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Sue Pelletier MeetingsNet mad blogger, and editor of Medical Meetings magazine After spending my first 10 journalistic years mired in sewage sludge and garbage as a writer and editor of...more

Archive for December, 2011

Survey says some docs see quality slide as commercial support declines

A survey conducted by MDlinx earlier this month came up with some shouldn’t-be-unexpected results: That a quarter of the docs surveyed say they’re seeing the quality of their continuing medical education activities decrease as pharma pumps fewer dollars into commercially supporting CME. Two-thirds didn’t notice any change, and a scant 9 percent thought quality was improving, according to an article in Medical Marketing & Media. Most notably on the decline was faculty, they said, though they also said it was harder to find the education they needed, and that they had to pay for more of it themselves.


This quote at the end of the article is really interesting, I thought: [Stephen Smith, chief strategist, MDLinx] called the perceptions of lesser quality an unintended consequence of the increase in regulation on pharmaceutical companies’ communications and their resulting pull-out from CME. “We’ve squeezed everything toward mediocrity to prevent abuses.”

CMS’s new rules around the Sunshine Act

Some pretty big news came out last week while I was in San Diego for our West Coast Life Sciences Meeting Management Forum: The Centers for Medicare & Medicaid Services announced a proposed rule designed to increase public awareness of financial relationships between drug and device manufacturers and certain healthcare providers, as required by the Sunshine Act provision of healthcare reform.


From a pharmaceutical/device meeting manager’s perspective (which I got last week in spades, being surrounded by these good folks), no one seemed to be anticipating it making much of a difference in their lives. The biggest issue for them was CMS’s delaying the collection of data on physician spend from Jan. 1, 2012, until after final regulations are issued.


I heard over and over again that if they weren’t already tracking physician and other healthcare worker spend as a requirement of a corporate integrity agreement, they have been working since healthcare reform passed to get a system up and running. In fact, a survey of the forum’s participants found that 88 percent had a system already to track their spend on physicians and other healthcare professionals, and 76 percent were either already testing their system or were confident that their system was ready to roll with the new year.


But that’s about as far as I’ve had time to get with CMS’ announcement. I’m not sure whether it’s a blessing (so thankful someone’s keeping on top of all this!) or a curse (ain’t no way I can keep up with the flow of information the dude puts out, much less beat him to the punch, so I have to live with being continually scooped!), but Tom Sullivan has been churning and burning all this up on his Policy and Medicine blog. Keep in mind that he comes at it from a pro-collaboration perspective, but he provides a great overview of possible affects this announcement could have on the CME community. Some posts to check out:


Physician Payment Sunshine Act: CMS Proposed Rule - Impact on Continuing Medical Education, Medical Societies and Patient Organizations


Physician Payment Sunshine Act: CMS Proposed Regulations — Public Posting, Data Submission and Correction


Physician Payment Sunshine Act: CMS Proposed Regulations Delayed Reporting for Clinical Trials, Penalties and Preemption




Physician Payment Sunshine Act: CMS Proposed Regulations – The Cost for Sunshine


Physician Payment Sunshine Act: CMS Proposed Rule Overview




Physician Payment Sunshine Act: CMS Releases Proposed Regulations


Update:Daniel Carlat, MD, has a different take on how the new rules could affect CME (namely, he’s ecstatic that the language could include faculty honoraria in reportable income) on his Carlat Psychiatry blog.

ACCME responds to REMS blueprint and other news

The Accreditation Council for CME’s latest monthly e-newsletter includes a link to the ACCME’s response to the FDA’s release of a blueprint for the prescriber education component of the Risk Evaluation and Mitigation Strategy (REMS) for long-acting and extended-release opioid medications (ACCME Standards for Commercial Support.


The ACCME also has added some new examples to its compendium of complaint summaries (PDF download). If you haven’t check it out yet, I highly recommend that you do—it’s a good way to see how the ACCME handles potential problems, and is something you can check your own work against to make sure you’re not doing something it may find suspect (though, as one confessional medical educator points out, the mistakes in the compendium are so boneheaded that it’s hard to believe the providers at issue could actually be making them at this stage in the game).


The accreditor also announced its new board of director lineup: Sandra Norris, MBA, and James Burke, MD, are the 2012 Chair and Vice-Chair of the ACCME. Other board members include Todd Dorman, MD; Mira Irons, MD; David Pieper, PhD; and Carol Havens, MD.


The e-newsletter also reminds ACCME-accredited providers that it’s never too soon to get the jump on entering your data into the Program and Activity Reporting System (PARS). I get the feeling they’re really prefer you not to wait until the March 30, 2012, deadline to enter your 2011 data. Another deadline is coming up January 31, 2012, when your 2012 ACCME annual accreditation fee is due.

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Twitter fountain for the 4th Annual Life Sciences Meeting Management Forum


Yep, there was a whole lot of tweeting going on (mostly by our staff and speakers, but still…)

Twitter fountain for the 4th Annual Life Sciences Meeting Management Forum


Yep, there was a whole lot of tweeting going on (mostly by our staff and speakers, but still…)

Summary of #CMEChat 35: Re-engineering the Data Stream

Continuing medical education professionals from around the world gathered via the #CMEChat hashtag on Twitter on December 7 to talk about what can be done to improve how new information flows from annual conferences to local practices. They used Medical Meetings’ November/December issue’s cover story as a jumping-off point. As one person pointed out, we need to find a way to curate the data presented at annual meetings more effectively.


They began by looking at what might be the best models for disseminating new medical information beyond major medical meetings, with “best” defined as being able to spread the word quickly to the widest possible audience while maintaining the integrity of the data. For the sake of discussion, the group decided not to complicate the process by saying the data would have to be available for CME credit; as one person said, “Credits have never been proven to motivate learning. They have been proven to complicate education.” Another chimed in to say that adding accreditation to the mix would just slow the dissemination process.


Most appeared to agree that medical societies and associations should develop clearinghouse models that enable rapid and open access, and that authors should take responsibility for ensuring that questions about the data they present are answered, at least during a specified period of time. Chat moderator and MM columnist Brian S. McGowan, PhD, suggested that local institutions could use technology to pull new medical information into their networks, and that these institutions could then stream feedback into the clearinghouse system to refine the model over time. One person suggested using bloggers as disseminators. While one participant was concerned about the possibility of bias that could come from filtering the information through a blogger, another pointed out that there could be value in having that personal point of view.


It’s vital, said one, that the data go where the learners are, instead of trying to make learners come to the content. Learners also should be able to access the system whenever is convenient for them.


Pros and Cons of Slide Decks

The moderator then asked about the pros and cons involved in having medical associations create and archive core slide decks that would become available when the data is released. “Archiving is critical,” said one person, as is organization and searchability so it’s easy to pull up X talk at Y meeting about Z topic. Otherwise it can be too challenging to find information that is applicable to the specific needs of someone’s practice.


Having a data clearinghouse as the core model not only would ensure data fidelity, but it also “would save tens of millions of dollars,” said one participant. However, said another, while a clearinghouse model works in an ideal world, there already are “10 million ‘clearinghouses’ for primary care docs.” Another countered that, while there are many channels, there currently is no true clearinghouse for new medical content. One possibility would be for each medical society to have its own clearinghouse. It would be up to the medical society to control the quality from the start, so that the data stream doesn’t become polluted with too many insignificant data points. Of course, there still can be disagreement among associations, such as the difference between the American College of Physicians and the American College of Radiology on when to require mammograms.


Of course, one practice’s insignificant data points is another’s very significant data points, depending on that practice’s needs. This led the moderator to ask the chatters to guesstimate the balance of core content to local content in an average CME program. They seemed to agree that for national meetings, the core-to-local ratio would be high, “at least 90-to-10 if not higher.” But that’s as it should be, said one person: “Local content = context. Core content shouldn’t be different anywhere.” At a minimum, said another, the intro and background sections could be shared. While one would think that there would be more contextual information coming from regional meetings, that’s not always the case, said one person.


Authors as Data Shepherds

One point that kept recurring was that it would be key to any data dissemination model to have faculty easily accessible to answer questions. “In many cases, Q&A has the most valuable information for the learner,” said one person. And, said another, it’s when “participants wake up.” Data shepherding currently is done through things like letters to the editor in a journal. The problem is that it can take five months to get an answer, and it’s behind a paywall to boot, which further limits access. A better way would be to have faculty or an editor on retainer to prompt timely responses to questions, say up to six months post-release. Learners could ask their questions online (possibly even through social media), then their answered questions could be included in the archive, along with the data. One of the CME chat participants mentioned he has been doing this on his blog by posting questions he has posed to the Accreditation Council for CME, along with their answers. (Here are a few examples: Needs assessment collaboration and independence; incentivizing surveys; accreditation language; defining commercial interest). But, he added, it would be better if the ACCME did the archiving. “Without curation, the system fails to help.”


But who is to do the curation? Should/could the vetting of core slides be done via crowdsourcing? The crowdsourcing could be done through Slideshare, blogs, tweets, Prezi, podcasts, simulations, etc. But then someone would have to take it all in and organize it. One person thought it should be up to each “house of medicine” to control and refine the new medical knowledge as it is vetted; “We can then use this data to educate.” Another participant thought the CME community could use an “uber curator” (which, along with being a good idea, someone thought would make a great name for a rock band). What we need, said one person, is to put a mashup of ACCME, PubMed, SoMe sites, and IBM’s Watson into a blender. Once we work through the barriers of cost, determining what the core content would be, gaining faculty support, etc., what would we end up with? A newly re-engineered data stream.

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Pfizer’s reorganization: Bye-bye, unsolicited grants

Pfizer recently reorganized its Medical Education Group in a pretty dramatic way, including moving 90 percent of its budget into a request-for-proposal model, rather than one based on unsolicited grant requests (here’s a fairly thorough run-down of the changes). Another big change is that the model is no longer going to be CME-centric; CME, accredited or not, may not get a very big piece of the Pfizer pie moving forward. While MEG leader Maureen Doyle-Scharff tells me that this is actually an opportunity for CME providers to prove their relevance to the big performance-improvement picture, I’m not so sure everyone would agree.


First GlaxoSmithKline limited the possible field of contenders to just 20, then Pfizer decided to eliminate medical education companies from their grantee mix, and now this. Like it or not, the grant-making models are changing.


What do you think of the evolution of commercial support models? How have these changes affected the CME community? What else do you think will be coming down the pike? (If you don’t want to leave a comment below, please e-mail me at spelletier@meetingsnet.com. I really want to know what people think about all this.)

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