agree in principal. however, for rare diseases where to have RCT is not feasible, we have to compare with historical control or data from observational studies. Propensity score matching is no worse than cherry picking match
@jekamito5 жыл бұрын
dude, that was FANTASTIC!!!
@ibipoabdurraheemsalami37093 жыл бұрын
So good, I forgot I had a journal club to prepare for!
@MrSpiritmonger2 жыл бұрын
but what about situations where you cannot randomize because of ethical concerns (e.g. smoking cause lung cancer)? PSM works right?
@pirasa54 жыл бұрын
Excellent! Really fantastic! Looking forward to the ones to come.
@brotherstandage4 жыл бұрын
Thank you. This was helpful.
@Actanonverba014 жыл бұрын
Clear and concise, Thank you
@sunnyboy2886 жыл бұрын
I was wondering why should effect size be only smaller with more variables. Couldnt it get larger too?
@davidaustin69624 жыл бұрын
Since the confidence goes down as you add potentially spurious data from additional variables, at a given confidence the measured effect also goes down.
@gbr41675 жыл бұрын
awesome explanation! thank you so much
@Dadlummusue4 жыл бұрын
Very clear. Thank you.
@HusainAlnasser4 жыл бұрын
thanks just came from your coursera for more info 😁
@GrifiN427 ай бұрын
That was very informative! Tell me more
@flavialan45442 жыл бұрын
Very Good!
@MK-xc6df9 ай бұрын
If you think it is in theory possible to create a model which accurately predicts everyone who smokes marijuana, you simultaneously deny the notion of free will and the nondeterminism and randomness.
@hisaurav20075 жыл бұрын
In Real world evidence propensity score contribute lot.
@davidaustin69624 жыл бұрын
Disappointing. Nobody is suggesting that they are anywhere as good as RCTs. At worse Propensity Scores is a flawed system to test for correlation for which doing an RCT is unconscionable (imagine assigning half of your non-pot-smoking participants to smoke pot), but in the case of such an unconscionable RCT, a propensity score is all we're left with to use (at least for doing weighting for example, note that it is inferior to other methods for matching datapoints). In the absence of being able to do an RCT it's better than nothing. Sadly in the last dozen years Dr. Wilson's opinion here has become so commonplace and popular ... like a clap trap really, that the medical community has become almost giddy with the prospect of disparaging any study that isn't an RCT. This prejudice against Propensity Scores where RCTs are not suitable is really shameful, and the prejudice has been doing a lot of damage in the field of medical research. Tremendous progress has already been held back as a result of doctors insisting on RCT's before they make a change when in fact an RCT is impractical or imprudent. It almost seems scripted since it leaves all decision making only to those funded enough to run RCT's, ie. pharmaceutical companies, who will only do RCTs on their drugs.