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Epidemiology
SOBANA.M, M.Sc(N).,
DEFINITION
"The study of the distribution and determinants of health related
states or events in specified population and application of this
study to control of diseases and other health problems“
(J.M. Last 1988)
USES OF EPIDEMIOLOGY
• Study of the History of disease.
• Planning
• Community diagnosis
• Assessment of individuals risk.
• Identification of syndrome
• Completion of the clinical picture of
chronic disease
• Searching for causes
• Evaluation.
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Scope of epidemiology
Epidemiology covers the various types of field in different types of
activities. It is applied in every field as agricultural, economics, statistics
etc. They are as
• Clinical epidemiology
• Sub-clinical epidemiology
• Infectious disease epidemiology
• Geographical epidemiology
• Social epidemiology
• Chronic disease epidemiology
• Serological epidemiology
• Cancer epidemiology
• Malaria epidemiology
• Neuro epidemiology
• Genetic epidemiology
• Occupational epidemiology
• Psychosocial epidemiology
• Computational epidemiology
• Field epidemiology
• Participative epidemiology
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• Molecular epidemiology
• Environmental epidemiology
• Micro- epidemiology
• Macro-epidemiology
• Nutritional epidemiology
• Statistical epidemiology
• Descriptive epidemiology
• Analytical epidemiology
• Experimental epidemiology
• Infectious diseases epidemiology
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Components of
Epidemiology
Epidemiology
Components of epidemiology
Disease frequency:
• The core characteristics of epidemiology are to
measure the frequency of diseases, disability or
death in a specified population. it is always as the
rate, ratio and proportion.
• This helps to development of strategies for
prevention or control of health related problems.
Distribution of diseases:
• Health events occur in pattern in community and this pattern varies
from community to community.
• Also health events or diseases condition affect population at various
age groups, different sexes, different subgroups of population.
• Distributions of events are based on time, place, and person. We
can analyze whether any increases or decreases occur for a
particular condition. Epidemiology addresses itself to a study of
these variations or patterns, which may suggest or lead to measure
to control or prevent the diseases. An important outcome of this
study is formulation of etiological hypothesis.
Determinants of diseases
• Epidemiology helps in identifying the
causative agent or the risk/predisposing
factors of diseases .
• This is one of the real uses of
epidemiology. Understanding the factors
leading to any programs for the control
of those diseases.
Dynamics of disease transmission
Epidemiology
Source:
The source of infection defined as the person, animal,
object or substance from which an infectious agent passes
or is disseminated to the host.
Reservoir:
A reservoir is defined as any person, animal, arthropod,
plant, soil or combination of these, in which an infectious
agent lives and multiplies , on which it depends primarily for
survival, where it is reproduce itself in such manner that it can
be transmitted to a susceptible host.
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Types of reservoir
Reservoir
Human
reservoir
Cases Carriers
Animal
reservoir
Reservoir of
non-living
things
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Cases
Clinical
Sub-
clinical
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CARRIERS
By type
Incubator
y
Convales
cent
Healthy
By duration
temporar
y
Chronic
By portal of
exist
urinary Intestinal
Respirato
ry
Skin blood
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MODE OF TRANSMISSION
MODE OF
TRANSMISSION
DIRECT
TRANSMISSION
INDIRECT
TRANSMISSION
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DIRECT
TRANSMISSION
DIRECT CONTACT
DROPLET
INFECTION
CONTACT WITH
SOIL
INOCULATION
INTO SKIN
TRANSPLACENTAL
TRANSMISSION
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INDIRECT
TRANSMISSION
VEHICLE BORNE VECTOR BORNE AIR BORNE FOMITE BORNE
UNCLEAN
HANDS AND
FINGERS
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I.SUCCESSFUL PARASITISM
• The infectious agent must find a portal of entry by which it may enter
the host
• Ongoing entry into the host, the organism must reach the
appropriate tissue or site of election in the body of host where it may
find optimum conditions for its multiplication and survival.
• The disease agent must find the portal of exist.
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• After leaving the human body the organism must
survive in the external environment for sufficient
period till a new host is found.
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II. INCUBATION PERIOD:
• It is defined as the time interval between invasion by
an infectious agent and appearance of the first signs
and symptoms of the disease in question.
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EPIDEMILOLOGICAL TRIAD
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AGENT
HOST
ENVIRON
MENT
AGENT FACTORS:
• The disease agent is defined as a substance, living
and non-living, tangible or intangible, the excessive
presence or relative lack, which may initiate a disease
process.
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Classification of disease agents:
1. Biological agent
2. Nutrient agent
3. Physical agent
4. Chemical agent
5. Mechanical agent
6. Absence or insufficiency or excess of factors necessary
to health
7. Social agent
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HOST FACTORS:(INTRINSIC HOST)
In epidemiological terminology, the human host is
referred to as soil and disease agent is seed.
The host factors may be classified as:
1. Demographic characteristics – ( age and gender)
2. Biological characteristics – (genetic factors, biochemical level of
blood, blood groups)
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• Social and economic characteristics – (socio-economic
status, education, occupation, marital status, housing)
• Life style factors – personality traits, physical exercise,
use of alcohol/drugs and smoking etc…..
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ENVIRONMENTAL FACTORS (EXTRNSIC)
• The environment has been divided into 3
components:
– Physical
– Biological
– psychosocial
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MEASUREMENTS OF MORBIDITY AND
MORTALITY
• MORTALITY MEASUREMENTS: (the commonly used measures are;)
1. Crude death rate
2. Specific death rate
A. Specific death rate due to TB
B. Specific death rate for males
C. Specific death rate in age group
D. Death rate for month
E. Weekly death rate
3. Case fatality rate
4. Proportional mortality rate
5. Survival rate
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1. Crude death rate:(CDR)
No.of death during the year
CDR=--------------------------------------------X 1000
Mid- year population
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2. Specific death rate:
• 1. Specific Death Rate Due To TB:
No.of deaths from TB during a
calendar year
SDR(TB)=------------------------------------------X 1000
Mid-year population
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2. Specific Death Rate For Males:
No.of deaths among males during a
calendar year
SDR(M)=-------------------------------------------------X1000
Mid-year population of males
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• 3. Specific Death Rate In The Age Group Of 15-20 Years:
No.of deaths of persons aged 15-20
years during a calendar year
SDR=----------------------------------------------------X1000
Mid-year population of
persons aged 15-20 years
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4. Death rate for January:
No.of deaths in January X 12
SDR=-----------------------------------------------X1000
Mid-year population
The death rate are multiplied by 12 in order to make the monthly
death rate comparable with the annual death rate.
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5. Weekly Death rate :
No.of deaths in a week X 52
SDR=--------------------------------------------X1000
Mid-year population
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3. Case fatality rate:
No.of deaths due to particular
disease
CFR=---------------------------------------------------------X1000
Total no.of cases due to same disease
CFR represents the killing power of disease. It is typically used in acute
infectious diseases.
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4.Proportional mortality rate:
• It is sometime useful to know what proportion of total deaths
are due to particular cause or what proportion of deaths are
occurring in a particular age group.
• PMR expresses no.of death due to particular cause or in
specific age group per 100 or 1000 total deaths.
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A) PMR For Specific Disease:
No.of deaths from the specific disease
in a year
PMR=-----------------------------------------------------X1000
Total deaths from all causes in
that year
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B) UNDER FIVE PMR:
No.of deaths under five years of age
in a given year
Under Five PMR=--------------------------------------------x1000
Total no.of deaths during the
same year
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C) PMR FOR AGE 50 YEARS AND ABOVE:
No.of deaths of persons aged
50 years and above in a given year
=--------------------------------------------------x1000
Total no.of deaths of all age group
during the same year
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5. SURVIVAL RATE:
It is the proportion of survivors in a age group (patients) studied and
follow over a period.
Total no.of patients alive after 5 years
SR=--------------------------------------------------------------X1000
Total no.of patients diagnosed and treated
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MEASUREMENTS OF MORBIDITY:
• Morbidity has been defined as any departure,
subjective or objective, from a state of physiological
well being.
• Morbidity commonly measured by 3 aspects:
» Frequency
» Duration
» Severity
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1. Disease frequency:
• Disease frequency is measured by incidence and
prevalence rates.
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INCIDENCE RATE:
• It is defined as the no.of new cases occuring in a
defined population during a specified period of time.
No.of new case of specific disease
during a given time period
IR=------------------------------------------------------X1000
Population risk during that period
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IR REFERS TO:
• Only to new cases
• During a given period ( usually a year)
• In a specified population or population at risk
• It can also refers to spells or episodes of disease
arising in a given period of time per 1000 population.
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PREVALENCE RATE:
• The term disease prevalence refers specifically to all
current cases (old and new) existing at given point in
time or over a period of time in a given population.
• Prevalence is of 2 types:
» Point prevalence
» Period prevalence
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Point prevalence:
• It is defined as no.of of all current cases (old and
new) of a disease at 1 point of time, in relation to a
defined population.
• The point- a day, several days, week; depending upon
the time it takes to examine the population sample.
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No.of all current cases (old and new) of a specified
disease existing at a given point in time
PP=-------------------------------------------------------------X100
Estimated population at the same point
in time
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Period prevalence:
• It measures the frequency of all current cases (old and new) existing during a
defined period of time.
No.of all existing cases (old and new) of a specified disease
during a given period of time interval
PP=--------------------------------------------------------------------X100
Estimated mid-interval population at risk
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2.DURATION
• The average duration per case or the disability rate,
which is the average no.of days of disability per
person, may serve as a measure of the duration of
illness.
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3.SEVERITY:
• The case fatality rate may be used as the index of
severity.
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Levels of prevention
Levels of prevention
• Introduction:
– The successful prevention depends on knowledge of
causation, dynamics of transmission, identification of risk
factors and risk groups, early diagnosis and frequent
measures an organization for applying these measures to
appropriate persons or groups and continuous evaluation of
and development of procedures applied.
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There are 4 levels of prevention:
Tertiary
prevention
Secondary
prevention
Primary prevention
Primordial prevention
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i. Primordial prevention:
• This is primary prevention in its purest sense.
• It is prevention of the emergence of or development
of risk factors in population group in which they have
not yet appeared
• A new concept, is receiving a special attention in
prevention of chronic diseases.
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Example:
• Many adult health problem (obesity, HT) have their
origin in childhood practices like smoking, eating
pattern, physical exercise.
• In primordial prevention, efforts are directed towards
discouraging children from adopting harmful
lifestyles.
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Interventions:
• Individual and mass health education
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HARMFUL LIFESTYLE
PRACTICES OF
CHILDHOOD
CONTROL
PREVENT FUTURE
HEALTH PROBLEMS
ii. Primary prevention:
• Primary prevention can be defined as action taken
prior to the onset of disease which removes the
possibility of disease will ever occur.
• It signifies intervention in the pre-pathogenesis
phase of a disease or health problems.
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Approaches for primary prevention of chronic diseases:
(WHO recommendations)
• 1. Population (mass) strategy
• 2.High risk strategy
1. Population (Mass) Strategy
– Which is directed at the whole population
irrespective of individual risk levels.
2.High Risk Strategy
– It aims to bring preventive care to individuals at
specific risk.
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Public health measures and activities of primary
prevention:
• Sanitation
• Infection control
• Immunization
• Protection of food, milk and water supply
• Environmental protection
• Protection against occupational hazards and
accidents.
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iii. Secondary prevention:
• It can be defined as action which halts the progress
of a disease at its incipient stage and prevent
complications.
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Interventions:
• Early diagnosis
• Adequate treatment
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iv. Tertiary prevention:
• It can be defined as all measures available to reduce or limit
impairments and disabilities, minimize suffering caused by existing
departures from good health and to promote the patient’s adjustment
to irremediable conditions.
• when the disease process has advanced beyond it’s early stage , it is still
possible to accomplish prevention by what might be called tertiary
prevention.
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Interventions:
• 1. Disability limitation
• 2. Rehabilitation
» Includes medical, psychosocial, vocational rehabilitations.
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Levels of
prevention
Primordial
prevention
Primary
prevention
Secondary
prevention
Tertiary
prevention
Modes of
intervention
1. Health
education
(individual &
mass)
1.Health
promotion
2.Specific
protection
1.Early diagnosis
2.Appropriate
treatment
1.Diability
limitation
2.rehabilitation
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METHODS OF EPIDEMIOLOGY
METHODS OF EPIDEMIOLOGY
• INTRODUCTION:
– The primary concern of the epidemiologist is to study
disease occurrence in people. Epidemiological studies can
be classified into
• 1. OBSERVATIONAL STUDIES
• 2. EXPERIMENTAL STUDIES (INTERVENTIONAL STUDIES)
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• Observational Study
– Descriptive studies
– Analytical Studies
• Ecological Study: - Correlation Study unit is a population.
• Cross-Sectional Study: - prevalent Study Individual is a unit
of study.
• Case-Control Study: - case-reference with individual is a
unit of study.
• Cohort study:-Follow up study with individual is a unit of
study.
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• Experimental Studies
–Randomized Control Trials
–Field Trials
–Community Trials
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OBSERVATIONAL STUDY:
1.DESCRIPTIVE STUDY
• It is descriptive epidemiology/descriptive study.
• It is the first phase of epidemiological investigation
• The studies are concerned with observing the distribution of
disease.
• By:
– Time distribution – when the disease is occurring?
– Place distribution- where it is occurring?
– Person distribution-who is getting the disease?
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PROCEDURE IN DESCRIPTIVE STUDY
• Define the population
• Define the disease under study
• Describing the disease by
• TIME
• PLACE
• PERSON
• Measurement of diseases
• Comparing with known indices.
• Formulation of an etiological hypothesis
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1.Define the population
• The population can be the whole population in a
geographic area. It can also be a specially selected
group such as age, gender, school children, small
communities.
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2.Define the disease under study:
• Define the disease or condition being investigated.
• A definition must be precise and valid to enable
epidemiologist to identify those who have the
disease from who don’t have.
• Operational definition- used to define the disease.
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3. Describing the disease
TIME PLACE PERSON
year,
Season
Month
Week
Day
Hours
Duration
Climatic zones
Country
Region
Urban
Rural
Town
Cities
Institution
Age
Gender
Marital status
Birth
Occupation
Social status
Education
Family size
Height
Weight
B.P
Personal habits9/29/2017 76
1. Time distribution:
3 types of time trends/ fluctuations in disease
occurrences.
1. Short term fluctuations – Epidemic diseases
2. Periodic fluctuations
1. Seasonal trend - URTI in summer, GI infections-summer
2. Cyclic trend- cycle spread over short period of time eg:
measles in every 2 – 3 years
3. Long term and secular trend - changes in the
occurrences of disease i.e a progressive increase or
decrease over a long period of time ( years /
decades)
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2. Place distribution ( Geographical comparison)
• The variations may be classified as;
– International variations – E.g : CVDs, Cancers.
– National variations – E.g: nutritional deficiencies,
epidemic goiter
– Urban and rural variations – E.g: accidents, lung
cancer, HT- urban area; zoonotic diseases – rural
areas.
– Local distribution- inner and outer city variations.
“ spot maps”/” shaded maps” is used.
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3. Person distribution:
• In descriptive study, the disease is further characterized by
defining the person who developed the disease by age,
gender, marital status, occupation, social status etc….
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4. Measurement of disease:
• Morbidity and mortality measurements gives clear picture of
disease load.
• Measurement of mortality is straight forward.
• Morbidity has 2 aspects:
1. Incidence – obtained from longitudinal studies
2. Prevalence – obtained from cross sectional
studies
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Cross sectional studies:
• It is a single examination of cross-section of
population at one point in time
• The results of which can be projected the whole
population
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Longitudinal studies:
• Observation of same population over a prolonged
period of time by means of follow-up examination.
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5. Comparing with known indices:
• By making comparison between different population
and sub-group of the same population, it is possible
to arrive at clues to disease etiology.
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6. Formulation of hypothesis
• Hypothesis is a supposition, arrived at from observation. An
epidemiological hypothesis should explain;
• Specific cause
• The expected outcome
• The dose response
• The time response
• E.g: smoking causes lung cancer ( incomplete)
• Smoking of 30-40 cigarette/day cause lung cancer in 10% of
smoker after 20 years of exposure – (complete).
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Uses of descriptive epidemiology:
• Provide data regarding magnitude and type of disease in
community.
• Provide clues to disease etiology & helps in the
formulation of etiological hypothesis
• Provide background data for planning, organizing &
evaluating preventive & curative services
• The contribute to research by describing variations in
disease occurrence by time, place, person.
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II. ANALYTICAL EPIDEMIOLOGY
• Analytical study are the second major type of epidemiological
study.
• The objective is not to formulate but to test the hypothesis.
• The individual subject are evaluated in analytical study.
• 2 types:
– Case control studies
– Cohort studies
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1. CASE CONTROL STUDIES:
• It is often called retrospective studies.
• Features of case control studies:
– Both exposure and outcome have occurred before the
start of study
– The study proceeds backwards from effect to cause
– it uses a control or comparison group to support or
refute an inference
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• By definition a case control study involves two
population
• cases and controls
• In CCSs the unit is individual rather than the group.
• The focus is on disease that has already developed
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Basic steps in case control study:
• There are 4 basic steps :
– Selection of cases and controls
– Matching
– Measurement of exposure
– Analysis and interpretation
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i) Selection of cases and controls:
• Selection of cases:
– Cases are selected based on diagnostic criteria
and eligibility criteria.
• Sources of cases:
– Hospital
– General population
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Selection of controls:
• The controls may be free from disease under study.
These may be as similar to the cases as possible,
except for the absence of disease under study
• As a rule, a comparison group is identified before a
study is done.
• Sources of controls:
• Hospitals, relatives, neighbors and general population.
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ii) matching:
• The control may differ from cases in a no.of factor
such as age, gender, occupation & social status. An
important consideration is to ensure comparability
between cases and controls. This is known as
matching.
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iii) Measurement of exposure:
• Information about exposure should be obtained
precisely the same manner both for cases and
controls.
• This may be obtained by interviews, questionnaires,
studying of past record of cases such as hospital
records and employment records.
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iv) Analysis :
• The final step is analysis to find out
• Exposure rate among cases and controls to
suspected factors
• Estimation of disease risk associated with
exposure
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2.COHORT STUDY
• In epidemiology the term cohort is defined as a
group of people who share a common characteristics
or experience within a defined time period.
– Example: age cohort, occupational cohort,
marriage cohort, pregnancy cohort, birth cohort.
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• Cohort study is known by variety of names:
• Prospective longitudinal study
• Incidence study
• Forward looking study
• The features of cohort studies:
– Cohorts are identified prior to the appearance of
disease under investigation.
– The study group observed over a period of time to
determine the frequency of disease among them.
– The study proceeds forward from cause to effect.
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Types of cohort studies:
• Prospective cohort study
• Retrospective cohort study
• Combination of retrospective and prospective cohort
study
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Prospective or current cohort study:
• It is one in which the outcome has not yet occurred
at the time the investigation begins.
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Retrospective cohort study:
• Or historical is one in which the outcome have all
occur before the start of the investigation.
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Combination of retrospective and prospective
cohort study
• In this type of study both the prospective and retrospective
elements are combined. The cohort is identified from past
records and the same cohort is followed prospectively in
future for further assessment outcome.
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Steps of cohort study:
• Selection of study subjects
• Obtain data on exposure
• Selection of comparison group
• Follow-up
• Analysis
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1. Selection of study subjects
• General population
• Special groups
• Select groups
• Exposure groups
• Select groups
– These may be professional groups ( doctors/nurses), insured
persons, college alumni, government employee and volunteers
etc…
• Exposure groups
– Cohort may be selected because of special exposure to physical,
chemical or other disease agent.
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2. Obtaining data on exposure:
• Information about exposure may be obtain directly from
cohort members through personal interviews, mailed
questionnaires, preview of records, medical examination or
special tests, environmental surveys.
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3. Selection of comparison groups:
• There are many ways of assembling comparison
groups:
– Internal comparison
– External comparison
– Comparison with general population
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• Internal comparison: In some cohort studies, no outside
comparison group is required. The comparison groups are inbuilt
within the individual study itself.
• External comparison: When information on degree of
exposure is not available, it is necessary to put-up an external
control, to evaluate the experience of the exposed groups.
• Comparison with general population: If none is available, the
mortality experience of the exposed groups is compared with the
mortality experience of the general population in the same
geographic area as exposed peoples.
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4. follow-up:
• One of the problem of cohort study is the regular follow-
up of all the participants.
• The procedure required comprises of:
– Periodical medical examination of each cohort
members
– Reviewing physician and hospital record
– Routine surveillance of death records
– Mailed questionnaires, telephonic calls
– Periodic home visit
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5. Analysis :
• The data are analyzed in terms of
–Incidence rates of outcome among exposed
and non-exposed
–Estimation of risk associated with disease.
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Experimental Studies Or Experimental
Epidemiology:
• These are also called as interventional studies.
• Experimental studies involves some actions, interventions or
manipulation such as deliberate application or withdrawal of the
suspected cause in the experimental group while making no change
in the control group, and observing & comparing the outcome of
the experiment in both the groups.
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Aims :
• To provide scientific proof of etiological factors
• To provide a method of measuring the effectiveness and
efficiency of health services for prevention, control and
treatment of disease and improve the health of the
community.
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Types of experimental studies:
1. Randomized Controlled Trials
2. Non-randomized Controlled Trials
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Randomized controlled trials (RCT)
• Those involving the process of random allocation
• Randomization means- giving equal chance to all
samples
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The basic steps in conducting RCT:
1. Drawing up of protocol
2. Selecting reference and experimental population
3. Randomization
4. Manipulation or intervention
5. Follow-up
6. Assessment of outcome
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1. Drawing up of protocol
• One of the essential features of RCT is the study is conducted
under strict protocol.
• The protocol specifies the aims and objectives of the study,
questions to be answered, criteria for the selection of study
groups and control groups, size of the sample, the procedure for
allocation of subjects into study and control groups, treatment to
be applied when and where?, standardization of working
procedures and schedules and responsibilities of researcher,
evaluation of outcome of the study.
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2. Selecting reference and experimental population
 Reference / target population: it is the population to which the
findings of the trials are expected to be applicable.
 Experimental or study population: it is derived from target
population. It is the actual population that the participants in the
experimental study. It should be randomly chosen from the
reference population
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3. Randomization :
• Randomization is a statistical procedure by which the
participants are allocated into groups usually called study
or control groups, to receive or not to receive an
therapeutic procedure or intervention.
• Randomization is an attempt to eliminate “bias”
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4. Manipulation / Intervention:
• Manipulation means doing something.
• Having formed the study and control groups, the next step is
to intervene / manipulate the study(experimental) group by
deliberate application or withdrawal of procedure.
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5. Follow-up :
• This implies examination of the experimental and control
group subjects at defined interval time, till the final
assessment of outcome.
• The duration of the trial is usually based on the expectation
that a significant different will be demonstrated at a given
point in time after the start of the study.
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6. Assessment Of Outcome:
• The final step is assessment of the outcome of the trial in
terms of ;
• Positive results
• Negative results
• Positive results – i.e benefits of the experimental measures.
• Negative results – i.e severity and frequency of side-effects
and complications, including death.
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2. Non- Randomized Controlled Trials:
• Although the experimental method is almost always to be preferred, it is
not always possible for ethical, administrative and other reasons to
randomized controlled trials in human beings.
• Example:
– Smoking and lung cancer
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• The cost and logistics are often prohibited
• These trials are rare
In such situations, we must depend upon non-
randomized trials designs.
Examples of NRCTs:
1. Uncontrolled trials
2. Natural experiments
3. Before and after comparison studies
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1.Uncontrolled Trials
• Uncontrolled trial is the trials with no comparison groups.
• Eg : screening of cervical cancer by PAP smear test is effective in
reducing mortality from this disease.
• Initially the uncontrolled trials useful in evaluating specific therapy
on particular diseases, appropriate dose, investigate adverse
reactions.
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2. Natural experiments
• Where experimental studies are not possible in
human population, the epidemiologist seeks to
identify “ natural circumstances” that mimic an
experiment.
• Eg: a major earth quake in Athens in 1981 provided a
natural experiment to epidemiologist to study the
effect of acute stress on cardiovascular mortality.
9/29/2017 124
3. Before and after comparison studies
• Before and after comparison studies without
controls.
• Before and after comparison studies with controls.
9/29/2017 125
Before and after comparison studies
without controls.
• These studies centered round comparing the
incidence of disease before and after introduction of
preventive measures.
• The events which took place prior to the use of new
treatment or preventive procedure are used as a
standard for comparison.
9/29/2017 126
Before and after comparison studies with
controls.
• In the absence of control group, between before and after the use
of new treatment or procedure may be misleading. In such
situations the epidemiologist tries to utilize a natural control group
i.e one provided by the nature or natural circumstances.
• If preventive programme is to be applied to an entire community
we would select another community as similar as possible.
9/29/2017 127
Reference :
• K Park (2015) Park's textbook of preventive and social
medicine , Twenty-third edition, Bhanot Publishers, India.
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Epidemiology

  • 2. DEFINITION "The study of the distribution and determinants of health related states or events in specified population and application of this study to control of diseases and other health problems“ (J.M. Last 1988)
  • 3. USES OF EPIDEMIOLOGY • Study of the History of disease. • Planning • Community diagnosis • Assessment of individuals risk. • Identification of syndrome • Completion of the clinical picture of chronic disease • Searching for causes • Evaluation.
  • 4. 9/29/2017 4 Scope of epidemiology Epidemiology covers the various types of field in different types of activities. It is applied in every field as agricultural, economics, statistics etc. They are as • Clinical epidemiology • Sub-clinical epidemiology • Infectious disease epidemiology • Geographical epidemiology • Social epidemiology • Chronic disease epidemiology • Serological epidemiology • Cancer epidemiology
  • 5. • Malaria epidemiology • Neuro epidemiology • Genetic epidemiology • Occupational epidemiology • Psychosocial epidemiology • Computational epidemiology • Field epidemiology • Participative epidemiology 9/29/2017 5
  • 6. • Molecular epidemiology • Environmental epidemiology • Micro- epidemiology • Macro-epidemiology • Nutritional epidemiology • Statistical epidemiology • Descriptive epidemiology • Analytical epidemiology • Experimental epidemiology • Infectious diseases epidemiology 9/29/2017 6
  • 9. Components of epidemiology Disease frequency: • The core characteristics of epidemiology are to measure the frequency of diseases, disability or death in a specified population. it is always as the rate, ratio and proportion. • This helps to development of strategies for prevention or control of health related problems.
  • 10. Distribution of diseases: • Health events occur in pattern in community and this pattern varies from community to community. • Also health events or diseases condition affect population at various age groups, different sexes, different subgroups of population. • Distributions of events are based on time, place, and person. We can analyze whether any increases or decreases occur for a particular condition. Epidemiology addresses itself to a study of these variations or patterns, which may suggest or lead to measure to control or prevent the diseases. An important outcome of this study is formulation of etiological hypothesis.
  • 11. Determinants of diseases • Epidemiology helps in identifying the causative agent or the risk/predisposing factors of diseases . • This is one of the real uses of epidemiology. Understanding the factors leading to any programs for the control of those diseases.
  • 12. Dynamics of disease transmission
  • 14. Source: The source of infection defined as the person, animal, object or substance from which an infectious agent passes or is disseminated to the host.
  • 15. Reservoir: A reservoir is defined as any person, animal, arthropod, plant, soil or combination of these, in which an infectious agent lives and multiplies , on which it depends primarily for survival, where it is reproduce itself in such manner that it can be transmitted to a susceptible host. 9/29/2017 15
  • 16. Types of reservoir Reservoir Human reservoir Cases Carriers Animal reservoir Reservoir of non-living things 9/29/2017 16
  • 18. CARRIERS By type Incubator y Convales cent Healthy By duration temporar y Chronic By portal of exist urinary Intestinal Respirato ry Skin blood 9/29/2017 18
  • 19. MODE OF TRANSMISSION MODE OF TRANSMISSION DIRECT TRANSMISSION INDIRECT TRANSMISSION 9/29/2017 19
  • 21. INDIRECT TRANSMISSION VEHICLE BORNE VECTOR BORNE AIR BORNE FOMITE BORNE UNCLEAN HANDS AND FINGERS 9/29/2017 21
  • 22. I.SUCCESSFUL PARASITISM • The infectious agent must find a portal of entry by which it may enter the host • Ongoing entry into the host, the organism must reach the appropriate tissue or site of election in the body of host where it may find optimum conditions for its multiplication and survival. • The disease agent must find the portal of exist. 9/29/2017 22
  • 23. • After leaving the human body the organism must survive in the external environment for sufficient period till a new host is found. 9/29/2017 23
  • 24. II. INCUBATION PERIOD: • It is defined as the time interval between invasion by an infectious agent and appearance of the first signs and symptoms of the disease in question. 9/29/2017 24
  • 26. AGENT FACTORS: • The disease agent is defined as a substance, living and non-living, tangible or intangible, the excessive presence or relative lack, which may initiate a disease process. 9/29/2017 26
  • 27. Classification of disease agents: 1. Biological agent 2. Nutrient agent 3. Physical agent 4. Chemical agent 5. Mechanical agent 6. Absence or insufficiency or excess of factors necessary to health 7. Social agent 9/29/2017 27
  • 28. HOST FACTORS:(INTRINSIC HOST) In epidemiological terminology, the human host is referred to as soil and disease agent is seed. The host factors may be classified as: 1. Demographic characteristics – ( age and gender) 2. Biological characteristics – (genetic factors, biochemical level of blood, blood groups) 9/29/2017 28
  • 29. • Social and economic characteristics – (socio-economic status, education, occupation, marital status, housing) • Life style factors – personality traits, physical exercise, use of alcohol/drugs and smoking etc….. 9/29/2017 29
  • 30. ENVIRONMENTAL FACTORS (EXTRNSIC) • The environment has been divided into 3 components: – Physical – Biological – psychosocial 9/29/2017 30
  • 31. MEASUREMENTS OF MORBIDITY AND MORTALITY • MORTALITY MEASUREMENTS: (the commonly used measures are;) 1. Crude death rate 2. Specific death rate A. Specific death rate due to TB B. Specific death rate for males C. Specific death rate in age group D. Death rate for month E. Weekly death rate 3. Case fatality rate 4. Proportional mortality rate 5. Survival rate 9/29/2017 31
  • 32. 1. Crude death rate:(CDR) No.of death during the year CDR=--------------------------------------------X 1000 Mid- year population 9/29/2017 32
  • 33. 2. Specific death rate: • 1. Specific Death Rate Due To TB: No.of deaths from TB during a calendar year SDR(TB)=------------------------------------------X 1000 Mid-year population 9/29/2017 33
  • 34. 2. Specific Death Rate For Males: No.of deaths among males during a calendar year SDR(M)=-------------------------------------------------X1000 Mid-year population of males 9/29/2017 34
  • 35. • 3. Specific Death Rate In The Age Group Of 15-20 Years: No.of deaths of persons aged 15-20 years during a calendar year SDR=----------------------------------------------------X1000 Mid-year population of persons aged 15-20 years 9/29/2017 35
  • 36. 4. Death rate for January: No.of deaths in January X 12 SDR=-----------------------------------------------X1000 Mid-year population The death rate are multiplied by 12 in order to make the monthly death rate comparable with the annual death rate. 9/29/2017 36
  • 37. 5. Weekly Death rate : No.of deaths in a week X 52 SDR=--------------------------------------------X1000 Mid-year population 9/29/2017 37
  • 38. 3. Case fatality rate: No.of deaths due to particular disease CFR=---------------------------------------------------------X1000 Total no.of cases due to same disease CFR represents the killing power of disease. It is typically used in acute infectious diseases. 9/29/2017 38
  • 39. 4.Proportional mortality rate: • It is sometime useful to know what proportion of total deaths are due to particular cause or what proportion of deaths are occurring in a particular age group. • PMR expresses no.of death due to particular cause or in specific age group per 100 or 1000 total deaths. 9/29/2017 39
  • 40. A) PMR For Specific Disease: No.of deaths from the specific disease in a year PMR=-----------------------------------------------------X1000 Total deaths from all causes in that year 9/29/2017 40
  • 41. B) UNDER FIVE PMR: No.of deaths under five years of age in a given year Under Five PMR=--------------------------------------------x1000 Total no.of deaths during the same year 9/29/2017 41
  • 42. C) PMR FOR AGE 50 YEARS AND ABOVE: No.of deaths of persons aged 50 years and above in a given year =--------------------------------------------------x1000 Total no.of deaths of all age group during the same year 9/29/2017 42
  • 43. 5. SURVIVAL RATE: It is the proportion of survivors in a age group (patients) studied and follow over a period. Total no.of patients alive after 5 years SR=--------------------------------------------------------------X1000 Total no.of patients diagnosed and treated 9/29/2017 43
  • 44. MEASUREMENTS OF MORBIDITY: • Morbidity has been defined as any departure, subjective or objective, from a state of physiological well being. • Morbidity commonly measured by 3 aspects: » Frequency » Duration » Severity 9/29/2017 44
  • 45. 1. Disease frequency: • Disease frequency is measured by incidence and prevalence rates. 9/29/2017 45
  • 46. INCIDENCE RATE: • It is defined as the no.of new cases occuring in a defined population during a specified period of time. No.of new case of specific disease during a given time period IR=------------------------------------------------------X1000 Population risk during that period 9/29/2017 46
  • 47. IR REFERS TO: • Only to new cases • During a given period ( usually a year) • In a specified population or population at risk • It can also refers to spells or episodes of disease arising in a given period of time per 1000 population. 9/29/2017 47
  • 48. PREVALENCE RATE: • The term disease prevalence refers specifically to all current cases (old and new) existing at given point in time or over a period of time in a given population. • Prevalence is of 2 types: » Point prevalence » Period prevalence 9/29/2017 48
  • 49. Point prevalence: • It is defined as no.of of all current cases (old and new) of a disease at 1 point of time, in relation to a defined population. • The point- a day, several days, week; depending upon the time it takes to examine the population sample. 9/29/2017 49
  • 50. No.of all current cases (old and new) of a specified disease existing at a given point in time PP=-------------------------------------------------------------X100 Estimated population at the same point in time 9/29/2017 50
  • 51. Period prevalence: • It measures the frequency of all current cases (old and new) existing during a defined period of time. No.of all existing cases (old and new) of a specified disease during a given period of time interval PP=--------------------------------------------------------------------X100 Estimated mid-interval population at risk 9/29/2017 51
  • 52. 2.DURATION • The average duration per case or the disability rate, which is the average no.of days of disability per person, may serve as a measure of the duration of illness. 9/29/2017 52
  • 53. 3.SEVERITY: • The case fatality rate may be used as the index of severity. 9/29/2017 53
  • 55. Levels of prevention • Introduction: – The successful prevention depends on knowledge of causation, dynamics of transmission, identification of risk factors and risk groups, early diagnosis and frequent measures an organization for applying these measures to appropriate persons or groups and continuous evaluation of and development of procedures applied. 9/29/2017 55
  • 56. There are 4 levels of prevention: Tertiary prevention Secondary prevention Primary prevention Primordial prevention 9/29/2017 56
  • 57. i. Primordial prevention: • This is primary prevention in its purest sense. • It is prevention of the emergence of or development of risk factors in population group in which they have not yet appeared • A new concept, is receiving a special attention in prevention of chronic diseases. 9/29/2017 57
  • 58. Example: • Many adult health problem (obesity, HT) have their origin in childhood practices like smoking, eating pattern, physical exercise. • In primordial prevention, efforts are directed towards discouraging children from adopting harmful lifestyles. 9/29/2017 58
  • 59. Interventions: • Individual and mass health education 9/29/2017 59 HARMFUL LIFESTYLE PRACTICES OF CHILDHOOD CONTROL PREVENT FUTURE HEALTH PROBLEMS
  • 60. ii. Primary prevention: • Primary prevention can be defined as action taken prior to the onset of disease which removes the possibility of disease will ever occur. • It signifies intervention in the pre-pathogenesis phase of a disease or health problems. 9/29/2017 60
  • 61. Approaches for primary prevention of chronic diseases: (WHO recommendations) • 1. Population (mass) strategy • 2.High risk strategy 1. Population (Mass) Strategy – Which is directed at the whole population irrespective of individual risk levels. 2.High Risk Strategy – It aims to bring preventive care to individuals at specific risk. 9/29/2017 61
  • 62. Public health measures and activities of primary prevention: • Sanitation • Infection control • Immunization • Protection of food, milk and water supply • Environmental protection • Protection against occupational hazards and accidents. 9/29/2017 62
  • 63. iii. Secondary prevention: • It can be defined as action which halts the progress of a disease at its incipient stage and prevent complications. 9/29/2017 63
  • 64. Interventions: • Early diagnosis • Adequate treatment 9/29/2017 64
  • 65. iv. Tertiary prevention: • It can be defined as all measures available to reduce or limit impairments and disabilities, minimize suffering caused by existing departures from good health and to promote the patient’s adjustment to irremediable conditions. • when the disease process has advanced beyond it’s early stage , it is still possible to accomplish prevention by what might be called tertiary prevention. 9/29/2017 65
  • 66. Interventions: • 1. Disability limitation • 2. Rehabilitation » Includes medical, psychosocial, vocational rehabilitations. 9/29/2017 66
  • 67. Levels of prevention Primordial prevention Primary prevention Secondary prevention Tertiary prevention Modes of intervention 1. Health education (individual & mass) 1.Health promotion 2.Specific protection 1.Early diagnosis 2.Appropriate treatment 1.Diability limitation 2.rehabilitation 9/29/2017 67
  • 69. METHODS OF EPIDEMIOLOGY • INTRODUCTION: – The primary concern of the epidemiologist is to study disease occurrence in people. Epidemiological studies can be classified into • 1. OBSERVATIONAL STUDIES • 2. EXPERIMENTAL STUDIES (INTERVENTIONAL STUDIES) 9/29/2017 69
  • 70. • Observational Study – Descriptive studies – Analytical Studies • Ecological Study: - Correlation Study unit is a population. • Cross-Sectional Study: - prevalent Study Individual is a unit of study. • Case-Control Study: - case-reference with individual is a unit of study. • Cohort study:-Follow up study with individual is a unit of study. 9/29/2017 70
  • 71. • Experimental Studies –Randomized Control Trials –Field Trials –Community Trials 9/29/2017 71
  • 72. OBSERVATIONAL STUDY: 1.DESCRIPTIVE STUDY • It is descriptive epidemiology/descriptive study. • It is the first phase of epidemiological investigation • The studies are concerned with observing the distribution of disease. • By: – Time distribution – when the disease is occurring? – Place distribution- where it is occurring? – Person distribution-who is getting the disease? 9/29/2017 72
  • 73. PROCEDURE IN DESCRIPTIVE STUDY • Define the population • Define the disease under study • Describing the disease by • TIME • PLACE • PERSON • Measurement of diseases • Comparing with known indices. • Formulation of an etiological hypothesis 9/29/2017 73
  • 74. 1.Define the population • The population can be the whole population in a geographic area. It can also be a specially selected group such as age, gender, school children, small communities. 9/29/2017 74
  • 75. 2.Define the disease under study: • Define the disease or condition being investigated. • A definition must be precise and valid to enable epidemiologist to identify those who have the disease from who don’t have. • Operational definition- used to define the disease. 9/29/2017 75
  • 76. 3. Describing the disease TIME PLACE PERSON year, Season Month Week Day Hours Duration Climatic zones Country Region Urban Rural Town Cities Institution Age Gender Marital status Birth Occupation Social status Education Family size Height Weight B.P Personal habits9/29/2017 76
  • 77. 1. Time distribution: 3 types of time trends/ fluctuations in disease occurrences. 1. Short term fluctuations – Epidemic diseases 2. Periodic fluctuations 1. Seasonal trend - URTI in summer, GI infections-summer 2. Cyclic trend- cycle spread over short period of time eg: measles in every 2 – 3 years 3. Long term and secular trend - changes in the occurrences of disease i.e a progressive increase or decrease over a long period of time ( years / decades) 9/29/2017 77
  • 78. 2. Place distribution ( Geographical comparison) • The variations may be classified as; – International variations – E.g : CVDs, Cancers. – National variations – E.g: nutritional deficiencies, epidemic goiter – Urban and rural variations – E.g: accidents, lung cancer, HT- urban area; zoonotic diseases – rural areas. – Local distribution- inner and outer city variations. “ spot maps”/” shaded maps” is used. 9/29/2017 78
  • 79. 3. Person distribution: • In descriptive study, the disease is further characterized by defining the person who developed the disease by age, gender, marital status, occupation, social status etc…. 9/29/2017 79
  • 80. 4. Measurement of disease: • Morbidity and mortality measurements gives clear picture of disease load. • Measurement of mortality is straight forward. • Morbidity has 2 aspects: 1. Incidence – obtained from longitudinal studies 2. Prevalence – obtained from cross sectional studies 9/29/2017 80
  • 81. Cross sectional studies: • It is a single examination of cross-section of population at one point in time • The results of which can be projected the whole population 9/29/2017 81
  • 82. Longitudinal studies: • Observation of same population over a prolonged period of time by means of follow-up examination. 9/29/2017 82
  • 83. 5. Comparing with known indices: • By making comparison between different population and sub-group of the same population, it is possible to arrive at clues to disease etiology. 9/29/2017 83
  • 84. 6. Formulation of hypothesis • Hypothesis is a supposition, arrived at from observation. An epidemiological hypothesis should explain; • Specific cause • The expected outcome • The dose response • The time response • E.g: smoking causes lung cancer ( incomplete) • Smoking of 30-40 cigarette/day cause lung cancer in 10% of smoker after 20 years of exposure – (complete). 9/29/2017 84
  • 85. Uses of descriptive epidemiology: • Provide data regarding magnitude and type of disease in community. • Provide clues to disease etiology & helps in the formulation of etiological hypothesis • Provide background data for planning, organizing & evaluating preventive & curative services • The contribute to research by describing variations in disease occurrence by time, place, person. 9/29/2017 85
  • 86. II. ANALYTICAL EPIDEMIOLOGY • Analytical study are the second major type of epidemiological study. • The objective is not to formulate but to test the hypothesis. • The individual subject are evaluated in analytical study. • 2 types: – Case control studies – Cohort studies 9/29/2017 86
  • 87. 1. CASE CONTROL STUDIES: • It is often called retrospective studies. • Features of case control studies: – Both exposure and outcome have occurred before the start of study – The study proceeds backwards from effect to cause – it uses a control or comparison group to support or refute an inference 9/29/2017 87
  • 88. • By definition a case control study involves two population • cases and controls • In CCSs the unit is individual rather than the group. • The focus is on disease that has already developed 9/29/2017 88
  • 90. Basic steps in case control study: • There are 4 basic steps : – Selection of cases and controls – Matching – Measurement of exposure – Analysis and interpretation 9/29/2017 90
  • 91. i) Selection of cases and controls: • Selection of cases: – Cases are selected based on diagnostic criteria and eligibility criteria. • Sources of cases: – Hospital – General population 9/29/2017 91
  • 92. Selection of controls: • The controls may be free from disease under study. These may be as similar to the cases as possible, except for the absence of disease under study • As a rule, a comparison group is identified before a study is done. • Sources of controls: • Hospitals, relatives, neighbors and general population. 9/29/2017 92
  • 93. ii) matching: • The control may differ from cases in a no.of factor such as age, gender, occupation & social status. An important consideration is to ensure comparability between cases and controls. This is known as matching. 9/29/2017 93
  • 94. iii) Measurement of exposure: • Information about exposure should be obtained precisely the same manner both for cases and controls. • This may be obtained by interviews, questionnaires, studying of past record of cases such as hospital records and employment records. 9/29/2017 94
  • 95. iv) Analysis : • The final step is analysis to find out • Exposure rate among cases and controls to suspected factors • Estimation of disease risk associated with exposure 9/29/2017 95
  • 96. 2.COHORT STUDY • In epidemiology the term cohort is defined as a group of people who share a common characteristics or experience within a defined time period. – Example: age cohort, occupational cohort, marriage cohort, pregnancy cohort, birth cohort. 9/29/2017 96
  • 97. • Cohort study is known by variety of names: • Prospective longitudinal study • Incidence study • Forward looking study • The features of cohort studies: – Cohorts are identified prior to the appearance of disease under investigation. – The study group observed over a period of time to determine the frequency of disease among them. – The study proceeds forward from cause to effect. 9/29/2017 97
  • 99. Types of cohort studies: • Prospective cohort study • Retrospective cohort study • Combination of retrospective and prospective cohort study 9/29/2017 99
  • 100. Prospective or current cohort study: • It is one in which the outcome has not yet occurred at the time the investigation begins. 9/29/2017 100
  • 101. Retrospective cohort study: • Or historical is one in which the outcome have all occur before the start of the investigation. 9/29/2017 101
  • 102. Combination of retrospective and prospective cohort study • In this type of study both the prospective and retrospective elements are combined. The cohort is identified from past records and the same cohort is followed prospectively in future for further assessment outcome. 9/29/2017 102
  • 103. Steps of cohort study: • Selection of study subjects • Obtain data on exposure • Selection of comparison group • Follow-up • Analysis 9/29/2017 103
  • 104. 1. Selection of study subjects • General population • Special groups • Select groups • Exposure groups • Select groups – These may be professional groups ( doctors/nurses), insured persons, college alumni, government employee and volunteers etc… • Exposure groups – Cohort may be selected because of special exposure to physical, chemical or other disease agent. 9/29/2017 104
  • 105. 2. Obtaining data on exposure: • Information about exposure may be obtain directly from cohort members through personal interviews, mailed questionnaires, preview of records, medical examination or special tests, environmental surveys. 9/29/2017 105
  • 106. 3. Selection of comparison groups: • There are many ways of assembling comparison groups: – Internal comparison – External comparison – Comparison with general population 9/29/2017 106
  • 107. • Internal comparison: In some cohort studies, no outside comparison group is required. The comparison groups are inbuilt within the individual study itself. • External comparison: When information on degree of exposure is not available, it is necessary to put-up an external control, to evaluate the experience of the exposed groups. • Comparison with general population: If none is available, the mortality experience of the exposed groups is compared with the mortality experience of the general population in the same geographic area as exposed peoples. 9/29/2017 107
  • 108. 4. follow-up: • One of the problem of cohort study is the regular follow- up of all the participants. • The procedure required comprises of: – Periodical medical examination of each cohort members – Reviewing physician and hospital record – Routine surveillance of death records – Mailed questionnaires, telephonic calls – Periodic home visit 9/29/2017 108
  • 109. 5. Analysis : • The data are analyzed in terms of –Incidence rates of outcome among exposed and non-exposed –Estimation of risk associated with disease. 9/29/2017 109
  • 110. Experimental Studies Or Experimental Epidemiology: • These are also called as interventional studies. • Experimental studies involves some actions, interventions or manipulation such as deliberate application or withdrawal of the suspected cause in the experimental group while making no change in the control group, and observing & comparing the outcome of the experiment in both the groups. 9/29/2017 110
  • 111. Aims : • To provide scientific proof of etiological factors • To provide a method of measuring the effectiveness and efficiency of health services for prevention, control and treatment of disease and improve the health of the community. 9/29/2017 111
  • 112. Types of experimental studies: 1. Randomized Controlled Trials 2. Non-randomized Controlled Trials 9/29/2017 112
  • 113. Randomized controlled trials (RCT) • Those involving the process of random allocation • Randomization means- giving equal chance to all samples 9/29/2017 113
  • 114. The basic steps in conducting RCT: 1. Drawing up of protocol 2. Selecting reference and experimental population 3. Randomization 4. Manipulation or intervention 5. Follow-up 6. Assessment of outcome 9/29/2017 114
  • 115. 1. Drawing up of protocol • One of the essential features of RCT is the study is conducted under strict protocol. • The protocol specifies the aims and objectives of the study, questions to be answered, criteria for the selection of study groups and control groups, size of the sample, the procedure for allocation of subjects into study and control groups, treatment to be applied when and where?, standardization of working procedures and schedules and responsibilities of researcher, evaluation of outcome of the study. 9/29/2017 115
  • 116. 2. Selecting reference and experimental population  Reference / target population: it is the population to which the findings of the trials are expected to be applicable.  Experimental or study population: it is derived from target population. It is the actual population that the participants in the experimental study. It should be randomly chosen from the reference population 9/29/2017 116
  • 117. 3. Randomization : • Randomization is a statistical procedure by which the participants are allocated into groups usually called study or control groups, to receive or not to receive an therapeutic procedure or intervention. • Randomization is an attempt to eliminate “bias” 9/29/2017 117
  • 118. 4. Manipulation / Intervention: • Manipulation means doing something. • Having formed the study and control groups, the next step is to intervene / manipulate the study(experimental) group by deliberate application or withdrawal of procedure. 9/29/2017 118
  • 119. 5. Follow-up : • This implies examination of the experimental and control group subjects at defined interval time, till the final assessment of outcome. • The duration of the trial is usually based on the expectation that a significant different will be demonstrated at a given point in time after the start of the study. 9/29/2017 119
  • 120. 6. Assessment Of Outcome: • The final step is assessment of the outcome of the trial in terms of ; • Positive results • Negative results • Positive results – i.e benefits of the experimental measures. • Negative results – i.e severity and frequency of side-effects and complications, including death. 9/29/2017 120
  • 121. 2. Non- Randomized Controlled Trials: • Although the experimental method is almost always to be preferred, it is not always possible for ethical, administrative and other reasons to randomized controlled trials in human beings. • Example: – Smoking and lung cancer 9/29/2017 121
  • 122. • The cost and logistics are often prohibited • These trials are rare In such situations, we must depend upon non- randomized trials designs. Examples of NRCTs: 1. Uncontrolled trials 2. Natural experiments 3. Before and after comparison studies 9/29/2017 122
  • 123. 1.Uncontrolled Trials • Uncontrolled trial is the trials with no comparison groups. • Eg : screening of cervical cancer by PAP smear test is effective in reducing mortality from this disease. • Initially the uncontrolled trials useful in evaluating specific therapy on particular diseases, appropriate dose, investigate adverse reactions. 9/29/2017 123
  • 124. 2. Natural experiments • Where experimental studies are not possible in human population, the epidemiologist seeks to identify “ natural circumstances” that mimic an experiment. • Eg: a major earth quake in Athens in 1981 provided a natural experiment to epidemiologist to study the effect of acute stress on cardiovascular mortality. 9/29/2017 124
  • 125. 3. Before and after comparison studies • Before and after comparison studies without controls. • Before and after comparison studies with controls. 9/29/2017 125
  • 126. Before and after comparison studies without controls. • These studies centered round comparing the incidence of disease before and after introduction of preventive measures. • The events which took place prior to the use of new treatment or preventive procedure are used as a standard for comparison. 9/29/2017 126
  • 127. Before and after comparison studies with controls. • In the absence of control group, between before and after the use of new treatment or procedure may be misleading. In such situations the epidemiologist tries to utilize a natural control group i.e one provided by the nature or natural circumstances. • If preventive programme is to be applied to an entire community we would select another community as similar as possible. 9/29/2017 127
  • 128. Reference : • K Park (2015) Park's textbook of preventive and social medicine , Twenty-third edition, Bhanot Publishers, India.