Lecture 11-12 Flashcards

1
Q

Define Counterfactual Theory

A

Loosely: The opposite.

  • The effect of the exposure difference in the counterfactual outcome
  • Counterfactual outcome for smokers is estimated by non-smokers
  • In other words, it has to be agreed that the group you’re comparing against is EXCHANGEABLE, or comparable.
  • If there’s no exchangeability, CONFOUNDING occurs. And that’s bad.
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2
Q

What is internal validity?

A

Researchers are “required” to check 3 aspects of their study before declaring whether two events are truly associated/comparable.

  1. Check for Confounding, or Effect Modification
  2. Check for Biases
  3. Check for Statistical Significance
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3
Q

What is a confounding variable, or a confounder?

A
  • A 3rd variable that distorts an association (RR/OR/HR) between the Exposure and the Outcome
  • A 3rd variable that makes the groups not exchangeable in terms of their associations
  • An alternative explanation of the association (findings)
  • Normally it should be Exposure Leads to Outcome. But by that Direct Acyclic Graph (D.A.G.), It becomes that and also Confound Affects Exposure and/Or Outcome
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4
Q

What are some other Choicey Keywords for describing Confounding Factors?

A
  • MIXING OF EFFECTS - an association (between Exposure and Outcome) is DISTORTED due to them being mixed with another (3rd) factor which is also associated with the Outcome…at the same time
  • CONFUSION OF EFFECTS, where effect of Exposure is DISTORTED because the effect of an extraneous (3rd) factor is mistaken for the effect of the Exposure
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5
Q

What 3 Requirements must something have to be a Confounder

A
  1. Associated with the Exposure
  2. Associated with the Outcome
  3. Not directly in the causal-pathway linking Exposure to Outcome (Independent)
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6
Q

What’s an example of a confounder

A

If the Exposure was studying the prevalence of smoking among people with CHD, the confounder might be the AGE of the population if they weren’t even.

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7
Q

How does one test for confounding presences?

A

Process called STRATIFICATION, or Regression…I think.

  1. Step One: Calculate your Crude, or your unadjusted OR/RR
  2. Step Two: Calculate outcome measure of association (OR/RR) between Exposure and Outcome for ALL STRATA (layers) of the 3rd variable (potential confounder)
    - Create a weighted-average of all strata (if near-equal)
    - Commonly called ADJUSTED association
  3. Step Three: Compare the Crude vs. Adjusted measures of association between Exposure and Outcome
    - The Crude & Adjusted estimates (RR/OR) of measure of association will be different by ~10%-20% (15%) if confounding IS present
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8
Q

What are two main impacts of confounders

A
  1. Intensity/Magnitude/Strength of Association
    - An association more/less extreme than true association
  2. Direction of Association
    - Produces association in an opposite direction o
    - Towards or away from a null association (RR/OR/HR=1.0)
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9
Q

Name 2 Ways to Control Confounding

A
  1. STUDY DESIGN STAGE
    - Randomization (Simple or Stratified versions)
    - Restriction
    - Matching
  2. ANALYSIS OF DATA STAGE
    - Stratification (w/ Weighting)
    - Multivariate statistical analysis (Regression analyses)
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10
Q

What is randomization?

Describe it’s strengths and weaknesses?

A

Randomization technique hopefully allocates an equal number of subjects with the known (and unknown) confounders into each intervention group
Strengths: With sufficient sample size (N), randomization will likely be successful in serving its purpose (making groups “equal”)
- Stratified version more precisely assures equal-ness

Weaknesses: Sample size (N) may not be large enough to control for all known and unknown confounders

  • Process doesn’t guarantee successful, equal allocation between all intervention groups for all known and unknown confounders
  • Practical only for Interventional studies
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11
Q

Describe Restriction.

What are some of Restriction’s strengths and weaknesses.

A

Study participation is restricted to only subjects who do not fall within pre-specified category(-ies) of confounder

  • Strength: Straight forward, convenient and inexpensive
  • Does not negatively impact Internal Validity
  • Weakness: Sufficiently narrow restriction criteria may negatively impact ability to enroll subjects (reduced sample size (N)).
  • If restriction criteria is not sufficiently narrow it will allow the introduction of residual confounding effects
  • Eliminates researchers ability to evaluate varying levels of the factor being excluded
  • Can negatively impact External Validity (Generalizability)
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12
Q

Describe Matching

What are the strengths and weaknesses of matching?

A

Study subjects selected in matched-pairs related to the confounding variable to equally distribute confounder among each study group

  • Strength: Intuitive, some feel it gives greater analytic efficiency
  • Weakness: Difficult to accomplish, very time consuming, and potentially expensive
  • Doesn’t control for any confounders other than those matched on
  • Over-matching possible; this will mask findings
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13
Q

Describe Stratification

What are the strengths and weaknesses of stratification?

A

Descriptive & Statistical analysis of data evaluating association between Exposure and Outcome within the various strata (layers) within the confounding variable(s), such as Young vs. Old; in the Smoking & CHD example)

  • Strength: Intuitive (to some), straight-forward and enhances understanding of data
  • Weakness: Impractical for simultaneous control of multiple confounders, especially those with multiple strata within each variable being controlled
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14
Q

Describe Multivariate Analysis.

What are multivariate analysis’s strengths and weaknesses?

A

Statistical analysis of data by mathematically factoring out the effects of the confounding variable(s)

  • Strength: Can simultaneously control for multiple confounding variables
  • In Regressions, beta coefficients can be converted to OR’s
  • Weakness: Process requires all individuals to clearly understand (interpret) the data (results)
  • Can be very time consuming for researcher/biostatistician
  • Examples: (FYI for now; not on exam #1)
  • Regressions (Linear & Logistic versions)
  • Cox Proportional Hazards
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15
Q

What is effect modification?

How is it different than confounding?

A
  • A 3rd variable, that when present, modifies the magnitude of effect of a TRUE association by varying it within different levels of a 3rd variable (modifies the effect across the strata)
  • If an interaction is present, the researcher MUST report the measures of association for each strata individually
  • So, unlike confounding, an effect modifying variable should be described and reported at each level of the variable, rather than controlled-for.
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16
Q

How does one check the effect modification OR across multiple strata (such as the singleton fetus example on slide 33)

A
  • Tentative Slide…not sure about this one

I’m not totally sure…but I think you would take the OR of the highest value, and the lowest value

(Highest - Lowest) / Highest Value

17
Q

How does one test for Effect Modification?

See slide 33 for details

A
  • Step One: Calculate CRUDE measure of association between Exposure and Outcome (OR/RR)
  • Step Two: Calculate measure of association (OR/RR) between Exposure and Outcome FOR EACH STRATA (layers)
  • Step Three: Compare each of the STRATUM-SPECIFIC measures of associations (OR/RR) between each other [while referencing the ADJUSTED measure of association]
  • The measure of association (RR/OR) between the Lowest and Highest strata (layers) of the effect-modifying variable will be ~10%-20% (15%) different if effect modification (interaction) IS present k