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Title: Public Health Information Network PHIN Series I


1
Public Health Information Network (PHIN) Series
I
2
(No Transcript)
3
Series Overview
  • Introduction to
  • The history of Epidemiology
  • Specialties in the field
  • Key terminology, measures, and resources
  • Application of Epidemiological methods

4
Series I Sessions
5
What to Expect. . .
  • Today
  • Understand the basic terminology and measures
    used in descriptive and analytic Epidemiology

6
Session I V Slides
  • VDH will post PHIN series slides on the
    following Web site
  • http//www.vdh.virginia.gov/EPR/Training.asp
  • NCCPHP Training Web site
  • http//www.sph.unc.edu/nccphp/training

7
Site Sign-in Sheet
  • Please submit your site sign-in sheet to
  • Suzi Silverstein
  • Director, Education and Training
  • Emergency Preparedness Response Programs
  • FAX (804) 225 - 3888

8
Series ISession III
  • Descriptive and Analytic Epidemiology

9
Todays Presenter
  • Kim Brunette, MPH
  • Epidemiologist
  • North Carolina Center for Public Health
    Preparedness, Institute for Public Health, UNC
    Chapel Hill

10
Session Overview
  • Define descriptive epidemiology
  • Define incidence and prevalence
  • Discuss examples of the use of descriptive data
  • Define analytic epidemiology
  • Discuss different study designs
  • Discuss measures of association
  • Discuss tests of significance

11
Todays Learning Objectives
  • Understand the distinction between descriptive
    and analytic Epidemiology, and their utility in
    surveillance and outbreak investigations
  • Recognize descriptive and analytic measures used
    in the Epidemiological literature
  • Know how to interpret data analysis output for
    measures of association and common statistical
    tests

12
Descriptive Epidemiology
  • Prevalence and Incidence

13
What is Epidemiology?
  • Study of the distribution and determinants of
    states or events in specified populations, and
    the application of this study to the control of
    health problems
  • Study risk associated with exposures
  • Identify and control epidemics
  • Monitor population rates of disease and exposure

14
What is Epidemiology?
  • Looking to answer the questions
  • Who?
  • What?
  • When?
  • Where?
  • Why?
  • How?

15
Case Definition
  • A case definition is a set of standard diagnostic
    criteria that must be fulfilled in order to
    identify a person as a case of a particular
    disease
  • Ensures that all persons who are counted as cases
    actually have the same disease
  • Typically includes clinical criteria (lab
    results, symptoms, signs) and sometimes
    restrictions on time, place, and person

16
Descriptive vs. Analytic Epidemiology
  • Descriptive Epidemiology deals with the
    questions Who, What, When, and Where
  • Analytic Epidemiology deals with the remaining
    questions Why and How

17
Descriptive Epidemiology
  • Provides a systematic method for characterizing a
    health problem
  • Ensures understanding of the basic dimensions of
    a health problem
  • Helps identify populations at higher risk for the
    health problem
  • Provides information used for allocation of
    resources
  • Enables development of testable hypotheses

18
Descriptive EpidemiologyWhat?
  • Addresses the question How much?
  • Most basic is a simple count of cases
  • Good for looking at the burden of disease
  • Not useful for comparing to other groups or
    populations

http//www.vdh.virginia.gov/epi/Data/race03t.pdf
19
Prevalence
  • The number of affected persons present in the
    population divided by the number of people in the
    population
  • of cases
  • Prevalence -------------------------------------
    ----
  • of people in the population

20
Prevalence Example
  • In 1999, Virginia reported an estimated 253,040
    residents over 20 years of age with diabetes.
    The US Census Bureau estimated that the 1999
    Virginia population over 20 was 5,008,863.
  • 253,040
  • Prevalence 0.051
  • 5,008,863
  • In 1999, the prevalence of diabetes in Virginia
    was 5.1
  • Can also be expressed as 51 cases per 1,000
    residents over 20 years of age

21
Prevalence
  • Useful for assessing the burden of disease within
    a population
  • Valuable for planning
  • Not useful for determining what caused disease

22
Incidence
  • The number of new cases of a disease that occur
    during a specified period of time divided by the
    number of persons at risk of developing the
    disease during that period of time
  • of new cases of disease over a
    specific period of time
  • Incidence --------------------------------------
    -----
  • of persons at risk of disease
    over that specific period of time

23
Incidence Example
  • A study in 2002 examined depression among persons
    with dementia. The study recruited 201 adults
    with dementia admitted to a long-term care
    facility. Of the 201, 91 had a prior diagnosis
    of depression. Over the first year, 7 adults
    developed depression.
  • 7
  • Incidence 0.0636
  • 110
  • The one year incidence of depression among adults
    with dementia is 6.36
  • Can also be expressed as 63.6 (64) cases per
    1,000 persons with dementia

24
Incidence
  • High incidence represents diseases with high
    occurrence low incidence represents diseases
    with low occurrence
  • Can be used to help determine the causes of
    disease
  • Can be used to determine the likelihood of
    developing disease

25
Prevalence and Incidence
  • Prevalence is a function of the incidence of
    disease and the duration of disease

26
Prevalence and Incidence
Prevalence
prevalent cases
27
Prevalence and Incidence
New prevalence
Incidence
Old (baseline) prevalence
No cases die or recover
prevalent cases
incident cases
28
Prevalence and Incidence
prevalent cases
incident cases
deaths or recoveries
29
Time for you to try it!!!
30
Descriptive Epidemiology
  • Person, Place, Time

31
Descriptive EpidemiologyWho? When? Where?
  • Related to Person, Place, and Time
  • Person
  • May be characterized by age, race, sex,
    education, occupation, or other personal
    variables
  • Place
  • May include information on home, workplace,
    school
  • Time
  • May look at time of illness onset, when exposure
    to risk factors occurred

32
Person Data
  • Age and Sex are almost always used in looking at
    data
  • Age data are usually grouped intervals will
    depend on what type of disease / event is being
    looked at
  • May be shown in tables or graphs
  • May look at more than one type of person data at
    once

33
Data Characterized by Person
http//www.vahealth.org/civp/Injury20in20Virgini
a_Report_2004.pdf
34
Data Characterized by Person
http//www.vdh.virginia.gov/std/AnnualReport2003.p
df
35
Data Characterized by Person
http//www.vdh.virginia.gov/epi/cancer/Report99.pd
f
36
Data Characterized by Person
http//www.vahealth.org/chronic/Data_Report_Part_3
.pdf
37
Time Data
  • Usually shown as a graph
  • Number / rate of cases on vertical (y) axis
  • Time periods on horizontal (x) axis
  • Time period will depend on what is being
    described
  • Used to show trends, seasonality, day of week /
    time of day, epidemic period

38
Data Characterized by Time
http//www.dhhs.state.nc.us/docs/ecoli.htm
39
Data Characterized by Time
http//www.vdh.virginia.gov/std/HIVSTDTrends.pdf
40
Data Characterized by Time
http//www.cdc.gov/mmwr/preview/mmwrhtml/mm5153a1.
htm
41
Data Characterized by Time
http//www.health.qld.gov.au/phs/Documents/cdu/127
76.pdf
42
Place Data
  • Can be shown in a table usually better presented
    pictorially in a map
  • Two main types of maps used
  • choropleth and spot
  • Choropleth maps use different shadings/colors to
    indicate the count / rate of cases in an area
  • Spot maps show location of individual cases

43
Data Characterized by Place
http//www.vdh.virginia.gov/epi/Data/region03t.pdf
44
Data Characterized by Place
http//www.vdh.virginia.gov/epi/Data/Maps2002.pdf
45
Data Characterized by Place
http//www.vahealth.org/civp/preventsuicideva/epip
lan202004.pdf
46
Data Characterized by Place
http//www.vahealth.org/civp/preventsuicideva/epip
lan202004.pdf
47
Data Characterized by Place
Source Olsen, S.J. et al. N Engl J Med. 2003
Dec 18 349(25)2381-2.
48
5 Minute Break
49
Analytic Epidemiology
  • Hypotheses and Study Designs

50
Descriptive vs. Analytic Epidemiology
  • Descriptive Epidemiology deals with the
    questions Who, What, When, and Where
  • Analytic Epidemiology deals with the remaining
    questions Why and How

51
Analytic Epidemiology
  • Used to help identify the cause of disease
  • Typically involves designing a study to test
    hypotheses developed using descriptive
    epidemiology

52
Borgman, J (1997). The Cincinnati Enquirer.
King Features Syndicate.
53
Exposure and Outcome
  • A study considers two main factors
  • exposure and outcome
  • Exposure refers to factors that might influence
    ones risk of disease
  • Outcome refers to case definitions

54
Case Definition
  • A set of standard diagnostic criteria that must
    be fulfilled in order to identify a person as a
    case of a particular disease
  • Ensures that all persons who are counted as cases
    actually have the same disease
  • Typically includes clinical criteria (lab
    results, symptoms, signs) and sometimes
    restrictions on time, place, and person

55
Developing Hypotheses
  • A hypothesis is an educated guess about an
    association that is testable in a scientific
    investigation
  • Descriptive data provide information to develop
    hypotheses
  • Hypotheses tend to be broad initially and are
    then refined to have a narrower focus

56
Example
  • Hypothesis People who ate at the church picnic
    were more likely to become ill
  • Exposure is eating at the church picnic
  • Outcome is illness this would need to be
    defined, for example, ill persons are those who
    have diarrhea and fever
  • Hypothesis People who ate the egg salad at the
    church picnic were more likely to have
    laboratory-confirmed Salmonella
  • Exposure is eating egg salad at the church picnic
  • Outcome is laboratory confirmation of Salmonella

57
(No Transcript)
58
Types of Studies
  • Two main categories
  • Experimental
  • Observational
  • Experimental studies exposure status is
    assigned
  • Observational studies exposure status is not
    assigned

59
Experimental Studies
  • Can involve individuals or communities
  • Assignment of exposure status can be random or
    non-random
  • The non-exposed group can be untreated (placebo)
    or given a standard treatment
  • Most common is a randomized clinical trial

60
Experimental Study Examples
  • Randomized clinical trial to determine if giving
    magnesium sulfate to pregnant women in preterm
    labor decreases the risk of their babies
    developing cerebral palsy
  • Randomized community trial to determine if
    fluoridation of the public water supply decreases
    dental cavities

61
Observational Studies
  • Three main types
  • Cross-sectional study
  • Cohort study
  • Case-control study

62
Cross-Sectional Studies
  • Exposure and outcome status are determined at the
    same time
  • Examples include
  • Behavioral Risk Factor Surveillance System
    (BRFSS) - http//www.cdc.gov/brfss/
  • National Health and Nutrition Surveys (NHANES) -
    http//www.cdc.gov/nchs/nhanes.htm
  • Also include most opinion and political polls

63
Cohort Studies
  • Study population is grouped by exposure status
  • Groups are then followed to determine if they
    develop the outcome

64
Cohort Studies
Study Population
Exposure is self selected
Non-exposed
Exposed
Follow through time
Disease
No Disease
No Disease
Disease
65
Cohort Study Examples
  • Study to determine if smokers have a higher risk
    of lung cancer
  • Study to determine if children who receive
    influenza vaccination miss fewer days of school
  • Study to determine if the coleslaw was the cause
    of a foodborne illness outbreak

66
Case-Control Studies
  • Study population is grouped by outcome
  • Cases are persons who have the outcome
  • Controls are persons who do not have the outcome
  • Past exposure status is then determined

67
Case-Control Studies
Study Population
Controls
Cases
Had Exposure
No Exposure
No Exposure
Had Exposure
68
Case-Control Study Examples
  • Study to determine an association between autism
    and vaccination
  • Study to determine an association between lung
    cancer and radon exposure
  • Study to determine an association between
    salmonella infection and eating at a fast food
    restaurant

69
Cohort versus Case-Control Study

70
Classification of Study Designs
Source Grimes DA, Schulz KF. Lancet 2002 359
58
71
Time for you to try it!!!
72
5 Minute Break
73
Analytic Epidemiology
  • Measures of Association
  • and
  • Statistical Tests

74
Measures of Association
  • Assess the strength of an association between an
    exposure and the outcome of interest
  • Indicate how more or less likely one is to
    develop disease as compared to another
  • Two widely used measures
  • Relative risk (a.k.a. risk ratio, RR)
  • Odds ratio (a.k.a. OR)

75
2 x 2 Tables
  • Used to summarize counts of disease and exposure
    in order to do calculations of association

76
2 x 2 Tables
  • a number who are exposed and have the outcome
  • b number who are exposed and do not have the
    outcome
  • c number who are not exposed and have the
    outcome
  • d number who are not exposed and do not have
    the outcome

  • a b total number who are exposed
  • c d total number who are not exposed
  • a c total number who have the outcome
  • b d total number who do not have the outcome
  • a b c d total study population

77
Relative Risk
  • The relative risk is the risk of disease in the
    exposed group divided by the risk of disease in
    the non-exposed group
  • RR is the measure used with cohort studies
  • a
  • a b
  • RR
  • c
  • c d

78
Relative Risk Example
a / (a c) 23 / 33 RR
6.67 c / (c d) 7 / 67
79
Odds Ratio
  • In a case-control study, the risk of disease
    cannot be directly calculated because the
    population at risk is not known
  • OR is the measure used with case-control studies
  • a x d
  • OR
  • b x c

80
Odds Ratio Example
a x d 130 x 135 OR 1.27 b
x c 115 x 120
81
Interpretation
  • Both the RR and OR are interpreted as follows
  • 1 - indicates no association
  • 1 - indicates a positive association

82
Interpretation
  • If the RR 5
  • People who were exposed are 5 times more likely
    to have the outcome when compared with persons
    who were not exposed
  • If the RR 0.5
  • People who were exposed are half as likely to
    have the outcome when compared with persons who
    were not exposed
  • If the RR 1
  • People who were exposed are no more or less
    likely to have the outcome when compared to
    persons who were not exposed

83
Tests of Significance
  • Indication of reliability of the association that
    was observed
  • Answers the question How likely is it that the
    observed association may be due to chance?
  • Two main tests
  • 95 Confidence Intervals (CI)
  • p-values

84
95 Confidence Interval (CI)
  • The 95 CI is the range of values of the measure
    of association (RR or OR) that has a 95 chance
    of containing the true RR or OR
  • One is 95 confident that the true measure of
    association falls within this interval

85
95 CI Example
Grodstein F, Goldman MB, Cramer DW. Relation of
tubal infertility to history of sexually
transmitted diseases. Am J Epidemiol. 1993 Mar
1137(5)577-84
86
Interpreting 95 Confidence Intervals
  • To have a significant association between
    exposure and outcome, the 95 CI should not
    include 1.0
  • A 95 CI range below 1 suggests less risk of the
    outcome in the exposed population
  • A 95 CI range above 1 suggests a higher risk of
    the outcome in the exposed population

87
p-values
  • The p-value is a measure of how likely the
    observed association would be to occur by chance
    alone, in the absence of a true association
  • A very small p-value means that you are very
    unlikely to observe such a RR or OR if there was
    no true association
  • A p-value of 0.05 indicates only a 5 chance that
    the RR or OR was observed by chance alone

88
p-value Example
Grodstein F, Goldman MB, Cramer DW. Relation of
tubal infertility to history of sexually
transmitted diseases. Am J Epidemiol. 1993 Mar
1137(5)577-84
89
Time for you to try it!!!
90
Questions???
91
Epidemiology Pocket GuideQuick Review Any Time!
  • Measures of Disease Frequency
  • Classification of Study Designs
  • 2 x 2 Tables
  • Measures of Association
  • Tests of Significance
  • http//www.vdh.virginia.gov/EPR/Training.asp

92
Session III Slides
  • Following this program, please visit the Web
    site below to access and download a copy of
    todays slides
  • http//www.vdh.virginia.gov/EPR/Training.asp

93
Site Sign-in Sheet
  • Please submit your site sign-in sheet to
  • Suzi Silverstein
  • Director, Education and Training
  • Emergency Preparedness Response Programs
  • FAX (804) 225 - 3888

94
References and Resources
  • Centers for Disease Control and Prevention
    (1992). Principles of Epidemiology 2nd Edition.
    Public Health Practice Program Office Atlanta,
    GA.
  • Gordis, L. (2000). Epidemiology 2nd Edition.
    W.B. Saunders Company Philadelphia, PA.
  • Gregg, M.B. (2002). Field Epidemiology 2nd
    Edition. Oxford University Press New York.
  • Hennekens, C.H. and Buring, J.E. (1987).
    Epidemiology in Medicine. Little, Brown and
    Company Boston/Toronto.

95
References and Resources
  • Last, J.M. (2001). A Dictionary of Epidemiology
    4th Edition. Oxford University Press New York.
  • McNeill, A. (January 2002). Measuring the
    Occurrence of Disease Prevalence and Incidence.
    Epid 160 lecture series, UNC Chapel Hill School
    of Public Health, Department of Epidemiology.
  • Morton, R.F, Hebel, J.R., McCarter, R.J. (2001).
    A Study Guide to Epidemiology and Biostatistics
    5th Edition. Aspen Publishers, Inc.
    Gaithersburg, MD.
  • University of North Carolina at Chapel Hill
    School of Public Health, Department of
    Epidemiology, and the Epidemiologic Research
    Information Center (June 1999). ERIC Notebook.
    Issue 2. http//www.sph.unc.edu/courses/eric/eric_
    notebooks.htm

96
References and Resources
  • University of North Carolina at Chapel Hill
    School of Public Health, Department of
    Epidemiology, and the Epidemiologic Research
    Information Center (July 1999). ERIC Notebook.
    Issue 3. http//www.sph.unc.edu/courses/eric/eric_
    notebooks.htm
  • University of North Carolina at Chapel Hill
    School of Public Health, Department of
    Epidemiology, and the Epidemiologic Research
    Information Center (September 1999). ERIC
    Notebook. Issue 5. http//www.sph.unc.edu/courses
    /eric/eric_notebooks.htm
  • University of North Carolina at Chapel Hill
    School of Public Health, Department of
    Epidemiology (August 2000). Laboratory
    Instructors Guide Analytic Study Designs. Epid
    168 lecture series. http//www.epidemiolog.net/epi
    d168/labs/AnalyticStudExerInstGuid2000.pdf

97
2005 PHIN Training Development Team
  • Pia MacDonald, PhD, MPH
  • Director, NCCPHP
  • Jennifer Horney, MPH
  • Director, Training and Education, NCCPHP
  • Kim Brunette, MPH
  • Epidemiologist, NCCPHP
  • Anjum Hajat, MPH
  • Epidemiologist, NCCPHP
  • Sarah Pfau, MPH
  • Consultant
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