Setting up Hematology and Biochemistry lab Dr. Avinash Phadke President SRL & Piramal Labs
Setting up Hematology and Biochemistry lab
Dr. Avinash PhadkePresidentSRL & Piramal Labs
A view to Haematology
ErythrocyteLeukocyte
Thrombocytes
Haematology
Haematology - the scientific study of blood, its formation and disease
Hematology
Hematology, also spelled haematology (from the Greek α μαἷ haima "blood" and -λoγία), is the branch of internal medicine, physiology, pathology, clinical laboratory work, and pediatrics that is concerned with the study of blood, the blood-forming organs, and blood diseases.
Hematology includes the study of etiology, diagnosis, treatment, prognosis, and prevention of blood diseases.
The laboratory work that goes into the study of blood is frequently performed by a medical technologist.
Blood diseases affect the production of blood and its components, such as blood cells, hemoglobin, blood proteins, the mechanism of coagulation, etc
Automation in hematology
Cell counting is reliable in automated method than manual method, since large number of cells a re counted rapidly.
Although better precision is obtained by automated cell counting, simultanoeus accuaracy can be obtained by microscopy.
Advantages -automation
Automated cell counters determines 8-40 different parameters of a complete hemogram, which are not possible by manual methods.
Samle recognition by barcode, automatic mixing of ample & diluent.
Automated cell counters are calibrated and controls are available for precision & accuracy.
Different principles …. Various Technologies for Differential Enumeration Impedance measurement Flow-cytometry Fluorescence Flow-cytometry
Types of analysers-1.Semi-autoanalysers
Semi-automatic analysers ( where the sample is diluted manually and only few parameters like Hb, PCV, WBC and or Platelets are given)
3-part analysers
Sample is aspirated directly and diluted by the equipment. Parameters depending on the equipment are given with calculated indices …18-22 parameters.
Differential count graph is plotted approximately. Manual differential is indicated for WBC and morphology of RBC).Abnormal results are flagged . They indicate possibility of blasts, promyelocytes or myelocytes.
Flags or alerts indicate further examination of the specimen
Impedance measurement
The principle takes advantage of the fact that blood cells are less conductive to electrical current than the cell diluting fluid.
Each change in the current is measured as pulse;indicating passage of a particle through the aperture. This allows the cells to be counted and the magnitude of pulse is proportional to the size of each cell.
Impedance Method
Vacuum
Resist ance
(ca. 100 V)
I nt er nal elect r ode Ext er nal elect r ode
Aper t ur e
Blood suspension
Impedance Method
Limit at ions
Ø Only size not suff icient to differentiate f ive types of WBCs
Ø Interference from NRBCs, Lyse Resistance RBCs etc.
Ø Inability to identify abnormal cellsØ Low linearity
CBC
Errors ….which can occur
Due to fibrin clots Sample deterioration Sample leakage(concentrated sample) Hemolysed sample
5-part analysers
.Along with the parameter s of 3 part , WBC differentials are plotted on the graph.
Depending on the technology which is used either a laser or scattered light technology or flow cytometry based method.
Newer parametrs like RDW, MPV are also given by these equipments.
RDW:RDW in conjunction with RBC count and MCV is useful in interpretation of several hematological disorders.
MPV is derived from platelet histogram . There is an inverse elationship between number & size of platelets.Various hematological contions like ITP, aplastic states, B12 and folate deficiencies .
Basic Laser Flow Cytometry
Basic Laser Flow Cytometry
Limit at ions
Ø Ability to differentiate only basic f ive types of WBCs
Ø Limited ability to identify abnormal cells – hence unable to separate abnormal cells from normal cells
Ø Interference from NRBCs & Lyse Resistance RBCs
Latest ....Benefits of 6-part diff analysis
Reduces review rate significantly
User definable setting for diff review is still possible (IG > 2%, 3%, 4% or 5%)
Reduces operators‘ costs (FTEs)
Reduces TAT
Increases precision of the reported WBC differential (thousand of cells counted)
FLOURESCENCE FLOW CYTOMETRY
When the laser light beam strikes a flourescent stained cell, the light of various intensity is scattered with respect to the physical characteristics of the cell.
i.e the following characteristics are determined:
Ø Cell size, Cell volume from forward scatterØ Internal structure, e.g. granulation or
vacuoles from side scatterØ Content of nucleic acids, i.e. RNA and DNA
from side flourescence
Fluorescence Flow Cytometry
Laser Fluorescence Flow Cytometry
Benefits
Ø 5 Part Differentiation of WBCs using patented Polymethine dyeØ Unmatched linearity of WBC from 0 - 4,40,000 cells / µL
ü Clear cut demarcation between normal and abnormal cells
ü Covers almost all the clinical conditionsü Dilution of samples is not requiredü Interference from lyse resistance RBC’s eliminatedü NRBC’s & PLT clumps are flagged and quantified
Differential Channel Fluorescent Stain Effect Laser (By Fluorescence Flow Cytometry )
Ø A surfactant lyses and dissolves RBCs and PLTs and perforates WBCs.
Ø Afterwards, Fluorescence stainer, polymethine dye enters perforated WBCs and stains their nucleic acids (RNA/DNA).
Ø Reactive cells (ATL, IG ) absorb more stain and emit more flourescence
Differential Scattergram(Laser Fluorescence Flow Cytometry )
Differential Scattergram (By Fluorescence Flow Cytometry )
SUMMARY
Flourescence Flow Cytometry ascertain
Ø Accurate 5 part Differentials Ø Precise demarcation between normal &
abnormal cellsØ Eliminates interferences from lyse resistance RBC’s,
NRBC’s, microcytic RBC’s & PLT clumpsØ Identification of Morphological abnormalities such
as IG, ATL & Blasts
Clinical Utility of IG Count
• Presence of IG in blood indicates a response to infection, inflammation or some other stimulus to the bone marrow.• XE IG master provides accurate and valuable information for immediate action.
58 ICU Patients
58 ICU Patients
Through the use of the Sysmex XE-2100 analyser the IT Ratio could be used as
a FAST INEXPENSIVE RELIABLE indicator of sepsis
Reticulocyte Count• Ret # , Ret %
RET-He (Hemoglobinization of Reticulocytes)• Reflects the actual iron supply for hemoglobin synthesis in the bone marrow. • Early detection of iron depletion in erythropoiesis.• Distinguish Fe def (ID) and functional Fe Def (FID). • In FID the iron stores are replete, but the iron is not sufficiently available for Hb
systhesis
RET-Quantity
RET-Quality
Clinical Significance of RET-He
Clinical Untility of RET-He
Diagnostic• Help to distinguish classical iron deficiency and functional iron deficiency
in anemia of chronic disease• Detect early state of iron deficiency when biochemical markers are
influenced (acute-phase response, pregnancy)
Therapeutic• Monitoring of erythropoietin and / or iron therapy
Reference range : 28 - 35 pg
Coagulation …
Equipments available are manual , semiautomatic and fully automatic equipments.
Parameters like PT, PTT, APTT , Fibrinogen ,FDP are routinely done in a medium size laboratory.
Blood coagulation factors like Factor V, VIII, Thrombin etc are availbale on fully automated equipments with good quality control data and calibrations.
AUTOMATION IN BIOCHEMISTRY
Why automation is required?
Since last few decades, in clinical biochemistry there has been increase in clinical demand for laboratory investigations.
When the volume of work is increased, there arose a need for work simplification.
Automation helps us to give correct results in short TAT
AUTOMATION IN BIOCHEMISTRY
What is automation?
Automation is a self – regulating process , where the specimen is accurately pipetted by a mechanical probe and mixed with the particular volume of the reagent and the results are displayed in digital forms and also printed by the printer.
DEVELOPMENT OF AUTOMATION IN BIOCHEMISTRY Initially Mono-step methods were introduced to replace
multistep cumbersome and inaccurate methods. The efficiency of mono-step methods was further
increased by the introduction of automatic dispensers and diluters.
In large labs for the common tests the above mentioned approach is still inadequate. Thus, instruments were developed which can handle the whole analytical process in a mechanized manner.
HISTORICAL ASPECTS OF AUTOMATIONFirst automated system was introduced in 1957 by
L. T. Skeggs.
1.Initially Continuous flow analyzers– Two types Single channel continuous flow analyzers Multi channel continuous flow analyzers e.g. SMA
2.Discrete Auto-analyzers- These analyzers co-ordinate multiple operations into a smoothly functioning system. Semi automated Fully automated
TYPES OF ANALYZERS
Semi automated analyzers-
These analyzers are called semi automated, because the initial stages of a specimen analysis are performed by Laboratory technician. These analyzers are suitable for medium complexity level laboratories.
SEMI AUTOMATED ANALYZERS
SEMI AUTOMATED ANALYZERS
SEMI AUTOMATED ANALYZERS
SEMI AUTOMATED ANALYZERS
TYPES OF ANALYZERSFully automated discrete analyzers-
These auto analyzers perform all the functions of semi automated analyzers and in addition to that , they also perform many functions like automatic dispensing of reagents & samples, mixing & incubation of reaction mixtures.
Batch Analysers & Random access Analysers
Batch analyzers perform only one type of test at a time.
Advantages…large no of sample batches can be tested accurately & precisely with appropriate quality control
Disadvantages…Not patient oriented , not equippped for stat samples, not equipped with facilities like “random access analysers”
RAA(random access analyser)
RAA perform all the functions of batch analyser & additionaly they are equipped with random access mode .
Additional facilities like : cuvette disk with temperature control , on board refrigerator , level sensors for samples and reagents,sample rack system, bar code identification, continous loading of samples, faciltiy for autodilution, automatic plotting of daily & monthly QC charts.
Dry chemistry…
Analysers do not use wet chemicals, the chemicals are incorporated in to a series of thin films on a single use slide.
Patients samples permeated through the various layers on the slide and the end results are determined colorimetrically
Sample carry over is avoided because test recation takes place entirely within the slide.
Flex technology & disposable cuvette technology…
Analysers are discrete, random access clinical chemistry analysers, use test reagents as flex, have integrated multisensor technology to provide accurate and precise test results.
For each tests, a cuvette is manufactured on board and sealed and discarded seperately for each parameter
Biochip array tests…
Biochip array consists of a single biochip which has many reagents coated.
Multiple tests can be done from a single chip. Convinient for panels of tests on a single sample
Automated floor models
Continous sample loading facility Ion –selective electrode options On board laundry for cuvettes Facility for urgent samples Measures icteric, hemolytic or lipaemic index
ADVANTAGES OF AUTOMATION Large number of samples can be tested in a short time. Variety of tests can be performed by using various
methods such as end point and rate of reactions. Most of the methods performed on automation are
accurate , precise, sensitive and specific. Although the various types of auto-analyzers are
expensive, in the long run , they prove to be cost effective because he amount of reagent and specimens required can be as low as 300 and 5 micro-liters respectively.
ADVANTAGES OF AUTOMATION Automation allows laboratories to process much larger
workload without a comparable increase in number of staff members.
Internal and external quality control programs can be implemented efficiently and effectively by using auto-analyzers.
In the case of fully-automated analyzers, the laboratory staff members do not come in contact with specimens and reagents and hence working on these analyzers is very safe.
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