Anthrax Information for Health Care Providers
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Department of Health and Mental Hygiene
S. Anthony McCann, Secretary
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Community Health Administration
Diane Matuzak, Director
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Office of Epidemiology and Disease Control Programs
John P. Krick, Ph.D., Director
September 26, 2001
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TO REPORT: Any confirmed or suspected case of anthrax
(Bacillus anthracis) must be reported IMMEDIATELY to the local
Health Department or the Department of Health and Mental Hygiene
at 410-767-5866
Anthrax
- Caused by Bacillus anthracis, a large, encapsulated,
gram-positive, aerobic, non-motile, spore-forming bacillus
- Transmission to humans usually occurs through occupational
contact with infected animals or animal products
- Naturally acquired anthrax in humans most commonly involves
the skin (cutaneous anthrax); inhalation anthrax and gastrointestinal
(GI) anthrax are rare
- B. anthracis is considered one of the most likely biological
warfare or terrorist threat agents
Inhalation anthrax, caused by inhaling aerosolized spores,
will be the most likely outcome of an intentional (bioterrorist)
exposure
- Person-to-person transmission does NOT occur with inhalation
or GI anthrax
Inhalation anthrax
Incubation: 1-5 days (may be as long as 60 days
with low inoculum exposures)
Sign and Symptoms: Typically a bi-phasic illness:
Iitial Phase: Characterized by flu-like symptoms:
Low grade fever, non-productive cough, malaise, fatigue,
myalgias, mild chest discomfort. Rhonchi may be present,
otherwise normal exam.
Acute Phase: Develops 1-5 days after initial symptoms.
May be preceded by <1-3 days of improvement. Characterized
by abrupt development of severe respiratory distress with
dyspnea, stridor, cyanosis, and high fever. Shock and death
usually follow within 24-36 hours after onset of respiratory
distress. The average interval between onset of initial
phase and death is 3 days.
| CXR:
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Mediastinal
widening, often with pleural effusion, but usually no
infiltrates (highly suspicious for anthrax) |
Autopsy Clues: Hemorrhagic necrotizing mediastinitis and
thoracic hemorrhagic necrotizing lymphadenitis. Hemorrhagic
meningitis may also be present.
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IF YOU HAVE REASON TO SUSPECT
ANTHRAX, ALERT YOUR LABORATORY AND LOCAL OR STATE
PUBLIC HEALTH PERSONNEL IMMEDIATELY
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Laboratory Clues to Bacillus anthracis:
Peripheral blood smear: gram-positive bacilli on an unspun
smear.
Microbiology: Aerobic blood culture growth of large, gram-positive
bacilli with preliminary identification of Bacillus species
Laboratory Confirmation of Diagnosis
- Should be performed by the State Department of Health
(DOH) Public Health Laboratory
Appropriate clinical samples for testing at DOH include:
blood (most important); pleural fluid and CSF may be helpful
- Transport and packaging of clinical specimens must be
coordinated with local and State health departments
- DOH has the capacity to report some preliminary results
within 2 to 4 hours
Treatment of Inhalation Anthrax
Early (during the initial phase) antibiotic treatment is
essential. Mortality may still be high (~90%) after the
onset of symptoms even with treatment
Natural strains of anthrax are resistant to extended-spectrum
cephalosporins, sulfamethoxizol, and trimethoprim: these
should not be used for treating (or prophylaxing for) anthrax
Physicians may be asked to get an informed consent signed
for administration of certain medications supplied by the
National Pharmaceutical Stockpile (NPS)
Anthrax Treatment Protocol (**indicated
medications which
will be supplied as part of the NPS maintained at the CDC)
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Adults:
Intravenous
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**Ciprofloxacin 400 mg BID
OR
**Doxycycline 200 mg x 1, then 100 mg BID
OR
Erythromycin 15-20 mg/kg/day in divided doses
OR
**Penicillin G 20 MU/day in divided doses (if in vitro
sensitivity indicates susceptibility)
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Estimated for 7 days. (Switch to oral antibiotic therapy
when clinically appropriate to complete 60-day regimen.) |
| Oral |
**Ciprofloxacin 500 mg BID
OR 2
**Doxycycline 100 mg BID |
Estimated for 60 days |
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Children
Intravenous
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**Ciprofloxacin 15 mg/kg IV Q12hrsOR
**Doxycycline4:
> 8 yrs and > 45 kg: 200mg x 1 dose, then 100
mg BID
> 8 yrs and 45 kg: 4.4 mg/kg x 1 dose, then 2.2-4.4
mg/kg/day in 2 divided doses
8 yrs: (same as > 8 yrs and 45 kg)
OR
Erythromycin 15-20 mg/kg/day IV in divided doses
OR
**Penicillin G 400,000 Units/kg/day in divided doses
(if in vitro sensitivity indicates susceptibility) |
Estimated for 7-14 days. (Switch to oral antibiotic
therapy when clinically appropriate to complete 60-day
regimen.) |
| Oral |
**Ciprofloxacin 15-20 mg/kg Q12 hrs3
OR
Estimated for 60 days
**Doxycycline4:
> 8 yrs and > 45 kg: 100 mg BID
> 8 yrs and 45 kg: 2.2 mg/kg BID
8 yrs: same as above |
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| Pregnancy |
Same as for non-pregnant adults (the high mortality
rate from the infection outweighs the risk posed by
the antibiotic)
**Doxycycline oral not recommended for more than 14
days of therapy. |
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| Immuno-compromised |
Same as for non-immunocompromised adults and children
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Therapy with ciprofloxacin may be initiated either as intravenous
or oral dosage form. The pharmacokinetics are such that
oral ciprofloxacin is rapidly and well absorbed from the
GI tract with no substantial loss by first-pass metabolism.
Maximum serum concentrations are attained 1-2 hours after
oral dosing.
If susceptibility testing allows, therapy should be changed
to IV penicillin for treatment or oral amoxicillin for post-exposure
prophylaxis to continue therapy out 60 days. Ciprofloxacin
dose should not exceed 1gram/day in children.
In 1991, the American Academy of Pediatrics amended their
recommendation to allow treatment of young children with
tetracyclines for serious infections, such as, Rocky Mountain
Spotted Fever, for which doxycycline may be indicated. Doxycycline
is preferred for its twice-a-day dosing low incidence of
gastrointestinal side effects.
Although tetracyclines are not recommended during pregnancy,
its use may be indicated for life-threatening illness. Adverse
affects on developing teeth and bones are dose related,
therefore, doxycycline might be used for a short course
of therapy (7-14 days) prior to the 6th month of gestation.
Please consult physician after the 6th month of gestation
for recommendations.
Cutaneous Anthrax (a possible, though unlikely outcome
of a terrorist release of B. anthracis)
- Local skin involvement after direct contact with spores
or bacilli
- Commonly seen on exposed areas: face, neck, forearms,
hands
- Localized itching, followed by a papular lesion that
turns vesicular, followed by development of a black eschar
within 7-10 days of onset of the initial lesion
- Usually non-fatal if treated with appropriate antibiotics
for 7-10 days
- Wound or wound drainage may be contagious (direct contact):
follow standard wound precautions
Gastrointestinal Anthrax(very unlikely outcome of
a terrorist release of B. anthracis)
- Abdominal pain, nausea, vomiting, and fever following
ingestion of contaminated food, usually meat
Bloody diarrhea, hematemesis
- Gram-positive bacilli on blood or stool culture, usually
after 2-3 days of illness
- Usually fatal after progression to septicemia
- Treatment is the same as for Inhalation Anthrax (see
Inhalation Anthrax Treatment Protocol)
Post-Exposure Prophylaxis
- Antibiotic prophylaxis should be initiated when exposure
to aerosolized anthrax spores is suspected
- Initiation of prophylaxis, especially in children, should
be coordinated with the local health jurisdiction or the
DOH
- Prophylaxis should continue for at least 60 days if
the exposure is confirmed
- Physicians may be asked to get an informed consent signed
for administration of certain medications supplied by
the National Pharmaceutical Stockpile (NPS)
Post-Exposure Prophylaxis Protocol (**indicated medications
which will be supplied as part of the NPS maintained at
the CDC)
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Initial Therapy
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Duration
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| Adults, including pregnant women and Immuno-compromised |
**Ciprofloxacin 500 mg po BID OR
**Doxycycline 100 mg po BID
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60 days |
| Children |
**Ciprofloxacin 15-20 mg/kg po Q12 hrs
OR
**Doxycycline5:
> 8 yrs and > 45 kg: 100 mg po BID
> 8 yrs and 45 kg: 2.2 mg/kg po BID
8 yrs: (same as > 8 yrs and 45 kg)
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60 days |
If susceptibility testing allows, therapy should be changed
oral amoxicillin for post-exposure prophylaxis to continue
therapy out to 60 days.
Although tetracyclines are not recommended during pregnancy,
its use may be indicated for life-threatening illness. Adverse
affects on developing teeth and bones are dose related,
therefore, doxycycline might be used for a short course
of therapy (7-14 days) prior to the 6th month of gestation.
Please consult physician after the 6th month of gestation
for recommendations.
Use of tetracyclines and fluoroquinolones in children has
well-known adverse effects; these risks must be weighed
carefully against the risk for developing life-threatening
disease. If a release of B. anthracis is confirmed, children
should be treated initially with ciprofloxacin or doxycycline
as prophylaxis but therapy should be changed to oral amoxicillin
40 mg per kg of body mass per day divided every 8 hours
(not to exceed 500 mg three times daily) as soon as penicillin
susceptibility of the organism has been confirmed.
Ciprofloxacin dose should not exceed 1gram/day in children.
In 1991, the American Academy of Pediatrics amended their
recommendation to allow treatment of young children with
tetracyclines for serious infections, such as, Rocky Mountain
Spotted Fever, for which doxycycline may be indicated. Doxycycline
is preferred for its twice-a-day dosing low incidence of
gastrointestinal side effects.
Anthrax Vaccine
- An inactivated cell-free vaccine that is used primarily
by the military and those at occupational risk
- Is only licensed for use in healthy adults aged 18-65
- Anthrax vaccine should be administered at 0, 2 and 4
weeks following exposure.
- Supplies are very limited, however, and it is unlikely
that the vaccine will be available for the general public
in the future
- If vaccine is not available, antibiotic treatment should
be continued for at least 30 days and possibly up to 60
days
Infection Control
Standard (Universal) Precautions for care and transport
of patients and during post-mortem care
- Wound precautions for patients with cutaneous anthrax
- Isolation of patients is NOT necessary; however, the
following extra precautions are advised:
- After an invasive procedure, instruments used should
be autoclaved
- Contaminated clothing/bedding should be placed in labeled,
plastic bags for later incineration or steam sterilization
Spills of potentially infected body fluid or tissue:
- Gently cover, then liberally apply 0.5% hypochlorite
( a 1:10 dilution of household bleach)
- Let sit for at least 20 minutes before cleaning up (work
from perimeter to center)
- Any materials used in the clean-up must be autoclaved
or incinerated
- Rinse off the concentrated bleach to avoid its caustic
effects
Contamination of personnel
- Remove outer clothing carefully where spill occurred
and place in a labeled, plastic bag
- Remove rest of clothing in the locker room and place
in a labeled, plastic bag
- Shower thoroughly with soap and water
If exposure to contaminated sharps occurs:
Follow standard reporting procedures for sharps exposures
- Thoroughly irrigate site with soap and water and apply
a disinfectant solution such as hypochlorite solution.
DO NOT SCRUB AREA.
- Promptly begin therapy for cutaneous anthrax
- Recommended treatment for cutaneous exposure: prophylaxis
with Ciprofloxacin 500 mg Po BID x 7-10 days
- Notify the DOH
Decontamination of environment
Use a decontamination solution , 0.5% hypochlorite ( a
1:10 dilution of household bleach) for surfaces
Let sit for at least 20 minutes before cleaning up (work
from perimeter to center)
Routinely clean non-sterilizable equipment with a sterilizing
solution
Cremation should be considered due to potential risks associated
with embalming
References
- Inglesby TV, Henderson DA, Barlett JG, Ascher MS, et
al. Anthrax as a biological weapon: Medical and public
health management (consensus statement). JAMA, May 12,
1999;281(18):1735-1745.
- No authors listed. Biological warfare and terrorism:
the military and public health response. U.S. Army, Public
Health Training Network, Centers for Disease Control,
and Food and Drug Administration Satellite broadcast,
September 21-23, 1999.
- Physicians Desk Reference, 53rd edition, 1999.
Medical Economics Co., Montvale, NJ.
WHO Guidelines
- Emerging Bacterial and Mycotic Disease Branch, DBMD,
NCID, CDC: (February 12, 1999)
AHFS Drug Information® 1999
- Drugs Facts and Comparisons® 2000
- 2000 Red Book, Report of Committee on Infectious Diseases,
25th Edition, American Academy of Pediatricians
- Mandell, Douglas, and Bennetts, Principles and
Practices of Infectious Diseases, 5th Edition
Benenson AS. Control of Communicable Diseases Manual,
American Public Health Association, Washington, DC 16th
Edition, 1995.
- Abramson J, Jon S, Givner LB. Rocky Mountain Spotted
Fever. [Review] Ped Inf Dis J. 18(6):539-540, June 1999.
- Centers for Disease Control and Prevention: Anthrax:
Recommendations of the Immunization Practices Advisory
Committee (ACIP), in press.
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