automation and poct

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    PRINCIPLES OF CLINICAL

    CHEMISTRY AUTOMATION

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    AUTOMATION IN CLINICAL

    CHEMISTRY

    The modern clinical chemistrylaboratory uses a high degree ofautomation.

    Many steps in the analytic process thatwere previously performed manuallycan now be performed automatically.

    This Permits the operator to focus ontasks that cannot be readilyautomated and increasing bothefficiency and capacity.

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    AUTOMATION IN CLINICAL

    CHEMISTRY

    The analytic process can be divided intothree major phases preanalytic,analytic, and postanalyticcorresponding

    to sample processing, chemical analysis,and data management, respectively.

    Substantial improvements have occurredin all three areas during the past decade.

    The analytic phase is the mostautomated, and more research anddevelopment efforts are focusing onincreasing automation of the preanalytic

    and postanalytic processes.

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    WHY AUTOMATION?

    Increase the number of tests by oneperson in a given period of time

    Minimize the variations in results from

    one person to anotherMinimize errors found in manual

    analyses equipment variations pipettes

    Use less sample and reagent for eachtest

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    TYPES OF ANALYZERS

    Continuous FlowTubing flow of reagents and patients

    samples

    Centrifugal AnalyzersCentrifuge force to mix sample and

    reagents

    DiscreteSeparate testing cuvets for each test and

    sample

    Random and/or irregular access

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    CONTINUOUS FLOW

    This first AutoAnalyzer (AA) was acontinuous-flow, single-channel,sequential batch analyzer capable of

    providing a single test result onapproximately 40 samples per hour.

    Analyzers with multiple channels (fordifferent tests), working synchronously

    to produce 6 or 12 test resultssimultaneously at the rate of 360 or720 tests per hour.

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    In continuous flow analyzers,samples were aspirated into tubing

    to introduce samples into a sample

    holder,bring in reagent,

    create a chemical reaction,

    and then pump the chromagensolution into a flow-through cuvettefor spectrophotometric analysis.

    CONTINUOUS FLOW

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    CONTINUOUS FLOW

    The major drawbacks that contributed to theeventual demise of traditional continuous-flowanalyzers in the marketplace were significant

    carry-over problems and wasteful use ofcontinuousl flowin rea ents.

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    CONTINUOUS FLOW

    Continuous flow is also used in somespectrophotometric instruments inwhich the chemical reaction occurs in

    one reaction channel and then isrinsed out and reused for the nextsample, which may be an entirelydifferent chemical reaction.

    CENTRIFUGAL

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    CENTRIFUGAL

    ANALYZERS

    Discrete aliquots of specimens and reagentsare piptted into discrete chambers in a rotor

    The specimens are subsequently analyzed inparallel by spinning the rotor and using theresultant centrifugal force to simultaneouslytransfer and mix aliquots of specimens andreagents into radially located cuvets.

    The rotary motion is then used to move the

    cuvets through the optical path of an opticalsystem

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    DISCRETE ANALYZERS

    Discrete analysis is the separation ofeach sample and accompanyingreagents in a separate container.

    Discrete analyzers have the capabilityof running multiple tests on onesample at a time or multiple samplesone test at a time.

    They are the most popular andversatile analyzers and have almostcompletely replaced continuous-flow

    and centrifugal analyzers.

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    DISCRETE ANALYZERS

    Sample reactions are kept discretethrough the use of separate reactioncuvettes, cells, slides, or wells that are

    disposed of following chemicalanalysis.

    This keeps sample and reactioncarryover to a minimum but increases

    the cost per test due to disposableproducts.

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    HITACHI 902 ANALYZER

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    WITH AUTOMATION THERE IS

    STILL SOME VERY BASIC STEPS

    Specimen preparation and IdentificationLabeling still critical

    Programming of instrument

    Laboratory personnel must perform andobserve:

    Quality AssuranceQuality Control

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    TOTAL LABORATORY AUTOMATION

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    SELECTION PROCESS

    What is your labs workload like?Discrete or large batch testing?

    Single instrument or multiples?

    Storage of reagentsNeed refrigeration or freezing?

    expense

    Kept at room temperature untilreconstituted

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    http://www.youtube.com/watch?v=iqSpmwiNTHo

    http://www.youtube.com/watch?v=FyLOTBicYbk

    http://www.youtube.com/watch?v=iqSpmwiNTHohttp://www.youtube.com/watch?v=FyLOTBicYbkhttp://www.youtube.com/watch?v=FyLOTBicYbkhttp://www.youtube.com/watch?v=iqSpmwiNTHo
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    POINT OF CARE

    TESTING

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    DEFINITION

    Point-of-care testing (POCT) has beendefined by the College of AmericanPathologists (CAP) as those analytical

    patient-testing activities providedwithin the institution, but performedoutside the physical facilities of theclinical laboratories.

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    PLACE OF ANALYSIS

    Physicians offices

    Operating rooms

    Emergency rooms

    Intensive Care Units Home health care

    Patient performed

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    PERSONNEL ISSUES

    Most often performed by non-laboratorians

    Physicians

    Nurses or nurses aides

    Respiratory technicians Not specifically trained in the requirements for

    accurate testing and interpretation

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    LABORATORY SUPPORT

    Laboratory still responsible forresults

    Therefore responsible for trainingand management of POCTprograms

    Laboratory must build a structure

    to support and facilitate POCT

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    SUPPORT STAFF

    Director - PhD, MD or laboratoryscientist or pathologist

    POC Coordinator laboratory scientist

    with high level technical &interpersonal skills

    POC Trainers designated person(s)for problem solving etc.

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    COMMON APPLICATIONS

    Glucose Testing

    Chemistries

    Electrolytes

    Blood gases Hematology

    Coagulation ACT

    Hematocrit