Exam 7: Quality Assurance and Quality Control

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MATCHING Match the term with the definition. -Precision

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D

Specificity is defined as the:

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B

Match the term with the appropriate definition. -Mode

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B

If the control value in a determination is out of the acceptable range,lack of attention to timing or incubation temperature may be the factor responsible.

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Sensitivity is defined as the:

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Required regulation of clinical laboratories is achieved by (the):

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If the control value in a determination is out of the acceptable range,the deterioration of reagents or standards may be the factor responsible.

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If the control value in a determination is out of the acceptable range,use of poor technique by the technologist doing the test may be the factor responsible.

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Using the Clinical and Laboratory Standards Institute (CLSI)protocol for a procedural format,insert the missing elements in the following written procedural protocol: Procedure name Name of test method -Specimen collection and storage

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MATCHING Match the term with the definition. -Accuracy

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For testing of moderate complexity,quality control requires:

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An example of a preanalytical error is:

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Using the Clinical and Laboratory Standards Institute (CLSI)protocol for a procedural format,insert the missing elements in the following written procedural protocol: Procedure name Name of test method -Reagents,supplies,and equipment

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Quality assessment programs include:

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If the control value in a determination is out of the acceptable range,faulty instrument or equipment may be the factor responsible.

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Match the term with the appropriate definition. -Mean

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MATCHING Match the term with the definition. -Standard

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A control specimen should be:

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Using the Clinical and Laboratory Standards Institute (CLSI)protocol for a procedural format,insert the missing elements in the following written procedural protocol: Procedure name Name of test method -Expected or normal (reference)values

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MATCHING Match the term with the definition. -Control

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