Exams and Tests
If you have symptoms that could be
caused by
anthrax, your doctor will use a medical history and
tests to find out whether you may have been exposed to anthrax spores. He or
she will ask where you work and about other environmental exposures that may
have put you at risk. Postal workers, for example, were at risk of exposure to
spores in the 2001 bioterrorism attacks.
If your doctor is at all
suspicious that you may have been exposed to anthrax, you will be treated with
antibiotics until a diagnosis can be confirmed or ruled out.
Doctors diagnose anthrax when Bacillus anthracis
bacteria are identified from a
culture and sensitivity test of the blood, spinal
fluid, skin sores, or respiratory fluids. The Anthrax Quick ELISA test has been
approved by the U.S. Food and Drug Administration (FDA) to identify the
Bacillus anthracis bacteria. This test of the blood can
be completed faster than previous tests for anthrax. Most doctors will not have
the Anthrax Quick ELISA test in their office and will send blood samples to a
laboratory to be tested.
Biopsy of a
skin ulcer also may be done to diagnose cutaneous anthrax.
If
results of a culture are not clear, blood tests or
polymerase chain reaction (PCR) may be done.
Nose swabs may help state and federal health departments determine how
many people in an area have been recently exposed to anthrax. But they are not
used to diagnose anthrax or to assist a doctor in deciding how to treat
it.
You may have imaging tests to look for signs of inhalational
anthrax infection.
- A
chest X-ray may reveal widening of the structures in
the middle of the chest, and fluid (pleural effusion) between the thin tissues
that separate the lungs from the chest wall.
- A
computed tomography (CT) scan may show these changes
and bleeding from lymph nodes in the chest.