To: Lane3 who wrote (16099 ) 4/7/2010 7:12:35 PM From: TimF Read Replies (1) | Respond to of 42652 Govt Muzzles More By Robin Hanson · March 31, 2010 1:30 pm Sponsorship [of pharmaceutical research and drug trials] by manufacturers has been found to be associated with a reduced likelihood of the reporting of adverse results. Likewise, a significant link has been found between industry funding and the likelihood that results of a randomized trial will support a new therapy. … One proposed solution to this problem is to increase public funding for the conduct of research on therapeutic effectiveness. Ironically, that may well aggravate the problem. In July 2007, AcademyHealth, a professional association of health services and health policy researchers, published results of a study of sponsor restrictions on the publication of research results. Surprisingly, the results revealed that more than three times as many researchers had experienced problems with government funders related to prior review, editing, approval, and dissemination of research results. In addition, a higher percentage of respondents had turned down government sponsorship opportunities due to restrictions than had done the same with industrial funding. Much of the problem was linked to an “increasing government custom and culture of controlling the flow of even non-classified information.” Of particular concern is a provision of the Senate-passed Patient Protection and Affordable Care Act, [regarding] the … new Patient-Centered Outcomes Research Institute to conduct comparative-effectiveness research. The bill allows the withholding of funding to any institution where a researcher publishes findings not “within the bounds of and entirely consistent with the evidence,” a vague authorization that creates a tremendous tool that can be used to ensure self-censorship and conformity with bureaucratic preferences. This appears to be an effort in part to bypass the court order in Stanford v. Sullivan, a case involving federal contractual requirements that would have banned researchers from any discussion of their work without pre-approval by the Department of Health and Human Services. The order held that such blanket bans are “overly broad” and constitute “illegal prior restraint” on speech. The language in the Senate bill attempts to overcome this hurdle by eliminating prior restraint, but using the threat of post hoc punishment as an incentive for self-censorship. That was written Feb 8; I just contacted its author and he doesn’t know if this made it into the final med bill or not. Alas this bodes poorly for the new comparative-effectiveness research program.overcomingbias.com Steven March 31, 2010 at 2:15 pm | Reply It’s in the final version of the bill. Section 6301 of the Patient Protection Act (Public Law No: 111-148) adds the following section to the Social Security Act: “Any research published under clause (ii)(IV) shall be within the bounds of and entirely consistent with the evidence and findings produced under the contract with the Institute under this subparagraph. If the Institute determines that those requirements are not met, the Institute shall not enter into another contract with the agency, instrumentality, or entity which managed or conducted such research for a period determined appropriate by the Institute (but not less than 5 years).” This act was subsequently modified by reconciliation, but looking at the table of contents reveals that Section 6301 was not among the modified sections.overcomingbias.com Michael Caton April 1, 2010 at 3:46 pm | Reply RE the meta-finding that sponsored drug studies more frequently have positive answers regarding the treatments of the sponsors – this not necessarily indicative of twisting the truth and is better explained as a form of editorial control over research questions. That is, if you spend money developing a drug, you’re going to try to develop uses of it that you have a pretty good feeling in advance WILL WORK, and you’ll ask limited questions appropriate to that. You can have a better than 50% sense of whether something will work before you investigate it with rigor to get a MUCH better than 50% answer that it works. So I would argue the effect we’re seeing is more the result of conservative investigations than bias, and this is not inappropriate. But it’s worth thinking of ways to distinguish the two possibilities.overcomingbias.com