely Decreased Microhematocrit
Tissue Fluids Severe Edema Milking Fingerstick Hemolysis Excessive Anticoagulants Improper Clay Seal Cells Lost During Centrifugation
Microhematocrit Procedure
Fill 2 capillary tubes 3/4 way full with EDTA or from a finger stick.
Seal 1 end with clay
Put in centrifuge with open end toward the center
Results must be within +/-1% of each other
Report Avg as percent of packed RBCs compared to blood volume
ESR
Measurement of rate that RBCs sediment in the period of 1 Hr.
A NON-SPECIFIC test for inflammatory processes.
Aggregation Phase
1 of 3 Phases of ESR.
RBCs come together & form a rouleaux
Sedimentation Phase
2 of 3 Phases of ESR.
Aggregates fall out of solution
Packing Phase
3 of 3 Phases of ESR.
Aggregates pack together
ESR Procedure
- Slowly push pipette through the top of the well.
- Fill pipette to or beyond 0 mark at the top
- Make sure there’s no air bubbles
- Place onto rack & let it sit undisturbed for 1 Hr
- Record mm’s of sedimentation.
DO NOT include Buffy Coat!
What causes elevated ESR?
Too Warm of Room Temperature
Tilted Tube
Agitation
ESR Red Range (male >50)
0-20 mm/Hr
ESR Ref Range (women <50)
0-20 mm/Hr
ESR Ref Range (child)
0-10 mm/Hr
ESR Ref Range (male <50)
0-15 mm/Hr
ESR Ref Range (woman >50)
0-30 mm/Hr
Characteristics of a well-made smear
No lines and holes
Thick & thin areas with gradual transition
Feathered Edge with Rainbow effect
What are the components of the Wright Stain?
For Peripheral Smear & Bone Marrow Films, they contain Eosin (Red) & Methylene (Blue)
What is the formula for the Platelet Estimate?
Average x 15 = PLT Count/uL
or
Average x 15,000 = PLT Count/uL
What is the formula for WBC Estimate?
Average x 2 = WBC Count/uL
or
Average x 2000 = WBC Count/uL
Proper peripheral smear technique examination
Scan on 10x, look for unusual distribution of cells
Look for platelet clumps in feathered edge (Redraw if you see any clumps - Blue tube and multiply by 1.1)
Go to 40x, find a “good area” where 1/2 RBCs are overlapping
Do manual WBC estimate if necessary
Go to 100x with oil & perform- Manual WBC Diff, RBC morphology eval, PLT estimation (abnormally shaped)
Battlement Pattern
Used to scan for cells during a differential. Following this pattern helps to ensure that we do not count the same cell more than once
Start from the feathered edge
Where are the lymphocytes in the Battlement Pattern?
Center
Where are the Neutrophils in the Battlent Pattern?
Near the Edge
Which WBCs are granulocytes?
N, E, B
Neutrophil
Eosibophil
Basophil
Which WBCs are NON-Granulocytes?
Lymphocyte
Monocyte
Characteristics of basophil
Segmented nucleus, abundant dark blue or purple granules
Characteristics of neutrophil
Polymorphonuclear and Seg, 2-5 Lobes
Characteristics of lymphocyte
Round/Oval shaped nucleus
Nucleus size of RBC.
N:C - Nucleus ratio > Cytoplasm
Characteristics of monocyte
Nucleus larger than RBC
Butt/kidney shaped nucleus
Lots of Vacuoles, Pseudopods
Hemocytometer Formula
(# Cells Counted)(Dilution Factor) / (# Sq Counted)(Sq Volume) = cells/mm3
What is the square volume of WBC?
Hint: Hemocytometer Cell Count
0.1 mm^3
What is the square volume of RBC?
Hint: Hemocytometer Cell Count
0.004 mm^3
LEVEY-JENNINGS CHART
A graph used to plot and visualize the results of control over time.
What is a “Shift” in Levey-Jennings Chart?
A sudden change in values that remain consistent
Which is the correct match of each component of VCS technology with what the WBCs are hit with?
A. Conductivity - Laser Beam, Nuclear Lobularity
Volume - Alternating Current, Measures Nucleus Volume
Light Scatter - Direct Current
B. Volume - Direct Current
Conductivity - Alternating Current, Measures Nucleus Volume
Light Scatter - Laser Beam, Nuclear Lobularity
C. Conductivity - Direct Current
Volume - Laser Beam, Nuclear Lobularity
Light Scatter - Alternating Current, Measures Nucleus Volume
B
Volume - Direct Current
Conductivity - Alternating Current, Measures nucleus volume
Light Scatter - Laser Beam, Nuclear Lobularity
What is VCS? What does it stand for?
Volume
Conductivity
Light Scatter
It allows the instrument to analyze WBC immediately (That’s a basophil! Thats a neutrophil!) & can be accurately identified. WBCs pass single filed through aperture & hit by (electrical currents, laser beam, radio waves)
Delta Check
Automatic check performed by LIS to notify tech of significant difference btwn recent test results
What should you do if the LIS notifies you of a Delta Check?
Check sample quality (clots, vole etc)
Check if patient had a tranfusion, surgery, etc
Make sure tube is properly labeled
What is QC?
Ensuring test work is done properly
- Controls frequently ran
- Controls have defined value
What is QA?
Making sure final results we report are correct (right test on right sample, right result reported on right pt)
- Maintenance
- Validation & Calibration of Instrument
- SOP
- Quality Control
How is Hemoglobin measured?
Hgb is directly measured using Cyanmethemoglobin test methodology
The _______ is an analyzer’s method of measure RBCs, which impede the _______ because they are ______ conductors.
Coulter Principle,
Direct current,
Poor
A Hgb molecule is tetrameric (4 Globin molecules placed in a quaternary structure). True or False?
True
Where is the iron ion found?
In the Fe2+ Ferrous state
Cyanmethemoglobin Method
Considered a Gold Standard.
Methemoglobin combines with residual cyanide ions to form cyanmethgb.
Hemoglobin
A molecule inside RBC that carries O2 & CO2
Where is oxyhemoglobin found?
In the ferric (Fe3+) state
MCV is directly measured. True or False?
False
MCV is directly measured
MCH, MCHC is Calculated Results. True or False?
True
What is the Ferric State of Hgb Formation?
Fe3+
What is the Reduced State of Hgb Formation?
Fe2+
An adult patient’s CBC shows a WBC count of 12.4x10^3 and a relative monocyte count of 8%. What is the absolute monocyte count?
What does it show?
0.9 Absolute Monocytosis
An adult patient’s CBC result shows a WBC count of 15.7x10^3 and the automated diff shows 30% Neutrophils. To describe this patient’s result, you would say this patient has ______ and ______.
Absolute Leukocytosis and Relative Neutropenia
You walk into a lab where a tech is performing an ESR. Upon closer examination, you realize the testing is being performed directly adjacent to a centrifuge. You tell the tech this may cause a _____ test result.
A. Falsely Decreased
B. Falsely Increased
C. Normal
D. None of the above
B. Falsely Increased