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BIOTERRORISM

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Yersinia pestis (plague) Class B agents: less potential. Class C agents: future threats ... Yersinia pestis (Pneumonic plague) Incubation: 2-3 days. S&S: ... – PowerPoint PPT presentation

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Title: BIOTERRORISM


1
BIOTERRORISM
  • June 15, 2006
  • Christina M. Cabott D.O.

2
Introduction
  • Bioterrorist event
  • Release of biological agent into civilian
    population
  • Purpose
  • Creating fear
  • Illness
  • Death
  • Disruption of social and economic infrastructure

3
Introduction
  • Biological agents
  • Infectious agents
  • Contagious
  • Noncontagious
  • Biologically produced toxins
  • Act as chemical agents within human body

4
Agents of Concern
  • Agent selection
  • 1. Potential for public health impact
  • 2. Delivery potential
  • Estimation of ease for development and
    dissemination
  • Potential for person-to-person transmission of
    infection
  • 3. Public perception (fear) of the agent
  • 4. Special requirements for public health
    preparedness

5
Agents of Concern
  • Ranking category
  • Class A agents most severe potential for
    widespread illness and death
  • Variola major (small pox)
  • Bacillus anthracis (anthrax)
  • Yersinia pestis (plague)
  • Class B agents less potential
  • Class C agents future threats

6
Class A Agents
  • Variola major (small pox)
  • Incubation 12-14 days
  • SS
  • Initially fever, severe myalgias, prostration
  • Within 2 days papular rash on face spreading to
    extremities ? rash on palms and soles ? trunk
  • Lesions progress at same rate
  • Vesicular ? pustular ? scabs

7
Class A Agents
  • Bacillus anthracis (Cutaneous anthrax)
  • Incubation usually lt 1 day, up to 2 weeks
  • SS
  • Macule or papule enlarging into eschar
  • Surrounding vesicles and edema
  • Sepsis possible

8
Class A Agents
  • Bacillus anthracis (GI anthrax)
  • Incubation usually 1-7 days
  • SS
  • Abdominal pain
  • Vomiting
  • GI bleeding leading to sepsis
  • Mesenteric adenopathy on CT

9
Class A Agents
  • Bacillus anthracis (Oropharyngeal anthrax)
  • Incubation usually 1-7 days
  • SS
  • Sore throat
  • Ulcers on base of tongue
  • Marked unilateral neck swelling

10
Class A Agents
  • Bacillus anthracis (Inhalational anthrax)
  • Incubation usually lt 1 week
  • SS
  • 1st stage fever, dyspnea, cough, headache,
    vomiting, abdominal pain, chest pain
  • 2nd stage dyspnea, diaphoresis, shock
  • Hemorrhagic mediastinitis with widened
    mediastinum on CXR

11
Class A Agents
  • Yersinia pestis (Bubonic plague)
  • Incubation 2-8 days
  • SS
  • Fever, chills, painful swollen lymph nodes
  • Nodes progress to bubo (possibly suppurative)

12
Class A Agents
  • Yersinia pestis (Pneumonic plague)
  • Incubation 2-3 days
  • SS
  • Fever, chills, cough, dyspnea, nausea, vomiting,
    abdominal pain
  • Clinical condition consistent with gram-negative
    sepsis

13
Class A Agents
  • Yersinia pestis (Primary septicemic plague)
  • Incubation 2-8 days
  • SS
  • After bubo formation, clinical condition
    consistent with gram-negative sepsis, DIC

14
Class A Agents
  • Clostridium botulinum (Food-born botulism)
  • Incubation 1-5 days
  • SS
  • GI symptoms
  • Followed by symmetric cranial neuropathies,
    blurred vision
  • Progresses to descending paralysis

15
Class A Agents
  • Clostridium botulinum (Inhalational botulism)
  • Incubation 12-72 hours
  • SS
  • Symmetric cranial nerve palsies
  • Progresses to descending paralysis

16
Class A Agents
  • Francisella tularensis (Tularemia)
  • Incubation 2-5 days
  • SS
  • Abrupt nonspecific febrile illness
  • Progressing to pleuropneumonitis
  • May have mucocutaneous lesions

17
Class A Agents
  • Filoviruses and arenaviruses (Ebola virus)
  • Viral hemorrhagic fevers
  • Incubation 2 days 3 weeks, depending on the
    virus
  • SS
  • Initial nonspecific febrile illness, sometimes
    with rash
  • Progresses to hematemesis, diarrhea, shock

18
Class B Agents
  • Coxiella burnetii (Q fever)
  • Incubation 2-3 weeks
  • SS
  • Fever, myalgias, headache
  • 30 develop pneumonia

19
Class B Agents
  • Brucella spp (Brucellosis)
  • Incubation 2-4 weeks
  • SS
  • Fever, myalgias, back pain
  • Possible CNS infections, endocarditis

20
Class B Agents
  • Burkholderia mallei (Glanders)
  • Incubation 10-14 days
  • SS
  • Suppurative ulcers
  • Pneumonia
  • Pulmonic abscesses
  • Sepsis

21
Class B Agents
  • Alpha viruses (VEE, EEE, WEE)
  • Encephalitis
  • Incubation variable
  • SS
  • Fever
  • Headache
  • Aseptic meningitis
  • Encephalitis
  • Focal paralysis
  • Seizures

22
Class B Agents
  • Rickettsia prowazekii (Typhus fever)
  • Incubation 7-14 days
  • SS
  • Fever
  • Headache
  • Rash

23
Class B Agents
  • Chlamydia psittaci (Psitticosis)
  • Incubation 6-19 days
  • SS
  • Fever
  • Headache
  • Dry cough
  • Pneumonia
  • Endocarditis

24
Class B Agents
  • Toxins
  • Ricin, Staphlococcus, Enterotoxin B
  • Food safety threats
  • Salmonella, Eschericia coli O157H7
  • Water safety threats
  • Vibrio cholera, Cryptosporidium parvum

25
Class C Agents
  • Emerging threats
  • Nipah virus
  • Hanta virus

26
Recognition of Bioterrorist Event
  • Patient presents with signs, symptoms, or
    immediately available diagnostic results that
    obviously indicate a suspect disease process.

27
Recognition of Bioterrorist Event
  • 2. Patient presents with protean symptoms, but
    an astute clinician establishes enough criteria
    (suspicious historical information, signs,
    symptoms, short turn-around lab results, public
    health corroborative information, etc.) to
    designate the patient as a presumptive case until
    diagnostic confirmation can be accomplished.

28
Recognition of Bioterrorist Event
  • 3. Patient presents, is evaluated and admitted
    or released, but not suspected as being a victim
    of bioterrorism. Diagnostic test results (blood
    cultures, immunoassays, etc.) subsequently
    establish a diagnosis, potentially even post
    mortem.

29
Recognition of Bioterrorist Event
  • 4. Multiple patients present over a defined
    period with similar symptoms or historical
    characteristics, raising the suspicions of a
    practitioner and causing that individual to
    report the concern. Further investigation with
    diagnostic testing and/or public health
    epidemiological investigation of the cohort
    establishes the cause.

30
Recognition of Bioterrorist Event
  • 5. Public health surveillance systems establish
    unusual patterns of signs, symptoms, or disease
    in the community and correlate with further
    investigation to establish the etiology.

31
Recognition of Bioterrorist Event
  • Emergency physician should know
  • Basic pathological principles for each agent
  • Modes of dissemination and transmission
  • Disease signs and symptoms
  • Recommended diagnostic testing
  • Recommended therapy
  • Immunizations, medicines, or prophylaxis
  • Infectious control practices

32
Recognition of Bioterrorist Event
  • Pictorial resources
  • Confirmatory tests
  • Respond to notification of potential disease by
    another health or medical professional
  • Querying the source for methodology of testing
    that produced the concern

33
Recognition of Bioterrorist Event
  • Exposure to an unidentified substance
  • Source substance and where obtained
  • Coordination with outside agencies, such as law
    enforcement and public health
  • Patient exposure risk stratification

34
Design and Implementation of Community
Surveillance Systems
  • Clinical duties are minimally affected
  • Does not consume valuable clinician or support
    staff time and attention
  • Financial investment is not carried by the
    hospital or professional staff

35
Design and Implementation of Community
Surveillance Systems
  • Patient privacy and hospital proprietary issues
    are addressed appropriately
  • Participation in the system provides direct
    benefit to the acute care medical community
  • - All pertinent epidemiologic information is
    disseminated in real time to the practitioners

36
Initial Response to a Potential Bioterrorist
Threat
  • Within hospital environment
  • Infection control procedures
  • Notification of hospital departments
  • Administration
  • Infectious disease
  • Infection control
  • Laboratory services
  • Security
  • Environmental services

37
Initial Response to a Potential Bioterrorist
Threat
  • Within hospital environment
  • Activation of Emergency Operations Plan (EOP)
  • Preplanned surge capacity configuration
  • Security dept aid in protection of facility and
    staff
  • Media relations
  • Outside of hospital environment
  • Notification of jurisdictional public health
    department

38
Initial Response to a Potential Bioterrorist
Threat
  • Information that needs to be conveyed to public
    health department
  • 1. Diagnosed or suspected agent of concern
  • 2. Whether it is a presumed or definitive
    diagnosis and how many diagnosis were made
  • 3. Patient demographics (including occupation)
  • 4. Recent history of travel or participation in
    special events (i.e. mass gatherings,
    high-profile events, or at- risk gatherings)

39
Initial Response to a Potential Bioterrorist
Threat
  • Information that needs to be conveyed to public
    health department
  • 5. Patient condition
  • 6. Initial testing performed and further
    diagnostic testing being conducted
  • 7. Treatment being provided
  • 8. Public health assistance required (including
    testing)
  • 9. Preferred method of contacting hospital or
    treating physicians for follow-up

40
Initial Response to a Potential Bioterrorist
Threat
41
Initial Response to a Potential Bioterrorist
Threat
  • Protective equipment
  • Gowns, gloves, respiratory masks
  • Patient isolation
  • Patient decontamination
  • Removal of clothing
  • Soap and warm water
  • NO bleach

42
Integration with Local Department of Health
  • Development of community wide patient evaluation
    and treatment protocol
  • Screening
  • Testing
  • Treatment methodologies
  • Patient and public education

43
Integration with Local Department of Health
  • Clear and concise definition for the suspicious
    agent
  • Reporting requirements (surveillance) for
    suspected or diagnosed cases
  • Type of information
  • Method of reporting (e.g. phone, fax, Internet)
  • Contact methods (e.g. 24 hr access for technical
    advice)

44
Treatment, Prophylaxis, and Immunizations
  • Agent Variola major
  • Vaccination Vaccinia vaccination
  • Not recommended for general public use
  • Contraindicated in immunocompromised pts and pts
    with eczema
  • Useful in preventing disease if given within 4
    days of exposure

45
Treatment, Prophylaxis, and Immunizations
  • Agent Variola major
  • Prophylaxis Vaccinia immunoglobin
  • Within 2-3 days of exposure
  • Limited supplies available
  • Consider giving it to those with
    contraindications to the vaccine
  • Treatment
  • Mainly supportive

46
Treatment, Prophylaxis, and Immunizations
  • Agent Bacillus anthracis
  • Vaccination Anthrax vaccination
  • 6 part series at 0,2, and 4 week, then 6,12, and
    18 months
  • Annual boosters required
  • Not available to the public
  • Animal models efficatious in inhalational
    anthrax

47
Treatment, Prophylaxis, and Immunizations
  • Agent Bacillus anthracis
  • Prophylaxis
  • Cipro or doxy for 60 days
  • Amoxicilin if strain not resistant to treatment
  • Treatment
  • Cipro or doxy (amoxicillin if strain not
    resistant) in combo with 2 others, including
    clindamycin, rifampin, imipenem, aminoglycoside,
    chloramphenicol, vancomycin, streptomycin, and
    some macrolides

48
Treatment, Prophylaxis, and Immunizations
  • Agent Yersinia pestis
  • Vaccination none
  • Prophylaxis
  • Cipro or doxy for 7 days
  • Alt chloramphenicol
  • Treatment
  • Streptomycin or gentamycin
  • Alt doxy, cipro, chloramphenicol

49
Treatment, Prophylaxis, and Immunizations
  • Agent Clostridium botulinum
  • Vaccination
  • Not available to public
  • Pentavalent toxoid of C botulinum toxin types A-E
  • 3-part series, with yearly booster
  • Prophylaxis none

50
Treatment, Prophylaxis, and Immunizations
  • Agent Clostridium botulinum
  • Treatment
  • Antitoxin from local public health agency
  • Antitoxin may preserve remaining neurologic
    function, BUT does not reverse paralysis
  • May require prolonged, assisted mechanical
    ventilation and supportive care

51
Treatment, Prophylaxis, and Immunizations
  • Agent Francisella tularensis
  • Vaccination
  • Live, attenuated vaccine under FDA investigation
  • Prophylaxis
  • Cipro or doxy for 14 days

52
Treatment, Prophylaxis, and Immunizations
  • Agent Francisella tularensis
  • Treatment
  • Streptomycin or gentamycin
  • Alt doxy, cipro, chloramphenicol

53
Treatment, Prophylaxis, and Immunizations
  • Agent Filoviruses and arenaviruses (e.g. Ebola
    virus)
  • Vaccination none
  • Prophylaxis none
  • Treatment
  • Supportive therapy
  • Ribavirin may have applicability in arenaviruses

54
Treatment for Bioterrorism
  • General Emergency Operation Plans
  • Need to have enough staff to handle large surge
    in general patient volume
  • Specialty requirements
  • Patient with unusual medical conditions
  • Patients who may be contagious
  • Contamination risks to staff and other patients

55
Treatment for Bioterrorism
  • Disease containment
  • Isolation
  • Designation of staff to care for infected vs.
    noninfected patients
  • Proper personal protective equipment

56
Treatment for Bioterrorism
  • Management of personnel
  • Need more personnel to care for more patients
  • Staff reluctance to care for potentially
    infectious patients

57
Treatment for Bioterrorism
  • Logistics
  • Limited supply of drugs and medical supplies
  • Sharing of critical supplies, staff, and
    equipment among local hospitals
  • National Pharmaceutical Stockpile

58
Treatment for Bioterrorism
  • Patient Management
  • Addressing requirements of each patient encounter
  • Preprinted instructions
  • Category of risk stratification
  • Why patient placed in that category
  • How disease transmitted
  • Measures to prevent spread
  • Early signs and symptoms of disease
  • Appropriate steps if symptoms occur

59
Treatment for Bioterrorism
  • Patient Management
  • Appropriate follow-up
  • Proper record keeping
  • Organization of charts

60
Treatment for Bioterrorism
  • Vaccinations
  • Not to be given in a pre-event setting to general
    public
  • Recommended therapies
  • Usually not for pregnant or lactating women
  • Usually not approved for children
  • Should be given if risk of infection and its
    consequences exceeds risks of the medications or
    vaccines

61
Treatment for Bioterrorism
  • Fatality Management
  • Bodies are considered evidence
  • Processed through coroner or medical examiner

62
Sources of Expert Information
  • http//jama.ama-assn.org
  • http//www.bt.cdc.gov
  • http//chemdef.apgea.army.mil/textbook/contents.as
    p
  • http//www.apic.org
  • Local poison control center
  • CDCs emergency response center
  • 1-770-488-7100
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