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Title: Preparing for and Responding to Bioterrorism: Information for the Public Health Workforce


1
Preparing for and Responding to Bioterrorism
Information for the Public Health Workforce
2
Acknowledgements
This presentation, and the accompanying
instructors manual, were prepared by Jennifer
Brennan Braden, MD, MPH, at the Northwest Center
for Public Health Practice in Seattle, WA, for
the purpose of educating public health employees
in the general aspects of bioterrorism
preparedness and response. Instructors are
encouraged to freely use all or portions of the
material for its intended purpose. The
following people and organizations provided
information and/or support in the development of
this curriculum. A complete list of resources
can be found in the accompanying instructors
guide.
Patrick OCarroll, MD, MPH Project Coordinator
Centers for Disease Control and Prevention
Judith Yarrow Design and Editing Health Policy
and Analysis University of WA Washington State
Department of Health
Jeff Duchin, MD Jane Koehler, DVM,
MPH Communicable Disease Control, Epidemiology
and Immunization Section Public Health - Seattle
and King County Ed Walker, MD University of
WA Department of Psychiatry
3
Diseases of Bioterrorist Potential Plague and
Botulism
CDC, AFIP
4
Diseases of Bioterrorist Potential Learning
Objectives
  • Describe the epidemiology, mode of transmission,
    and presenting symptoms of disease caused by the
    CDC-defined Category A agents
  • Identify the infection control and prophylactic
    measures to implement in the event of a suspected
    or confirmed Category A case or outbreak

5
PlagueHistory Significance
  • 14th Century Black Death responsible for
    gt20million deaths in Europe
  • Used as a BW agent by Japan in WW II
  • Studied by Soviet and, to a smaller extent, U.S.
    BW programs
  • 1995 Larry Wayne Harris arrested for illicit
    procurement of culture via mail

6
PlagueEpidemiology
  • Caused by Yersinia pestis
  • About 10-15 cases/year U.S.
  • Mainly SW states
  • Human plague occurs from bite of an infected flea
    (bubonic)
  • Only pneumonic form of plague is spread
    person-to-person
  • Last case of person-to-person transmission in
    U.S. occurred in 1924

7
Yersinia Pestis
  • Gram negative, non-motile, non-spore-forming
    bacillus
  • Resistant to freezing temperature and drying,
    killed by heat and sunlight

Source Centers for Disease Control and
Prevention, Division of Vector-Borne Infectious
Diseases, Fort Collins, CO
8
Plague Case Definition
  • Characterized by fever, chills, headache,
    malaise, prostration, leukocytosis that
    manifests in one or more of the following
    clinical forms
  • Regional lymphadenitis (bubonic)
  • Septicemia w/o evident bubo (septicemic)
  • Plague pneumonia
  • Pharyngitis cervical lymphadenitis (pharyngeal)

MMWR 199746(RR-10)
9
PlagueCase Definition, cont.
  • Laboratory criteria for diagnosis
  • Presumptive
  • Elevated serum antibody titers to Y. pestis F1
    antigen (w/o documented 4-fold change) in a
    patient with no history of plague vaccination OR
  • Detection of F1 antigen in a clinical specimen by
    fluorescent assay
  • Confirmatory
  • Isolation of Y. pestis from a clinical specimen
    OR
  • 4-fold or greater change in serum antibody titer
    to Y. pestis F1 antigen

MMWR 199746(RR-10)
10
Plague Case Classification
  • Suspected Clinically compatible case w/o
    presumptive or confirmatory lab results
  • Probable Clinically compatible case with
    presumptive lab results
  • Confirmed Clinically compatible case with
    confirmatory lab results

MMWR 199746(RR-10)
11
PlagueClinical Forms
  • Bubonic plague
  • Most common naturally-occurring form
  • Mortality 60 untreated, lt5 treated
  • Primary or secondary septicemic plague
  • Pneumonic plague
  • Most likely BT presentation
  • From aerosol or septicemic spread to lungs
  • Survival unlikely if treatment not initiated w/in
    24 hours of the onset of symptoms

12
Pneumonic PlagueClinical Presentation
  • Incubation 1-6 days (usually 2-4 days)
  • Acute onset of fever with cough, dyspnea, and
    chest pain
  • Hemoptysis characteristic watery or purulent
    sputum also possible
  • Prominent GI symptoms may be present, including
    nausea, vomiting, diarrhea, and abdominal pain

13
Pneumonic PlagueClinical Presentation
  • Other symptoms include headache, chills, malaise,
    myalgias
  • Rarely, cervical bubo present
  • Rapid progression to respiratory failure shock

14
Bubonic Plague
  • Incubation 2-8 days
  • Sudden onset nonspecific symptoms fever, chills,
    malaise, muscle aches, headache
  • Regional lymphadenitis (buboes)
  • Swollen, very painful lymph nodes
  • Typically inguinal, femoral, axillary, or
    cervical
  • Erythema overlying skin
  • May have surrounding edema
  • Concurrent with or shortly after onset of other
    symptoms

15
Septicemic Bubonic Plague
Source CDC NVBID
16
PlagueInfection Control
  • Person-to-person transmission via respiratory
    droplets
  • Standard respiratory droplet precautions
  • Treatment 10 days antibiotics
  • Case isolation for at least the first 48 hrs of
    antibiotic treatment
  • Bubonic plague - standard precautions

17
PlagueInfection Control
  • Antibiotic prophylaxis for close contacts
  • Duration 7 days or duration of risk of exposure
    7 days
  • Close contacts refusing prophylaxis
  • Observe 7 days after last exposure and treat if
    fever or cough develop
  • Bubonic contacts
  • Observe 7d and treat if symptoms develop

18
Plague Summary of Key Points
  • The most likely presentation in a BT attack is
    pneumonic plague.
  • Unlike other forms of plague, pneumonic plague is
    transmitted person to person, and thus
    respiratory droplet precautions are indicated in
    suspected cases until 48 hours after the
    initiation of antibiotic therapy.

19
Case Reports
  • Plague

Plague Pneumonia - CA. MMWR 198433(34)
Pneumonic Plague -- Arizona, 1992. MMWR 41(40)

20
Clostridium Botulinum
  • C. botulinum spores found in soil worldwide
  • Toxin causative agent of botulism
  • Types A-G A,BE most commonly associated with
    human disease
  • Most potent toxin known (lethal dose 1ng/kg)
  • Inactivated by chlorine (20min) and sunlight
    (1-3hrs) destroyed by heat (5min at 85?C)
  • Absorbed into circulation via mucosal surface or
    wound, not intact skin
  • Interferes with nerve transmission ? paralysis

21
Clostridium BotulinumEpidemiology
  • Approximately 100 reported cases botulism/year
    in the U.S.
  • Infant most common (72)
  • Food-borne not common
  • Incubation (food-borne) 12-72hrs (range 2hr-8d)
  • Dose dependent
  • Could be less following a BT attack
  • No person-to-person transmission
  • Death 60 untreated lt5 treated

22
Botulism Bioterrorism
  • Weaponized by former U.S. and Soviet offensive BW
    programs
  • Iran, Iraq, N. Korea, Syria believed to have
    developed/be developing toxin as a weapon
  • Aerosol use or food supply sabotage most likely

23
BotulismClinical Forms
  • Food-borne
  • Toxin produced anaerobically in improperly
    processed or canned, low-acid foods contaminated
    by spores
  • Wound
  • Toxin produced by organisms contaminating wound
  • Infant
  • Toxin produced by organisms in intestinal tract
  • Inhalation botulism
  • No natural occurrence, developed as BW weapon

3 accidental cases in veterinary personnel, W.
Germany, 1962
24
Botulism Case Definition
  • Ingestion of botulinum toxin results in an
    illness of variable severity. Common symptoms
    are diplopia, blurred vision and bulbar weakness.
    Symmetric paralysis may progress rapidly.
  • Laboratory criteria for diagnosis
  • Detection of botulinum toxin in serum, stool or
    patients food (food-borne) or other clinical
    specimen (botulism, other) OR
  • Isolation of Clostridium botulinum from stool
    (food-borne) or other clinical specimen

Assay available at CDC some state public
health labs
MMWR 199746(RR-10)
25
Botulism Case Classification
  • Botulism, Food-borne
  • Probable Clinically compatible with an
    epidemiologic link
  • Confirmed Clinically compatible case that is
    laboratory confirmed or that occurs among persons
    who ate the same food as persons who have
    laboratory-confirmed botulism
  • Botulism, Other
  • Confirmed Clinically compatible case that is
    laboratory confirmed in a patient ? 1 yr who has
    no history of ingestion of suspect food and has
    no wounds

age parameter may not apply in BT
MMWR 199746(RR-10)
26
BotulismTreatment
  • Ventilatory assistance and supportive care
  • Standard precautions
  • Botulinum antitoxin
  • Most effective if given early does not reverse
    effect of toxin already bound to nerve receptor
  • Trivalent equine product against types A,B, and E
    currently available from CDC
  • Heptavalent (A-G) antitoxin - investigational
  • Monovalent human anti-serum for infant botulism
    -investigational

27
BotulismProphylaxis
  • Pre-exposure
  • Prophylaxis for at-risk lab workers and military
    with investigational vaccine
  • No pre-exposure prophylaxis recommended for
    general public
  • Post-exposure close monitoring of those exposed
    treat with antitoxin at first signs of illness

28
Botulism Summary of Key Points
  • An outbreak of botulism occurring with a common
    geographic factor, but with no common food
    exposure, would suggest a deliberate aerosol
    exposure.
  • Inhalational botulism does not occur naturally,
    and any potential cases suggest a deliberate
    source of infection.

29
Botulism Summary of Key Points
  • Gastrointestinal symptoms may not occur with
    inhalational botulism or with food-borne botulism
    (e.g., resulting from deliberate contamination of
    the food supply).
  • Botulinum antitoxin must be administered as soon
    as possible for optimum results.

30
BotulismCase Reports


MMWR Morb Mortal Wkly Rep 199948(21)



MMWR Morb Mortal Wkly Rep 199544(48)
31
Resources
  • Centers for Disease Control Prevention
  • Bioterrorism Web page
  • CDC Office of Health and Safety Information
    System (personal protective equipment)
  • USAMRIID -- includes link to on-line version of
    Medical Management of Biological Casualties
    Handbook
  • Johns Hopkins Center for Civilian Biodefense
    Studies

http//www.bt.cdc.gov/
http//www.cdc.gov/od/ohs/
http//www.usamriid.army.mil/
http//www.hopkins-biodefense.org
32
Resources
  • Office of the Surgeon General Medical Nuclear,
    Biological and Chemical Information
  • St. Louis University Center for the Study of
    Bioterrorism and Emerging Infections
  • Public Health - Seattle King County

http//www.nbc-med.org
http//bioterrorism.slu.edu
http//www.metrokc.gov/health
33
Resources
  • Washington State Department of Health
  • Communicable Disease Epidemiology
  • (206) 361-2914 OR
  • (877) 539-4344 (24 hour emergency)
  • Association for Professionals in Infection
    Control
  • MMWR Rec Rep. Case definitions under public
    health surveillance.

http//www.doh.wa.gov
http//www.apic.org/bioterror
199746(RR-10)1-55
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