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» LymeNet Flash » Questions and Discussion » Medical Questions » Credibility of ILADS guidelines -- can someone 'splain me?

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Author Topic: Credibility of ILADS guidelines -- can someone 'splain me?
minoucat
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So...I was speaking the other day to someone closely involved in the library-science end of biomedical research whose only connection to Lyme disease is...me. She said the ILADS guidelines would be perceived by academics and powers that be as not being particularly credible because of the way they were published -- not in a major peer reviewed journal, etc.

Can anyone tell me more about this? If it is so, is ILADS going to correct this with their new guidelines?

What does having the ILADS guidelines on the online National Guidelines Clearinghouse actually mean?

I realize that the politics of academic publishing can be fierce, and that journal editors with a strong viewpoint can and will refuse to publish articles that have a premise with which they don't agree, or that are not ammended to their satisfaction. What I don't know is how common this is, and if it is a factor for ILADS.

My PCP, when I gave him the guidelines, appeared to be much less concerned about who published the guidelines than who wrote it. The first thing he did was to read down the list of authors. He recognized many of the names, from conferences, other publications, and personal contacts, and that is what seemed to give the guidelines their credibility for him. (I know he later made some calls and did more research on his own.) He incorporates a lot of non-allopathic treatments in his practice; it wasn't the same situation as confronting the neurologist or other docs.

I'd just like to be forewarned...

[This message has been edited by minoucat (edited 13 April 2005).]


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Areneli
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In addition, this publication is based not only on published articles but also is partially based on Conference abstracts and speeches.


This will bring some question marks by these who are strictly biomedical.

Still, this is the best we can get these days.


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NP40
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If I'm not mistaken doesn't the National Guidelines Clearinghouse establish treatment protocol's for the NIH ?
Posts: 1632 | From Northern Wisconsin | Registered: Jan 2005  |  IP: Logged | Report this post to a Moderator
lou
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Well, if you know how to get anyone in the medical establishment to print anything other than the Steere/NIH/CDC view of lyme treatment, please clue us in! In the past, those journals have even refused to print letters in response to Steerite articles. Do you think they will print treatment guidelines?

Basically, those folks would not touch this with a ten foot pole.

So, ILADS did the best they could under these lousy circumstances.


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