SlideShare uma empresa Scribd logo
1 de 30
BLOOD SMEARS 
RAJESH MOHESS, CLT
BLOOD SMEARS 
• Peripheral blood smear is a very important tool in the 
hematology lab 
• It provides rapid, reliable access to information about a 
variety of hematologic disorders 
• Examination of the peripheral blood smear is an inexpensive 
but powerful diagnostic tool in both children and adults 
• The smear offers a window into the functional status of the 
bone marrow 
• Review of the smear is an important adjunct to other clinical 
data; in some cases, the peripheral smear alone is sufficient to 
establish a diagnosis
BLOOD SMEARS 
• An examination of the blood smear (or film) may be 
requested by physicians based on medical history or 
initiated by laboratory staff as part of their protocol 
• Majority of cases for blood smears are from laboratory 
protocol 
• With the development of sophisticated automated blood-cell 
analyzers, the proportion of blood-count samples that 
require a blood smear has steadily diminished and in many 
clinical settings is now 10 to 15 percent or less. 
• Nevertheless, the blood smear remains a crucial diagnostic 
aid
BLOOD SMEARS 
• For a true morphological interpretation, a trained 
person is required to review the smear, as automation 
in hematology will normally generalize the morphology 
• The indications for smear review differ according to the 
age and sex of the patient, whether the request is an 
initial or a subsequent one, and whether there has 
been a clinically significant change from a previous 
validated result (referred to as a failed delta check). 
• All laboratories should have a protocol for the 
examination of a laboratory-initiated blood smear
BLOOD SMEARS 
• Not all hematological disorder requires a 
peripheral blood smears for diagnosis. 
• Some conditions can be diagnosed by other 
laboratory data also. 
• For example, Iron deficiency anemia can be 
diagnosed by MCV, iron and ferritin levels
BLOOD SMEARS 
• There are numerous valid reasons for a clinician to request 
a blood smear and these differ somewhat from the reasons 
why laboratory workers initiate a blood-smear examination. 
• Sometimes it is possible for a definitive diagnosis to be 
made from a blood smear. 
• More often, the smear is an important tool in the provision 
of a differential diagnosis and the indication of further 
necessary tests. 
• The blood smear can have an important part in the speedy 
diagnosis of certain specific infections. 
• Otherwise, its major roles are in the differential diagnosis 
of anemia and thrombocytopenia and in the identification 
and characterization of leukemia and lymphoma.
BLOOD SMEARS 
Anemia: 
• In patients with anemia, physician-initiated 
examinations of blood smears are usually 
performed in response to clinical features or to a 
previously abnormal complete blood count 
• Laboratory-initiated examinations of blood 
smears for patients with anemia are usually the 
result of a laboratory policy according to which a 
blood smear is ordered whenever the 
hemoglobin concentration is unexpectedly low
BLOOD SMEARS 
Hemolytic Anemia: 
• In the hemolytic anemias, red-cell shape is of 
considerable diagnostic importance. 
• Some types of hemolytic anemia yield such a 
distinctive blood smear that the smear is often 
sufficient for diagnosis. 
• This is true of hereditary elliptocytosis, and 
ovalocytosis. 
• The presence of bite cells points to a Heinz body 
hemolytic anemia
BLOOD SMEARS 
Macrocytic Anemia: 
• Patients with vitamin B12 or folic acid 
deficiency, the blood smear shows 
macrocytes. 
• It may also show oval macrocytes and 
hypersegmented neutrophils. 
• When the anemia is more severe, there may 
be marked poikilocytosis, with teardrop and 
red-cell fragments
BLOOD SMEARS 
Microcytic Anemia: 
• Blood smear not very significant in diagnosis, 
although very useful. 
• Most common cause is iron deficiency anemia 
which can be diagnosed by other blood tests 
Sickle cells/Thalassemia: 
• A blood smear is useful. Usually shows target 
cells sickle cells
BLOOD SMEARS 
Thrombocytopenia/Thrombocytosis: 
• A blood smear should always be examined for 
patients with thrombocytopenia. 
• This is done to both confirm the 
thrombocytopenia and to look for the 
underlying cause. 
• Falsely low platelet counts may be the result 
of small clots, platelet clumping, platelet 
satellitism or abnormally large platelets
BLOOD SMEARS 
White Cell Disorders 
(Leukemia/Lymphoma/Bone Marrow Failure): 
• The precise disease classification may rely upon 
evaluation of abnormal circulating cells. 
• Blood smears must always be examined when 
there is unexplained leukocytosis, lymphocytosis, 
or monocytosis or when the flagging system of an 
automated instrument suggests the presence of 
blast cells 
• For example, the presence of Auer rods in a blast 
form in patients with acute myeloid leukemia
BLOOD SMEARS 
The role of the blood smear in the diagnosis 
of leukemia and lymphoma is to suggest: 
• A likely diagnosis or range of diagnoses 
• To indicate which additional tests should be 
performed 
• To provide a morphologic context without 
which immunophenotyping and other 
sophisticated investigations cannot be 
interpreted
BLOOD SMEARS 
Summary 
• The blood smear remains an important diagnostic tool, 
even in this age of molecular analysis 
• Physicians may and should request a blood smear 
when there are clinical indications for it. 
• The Laboratory technologist should make and examine 
a blood smear whenever the results of the CBC indicate 
that a blood smear is necessary for the validation or to 
further investigate an abnormality 
• To avoid errors and miss any diagnoses, hematological 
disorders should be investigated by both clinical data 
and the peripheral smear
PREPARATION OF A BLOOD SMEAR 
Principle: 
• A peripheral smear may be requested by the clinician. 
• It may also be performed as part of the laboratory 
protocol from reflex or if there are discrepancies from 
prior results. 
• We will discuss the ‘Wedge Smear’ 
• Smears are prepared by placing a drop of blood on a 
clean glass slide and spreading the drop using another 
glass slide at an angle. 
• The slide is then stained and observed microscopically, 
mainly to determine differential count and morphology 
study
PREPARATION OF A BLOOD SMEAR 
Principle: 
• A well-stained peripheral smear will show the red cell 
background as red orange. 
• White cells will appear with blue purple nuclei with red 
purple granules throughout the cytoplasm. 
• A well made, well distributed peripheral smear will have a 
counting area at the thin portion of the wedge smear which 
is approximately 200 red cells not touching. 
• A good counting area is an essential ingredient in a 
peripheral smear for evaluating the numbers of and types 
of white cells present and evaluating red cell and platelet 
morphology.
PREPARATION OF A BLOOD SMEAR 
Principle: 
• Functions of the peripheral blood smear are: 
- provide information for diagnosis 
- provide information for further testing or to 
establish diagnosis 
- used as a guide for therapy 
- Used as an indicator to monitor the harmful 
effects for chemotherapy and radiation therapy
PREPARATION OF A BLOOD SMEAR 
Materials: 
- Glass slides 
- Applicator sticks 
- Capillary tubes 
- EDTA specimen (smear should be made within 4 
hours of blood collection) 
- Capillary blood specimen collected in 
heparinized tubes
BLOOD SMEAR PROCEDURE 
• Mix blood properly 
• Place a small drop of blood (about 2-3 mm) about 1 cm from 
the frosted end of a clean slide (slide must be completely 
clean) 
• Using a spreader (another slide), draw backwards into the 
drop of blood (while applying pressure) – maintain an angle of 
30-45 degrees
BLOOD SMEAR PROCEDURE 
• When the spreader touches the blood, allow the 
blood to spread across the edge of the spreader 
• Move the spreader forward on the slide (in one 
smooth motion), so a smear is made 
approximately 3 to 4 cm in length. 
• The smear should be half the size of the slide, 
with no ridges, and a “feather edge” should be 
toward the end of the smear.
BLOOD SMEAR PROCEDURE
BLOOD SMEAR PROCEDURE 
• Label the frosted end of the slide with the 
patient’s last name and first initial, specimen 
number, and the date 
• Allow the smear to air dry completely (about 5 
minutes) 
• Specimen can now be stained
BLOOD SMEAR PROCEDURE
BLOOD SMEAR 
Good smear 
A good smear should have the following 
appearance: 
• Appear smooth and uninterrupted 
• Start thick and gradually thinning out (feather-edge) 
• The film should take up ½ to ¾ the length of 
the slide
BLOOD SMEAR LIMITATIONS 
• The angle between the slides is dependent upon the size of the 
blood drop and viscosity of the blood. 
The optimal angle is 45 degrees 
• The larger the drop of blood and lower the hematocrit, the higher 
the angle needs to be so the blood smear is not too long 
• Blood with a higher hematocrit needs to have a lower angle so the 
smear is not too short and thick 
• Glass slides must be clean; otherwise, this results in imperfect 
distribution of cells and improper staining 
• Smears should not be made from blood remaining on the tube 
stopper as the lubricant on the stoppers can interfere with the 
drying process
BLOOD SMEAR LIMITATIONS 
• Once the drop of blood has contact on the slide, the smear 
needs to be made immediately. 
• Otherwise, the blood will clump and dry, again resulting in 
uneven distribution of WBC and platelets (granulocytes will 
accumulate at the edges)
POOR SMEARS 
Poor smears can results from a number of 
reasons, such as: 
• Too large or small blood drop 
• Not pushing the spreader in an even motion 
• Pressing down heavily on the spreader 
• Too great or small an angle of the spreader 
• Speed of stroke used to move the spreader 
• Clots in the blood 
• Dirty (oily) slides
BLOOD SMEAR
BLOOD SMEAR
BLOOD SMEAR 
THE END

Mais conteúdo relacionado

Mais procurados

Mais procurados (20)

Hemoglobin estimation
Hemoglobin estimationHemoglobin estimation
Hemoglobin estimation
 
Thick and thin blood smear Procedure
Thick and thin blood smear ProcedureThick and thin blood smear Procedure
Thick and thin blood smear Procedure
 
Blood cell count
Blood cell countBlood cell count
Blood cell count
 
Blood sample collection procedure ppt
Blood sample collection procedure pptBlood sample collection procedure ppt
Blood sample collection procedure ppt
 
Bone Marrow Examination, BMA
Bone Marrow Examination, BMABone Marrow Examination, BMA
Bone Marrow Examination, BMA
 
Rbc count
Rbc countRbc count
Rbc count
 
Blood collection and anticoagulants
Blood collection and anticoagulantsBlood collection and anticoagulants
Blood collection and anticoagulants
 
Bone marrow biopsy
Bone marrow biopsyBone marrow biopsy
Bone marrow biopsy
 
Blood collection and its types
Blood collection and its typesBlood collection and its types
Blood collection and its types
 
Blood smear staining
Blood smear stainingBlood smear staining
Blood smear staining
 
stains
stainsstains
stains
 
Erythrocyte Sedimentation Rate (ESR)
Erythrocyte Sedimentation Rate (ESR)Erythrocyte Sedimentation Rate (ESR)
Erythrocyte Sedimentation Rate (ESR)
 
Crossmatching
CrossmatchingCrossmatching
Crossmatching
 
Blood grouping
Blood groupingBlood grouping
Blood grouping
 
Pleural fluid
Pleural fluidPleural fluid
Pleural fluid
 
Total leukocyte count - TLC
Total leukocyte count - TLCTotal leukocyte count - TLC
Total leukocyte count - TLC
 
Bm examination
Bm examinationBm examination
Bm examination
 
Sputum examination
Sputum examinationSputum examination
Sputum examination
 
Pcv
PcvPcv
Pcv
 
Differential Leukocyte Counts
Differential Leukocyte Counts Differential Leukocyte Counts
Differential Leukocyte Counts
 

Destaque (10)

Preparation of blood films for malaria parasites
Preparation of blood films for malaria parasitesPreparation of blood films for malaria parasites
Preparation of blood films for malaria parasites
 
clinical chemistry
clinical chemistry clinical chemistry
clinical chemistry
 
Blood film for malaria
Blood film for malariaBlood film for malaria
Blood film for malaria
 
05 peripheral blood smear examination
05 peripheral blood smear examination 05 peripheral blood smear examination
05 peripheral blood smear examination
 
CBC Interpretition
CBC InterpretitionCBC Interpretition
CBC Interpretition
 
Special Investigation
Special InvestigationSpecial Investigation
Special Investigation
 
Interpretation of cbc
Interpretation of cbcInterpretation of cbc
Interpretation of cbc
 
Complete Blood Count, Interpretations
Complete Blood Count, InterpretationsComplete Blood Count, Interpretations
Complete Blood Count, Interpretations
 
anemia classification
 anemia classification anemia classification
anemia classification
 
laboratory investigations
 laboratory  investigations laboratory  investigations
laboratory investigations
 

Semelhante a Blood smear

bloodsmear-141130214419-conversion-gate02.pdf
bloodsmear-141130214419-conversion-gate02.pdfbloodsmear-141130214419-conversion-gate02.pdf
bloodsmear-141130214419-conversion-gate02.pdf
jnrkwesi
 
4_2018_02_21!02_23_11_PM.ppt
4_2018_02_21!02_23_11_PM.ppt4_2018_02_21!02_23_11_PM.ppt
4_2018_02_21!02_23_11_PM.ppt
ssuser75fd45
 
1._BLOOD_Donation_and_Testing_Blood_Transfusion.pptx_5.pptx
1._BLOOD_Donation_and_Testing_Blood_Transfusion.pptx_5.pptx1._BLOOD_Donation_and_Testing_Blood_Transfusion.pptx_5.pptx
1._BLOOD_Donation_and_Testing_Blood_Transfusion.pptx_5.pptx
JoshuaKweka
 

Semelhante a Blood smear (20)

bloodsmear-141130214419-conversion-gate02.pdf
bloodsmear-141130214419-conversion-gate02.pdfbloodsmear-141130214419-conversion-gate02.pdf
bloodsmear-141130214419-conversion-gate02.pdf
 
Peripheral smear
Peripheral smear Peripheral smear
Peripheral smear
 
Biomedical Instrumentation
Biomedical InstrumentationBiomedical Instrumentation
Biomedical Instrumentation
 
Laboratory_Investigation_(guru n navya).pptx
Laboratory_Investigation_(guru n navya).pptxLaboratory_Investigation_(guru n navya).pptx
Laboratory_Investigation_(guru n navya).pptx
 
1a hematology slides
1a hematology slides1a hematology slides
1a hematology slides
 
Hematological. exam
Hematological. examHematological. exam
Hematological. exam
 
Peripheral smear staining and morphology
Peripheral smear  staining and morphologyPeripheral smear  staining and morphology
Peripheral smear staining and morphology
 
Laboratory Investigation in microbiology FINAL 123.pptx
Laboratory Investigation in microbiology FINAL 123.pptxLaboratory Investigation in microbiology FINAL 123.pptx
Laboratory Investigation in microbiology FINAL 123.pptx
 
Determination of Haematocrit in diagnostic hematology
Determination of Haematocrit in diagnostic hematologyDetermination of Haematocrit in diagnostic hematology
Determination of Haematocrit in diagnostic hematology
 
Counting of rbc and wbc
Counting of rbc and wbcCounting of rbc and wbc
Counting of rbc and wbc
 
Peripheral blood smear examination
Peripheral blood smear examinationPeripheral blood smear examination
Peripheral blood smear examination
 
4_2018_02_21!02_23_11_PM.ppt
4_2018_02_21!02_23_11_PM.ppt4_2018_02_21!02_23_11_PM.ppt
4_2018_02_21!02_23_11_PM.ppt
 
Blood count
Blood countBlood count
Blood count
 
PCV.pptx
PCV.pptxPCV.pptx
PCV.pptx
 
blood practical CBC
blood practical CBCblood practical CBC
blood practical CBC
 
Thrombocytopenia
ThrombocytopeniaThrombocytopenia
Thrombocytopenia
 
synopsis
synopsissynopsis
synopsis
 
Laboratory Investigation particular for Dentistry.pptx
Laboratory Investigation particular for Dentistry.pptxLaboratory Investigation particular for Dentistry.pptx
Laboratory Investigation particular for Dentistry.pptx
 
1._BLOOD_Donation_and_Testing_Blood_Transfusion.pptx_5.pptx
1._BLOOD_Donation_and_Testing_Blood_Transfusion.pptx_5.pptx1._BLOOD_Donation_and_Testing_Blood_Transfusion.pptx_5.pptx
1._BLOOD_Donation_and_Testing_Blood_Transfusion.pptx_5.pptx
 
Blood investigations in Dental Practice.Dr Ayesha
Blood investigations in Dental Practice.Dr AyeshaBlood investigations in Dental Practice.Dr Ayesha
Blood investigations in Dental Practice.Dr Ayesha
 

Mais de Shabab Ali

Mais de Shabab Ali (20)

Preanalytical variables in coagulation testing
Preanalytical variables in coagulation testingPreanalytical variables in coagulation testing
Preanalytical variables in coagulation testing
 
Overview of platelet physiology
Overview of platelet physiologyOverview of platelet physiology
Overview of platelet physiology
 
Lecture 9, fall 2014
Lecture 9, fall 2014Lecture 9, fall 2014
Lecture 9, fall 2014
 
Lecture 8, fall 2014
Lecture 8, fall 2014Lecture 8, fall 2014
Lecture 8, fall 2014
 
Lecture 7, fall 2014
Lecture 7, fall 2014Lecture 7, fall 2014
Lecture 7, fall 2014
 
Lecture 6, coagulation fall 2014
Lecture 6, coagulation fall 2014Lecture 6, coagulation fall 2014
Lecture 6, coagulation fall 2014
 
Lecture 5, part 2 fall 2014
Lecture 5, part 2 fall 2014Lecture 5, part 2 fall 2014
Lecture 5, part 2 fall 2014
 
Lecture 5, fall 2014 pdf
Lecture 5, fall 2014 pdfLecture 5, fall 2014 pdf
Lecture 5, fall 2014 pdf
 
Lecture 4, fall 2014 pdf
Lecture 4, fall 2014 pdfLecture 4, fall 2014 pdf
Lecture 4, fall 2014 pdf
 
Lecture 3, spring 2014
Lecture 3, spring 2014Lecture 3, spring 2014
Lecture 3, spring 2014
 
Lecture 2, fall 2014 pdf
Lecture 2, fall 2014 pdfLecture 2, fall 2014 pdf
Lecture 2, fall 2014 pdf
 
Lecture 1, fall 2014
Lecture 1, fall 2014Lecture 1, fall 2014
Lecture 1, fall 2014
 
Lab parasites sections 1 xbc-!xcs
Lab parasites   sections 1 xbc-!xcsLab parasites   sections 1 xbc-!xcs
Lab parasites sections 1 xbc-!xcs
 
Colonial morphology
Colonial morphologyColonial morphology
Colonial morphology
 
Bio265 lab 6 1 xbc and 1xcs _dr di bonaventura
Bio265 lab 6  1 xbc and 1xcs _dr di bonaventuraBio265 lab 6  1 xbc and 1xcs _dr di bonaventura
Bio265 lab 6 1 xbc and 1xcs _dr di bonaventura
 
13 bio265 disease of gastrointestinal, urogenital systems instructor dr di bo...
13 bio265 disease of gastrointestinal, urogenital systems instructor dr di bo...13 bio265 disease of gastrointestinal, urogenital systems instructor dr di bo...
13 bio265 disease of gastrointestinal, urogenital systems instructor dr di bo...
 
12 bio265 disease of circulatory system instructor dr di bonaventura
12 bio265 disease of circulatory system instructor dr di bonaventura12 bio265 disease of circulatory system instructor dr di bonaventura
12 bio265 disease of circulatory system instructor dr di bonaventura
 
11 bio265 disease of respiratory system instructor dr di bonaventura
11 bio265 disease of respiratory system instructor dr di bonaventura11 bio265 disease of respiratory system instructor dr di bonaventura
11 bio265 disease of respiratory system instructor dr di bonaventura
 
10 bio265 disease of skin and cns instructor dr di bonaventura
10 bio265 disease of skin and cns instructor dr di bonaventura10 bio265 disease of skin and cns instructor dr di bonaventura
10 bio265 disease of skin and cns instructor dr di bonaventura
 
9 bio265 viruses, fungi, protozoa, helminths instructor dr di bonaventura
9 bio265 viruses, fungi, protozoa, helminths instructor dr di bonaventura9 bio265 viruses, fungi, protozoa, helminths instructor dr di bonaventura
9 bio265 viruses, fungi, protozoa, helminths instructor dr di bonaventura
 

Último

POGONATUM : morphology, anatomy, reproduction etc.
POGONATUM : morphology, anatomy, reproduction etc.POGONATUM : morphology, anatomy, reproduction etc.
POGONATUM : morphology, anatomy, reproduction etc.
Silpa
 
Porella : features, morphology, anatomy, reproduction etc.
Porella : features, morphology, anatomy, reproduction etc.Porella : features, morphology, anatomy, reproduction etc.
Porella : features, morphology, anatomy, reproduction etc.
Silpa
 
Module for Grade 9 for Asynchronous/Distance learning
Module for Grade 9 for Asynchronous/Distance learningModule for Grade 9 for Asynchronous/Distance learning
Module for Grade 9 for Asynchronous/Distance learning
levieagacer
 
Conjugation, transduction and transformation
Conjugation, transduction and transformationConjugation, transduction and transformation
Conjugation, transduction and transformation
Areesha Ahmad
 
development of diagnostic enzyme assay to detect leuser virus
development of diagnostic enzyme assay to detect leuser virusdevelopment of diagnostic enzyme assay to detect leuser virus
development of diagnostic enzyme assay to detect leuser virus
NazaninKarimi6
 
Biogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune Waterworlds
Biogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune WaterworldsBiogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune Waterworlds
Biogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune Waterworlds
Sérgio Sacani
 
Human genetics..........................pptx
Human genetics..........................pptxHuman genetics..........................pptx
Human genetics..........................pptx
Silpa
 
(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...
(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...
(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...
Scintica Instrumentation
 

Último (20)

POGONATUM : morphology, anatomy, reproduction etc.
POGONATUM : morphology, anatomy, reproduction etc.POGONATUM : morphology, anatomy, reproduction etc.
POGONATUM : morphology, anatomy, reproduction etc.
 
Factory Acceptance Test( FAT).pptx .
Factory Acceptance Test( FAT).pptx       .Factory Acceptance Test( FAT).pptx       .
Factory Acceptance Test( FAT).pptx .
 
Bhiwandi Bhiwandi ❤CALL GIRL 7870993772 ❤CALL GIRLS ESCORT SERVICE In Bhiwan...
Bhiwandi Bhiwandi ❤CALL GIRL 7870993772 ❤CALL GIRLS  ESCORT SERVICE In Bhiwan...Bhiwandi Bhiwandi ❤CALL GIRL 7870993772 ❤CALL GIRLS  ESCORT SERVICE In Bhiwan...
Bhiwandi Bhiwandi ❤CALL GIRL 7870993772 ❤CALL GIRLS ESCORT SERVICE In Bhiwan...
 
Porella : features, morphology, anatomy, reproduction etc.
Porella : features, morphology, anatomy, reproduction etc.Porella : features, morphology, anatomy, reproduction etc.
Porella : features, morphology, anatomy, reproduction etc.
 
Module for Grade 9 for Asynchronous/Distance learning
Module for Grade 9 for Asynchronous/Distance learningModule for Grade 9 for Asynchronous/Distance learning
Module for Grade 9 for Asynchronous/Distance learning
 
PATNA CALL GIRLS 8617370543 LOW PRICE ESCORT SERVICE
PATNA CALL GIRLS 8617370543 LOW PRICE ESCORT SERVICEPATNA CALL GIRLS 8617370543 LOW PRICE ESCORT SERVICE
PATNA CALL GIRLS 8617370543 LOW PRICE ESCORT SERVICE
 
An introduction on sequence tagged site mapping
An introduction on sequence tagged site mappingAn introduction on sequence tagged site mapping
An introduction on sequence tagged site mapping
 
Conjugation, transduction and transformation
Conjugation, transduction and transformationConjugation, transduction and transformation
Conjugation, transduction and transformation
 
Human & Veterinary Respiratory Physilogy_DR.E.Muralinath_Associate Professor....
Human & Veterinary Respiratory Physilogy_DR.E.Muralinath_Associate Professor....Human & Veterinary Respiratory Physilogy_DR.E.Muralinath_Associate Professor....
Human & Veterinary Respiratory Physilogy_DR.E.Muralinath_Associate Professor....
 
development of diagnostic enzyme assay to detect leuser virus
development of diagnostic enzyme assay to detect leuser virusdevelopment of diagnostic enzyme assay to detect leuser virus
development of diagnostic enzyme assay to detect leuser virus
 
GBSN - Microbiology (Unit 2)
GBSN - Microbiology (Unit 2)GBSN - Microbiology (Unit 2)
GBSN - Microbiology (Unit 2)
 
FAIRSpectra - Enabling the FAIRification of Analytical Science
FAIRSpectra - Enabling the FAIRification of Analytical ScienceFAIRSpectra - Enabling the FAIRification of Analytical Science
FAIRSpectra - Enabling the FAIRification of Analytical Science
 
pumpkin fruit fly, water melon fruit fly, cucumber fruit fly
pumpkin fruit fly, water melon fruit fly, cucumber fruit flypumpkin fruit fly, water melon fruit fly, cucumber fruit fly
pumpkin fruit fly, water melon fruit fly, cucumber fruit fly
 
PSYCHOSOCIAL NEEDS. in nursing II sem pptx
PSYCHOSOCIAL NEEDS. in nursing II sem pptxPSYCHOSOCIAL NEEDS. in nursing II sem pptx
PSYCHOSOCIAL NEEDS. in nursing II sem pptx
 
Biogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune Waterworlds
Biogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune WaterworldsBiogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune Waterworlds
Biogenic Sulfur Gases as Biosignatures on Temperate Sub-Neptune Waterworlds
 
Human genetics..........................pptx
Human genetics..........................pptxHuman genetics..........................pptx
Human genetics..........................pptx
 
Zoology 5th semester notes( Sumit_yadav).pdf
Zoology 5th semester notes( Sumit_yadav).pdfZoology 5th semester notes( Sumit_yadav).pdf
Zoology 5th semester notes( Sumit_yadav).pdf
 
(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...
(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...
(May 9, 2024) Enhanced Ultrafast Vector Flow Imaging (VFI) Using Multi-Angle ...
 
300003-World Science Day For Peace And Development.pptx
300003-World Science Day For Peace And Development.pptx300003-World Science Day For Peace And Development.pptx
300003-World Science Day For Peace And Development.pptx
 
GBSN - Microbiology (Unit 1)
GBSN - Microbiology (Unit 1)GBSN - Microbiology (Unit 1)
GBSN - Microbiology (Unit 1)
 

Blood smear

  • 1. BLOOD SMEARS RAJESH MOHESS, CLT
  • 2. BLOOD SMEARS • Peripheral blood smear is a very important tool in the hematology lab • It provides rapid, reliable access to information about a variety of hematologic disorders • Examination of the peripheral blood smear is an inexpensive but powerful diagnostic tool in both children and adults • The smear offers a window into the functional status of the bone marrow • Review of the smear is an important adjunct to other clinical data; in some cases, the peripheral smear alone is sufficient to establish a diagnosis
  • 3. BLOOD SMEARS • An examination of the blood smear (or film) may be requested by physicians based on medical history or initiated by laboratory staff as part of their protocol • Majority of cases for blood smears are from laboratory protocol • With the development of sophisticated automated blood-cell analyzers, the proportion of blood-count samples that require a blood smear has steadily diminished and in many clinical settings is now 10 to 15 percent or less. • Nevertheless, the blood smear remains a crucial diagnostic aid
  • 4. BLOOD SMEARS • For a true morphological interpretation, a trained person is required to review the smear, as automation in hematology will normally generalize the morphology • The indications for smear review differ according to the age and sex of the patient, whether the request is an initial or a subsequent one, and whether there has been a clinically significant change from a previous validated result (referred to as a failed delta check). • All laboratories should have a protocol for the examination of a laboratory-initiated blood smear
  • 5. BLOOD SMEARS • Not all hematological disorder requires a peripheral blood smears for diagnosis. • Some conditions can be diagnosed by other laboratory data also. • For example, Iron deficiency anemia can be diagnosed by MCV, iron and ferritin levels
  • 6. BLOOD SMEARS • There are numerous valid reasons for a clinician to request a blood smear and these differ somewhat from the reasons why laboratory workers initiate a blood-smear examination. • Sometimes it is possible for a definitive diagnosis to be made from a blood smear. • More often, the smear is an important tool in the provision of a differential diagnosis and the indication of further necessary tests. • The blood smear can have an important part in the speedy diagnosis of certain specific infections. • Otherwise, its major roles are in the differential diagnosis of anemia and thrombocytopenia and in the identification and characterization of leukemia and lymphoma.
  • 7. BLOOD SMEARS Anemia: • In patients with anemia, physician-initiated examinations of blood smears are usually performed in response to clinical features or to a previously abnormal complete blood count • Laboratory-initiated examinations of blood smears for patients with anemia are usually the result of a laboratory policy according to which a blood smear is ordered whenever the hemoglobin concentration is unexpectedly low
  • 8. BLOOD SMEARS Hemolytic Anemia: • In the hemolytic anemias, red-cell shape is of considerable diagnostic importance. • Some types of hemolytic anemia yield such a distinctive blood smear that the smear is often sufficient for diagnosis. • This is true of hereditary elliptocytosis, and ovalocytosis. • The presence of bite cells points to a Heinz body hemolytic anemia
  • 9. BLOOD SMEARS Macrocytic Anemia: • Patients with vitamin B12 or folic acid deficiency, the blood smear shows macrocytes. • It may also show oval macrocytes and hypersegmented neutrophils. • When the anemia is more severe, there may be marked poikilocytosis, with teardrop and red-cell fragments
  • 10. BLOOD SMEARS Microcytic Anemia: • Blood smear not very significant in diagnosis, although very useful. • Most common cause is iron deficiency anemia which can be diagnosed by other blood tests Sickle cells/Thalassemia: • A blood smear is useful. Usually shows target cells sickle cells
  • 11. BLOOD SMEARS Thrombocytopenia/Thrombocytosis: • A blood smear should always be examined for patients with thrombocytopenia. • This is done to both confirm the thrombocytopenia and to look for the underlying cause. • Falsely low platelet counts may be the result of small clots, platelet clumping, platelet satellitism or abnormally large platelets
  • 12. BLOOD SMEARS White Cell Disorders (Leukemia/Lymphoma/Bone Marrow Failure): • The precise disease classification may rely upon evaluation of abnormal circulating cells. • Blood smears must always be examined when there is unexplained leukocytosis, lymphocytosis, or monocytosis or when the flagging system of an automated instrument suggests the presence of blast cells • For example, the presence of Auer rods in a blast form in patients with acute myeloid leukemia
  • 13. BLOOD SMEARS The role of the blood smear in the diagnosis of leukemia and lymphoma is to suggest: • A likely diagnosis or range of diagnoses • To indicate which additional tests should be performed • To provide a morphologic context without which immunophenotyping and other sophisticated investigations cannot be interpreted
  • 14. BLOOD SMEARS Summary • The blood smear remains an important diagnostic tool, even in this age of molecular analysis • Physicians may and should request a blood smear when there are clinical indications for it. • The Laboratory technologist should make and examine a blood smear whenever the results of the CBC indicate that a blood smear is necessary for the validation or to further investigate an abnormality • To avoid errors and miss any diagnoses, hematological disorders should be investigated by both clinical data and the peripheral smear
  • 15. PREPARATION OF A BLOOD SMEAR Principle: • A peripheral smear may be requested by the clinician. • It may also be performed as part of the laboratory protocol from reflex or if there are discrepancies from prior results. • We will discuss the ‘Wedge Smear’ • Smears are prepared by placing a drop of blood on a clean glass slide and spreading the drop using another glass slide at an angle. • The slide is then stained and observed microscopically, mainly to determine differential count and morphology study
  • 16. PREPARATION OF A BLOOD SMEAR Principle: • A well-stained peripheral smear will show the red cell background as red orange. • White cells will appear with blue purple nuclei with red purple granules throughout the cytoplasm. • A well made, well distributed peripheral smear will have a counting area at the thin portion of the wedge smear which is approximately 200 red cells not touching. • A good counting area is an essential ingredient in a peripheral smear for evaluating the numbers of and types of white cells present and evaluating red cell and platelet morphology.
  • 17. PREPARATION OF A BLOOD SMEAR Principle: • Functions of the peripheral blood smear are: - provide information for diagnosis - provide information for further testing or to establish diagnosis - used as a guide for therapy - Used as an indicator to monitor the harmful effects for chemotherapy and radiation therapy
  • 18. PREPARATION OF A BLOOD SMEAR Materials: - Glass slides - Applicator sticks - Capillary tubes - EDTA specimen (smear should be made within 4 hours of blood collection) - Capillary blood specimen collected in heparinized tubes
  • 19. BLOOD SMEAR PROCEDURE • Mix blood properly • Place a small drop of blood (about 2-3 mm) about 1 cm from the frosted end of a clean slide (slide must be completely clean) • Using a spreader (another slide), draw backwards into the drop of blood (while applying pressure) – maintain an angle of 30-45 degrees
  • 20. BLOOD SMEAR PROCEDURE • When the spreader touches the blood, allow the blood to spread across the edge of the spreader • Move the spreader forward on the slide (in one smooth motion), so a smear is made approximately 3 to 4 cm in length. • The smear should be half the size of the slide, with no ridges, and a “feather edge” should be toward the end of the smear.
  • 22. BLOOD SMEAR PROCEDURE • Label the frosted end of the slide with the patient’s last name and first initial, specimen number, and the date • Allow the smear to air dry completely (about 5 minutes) • Specimen can now be stained
  • 24. BLOOD SMEAR Good smear A good smear should have the following appearance: • Appear smooth and uninterrupted • Start thick and gradually thinning out (feather-edge) • The film should take up ½ to ¾ the length of the slide
  • 25. BLOOD SMEAR LIMITATIONS • The angle between the slides is dependent upon the size of the blood drop and viscosity of the blood. The optimal angle is 45 degrees • The larger the drop of blood and lower the hematocrit, the higher the angle needs to be so the blood smear is not too long • Blood with a higher hematocrit needs to have a lower angle so the smear is not too short and thick • Glass slides must be clean; otherwise, this results in imperfect distribution of cells and improper staining • Smears should not be made from blood remaining on the tube stopper as the lubricant on the stoppers can interfere with the drying process
  • 26. BLOOD SMEAR LIMITATIONS • Once the drop of blood has contact on the slide, the smear needs to be made immediately. • Otherwise, the blood will clump and dry, again resulting in uneven distribution of WBC and platelets (granulocytes will accumulate at the edges)
  • 27. POOR SMEARS Poor smears can results from a number of reasons, such as: • Too large or small blood drop • Not pushing the spreader in an even motion • Pressing down heavily on the spreader • Too great or small an angle of the spreader • Speed of stroke used to move the spreader • Clots in the blood • Dirty (oily) slides