From March
13 to 15, 2013, the International College of Integrative Medicine (ICIM) held a
summit meeting about what should be accomplished next, now that EDTA chelation therapy
has been supported as a useful treatment for vascular disease by the Trial to
Assess Chelation Therapy (TACT). Experts
from around the world were invited. This
paper is a summary of the conclusions and recommendations of this gathering. Key presentations were given by Drs. John
Trowbridge, Efrain Olzsewer, and Eleonore Blaurock-Busch. Representatives from the U.S., Canada,
Indonesia, Brazil, Denmark, the Netherlands, Germany, Ecuador, and New Zealand
participated, as well as the attendees for the Advanced Metals Workshop that
was part of the spring meeting of ICIM.
Recordings of the lectures are available from icimed.com. This paper was prepared prior to articles on TACT
published in the Journal of the American Medical Association in the March 27,
2013 issue.
Background
EDTA has
been used as a treatment for vascular disease since Norman Clarke, Jr.’s work
in 1952. For a timeline of the many
studies that have supported its effectiveness, see chelation.me. In 1981, the
AMA challenged the proponents of chelation therapy to produce a large-scale,
randomized, controlled, clinical trial to prove its safety and
effectiveness. The members of the
American College of Advancement in Medicine (ACAM) led by president Ross Gordon
collaborated with Walter Reed Hospital to begin such a study for treatment of
peripheral vascular disease in 1987.
Unfortunately, the first Gulf War took the investigators away from the
study, and it was not completed. In
1999, Congressman Dan Burton, Chair of the Committee on Oversight, held a
hearing bringing together the head of the Heart, Lung, and Blood section of the
National Institutes of Health and several physicians who testified about their
experiences with chelation. NIH
subsequently called for proposals, and eventually TACT was funded, with Gervasio
Lamas as chief investigator.
TACT was
unique in that it combined university research cardiologists and experienced
chelation specialists with private offices.
134 sites from the U.S. and Canada participated in the randomized,
placebo-controlled, double-blind, clinical trial. TACT continued for 7 years, and included 1708
patients with documented previous heart attacks who continued to receive
evidence-based therapy. The primary end
point was a composite of new cardiac events to include death, heart attack,
stroke, hospitalization for unstable angina, and need for revascularization
surgery. TACT showed that the therapy
was unquestionably safe, and the group treated with chelation therapy had fewer
cardiac events, which was statistically significant. The results were announced by Lamas at the
American Heart Association meeting on November 4, 2012 in Los Angeles. Publication of the results is pending. The authors called for further studies to
confirm the results and explore the mechanisms of action.
Where we stand now,
according to the Summit
1. TACT
conclusively showed that chelation therapy used according to the recommended
protocol is safe.
2. TACT
and the many other studies that proceeded it support the use of chelation
therapy as an option for patients with vascular disease, especially for those
who also have diabetes and those with a history of anterior wall myocardial
infarction.
3. There
is not yet enough evidence to state that chelation therapy should be given to
all cardiac patients. More studies need
to be done. A duplication of TACT would
be ideal, as long as it included heavy metal testing. However, another $30 million to repeat the
study might be difficult to find.
4. Strong
consideration should be given to doing a challenge test for heavy metals
(especially lead) for all patients with vascular disease. If high levels are found, the patients should
be treated with chelating agents.
5. Regulatory
agencies, such as medical boards, should immediately stop harassing physicians
who offer chelation therapy to their patients who give appropriate informed
consent. Physicians who offer chelation
therapy have accomplished exactly what the AMA asked them to do in 1981 to
justify its use.
6. Most
physicians who offer chelation therapy are happy to serve as consultants for
placebo-controlled RCT’s, but are uncomfortable with the ethics of giving
placebos to patients who have come to them for help. Certainly, patients should not be asked to
pay to receive placebos, especially for a potentially life-threatening
illness. Physicians who provide
chelation are almost always convinced that in their experience the therapy is
very effective.
7. Many
chelation doctors feel that their primary goals of showing efficacy and safety
with a RCT have been accomplished with TACT.
Gaining FDA approval of EDTA for use in vascular disease is secondary, and
they encourage qualified investigators to move in that direction.
Recommendations of the Summit
1. More
research should indeed be done on metal toxicity, free radical pathology, and
on various diseases that have been linked to free radical pathology, especially
vascular disease.
2. Chelation
doctors do not have the resources to fund or carry out clinical trials, but
they do have the expertise to help plan them.
3. The
conditions that are most likely to show benefit with chelation treatment and
thus should have the greatest research priority are as follows:
a. Patients
waiting to have limbs amputated due to non-infected vascular disease. For end points, all that is needed is to
count the remaining limbs. Claus
Hancke’s work is most impressive in this regard.
b. Walking distance and A/B index
in patients with peripheral vascular disease.
In our experience, a very high percentage of patients improve. Ffrain Olzsewer and Jim Carter documented
this. There have been a couple of
negative studies published on this subject in prominent journals, but they have
been seriously flawed. Stephen Olmstead
has written a good research protocol to evaluate chelation treatment for
peripheral artery disease that is almost ready to go. He is willing to share his work with others. Attendees
to the summit expressed significant concern that opponents of the therapy might
proceed with new studies that are designed to fail, which has happened in the
past.
c. Brachial
artery stiffness and other measurements of vulnerable plaque. Peter van der Schaar is beginning a study on
arterial stiffness.
d. Diabetic
patients who have evidence of vascular disease.
e. Patients
who have suffered an anterior wall MI.
f. Patients
who have angina that is difficult to control with drugs.
g. Macular
degeneration.
h. Patients
who have been told that revascularization surgery is an option
i.
Quality of Life measurements should be included
in all research projects. Chelating
physicians insist that their patients feel considerably better with long-term
treatment, even though the relatively short follow-up in TACT detect
significant improvement.
4. Other
areas that are important to study and are likely to show successful outcomes:
a. Patients
with hypertension and elevated lead levels
b. Arterial
intimal thickness and high resolution ultrasound of the carotid arteries (see
the work of Robert Bard)
c. Osteoporosis
d. Mild
to moderate Alzheimer’s disease associated with heavy metal toxicity
e. Autoimmune
diseases, especially scleroderma
f. Fibromyalgia
with high levels of toxic metals detected with a challenge test
g. Diseases
that are familiar to the public should be studied in order to raise awareness
and support for chelation.
5. There
are many biomarkers in the laboratory that can help examine the mechanisms of
action of chelation therapy. Expert biochemists
(Blaurock-Busch, Jaffe, Quig) are happy to consult with investigators as to
which ones are most appropriate to utilize in this assessment.
6. Various
combinations of chelating agents, and different doses of such entities as EDTA
and vitamin C are important to study.
7. Chelation
therapy is useful to study at all stages, to include
a.
Preventive
b.
Pre-emptive (early signs of disease)
c.
Treatment of established disease
d.
Treatment following revascularization procedures
e.
Maintenance treatments are very important
8. Such
international lecturers as van der Schaar, Olzsewer, Rozema, Hancke, Dooley,
and Godfrey continue to teach physicians on how to use chelation therapy safely
and effectively. Organizations such as
ACAM, ICIM, and A4M hold workshops in the United States. Excellent recent textbooks have been
published by van der Schaar and Blaurock-Busch (both are available through the
International Board of Clinical Metal Toxicology). There is a need to move toward consistent
protocols and best practices.
9. Studies
must be well-designed and conducted so that clear outcomes can be readily
understood and will resonate with a large portion of the population, as well as
stimulate Congressional action.
10. Use
of NBMI—a compound being studied by Boyd Haley might turn out
to be a powerful therapeutic modality.
Conclusion
Raising public, political, and
media awareness is now essential. Experienced
chelating physicians can help provide solid data to support general
understanding of efficacy, mechanisms, and positive outcomes in the treatment
of vascular diseases. Registries might be the best way for clinicians to
collect data without the constraints of a RCT. Self-insured corporations, such as
Parker-Hannifin are now paying for chelation therapy. Cooperation among organizations with similar
interests, such as ICIM, ACAM, AAEM A4M, ABCMT, IBCMT, and specialized
laboratories is strongly encouraged to standardize protocols and set up
registries. This can be done quickly and
with minimal expense. Physicians from around
the world should be included. Experienced
chelating physicians can serve as consultants for researchers who are qualified
to perform RCTs. NIH and various
foundations are encouraged to fund projects discussed in this paper. Pollution with heavy metals continues to get
worse, and evidence is mounting that their toxicity is an important factor in
the development of chronic degenerative diseases.
No comments:
Post a Comment