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BD Veritor System Reader Quality Control Procedure
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BD Veritor System Reader Quality Control Procedure

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Questions and Answers

What is the minimum duration for plunging the swab up and down in the fluid?

  • 5 seconds
  • 20 seconds
  • 15 seconds (correct)
  • 10 seconds
  • When should external positive and negative swab controls be run?

  • Never required for quality control
  • Only when a new shipment is received
  • For each new lot, each newly trained operator, and each new shipment (correct)
  • Only when a new lot is opened
  • How are internal controls evaluated by the BD Veritor System Reader?

  • After inserting each test device (correct)
  • Before inserting each test device
  • Only after receiving a new shipment
  • Not evaluated by the system reader
  • What action should be taken if the internal/procedural controls fail?

    <p>Generate an invalid test result</p> Signup and view all the answers

    How should the absence of a new lot or shipment be documented?

    <p>'No new lot, no new shipment' on the log</p> Signup and view all the answers

    What must be noted whenever external positive and negative swab control is run?

    <p>The internal control evaluation</p> Signup and view all the answers

    What is the purpose of applying a pink sticker and marking the box with date opened/QC completed in the quality control procedure for nasal swabs?

    <p>To differentiate between boxes of the same lot</p> Signup and view all the answers

    When should internal control be noted in the quality control procedure for nasal swabs?

    <p>Whenever external positive and negative swab control is run</p> Signup and view all the answers

    What action should be taken if there is a failure of the internal/procedural controls during quality control of nasal swabs?

    <p>Document the failure and proceed with the testing</p> Signup and view all the answers

    How should quality control documentation be handled if no new lot is opened in a given month?

    <p>Record 'No new lot' and the box lot number and expiration date</p> Signup and view all the answers

    In the CardioChek Plus Quality Control Guidance, what must be reviewed before performing tests on patients?

    <p>Optics Check and package insert</p> Signup and view all the answers

    What is the purpose of running Quality Control for CardioChek Plus per manufacturer’s recommendations?

    <p>To ensure accurate test results and quality of care</p> Signup and view all the answers

    What is the consequence if the control line does not appear or the background is not clear during quality control testing?

    <p>The test is invalid and needs to be rerun.</p> Signup and view all the answers

    What should be done before performing tests on patients with BD Veritor Influenza?

    <p>Review the package insert and quality control log to ensure proper controls.</p> Signup and view all the answers

    What is the purpose of applying a pink sticker and marking the box with the date opened and QC completed?

    <p>To document completion of quality control procedures.</p> Signup and view all the answers

    What is the role of the red control line in BD Veritor Influenza quality control?

    <p>It serves as an internal positive control.</p> Signup and view all the answers

    If no new lot is received in a given month, what documentation should be done?

    <p>Record box lot number, expiration date, and 'No new lot, no new shipment'.</p> Signup and view all the answers

    Why is it crucial to run quality control for BD Veritor Flu A+B according to the manufacturer’s recommendations?

    <p>To ensure accurate test results and quality of care.</p> Signup and view all the answers

    Study Notes

    Swab Control Procedures

    • Minimum duration for plunging the swab is typically a specified period, often around 10 times up and down, depending on the protocol.
    • External positive and negative swab controls are run whenever a new lot is opened or when a new shipment is received.

    Internal Controls Evaluation

    • Internal controls are evaluated by the BD Veritor System Reader which checks for the correct appearance of control lines.
    • If internal or procedural controls fail, the test results should be considered invalid and must be repeated.

    Documentation for Quality Control

    • Absence of a new lot or shipment must be documented in quality control logs to ensure traceability.
    • Whenever external positive and negative swab control is run, the results must be logged and reviewed.

    Quality Control Procedure

    • Applying a pink sticker and marking the box with the date opened/QC completed serves to indicate when the quality control was performed and ensures accuracy in tracking.
    • Internal control results should be noted in the quality control procedure for nasal swabs to confirm their validity.

    Actions on Control Failures

    • If there is a failure of internal/procedural controls during nasal swab quality control, the tests using that lot should be discarded, and a new test run should be initiated.

    Monthly Quality Control Documentation

    • If no new lot is opened in a given month, a note should be made in quality control documentation for record-keeping.

    CardioChek Plus Quality Control

    • Before performing tests on patients, review all QC results to ensure reliability and accuracy of testing systems.
    • Running quality control for CardioChek Plus as per the manufacturer’s recommendations ensures that the device functions correctly and safely.

    Consequences of Control Line Failure

    • If the control line does not appear or the background is unclear during quality control testing, the test is deemed invalid and must not be used for patient testing.

    Patient Testing Protocol for BD Veritor Influenza

    • Prior to performing tests on patients with BD Veritor Influenza, confirm the validity of the internal controls to ensure accurate results.
    • The red control line in BD Veritor Influenza quality control indicates whether the test has functioned properly.

    Documentation for New Lots

    • If no new lot is received in a month, appropriate documentation should still be made to maintain quality assurance.

    Importance of Quality Control Compliance

    • Running quality control for BD Veritor Flu A+B according to manufacturer’s recommendations is crucial to ensure test accuracy and reliability, safeguarding patient health.

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    Description

    Learn about the quality control procedure for the BD Veritor System Reader, including the steps to follow for nasal swabs and documentation requirements. Understand how internal controls are evaluated to ensure accurate test results.

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