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re: RE: st: RE: MCNEMAR test or Average treatment effects in matched data.
From
"Ariel Linden" <[email protected]>
To
<[email protected]>
Subject
re: RE: st: RE: MCNEMAR test or Average treatment effects in matched data.
Date
Wed, 8 Jan 2014 11:01:07 -0500
Let me weigh in here, since I was the poster of that previous thread on this
subject (http://www.stata.com/statalist/archive/2012-08/msg00985.html)
The questions that are being asked here are somewhat difficult to follow, so
I'll attempt to answer them, given what I understand:
" So if I understood well, you simply would use the log.regression to see
the effect of the my treatment. What about the average treatment effects?
Are they usefull? In my case?(the incidence of mediastinitis is the outcome
) Maybe the interpretaion in medical issues is not so clear?So should I
avoid it?"
If your outcome is binary, then yes, you can use a logistic regression.
Which type of treatment effect you'll be estimating depends on how you do
your matching/weighting. In general, matching untreated individuals to
treated individuals provides an average treatment effect on the treated
(ATT). Why, because you are choosing untreated units that have the same
characteristics as the treated. You can use weighting strategies instead of
matching, and choose your treatment effect estimator, if you are not happy
with the matching approach.
" It is very frequent that many paper using propensity score (not necessary
should be right) they show the new propensity score groups that they are
balanaced using parametric tests or non parametric test(even then they use
standarizes mean differences). What would you advice me to use if I want to
compare baseline caracteristic of my population before and after the
propensity score ? Note that I want to show all the baseline variables and
many of them are not included in the propensity score model. Should. I
simply use parametric tests weighted by psmatch2?"
As common practice, you should show a "table 1" before and after matching.
This will provide "evidence" that matching resulted in balance on observed
pre-intervention characteristics. As per my previous thread, you should NOT
be using t-tests to assess balance. This is not inferential statistics, and
thus we are not attempting to draw assumptions to a population. Moreover,
sample size will influence the statistics, which we hope to avoid. You
should use standardized differences for calculating balance, with the intent
of reducing the value as far as possible (down to zero). You should also
review Q-Q plots, box plots, density plots, etc. to visually inspect the
distributions of each covariate.
Lastly, you write that you want to show baseline variables that are not
included in the propensity score model? Why would you not include them in
the model? If you read the Elizabeth Stuart article that Joe referenced, you
will see that the rule of thumb is to include as many covariates as
available into the propensity score. This increases the likelihood that
you've balanced all observable characteristics, thereby reducing the
possibility of bias from omitted variables.
In summary, you should spend some time reading about these issues. Blindly
running statistics without a firm understanding of the underlying principles
is not a recommended practice for researchers.
I hope this helps
Ariel
Date: Tue, 7 Jan 2014 17:28:37 +0000
From: Joe Canner <[email protected]>
Subject: RE: st: RE: MCNEMAR test or Average treatment effects in matched
data.
Dr. Ayaon,
I am not an expert on propensity score matching; I have used it occasionally
and was sharing a few insights and experiences since no one else had
replied. I would recommend that you familiarize yourself with the recent
literature on the subject. A good start would be: Stuart, E.A. (2010).
Matching Methods for Causal Inference: A review and a look forward.
Statistical Science 25(1): 1-21.
In a recent thread on this subject, someone recommended against checking for
balance using methods like t-tests which are dependent on sample size. This
is certainly a useful caution, depending on the size of your study. If
balance is determined by not rejecting the null hypothesis of no difference,
you need to be careful that this result is due to the lack of difference
between the groups rather than to insufficient sample size. If sample size
is an issue for you in this regard, then perhaps you can try a
non-parametric test.
Regards,
Joe
________________________________________
From: [email protected]
[[email protected]] on behalf of mccali mccalister
[[email protected]]
Sent: Tuesday, January 07, 2014 8:17 AM
To: [email protected]
Subject: Re: st: RE: MCNEMAR test or Average treatment effects in matched
data.
Dear Dr.Canner,
I really apreciate your replay. So if I understood well, you simply would
use the log.regression to see the effect of the my treatment. What about the
average treatment effects? Are they usefull? In my case?(the incidence of
mediastinitis is the outcome ) Maybe the interpretaion in medical issues is
not so clear?So should I avoid it?
It is very frequent that many paper using propensity score (not necessary
should be right) they show the new propensity score groups that they are
balanaced using parametric tests or non parametric test(even then they use
standarizes mean differences). What would you advice me to use if I want to
compare baseline caracteristic of my population before and after the
propensity score ? Note that I want to show all the baseline variables and
many of them are not included in the propensity score model. Should. I
simply use parametric tests weighted by psmatch2?
Best regards
Dr. Ayaon
Cardiovascular resident
Enviado desde mi iPad
> El 06/01/2014, a las 23:12, "Joe Canner" <[email protected]> escribió:
>
> Dear Dr. Ayaon,
>
> According to a previous thread on this subject
(http://www.stata.com/statalist/archive/2012-08/msg00985.html) it is not
necessary to used a matched analysis in a 1:k propensity score matched
analysis. In fact, I'm not even sure how one would do a McNemar test for
1:5 matching (although with a little work it might be possible for a 1:1
match). More to the point, as mentioned in the previous thread, I would
question whether propensity score matching truly qualifies as a matched
analysis for McNemar purposes. Two people can have the same (or similar)
propensity score even if they have a quite different set of characteristics.
>
> As noted in the previous thread, it should be sufficient (if not
preferable) to do a logistic regression of your outcome variable versus the
treatment group, weighted using the _weight variable provided by -psmatch2-,
and including all of the matching variables (and any other relevant
variables) as covariates.
>
> Regards,
> Joe Canner
> Johns Hopkins University School of Medicine
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