qa and qc in histopathology 2 by fehmi

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  • 7/30/2019 Qa and Qc in Histopathology 2 by Fehmi

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    1

    QUALITY

    ASSURANCE/QUALITY

    CONTROL IN

    HISTOPATHOLOGY

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    2

    TOTAL QUALITY MANAGEMENT Quality control

    Quality

    assurance

    Quality

    improvement

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    3

    OUR VALUES OUR QUALITY

    SERVICES

    vision

    mission Core values

    Safety policy Quality policy

    AKUH

    FOUNDADTION

    Hospital

    services

    SATISFIEDCUSTOMER

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    4

    Quality improvement

    is the practice of

    Continuously assessing

    And adjusting performance

    Using scientifically

    Accepted procedure.

    Quality control,Is an integral component of

    Quality assurance and is the

    aggregate of process

    And techniques to detect,

    reduce, and correct

    Deficiencies in an analytic

    Process

    Quality AssuranceIn pathology and laboratory

    Medicine is the practice of

    Assessing performance in

    All steps of the laboratory

    Testing cycle including

    Pre- analytic, analytic, and

    Post analytic phases to

    Promote excellent outcomes

    In medical care

    TOTAL QULAITY PLAN OFHISTOPATHOLOGY

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    QUALITY CONTROLQC aims to identify defects in the finished product. Quality control,

    therefore, is a reactive process

    GOAL ----- The goal of QC is to identify defects after a product is

    developed and before its released..

    QUALITY ASSURANCEQA is aims to prevent defects with a focus on the processused to make the product .it is a proactive quality processGoal---- The goal of QA is to improve development and

    test processes so that defects do not arise when the productis being developed.

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    QUALITY CONTROL EMPHASISES ON THREE

    ASPECTS

    .Hitopathology

    Q/C

    1.Elements such as controls, job management,

    defined and well managed

    processes,[performance and integrity criteria, andidentification of records

    2.Competence, such as knowledge, skills,

    experience, and qualifications

    3.Soft elements, such as personnel integrity,

    confidence, organizational culture, motivation,team spirit, and quality relationships.

    http://en.wikipedia.org/wiki/Integrityhttp://en.wikipedia.org/wiki/Confidencehttp://en.wikipedia.org/wiki/Organizational_culturehttp://en.wikipedia.org/wiki/Motivationhttp://en.wikipedia.org/wiki/Team_spirithttp://en.wikipedia.org/wiki/Team_spirithttp://en.wikipedia.org/wiki/Motivationhttp://en.wikipedia.org/wiki/Organizational_culturehttp://en.wikipedia.org/wiki/Confidencehttp://en.wikipedia.org/wiki/Integrity
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    TWO

    PRINCIPLE OF

    QUALITY

    ASSURANCE

    ASPECTS OF QUALITY ASSURANCE

    "Fit for purpose", the service

    should be suitable for the intended

    purpose; and "Right first time",

    mistakes should be eliminated.

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    following are the continuous QA

    parameters are recommended:

    1-Intradepartmental consultation

    review

    2-frozen section review3-Histopathology case review

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    4-incident reporting

    5-histopathology QC

    6 -turn around time

    7-vertical case review/audit-

    8-autopsy QA

    9-cytology QA

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    ALL RECOMMENDED PROGRAMME AREANALYZED FROM THREE ASPECTS INHISTOPATHOLOGY:

    A- Pre analytical aspects (before analysis)pre-steps as equipment/reagent Q.C, control run,request confirmation of test/stain and correctidentification.

    B- Analytical aspects (during analysis)

    procedural Q.C how we are performing test.C- Post analytical aspects (after analysis )such as reporting right patient should have right

    report

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    RECIVINGBENCH

    H$E BENCH

    SEMEN DR CYTOGENETICS

    SPECIALPATHOLOGY

    GROSS BENCHCUTTING AND

    EMBEDDING

    CYTOLOGY

    FLOW

    CYTOMETERY

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    Receiving is the first step where we assure allconfirmations regarding any sample received in

    histopathologyWe assure biopsy sample should received in formalin.If not, PS# C/P /M.R# with patient name is entered inquality control log book, dictate as without formalin,and without formalin letter is sent to respective doctors

    to reduce this error.We have to make sure that sample (either biopsy/cytology)must be received with required information(history ,confirm age name ,gender, clinical diagnosisand biopsy/cytology site ).

    Sample is hold and entered in hold log book in case of

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    make sure correct charging correct reporting date

    (LB/SB/MB).

    Ensue receiving of X-ray where it is required (bone

    specimen).

    PBCR must required block as well as previous reports ensure

    it if not available as per protocol rejection may consider.

    Receiving bench ensure sample not received in formalin .

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    After receiving sample has to move toward respective benches.where we consider bench related quality aspects.

    Gross Benchensure proper working of gross station.Ensure gross room cleaning before work.Change formalin if needed.Perform daily Q.C of gross station after checking it.Entered sample information in Q.C log book if received withoutformalin.

    Entered B.T # in B.T quality control file.Always make sure negative pressure of exhaust system forEffective quality and safety as well.Ensure formalin Q.C for effective fixation where required usezinc formalin.

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    One of the very important aspect of histopathology is

    frozen section.

    Ensure time management for frozen (reporting 20 minutes

    /frozen)

    Cryostat Q.C is done before frozen.Entry is done in frozen log book.

    Indicator data is maintained for confirmation of timely

    reporting of frozen and to check delay of frozen to cause-

    effect analysis.

    As frozen received inform to doctor immediately for frozen.One of the most important thing is frozen should not

    received in formalin or saline or any other solvent other

    wise it will be rejected for frozen.

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    Ensure equipment Q.C on all benches check PPM.(check

    equipment temperature/working/reagents/daily maintenance)

    Follow bench protocol for quality assurance .

    Run control to ensure equipment/reagent are in excellentworking condition.

    Keep a record of control.

    If any error is noticed in control search cause of it, eliminate it

    than perform test or stain.

    we assure that which reagent should store on roomtemperature /refrigerator and marked them with temperature

    tag to avoid any quality error.

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    For wrong addressograph and for wrong labeling we entered the

    copy of form and information in tissue committee file.Any issue regarding quality is discussed during QICC meeting andcorrective and preventive action are taken.Qualified staff is trained for work after multiple test judgmentshe/she will be allowed to work independently.There is no compromise in quality assurance in histopathology dueto the most sensitive nature of manual work. Incase of anymajor/minor nonconformities it has to be informed to supervisorand immediate investigation has to be done.

    Delayed report is informed to patient with specific reason and it isentered in comments section of Sample in order to have a record ofit.

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    QICC (QUALITY INDICATOR

    COORDINATION COMMITTEE)

    QUALITYINDICATORS

    APPROVAL OF

    NEW TEST AND

    PROCEDURE

    REVIEW AND

    REPORT

    ANALYSIS

    1. internal q.c as equipment PPMreagents accuracy

    2. Appraising. introduction of standards

    innovative test procedure

    3. Providing feedback .how quality is

    improving if any suggestion any

    issues in QICC meeting it is

    discussed

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    OUR ACHIEVEMENTSTOWARD QUALITY

    ASSURANCE

    ISO CERTIFIED

    JCIA CERTIFIED

    MOVING TOWARDCAP

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    Thank You!!!

    Fahmida umer shaikh