Exam 2 Flashcards

1
Q

Equation for Prevalence

A

of individuals with disease/# of individuals considered

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2
Q

Equation for incidence density (rate)

A

of new individuals with disease or disease onset/sum of person-time at risk

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3
Q

Equation for cumulative incidence (proportion)

A

of disease onsets/# at risk at beginning of follow-up

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4
Q

What ratio does this apply to?

The odds of exposure (1 row) to (1 column) is 2.0 times the odds among those without ( 2 column)

A

Odds Ratio

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5
Q

What ratio does this apply to?

The risk of (what’s being studied) among those with (primary exposure or 1 row) is 2.0 times the risk among those with (2 row)

A

Risk Ratio

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6
Q

What are quasi-experimental studies?

A

Community trials that are focused on groups

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7
Q

Are randomized clinical trials primarily focused on groups or individuals?

A

individuals

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8
Q

What’s the equation measure for randomized clinical trials? And what is needed to calculate?

A

Relative Risk is the measure and incidence measure calculations are needed first

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9
Q

Whats the equation for relative risk

A

A/A+B/C/C+B

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10
Q

Are cohort observational study participants disease free at baseline? why?

A

yes, because the study is to see if exposure causes the disease

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11
Q

What is the equation used in cohort studies?

A

Relative Risk

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12
Q

What kind of a study is a population-based study followed through time?

A

Cohort

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13
Q

how many time points are there in cohort studies?

A

at least 2

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14
Q

Are cohort studies exposure or outcome based or both?

A

cohort studies are exposure based

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15
Q

Are cross-sectional studies exposure or outcome based or both?

A

cross-sectional studies are both

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16
Q

Are case-control studies exposure or outcome based or both?

A

case-control studies are outcome based (disease)

17
Q

What is the equation for cross-sectional studies?

A

Odds Ratio

18
Q

What is the equation for case-control studies?

A

Odds Ratio

19
Q

What do case-control studies measure?

A

they measure beyond exposure

20
Q

What study design has potential for recall bias?

A

case-control studies

21
Q

What is a retrospective study?

A

A retrospective looks at historical data but at that past point in time of the study the group was disease free

22
Q

What is a prospective study?

A

A prospective study watches for outcomes, such as the development of a disease, during the study period and relates this to other factors such as suspected risk or protection factor(s). The study usually involves taking a cohort of subjects and watching them over a long period.

23
Q

What is recall bias?

A

this means that there is always a measurement error when recalling something in the past and bias comes in when there is exposure to the disease that could come out as feeling towards a diagnosis (could be different in disease group vs. the control group)

24
Q

Is cross-sectional studies representative of incidence or prevalence?

A

prevalence

25
Q

Does risk ratio represent incidence or prevalence?

A

incidence

26
Q

Does odds ratio represent incidence or prevalence?

A

prevalence

27
Q

What does Bradford Hill’s criteria do with study designs?

A

fits into interpreting the strength of the evidence for causal relationships

28
Q

What is temporality?

A

It is solid evidence that exposure happened before the disease

where exposure preceded development of disease by a period consistent with proposed biologic mechanism

when a sufficient induction / latent period exists

29
Q

What does strength of association mean?

A

the stronger the association the more likely the exposure-disease relationship is causal

a strong association is less likely than a weak association to be due to confounding bias

RR or OR quantifies the association between exposure and outcome - generally there is a large relative risk or large odds ratio here

30
Q

What is biological gradient/dose response?

A

the higher the exposure (perhaps to a dose) the higher the risk

strength of association increases with intensity or duration of exposure, as predicted

31
Q

What is plausability?

A

when there are known or postulated biological mechanisms that help explain exposure-disease relationship - when there is evidence to support and association

examples: contaminated water / cholera, cigarette smoke / lung cancer, promiscuity / AIDS

32
Q

What is consistency?

A

when other studies using different populations and methodology show similar results

33
Q

What is coherence?

A

when an association must not seriously conflict with what is already known about natural history or biology of disease

34
Q

What is specificity?

A

when a specific exposure is associated with only one disease - this may not be applicable to chronic diseases since a specific exposure may be associated with several diseases

35
Q

What is internal validity?

A

Internal validity refers to how well an experiment is done, especially whether it avoids confounding (more than one possible independent variable [cause] acting at the same time). The less chance for confounding in a study, the higher its internal validity is