EDTA has been successfully used in the treatment of atherosclerosis and arteriosclerosis for over 50 years. Yet there is a very select few Medical Doctors and even fewer Naturopathic Doctors who have received proper training in this wonderful technology. It will be difficult to find a doctor who practices EDTA because the AMA and FDA do not promote this technology to Medical Doctors. EDTA is administered directly into the blood veins and must be administered in a medical office, hopefully under the direction of a doctor who has been trained in EDTA IV chelation therapy. Available from: a few, very special and open mined doctors who believe in Alternative Care Medicine.
Orally administered EDTA is only absorbed 5% into the bloodstream, limiting It's use as a treatment. Therefore oral EDTA is best if only used for prevention of re-absorption of heavy metals during a regular chelation session. Most heavy metals are imbedded within various cell walls where they do their damages to those cell, and are not freely moving around in the body. All heavy metals have varying stability constants with the chelation molecules. During the normal chelation process, the chelator picks up heavy metals, then when a metal with a higher stability constant comes in contact with the chelator molecule, the chelator will drop the metal with the weaker stability constant in favor for the metal with the higher stability constant. Thus, during a normal chelation session, some unbound heavy metals will be freely moving around in the body. Due to the normal perfusion of blood and body fluids through the intestines, some heavy metals will find their way into the intestines where they will eventually be re-absorbed back into the blood stream. The very fact that oral EDTA is only absorbed 5% makes taking oral EDTA good preventative practice under these conditions. If oral EDTA is taken shortly after a normal chelation session, any unbound heavy metal toxins found in the gut will be bound (chelated) by the oral EDTA, and then safely excreted. Depending on the dosage, these oral EDTA capsules could be sold as a food supplement, or a prescription. If the dose is high and a prescription is needed, it must be through a doctor who is licensed to prescribe EDTA in the state of his or her licensure. Oral EDTA can also prevent normal absorption of needed minerals in your diet. Therefore, taking oral EDTA on a daily basis is contraindicated. Oral EDTA is best used under the direction of a doctor who has this understanding. Available from: Currently only from a few selected Alternative Care minded doctors.
Each suppository is 1/10 a normal IV dose. Suppositories come packaged ten to a box. Therefore one box is equivalent to one medically administered EDTA chelation IV therapy. The suppositories can be administered in the privacy of your home. There are a few doctors who do not agree with this delivery method because they feel the EDTA is not very well absorbed via the rectum. (It is only minutely absorbed in the stomach, which is why the manufacturer produced the suppositories.) The manufacturer has doctors who do believe, and some evidence to back up their claims, that suppositories deliver 90% of their EDTA into the bloodstream. Available from: a few selected Alternative Care minded doctors.
- 750 mg. up to 165# body weight. Insert every other day - always take essential minerals
- 1,00 mg. 165 to 200#. Insert every other day - always take essential minerals
- 1,500 mg. above 200#. Insert every other day - always take essential minerals
An IV push form of chelation therapy which must be administered under the supervision of a doctor who is licensed to use DMPS in the state of his licensure. The Journal of Chelation Therapy, produced by the American College for Advancement in Medicine, advises that DMPS be used only as a diagnostic tool to determine current levels of heavy metal toxicity. Also, if you have old silver amalgam dental fillings, it is strongly advised you do NOT receive DMPS as DMPS has been found in saliva and is believed may actually leach out mercury from the old fillings, thus causing a RISE in mercury toxicity in the body.
An oral form of chelation therapy which is the most gentle form of chelation, yet is highly effective. DMSA must be administered under the supervision of a doctor who is licensed to use DMSA in the state of his or her licensure.
Chelation therapy is a treatment that is approved by the Food and Drug Administration (FDA) as a treatment for heavy metal poisoning. An estimated 1 million people in the United States are treated with chelation therapy, every year. About 10% of this total are treated for heart disease (not FDA approved). Many of the providers of this therapy are trained and certified by the American College for Advancement in Medicine(ACAM).
Proponents of chelation therapy for heart disease claim that EDTA, in combination with vitamins and minerals, helps dissolve plaques and mineral deposits associated with atherosclerosis (blockage of arteries that can lead to heart attack or stroke).
Some uses of EDTA are listed below:
- Heavy Metal Toxicity
Chelation therapy using EDTA is the medically accepted treatment for lead poisoning. EDTA is injected intravenously in a medical setting such as a clinic or a hospital. Once in the bloodstream, EDTA latches onto lead and other heavy metals, to form a compound that can be excreted in the urine. The process generally takes between 1 to 3 hours. Other heavy metal toxicities treated with chelation include mercury, arsenic, aluminum, chromium, cobalt, manganese, nickel, selenium, zinc, tin, and thallium. Chelating agents other than EDTA are also used to clear several of these agents from the bloodstream. In the case of chromium, selenium and zinc, which are essential elements, they must be added back, as they are essential for life itself.
- Digoxin Toxicity
Although not considered standard therapy, EDTA has also been used to treat digoxin toxicity. In this case, EDTA helps remove excess levels of digoxin, a medication known as a digitalis glycoside, that is used to treat abnormal rhythms of the heart. digoxen toxicity occurs when the body accumulates more digitalis, than it can tolerate.
Proponents of EDTA chelation therapy for heart disease, believe that this process may help with atherosclerosis or peripheral vascular disease (namely, decreased blood flow to the legs) by clearing clogged arteries and improving blood flow.
- Available Forms
EDTA is synthetic and not found naturally. Most doctors will administer EDTA chelation intravenously. However, some doctors use oral chelation which is generally considered to be less than 10% as effective as intravenous. There is also a lesser known form of chelation therapy Called (DETOXAMIN SUPPOSITORIES) or (MEDICARDIUM SUPPOSITORIES), that are administered rectally and is generally considered to be about 90 % as effective, as IV chelation.
EDTA treatments will remove both toxic and essential elements. So, caution should be taken to make sure essential elements are not depleted. This can be assured by testing the blood levels, before chelation is started and after chelation has been completed.
There are also some food products that add to the process of chelation. These products would be classified as mild chelators. Apples and chlorella are just two of these foods. Apple pectin reportedly helps retain cholesterol in the stomach, binding cholesterol to itself and carrying it through the digestive tract to be eliminated and is also reported to help the body rid itself of lead, mercury and other heavy metals prevalent in modern water, food, and air. Chlorella reportedly does the same thing, or has the same result.
Alfred Werner proposed the theory of metal-ligand binding ("the pincer-like fashion"), which provided the foundation for modern chelation chemistry and development of treatment.
The textile industry required a chelating agent to remove calcium during textile processing and this led to the synthesis of polyamino-carboxylic acids, one of which was EDTA. A patent was filed for EDTA in Germany in 1935.
Martin Rubin, PhD, professor at Georgetown University, who was involved in getting a patent for EDTA (along with chemist Frederick Bersworth), discovered its biological effects on calcium homeostasis. This led to its laboratory use as an anticoagulant, for which it is still used today ("purple-top tubes"). Dr. Rubin helped to achieve approval by the FDA for the treatment of lead poisoning (CaEDTA) and hypercalcemia (disodiumEDTA), and later collected the world literature on chelation.
Norman E. Clarke, Sr. and Albert Boyle separately published several articles showing improvement in patients with heart disease who were being treated for lead poisoning.
Foreman reported that high doses of disodium EDTA over a short period of time can cause kidney damage, leading to the development of safe treatment protocols.
In 1960, Dr. Marvin Seven and other authors edited a book entitled "Metal Binding in Medicine", which contained papers on chelation that had been presented at two major symposia. Dr. Seven, who was associated with the National Institutes of Health, was killed in auto accident in 1961. This was considered by many to be a major blow to the development of EDTA chelation therapy, because he was a leading advocate of the therapy.
Kitchell and Meltzer wrote several articles reporting on positive effects of EDTA treatment for heart disease but their last article had a negative conclusion(not supported by their reported data), which discouraged further research by conventional doctors. A 1980's re-examination and critique pointing out glaring errors in this negative article, by Cranton and Frackelton, was ignored by mainstream medicine.
Ray Evers and Carlos Lamar each collected huge volumes of anecdotal data showing vascular improvements with chelation therapy. Lamar published his experiences in a series of articles, particularly documenting the salvage of legs with diabetic peripheral vascular disease. Evers won a precedent-setting court case establishing that once a drug is approved for any purpose, it can be used for other indications at the discretion of a physician, which allowed the use of EDTA for vascular disease as well as for the use of dozens of other drugs by all American specialists.
In 1969, Abbott's patent for EDTA expired, which resulted in decreased motivation to promote EDTA as a treatment for cardiovascular disease.
The American Institute of Medical Preventics, later called the American College for the Advancement in Medicine (ACAM), was formed in 1973 by Harold Harper, Ross and Garry Gordon and others to promote and teach chelation therapy. Since that time, ACAM has sponsored conferences and workshops on cutting edge subjects involving nutritional medicine and chelation therapy twice a year. Many physicians were trained in the safe administration of EDTA chelation therapy.
Garry Gordon and Robert Vance wrote an article about the mechanisms of action of EDTA chelation therapy.
Bruce Halstead wrote the book Scientific Basis of Chelation Therapy, This book was later updated by Ted Rozema.
Richard Casdorph, a practicing cardiologist, showed improvements in ejection fractions of the heart and in cerebral blood flow with chelation therapy in several articles.
McDonagh, Rudolph, and Cheraskin published about 30 articles documenting various positive effects with chelation therapy, including improvement in lipids, carotid blood flow, and lung function and no adverse effect on bone density. This group and Cranton each wrote articles showing no problems with kidney function in patients treated with EDTA according to the published protocol.
The American Medical Association called for studies to see if chelation worked. At the same time, conventional cardiologists wrote several editorials against the therapy.
The American Board of Chelation Therapy in 1983 was formed to certify doctors who give the therapy. It was later called the American Board of Clinical Metal Toxicology. ACAM also certified doctors who took its workshop on chelation therapy and passed its written and oral examinations.
The Great Lakes College of Clinical Medicine, later called the International College of Integrative Medicine (ICIM) was formed in 1983 to teach and do research on chelation and other integrative therapies.
After complex negotiations, in the late 1980's Walter Reed Army Hospital agreed to do a randomized clinical trial on EDTA chelation therapy, but part way through the study it was discontinued, allegedly because the investigators were called to serve in the Gulf war and did not return to complete the study.
Frackelton and Cranton published a landmark study about free radical control as the primary mechanism for chelation therapy in 1984.
Olszewer and Carter published a study in in 1988 in Medical Hypothesis documenting 87% of vascular patients showing improvement with chelation therapy. They later published a small cross-over clinical trial in 1990, documenting significant results in peripheral vascular disease, in the Journal of the National Medical Association.
Arlene Brecher lectured throughout the country and wrote a popular book (Forty Something Forever) promoting chelation therapy from the patient's point of view.
Blumer and Cranton raised the possibility that EDTA therapy might prevent cancer in a population exposed to environmental lead exposure in a study with an 18-year follow-up.
Three groups of cardiovascular surgeons published small clinical trials on chelation therapy. None had enough subjects to come close to clinical significance. All were severely criticized in letters to the editor because of procedural errors. All came to negative conclusions. One even admitted that their purpose was to disprove the therapy. At the initiative of Claus Hancke, the Guldager study was criticized for its shortcomings by the Danish supreme court. Hancke and Flytlie published an article showing that 58/65 patients on the waiting list for cardiac bypass and 24/27 peripheral vascular patients also on a surgical waiting list were able to cancel their surgeries after receiving EDTA chelation therapy.
Peter van der Schaar, a Dutch cardiovascular surgeon, published several favorable studies and wrote a massive textbook on the therapy, recently in its 10th edition.
Michael Schachter had an article published titled: "Overview, Historical Background and Current Status of EDTA Chelation Therapy for Atherosclerosis" in 1996.
Elmer Cranton published a Textbook on Chelation Therapy, into its 2nd edition in 2001.
Terry Chappell published two meta-analyses summarizing the literature to date and coming to the conclusion that treatment with EDTA chelation therapy was very closely correlated to measurable improvement in vascular function
Opponents of chelation therapy, as well as almost all alternative therapies, call themselves "quackbusters". This small group of doctors has infiltrated the Federation of State Medical Boards and travels around the country making formal complaints about doctors who provide the therapy.
They tried to outlaw the therapy in California. ACAM testified in defense of chelation and the California Medical Board voted down the proposal.
The Federal Trade Commission filed a complaint against ACAM for making a claim in a brochure that chelation was effective for vascular disease. ACAM submitted almost 100 articles in support of the claim, but the FTC insisted that a large randomized trial was required to make that claim. ACAM finally gave up after spending a million dollars in legal fees and signed a consent order saying they would not make such a claim any more, based on the evidence at that time.
Articles began appearing in the conventional medical literature that too much heart surgery was being done in the United States. The outcomes from medical therapy were just as good for many patients, if not better.
Steve Olmstead, a research cardiologist from the University of Washington Medical School, wrote a 100 page monograph discussing in detail the mechanisms, chemistry, and scientific evidence on chelation therapy. One of his conclusions was that the preponderance of the evidence was in favor of the therapy for peripheral vascular disease. This document was distributed to every medical school library in the United States.
Representative Daniel Burton, chairman of the Congressional Oversight Committee held a hearing with testimony from the NIH and from experienced chelation physicians. The conclusion was that a large study was clearly indicated. Subsequently, the NIH sent out a call for proposals. A review panel turned down the first proposal, but approved the second one, called the Trial to Assess Chelation Therapy (TACT). The chief investigator is Gervasio A. Lamas, who is a world-renowned researcher. Several prominent medical schools (Miami, Duke, Harvard) and experienced chelation physicians agreed to participate.
Several articles appeared in major journals showing that even small amounts of lead can increase the risk for hypertension and vascular disease.
Lin and Lin Tan published a leading article in the New England Journal of Medicine that chelation can improve moderate non-diabetic kidney failure, presumably by removing lead and improving circulation to the kidneys.
Terry Chappell and seven colleagues published a study showing that patients with known vascular disease treated with chelation therapy had a much lower incidence of subsequent cardiac events, such as heart attacks and the need for surgery, than a comparable group of patients treated with conventional cardiac care. These were the same end points as TACT, but the study was much smaller and was not a randomized, double-blind study.
It was reported by the Center for Disease Control (CDC) that a child died after receiving the wrong medication, disodium EDTA, in a short intravenous push. It is very important to know that calcium EDTA, which is approved to treat lead toxicity can be given as a short IV push, but that disodium EDTA, which has been described in this timeline as a potential treatment for vascular disease, must always be given by a slow intravenous drip, at a rate no more than 1 gram per hour. Otherwise, the calcium blood level can drop dangerously fast. The unfortunate child was given the wrong preparation, and that is the reason for the death.
Because many cardiologists discouraged patients from participating in TACT, enrollment proceeded slowly. For several months, the study was delayed because a complaint by the "quackbusters" saying that it should be stopped immediately. The same group convinced a reporter from the Chicago Tribune to write a negative article about the study, even though no data had yet been released. However, after seven years the study was finally completed on October 31, 2011. The findings of the study are to be presented at the American Heart Association meeting in Los Angeles on November 4, 2012. All we know at this point is that over 1700 patients enrolled nationwide, and the safety committee, which was active throughout the study, found no concerns for safety, using the study protocol.
Virtually all of the studies noted in the timeline used intravenous disodium EDTA with various vitamins and minerals. The protocol for the safe administration of intravenous EDTA chelation therapy has been published by ACAM and ICIM in their training courses, and is used in certifications by ACAM and ABCMT. Despite numerous claims, that oral EDTA might be similarly effective, there is no published evidence that oral EDTA might be helpful for treating vascular disease. Oral EDTA is only about 5% absorbed, which might make it useful for prevention for those exposed to high levels of lead on an ongoing basis, but most doctors who utilize intravenous disodium EDTA for vascular disease do not recommend oral EDTA for primary treatment.
The references for the articles cited in this timeline are available in Schachter's historical article, in Chappell's meta-analysis, and from L. Terry Chappell at P.O. Box 248, Bluffton, Ohio 45817 or at email@example.com. A good number of additional articles and events were not included in the timeline for lack of space.
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