Sepia Mutiny on CRUDE
See http://www.sepiamutiny.com/sepia/archives/004996.html#more
The History Channel is re-airing CRUDE on Friday Feb 22 at 8 am. You can also watch it online here.
See http://www.sepiamutiny.com/sepia/archives/004996.html#more
The History Channel is re-airing CRUDE on Friday Feb 22 at 8 am. You can also watch it online here.
A few years ago, a documentary fillmmaker from the ABC in Sydney (that’s the Australian public television network) spent a day with me in Boston, talking about oil politics. His film, which he dubbed “Crude” (after kindly discussing it with me), came out in Australia a few years ago, and won a slew of awards. It has some amazing footage in it, the least of which are some clips from that day in Boston with me. (A film crew followed me around at the grocery store while I pretended to shop. Slightly embarassing.)
This Sunday, the film airs on the History Channel here in the US. The New York Sun previewed it and mentioned the appearance of yours truly:
“The investigative journalist Sonia Shah,who wrote the equally sweeping 2004 book “Crude: The Story of Oil,”lends an ever-so-slight analytic edge with trenchant demonstrations of oil’s inescapability: Plastic-wrapped supermarket veggies from distant farms, for example, pack the double whammy of petroleum-based packaging and gas-guzzling truck transport.”
The film CRUDE airs on the History Channel on January 27, 2008 at 8 pm.
But that wasn’t quite it, either. The “study” had no control group,because nobody wanted to NOT use the checklists. In other words, theerstwhile researchers felt they knew that it WOULD work. In which case,they were simply trying to improve patient care with a provenintervention and no IRB or informed consent was required.
So was it really a “study” or was it actually a “program”? Did they know it would work or didn’t they? How confused were they?
Well, in the actual doing of the thing, the clinicians conductedthemselves as if it were a program of improved care, but then when theywrote up their results in the NEJM, they cast their work as anexperimental ’study.’
That’s not right, either: you can’t have it both ways. Someonecomplained to the OHRP, which opened some kind of investigation, whichthen led to Gawande’s complaint, and a flood of angry letters to theOHRP. Phew!
All of which is to say: there’s a shifting line between what we say weknow and what we say we need more research on. When there’s somethingwe want to do, when there’s political will and money to do it, wedispense with “research” quickly and move on to implementation. Inother areas–say, the administration of expensive drugs to poorpeople–there are endless calls for studies and experiments to provethe same thing over and over again, putting subjects at some risk everytime, because intransigent authorities (drug companies, healthministries) find it politically more expedient to say “we need moreresearch” instead of “sorry, no” (or “absolutely not, who cares aboutpoor people who don’t buy lots of stuff.”)
Fyi, these were the checklisted items, as reported in the NEJM, used inthe ICU on patients with catheters: hand washing, using full-barrierprecautions during the insertion of central venous catheters, cleaning the skin with chlorhexidine, avoiding the femoral site if possible, andremoving unnecessary catheters. The implementation of these procedurescoincided with a precipitous drop in the number of catheter-relatedinfections, but without the control group, no cause and effect can bedetermined, at least not by this study.
Canada.cominterviewed the curator of a new exhibit on energy and oil, who verykindly mentioned my book CRUDE as one of 2 interesting books on thehistory of oil….the other being Yergin’s The Prize! Good company.Thanks for that.
I find this interesting, given that the French actually have some of the very best laws protecting clinical trial subjects in the world. Could reader interest in this topic be viewed as some version of rubbernecking? Perhaps so.
Well, Pfizer’s drug, Exubera, was a bust. They “only” sold $12 million worth of it, and so now they are going to stop selling it! First it was the best thing since sliced bread, but now…since they aren’t making the billions they foresaw, they’re dumping it. So much for those users who did switch and actually liked it. They’re screwed.
Basically, the drug was a bust because it was no better than injected insulin and on top of that, it messed up patients’ lungs. A total disaster.
Now, a new company called Mannkind, backed by a billionaire investor, is launching a new inhaled insulin called Technosphere Insulin, similarly gloating–while the drug is still in clinical trials–that they will make billions on the thing. The New York Times business section featured their glossy PR in an article this morning, replete with a large pic of the billionaire investor looking smug in his grand digs. He might as well have had dollar signs tattooed on his eyeballs.
Buried near the end of the story we learn that–already!–more patients taking the inhaled insulin have dropped out of clinical trials than patients taking the old standby, injected insulin! “For reasons that are not yet clear”! Well, there can’t be any reason, in my mind, that doesn’t bode poorly for the inhaled insulin. They didn’t like it, they had adverse effects, or whatever.
And, the chief medical officer has accused the company of hiding information about the drug from the FDA! The company, in response, fired him. But we’ll never learn about the dirt he found because his wrongful termination suit has been settled out of court!
This thing seriously stinks. And it is all the more remarkable for the fact that all of this dirty laundry about the drug is tucked into what is overall a glowing business story.
Check it out: http://www.nytimes.com/2007/11/16/business/16mannkind.html?_r=1&oref=slogin
When I went to Cameroon, I visited villages where ExxonMobil had said it had distributed thousands of free nets; and yet the people I met at the malaria clinic there said they didn’t know a single person who actually used one. I got the same response when I asked people at a malaria clinic in Malawi, and in Panama. They said the nets are hot, that people have different priorities (like using the netting for fishing, wedding veils, curtains), that the nets get holes in them, that malaria isn’t taken seriously enough, and so on.
It sounds nice for donors to be able to say they distributed lots and lots of free nets (marketing the nets is slower), but they should also track how many people actually use the nets.
What’s really needed is greater transparency, but the Nigerian authorities are not asking for that. They’re asking for payback. The bad PR that Pfizer will inevitably get may very well make drug companies more secretive about their activities in poor countries–which will make clinical trials more dangerous for trial subjects everywhere.