Core Epidemiology Concepts: Definitions, History, and Measures

Lectures 1–2 – Intro to Epidemiology

Key Definitions:

Epidemiology: study of frequency, distribution, determinants of health/disease in populations + application to control.
Frequency: how often events occur (counts, proportions, rates).
Distribution: patterns by person/place/time.
Determinants: factors influencing occurrence (host/agent/environment).

Historical Figures (name + contribution):

  • Edward Jenner: cowpox → smallpox vaccine (1st vaccination).

  • James Lind: scurvy + citrus trial.

  • Percival Pott: chimney sweeps + scrotal cancer (carcinogens).

  • John Snow: cholera + Broad Street pump (natural experiment).

  • Ignaz Semmelweis: handwashing → puerperal fever reduction.

Epi helps: identify patterns, test hypotheses, evaluate interventions, guide prevention/control.


Lecture 3-4: Health, Disease, Prevention

  • Health: complete physical/mental/social well-being (not just no disease).

  • Disease: deviation from normal structure/function w/ specific signs/symptoms.

  • Infected: pathogen present. Asymptomatic: infected, no clinical signs.

  • Epidemiologic Triad:

  • Host: gets disease (age, immunity, genetics).

  • Agent: causes disease (infectious/non-infectious).

  • Environment: enables transmission (climate, crowding).

Natural History Timeline:
Exposure → Latent period (infection→infectious) → Incubation (infection→symptoms) → Infectious period → Recovery/disability/death.

Prevention Levels:

  • Primary: prevent occurrence (vaccination, sanitation).

  • Secondary: early detection (screening)
    .

  • Tertiary: reduce complications (rehab).

5 Ws (Descriptive Epi): What/Who/Where/When/Why-How.

Temporal Patterns:

  • Sporadic: occasional/irregular.

  • Endemic: constant expected level (ex: 14% osteoarthritis).

  • Epidemic: > expected. Pandemic: worldwide.

Transmission:

  • Direct: immediate (bite, contact).

  • Indirect: airborne/vehicle/vector.

  • Common vehicle: single contaminated source (salad mix).
    Herd immunity: susceptibles protected when enough immune (random mixing assumption).


Lecture 5 – One Health

Interconnected health of humans/animals/environment requiring collaborative, transdisciplinary approach.

Principles:

  • Systems thinking: interconnected components w/ feedback loops.

  • Transdisciplinarity: integrate disciplines + stakeholder knowledge.

Benefits: Early zoonosis detection, better resources, complex problem solutions (AMR).
Challenges: Coordination, funding, data sharing, power imbalances.

Lectures 6–8 – Disease Frequency

Why measure? Describe burden, compare groups/time, evaluate interventions.
Proportion = cases/population (0-1 or %). Rate = events/person-time (has time unit).

Prevalence = Existing cases / Population

  • Point: at single time. Period: during interval.

  • Tells: probability of HAVING disease (healthcare burden).

  • Ignores: when disease occurred (not risk of getting).

Incidence Risk = New cases / (Initial NAR – 0.5 × Withdrawals)

  • Probability of DEVELOPING disease in time t.

  • NAR = disease-free + susceptible at t=0.

  • Ex: “67% incidence risk” = 67% initially healthy develop it.

  • Incidence Rate = New cases / Total person-time at risk


Exact denominator: sum individual time-at-risk.
Approximate: [0.5 × (initial NAR + final NAR)] × ITC
ITC = observation period length.

Interpretation: “X cases per Y person-months” = expect X cases if follow Y people 1 month.

Quick Comparison Table

Measure

What

Numerator

Denominator

Time?

Prevalence

Existing

All cases

Population

No

Inc Risk

New prob

New cases

At-risk pop

Implicit

Inc Rate

New speed

New cases

Person-time

Yes

Relationship (steady state): Prevalence ≈ Incidence × Duration

Other Measures (all incidence unless noted)

Attack Rate = New cases among exposed / Total exposed

Case Fatality = Deaths from X / Cases of X

Morbidity Risk = New illness cases / At-risk pop

Mortality Risk = New deaths / At-risk pop

  • Crude: all causes. Cause-specific: one cause.

CFR/attack rate: NOT true rates (no time denominator).


Screening: healthy → detect unrecognized disease. Diagnostic: sick → confirm/treat.

2×2 Table

        Disease+  Disease-  Total

Test+       a(TP)    b(FP)    a+b

Test-       c(FN)    d(TN)    c+d

Total     a+c      b+d       n

Formulas (know calc + interpret):

True Prev  = (a+c)/n

App Prev   = (a+b)/n

Sensitivity = a/(a+c)     [Of diseased, % test+]

Specificity = d/(b+d)     [Of non-diseased, % test-]

PPV = a/(a+b)             [Of test+, % truly diseased]

NPV = d/(c+d)             [Of test-, % truly disease-free]

False Results:
1-Sn = False Neg fraction. 1-Sp = False Pos fraction.

Choose test by context:

  • Minimize FN → High Sn (ex: contagious MRSA).

  • Minimize FP → High Sp (ex: cull entire flock).

Predictive values depend on: Prevalence ↑ → PPV ↑, NPV ↓.

Series vs Parallel

Series: Both+ to call positive → ↑Sp (↓FP), ↓Sn (↑FN)  [Rule-IN]

Parallel: Any+ to call positive → ↑Sn (↓FN), ↓Sp (↑FP) [Rule-OUT]

Validity/Precision:

  • Validity = distinguishes D vs D- (Sn/Sp).

  • Precision = repeatability (SD for continuous, Kappa for categorical).

Kappa (agreement beyond chance):
0-0.2 slight, 0.4-0.6 moderate, 0.6-0.8 substantial, 0.8-1 perfect.