Medical Revisionists Threaten Effective Lyme Treatment
DR.
RAPHAEL B. STRICKER
HARTFORD COURANT
July
31st, 2006
A
small group of scientists is turning the world of Lyme
disease on its head. They deny the existence of chronic
Lyme disease.
They insist there is no "credible scientific evidence"
for persistent infection after a short course of
antibiotic treatment because the corkscrew-shaped
bacteria that causes Lyme disease, Borrelia burgdorferi,
cannot survive this treatment.
Fearing "over-diagnosis," they publish guidelines
endorsing an insensitive testing program that misses
half the patients with the tick-borne illness.
Fearing "over-treatment," they recommend antibiotic
therapy barely adequate for acute infection and wholly
inadequate for chronic Lyme disease.
Soon they will publish the latest version of an already
restrictive set of guidelines that will further pressure
the Centers for Disease Control and Prevention and
academic institutions to ignore chronic Lyme disease.
The guidelines will encourage insurance companies to
embrace up-front cost savings inherent in shorter
treatment and deny payment for longer treatment, even if
the Lyme patient is still sick but showing signs of
improvement.
Although the Lyme denialists claim support from
mainstream medical groups, the reality is that the
handful of them have managed to dictate policy to larger
health care organizations through a closed process that
rejects dissenting views. Unaware of this one-sided
process, the rest of the medical industry blindly
follows their lead while patients suffer.
Lyme disease is the most common tick-borne illness in
the world. Named after the town where it was discovered
in 1975, the disease is transmitted by the bite of an
infected tick. Research has demonstrated that the Lyme
bacteria is one of the most invasive and elusive
pathogens known to man. After causing a telltale
"bulls-eye" rash, the bacteria screws its way into
multiple organs and tissues to produce
often-debilitating muscle, joint, nerve, brain and heart
ailments.
Although New England remains the epicenter of the
disease, with up to 20 percent of new cases reported in
Connecticut alone, Lyme disease and associated
infections are popping up in new locations around the
globe. Where you live doesn't accurately reflect your
risk of catching Lyme disease because people travel on
planes, trains and automobiles, while ticks travel on
deer, birds and household pets. As a result, the risk of
acquiring the disease is increasing unpredictably.
We know treatment is effective when instituted early,
but fewer than half the people with Lyme disease even
remember getting a tick bite or seeing a rash. The
resulting infection may spread and become chronic before
the victim has a chance to seek treatment.
Research over the past two decades suggests the key to
eliminating chronic Lyme disease is prolonged antibiotic
therapy. Lyme-treating physicians recognize this fact
and studies support it.
The Lyme denialists refuse to accept this point of view.
Imagine if "AIDS denialists" had won out in the early
1990s. Doctors would have refused to prescribe antiviral
medications and insurance companies would have refused
to pay for them. How many millions of patients would
have gone undiagnosed and untreated?
Sound scary? Welcome to the world of Lyme disease run by
Lyme denialists.
Today many Lyme patients are going undiagnosed and
untreated because of the Lyme denialist agenda. Although
Lyme disease is usually not fatal, the disability
associated with a chronic case is equivalent to
congestive heart failure.
Health care providers, government agencies and Lyme
patients must confront the Lyme denialists and fight for
better recognition and treatment of Lyme disease.
Raphael B. Stricker, MD, of California is
president of the International Lyme & Associated
Diseases Society.
Article published in the HARTFORD COURANT. July
31st, 2006.