Clinical Chemistry 1.2 Flashcards

Quality Assurance to Blood Collection and Specimen Considerations

1
Q

All steps done PRIOR to sample analysis. From test requisition to patient preparation, patient identification, specimen collection, labelling and transport, reception, handling, preparation of processing.

A

Pre-analytical

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2
Q

What are the 5 components in analytical phase?

A

reagents, preventive maintenance of equipment, calibrator, quality control, and sample analysis

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3
Q

Special aspect of analytical testing or laboratory testing

A

Quality Control

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4
Q

include verification of calculations and reference ranges, flagging and not of panic/critical values, delta checks, reporting of results

A

Post-analytical

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5
Q

an algorithm in which a current laboratory result is compared with results on a previous specimen from the same patient

A

Delta check

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6
Q

What is the goal of quality control?

A

To maintain reliability, accuracy, and precision.

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7
Q

Ability to maintain accuracy and precision over an extended period of
time during which equipment, reagents, and personnel may change

A

Reliability

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8
Q

closeness of the result to the true or actual value.

A

Accuracy

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9
Q

the ability to produce a series of results that agree closely with each
other; commonly expressed in terms of coefficient of variation; also
called repeatability or reproducibility

A

Precision

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10
Q

→ Also called Intralab
→ Involves the analysis of at least 2 levels of control every 24 hours
→ Initial control limits are established by analyzing control materials for at
least 20 consecutive days or runs
→ Important for the daily monitoring of accuracy and precision of analytical
methods

A

Internal QC

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11
Q

→ Also called Interlab - Proficiency testing
→ Involves testing blind samples (unknown concentration of analytes) sent
periodically by regulatory agencies to participating laboratories
→ Important for maintaining the long-term accuracy of analytical methods
→ SDI = (Lab Result – Group Mean)/Group SD

A

External QC

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12
Q

the regulatory agency administered by National Representatives (NRs)

A

National External Quality Assessment Scheme (NEQAS)

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13
Q

national reference laboratory for clinical chemistry or biochemistry

A

Lung Center of the Philippines

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14
Q

SDI >2 indicates ______

A

poor performance

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15
Q

An error that is due to chance or an unpredictable cause; does not recur in regular pattern.

A

Random Error

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16
Q

Recurring error inherent in test
procedure; influences observations
in one direction; Recurring error with a predictable
pattern

A

Systematic Error

17
Q

Random error affects ______; indicated by violation of the 1(2s), 1(3)s, R4s Westgard rules.

A

precision

18
Q

Affects _____; indicated by shift,
trend, or violation of the 2(2)s, 4(1)s, 8(1)s,
and 10x Westgard rules

A

accuracy

19
Q

Causes of random error

A

instrument instability (e.g.
temperature and voltage
fluctuations), dirty glassware,
sampling error, improper mixing of
sample and reagent, operator
variability (e.g. pipetting error),
anticoagulant or drug interference

20
Q

Causes of systematic error

A

deterioration of reagents,
change in reagent lot, unstable
reagent blanks, calibration error,
changes in standard concentration,
contaminated control solutions,
diminishing lamp power, dirty
photometer, faulty ISE, and pipettor
maintenance error

21
Q

abrupt change in the distribution of control values such that they accumulate on one side or either side of the mean for 6 consecutive days; major cause calibration error/error in standard preparation.

A

Shift

22
Q

gradual change in the distribution of control values such that they
continue to increase or decrease over a period of 6 consecutive days passing
through the mean; major cause deterioration of reagents.

A

Trend

23
Q

highly deviating control values caused by random or systematic
errors

A

Outliers

24
Q

What is the most commonly used QC chart?

A

Shewhart Levey-Jennings chart (LJ Chart)