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July 2008 Health in the News Archive

[ Monthly Index of New Briefs ]


Chelation therapy for autistic kids called "Fringe"

July 2008

An AP article reprinted in the Arizona Republic said use of chelation with autistic children "is a move some scientists see as an unethical experiment in voodoo medicine. The treatment removes heavy metals from the body and is based on the fringe theory that mercury in vaccines triggers autism – a theory never proved and rejected my mainstream science."

The article relates the story of a boy named Charlie who started chelation at 5 and three weeks later "looked at (his mom) and waved and gave a thumbs-up sign and walked into school. All the moms who had been watching burst into tears (of joy)." The writer said there was no way to prove whether chelation made a difference or whether Charlie simply adjusted to the school routine.

Dr. Grout's Comment:
This article so moved me I fired off a letter to the editor at the Republic. It says, in part, "How can I take seriously an article written as though it were "news", when even the headline contains emotionally charged words aimed at steering the reader toward the writer's opinion? In medicine, informed consent involves presenting the facts to patients, discussing the pros and cons, and allowing them to make their own decisions about whether to undergo the proposed treatment. We try very hard not to say that ours is the only way, that other ways are "quackery".

Medical history is full of cases where those who, early on saw value in new ways, were at first ridiculed, then later awarded the Nobel Prize. Linus Pauling of vitamin C fame is one such example. In the case of chelation's use in autism, the writer miserably failed to present both sides of the story.

Chelation is a proven therapy. It was used by the U.S. Navy to successfully remove lead from poisoned sailors and has been used since successfully to treat heart disease. This is not a "fringe" treatment. It is a tried and true treatment now being applied to children because studies show children's bodies are loaded with metals and environmental chemicals.

Of course, parents of autistic children are desperate. An estimated 1 in 150 children now has autism. Conventional medicine, as the article points out, says there is no cure and offers a few prescription drugs. If chelation can bring autistic children back into the world, then the media deserves to give it an honest look and stop merely repeating old dogma. Here at the Arizona Center for Advanced Medicine, autistic children use chelation often with great success and we celebrate those successes.

Statin Drugs Recommended for Kids

July 2008

The nation's pediatricians are recommending wider cholesterol screening for children and more aggressive use of cholesterol-lowering drugs starting as early as the age of 8 in hopes of preventing adult heart problems.

New guidelines issued by the American Academy of Pediatrics (AAP) are a push to aggressively screen and medicate children for high cholesterol. The recommendations call for cholesterol screening of children and adolescents, starting as early as the age of 2 and no later than the age of 10, if they come from families with a history of high cholesterol or heart attacks before 55 for men and 65 for women.

Proponents say there is growing evidence that the first signs of heart disease show up in childhood, and with 30 percent of the nation's children overweight or obese, many doctors fear that a rash of early heart attacks and diabetes is on the horizon as these children grow up.

Dr. Jatinder Bhatia, a member of the academy's nutrition committee, said that although there was not "a whole lot" of data on pediatric use of cholesterol-lowering drugs, recent research showed that the drugs were generally safe for children.

Surprisingly, the paper published in the medical journal Pediatrics that explains the new guidelines notes that among adolescents, average total cholesterol levels as well as LDL and HDL cholesterol have remained stable, while triglyceride levels have dropped, based on data collected from 1988 to 2000.

Dr. Grout's Comment:
This is another curious recommendation from the AAP. Statins have been around since only the mid-1980s; there is no evidence to show whether giving statins to a child will lower the risk for heart attack in middle age. Despite Dr. Bhatia's breezy endorsement of these drugs, there is evidence that statins cause muscle pain and weakness, and interfere with the mental ability to concentrate and think clearly.

Decades ago, a few studies caused the medical world to think high cholesterol is linked to heart disease. We know now those studies were flawed. We also now know enough that before we prescribe drugs for young children that alter the body's basic processes, we should first look at whether "high" cholesterol is caused perhaps by low thyroid, exposure to chlorine, lack of sun exposure, lack of vitamin c, or hydrogenated oils in the diet.

The AAP also recommends giving children low-fat milk after 12 months if a doctor is concerned about future weight problems. The AAP says that because children often consume so much fat, low-fat milk is now appropriate. Truth is, children absolutely need fat - and cholesterol - for brain development.

But too many kids eat the wrong kids of fats, trans fatty acids from fast foods. What kids need more than anything is DHA, especially when they are very young, to build up their brain function and neural connections. Mother's milk has the highest levels of DHA. It would be a shame to deprive toddlers and growing children of the most helpful part of cow's milk - the full fat - in the mistaken belief that high cholesterol levels are the cause of heart disease.

FDA to regulate cancer-causing cigarettes?

July 2008

The U.S. House of Representatives has approved a bill that would give the FDA the power to regulate tobacco products. The bill still has to be approved by the Senate and the President.

The show of support in the House, which passed the bill by a vote of 326 to 102, illustrated not only the strength of antismoking sentiment in the country but the benefit of enlisting a powerful ally. The legislation was partly the result of negotiations with Philip Morris USA, the nation's largest cigarette company, which split with other companies by endorsing it.

Most large public health groups supported the measure, including the American Lung Association, but some antismoking advocates said the bargain struck with Philip Morris gave too many concessions to industry.

The bill specifically states that the F.D.A.'s new powers would stop short of the ability to order the elimination of nicotine from tobacco products or place an outright ban on all tobacco products.

The agency could reduce nicotine to nonaddictive levels if it determined that doing so would benefit public health. The bill bans flavored cigarettes that appeal to young people but exempts menthol from that ban. The bill requires cigarette makers to provide detailed disclosure about the type and quantities of ingredients in their products — like ammonia and acetaldehyde — which are believed to work with nicotine to increase the addictiveness of cigarettes and smokeless tobacco. The requirements mean that companies would be required to disclose internal research on the biological effects of those additives.

If the legislation is enacted, consumers would see a wholesale revamping of the warning labels on tobacco products. The current warning message would be replaced by graphic images of the physical ravages often caused by cigarettes, such as lung tumors and mouth growths.

Dr. Grout's Comment:
This bill would put the FDA in the interesting position of approving the sale of something that kills people and has no medical benefit. According to the CDC, tobacco kills 438,000 people each year in the United States alone. According to conservative figures from the American Medical Association, FDA-approved drugs kill about 100,000 Americans a year. By contrast, 2751 people died in the 9-11 World Trade Center tragedy.

The White House is promising to veto the legislation because "the bill will unfortunately undermine one of the nation's premier public health and regulatory institutions and potentially lead the public to mistakenly conclude some tobacco products are safe." Meanwhile, Barack Obama promises a national ban on smoking in public places.

Politics aside, one thing is for sure. The FDA is undermanned and unable to protect the public health as it is. FDA-approved Vioxx killed 60,000 people and headlines about salmonella in tomatoes and e.coli in the beef just keep coming.

Are Pediatricians Industry Shills?

July 2008

Writing in the San Francisco Chronicle, author and pediatrician Lawrence Diller paints a chilling picture of how so many children came to be on behavior modifying prescription drugs.

"Most parents have never heard of him, but Joseph Biederman of Harvard may be the United States' most influential doctor when it comes to determining whether their children are normal or mentally ill," Diller wrote. "The science of children's psychiatric medications is so primitive and Biederman's influence so great that when he merely mentions a drug during a presentation, tens of thousands of children within a year or two will end up taking that drug, or combination of drugs. This happens in the absence of a drug trial of any kind…

"That's why Iowa Sen. Charles Grassley's recent revelation that Biederman did not declare $1.6 million in drug company consulting fees is so important, scary and tragic … drug company money is corrupting medical practice and the maintenance of our country's health."

Diller explains that the $1.6 million that Biederman didn't declare is only a small fraction of the full amount of research funding that his clinic receives from nearly a dozen companies that pay for not only the cost of running studies but also the salaries of the doctors involved. "Virtually all doctors who receive drug company money say they are not influenced, but every independent study examining the effects of such money says they are."

Dr. Grout's Comment:
Dr. Lawrence Diller is the author of "The Last Normal Child" (Praeger, 2006). He is to be applauded for bringing attention to the gross conflicts of interests which now permeate standard medicine. These conflicts are hidden from American public by an unquestioning media.

Many times Dr. Paul Offit for example been quoted as an expert doctor when it comes to vaccines, yet rarely does the news mention that he is a paid consultant to Merck Pharmaceuticals who makes vaccines.

Dr. Diller's essay is excellent and can be found in its entirely at http://sfgate.com/cgi-bin/article.cgi?f=/c/a/2008/07/13/IN7G11L6TL.DTL

Also see our recent news item on the American Academy of Pediatrics recommending cholesterol lowering drugs for children beginning at age 8.

Inappropriate childhood behavior ranging from aggressiveness to autism, from inability to focus to severe stomach pains is our specialty. Read how we examine the whole body – from brain function to gut function and everything in between – and how we apply non-drug based answers at http://www.arizonaadvancedmedicine.com/therapies/brain_advantage.html

Secret Toxic Laundry Products

July 2008

A University of Washington study of six top-selling laundry products and air fresheners found they all gave off at least one chemical regulated as toxic or hazardous, but none of those chemicals was listed on the product labels.

"People were telling me that the air fresheners in public restrooms and the scent from laundry products vented outdoors were making them sick," said Anne Steinemann, a UW professor of civil and environmental engineering and of public affairs. She analyzed the products to discover the chemicals' identity.

"I was surprised by both the number and the potential toxicity of the chemicals that were found," Steinemann said. Chemicals included acetone, the active ingredient in paint thinner and nail-polish remover; limonene, a molecule with a citrus scent; and acetaldehyde, chloromethane and 1,4-dioxane.

"Nearly 100 volatile organic compounds were emitted from these six products, and none were listed on any product label. Plus, five of the six products emitted one or more carcinogenic 'hazardous air pollutants,' which are considered by the EPA to have no safe exposure level," Steinemann said.

Her study was published online July 23 by the journal Environmental Impact Assessment Review. Steinemann chose not to disclose the brand names of the six products she tested. In a larger study of 25 cleaners, personal care products, air fresheners and laundry products, now submitted for publication, she found that many other brands contained similar chemicals.

Dr. Grout's Comment:
Manufacturers of consumer products are not required to disclose the ingredients The European Union recently enacted legislation requiring products to list 26 fragrance chemicals when they are present above a certain concentration in cosmetic products and detergents. No similar laws exist in the United States.

If we had better in truth in labeling, we wouldn't be in the dark about toxic chemicals in our environment.

FDA funding increases despite complaints of incompetence

July 2008

For the second year in a row legislators have scolded the Food and Drug Administration for doling out most of its bonus money to top managers instead of field inspectors.

President Bush signed an Iraq war spending bill into law June 30th that also included an extra $150 million for the FDA to hire more staff and conduct more food inspections.

Meanwhile, a House Energy and Commerce Committee report said "retention" bonuses were created to keep coveted field inspectors, analysts and scientists from ditching the federal government for greener paychecks at private sector posts. But most of the money has ended up in the hands of upper-level management, the report said.

The House committee issued a similar report criticizing the FDA in 2007.

By way of example, the FDA's chief of regulatory affairs received $48,663 in bonuses last year—more than half the salary of the average federal employee, according to the committee report.

The Western Growers Association has asked Rep. Dennis Cardoza, D-Calif, to seek a congressional investigation of the FDA's handling of the tomato recall. The group sees the singling out of tomatoes as part of a trend in which the FDA puts out information too quickly to merely quash public panic.

Dr. Grout's Comment:
I give a big thumbs up to the words of Committee Chairman John Dingell, D-Mich, who called the FDA's funding distribution pattern a "failure of FDA management to understand that its sole purpose for existence is to protect the American people."

FDA orders Cipro warning

July 2008

The Food and Drug Administration (FDA) has ordered drug manufacturers to add a stronger black-box warning label to fluoroquinolone antibiotics. The new labels must highlight the increased risk of tendonitis and tendon rupture for people using the drugs.

According to a July 8, 2008 FDA statement, the agency analyzed available literature and postmarketing reports of adverse events. Their latest research confirmed that use of fluoroquinolone is associated with an increased risk of tendon rupture.

And despite the current label warnings regarding possible tendon rupture—the agency continues to receive numerous reports of tendon-related adverse events.

"Fluoroquinolones are effective in treating certain bacterial infections, but health care professionals and patients need to be aware of the increased risk associated with the use of these drugs of developing tendonitis and tendon rupture, particularly for certain patient populations," said Edward Cox, M.D., director of the Office of Antimicrobial Products, Center for Drug Evaluation and Research.

People over 60 years of age have an increased risk of developing tendonitis and tendon rupture associated with the use of fluoroquinolone. The risk also increases for kidney, heart, and lung transplant recipients, and for people taking corticosteroid drugs.

Dr. Grout's Comment:
When we are dying, antibiotics are a good choice to debulk the infection so that the body can deal with the clean-up. But the casual use of antibiotics has led to the growth of "superbugs." And all pharmaceutical drugs carry risk. We think we know the effects of drugs, but their effects have not tested on every metabolic process in the body. Only "post-marketing" reports will reveal some of these side effects, which may well turn out to be affecting essential metabolic processes as we have found out with Cipro.

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