I am performing propensity score matching using teffects psmatch. I would like to generate a table containing the baseline characteristics of patients after propensity score matching. To do this, I generated a match variable [teffects psmatch (outcome) (treatment X1 X2 X3 etc.), atet gen(match)]. Is it correct to use all 'treated' patients with a non-missing match value and all 'control' patients with a non-missing match value to generate this table? If not, how can I identify patients belonging to the post-propensity score matching treatment and control groups?
In addition, when using default settings, I am getting up to 10 matches (controls being used as matches up to 10 times) despite specifying 1:1 matching. Could this just be a feature of the sample size of my control/treatment groups (treatment several times smaller than control), or is there an additional term I should add to my code? Stata output attached.
Thank you for your time and effort.
In addition, when using default settings, I am getting up to 10 matches (controls being used as matches up to 10 times) despite specifying 1:1 matching. Could this just be a feature of the sample size of my control/treatment groups (treatment several times smaller than control), or is there an additional term I should add to my code? Stata output attached.
Thank you for your time and effort.
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