board review intro/biostatistics Flashcards

1
Q

diagnostic error

A

missed opportunity

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2
Q

types of studies

A
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3
Q

cross-sectional

A

moment in time

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4
Q

case control

A

generally retrospective

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5
Q

cohort

A

2 groups - based on presence or absence of risk factor

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6
Q

RCT

A
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7
Q

systematic review with meta analysis

A
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8
Q

which study is best for studing rare disease

A

case control

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9
Q

strongest experimental design

A

rct

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10
Q

best to determine disease prevalence

A

cross-sectional

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11
Q

studying outcomes that develop over time or survival analyses

A

cohort

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12
Q

heterogeneity

A

most important limitation of meta-analysis

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13
Q

confounding

A

try to account for it with randomization

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14
Q

validity

A

internal – how well study error is minimized (ie, errors in sampling, measurement, and analysis)

external – aka generalizability
–extent to which study results can be applied to other settings

threats to validity
–systematic error and random error

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15
Q

systematic error

A

attempt to min via study design
1. confounders - factors other than variables being studied that are associated with the study population
mitigate: matching, statistical technique

  1. bias – presence of factors that skew results in a specific direction
    mitigate: study design
    —ie, appropriate selection of particpants
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16
Q

randomization

A

minimize systematic error
– try to ensure the groups being studied differ only in terms of intervention

17
Q

random error

A

error introduced by chance
–assess via CI and p-values

mitigate: increase study size, use precise measurement techniques

18
Q

statistical analysis

A

indicates likelihood of study result being caused by chance alone

does not compensate for bias

the larger the sample size the more likely you are to detect a difference
-always consider practical significance

19
Q

CI

A

range of values which the true results fall
-95% confidence that true value is within range

a CI that crosses the null value (ie, 1 for RR and OR) is not statistically significant

20
Q

assessing the value of a diagnostic test

A

sensitivity
specificity
PPV
NPV
LR

21
Q

sn and sp

A

inherent to test themselves and does not change with prevalence of disease in population

sensitivity - proportion of patients with dz who test positive snout
ie, high sensitvity –> low false neg

spec – proportion of patients without dz who test negative
high sp –> low false positive
-spin

22
Q

as sensitivity increases

A

false negative ratio decreases
npv

23
Q

as sensitivity increases

A

false negative ratio decreases
npv increases

24
Q

as specificity increases

A

false positive rate decreases
ppv increases

25
Q

predictive values

A

reflects the validity of a positive or negative test result
-used to interpret a test result
-determined by sensitivity, specificity, and prevalence of disease

PPV–% of pt with pos test who have dz
NPV–% of pt with neg test who do not have dz

26
Q

as prevalence increases

A

PPV increases and NPV decreases

27
Q

LRs

A

also assess performance of a diagnostic test
-independent of dz preva

28
Q

LRs

A

also assess performance of a diagnostic test
-independent of dz prevalence

how much more or less likely is a disease based on the test result

pret test probability xLR = post-test probability
the magnitude of LR suggests how strongly a test will increase or decrease the likelihood of the disease

LR+ used when test is positive
sens/(1-sp)
2,5,10 increases post test probability by 15, 30 and 45%

LR- used when test is neg
1-sen/sp
0.5, 0.2, 0.1 decreases post test probability by 15, 30, and 45%

29
Q

risk estimates–NNT/NNH

A
30
Q

risk estimates ARR and RRR

A