Epidemic of Mental Illness — Yes or No?

Fascinating review of three books on psychiatry, conflicts of interest, over medication and ultimately the culture of U.S. money driven medicine in the N.Y. Review of Books by Marcia Angell. This is a two part series. Part 2 is here. Comments here.

Among other issues Angell looks at:

What is going on here? Is the prevalence of mental illness really that high and still climbing? Particularly if these disorders are biologically determined and not a result of environmental influences, is it plausible to suppose that such an increase is real? Or are we learning to recognize and diagnose mental disorders that were always there? On the other hand, are we simply expanding the criteria for mental illness so that nearly everyone has one? And what about the drugs that are now the mainstay of treatment? Do they work? If they do, shouldn’t we expect the prevalence of mental illness to be declining, not rising?

She discusses that there is a misunderstanding of the basis of these diseases; that they are over diagnosed; that neurotransmitter theories are unproven and probably wrong; that the pharmaceutical industry is funding (Medicynical Note: corrupting) psychiatry and psychiatrists more than any other specialty; placebo treatment in depression is virtually as effective as antidepressants; these drugs have serious long term side effects; and so on.

She concludes:

At the very least, we need to stop thinking of psychoactive drugs as the best, and often the only, treatment for mental illness or emotional distress. Both psychotherapy and exercise have been shown to be as effective as drugs for depression, and their effects are longer-lasting, but unfortunately, there is no industry to push these alternatives and Americans have come to believe that pills must be more potent. More research is needed to study alternatives to psychoactive drugs, and the results should be included in medical education.

In particular, we need to rethink the care of troubled children. Here the problem is often troubled families in troubled circumstances. Treatment directed at these environmental conditions—such as one-on-one tutoring to help parents cope or after-school centers for the children—should be studied and compared with drug treatment. In the long run, such alternatives would probably be less expensive. Our reliance on psychoactive drugs, seemingly for all of life’s discontents, tends to close off other options. In view of the risks and questionable long-term effectiveness of drugs, we need to do better. Above all, we should remember the time-honored medical dictum: first, do no harm (primum non nocere).

Read the articles and comments.


Avastin for Breast Cancer: NCCN Cost/Efficacy Not Our Department

Value in medicine appear to be an oxymoron. Despite having little evidence of efficacy but strong evidence of great cost, the National Comprehensive Cancer Network (NCCN) an ad hoc outfit that provides guidelines for cancer treatment has decided that Avastin should be available to treat cancer patients.

Apparently $80,000-$90,000 for treatment, for the drug alone, does not make them pause even a second on their recommendation.

Of course a significant number of the panel members who decided this, including the chairman are on Genentech/Roche’s payroll. (FYI Genentech/Roche makes Avastin)

The organization’s “quote” conflict of interest rules state:

Per NCCN policy (also on the website), disclosure of a relationship with an external party does not automatically disqualify an individual from committee membership.

The policy also states that committee members who have a “significant and direct or indirect interest with an external entity which constitutes a conflicting interest shall not participant in the NCCN Guidelines Panel’s discussion when the NCCN Guidelines Panel’s action or topic under discussion may advantage or disadvantage an external entity.”

However, the NCCN disclosure policy gives committee chairs discretion to allow panelists with potential conflicts to “participate for the purpose of providing or presenting information to the NCCN Guidelines Panel.”

Medicynical Note: Cost-efficacy doesn’t appear to be anyone’s responsibility. No wonder our non-system of health care is the most expensive by far in the world.

And no wonder our dysfunctional pathetic political non-system which oversees health care (as well as our national budget and debt “ceiling”) is the laughing stock of the world.


Medical Info Tainted by Drug Companies Bias — So What Else is New?

Not surprisingly drug companies do everything they can to get doctors to prescribe their products. It matters not that their medications are no better than generics, that their medications cost more than the annual average income in the U.S., that there are other better drugs available. They pay for the ads and for the prominence of the drug recommendations. Take the “wonderful” free app Epocrates: Please.

But like so much else on the Web, “free” comes with a price: doctors must wade through marketing messages on Epocrates that try to sway their choices of which drugs to prescribe.

and:

However, the marketing through Epocrates is more insidious, according to Dr. Adriane Fugh-Berman, an associate professor of medicine at Georgetown University and founder of PharmedOut, a nonprofit group critical of drug companies’ marketing practices.

“With targeted ads in Google, you may buy something that’s an unwise purchase,” she said. “But when a physician is influenced in Epocrates, it’s the patient (Medicynical addendum: and insurer) who’s bearing the financial and health risk.”

Dr. Fugh-Berman and other critics of drug marketing say the apps promote more expensive and sometimes less effective drugs. The companies say they are helping doctors find the best medicines.

Medicynical Note: This type advertising costs us all money, whether we pay directly for the medication or our insurer covers the cost. Doctors have lived too long in the world where cost is not a consideration in their treatment options. We need to encourage value, as well as efficacy, in health care. The U.S. has the most expensive, most inefficient and perhaps only non system of health care operational in the industrialized world. We can do better……..maybe.


People Will Die (I don’t know How Else to Put it)

This chart tells it all. Republicans had no problem with Bush but are determined to continue our recession/depression and health care by by cutting programs that benefit the poor, lower middle class, the sick and infirm the most. It’s letting them eat cake.


The Boehner bill to be voted on today will cut 1.6 trillion from “entitlements” which will include cuts in Medicare, Medicaid and Social Security. Meanwhile his party has vowed there will be no increase in taxes on anyone, including the weathiest individuals and corporations. Just to refresh your memory in the US the distribution of wealth is highly skewed to the wealthiest and has gotton more out of balance the last ten years:

Top 1% own 38.1%
Top 96-99% own 21.3%
Top 90-95% own 11.5%
And it gets much uglier as you proceed downward. Bottom 40% of population has 0.2% of all wealth.

Medicynical note: The cuts proposed by Boehner, the tea party, and the republicans in Medicare and Medicaid will result in much pain, suffering and deaths in the lowest income groups who cannot afford healthcare and rely on publically funded programs. Yes people will die.

We can and should do better by implementing health reform; providing rational coverage to the uninsured; controlling costs by evaluating treatment options and using the most cost effective; negotiating with suppliers on price; cutting the cost of administration.


Pervasive conflicts of interest in Medical Journal Reports

More on conflicts of interest: and here too:

Economic ties that could bias drug trials and patient care might remain hidden due to tangled disclosure rules at medical journals, a new study reveals.

Researchers found that of 131 cancer journals, only 112 had policies requiring researchers to state conflicts of interest, such as drugmaker stock ownership or speaker fees. And among journals that did have such policies, the rules were all over the map.

“Journals can’t even agree on what a conflict of interest means,” said Dr. Aaron S. Kesselheim of the Harvard Medical School in Boston. “It is certainly confusing to authors and to readers.”

Scores of studies have shown that when researchers have a financial stake in their work, their reports are more likely to promote drugs and downplay side effects.

Medicynical note: It’s hard not to be a little cynical. There’s nothing new here. We’ve the perfect system to make money not to deliver effective health care. In our country big money trumps reason.

Hospice Care – It’s About The Monry

Health, once a charitable calling has become a “business” opportunity.

As hospice care has evolved from its charitable roots into a $14 billion business run mostly for profit, patients like Covington and their families have paid a steep price, according to lawsuits and federal investigations. Providers have been accused of boosting their revenues with patients who aren’t near death and not eligible for hospice — people healthy enough to live a long time with traditional medical care. In hospices, patients give up their rights to “curative” measures because they are presumed to be futile.

And:

In 2009, a Medicare oversight report found nearly a third of hospice patients were not getting services in care plans that describe the treatment and visits providers promise to give them.

Medicynical Note: Left to themselves without standards or oversight, businesses work to maximize profit. In other areas, competition may work to assure quality.  In hospice care such competition may work as well but that remains to be seen.  What is certain, however, is that in the rush for immediate profit patients suffer needlessly.

In our local area, our “non-profit” hospice recently opened an inpatient facility. It was a financial stretch. To pay for it the hospice, it appears, is emphasizing the need for patients to reside in their facilty rather than remain in their home. This increases their payments from medicare and supports the inpatient facility but undermines the desire of many patients to be in their familiar home setting during the last stage of their illnesses.

And, the remarkably dysfunctional House of Representatives voted thursday to decrease the reach and function of the new consumer protection agency. They find it unimaginable that consumers should be protected.

 

Multiple Sclerosis Medications — Overpriced? Effective?

Drug companies take advantage of chronically ill patients and their families by aggressively marketing modestly effective drugs at inflated prices, especially in the U.S. This is commonplace for cancer patients who are coerced into paying $50,000-$100,000/year for drugs offering very limited benefit.

The same appears to be true in multiple sclerosis:

The drugs include beta interferons (brand-names like Avonex, Rebif and Betaseron), glatiramer (Copaxone) and natalizumab (Tysabri). They are given by injection or infusion and can help prevent MS symptom flare-ups and delay long-term disability from the disease. But the price tag is large, with each drug now costing upwards of $3,000 a month in the U.S.

And a study in the journal Neurology estimates:

They would gain an extra two months or less of good health over 10 years, the researchers say, compared with using only therapies that help ease MS symptoms — like medications for pain, fatigue and muscle spasms. Overall, the study estimated, DMDs cost close to $1 million for each year of relatively healthy life a person with MS could expect to gain with 10 years of use.

And if the drug is started earlier in the course of the disease:

The researchers estimate that starting the drugs before any noticeable disability makes the medications more cost-effective — though they still hover above $700,000 for each good-quality year of life gained.

It should be noted that while there is no hard and fast rule regarding cost-effectiveness in the U.S., costs exceeding $150,000 for a year of good quality life are consider excessive. Consider also that the average and median incomes in the U.S. are in the $50,000-$60,000 range.

And in the U.S. we get to pay more for the drugs!

Both Noyes and Smyth said the findings highlight a wider issue: the high price Americans pay for prescription drugs.

Avonex, for example, cost Americans with MS about $34,000 for the year in 2010. The price in the UK was equivalent to about $12,000 — because that’s all the National Health Service will pay for the drug.

Medicynical Note: Is it any wonder the PHarma doesn’t want to negotiate prices with Medicare and pays our congressmen and women handsomely in the form of campaign support to maintain the pricing structure in the U.S. It may be “speech” of some sort, but it certainly isn’t free.


Medical Conflicts of Interest: Part of the Problem

It’s difficult to measure the insidious effect of money on medical practices but this case provides evidence that we have a problem. The medical board of Maryland revoked a cardiologists medical license for implanting unnecessary medical stents.

The issue was first brought to the public’s attention in late 2009, when St. Joseph Medical Center sent letters to Midei’s stenting patients, explaining that their stents may have been implanted unnecessarily. The letters became the subject of an article in the Baltimore Sun.

“This report sets forth alarming evidence that patients at St. Joseph Medical Center received unnecessary and potentially harmful stent implants time and again -– a pattern that is shocking, disturbing and shameful,” wrote Sen. Max Baucus (D-Mont.), chairman of the committee.

Abbott paid Midei nearly $31,000, put him on its list of top stent volume cardiologists, and paid for a barbecue and a crab dinner at his home, according to the Finance Committee report. (Medicynical emphasis)  After St. Joseph barred him from practicing in 2009, Abbott hired him to prepare safety reports in China and Japan.

Medicynical Note: Previous posts have highlighted similar unethical behavior of psychiatrists, urologists, and researchers.

The medical industrial complex’s interest is in making money. Quality of care, ethics and value are not their concern.

Our republican congress wants less regulation.  This case would seem to indicate we need more and closer oversight.

 

Less for More–A System to Assure PHarma’s Profits Not Our Health

A a graph says it best:

20110715-123720.jpg

Medicaid: An Ongoing Public Health Disaster

The NEJM reviews the limitations of Medicaid, which is about to get worse whether or not there is agreement on debt extension:

Since Medicaid was enacted in 1965, its coverage guarantee for millions of the poorest Americans has faced a substantial vacuum in actual access to health care. Multiple factors contribute to this problem: severe shortages of physicians and hospitals in many low-income inner-city and rural communities; low rates of participation in Medicaid among available providers, owing to low payment rates; state administrative practices that drive providers away; and the economic, clinical, educational, and cultural characteristics of Medicaid beneficiaries. Where they are operating, federal programs such as community health centers, federally funded family planning agencies, the National Health Service Corps, local public health agencies, and public and children’s hospitals help to mitigate the situation. But thousands of U.S. communities lack such programs, and even where they do exist, they don’t address the specialized long-term care needs of beneficiaries with severe disabilities.

Medicynical note: This in the “best” and most expensive non-system of healthcare in the world.