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    SEARO CSR Training on Outbreak Investigation

    Outbreak Investigation

    Best Practice/MethodsPractical Reference Points

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    Learning Objectives

    At the end of the session, the participants

    will be able to:

    List down the objectives of outbreak

    Describe steps in outbreak investigation

    Explain the importance of conducting timely

    outbreak investigation

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    Detecting an outbreak

    DetectionRoutine surveillance

    Clinical/laboratory

    Rumor verification

    General public

    Media

    Is this an

    Outbreak?

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    Is it an outbreak?

    More than expected cases Illustrates the importance of surveillance and timely

    analysis

    Clustered in time, place or person

    Pattern recognition

    Concern from a HCW, school or media

    Rumour verification

    Encourage participation in the system

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    Why investigate outbreaks?

    Stop the outbreak (new cases)

    Increase our knowledge

    Prevent new episodes Evaluate the surveillance system

    Establish a surveillance system

    L

    earn field epidemiology by doing

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    Specific objectives of an investigation

    Identify:

    Causal agent

    Mode of transmission

    Source

    Carrier

    Population at risk

    Exposure causing disease (risk factors)

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    Real time vs. retrospective

    investigation

    Outbreaks in existence for several

    days, weeks, months.

    Based on the memory of the people

    Data already collected

    To be or not to be used

    It is never to late,

    but it can also be more difficult

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    Preparation

    Collect preliminary information Available data

    Consult experts (microbiologist, veterinarian,entomologist etc)

    Check search engines e.g., PUBmed

    Search from both formal and informal surveillancesystem (event based and indicator based)

    Prepare a short memo

    Inform the concerned

    Get authorization, travel itinerary

    Investigation committee

    Multidisciplinary Assign person in charge

    Define tasks

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    Example: Community epidemic due to S.

    Typhimurium, Jura, May-June 1997

    Context

    Alert: PH medical officer

    80 cases of salmonellosis in 5 weeks

    Salmonella Typhimurium

    Clustered in the South department of Jura

    No connection (a priori) among cases

    Pressure of media, of politicians

    L

    ocal Department of Public Health, VeterinaryServices, Centre National Reference, National

    Institute of Public Health

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    Steps in Outbreak Investigation

    Descriptive steps

    1) Determine existence of an outbreak

    2) Confirm the diagnosis:

    Which diseases are we talking about?

    3) Define a case; find and count cases

    4) Orient data as to:

    Time (When?) Place (Where?)

    Person (Who?)

    the sequence is not important !

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    Analyse5) Generate hypotheses

    6) Test the hypotheses

    7) Compare each hypothesis with facts

    8) Plan a more systematic study

    Synthesis and action

    9) Write a report, communicate findings10) Control measure and prevention

    Steps in Outbreak Investigationthe sequence is not important !

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    1. Determine existence of an outbreak

    Outbreak n observed cases > n expected cases

    Expected cases? Surveillance data

    Clinicians, hospital registers Hospital investigation, lab, doctors, schools..

    Be careful of artefacts! Seasonal variation: (diarrhoea)

    Notification variation: (new surveillance system inplace) Diagnostic variation: (new technique) Diagnostic mistake: (false epidemic")

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    Number ofLegionella cases per week, France

    January 1996 August 1997

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    2. Confirm the diagnosis

    Laboratory serology

    isolation, serotype, lysotype, etc.

    toxic agent

    Meet the doctors

    See the patients

    Visit the laboratories

    It is not necessary to confirm all the cases

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    3. Define a case; find and count cases

    A case definition is a standard set of criteria for

    deciding whether an individual should be

    classified as having the health condition of

    interest Includes:

    clinical criteria

    restrictions by time, place and person (epidemiological

    link)

    laboratory findings (generally)

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    Suspected

    cases clinical case

    definition enough for

    immediate action

    Confirmed

    cases Collect relevant

    samples laboratory

    few cases (10-20)

    Do not wait for laboratory results tostart treatment and control activities!

    3.1. Define a case

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    Example: Case DefinitionOutbreak of S. Typhimurium, Jura, May-June 1997

    Confirmed Probable

    Clinical Diarrhoea (> 2 liquidstools/day)

    or Fever > 38C ( + one

    day)

    Diarrhoea (> 2 liquid

    stools/day)

    or Fever > 38C ( + one

    day)

    AND

    Place,

    Person

    resident in Jura or

    neighbourhood

    resident in Jura or

    neighbourhood

    Time Since 12 May 1997 Since 12 May 1997

    Biological Identification of S.Typhimurium

    None, but contact with

    confirmed case

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    3.2. Find and count the cases

    Information sources All possible sources (NGOs, local leaders, etc) Hospitals, health centres, laboratories, doctors,

    nurses schools, camps, settlements Radio, door to door

    snow ball Laboratory

    How many? No strictly all

    Collected information

    Demographics clinical and biological

    eventual exposure

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    4. Orient data as to:

    Time

    Place

    Persons

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    4.1 Data description: TIME

    epidemic curve

    Case distribution over time (according tothe date - hour, week - of onset of signs)

    Onset, peak, importance, time, end of

    epidemic Abnormal cases

    Allow to make hypothesis: incubation period, pathogen responsible

    source, mode of transmission time of exposure

    Epidemic evolution

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    Example: Epidemic curve of Cases due to S.Typhimurium

    by week of onset of symptoms of isolated bacteria,

    Jura, May- June 1997.N o m b r e d e c a s

    3 0

    1 c a s

    2 5

    2 0

    1 5

    1 0

    5

    1 4 1 5 1 6 1 7 1 8 1 9 2 0 2 1 2 2 2 3 2 4 2 5 2 6 2 7 2 8

    A v r i l M a i J u in J u i l le t

    S e m a i n e s d is o l e m e n t o u d e d b u t d e s s y m p t m e s

    One Case

    April May June July

    Number of Cases

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    4.2 Data description: PLACE

    Residence

    Place of exposure

    work, food places, journeys, tour Maps (mud maps, points, attack rate)

    Identify areas at risk,Identify population at risk

    Identify priority areas for control activities

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    4.3 Data description: PERSON

    Distribution of cases by age, sex, profession,etc (Numerator) ex: 50 women, 100 men

    Distribution of variables in the population from

    where cases are coming (Denominator) ex: 1500 women, 1000 men

    Compute attack rate ex: women 50/1500 , men 100/1000

    => Identification of sub-group(s) at risk

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    Example: Data Description - Person

    Infection by S.Typhimurium

    Attack Rate by age group, Jura, May-June 1997

    Age group

    (years)

    Number of

    Cases

    65 9Total 98

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    Example: Data Description - Person

    Infection by S.Typhimurium,

    Attack Rate by age group, Jura, may-June 1997

    Age Group

    (years)

    Number of Cases Population Attack Rate/

    100,000

    65 9 41,948 22Total 98 246,858 40

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    5. Generate hypotheses

    Starting from: Descriptive information (TPP) Knowledge of the disease

    Exploratory study on some cases

    Explaining: Causal agent

    Source

    Way of transmission

    Carrier

    DIFFICULT !!!!

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    Example: Generating Hypothesis

    Infection of S.Typhimurium

    Descriptive data: Agent: S. Typhimurium lysotype 12 atypical

    Time, epidemic curve: persistent commonsource

    Place: cases clustered in the south of Jura

    Persons: Attack rate higher among children

    All ages affected

    Muslim among the cases

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    Example: Formulating Hypothesis

    Infection S.Typhimurium

    May June 1997

    Descriptive information Hypothesis

    S. Typhimurium Meat (cow), salami, poultry,

    milk products, etc

    South of Jura Regional products, local

    distribution

    Children more affected Consumed products (also) by

    some children

    Muslim among cases Pork less probable

    Good weather condition Barbecue, poultry

    Documentation Epidemic of roasted poultry

    described

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    5. Generate HypothesisExploratory Survey

    Formulate hypothesis

    Interview some cases:

    Open questionnaire and complete

    Common exposure?

    Example Jura:

    Big questionnaire, inclusion of regionalproducts (cheese)

    17 cases interviewed

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    Example: Results of Exploratory Survey

    Exposure of cases to specific food

    Jura, May - June 1997

    Food No. of cases

    who ate

    No. of

    respondents

    % of cases

    exposed

    Chipolatas 6 15 40

    Cooked chicken 5 17 29

    Raw chicken 7 16 44

    Minced beef 7 17 41

    Pork 9 17 53

    Veal 8 17 47

    Cheese (comte) 13 17 77Cheese A

    (Fromage a)14 16 88

    Rochfort (Bleu de

    Gex)6 10 60

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    6. Test the hypothesis

    Objectives

    Specific exposure: the carrier and the source Factors facilitating or protective

    host, agent, environment

    Survey to identify aetiology:

    Cohort uses attack rates best in a small, well-defined population

    Case-control odds ratio quantifies the relationship b/w exposure and

    disease

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    6. Test the hypothesis

    Case-control

    Compare Proportion of exposed among cases

    Proportion of exposed among the non cases (controls)

    Compute Odds Ratio (OR) and Confidence Interval(CI) at 95%

    Select controls Not sick

    Susceptible (e.g., not immunised)

    Coming from the same population of cases

    The same chances of being exposed

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    Exposure of Cases and Controls to specific food

    Jura, May - June 1997

    Food No (%) of

    exposed cases

    Odds Ratio CI 95%

    (N = 42) (N = 42)

    Pats 11 (26) 17 (40) 0.5 0.2 1.3

    Sausage 24 (57) 28 (67) 0.7 0.3 1.6

    Beef 32 (78) 33 (79) 1 0.3 3.5

    Pork 23 (59) 29 (76) 0.5 0.2 1.5

    Veal 22 (54) 19 (46) 1.4 0.6 3.4

    Chicken 30 (71) 34 (81) 0.6 0.2 1.7

    Munster(cheese)

    4 (10) 1 (2) 4.0 0.5 35.8

    Bleu de Gex(blue cheese)

    12 (35) 10 (24) 3.0 0.6 14.9

    Comt (cheese) 36 (86) 37 (88) 0.8 0.3 2.7

    Fromage A(cheese)

    33 (83) 23 (55) 6.5 1.4 28.8

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    7. Compare the hypothesis with facts

    Compare the results clinical observation

    biological examinations

    epidemiological studies

    statistical tests

    The hypothesis should be:

    plausible

    biologically acceptable explain causal agent, source,

    mode transmission, time of exposure

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    Example:

    Comparison of hypotheses with observed facts,

    Jura, May-June 1997

    Cheese A

    Raw milk (plausible)

    Consumed by children (meets personsaffected by the outbreak)

    Regional product(meets place affected)

    Collect cheese among the cases (datamicrobiological) S. Typhimurium identified in 3 cheeses A

    Other cheeses negatives

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    8. Plan a more systematic study

    At the same time, and oriented by theepidemiological survey

    Environmental survey

    Microbiological survey

    Plan more systematic studies (if needed)

    More cases, more controls

    Dose-effect, facilitating factors..

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    Example: Complementary studies

    Epidemic of S. Typhimurium

    Jura, May-June, 1997

    Microbiological survey: Food collection among cases

    Sample collection among cases suppliers

    Comparison of human specimens and food

    products

    Survey on the distribution network of cheese A

    Survey among the producers: Veterinary Labour medicine

    Environmental

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    Survey distribution network

    CREMERIE

    Wholesaler

    Cheese

    dairy

    Example: Complementary studiesEpidemic of S. Typhimurium

    Jura, May-June, 1997

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    9. Write a report; communicate findings

    To be written on site

    Promotes synthesis (of the objectives)

    Documents the event(for evaluation/ legalpurposes)

    Allows communication of results

    Provides recommendations

    Pedagogical tool (training material)

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    10. Control measures and prevention

    Dont wait for the end of the investigation : General measures at beginning Specific measures according to the results

    Kinds of measures to control : The source (e.g.: chlorination of water)

    The transmission (e.g.: hygiene measures) The carrier (e.g.: recall a lot of suspected cheese)

    Reduce the susceptibility of host (e.g.: vaccination)

    Communicate risk if outbreak is affecting the public

    Example Jura:

    Personal Hygiene Adequate cooking of meat

    Recall of the incriminated product (Fromage A)

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    " The art of epidemiological reasoning is tomake some reasonable conclusions

    starting from imperfect data"

    George W. Comstock (1915-2007)Physician and Professor Emeritus

    Johns Hopkins Bloomberg School ofPublic Health

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    But better information leads to better results

    This means having: A good description of Time, Place, Person

    (TPP)

    Good data collection and preservation ofsamples

    A well coordinated multidisciplinary team

    Immediate

    detection

    Immediate

    response

    Reduced morbidity

    and mortality

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    0

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    6070

    80

    90

    1 4 7 10 13 16 19 22 25 28 31 34 37 40

    DAY

    CASES

    LabConfirmation

    Outbreak Detection and Response

    Response

    Opportunity

    for control

    Detection/Reporting

    First

    Case

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    0

    10

    20

    30

    40

    50

    60

    70

    80

    90

    1 4 7 10 13 16 19 22 25 28 31 34 37 40

    DAY

    CASES

    Outbreak Detection and Response

    First

    CaseDetection/

    ReportingLabConfirmationResponse Opportunity

    for control

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    Ethical Aspect

    Securing consent (participants)

    Informing local authorities,

    communities

    Ethical treatment of animals

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    Best practices

    Establish clear and concise policies andprocedures

    Careful documentation and proper

    recording of events/results Effective communication skills

    Evaluate and review responses

    Expect the unexpected Key people away, new, emerging pathogen,

    demystifying rumour, etc.

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    References

    De Valk, Henriette, French Institute for

    Public Health Surveillance (Institut de veille

    sanitaire, InVS)

    European Programme on Intervention

    Epidemiology Training

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