Re: EBM -- was Testerone

From: art fougner, md (evsono@pipeline.com)
Sun Mar 4 10:21:42 2001


No doubt smallpox vaccination would have not been reimbursed since it was not validated by EBM.

art

At Sun, 4 Mar 2001, DoctorJoe@aol.com wrote: >
>In a message dated 3/4/01 8:34:51 AM, mperloe@ivf.com writes:
>
><< While evidence based medicine (EBM) has allowed us to abandon many
>ineffective treatment regimens, unfortunately it has been used to refuse
>coverage for many treatments that have not yet undergone EBM validation. We
>must be careful not to fall into the trap that equates a lack of evidence
>(EBM double blind randomized clinical trial) with lack of clinical benefit.
>If we remove clinical judgement from the picture and reduce medicine to
>merely allocating patients to the appropriate EBM clinical pathway, we will
>be become medical technicians and provides and not healers. >>
>
>Ditto that.
>
>What the EBM clinical pathways are basically SUPPOSED to do is set a
>"standard" so a patient won't get SUBstandard care. However, if an EBM
>pathway doesn't exist, or a physician individualizes a patient outside of the
>pathway (giving, in effect, SUPERstandard care), then he/she is at risk from
>the reimbursement angle, as well as the "peer-review" angle (other physicians
>taking aim at a competitor for doing "unnecessary" medicine).
>
>So while EBM clinical pathways, or just clinical protocols and pathways of
>any kind, are good to keep mediocre doctors from falling below standard, they
>also run the risk of "dumbing down" medicine and also perhaps helping to run
>the best doctors out of town.
>
>Joe P.
>
>P.S. Just as an aside... (or a post script... hehe)
>
>The "evidence" which makes up many EBM protocols is not always applicable to
>the patient in question, depending upon where you are. A good example is the
>Canadian tocolytic study (by Hannah et al?), which used ritodrine and
>concluded that tocolytics don't work for longer than 48 hours, etc, etc.
>This, and studies like it, are often used to define "standard", at least for
>protocol development, of tocolytic drugs.
>
>However, as we years ago decided in a resident journal club, that paper gave
>results of a study of a drug we DIDN'T use, on patients we WOULDN'T use it
>on, in a way we WOULDN'T use it.
>
>So how, if we were out in a private hospital, let's say, would we be held
>accountable for a protocol based on such data? We SHOULDN'T be, but we COULD
>be...

--
art fougner, md

A series of 1000 cases begins with but a single anecdote.





use when must restrict search to only the ob-gyn-l forum...
Enter search keywords:
Returns per screen: Require all keywords:

Return to  OB-GYN-L Mail a New Message to the Forum: ob-gyn-l@obgyn.net
Forum Administrator: geffrey.klein@obgyn.net
Report Technical Problems: webmaster@obgyn.net
Last Updated: Wed Dec 2 04:49:48 2009

The American Medical Association is no longer designating CME hours for AMA Category II CME credit. However, physicians themselves may self designate learning activities as Category II CME credit hours if they feel it is of sufficient educational merit and meets the formal definitions of continuing medical education. OBGYN.net believes these interaction in this forum meets these criteria. For further information see the AMA web site.