Biostats Flashcards

1
Q

Precision

A

Data points cluster around one POINT

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2
Q

Accuracy

A

Aka Validity - combo of specificity and sensitivity and it = “gold standard”
(Think of the targets)

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3
Q

Standard error of mean (as sample goes up or down what happens)

A

SEM becomes smaller as more samples are added to data set (power increase) so the data becomes more PRECISE

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4
Q

Z score

A

Shows how far above or below the mean for a given value (in standard deviations basically)

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5
Q

Median helps do what with outliers

A

Corrects for outliers

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6
Q

Confidence interval (CI)

A

Shows precision of a data set, it’s 2 times the SEM so if CI crosses 1 the results are not significant/precise enough to be useful

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7
Q

T-test good for what type of data?

A

Used to assess data from 2 groups (T for 2)

*same individual followed over time

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8
Q

ANOVA used in what situation?

A

To assess data from 3 or more groups

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9
Q

Chi square COMPARES what?

A

COMPARES multiple groups and indicates whether or not they’re statistically significant used when data comes in discrete CATEGORIES

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10
Q

What does randomization account for/do?

A
  • Accounts for selection bias
  • “intention to treat” preserves the benefit of randomization
  • minimizes confounding bias
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11
Q

Cohort study uses what equation/parameter?

A

Relative Risk = (exposure with dz / all exposed) / (no exposure with dz / all not exposed)

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12
Q

Case control uses what equation/parameter?

A

Odds Ratio = (exposed with dz X no exposure with no dz) / (no exposure with dz X exposure with no dz)
*Case-control is subject to recall bias

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13
Q

P-value means what?

A

If < 0.05 it’s significant, means that if study were repeated there’s 95% chance of same results
* also means there’s 5% probability there’s no association to the null hypothesis (meaning it’s rejected)

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14
Q

Type I error (alpha)

A
False Positive (you Accept alternate hypothesis when it’s false)
AKA P-value
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15
Q

Type II error (beta)

A
false Negative (Beta error, you’re Blinded to the fact the alt hypothesis is true)
POWER = (1-Beta)
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16
Q

Equation to figure TP using Prevalence

A

Sensitivity X Prevalence = TP

17
Q

Equation to figure FP using Prevalence

A

(1-Specificity) X Prevalence = FP

18
Q

Length-time bias VS. Lead-time bias

A

Length-time is when screening test detects less aggressive form of dz which = an apparent increase in survival time
Lead-time is when you find a dz earlier but it looks like increased survival time when really it’s not

19
Q

Number needed to Treat (NNT)

A

1/ARR

20
Q

Attributable Risk (AR)

A

AR = Incidence of exposed - Incidence of unexposed

21
Q

Absolute Risk Reduction

A

Controlled event rate (CER) - Exposed event rate (EER) = ARR

22
Q

RRR

A

CER-EER/CER