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CLS 706 > Biostatistics and QC > Flashcards

Biostatistics and QC Flashcards

1
Q

Sensitivity

A

% of sick who test positive

(TP/(total sick)) x 100

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2
Q

Specificity

A

% of people who test negative

(TN/(total healthy)) x 100

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3
Q

Predictive value (+)

A

Probability that positive result predicts patient has disease
(TP/(total positives)) x 100

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4
Q

Predictive value (-)

A

Probability that negative result predicts patient doesn’t have disease
(TN/(total negatives)) x 100

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5
Q

Efficiency

A

Percent of tests that correct lay reflect patient wellness or disease
((TP + TN)/total tests) x 100

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6
Q

Prevalence

A

Percent population who has disease

(Total sick/total tests) x 100

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7
Q

Proportional Error (PE)

A

(Slope - 1) x 100

Affects graph more at higher values

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8
Q

Constant Error (CE)

A

Y-intercept

Affects graph more at low values

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9
Q

Bias

A

Average of the differences between 2 sets of data (new method & old method)

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10
Q

Random Error (RE)

A

Error that cannot be predicted

One day of QC could be much higher or lower while all other days are normal

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11
Q

Systematic Error (SE)

A

SE = Constant Error (CE) + Proportional Error (PE)

Usually seen as trends or shifts in LJ charts

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12
Q

Standard Deviation (SD)

A

Describes “spread”, only applies to Gaussian spread

SD = sqrt((sum of ((data point - mean)^2) / (n - 1)))

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13
Q

Variance

A

SD^2

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14
Q

Coefficient of Variation (CV)

A

Helps compare SD’s of data with different units/different orders of magnitude
CV (%) = (SD/mean) x100

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15
Q

Precision

A

As little spread of data as possible, small SD

Use F-Test to compare precision of 2 sets of data

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16
Q

Accuracy

A

Measured values as close to true values as possible

Use paired T-test to compare accuracy of 2 sets of data

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17
Q

Reference Ranges

A

Expected range of values of an analyst in a healthy population

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18
Q

Reference Range Partitioning Factors

A

Age, Sex, Ethnicity, Diet, Pregnancy, Blood Group, Tobacco Use, Exercise, Geographic Location, etc

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19
Q

What value of R is acceptable?

A

Greater than .95

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20
Q

Analytical Measurement Range (AMR)

A

Smallest and largest values that can be reported from instrument without dilution, make sure smallest amount can be distinguished from a blank

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21
Q

Reference Interval Verification when given manufacturer’s existing reference interval

A

20-30 healthy individuals, if less than 10% fall outside proposed limit then reference interval is verified

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22
Q

Reference Interval Validation when establishing new interval with a Gaussian distribution

A

Test at least 40 healthy patients, reference interval is (+/-) 2 SD from mean

23
Q

Reference Interval Validation for establishing new interval for non-Gaussian distribution

A

At least 120 healthy patients, discard outliers if necessary, middle 95% of patient values is new reference interval

24
Q

Lower Limit of Detection (LLD)

A

Lowest concentration that can be detected

25
Q

Biological Limit of Detection (BLD)

A

Lowest concentration that can be detected in blood

26
Q

Functional Sensitivity (FS)

A

Lowest concentration that can be accurately measured

27
Q

What is good criteria for a screening test? (Sensitivity and Specificity)

A 
High Sensitivity (catch all people who are sick) 
Low Specificity (may catch some false positives)
28
Q

What is good criteria for a Confirmatory Test? (Sensitivity and Specificity)

A 
Sensitivity good (still want to catch all sick people) 
Specificity is high (weed out any false positives)
29
Q

What are some possible reasons for Systematic Error on a LJ chart? What can be done to fix it?

A

New reagent lot (try a different lot), wrong or deteriorating reagent (replace), out of reagent (replace), incorrect calibration (re-do)

30
Q

What are some causes of Random Error on an LJ chart? What can be done to fix it?

A

Erratic volume change of sample/reagents (replace analyzer pipette tips, check for loose component), temperature changes (use heater or AC)

31
Q

Paired T-test

A

Compares the accuracy of 2 sets of data, can confirm if new test is as accurate as old one

32
Q

F-test

A

Used to compare precision of 2 sets of data, can be used to determine if new test is as precise as old one

33
Q

Pre-analytic process

A

Ordering, collection, identification, transportation, separation

34
Q

Analytic process

A

Actual testing done in lab (usually less error than Pre- and Post-analytic)

35
Q

Post-Analytic Process

A

Reporting, interpretation, action

36
Q

Centers for Medicare and Medicaid Services (CMS)

A

CMS is federal agency that enforces CLIA, gives proxy status to others like CAP and JCAHO to inspect and accredit in order to give CLIA certification to receive repayment for Medicare/Medicaid testing

37
Q

Clinical Laboratory Improvement Amendments (CLIA)

A

Federal regulations, first passed 1967, updated 1988 and 2003, must have CLIA certification to get repaid by CMS

38
Q

College of American Pathologists (CAP)

A

Act as a proxy for CMS, regulate proficiency testing for labs

39
Q

Joint Commission on Accreditation of Healthcare Organizations (JCAHO)

A

Act as a proxy for CMS, regulate proficiency testing for laboratory and hospital

40
Q

CLIA Requirements for Waived Tests

A

Only requirement is to follow manufacturer’s written instructions

41
Q

CLIA requirements for Non-Waived tests

A

Moderate Complexity must show: accuracy, precision, reportable range, reference interval

High Complexity must show: all above, analytical sensitivity (detection limit), analytical specificity (interference and recovery)

42
Q

JCAHO requirements for Waived tests

A

Accuracy, precision, reportable range

43
Q

JCAHO requirements for Non-Waived tests

A

Moderate Complexity: accuracy, precision, reportable range, reference intervals

High Complexity: all above, analytical sensitivity, analytical specificity (including interferences)

44
Q

CAP Requirements for Waived tests

A

None, except verification of reference range if practical (manufacturer’s document)

45
Q

CAP requirements for Non-Waived tests

A

Moderate and High Complexity: accuracy, precision, reportable range, reference range, sensitivity, specificity (interferences)

46
Q

12s

A

Warning flag, can be systematic or random depending on other data

47
Q

13s

A

Automatic reject, can be random or systematic depending on other data

48
Q

22s

A

Can be 2 consecutive runs above 2s or 2 simultaneous runs on the same day on the same side of the mean, usually systematic error

49
Q

R4s

A

When there is a 4s difference within the same run, across 2 levels of control, always random error

50
Q

41s

A

Can be 4 consecutive measurements above 1s on 1 level of control, or 2 consecutive measurements on 2 levels of control, systematic error

51
Q

10x

A

Can be 10 consecutive measurements on 1 side of the mean on 1 level of control, or 5 consecutive measurements on the same side of the mean across 2 levels of control, systematic

52
Q

7T

A

7 control measurements that trend in one direction (progressively higher or lower)

53
Q

Equivalent Quality Control (EQC) vs. Individualized Quality Control Plans (IQCP)

A

IQCP are standards that must be follow/risk factors checked in order to use analyzers internal QC
Otherwise can use EQC which required 2 levels of external QC every day (more expensive)

54
Q

Rules for CAP proficiency testing

A
  • Test samples as you would any patient sample
  • Do not communicate results or share samples with other labs
  • If you get a test you normally send out, don’t sent it out
  • If you work at 2 labs you may not test the same sample at both labs
  • Can’t fail 2 consecutive surveys
  • Can’t fail 2 surveys per year
  • If you fail, documentation of corrective action
  • Records must be kept for 2 years

CLS 706 (4 decks)

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