WEEK 4: measures of association, measures of public health impact & errors Flashcards

1
Q

Weaknesses of an ecological study?

A
  • Ascertainment of the disease: quality of recording across time/place can vary
  • Idem info on exposure
  • Data obtained on non-representative samples
  • Often no adjustments for confounders apart from age, sex
  • Not good for rare exposures, because there is no good reliable data for this across countries
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2
Q

Which measure of association: RCT?

A

Incidence in exposed vs unexposed and compare with each other: incidence proportion ratio or incidence rate ratio

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3
Q

Which measure of association: Cross-sectional study?

A

Use prevalence proportion ratio to ‘count’ the cases (prevalence in exp/prevalence in unexp)

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4
Q

Which measure of association: Case-control?

A

Odds ratio = ad/bc (a = exposed)

(Exp diseased x not exp not diseased)/(exp not diseased x not exp diseased)

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5
Q

Which measure of association: cohort?

A

relative risk (incidence proportion ratio or incidence rate ratio)

IRR: IR in exp/IR in unexp
IPR: IP in exp/IP in unexp

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6
Q

Why should the cases in a case-control study be incidence cases?

A

 Survivor bias: if you do not choose the incidence cases and your disease is severe, you only look at prevalent cases that already have survived for a while. These are the less serious cases which results in a bias.

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7
Q

Examples of quasi-experimental study?

A

Example of quasi-experimental study = pre-post design, or intervention in one city, control in the other
Quasi-experimental study can also be (besides no randomization) an intervention that has not been introduced by the researcher or no control group

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8
Q

What is the background risk?

A

The natural occurrence of
disease in the unexposed population

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9
Q

What is the RD (rate difference)?

A

= Rate of exposed people (e.g. smoking) – Rate of non-exposed people (no smokers)

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10
Q

RR = ?

A

Relative risk = Rate exp (e.g. smoking)/Rate non-exposed (e.g. non- smoking)

(1 = no association). Per 100.000

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11
Q

What is the RR dependent on?

A
  1. Background risk:
    lower background risk -> stronger RR even when RD (rate difference) is constant
  2. Prevalence of other component causes (gene pool)
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12
Q

Why do you not use IPR or IRR with a case-control study design?

A

Incidence is not available, because it is a sample of the population

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13
Q

What does the odds ratio mean?

A

Odds ratio = the odds (not probability) of disease in the exposed relative to the odds of disease in unexposed.

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14
Q

What is a major problem in using the odds ratio with case-control studies?

A

Big problem is confounding (e.g. not adjusting for socio-economic status).

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15
Q

What does a RR of < 1 mean?

A

Negative association, decreased risk or protective effect

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16
Q

What is attributable risk? How is it measured?

A

Measures the actual amount of disease that can be attributed to a particular exposure

Can be
A. Incidence rate difference
B. Incidence proportion difference
C. Prevalence difference

17
Q

What is the difference between attributable and relative risk?

A

Attributable risk = measures the actual amount of disease
RR = How many times higher is the risk of disease in one group compared to the other?

18
Q

3 different ways to state attributable risk?

A

● How much extra disease occurs in group A vs B?

or
● What is the excess amount of disease occurring among those
exposed to a risk factor?

or
● How much disease among those who are exposed could
potentially be prevented by removing the exposure?

19
Q

What is the IRD (Incidence rate difference)? Or: excess rate

A

= IR in exp - IR in unexp

20
Q

What is the IPD (incidence proportion difference)? Or: risk difference/excess risk

A

= IP exp - IP unexp

21
Q

What is the prevalence difference (PD)? Or: risk difference/excess risk

A

prevalence proportion exp - prevalence proportion unexp

22
Q

What is the Attributable fraction (AF)?

A

= Attributable risk/incidence in exp * 100%

= Attributable risk/incidence rate or proportion in exposed * 100%

= (a - b)/a * 100

23
Q

What does the attributable fraction tell you?

A

-> Tells us the proportion of disease in those exposed that can be attributed to the exposure

24
Q

2 Differenct ways to state the PAR (population attributable risk)?

A

● How much extra disease occurs in the population compared to an unexposed group?

or
● How much disease among in the population could potentially be prevented by removing the exposure?

25
Q

How to use PAR with rate, proportion and prevalence?

A

PAR =

IR population - IR unexp
IP population - IP unexp

Or, using attributable risk and prevalence:
AR x P exposed

26
Q

What is the PAF and how is it measured?

A

PAF = population attributable fraction

(Pop. attributable risk (PAR)/ incidence in the total population) * 100%

Tells us the PROPORTION of disease in the population that can be attributed to the exposure

27
Q

For what purpose do you use relative risk vs attributable risk?

A

Relative risk: how many times higher is the risk of disease in group A compared to B
> is used for etiology
> note: high relative risk does not always reflect high impact

Attributable risk: Measures actual amount of disease attributed to an exposure
> used for policy decisions
> funding decisions (prevention programmes)
> Which disease should be targeted first?