flowchart LR Z[Z] --> A[A] A[A] --> Y{Y} U(U) --> A[A] U(U) --> Y{Y}
Notes from book: What if (Part x)
Instrumental variables
Instrumental variable estimation is one way that does not rely on the assumptions where all variables to adjust for confounding and selection bias to be identified and correctly measured.
- Z is the random assignment indicator (1 treatment 0 placebo)
- A is the treatment (1 yes 0 no), not all adhere to original assignment
- Y is the outcome
- U is the unmeasured variables that affect both treatment adherence and outcome
Conditions for instrument Z
- Z is associated with A (treatment)
- Z does not affect Y through its potential effect on A
- Z and Y do not share causes
The three conditions are satisfied in a double blind randomized controlled trial as
- those who are assigned to treatment (Z=1) are more likely to receive treatment (A=1), indicating association
- expected in double blind design
- expected by random assignment
There is a fourth condition of heterogeneity / monotonicity.
If an instrument is unmeasured, sometimes a proxy or surrogate instrument associated with the unmeasured instrument \(U_z\) can be used.
In observational studies
In observational studies we do not have the random assignment indicator Z. Some common categories of IV:
- genetic factors
- preference
- access to treatment
Compare with other methods
The conditional exchangeability required by IP weighting, standardization is replaced by other assumptions. The choice of method depends on whether it is easier to identify and measure the confounders, or find an instrument Z and expect monotonicity and heterogeneity.
Violation of assumptions 1-4 may result in large biases; IP weighting and standardization are more robust compared to IV.
When there are time varying treatment, IV is not ideal as it is suited for point intervention.
ivreg
package
Check out this post for an example. Only normal errors.