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TRANSCRIPT
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Examination of Peripheral Blood Smear
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A well Made and well Stained Smear can provide:
Estimates of cell count
Proportions of the different types of WBC
Morphology
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Peripheral Blood Smear
Objective
1. Specimen Collection
2. Peripheral Smear Preparation
3. Staining of Peripheral Blood Smear
4. Peripheral Smear Examination
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Specimen Collection
Venipuncture
should be collected on an EDTA Tube
EDTA liquid form preferred over the powdered form
Chelates calcium
Disodium or Tripotassium ethylenediamine tetra-acetic acid
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Advantages
1. Many smears can be done in just a single draw
2. Immediate preparation of the smear is not necessary
3. Prevents platelet clumping on the glass slide
Specimen Collection
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Disadvantages:
PLATELET SATELLITOSIS
causes pseudothrombocytopenia and pseudoleukocytosis
Cause: Platelet specific auto antibodies that reacts best at room temperature
Specimen Collection
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Platelet satellitosis
Specimen Collection
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Solution
recollect specimen using Sodium Citrate in a 9:1 dilution
Correction for dilution
2.7 ml blood
0.3 ml anticoagulant
9/10 dilution is reciprocal 10/9 = 1.1
Ergo, all computations for WBC and Platelet should be multiplied to 1.1
Specimen Collection
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Peripheral Smear Preparation
Wedge technique
Coverslip technique
Automated Slide Making
and Staining
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Peripheral Smear Preparation
Wedge technique
1. Easiest to master
2. Most convenient and most commonly used technique
Material needed
1. Glass slide 3 in X 1in
2. Beveled/chamfered edges
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Peripheral Smear Preparation
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Procedures:
1. Drop 2-3 mm blood at one end of the slide
Diff safe can be used
a. Easy dropping
b. Uniform drop
Peripheral Smear Preparation
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Precaution: Too large drop = too thick
smear
Too small drop = too thin
smear
Peripheral Smear Preparation
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2. The pusher slide be held securely with the dominant hand in a 30-45 deg angle.- quick, swift and smooth gliding motion to the other side of the slide creating a wedge smear
Peripheral Smear Preparation
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Peripheral Smear Preparation
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Wedge Technique
1. Push Type wedge preparation
2. Pull Type wedge prepartion
Peripheral Smear Preparation
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Precautions: Ensure that the whole drop of blood is
picked up and spread Too slow a slide push will accentuate
poor leukocyte distribution, larger cells are pushed at the end of the slide
Maintain an even gentle pressure on the slide
Keep the same angle all the way to the end of the smear.
Peripheral Smear Preparation
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Precautions:
Angle correction:
1. In case of Polycythemia: high Hct angle should be lowered
- ensure that the smear made is not to thick
2. Too low Hct: Angle should be raised
Peripheral Smear Preparation
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Feature of a Well Made Wedge Smear
Smear is 2/3 or ¾ the entire slideSmear is finger shaped, very slightly rounded at the feathery edge: widest area of examinationLateral edges of the smear visibleSmear is smooth without irregularities, holes or streaksWhen held up in light: feathery edge should show rainbow appearanceEntire whole drop of blood is picked up and spread
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Cover Slip Technique
rarely used
used for Bone marrow aspirate smears
Advantage: excellent leukocyte distribution
Disadvantage: labeling, transport, staining and storage is a problem
Peripheral Smear Preparation
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22 x 27mm clean coverslipMore routinely used for bone marrow aspirateTechnique: 1. A drop of marrow aspirate is placed on top of 1 coverslip2. Another coverslip is placed over
the other allowing the aspirate to spread.
3. One is pulled over the other to create 1 thin smears
Peripheral Smear Preparation
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4. Mounted on a 3x1 inch glass slidePrecautions:
Very lgiht pressure should be applied between the index finger and the thumbCrush preparation techniqueToo much pressure causes rupture of the cells making morphologic examination impossibleToo little pressure prevents the bone spicules from spreading satisfactorily on the slide
Peripheral Smear Preparation
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Automatic Slide Making and Staining
SYSMEX 1000i
Peripheral Smear Preparation
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Drying of Smears
Fan
Heating pans
No breath blowing of smears – may produce crenated RBCs or develop water artifact (drying artifact)
Peripheral Smear Preparation
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Wright Staing Method
Automated Slide Stainers
Quick Stains
Staining of Peripheral Blood Smear
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Pure Wright stain or Wright Giemsa stain
Blood smears and bone marrow aspirate
Polychrome stains: Eosin and Methylene blue stains
Purpose: see and evaluate cell morphology
Staining of Peripheral Blood Smear
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Eosin + Methylene Blue = thiazine eosinate complex
The complex will not stain any color unless a buffer is added: 0.05M sodium phosphate (pH 6.4) and aged distilled water (pH 6.4-6.8)
Methanol is added to fix the cells on the slide
Staining of Peripheral Blood Smear
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Free Methylene Blue: - basic- stains acidic cellular
components such as RNAFree Eosin
- acidic- stains basic cellular
components such as Hgb and eosinophilic granules
Staining of Peripheral Blood Smear
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Problem encountered during staining
Water artifact: moth eaten RBC, heavily demarcated central pallor on the RBC surface, crenation, refractory shiny blotches on the RBC
Staining of Peripheral Blood Smear
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What contributes to the problem:1. humidity in the air as you air dry the slides.2. Water absorbed from the humid air into the
alcohol based stainSolution:
1. Drying the slide as quickly as possible.2. Fix with pure anhydrous methanol before
staining.3. Use of 20% v/v methanol
Staining of Peripheral Blood Smear
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AUTOMATED SLIDE STAINERS1. It takes about 5-10 minutes to stain a batch of
smears2. Slides are just automatically dipped in the
stain in the buffer and a series of rinsesDisadvantages:
1. Staining process has begun, no STAT slides can be added in the batch
2. Aqueous solutions of stains are stable only after 3-6 hours
Staining of Peripheral Blood Smear
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Staining of Peripheral Blood Smear
HEMA-TEK STAINER
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QUICK STAINSFast, convenient and takes about 1 minute to be accomplishedModified Wrights-Giemsa Stain, buffer is aged distilled waterCost effectiveDisadvantage:
Quality of stains especially on color acceptanceFor small laboratories and for physician’s clinic
only
Staining of Peripheral Blood Smear
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Features of a well-stained PBS
Macroscopically: color should be pink to purple
Microscopically:
RCS: orange to salmon pink
WBC: nuclei is purple to blue
cytoplasm is pink to tan
granules is lilac to violet
Eosinophil: granules orange
Basophil: granules dark blue to black
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Features of a well-stained PBS
Troubleshooting:
1. RBC gray, WBC too dark Eosinophil granules are gray
Cause: stain or buffer is to alkaline
inadequate rinsing
Prolonged staining
heparinized sample
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Features of a well-stained PBS
Troubleshooting:
2. RBC too pale, WBC barely visible
Causes:Stain or buffer is too acidic
Underbuffering
Over rinsing
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Peripheral Smear Examination
Macroscopic
1. Overall bluer color: increased blood proteins (multiple myeloma, rouleaux formation)
2. Grainy appearance: RBC agglutination (cold hemagglutinin diseases)
3. Holes: increased lipid
4. Blue specks at the feathery edge: Increased WBC and Platelet counts
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Peripheral Smear ExaminationMicroscopic:10x Objective
1. Assess overall quality of the smear i.e feathery edge, quality of the color, distributin of the cells and the lateral edges can be checked for WBC distribution
2. Snow-plow effect: more than 4x/cells per field on the feathery edge: Reject
3. Fibrin strands: Reject4. Rouleaux formation, large blast cell
assessment
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Peripheral Smear Examination
Microscopic:
40x Objective1. Correct area where to star counting is
determined
2. WBC estimate: internal quality control
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Peripheral Smear ExaminationMicroscopic:
100x Objective; OIO1. Highest magnification
2. WBC differential counting
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Peripheral Smear ExaminationOptimal Assessment Area:
1. RBCs are uniformly and singly distributed
2. Few RBC are touching or overlapping
3. Normal biconcave appearance
4. 200 to 250 RBC per 100x OIO
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Too thin
Peripheral Smear Examination
Too thick
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Performance of a White Blood Cell Differential Count
Systematic
Choose the best area for assesment
Back and forth serpentine or battlement track patters in preferred
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Performance of a White Blood Cell Differential Count
100 WBCs are counted using a push down counters (Clay Admas Laboratory counters,Biovation diff counters
Accuracyof Diff Count:
Count 200 WBC if WBC>40 x 109/L
Extremely low WBC counts, do the Diff count under 50X OIO
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Performance of a White Blood Cell Differential Count
Extremely low WBC counts, do the Diff count under 50X OIO
Extremely low WBCs: WBC are concentrated, buffy coat smears are made
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RBC Morphology
Anisocytosis
Poikilocytosis
Cellular Inclusions
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Platelet Estimate
Choose an area where RBC barely touch
No. of platelet in 10 OIO fields is counted multiplied by 20,000
Anemia or Erythrocytosis
Average No. of Plts/field x total RBC count
200 RBCs/field
(200 is the average number of RBC/field)
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Summarizing WBC parameters
1. Total WBC counts per (WBC x 109/L)
2. WBC differential counts are percentages
3. WBC differential count values expressed as actual number of each type of cell
4. WBC morphology
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Summarizing WBC parameters
STEP 1
WBC increased : leukocytosis
WBC decreases: leukopenia
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Summarizing WBC parameters
STEP 2
Relative differential count
Cell Type Increases Decreases
Neutrophil Neutrophilia Neutropenia
Eosinophil Eosinophilia N/A
Basophil Basophilia N/A
Lymphocyte Lymphocytosis
Lymphopenia
Monocyte Monocytosis Monocytopenia
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Summarizing WBC parametersSTEP 3Absolute Cell CountsEx. WBC 13.6
PMNs 67Lym 26Eos 3Baso 3Mono 1
Absolute Neutrophil Count: 9.1 (NV: 2.4-8.2)Absolute Lymphocyte Cout: 3.5 ((NV: 1.4-4.0)Absolute Monocyte Count: 0.4 (NV: 0.1-1.2)
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Summarizing WBC parametersSTEP 4Examination for immature cellsYoung cells should not be seen in the peripheral blood smearImmature cells: possess a nucleus
do not lyse during testing
can be counted as WBC and falsely elevate WBC results
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LEFT SHIFT
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Summarizing RBC Parameters
RBC Count )RBC x 1012/L)Hb (g/dl)Hct (5 or L/L)Mean Cell Volume (MCV. Fl)Mean Cell Hb (MCH, pg)Mean Cell Hb Concentration (MCHC. %, g/dl)RBC distributionMorphology
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Step1
Examne Hb an Hct for anemia or polycythemia
If the RBC morphology is normal: Use rule of three to estimate the Hct
Step 2
MCV: to check and correlate to the morpholic apperance of the cells
Summarizing RBC Parameters
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Step 3Examine MCHCDescribes how well the cells are filled with HbHypochromic, normochromic2 conditions when MCHC should be evaluated:1. spherocytosis: slight elevation2. lipemia/icterus: markedly increase
Summarizing RBC Parameters
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Step 4
Examine MCHC
Describes how well the cells are filled with Hb
Hypochromic, normochromic
2 conditions when MCHC should be evaluated:
1. spherocytosis: slight elevation
2. lipemia/icterus: markedly increase
Summarizing RBC Parameters
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Step 5
Morphology
1. Size
2. Shape
3. Inclusions
4. Young rbcs
5. Color
6. Arrangement
Summarizing RBC Parameters
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Summarizing Platelet Parameters
Platelet count (x 109/L)
Mean Platelet Volume MPV, fl
Morphology