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“Sadly the world has changed.

The threat of bioterrorism is


Bioterrorism real and growing.”

Lester Kallus, MD Margaret Hamburg MD – Oct 12, 1999


Emergency Medicine Department Assistant Secretary
SUNY @ Stony Brook Department of Health and Human Services
(2009 FDA Commissioner)

New York Times – 9/23/01


“Whenever a new or  The nation is "woefully
unexpected disease emerges unprepared to deal with
in an outbreak such as this bioterrorism,“
[West Nile-
Nile-like epidemic], it Jerome M. Hauer,
would be irresponsible not to former head of emergency management for
at least consider the possibility New York City,
told Congress 7/01
of bioterrorism
bioterrorism.” .”
Dr. Margaret Hamburg – Oct 12, 1999, NY Times

Bioterrorism – CDC Category A Bioterrorism – CDC Category A


 High priority agent  Anthrax  Ebola
 Pose national security risk  Botulism  Marburg
 Easily transmitted & disseminated  Plague hemorrhagic fever
 Smallpox  Lassa fever
 High mortality
 Tularemia  Argentine
 Major public health impact hemorrhagic fever

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Bioterrorism – CDC Category B Bioterrorism – CDC Category B
 Easy to disseminate  Q fever  Ricin
 Brucellosis  Clostridium
 Low mortality rates
 Glanders perfringens
 Venezuelan  Staph enterotoxin B
encephalomyelitis
 SalmonellaShigella
 Eastern equine
encephalomyelitis dysenteria
 Western equine  E coli
encephalomyelitis  Vibrio cholerae
 Cryptosporidium
parvum

Bioterrorism – CDC Category C Bioterrorism – CDC Category C


 Emerging Pathogens  Nipah virus
 Possibly engineerable  Hantavirus
 Tickborne hemorrhagic fever
 Tickborne encephalitis virus
 Yellow fever
 Multi-drug resistant tuberculosis

Bioterrorism – Early History Bioterrorism – Early History


 Assyrians poisoned wells with  Romans
Rye Ergot ◦ Used dead animals to foul enemy’s water
◦ Lessened numbers
◦ Lowered morale
 Tartars
◦ Catapulted dead bubonic plague victims
◦ ? Caused medieval European plague epidemic

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Bioterrorism – Early History Bioterrorism – Modern Japanese
 British – French-Indian War  Japanese 1918 formed Unit 731
◦ “Gifts” of smallpox infected blankets ◦ Dedicated to BW
◦ Devastated # of Indians ◦ 1931 used Manchurian prisoners for BW
research
◦ 1941 sprayed bubonic plague over China
◦ 1942 “bacterial bombs” deployed in China
◦ Tested BW on US POWs

Bioterrorism – Modern British Bioterrorism – Modern US


 British  US Program – 1942
◦ Feared a German-Japanese advantage in WW II  Acquired Japanese data
◦ Studied anthrax dispersion  1956 – USSR accused US of using BW in
◦ Gruinard Island off the coast of Scotland Korea
◦ Too close to mainland  USSR threatened retaliatory
 infected coastal sheep Chemical & BW
◦ Gruinard Island still contaminated with spores

Bioterrorism – Modern US Bioterrorism – Modern Russian


 US shifted to “defensive” research 1979 – Sverdlosk factory exploded
followed by Anthrax outbreak – >66 dead
 Sprayed Serratia over populated areas
All accusations of BW research were denied
 San Francisco – 10 infected, 1 died
1992 – Yeltsin confirmed Anthrax research
 1966 B. subtilis dispersed in NY subways vowed to stop all BW research
Allegations of
“super virus” research

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Modern Bioterrorism Bioterrorism – advantages
 Rajneeshee Cult members Great killing efficiency
◦ sprayed salmonella on Oregon salad bars Botulinum 3 million x more potent
◦ >700 infected than Sarin
Cheap
Conventional weapons explode once
BW like the energizer bunny –
keeps on going

Bioterrorism cost to affect 1 km2 Bioterrorism dispersal equipment


Type of weapon Cost Piece of fruit
Conventional $2000 Missile
Nuclear $800 Aerosol equipment (e.g. farm equipment)
Chemical $600
Biological $1

Chemical – Biological Expert Panel


United Nations, 1969

Airplane with 50 kg agent, 2 km line


Bioterrorism – disadvantages
upwind of 500,000 people
Agent Downwind Dead Incapacitated Unpredictable
Reach Weather
Rift Valley Fever 1 400 35,000 ◦ Especially if worried about your own
Tick borne 1 9,500 35,000 troops
Encephalitis ◦ Gruinard Island (Scotland) is a prime
example
Typhus 5 19,000 85,000
Brucellosis 10 500 100,000
Lifespan of material
Q Fever >20 150 125,000
How soon can your troops rush in?
Tularemia >20 30,000 125,000
Horrible stigma – politically damaging
Anthrax >>20 95,000 125,000

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Bioterrorism detection Bioterrorism detection
 Covert event  Require outside assistance
◦ Persons unknowingly exposed
◦ County health officials
◦ Suspected only upon unusual clustering
of disease ◦ State health officials
 Announced event ◦ FBI
◦ Mostly hoaxes in US (so far)
 Must prepare for both types

Bioterrorism & capitalism Bioterrorism & capitalism


 Spam email from “Bayer said that it would increase
janne33@kol.co.kr 10/11/01 production of its antibiotic Cipro, which is
◦ We have Gas Masks the only medicine specifically approved
certified by Israeli Defense for the treatment of inhaled anthrax.”…
and the ONLY anthrax antibiotic available New York Times 10/11/01
(also Viagra)
[cipro = $3/pill doxycycline = $0.04/pill]
◦ “Stock up now while
supplies last worldwide

Epidemiologic features Epidemiologic features


 Rapid increase in disease incidence  Endemic disease in unusual pattern
(days or hours)  Lower attack rate in people who were
 Epidemic curve rises & falls in short indoors
period  Clusters of patients from one locale
 Large # of fatal cases
 Unusual increase in people seeking care
 Characteristic disease:
◦ Fever
◦ Pulmonary anthrax
◦ Respiratory
◦ Tularemia
◦ GI sx
◦ Plague

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Infection control practices Patient placement
Isolation precautions  Small scale event
 Generally not transmitted from person to ◦ Routine facility placement
person ◦ Routine infection control practices
(except pneumonic plague & smallpox)  Larger scale event
 Handwashing ◦ Practical alternatives
 Gloves (wash after removing gloves) ◦ Group affected patients
 Mask & Eye protection ◦ Set up a response center (controlled
entrance)
 Gowns

Discharge management Post--mortem care


Post
 Generally keep in hospital until non-  Path department should be informed!
infectious  Consider funeral directors when
 Consider need for home care - large scale developing plans
event

Psychology of biology of
Prophylaxis & immunization
bioterrorism
 Recommendations subject to change  Fear & panic in patients
 Consult local & state health departments  Minimize panic by clearly explaining risks
& CDC  Avoid unnecessary isolation or quarantine
 Maintain good records  Reassure unexposed patients with
somatic sx.

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Psychology of biology of Anthrax –
bioterrorism ? Safe type
 Fear & panic in staff
 Provide bioterrorism education
 Invite active, voluntary involvement in
planning
 Encourage participation in drills

Anthrax Anthrax – 3 forms


 Bacillus anthracis  Pulmonary – the bioterrorism form
 Spore forming gm(+) rod  Cutaneous
 Sheep, goats, cattle  GI
◦ Eat contaminated soil
 Humans infected from:
◦ Skin
◦ Ingestion
◦ Inhalation of spores (associated with
bioterrorism)

Pulmonary anthrax Anthrax - pulmonary


 1900 – 2000 – 18 cases (last in 1976)  Person to person transmission does not occur
 October 2001 – 22 cases  Person to person transmission does not occur
◦ 11 life-threatening infection  Person to person transmission does not occur
◦ 5 deaths from inhalational anthrax  Person to person transmission does not occur
 Person to person transmission does not occur
 Person to person transmission does not occur
 Person to person transmission does not occur

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Anthrax
Anthrax – pulmonary
Spores
 1st, a
non-specific prodrome – flu-like
symptoms
 Possible brief interim improvement
 2-4 days later
◦ Abrupt respiratory failure
 Transmitted by spores ◦ Hemodynamic collapse
◦ Inhalation of aerosolized spores ◦ Widened mediastinum (mediastinitis)
◦ Cutaneous contact with spores ◦ Gm(+) bacilli on blood culture
◦ Ingestion of contaminated food ◦ Tx too late after pulmonary sx

Anthrax diagnosis
 Isolation of B. anthracis from specimen
 4-fold or greater rise in Elisa
 Demonstration via immunofluorescence

Anthrax Incubation Period Anthrax Infection Control


 Vaccine available (Inactivated, cell-free)  Isolation precautions (use of gloves!)
 Routine procedure for military  Private room is not necessary
 Not recommended for civilians ◦ No human-human transmission
 Standard precautions used
 Standard disinfecting equipment

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Anthrax prophylaxis
Post Exposure Management
 Re-aerosolization risk is low Agent Adults Children
 In cases of high risk Ciprofloxacin 750 mg BID 10-15 mg/kg BID
◦ Cleanse skin Levofloxacin 500 mg OD NR
◦ Instruct patient to remove clothing Ofloxacin 400 mg BID NR
store in labeled plastic bag
◦ Patient must shower with soap & water Doxycycline 100 mg BID 2.5 mg/kg BID
◦ Standard precautions when handling
belongings  If exposure confirmed
◦ Decontaminate surfaces ◦ Rx for 8 weeks
◦ Rx with vaccine

Patient,Visitor & Public Information Botulism


 Exposed victims are NOT contagious  Clostridium botulinum
 Prophylactic antibiotics ARE available  Gm+ bacillus
 Vaccine IS available  Produces potent neurotoxin
 Toxin releases acetylcholine
 Results in flaccid paralysis

Botulism Botulism clinical features


 Food-born disease most common  Food-borne accompanied by GI sx
 Inhalation disease also possible  Both forms share:
◦ Responsive patient, no fever
 NOT transmitted from person to person ◦ Symmetric cranial neuropathies
◦ Blurred vision & diplopia
◦ Respiratory dysfunction (paralysis)
◦ No sensory deficit

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Botulism – Incubation period
Botulism – mode of transmission
Neuro symptoms
 Toxin-contaminated food  GI form – 12-36 hours
 Aerosolized – bioterrorism form  Inhaled form – 24-72 hours

Botulism confirmation Botulism prevention


 Clinically
compatible case  Vaccine currently under development
 Laboratory:  Immunization lasts at least 1 year

◦ Detection of botulinum toxin in  Routine immunization not recommended


serum, stool or food  Heat labile – so heat the food

Infection Control Practices Post exposure management


 Standard precautions  Suspicion even if just one case
 Patient-to-patient transmission does not  If not bioterrorism, maybe mass food
occur exposure
 Standard precautions for transport  Carefully monitor any suspected patient
 Decontamination not indicated
 Trivalent antitoxin available
 Prepare for ventilatory support

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Botulism lab support Pneumonic Plague
 Routine labs of limited value  Yersinia pestis
 Coordinate handling specimens  Gm(-) rod, non motile, pleomorphic
◦ Public Health Authorities
◦ FBI

Pneumonic Plague – clinical features Plague – mode of transmission


 Fever, cough, chest pain  Normally fleas from infected rodents
 Hemoptysis  Bioterrorism – aerosolized
 Lymphadenopathy  Person-to-person transmission
 Muco-purulent watery sputum possible
gm(-) rods on gm stain Large aerosol droplets
 X-ray shows bronchopneumonia
 Highly contagious
 Buboes possible, not necessary

Plague – incubation period Plague communicability


 2-8 days if flea borne  Cough produces infectious particle
 1-3 days if pulmonary exposure droplets
 Use mask for patient care
until 72 hrs of abx

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Plague confirmation Plague prevention
 Laboratory – presumptive:  Vaccine available – not effective for
◦ Elevated serum antibody titer to Y. pestis pneumonic
(in patient with no history of vaccination)  Not available in US
◦ Detection of F1 antigen by fluorescent assay  Involves multiple doses over several
 Laboratory – confirmatory weeks
◦ Isolation of Y. pestis *or*  Post exposure immunization useless
◦ 4fold or greater change in serum antibody
titer

Plague Infection Control Post Exposure Management


 Droplet precautions  Risk or re-aerosolization is low
 Large droplets (generally > 5µ in size)  Remove contaminated clothing – plastic
 Wear mask at least within 3 ft of patient bag
 Private room  Handle clothes minimally – avoid agitation
 Cohort placement  Patient should shower thoroughly
(if no private rooms available)  Standard Universal Precautions
 Maintain 3 feet between patients  Environmental surface decontamination

Plague Prophylaxis for 7 days Plague public information


Antibiotic Adults Children  Fact sheet should be prepared:
Doxycycline 100 mg BID 2.5 mg/kg BID  Description of droplet precaution
Ciprofloxacin 500 mg OD 10-15 mg/kg BID  Difference between prophylaxis &
treatment
 Decontamination by showering

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Smallpox Smallpox Mode of transmission
 Variola virus  Large & Small droplets = airborne!
 Can be transmitted via airborne route  Patient-to-patient transmission likely
 Single case is a  More infectious if coughing or bleeding
public health
emergency

Smallpox incubation period Smallpox prevention


 7-17 days  Vaccine available
 12 day average
 No longer recommended
last case 20 years ago
but…

 Immunization does not


confer lifelong immunity
but…

Smallpox original vaccine Smallpox Infection Control


 Prevent inhalation of particles ≤ 5µ

 Strict Universal Precautions

 Transfer to appropriate isolation room

 In large epidemic, may cohort patients

 Limit transportation
(but use mask on patient if necessary)

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Smallpox post exposure Steps to take upon initial suspicion
management
 Decontamination not indicated
 Post exposure immunization effective
 Vaccination alone if < 3 days
 IGG also if > 3 days
 Vaccination contraindicated:
◦ Pregnancy
◦ Immunocompromised patient

Sandia Laboratory –
Decontamination Foam
Application
new chem-
chem-bio
decontamination
foam from
pressurized
canister

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