Podcast
Questions and Answers
What is the minimum duration for plunging the swab up and down in the fluid?
What is the minimum duration for plunging the swab up and down in the fluid?
When should external positive and negative swab controls be run?
When should external positive and negative swab controls be run?
How are internal controls evaluated by the BD Veritor System Reader?
How are internal controls evaluated by the BD Veritor System Reader?
What action should be taken if the internal/procedural controls fail?
What action should be taken if the internal/procedural controls fail?
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How should the absence of a new lot or shipment be documented?
How should the absence of a new lot or shipment be documented?
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What must be noted whenever external positive and negative swab control is run?
What must be noted whenever external positive and negative swab control is run?
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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?
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?
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When should internal control be noted in the quality control procedure for nasal swabs?
When should internal control be noted in the quality control procedure for nasal swabs?
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What action should be taken if there is a failure of the internal/procedural controls during quality control of nasal swabs?
What action should be taken if there is a failure of the internal/procedural controls during quality control of nasal swabs?
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How should quality control documentation be handled if no new lot is opened in a given month?
How should quality control documentation be handled if no new lot is opened in a given month?
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In the CardioChek Plus Quality Control Guidance, what must be reviewed before performing tests on patients?
In the CardioChek Plus Quality Control Guidance, what must be reviewed before performing tests on patients?
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What is the purpose of running Quality Control for CardioChek Plus per manufacturer’s recommendations?
What is the purpose of running Quality Control for CardioChek Plus per manufacturer’s recommendations?
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What is the consequence if the control line does not appear or the background is not clear during quality control testing?
What is the consequence if the control line does not appear or the background is not clear during quality control testing?
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What should be done before performing tests on patients with BD Veritor Influenza?
What should be done before performing tests on patients with BD Veritor Influenza?
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What is the purpose of applying a pink sticker and marking the box with the date opened and QC completed?
What is the purpose of applying a pink sticker and marking the box with the date opened and QC completed?
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What is the role of the red control line in BD Veritor Influenza quality control?
What is the role of the red control line in BD Veritor Influenza quality control?
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If no new lot is received in a given month, what documentation should be done?
If no new lot is received in a given month, what documentation should be done?
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Why is it crucial to run quality control for BD Veritor Flu A+B according to the manufacturer’s recommendations?
Why is it crucial to run quality control for BD Veritor Flu A+B according to the manufacturer’s recommendations?
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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.