December 04, 2006

Atypicals Have No Advantages

As I mentioned on Friday, the latest results of the landmark, NIH-funded CATIE study, which measures the performance over 18 months of second-generation antipsychotics versus one first-generation antipsychotic in treating schziophrenia, came out in the American Journal of Psychiatry. This is the second--and final, I believe--phase of results from the study and this time out (I have blogged about the other phase here) what researchers tried to measure is whether there was any cost differential between using older drugs versus the newer ones and whether there was any quality of life differential between the two groups of drugs.

I have read the primary paper, the accompanying editorial, an accompanying paper assessing whether the same kind of potential differentials could be detected in other randomized studies of similar drugs in schizophrenia, as well as a final CATIE paper on the effectiveness of switching meds on patients. Needless to say, my head is full and my eyes are tired. AJP has not updated its website with the relevant links yet, so I'll pass those along later.

In addition, a recent somewhat-analogous British study came to much the same conclusions.

There is no need for a thorough treatise here. The atypical antipsychotics--Zyprexa, Seroquel, Risperdal and Geodon--proved to be much more expensive (to the tune of $300 a month) than was the lone old antipsychotic (perphenazine, a medium-core typical antipsyhcotic), once all associated health care costs (meds, inpatient and outpatient treatment) were taken into consideration. Second, the newer drugs did not improve patient quality of life--the researchers hit upon a complex index of symptoms, side effects, cognition--over perphenazine. What's more, regardless of the drug involved, patient quality of life didn't improve much at all, despite patients being med-compliant. Sigh.

At this point, the atypicals have lost whatever perceived value they once had, although their respective makers were out with lame attempts to spin the study's results soon after they became available. It is discouraging to me that after a decade-plus of feeding these meds to profoundly-ill schizophrenics, and offering up reams of promises in the process, that they have not turned out to be the silver bullet or the great hope that everyone in the mental health world thought them to be. I first noticed that the atypicals didn't seem to improve things for schziophrenics in 2004, when I did a bunch of reporting on community mental health work in the Seattle area and in Western State Hospital. The positive and negative symptoms were still as present as the first time I began paying attention to chronic schizophrenics in the mid-1990s. In fact, I was so confused by the discrepancy that I didn't explore it formally in print for another year. It's been interesting over the past year to see my reportorial hunches turn out this way.

I wish that I had been wrong. So do millions of schizophrenics.

Really, all that's left to be said is that, despite these findings, insurance companies and bean counters should not restrict access to these drugs for patients because of the cost imbalance. It should be a choice made by their doctors and themselves, and access should be open and equal.

That said, however, it is clear to me that the time has come for researchers, doctors, patients and health care systems to band together and press the pharma comapnies to dramatically cut the prices on the atypicals. These drugs cost anywhere from 8 to 20 times the cost of older, off-patent meds, but in no way is the cost differential justified in terms of clinical performance or patient quality of life.

NAMI and MHA and the American media have an important role to play in helping to make that happen. So far, they are silent. But, then, so is damn near everyone else.

There are other implications as well, but those are for another post.

Posted by Philip Dawdy at December 4, 2006 12:01 AM
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Comments

After watching my daughter live a non quality life on Zyprexa for nearly a decade, then see her unable to come off of it, reading the MHA news bulletin, and reviewing my own recent 8 week Seroquel trial, this entire thing, leaves me completely depressed.
I truly believe the drug companies have mislead the public with false hope and misrepresentation regarding products such as Seroquel and Abilify, among others. I think a class action lawsuit is in order beyond the diabetes angle.
When I called a Zyprexa attorney 2 years ago, I asked him if he was going to go after other side effects. (such as brain addiction, psychotic reaction, paradoxical schizophrenic reaction)the answer then was no.
I'm thinking of calling him back now.
Regarding the anon doctor? he wants his knee caps in place.
Yeah, being a whistle blower up against a billion dollar company isn't a good way to get a good nights sleep.

Any one unhappy with the last decade of lack of progress in the mental health system should start making a lot of noise.
As small as it sounds, and journalist's will disagree with me (right?) I say a 10 second TV sound bite could start something big. It could get other media outlets interested.

You know, such as "Woman sues drug manufacturer over false claims for a quality life and weight gain on bipolar medication.News at 6pm".

Forget the professionals , Nami, and all the rest remaining silent....

Hello consumers/patients!! speak up!!

Posted by: Stephany at December 4, 2006 07:57 AM

Part of a post of mine on my blog:

"Nearly a decade has gone by and look where we are. My daughter has had numerous horrific hospitalizations, a boatload of med trials that really stands alone as a chemical lobotomy of her mind, and now I am struggling as well to find the right med.
They told me false promises and lead me down the path believing meds were the end all be all answer to my life and my daughter's life, and now we are all ripping our hair out asking ourselves what the fuck happened."

Posted by: Stephany at December 4, 2006 08:04 AM

It's about time we started thinking about some radically different ways to treat schizophrenia frankly. Have you or your readers read "A Beautiful Mind"? It's certainly my opinion that John Nash was saved by having the bare minimum of pharmaceutical treatment, something that was grossly misrepresented in the movie. You can read a review of the book I wrote on Amazon entitled "The Unstated Lesson". Also read Dan Dorman's book "Dante's Cure" or Robert Whitaker's "Mad in America" or this article: http://psychrights.org/Research/Digest/Effective/MIrwinSxReversalNoDrugs.pdf. As long as we keep treating psychosis with mind altering drugs we are actually reducing the chances of healing.

Posted by: Sara at December 4, 2006 08:08 AM

Sara, I totally agree.

"As long as we keep treating psychosis with mind altering drugs we are actually reducing the chances of healing."

Posted by: Stephany at December 4, 2006 11:20 AM

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