EPIDEMIOLOGI DESKRIPTIF
Study of the occurrence and distribution of disease

Correlational Studies (Ecological Studies)

Uses measures that represent characteristics of entire populations

It describes outcomes in relation to age, time, utilization of services, or exposures

advantages

• We can generate hypotheses for case-control studies and environmental studies

• We can target high-risk populations, time-periods, or geographic regions for future studies

limitation

• Because data are for groups, we cannot link disease and exposure in individual

• We cannot control for potential confounders

• Data represent average exposures rather than individual exposures, so we cannot determine a dose-response relationship

• Caution must be taken to avoid drawing inappropriate conclusions, or ecological fallacy

pattern

disease (population) burden [ Y axis ]
vs. prevalence of “risk factor” [ X axis ]

Case Reports (case series)

Report of a single individual or a group of individuals with the same diagnosis

advantages

We can aggregate cases from disparate sources to generate
hypotheses and describe new syndromes

limitations

We cannot test for statistical association because there is no relevant comparison group

Based on individual exposure {may simply be coincidental}

Important interface between clinical medicine & epidemiology

Most common type of studies published in medical journals

Cross-Sectional Studies (prevalence studies)

Measures disease and exposure simultaneously in a well- defined population

advantages

• They cut across the general population, not simply those seeking medical care

• Good for identifying prevalence of common outcomes, such as arthritis, blood pressure or allergies

limitations

• Cannot determine whether exposure preceded disease

• It considers prevalent rather than incident cases, results will be influenced by survival factors

• Remember: P = I x D

Can be used as a type of analytic study for testing hypothesis, when;

Current values of exposure variables are unalterable over time

Represents value present at initiation of disease E.g. eye colour or blood group

If risk factor is subject to alterations by disease, only hypothesis formulation can be done

descriptive epidemiology

place

person

time

periodic

seasonal

secular

epidemic

The long-time trend of disease occurrence

Temporal interruption of the general trend of secular variation

A cyclic variation in disease frequency by time of year & season

seasonal fluctuation

Environmental factors

Occupational activities

Recreational activities

An increase in incidence above the expected in a defined geographic area within a defined time period

geographic area

example

action level

Age

Sex

Occupation

hobbies

pets

medication

socioeconomic factors

hypothesis formulation

4 methods {derived from 5 canons of
inductive reasoning by John Stuart Mill}

Method of difference

Method of agreement

Method of concomitant variation

Method of analogy

methods for measuring

Rate

measure

Morbidity: Refers to the presence of disease in a population

Mortality: Refers to the occurrence of death in a population

Compute Disease Rate

Number of persons at risk = 5,595,211

Number of persons with disease = 17,382

Rate = 17,382 persons with heart disease

5,595,211 persons

= .003107 heart disease / resident / year

Prevalence

Rates are usually expressed as integers and decimals for populations at risk during specified periods to make comparisons easier.

310.7 heart disease / 100,000 residents / year

is the number of existing cases of disease in the population during a defined period.

incidence

is the number of new cases of disease that develop in the population during a defined period.

Incidence rate is a measure of the probability of the event among persons at risk.

IR = # new cases during time period X K /
specified population at risk

mortalitiy rate

Mortality rates are used to estimate disease frequency when incidence data are not available, case-fatality rates are high, goal is to reduce mortality among screened or targeted populations

Crude mortality: death rate in an entire population
Rates can also be calculated for sub-groups within the population

Cause-specific mortality: rate at which deaths occur for a specific cause

Case-fatality: Rate at which deaths occur from a disease among those with the disease

Maternal mortality: Ratio of death from childbearing for a given time period per number of live births during same time period

Infant mortality: Rate of death for children less than 1 year per number of live births

Neonatal mortality: Rate of death for children less than 28 days of age per number of live births

PR = # existing cases during time period / population at same point in time

basic measure of association

relative risk

odds ratio

• Ratio of the incidence rates between two groups • Can only be calculated from prospective studies (cohort studies)

• Interpretation

• RR > 1: Increased risk of outcome among “exposed” group

• RR < 1: Decreased risk, or protective effects, among “exposed” group

• RR = 1: No association between exposure and outcome

RR = incidence rate among exposed /
incidence rate among non-exposed

Odds: ratio of the probability of an event occurring to the probability of an event not occurring

Odds = P/(1-P)

Probability: Chance or risk of an event occurring (a proportion)

Probability= no. of times an event occurs/
no. of times an event can occur

odds ratio = ad / bc

interpretations

OR > 1: Increased odds of exposure among those with outcome

OR < 1: Decreased odds, or protective effects, among those with outcome

OR = 1: No association between exposure and outcome