Now here are my "claimers:" recent media accounts of this novel approach border on the irresponsible, and point to serious problems with the way many media outlets cover translational clinical research. My second "claimer" is that such media coverage has important consequences for patients and the research community.
Finally, a point of clarification: my comments below concern the quality and consequences of media coverage, not the merits of the medical procedure discussed.
Here is the background: on November 20, the Globe and Mail ran a feature by veteran reporters André Picard and Avis Favaro titled "Researcher's labor of love leads to MS breakthrough." The story described a novel theory of an Italian researcher, Paolo Zamboni, that MS "is not, as widely believed, an autoimmune condition, but a vascular disease. More radically still, [an] experimental surgery offers hope that MS... can be cured and even largely prevented." Said Dr. Zamboni, "I am confident that this could be a revolution for the research and diagnosis of multiple sclerosis." The news story then describes an Italian study that performed the surgical procedure in 65 patients; the patients saw their disease virtually eradicated.
Like practically every other news article of this species, the reporters do two things. First, they truck out a few patients to proclaim the miracle cure (said one: "I don't remember what it's like to have MS"). Second, to establish credibility, the reporters throw in the perfunctory killjoy comments of a few scientists: "skeptics warn the evidence is too scant and speculative."
As observed on the excellent NPR program On the Media, media coverage of medical research and breakthroughs "overflow with optimism and excitement, offering hope for millions." According to long-time media analyst Gary Schwitzer, "What they don't overflow with is accuracy, context and journalistic responsibility." (Schwitzer, by the way, runs an excellent blog on health news coverage).
Here are some concerns I had about the Globe and Mail story:
• the story reports on clinical research findings. The story did not say, however, that the results have not been published and subjected to peer review.
• the story did not say whether the studies were well-designed: was there a control or placebo arm, for example? the story did not mention that placebo responses can be especially high in the setting of surgical interventions. Nor did it mention that placebo responses are often high in the context of remitting diseases like MS.
• the story wrapped logical fallacies within emotive proclamations. For example, what, precisely, could it possibly mean to say "I am confident this could be a revolution..."?
• the story was not linked in any way to any particular event. Usually reports like this follow from major scientific publications, or presentations at medical conferences. This story, however, is "free floating"- which makes it much more difficult to contextualize (why is it being reported now? how well have the findings been vetted? how did the researchers capture the attention of journalists?).
• the story contains statements that are deeply suspicious. One example is that Zamboni claims MS is not an autoimmune condition. Here is the very first line in the abstract of Professor Zamboni's most recent publication: "Multiple sclerosis is primarily an autoimmune disorder of unknown origin."
• the story did not address the correlation and causation problem. The story (and Zamboni) claim that vascular malformations cause MS symptoms, because the researcher discovered that many MS patients have "malformed or blocked" veins draining the brain. But an alternative explanation would be that malformations or blockages are themselves caused by MS- that they are symptomatic rather than causal. Any news coverage of correlation should always address the issue of cause.
And the consequences? Do a google search yourself on the procedure (CCVSI) to find out how much chatter there is among expectant patients, who (judging from discussions) are wondering whether they can travel to Italy to receive the "treatment." And today, the Globe and Mail reports that the MS Society of Canada- portrayed as sourpuss nabobs of negativism in the previous article- will now fund CCVSI "with significant research dollars" in response to "the overwhelming public response to the media stories."
Surely, more research, more trials, more basic science is needed. If indeed this approach is a promising as reported, it should be subject to rigorous clinical testing. But can anyone seriously argue that media coverage of this low quality should set the research agenda and decide how scarce research resources are allocated? (photo credit: xbloodsin, sepulcrum, 2008)
9 comments:
Interesting blog. I just randomly stumbled on to it. I may actually be involved in a study evaluating this "venous blockage" idea of MS (there is some theoretical science supporting it), but I totally agree with you. Without actual clinical trials it is irresponsible of the media to have such one-sided reports on "miracle cures" (this isn't the first case - it's all about ratings). The problem is that most science reporting is not done by scientists.
MXH- thank you for your kind words about my blog. While I agree with you about the problems with "one-sided" coverage, I actually think there are plenty of good science journalists who are not themselves scientists.
Whether covering politics, business, foreign affairs, or even art, key components of journalism include thinking skeptically, asking critical questions, and being nosy. Too often (though not always), science and medical journalists opt instead for the seductive narrative of miracle.
Yes, venous blocks can be due to MS. But what matters is that the procedure has given relief to lot of patients already. The fact of the matter is that the final proof are the people who have gained from this. If this was not the case, CCSVI theory would have died down by now.
You also talk about correlation and causation. A single person can hardly unravel such a complex question. It will take time. By the same token, how do you correlation explain smoking. All we have is statistics. We also N number of cases where smokers dont develop cancer.
The bottom line is simple, if it helps it is good. And if it placebo effect, so be it (and so is Tsyabri)
Sharan: Thanks for your response to my posting on CCVSI. I can't say I entirely agree with you. As I note on the blog, CCVSI remains unproven as an effective therapy for MS.
However, the surgical approach- like all surgical approaches- entails considerable risk and expense. So it is disturbing indeed if patients- already weakened by their illness- are made worse off medically and financially by submitting to a procedure that may not have any benefits at all.
Your response raises the possibility that CCVSI may work by triggering a placebo response. This is, indeed, a possibility. But then, the question is: how long does a placebo response last before it wears off? Are there other, less invasive and costly ways of achieving a similar placebo response? And do the practitioners who offer CCVSI to patients explain that they think the benefits (to the extent that they occur) may be entirely due to a placebo response? Of do they try to sell the procedure with theories and explanations that have not yet been validated?
Curiously...you speak of the cost and risk. There is CONSIDERABLE cost and risk involved in the drugs that neurologists put us on. If the buildup is caused by the MS, having the procedure to get back your life suits me just fine. I have endured taking shots that do other things to my body (one of which I believe caused a cancer...but again, of course...who knows). I don't remember what it is like to run anymore...bend and pick things up without needing help getting back up. I would love to have feeling in my hands again. If this procedure would give me back my life, then I would want this done. What say all you sufferers who are told these nasty shots are all you can do?
I actually think there are plenty of good science journalists who are not themselves scientists.
Nice points…I might notice that as someone who really doesn’t comment to blogs much (the truth is, this may be my first put up), I don’t suppose the term “lurker” is very flattering to a non-posting reader. It’s not your fault at all, but maybe the blogosphere could provide you with a better, non-creepy name for the 90% of us that take pleasure in studying the posts.
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