Journal of Advancement in Medicine

Volume 4, Number 3, Fall 1991 

A Non-Surgical Approach to Obstructive

Carotid Stenosis Using EDTA Chelation

C. J. Rudolph, DO, PhD E. McDonagh, DO,

ACGP; and R. K. Barber, BS, ACSM, ETT

Abstract: Thirty subjects with arteriosclerotic vascular disease were treated with 3 gram intravenous infusions of disodium ethylene diamine tetraacetic acid (EDTA). These patients were evaluated objectively for both right and left internal carotid atheromatous stenosis at the bifurcation, before and after EDTA chelation. Each subject had treatments over a period of approximately IO months. Overall intra-arterial obstruction decreased 20.9% +/- 2.3% (t--g.921. p<.001*). Subjects with greater than 33% (i.e. statistically + I i) above initial mean obstruction. experienced a reduction in stenosis of 35.00% +/- 4.3% after treatment (t-- S. 178, p<0.00 I * n= 16). (*Statistically significant change comparing the difference of the means).

 

Introduction

This continues a series of paper-s analyzing the effects of intravenous ethylene diamine tetraacetic acid (EDTA) therapy (1-13). Many physicians have successfully used EDTA to treat atherosclerotic vascular disease (14-16). In particular, this research studied stenosis at the bifurcation of the common carotid and in the internal carotid arteries before and after EDTA infusions.

Conclusion

Significant improvement in the treatment of carotid occlusive disease should be as effective as surgery. The results from this study demonstrate that EDTA chelation, together with appropriate nutritional supplements and diet management can significantly decrease atheromatous plaque and the chance of cerebral infarction, thus satisfying this requirement.

Moreover, it should be emphasized that the safety of treatment, repeatedly demonstrated in our studies (1-13), far outweighs the published risks of endarterectomy (23). If the end result is equal to, or better than surgery, chelation should be offered as the preferred treatment.

Dr. Rudolf practices and is a partner at the McDonagh Medical Center, Inc. in Kansas City, Mo. were Dr. McDonagh is founder and Miss Barber is Cardiac Director.

  Address reprint requests to: Charles J. Rudolph, D.O., PhD., 2800-A Kendalwood Pkwy, Kansas City, MO. 64119. (@1991 Human Science Press, Inc. (complete studies on file)



Journal of the National

Medical Association. Vol 82, No 3

A Pilot Double Blind Study of Sodium

Magnesium EDTA in Peripheral Vascular Disease

 Efrain Olszewer, MD, had Calil Sabbag, MD, and James P. Caner, MD, Dr. PH New Orleans, Louisiana

  Ten male patients with peripheral vascular disease, Type 2 (LaFontaine), were randomly assigned in a double-blind study to receive either Na2 ethylene diamine tetra acetic acid (EDTA) plus MgSO4, B complex, and vitamin C, or a placebo of MgSO4, B complex, and vitamin C in Ringer's lactate solution. A total of 20 intravenous infusions were planned for administration to each patient. Clinical and laboratory (noninvasive) tests showed dramatic improvements after 10 infusions in some patients, thus was broken the code indicating who receiving EDTA and who was receiving

placebo. The group that improved had been receiving EDTA; there was no change in the placebo group. The trial was then completed in single-blind fashion. Patients originally assigned to receive placebo then received IO EDTA infusions, while the group originally assigned to EDTA received 20 EDTA infusions. The group that had formerly received placebo showed improvements comparable to those seen in the first EDTA group after 10 treatments.

Key words - peripheral vascular disease - ethylene amine tetra acetic acid

To our knowledge, no one has yet published a double-blind study evaluating the effectiveness of  NaMg EDTA in the treatment of peripheral vascular disease. Some case reports and retrospective studies, including our recent review of 2870 cases of chronic degenerative disease treated with EDTA have been published.2-5 We, therefore, conducted a pilot double blind clinical trial of EDTA in peripheral vascular disease.

METHODOLOGY

Ten patients, all male, with a mean age of 47 years (range 41 to 53), and all with peripheral vascular disease from diabetes or arteriosclerosis, aggravated by smoking, were enrolled in the study. They were all stage 2 of the LaFontaine Classification, which means that they had intermittent claudication, but no pain at activity, at rest, or in the night and no gangrene. They included eight former heavy cigarette smokers, all of whom had quit at least 6 months before the study began.

From CEWO, Sac) Paulo, Brazil', an affiliate of the International Institute of Preventive Medicine, Rua Tamadi 320. Perdizes. 05002 Sao Paulo, Brazil. Requests for reprints should be addressed to Dr. James P. Carter, Tulane Univ. School of Public Heath and Tropical Medicine, 1501 Canal Street. suite 809. New Orleans. LA. 70112.

 


 

J. Cardiovase.Nurs 1996: 10(3):78-86

@ 1996 Aspen Publishers. Inc

 

EDTA Chelation Therapy in the Treatment of Vascular Disease

Ethylenediamine tetraacetic acid EDTA) chelation therapy has been used for decades for the treatment of vascular disease, alone or in combination with other treatments. This article includes a historical review of the research literature, current evidence of effectiveness, potential mechanisms of action EDTA, and some brief case reports. The authors conclude that EDTA Chelation therapy is a valuable therapeutic option for vascular disease, either alone or in conjunction with standard treatment protocols. Key words : angina, atherosclerosis, chelation, claudication , EDTA, vascular disease.

Chelation is defined as the incorporation of a metal ion into a heterocyclic ring structure. Living systems, use chelates commonly, for example, in many enzyme functions and in the structure and function of heme (a chelate of iron) and chlorophyll (a chelate of magnesium). Ethylenediamine tetraacetic acid (EDTA) is a synthetic amino acid with chelating properties. It was first used clinically for the treatment of lead toxicity before 1950 and was reportedly used for control of hyper-calcemia in 1950.

It was noted that patients being treated with EDTA for lead toxicity reported improvement, apparently coincidentally, in angina pectoris. That observation began

the investigation of the use of EDTA in the treatment of atherosclerotic vascular disease. As a result, the first study of the use of EDTA in atherosclerotic disease was published in 1956. Clarke, et al 2 reported on the results of chelation therapy in 20 patients with confirmed diseases 19 of whom improved as measured by physical activity. They stated "A placebo action seemed improbable for several reasons. There was slight if any clinical improvement until after the discomfort of 20, and with a few, 30 infusions. A patient's progress was based on measured physical activity rather than appraisal of subjective Symptoms. The improvement gained has been retained and expanded in all, and a few for as long as 2 years, The results have been uniformly good.

L.. Terry Chappell, MD Private Practice Bluffton, Ohio

Assistant Professor of Family Practice Wright State School of Medicine Dayton, Ohio

President-Elect of the American College for Advancement in Medicine

Michael Janson, MD Private Practice

Barnstable, Massachusetts, Chairman of the Scientific Advisory Committee, Program Chairman of the American College for Advancement In Medicine President of America Preventive Medical Association.


 

 

Journal of Advancement in Medicine    

@ 1993 Human Sciences Press, Inc. 

Volume 6, Number 3, Fall 1993

Benefits of EDTA Chelation Therapy in Arteriosclerosis: A Retrospective Study of 470 Patients.

C. Hancke, M.D, and K. Flytlie, M.D.

Abstract: In a retrospective study we report results of EDTA chelation in 470 patients, using a number of parameters, most of them objective. Although the patients acted as their own controls, we observed improvements of8O to 91%, depending on the measurement used. Of 92 patients referred for surgical intervention, only 10 required ultimate surgery after or during their chelation therapy, thus saving an estimated 3 million dollars of insurance money. Our experience covers a period of 6 years and we saw no severe side effects or casualties arising from the treatment. We conclude that EDTA chelation therapy is safe effective and cost saving.

Introduction: Intravenous administration of ethylene diamine tetraacetic acid (EDTA) has been used from the beginning of the 1950's by an increasing number of physicians throughout the world for the treatment of arteriosclerosis. In the last few years, there has been increasing criticism of surgical intervention in this disease, since it falls to prolong life, and is a temporary solution in treating a generalized, chronic condition (1). In addition, surgery damages vital tissue by means of reperfusion-released free radical bursts (2,3). Effective- ness of EDTA chelation therapy is cumulative over many years (4,90), and the recent association of iron in the etiology of cardiovascular disease (IO) makes the technique worthy of complete acceptance today.

Claus Hancke, M.D. received his medical education at the University of Copenhagen. He is in general practice and is the president of the Danish Chelation Doctors. He is an ABCT diplomat.

Knut Flytlie, M.D. received his medical education at the University of Gutenberg, Germany. He is in general practice and operates a clinic for Preventive Medicine and Chelation. He is an ABCT diplomat.

Address correspondence to Claus Hancke, M. D.,Hovedgade 17, 1, DK- 2800-LYNGBY, Denmark. Additional information may be obtained from ACAM. Phone number on contents page.

*In our view, the beneficial results that were observed were far in excess of the 10-15% improvement that is usually seen in the placebo group of a controlled study. Of 65 patients who were referred for coronary by-pass surgery, 58 did not require it after chelation therapy.


 

Journal of Advancement in Medicine

Volume 2. Numbers 1/2 Spring/Summer 1989

EDTA Chelation Therapy:

A Retrospective Study of 2,870 Patients

Efrain Olszewer, MD and James P. Carter, MD, Dr. PH