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Class 1 - 032024
Class 1 - 032024
Course Topics
Class 1
1. Introduction to Epidemiology & Its Role in Public
Health (Chapter 1, p1 -> p6)
2. Measuring Health and Disease (Chapter 2, p15 -> p31)
3. Types of Studies (Chapter 3: p39-p51)
Class 2
4. Causation in Epidemiology (Chapter 5: p89-p96)
5. Epidemiology and prevention: chronic
noncommunicable diseases (Chapter 6: p99-p113)
6. Communicable diseases: epidemiology surveillance
and response (Chapter 7: p117-p127)
Class 3
7. Understanding & Managing Errors in Studies (Chapter 3:
p51-p57)
2
8. Basic Biostatistics: concept and tools (Chapter 4: p63-p69)
Assessment components
ØUsing a 10-point scale for all assessment.
ØOngoing Assessment: Attendance 10% + In-class
individual exercises 10% = 20%
ØMid-term Assessment: Presentation 10% + Mid-
term exams 10% = 20%
ØFinal Exams: 60%
üMinimum passing point: 4/10
3
Class attendance (10%)
ØArriving late by 15 minutes: no points deducted
ØArriving late by more than 15 minutes but less than 1
hour: 25% deduction
ØArriving late by 1 hour or more: 50% deduction
ØMissing a class without permission: NOT allowed to
take the semester exam.
4
In-class individual exercises
ØFor each speech you make, you will receive 1
bonus point.
ØThe class monitor will compile the bonus points at
the end of the class and send them to me.
5
Presentation 10% (Class 2)
Group 1: Causation in Epidemiology
Group 2: Epidemiology and prevention: chronic
noncommunicable diseases
Group 3: Communicable diseases: epidemiology
surveillance and response
ØThe groups submit their list of members after
playtime.
ØEach group has 15-20 minutes for presentation, 5-
10’ Q&A.
ØPlease send your presentations to me 1 days
before class; students should prepare their own 6
laptops/computers.
Presentation score
6 points Content aligns with the textbook
+1 point Demonstrates creativity: content, visuals,…
+1 point Exhibits presentation skills
+1 point Capable of answering questions
7
Mid-term exams (10%) (Class 3)
- Take the test on Google Forms, 15 multiple choice
questions/15 minutes
- Please remember to bring your phone to class
8
Textbook
9
NGUYEN TAT THANH UNIVERSITY
NURSING FACULTY
17
18
Purposes Of Epidemiology
20
Causation of Disease
21
Natural History of Disease
üEpidemiology is also concerned with the course and
outcome (natural history) of diseases in individuals and
groups.
Risk factors
Death
disabled
23
Epidemiology VS Clinical medicine
27
Definition of Health
ØEpidemiologists are required to have some
knowledge of the disciplines of public health,
clinical medicine, pathophysiology, statistics, and
the social sciences.
28
Diagnostic Criteria
üDiagnostic criteria are usually based on symptoms,
signs, history and test results.
29
30
üDiagnostic criteria can change rapidly with
advancing knowledge and improving techniques,
as well as based on the context of their
application.
31
Measuring Disease Frequency
Population at risk
üThe people who are susceptible to a given disease, and
can be defined by demographic, geographic or
environmental factors.
32
Incidence and Prevalence
ü Diabetes: Low
incidence, high
prevalence
34
Attack Rate and Rates
• Rate =
!"#$%& '( ,+1%1
,'&&%1)'!.2!3 !"#$%& '( )%')*% 2! -/% )')"*+-2'! +- &214
35
Prevalence
Øhow common a disease is in a specific group at a particular
time, a "snapshot" of a disease in a community.
!"#$%& '( )%')*% +,-. -.% /,0%10% '& 2'3/,-,'3 1- 1 0)%2,(,%/ -,#%
P= !"#$%& '( )%')*% ,3 -.% )')"*1-,'3 1- &,04 1- -.% 0)%2,(,%/ -,#%
(x10n)
Have you had asthma during the last 2 years? Period prevalence
37
Incidence
!"#$%& '( 3%+ %5%3-0 ,3 1 0)%2,(,%/ )%&,'/
I= (x10 n)
!"#$%& '( )%&0'30 %6)'0%/ -' &,04 /"&,37 -.,0 )%&,'/
Cumulative Incidence
!"#$%& '( )%')*% +.' 7%- 1 /,0%10% /"&,37
1 0)%2,(,%/ )%&,'/
= !"#$%& '( )%')*% (&%% '( -.% /,0%10% ,3 -.% )')"*1-,'3 (x10 n)
38
Incidence and Prevalence
40
Health Data
Mortality
43
Mortality
Age-Specific Death Rates
='-1* 3"#$%& '( /%1-.0 '22"&&,37 ,3 1 0)%2,(,2 17% 13/ 0%6 7&'")
'( -.% )')"*1-,'3 ,3 1 /%(,3%/ 1&%1 /"&,37 1 0)%2,(,%/ )%&,'/
>0-,#1-%/ -'-1* )')"*1-,'3 '( -.% 01#% 17% 13/ 0%6 7&'") (x10 n)
'( -.% )')"*1-,'3 ,3 -.% 01#% 1&%1 /"&,37 -.% 01#% )%&,'/
Proportionate Mortality
A ratio: the number of deaths from a given cause per 100 or
1000 total deaths in the same period.
44
Mortality
45
Mortality
47
NGUYEN TAT THANH UNIVERSITY
NURSING FACULTY
52
The 5W's of descriptive epidemiology
53
Observational Studies
üAnalytical Studies: look at the relationships between a
health status and other factors.
E.g. Trying to find out if people who smoke are more
likely to get lung cancer.
• Cross-sectional
• Cohort
• Case-control
54
Analytic epidemiology
Tests hypotheses about:
• Why
• How
55
Experimental studies
üExperimental studies involve actively attempting
to change a disease determinant or its progression
through treatment.
• Randomized control trial
• Clinical trial
• Community trial
56
57
Epidemiology study
Time
Person
Epidemiology
60
Person
61
Time
• Changing or stable?
• Seasonal variation.
62
Place
• Geographically restricted or widespread
(pandemic)?
63
64
Ecological Studies
ØThe units of analysis are groups of people rather
than individuals.
ØThese studies compare populations in different
places at the same time or, in a time series, or one
place at different times.
ØThe shorter the time being studied, the less likely
other factors will confuse the results.
65
66
Limitations
ØDifficult to interpret since it is seldom possible to
examine directly the various potential explanations
for findings.
ØData on different exposures and on socioeconomic
factors may not be available.
ØThe unit of analysis is a group, the link between
exposure and effect at the individual level can not
be made.
ØThe ecological fallacy/bias occurs.
67
Cross-sectional Studies
ØCross-sectional studies take a "snapshot" of a
group at a specific time.
ØThese studies measure the prevalence of disease -
prevalence studies.
ØThey measure both the exposure and disease at
the same time.
68
69
70
Pros and Cons
ØAdvantages:
• quick to conduct and cost is moderate
compared with other study designs.
• useful for the health care needs of populations,
sudden outbreaks of disease
ØDisadvantages:
• cannot provide information on the incidence of
disease in a population only an estimate of
prevalence
• Difficult to investigate cause and effect
relationships
71
72
Case-control Studies
ØCase-control studies investigate causes of diseases.
ØThey include people with a disease (cases) and without
a disease (control/comparison/reference) group.
ØThe study compares the occurrence of the possible
cause in cases and in controls.
73
Ø The investigators collect data on disease occurrence at one
point in time and exposures at a previous point in time.
74
Ø Case-control studies are longitudinal, in contrast to
cross-sectional studies
75
= timing of data collection
79
OR=(50/11)÷(16/41)= (50 × 41)/(11 × 16)= 11.6
Ø The cases were 11.6 times more likely than the
controls to have recently eaten meat. 80
Pros and Cons
ØAdvantages:
• an efficient method for studying rare diseases
• subjects have experienced the outcome of interest
at the start of the study
• quick to run and cheaper than other study
ØDisadvantages:
• Can not provide information on the disease
incidence in a population
• Reliant on the quality of past records or recollection
of study participants
• Difficult to ensure an unbiased selection of the
control group 81
Cohort Studies
ØBegin with a group of healthy people are classified
into subgroups according to exposure to a potential
cause of disease and followed up to see how the
subsequent development of new cases in the
groups with and without exposure.
ØFollow-up or incidence studies
82
Ø the data on exposure and disease refer to different
points in time, cohort studies are longitudinal, like
case- control studies 83
Pros and Cons
ØAdvantages:
• monitored over time for disease occurrence
• estimates of the absolute incidence of disease in
exposed and non-exposed
ØDisadvantages:
• long follow-up period
• case of rare diseases large groups are necessary
• Losses to follow-up
• expensive
84
follow up study
participants for a long
time
86
confuse
89
Experimental Studies
ØIntervention/experimentation involves attempting to
change a variable in one or more groups of people.
• The elimination of a dietary factor thought to cause
allergy
• testing a new treatment on a selected group of patients
ØThe effects of an intervention are measured by
comparing the outcome in the experimental group with
that in a control group.
ØEthical considerations are of paramount importance in
the design of these studies.
90
Randomized controlled trials
Ø An epidemiological experiment designed to study
the effects of a particular intervention, usually a
treatment for a specific disease (clinical trial).
ØSubjects are randomly allocated to intervention
and control groups, and the results are assessed by
comparing outcomes.
91
Field Trials
ØField trials involve people who are healthy but
presumed to be at risk.
ØData collection takes place “in the field,” usually among
non-institutionalized people.
92
Field Trials
ØField trials are often logistically complicated and
expensive endeavours. E.g.
ØField trials can be used to evaluate interventions
aimed at reducing exposure without necessarily
measuring the occurrence of health effects. E.g.
ØSuch intervention studies involve a smaller scale,
and at lower cost, since lengthy follow-up or
measurement of disease outcomes.
93
The Salk polio vaccine
94
95
Community Trial
ØThe treatment groups are communities rather than
individuals.
ØThis is particularly appropriate for diseases that are
influenced by social conditions, and for which
prevention efforts target group behaviour.
96
Limitations of community trials
ØOnly a small number of communities can be
included and random allocation of communities is
usually not practicable.
ØOther methods are required to ensure that any
differences found at the end of the study can be
attributed to the intervention rather than to
inherent differences between communities.
ØIt is difficult to isolate the communities where
intervention is taking place from general social
changes that may be occurring.
97
Limitations of community trials
ØDesign limitations, especially in the face of
unexpectedly large, favourable risk factor changes
in control sites, are difficult to overcome.
ØAs a result, definitive conclusions about the overall
effectiveness of the community-wide efforts are
not always possible.
98