[PHNUTR-L] Carried by Immigrants, Leprosy in Heartland Surprises Clinicians

Kathrynne Holden fivestar at nutritionucanlivewith.com
Tue Dec 30 09:36:46 PST 2008


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Carried by Immigrants, Leprosy in Heartland Surprises Clinicians

By Michael Smith, North American Correspondent, MedPage Today
Published: December 29, 2008

Reviewed by Robert Jasmer, MD; Associate Clinical Professor of Medicine,
University of California, San Francisco
http://www.medpagetoday.com/InfectiousDisease/PublicHealth/12284

SIOUX CITY, Iowa, Dec. 29 -- The man from Guatemala was admitted to
Mercy Medical Center here with a fever of 109, swollen lymph nodes, and
enlarged liver and spleen.

Initially, his doctors suspected lymphoma or some other form of cancer,
says Bertha Ayi, M.D., an infectious diseases specialist, but they were
ruled out, one after another.

Dr. Ayi was called in to check for tuberculosis, but it took her almost
no time to rule that out as well and determine the correct diagnosis,
one that would not be expected in Iowa.
Action Points

* Explain to interested patients that Hansen's disease -- more
commonly known as leprosy -- is not easily transmissible and is readily
cured with antibiotics if it is diagnosed early.

* Note that the incidence of leprosy in the U.S. is stable, but the
pattern is changing, with new cases now being seen in places such as the
Midwest, where the disease has been rare.

"It didn't take more than five minutes to see the gentleman had Hansen's
disease," Dr. Ayi said, mainly because of telltale skin lesions.
Bacteriological tests quickly confirmed the diagnosis and the man was
started on antibiotics.

Now, Dr. Ayi said, "he's doing terrific."

Bu how was the diagnosis missed at presentation? For most U.S. doctors,
leprosy is the last thing on their minds -- particularly in the
heartland of America.

Even the Ghana-born Dr. Ayi -- aware of the disease through both
experience and training -- said she "wasn't expecting to find Hansen's
disease in Iowa."

Most leprosy in the U.S. is imported and -- until recently -- the
150-odd new cases a year were mainly found among immigrants clustered in
11 port cities, according to James Krahenbuhl, Ph.D., director of the
National Hansen's Disease Program (NHDP) in Baton Rouge, La., part of
the federal Health Resources Service Administration.

But the disease is now popping up in states like Iowa, "in places where
we hadn't seen it before," Dr. Krahenbuhl said. Immigrants -- usually
medically underserved -- "are going where the jobs are" and taking
leprosy with them.

Yet outside of those 11 ports, where there are long-established
surveillance and treatment programs, most doctors in the U.S. have a low
index of suspicion for the disease.

Samuel Moschella, M.D., of Lahey Clinic Medical Center in Burlington,
Mass., describes the shifting pattern of leprosy as a "geopolitical
phenomenon" that may catch clinicians by surprise.

"All of our doctors are not familiar with the disease," said Dr.
Moschella, a former president of the American Academy of Dermatology who
is involved in caring for about 100 active Hansen's disease patients.

That lack of familiarity is why Dr. Krahenbuhl led a symposium on the
topic at the recent meeting of the American Society for Tropical
Medicine and Hygiene in New Orleans.

It was a proactive effort to restore leprosy awareness, said Dr.
Krahenbuhl, in view of the shifting population patterns. As time goes
on, he said, he and other leprosy experts will be giving more and more
talks, seminars, and symposia on Hansen's disease.

Raising the index of suspicion is the first step, according to David
Scollard, M.D., chief of the clinical branch at the National Hansen's
Disease Program. "Physicians can easily miss it because they don't think
of it," he said.

The next step is making the diagnosis, and the "big clue" there is a
reduction or absence of sensation around the suspect lesion, he said.

"Most of the time this can be picked up fairly easily if people think to
test for it," Dr. Scollard said.

If physicians are not sure about their diagnosis or simply want some
additional guidance, they can take a biopsy and send it to the program's
Baton Rouge headquarters.

"We'll help manage the care," Dr. Scollard said.

The disease historically -- it's been known since the year 600-- was
feared as highly contagious and devastating. But in fact, it's not
highly transmissible, is now easily treatable, and, with early diagnosis
and treatment, is not disabling.

The Hansen's disease program is the successor to the National
Leprosarium, established in Carville, La., in 1917. The program still
has some elderly in-patients who were admitted to the leprosarium, but
most patients are now followed on an outpatient basis.

More than a century ago, when leprosy was endemic in Hawaii, patients
were forcibly repatriated for life to the remote nearly inaccessible
Kalaupapa colony on Molokai. It was there that Father Damien, the
legendary Belgian priest, held sway from 1873.

Few leprosy patients are at Kalaupapa today, and they are there by
choice. In Louisiana, Dr. Scollard said most patients are treated in
their home towns, but a few -- mainly those who need intensive
management -- will be brought to Baton Rouge for care.

All told, about 7,100 people in the U.S. were reported to have Hansen's
disease over the past 30 years, Dr. Krahenbuhl said, and of those about
6,500 are still alive and some 3,500 are under active management.

It's a chronic granulomatous disease, caused by infection with
Mycobacterium leprae that mainly affects the skin and peripheral nervous
system. Most people are immune to M. leprae.

Treatment recommendations vary depending on the type of disease.
Paucibacillary disease is treated for a year with dapsone at 100 mg a
day and rifampin (Rifadin) at 600 mg a day. Multibacillary disease gets
the same combination, but for two years and with the addition of
clofazimine (Lamprene) at 50 mg daily.

With those drugs, "we can cure the infection, full stop," Dr. Scollard
said, although some patients will have complications that make the
disease course "more rocky."

Indeed, from 10% to 20% of patients have hypersensitivity reactions,
characterized by systemic inflammation, that can occur up to a decade
after the end of treatment.

"So we never dismiss any of our patients," said Dr. Moschella.

Also, Dr. Krahenbuhl said, if treatment is started late, permanent nerve
damage may already have occurred, which will make care more complicated.

Humans are the main reservoir of the disease, although a related strain
found in armadillos is thought by some experts to be a possible source
for some home-grown U.S. cases.

Most home-grown leprosy occurs in southern states -- Louisiana, Texas,
and the Gulf Coast of Florida -- where armadillos are also present --
but "it's tremendously difficult to connect those dots" because the
disease can take years to develop after exposure, Dr. Krahenbuhl said.

New research on the DNA fingerprint of M. Leprae may allow the program's
experts to nail down the armadillo connection, if it is exists, he said.

In the meantime, physician awareness -- leading to early diagnosis and
treatment -- remains key to controlling the disease, he said.
--
Kathrynne Holden, MS, RD
"Ask the Parkinson Dietitian" http://www.parkinson.org/
"Eat well, stay well with Parkinson's disease"
"Parkinson's disease: Guidelines for Medical Nutrition Therapy"
http://www.nutritionucanlivewith.com/








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