BT EPIDEMIOLOGIC RESPONSE TEAM TRAINING SESSION 1 - PowerPoint PPT Presentation

1 / 41
About This Presentation
Title:

BT EPIDEMIOLOGIC RESPONSE TEAM TRAINING SESSION 1

Description:

BT EPIDEMIOLOGIC RESPONSE TEAM TRAINING SESSION 1 – PowerPoint PPT presentation

Number of Views:36
Avg rating:3.0/5.0
Slides: 42
Provided by: betty96
Category:

less

Transcript and Presenter's Notes

Title: BT EPIDEMIOLOGIC RESPONSE TEAM TRAINING SESSION 1


1
BT EPIDEMIOLOGIC RESPONSE TEAM TRAININGSESSION
1
2
Objectives of training
  • To understand clinical description and
    epidemiology
  • To understand the disease case definition, lab
    specimens needed, labs role, and lab tests needed
    for confirmation
  • To understand prevention and control procedures
    including available treatment and post-exposure
    prophylaxis, isolation and infection control
    procedures.
  • To understand contact tracing and surveillance
    procedures

3
Team Roles and Responsibilities
  • Outbreak management staff
  • Case Ascertainment staff/active surveillance
  • Face-to-face interviewers
  • Telephone interviewers
  • Data base support

4
Employee Health
  • Education of risks of disease from exposure to BT
    agents or infectious patients
  • Vaccination
  • Personal protective equipment (PPE)

5
BT AGENTS
6
Prioritization Categories
  • Category A
  • High public health impact and public perception
  • Variable dissemination potential
  • Comprehensive PH preparedness
  • Category B
  • Less public health impact
  • Variable dissemination potential
  • Less comprehensive PH preparedness
  • Category C
  • Addressed with current preparedness efforts
    (BT/EID)

7
Category A Agents
  • Variola virus - smallpox
  • Bacillus anthracis - anthrax
  • Yersinia pestis - plague
  • Francisella tularensis - tularemia
  • C. botulinum toxins - botulism
  • Filo and Arenaviruses - VHFs

8
Characteristics of Category A Agents
  • Infectious via aerosol
  • Organisms fairly stable in aerosol
  • Susceptible civilian populations
  • High morbidity and mortality
  • Person-to-person transmission
  • Difficult to diagnose and/or treat
  • Previous development for BW

Priority agents may exhibit all or some of the
above characteristics
9
Characteristics of Category B Agents
  • Coxiella burnetii Q fever
  • Brucella spp. - brucellosis
  • Burkholderia mallei - glanders
  • Alphaviruses (VEE, WEE, EEE) - encephalitis
  • Ricinus communis - Ricin
  • Epsilon toxin from clostridium perfingens
  • Staphylococcus enterotoxin B

10
Category C Agents
  • Emerging infectious disease agents (Hantavirus,
    Nipah virus, etc.)
  • Salmonella
  • E-coli O157H7
  • Vibrio cholerae cholera
  • Cryptosporidium parvum - cryptosporidiosis

11
OUTBREAK INVESTIGATION
12
Definition
  • Occurrence of more cases of disease than expected
  • Nosocomial outbreak-any group of illnesses of
    common etiology occurring in patients of a
    medical care facility acquired by exposure of
    those patients to the disease agent while
    confined in such a facility.

13
Reasons to investigate
  • Control/prevention
  • Research opportunities
  • Training
  • Public, political, or legal concerns
  • Program considerations

14
Control / Prevention
  • Where are we in the outbreak?
  • Goals will be different depending on answer(s)
  • Cases continuing to occur
  • Goal prevent further cases
  • Assess population at risk, implement control
    measures
  • Outbreak appears to be coming to an end
  • Goal prevent future outbreaks
  • Identify factors contributing to outbreak,
    implement measures to prevent similar events in
    the future

15
Steps of an Outbreak Investigation
16
1. Preparation
  • Investigation
  • Scientific knowledge
  • Review literature
  • Consult experts
  • Sample questionnaires
  • Supplies
  • Consult with laboratory
  • Equipment
  • Laptop, camera etc.

17
Preparation, cont.
  • Administration-assure personnel resources,
    funding
  • Travel arrangements (orders)
  • Approval
  • Personal matters
  • Consultation-make sure you know your role and its
    parameters
  • Lead investigator or just lending a hand?
  • Know who to contact when you arrive

18
2. Establish existence of an outbreak
  • Is an outbreak truly occurring?
  • True outbreak
  • Sporadic and unrelated cases of same disease
  • Unrelated cases of similar unrelated disease
  • Determine the expected number of cases before
    deciding whether the observed number exceeds the
    expected number

19
Establish outbreak existence, cont.
  • Comparing observed with expected
  • through surveillance records for notifiable
    diseases
  • hospital discharge data, registries, mortality
    statistics
  • data from other facilities, states, surveys of
    health care providers
  • community survey

20
3. Verify the Diagnosis
  • Ensure proper diagnosis and rule out lab error as
    the bias for increased diagnosis
  • Review clinical findings, lab results
  • Summarize clinical findings with frequency
    distributions
  • Characterize spectrum of disease
  • Verify diagnosis
  • Develop case definition

21
Verify the Diagnosis cont.
  • See and talk with patients if at all possible
  • Better understand clinical features
  • Mental image of disease and the patients affected
  • Gather critical information
  • Source of exposure
  • What they think caused illness
  • Knowledge of others with similar illness
  • Common denominators
  • Helpful in generating ideas for hypothesis about
    etiology and spread

22
4a. Establish a case definition
  • Case definition
  • Standard set of criteria for deciding whether an
    individual should be classified as having the
    health condition of interest
  • Includes clinical criteria and restrictions by
    time, place and person
  • Must be applied consistently and without bias to
    all persons under investigation
  • Must not contain an exposure of risk factor you
    want to test

23
4a. Establish a case definition, cont.
  • Classification
  • Definite (confirmed)
  • Laboratory confirmed
  • Probable
  • Typical clinical features without lab
    confirmation
  • Possible (suspected)
  • Fewer of the typical clinical features

24
4a. Establish a case definition, cont.
  • Early in investigation may use a loose case
    definition
  • Better to collect more than necessary so you
    dont need to make repeat visits
  • Identify extent of problem and population
    affected
  • Generating hypotheses
  • Later when hypotheses are sharpened investigator
    may tighten case definition

25
4b. Identify and count cases
  • Target health care facilities where diagnosis
    likely to be made
  • Enhanced passive surveillance e.g. letter
    describing situation and asking for reports
  • Active surveillance e.g. phone or visit facility
    to collect information
  • Alerting the public
  • Media alert to avoid contaminated food product
    and seek medical attention if symptoms arise

26
4b. Identify and count cases, cont.
  • OB population restricted and large proportion of
    cases are unlikely to be diagnosed e.g. on a
    cruise ship
  • Survey entire population
  • Always ask case-patients if they know of any
    others ill with the same symptoms

27
4b. Identify and count cases, cont.
  • Information to be collected about every case
  • Identifying information
  • Re-contact if additional questions come up
  • Notification of lab results and outcomes of
    investigation
  • Check for duplicate records
  • Map geographic extent
  • Demographics
  • Provide person characteristics for defining
    population at risk

28
4b. Identify and count cases, cont.
  • Information to be collected about every case
    cont.
  • Clinical findings
  • Verify case definition met
  • Chart time course
  • Supplemental date e.g. deaths
  • Risk factor information
  • Tailored to specific disease in question
  • Reporter information
  • Id of person making report

29
4b. Identify and count cases, cont.
  • Collection forms
  • Standard case report form
  • Questionnaire
  • Data abstraction form
  • Line listing
  • Abstraction of selected critical items from above
    forms
  • Contains key information

30
5. Perform Descriptive Epidemiology
  • After collection of data characterize the
    outbreak by
  • Time
  • Place
  • Person

31
Time
  • Epidemic curve
  • Histogram of the number of cases by their date of
    onset
  • Visual display of the outbreaks magnitude and
    time trend
  • Where you are in the time course of the outbreak
  • Future course?
  • Probable time period of exposure
  • Helps in development of questionnaire focusing on
    that time period
  • Common source vs. Propagated

32
Place
  • Geographic extent of problem
  • Clusters or patterns providing important
    etiologic clues
  • Spot maps
  • Where cases live, work or may have been exposed

33
Person
  • Determine what population at risk
  • Usually define population by host characteristics
    or exposure
  • Use rates to identify high-risk groups
  • Numerator number of case
  • Denominator number of people at risk

34
Develop Hypotheses
  • Hypotheses should address
  • Source of the agent
  • Mode of transmission
  • Vector or vehicle
  • Exposure that caused disease

35
Develop Hypotheses
  • Generating the hypothesis
  • What do you know about the disease?
  • Reservoir, transmission, common vehicles and
    known risk factors
  • Talk to several case-patients
  • Use open ended questions
  • Ask lots of questions
  • Talk to local health department staff
  • Use descriptive epidemiology e.g. epi curve

36
7. Test Hypotheses
  • Evaluate the credibility of your hypotheses
  • Compare with established facts
  • When clinical, lab, environmental and/or epi data
    undoubtedly support hypothesis
  • Use analytic epidemiology to quantify
    relationships and explore the role of chance
  • Cohort studies
  • Case control studies

37
7. Test Hypotheses, cont.
  • Cohort
  • Small, well defined population
  • Contact each attendee and ask a series of
    questions
  • Ill Vs not ill
  • Look for source exposure
  • Attack rate is high among those exposed
  • Attack rate is low among those not exposed
  • Most of the cases were exposed, so that the
    exposure could explain most, if not all, of the
    cases
  • Relative risk measure of association between
    exposure and disease

38
7. Test Hypotheses, cont.
  • Case-control
  • Population not well defined
  • Case patients and comparison group (controls)
    questioned about exposure(s)
  • Compute measure of association Odds Ratio
  • Quantify relationship between exposure and
    disease

39
8. Refine hypotheses and do additional studies
  • Epidemiologic
  • When analytical epi unrevealing need to
    reconsider your hypotheses
  • Go back and gather more information
  • Conduct different studies
  • Laboratory
  • Additional tests
  • Environmental studies

40
9. Implement Control /Prevention Measures
  • Implement control measures as soon as possible
  • May be aimed at agent, source, or reservoir
  • Short or long term

41
10. Communicate the Findings
  • Orally within facility/community
  • Local health authorities and persons responsible
    for implementation of control and prevention
    measures
  • Written reports (consider publication) for
    planning, record of performance, legal issues,
    reference, adding to knowledge base
Write a Comment
User Comments (0)
About PowerShow.com