Lecture 28: Confounding II Flashcards

1
Q

“Risk factors party together”. What does this mean?

A

people who have one risk factor for an outcome also tend to have other risk factors for that outcome

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2
Q

As well can controlling for confounding in the study design, when else can we control for confounding?

A

in the study analyses

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3
Q

What are three ways to control for confounding in the study analyses?

A
  • stratification
  • multivariable analysis
  • standardisation
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4
Q

What is stratification?

A

calculating the measure of association for each stratum (level of potential confounder eg age strata could be 20-29, 30-39) of potential confounder and comparing them

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5
Q

What are the steps to stratification?

A
  1. calculate the measure of association between the exposure and the outcome (the crude, univariate, unadjusted)
  2. divide the potential confounder into strata
  3. for each stratum, calculate the measure of association between the exposure and the outcome (ie. calculate the stratum specific measures of association)
  4. compare stratum specific measures of association
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6
Q

What are some advantages of stratification?

A
  • easy for a small number of potential confounders with limited strata
  • can evaluate the impact of confounding
  • can identify effect modification
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7
Q

What are some disadvantages of stratification?

A
  • can leave residual confounding (distortion that remains after controlling for confounding in the design and/or analysis of a study)
  • not feasible when dealing with lots of potential confounders with many strata
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8
Q

Define multivariate analysis

A

statistical method for estimating measure of association whilst controlling for multiple potential confounders

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9
Q

Define standardisation?

A

this is done when age differs between the populations and the disease risk varies by age

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10
Q

What are some potential issues with controlling for confounding in the study analysis?

A
  • residual confounding (using strata that are too wide eg. 65+)
  • you can only control what you have measured
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11
Q

If you controlled for confounding in the design phase by matching, what do you need to do in the analysis phase? Why?

A

a matched analysis otherwise you will underestimate the measure of association

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12
Q

How can you evaluate confounding?

A

you need to compare crude and adjusted measures of association

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13
Q

How do we know if confounding has occurred? Which MoA should we use?

A

When we compare the crude and adjusted MoA, if they are not equal, there is confounding present. You should calculate and use the adjusted MoA

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14
Q

How do we know if confounding has not occurred?

A

When we compare the crude and adjusted MoA, if they are equal, there has been no major confounding. We can therefore just use the crude MoA

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15
Q

How much change indicated confounding?

A

The general guideline is if controlling for confounding changes the MoA by more than 10%, confounding has occurred

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16
Q

What is effect modification? Give an example

A

it is all about stratification and occurs when an exposure has a different effect among different subgroups. Effect modification is associated with the outcome but not the exposure.
For example, imagine you are testing out a new treatment that has come onto the market, Drug X. If Drug X works in females but does not work in males, this is an example of effect modification.

17
Q

How can you identify effect modification?

A

if the stratum specific MoA are different to one another, this is an effect modifier (but if they are similar to one another, this is a confounder, and then you compare to the crude MoA)