Every patient tells a story by Lisa Sanders
Author:Lisa Sanders [Sanders, Lisa]
Language: eng
Format: mobi
Tags: Clinical medicine, Nursing, Medical, Differential, Physician-Patient Interaction, General, Diagnosis, Diagnostic Errors, Popular Works
ISBN: 9780767922463
Publisher: Random House, Inc.
Published: 2009-08-11T11:05:24+00:00
CHAPTER EIGHT
Testing Troubles
C arol Ann DeVries felt like she
was falling apart. A compact
woman with a cheerful, round face
and deep-set brown eyes, she had
been healthy all her life. Then, just
a few weeks after her fifty-ninth
birthday, everything changed. Out of
nowhere she got a rampant case of
hives. A short course of prednisone
cleared them up, but neither Carol
Ann nor her internist could figure
out where they’d come from.
Then, one Saturday morning, a
few days later, she awoke feeling
achy and hot, her throat was
sandpaper, and she had an odd red
rash near the base of her spine. Was
this more hives? Carol Ann had a
doctor’s appointment scheduled for
the next week, but she felt too awful
to wait. She drove herself to the
emergency room of her local
hospital.
The
ER
doctor
took
her
temperature, looked at the rash, and
briskly told her she had Lyme
disease. “An antibiotic will clear it
up,”
he
said,
scribbling
the
prescription. “One pill twice a day
for two weeks,” he told her, and he
headed out the door. “Wait a
second,” Carol Ann called after
him. “Aren’t you even going to get a
test to see if I have Lyme?”
“You don’t need it,” he told her,
ticking off the items that supported
his diagnosis. It was early summer,
when Lyme is most common. She
lived in suburban Connecticut—not
too far from the actual town of
Lyme, where the disease was first
identified. And she had a big, round
rash typical of those seen in the
early stages of Lyme disease.
He
acknowledged
that
her
symptoms weren’t the classic
headache and stiff neck, but, still,
she had the fever and body aches.
The odds were overwhelming that
this was Lyme, he told her.
“Besides, this early in the disease,
the Lyme test wouldn’t tell us a
thing.” Then he was gone, off to the
next room, the next patient, leaving
Carol Ann with his scrawled
prescription and a feeling of
uncertainty.
Every spring and summer some
version of this story is repeated tens
of thousands of times in states of the
Northeast, Midwest, and northern
West Coast. Often, as in Carol
Ann’s case, the diagnosis will be
made without a test, based on the
patient’s geography and symptoms,
and cinched by the presence of the
typical rash, known as erythema
migrans. The diagnosis will be
appropriate and reasonable, but not
definitive. And in Lyme disease,
that uncertainty has proved to be a
particularly noxious ingredient.
Carol Ann took the antibiotics as
prescribed.
By
the
following
weekend she felt almost back to her
usual self. For most patients with
Lyme disease, a single course of
antibiotics is curative. But if Carol
Ann had had a simple case of Lyme
disease, I wouldn’t be telling you
this story. Instead, a few weeks
later, Carol Ann developed pain
and stiffness in her knees and hips.
There was no swelling, no redness,
just this strange reluctance in the
joints of her lower body.
She went to her internist, who
thought the symptoms were from
Lyme
disease.
Untreated
or
inadequately treated, Lyme can
attack the joints, causing pain, and
usually swelling. He changed her to
another
antibiotic—doxycycline.
She stayed on that for three more
weeks but the stiffness continued.
Her internist was baffled; he sent
her to a rheumatologist. The
rheumatologist wasn’t sure what
was going on either. So she went
back to her internist. “He fobbed me
off on his physician’s assistant,”
Carol Ann said. “I was practically
crying over the phone because of
the pain. I told the PA I couldn’t
even sleep because the pain was so
bad. She wasn’t very sympathetic.”
Carol Ann felt abandoned. Her
doctor was a nice guy, she told me,
but he clearly didn’t know what
was causing her pain or what to do
about it.
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