It
is a pleasure to announce that a resolution
on iron overload/hemochromatosis awareness
which I wrote with the input of David
Porter, Director/Office of Specialty
Society Relations, American Medical
Association (AMA), was adopted by the
AMA House of Delegates at the AMA House
of Delegates Annual Meeting on June
22-26, 1997 in Chicago, Illinois.
Originally,
I submitted this resolution to the
Palm Beach County Medical Society (West
Palm Beach, Florida) which then proposed
it at the Florida Medical Association
(FMA) state convention in Miami in
May 1997. It was amended there and
then was proposed by the FMA to the
AMA House of delegates at its convention
in June where it was amended once again
and then adopted.
This
resolution now stands as an official
AMA directive. David Porter states
that to his knowledge (and according
to the 600+ pages of the AMA Policy
Compendium), there has never before
been an AMA directive on hereditary
hemochromatosis. Copies of this resolution
have been distributed by the AMA to
its state presidents, delegates, 54
states and territories, 95 national
specialty groups, and approximately
2000 county medical societies.
Anyone
wishing a copy of this resolution may
contact the AMA directly. Please note
that the official resolution in its
final adopted form ordered from the
AMA contains ONLY the last two "Resolved" sections
and not the "whereas" sections.
Therefore, you might prefer to simply
use the version below which contains
the original "whereas" sections
as well as the "resolved" sections,
to print, copy or share. This copy
of the iron overload/hemochromatosis
resolution would be of interest to
physicians treating HH patients as
well as patients who have HH.
Best
wishes,
Sandra Thomas, President/Founder
American
Hemochromatosis Society, Inc.

Resolution #525: "Routine
Screening for Iron Overload/Hemochromatosis"
D ate
Adopted: June 1997
Write: American
Medical Association 515 North State
Street Chicago, Illinois 60610
Call: 312-464-5000
Introduced
by: Florida Delegation (Florida
Medical Association)
Subject: Routine
Screening for Iron Overload/Hemochromatosis
Referred to: Reference Committee E--Ira
D. Godwin, MD, Chair Resolution #525: "Routine
Screening for Iron Overload/ Hemochromatosis"
Date
Adopted: June 1997
Whereas,
Recent studies have found hemochromatosis
(iron overload) is the most common
genetic disease in the Northern Hemisphere
which affects more than 1.25 million
Americans with the double gene (homozygotes)
and 32 million Americans who are single
gene carriers (heterozygotes) with
a prevalence of one in eight as single
gene and one in 200 as double gene;
and
Whereas;
Diagnosis of hemochromatosis, a condition
of abnormal metabolism of iron, is
often difficult due to the symptoms
of excess iron stored in organs and
tissues, which may cause heart failure,
chronic fatigue, cirrhosis, arthritis,
diabetes, cancer and ultimately premature
death; and
Whereas,
Deaths from iron overload are needless
and avoidable with early diagnosis
by proper testing and aggressive treatment
through drawing of blood from the patient
until normal levels of stored iron
are obtained; and
Whereas,
All blood relatives of a diagnosed
patient should be tested for the disease;
Whereas,
Simple and available blood tests for
iron overload are transferrin saturation
and serum ferritin as well as a new DNA
genetic test for the newly discovered
hemochromatosis gene; and
Whereas,
Recent studies have shown that routine,
universal screening for iron overload
is cost-effective; therefore be it
RESOLVED,
That the American Medical Association
encourage the development of guidelines
for screening patients for iron overload
and hemochromatosis in association
with the appropriate medical specialty
societies, and be it further
RESOLVED,
That the AMA work with the appropriate
specialty societies and voluntary health
agencies to disseminate information
about iron overload and hemochromatosis.