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  Vol. 301 No. 24, June 24, 2009 TABLE OF CONTENTS
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Clinical Practice Guideline Development and Antitrust Law

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

To the Editor: The Connecticut attorney general's antitrust investigation and settlement with the Infectious Diseases Society of America (IDSA) regarding its development of clinical practice guidelines for Lyme disease offers important guidance for strengthening the integrity of clinical practice guideline development and preserving clinical discretion. I believe that in their Commentary, Mr Kraemer and Mr Gostin1 mischaracterized fact and misread the relevant law in criticizing the attorney general's intervention as political and purporting to defend the supposed positive, scientific character of clinical practice guidelines against the imposition of normative goals. Contrary to their argument, the attorney general's intervention can in fact advance evidence-based medicine.

First, the authors misleadingly likened guideline development—which only faintly resembles the scientific method—to bench science.2 Guideline development has also proved vulnerable to due-process irregularities, through conduct and conflicts of interest, just as the attorney general found here.

Second, Kraemer and Gostin erroneously asserted that the attorney . . . [Full Text of this Article]

Richard Wolfram, JD
rwolfram@rwolframlex.com
New York, New York



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RELATED ARTICLES

Science, Politics, and Values: The Politicization of Professional Practice Guidelines
John D. Kraemer and Lawrence O. Gostin
JAMA. 2009;301(6):665-667.
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Why Guideline-Making Requires Reform
Allan D. Sniderman and Curt D. Furberg
JAMA. 2009;301(4):429-431.
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RELATED LETTER

Clinical Practice Guideline Development and Antitrust Law—Reply
John Kraemer and Lawrence Gostin
JAMA. 2009;301(24):2549-2550.
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