Lesson 6 Flashcards

1
Q

It refers to the overall process of guaranteeing
quality patient care and it is the continual monitoring of the entire process test
ordering and specimen collection through
reporting and interpreting results.

A

QUALITY ASSURANCE

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2
Q

What are the process that was included in Quality Assurance?

A

Procedure manuals
Pre-analytical factors
Analytical factors
Post-analytical factors

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3
Q

It contains all the procedures performed in
the urinalysis section

A

PROCEDURE MANUAL

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4
Q

What are the included procedures done in Procedure Manual?

A

 Principle or purpose of the test
 Patient preparation
 Specimen type and method of collection
 Reagents,standards and control
 Instrumentation calibration and maintenance
protocols and schedules
 Procedure
 Normal values
 Limitations of the test
 Reference

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5
Q

What are the Pre- Analytical Factors?

A

Test request
Patient preparation
Specimen collection and handling

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6
Q

It is the complete data of the patient

A

Test request

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7
Q

It is to give proper instructions to the
patients or relative of the patient

A

Patient preparation

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8
Q

It is where mostly mistakes happen

A

Specimen collection and handling

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9
Q

It is the processes that directly affect the testing of
the specimen

A

ANALYTICAL FACTORS

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10
Q

It refers to materials, procedures and
techniques that monitor the accuracy, precision and reliability of
a laboratory tests and it is also performed to ensure that acceptable
standards are met during the process of
patient testing.

A

Quality Control

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11
Q

It is used to verify accuracy and precision. Levy Jennings chart

A

Internal QC

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12
Q

It is the testing of unknown samples received
from outside agency and it provides unbiased validation of the
quality of patient test results.

A

External QC

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13
Q

What are the two type of Quality Control?

A

Internal Quality Control (Internal QC)
External Quality Control (External QC)

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14
Q

All reagents and reagent strip must be
properly labeled

A

Reagents

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15
Q

What are the way of proper labelling a reagent?

A

 Date of preparation or opening
 Purchase date
 Appropriate safety information

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16
Q

refractometers, automated reagent
strip readers, automated microscopy
instruments, what are these?

A

Instruments

17
Q

refrigerators, centrifuges, microscopes, water baths, what are these?

18
Q

This procedure is where detailed, concise testing instruction written
in a step by step manner

A

Testing procedure

19
Q

What are the Analytical Factors?

A

Quality Control
Reagents
Instrumentation and Equipment
Testing Procedure
Person and Facilities

20
Q

This is the processes that affect the reporting of results and correct interpretation of data.

A

POST ANALYTICAL FACTORS

21
Q

What are the Post-Analytical Factors?

A

Reporting of Results
Interpretation of Results

22
Q

Standardized reporting format, with reference ranges and written procedures should be available for reporting of critical values

A

Reporting of results

23
Q

What are the Pre Analytical Quality Assurance Errors?

A

 Patient misidentification
 Wrong test ordered
 Incorrect urine specimen type collected
 Insufficient urine volume
 Delayed transport of urine to the
laboratory
 Incorrect storage or preservation of urine

24
Q

What are the Analytical Quality Assurance Errors?

A

 Sample misidentification
 Erroneous instrument calibration
 Reagent deterioration
 Poor testing technique
 Instrument malfunction
 Interfering substances present  Misinterpretation of quality control

25
Q

What are the Post Analytical Quality Assurance Errors?

A

 Patient misidentification
 Poor handwriting
 Poor quality of instrument printer  Failure to send report  Failure to call critical values
 Inability to identify interfering substances