EPI 201 Midterm Flashcards

1
Q

Relationship between CI and IR

A

CI = 1 - e^(-IR*t)

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2
Q

Which interval does a censored person go in?

A

The one that ends soonest AFTER they are censored

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3
Q

What do you need to include with a CI?

A

Time period

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4
Q

What do you need to include with an IR?

A

Person-time

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5
Q

What do you need to include with a prevalence?

A

Point in time

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6
Q

Measures of association

A

Cumulative incidence ratios/differences, prevalence ratios/differences, incidence rate ratios/differences

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7
Q

Traditional definition of a confounder

A
  • Must be associated with exposure in the study base
  • Must be a cause or correlate of a cause of the outcome among the unexposed
  • Cannot be a downstream consequence of exposure or outcome
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8
Q

Definition of a prospective cohort study

A

Exposures measured for research purposes before the OUTCOME occcurs

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9
Q

Study base types

A

Primary, secondary

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10
Q

Types of case-control sampling

A

Density - IRR, risk-set (subset of density) - IRR, case-crossover - IRR, cumulative incidence - CI (under rare disease assumption), case-cohort - IRR

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11
Q

Measures of association for a closed cohort study

A

IRs, CIs, ORs…

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12
Q

Hill Criteria

A

Strength, consistency, specificity, temporality, biologic gradient, plausibility, coherence, experimental evidence, analogy

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13
Q

Popper postulates

A

Knowledge accumulates by falsification
Scientific theories can only be falsified, never proven
Scientific hypotheses must have empirical content and be falsifiable

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14
Q

Problems with random digit dialing

A

Probability of having a phone may relate to exposure
Probability of answering may relate to exposure
Different ratios of people to phone
Area codes no longer relate to geography

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15
Q

Key point with hospital matched controls

A

The control condition must be UNRELATED to the exposure of interest

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16
Q

Attributable risk

A

CID = CI_E+ - CI_E-

17
Q

Population attributable risk percent

A

Pr[A=1|Y=1] = (CI_tot = CI_E-)/CI_tot

18
Q

Number needed to treat

A

1/CID

19
Q

Population attributable risk

A

CI_tot - CI_E-

20
Q

Attributable rate

A

IRD

21
Q

Attributable risk percent

A

(CIR-1)/CIR * 100

22
Q

Measures of association for an open cohort study

A

Odds, IR, only approx CIs using exponential formula

23
Q

Definition of D-separation

A

Two variables in a DAG are D-separated if all paths between them are blocked

24
Q

What happens if you condition on a descendant of a collider?

A

This is just like conditioning on the collider itself – opens a path

25
Q

Problems with ecological studies

A

Often have poor measure of exposure
Often have no info on who is exposed
No info on if exposed are the ones getting the outcome
No data on individual-level confounding

26
Q

In what kind of study can you directly measure CI?

A

Closed cohort study (however, you would often use IR in a closed cohort situation due to LTFU, changes in exposure over time, etc). In an open cohort, you cannot measure CI directly, but you can estimate it using the exponential formula.

27
Q

Problems with CI

A

Tends towards 1
No info on when event occurred
Does not allow for changing population size
Does not allow for time-varying exposures
Events may not be observable due to censoring

28
Q

Probability tree notes

A

L=0 (0.33) 20

Non-treatment variables in circles

29
Q

Relationship between prevalence and IR

A

prevalence odds = IR * duration (under steady state)

30
Q

Difference between confounding and selection bias

A

Confounding occurs when there is a lack of exchangeability between exposed and unexposed groups. Selection bias occurs when we condition on a collider.

31
Q

When is it appropriate to use the NON-exponential formula?

A

To approximate CI using the IR, you can use the NON-exponential formula C=I*t when the product of I and t is small.