Chapter 2 Flashcards

1
Q

Validity

A

does the test accurately id whether a pt has a disease?

  • gold standard test
  • 2x2 table format
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2
Q

Sensitivity

A

probability that a person with disease has a positive test

- the true positive rate

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3
Q

Specificity

A

probability that a non-diseased person has a negative test

- the true negative rate

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4
Q

Positive Predictive Value

A

probability that a person w/ a + test has disease

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5
Q

Negative Predictive Value

A

probability that a person w/ a - test does not have disease

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6
Q

Prevalence of Disease

A

proportion of pts in the disease present column

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7
Q

Likelihood Ratio

A

probability of obtaining a given test result in a diseased patent divided by the probability of obtaining a given test result in a non-diseased patient
- tells us how much a test result changes the pre-test disease probability (prevalence) to the post-test disease probability

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8
Q

higher likelihood ratio for positive test

A

indicates that a positive test is more likely to be coming from a diseased person than from a non-diseased person, increasing confidence that a person w/ a + result has disease

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9
Q

lower likelihood ratio for negative test

A

negative test is much more likely to be coming from a non-diseased person than from a diseased person, increasing our confidence that a person w/ a - test does not have disease

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10
Q

Bayes Theorem

A

one way to use likelihood ratios to revise probabilities for disease

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11
Q

Ways to use Likelihood Ratios

A

Bayes Theorem
Fagan Nomogram
Natural Frequencies

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12
Q

Natural Frequencies

A

represent the joint frequency of 2 events, such as # of pts w/ disease and the # who have a + test result

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13
Q

Kappa Score

A

(reproducibility)

measures amount of agreement that occurs beyond chance (higher = better)

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14
Q

Precision

A

(reproducibility)

being able to apply the same test to the same unchanged person and obtain the same results

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15
Q

coefficient of variation

A

statistical test used to characterized precision

- the standard deviation divided by the mean value (lower = greater precision)

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16
Q

Primary Prevention

A

interventions designed to prevent disease

17
Q

Secondary Prevention

A

screening tests designed to find disease or disease processes at an early, asymptomatic stage

18
Q

Evidence Pyramid

A
  1. Systematic Reviews
  2. Randomized Control Trials - strongest health promotion recommendations are based on these results
  3. Cohort Studies
  4. Case-Control Studies
  5. Case Series, Case Reports
  6. Editorials, Expert Opinion
19
Q

Selection Bias

A
  • occurs when comparison groups have systematic differences in their baseline characteristics what can affect the outcome of the study
  • creates problems interpreting observed differences in outcomes n/c they could result from the interventions or the baseline differences between groups
  • randomly allocating subjects to the intervention is the best approach to minimize this
20
Q

Performance Bias

A
  • occurs when there are systematic differences in the care received between comparison groups (other than intervention)
  • creates problems in interpreting outcome differences
  • Minimize by: blinding subjects and providers to the intervention
21
Q

Detection Bias

A
  • Occurs: systematic difference in efforts to diagnoses ot ascertain outcome
  • Minimize by: blinding outcomes assessors (ensuring that they are unaware of the intervention received by h\the subject)
22
Q

Attrition Bias

A
  • Occurs: systematic differences in the comparison groups in the number of subjects who do not complete the study
  • failing to account for these difference can lead to incorrectly estimating the effectiveness of an intervention
  • Minimize by: using an intervention-to-treat analysis, where all analyses consider all subjects who are assigned to a comparison group, regardless of whether they received to completed the intervention
23
Q

statistics used to characterize the performance of a treatment of prevention intervention:

A
  • relative risks
  • relative risk difference (reduction or increase, reflecting benefit or harm)
  • absolute risk difference (reduction or increase, reflecting benefit or harm)
  • numbers needed to treat
  • numbers needed to harm
24
Q

Experimental Event Rate

A

probability that an intervention subject had the outcome

25
Control Event Rate
probability that a control subject had the outcome
26
Relative Risk
probability of an outcome in the intervention group compared to the probability of an outcome in the control group
27
Relative Risk Difference
proportion of baseline risk is reduced/increased by the therapy
28
Absolute Risk Difference
difference in outcome rates between the comparisons groups
29
Reciprocal of the absolute risk difference
number of subjects who need to be treated over a specific period of time to prevent one outcome - if intervention increases risk of a bad outcome this statistic becomes the number needed to harm
30
guideline recommendations: US Preventative Services Task Force Approach
assigns 1-5 ratings and a level of certainty regarding net benefits
31
guideline recommendations: Grading of Recommendations, Assessment, Development, and Evaluation (GRADE)
rates quality of the evidence and grades the strength of recommendations in clinical guidelines - primary goals (1) clearly separate quality of evidence and strength of recommendations [A,B,C] (2) provide clear, pragmatic interpretations of strong v. weak recommendations [1,2]