NLE Community Health Nursing — Epidemiology & BiostatisticsCheat Sheet
Cheat sheet for NLE Community Health Nursing — Epidemiology & Biostatistics. Compact, printable, and organised around the concepts Professional Regulation Commission (PRC) — Board of Nursing tests most frequently in the NLE 2026. Perfect for the week before exam day.
Exam context
For the Philippine Nurse Licensure Examination (PNLE), Professional Regulation Commission (PRC) — Board of Nursing tests Community Health Nursing under a "Core" label, with Epidemiology & Biostatistics in the 2nd slot across 6 chapters. NLE candidates must clear the 75% weighted average with no sub-test below 60% cut on the 2026 paper, which draws about 50 Community Health Nursing questions. Date to watch: Bi-annual.
Epidemiology & Biostatistics - Cheat Sheet
Your final 30-minute rapid-fire reference for all formulas, definitions, and high-yield facts in Epidemiology & Biostatistics. Focus on the formulas section, must_remember items, and comparison_tables—these are your exam winners.
Sections
Section Title
Core Epidemiology Definitions
Important Facts
- Epidemiology describes health by THREE dimensions: Person (who), Place (where), Time (when).
- Vector = organism that carries agent (mosquito, snail, tick). Add to triangle as needed.
- Web of Causation (non-communicable diseases) = multiple interacting risk factors, NOT single cause (e.g., HTN: diet, stress, genetics, obesity).
- Endemic vs. Epidemic: endemic is EXPECTED baseline; epidemic is EXCESS of expected.
- Incidence counts NEW cases only; prevalence counts ALL cases (existing at a point in time).
- Prevalence is influenced by BOTH incidence AND duration of disease.
- Three Levels of Prevention: Primary (before disease occurs—health ed, immunization), Secondary (early detection—screening, case-finding), Tertiary (after disease—rehabilitation, disability limiting).
Key Definitions
Term
Epidemiology
Example
Tracking TB cases across Barangay X to identify transmission sources and implement DOH interventions.
Definition
Study of the distribution and determinants of health-related states/events in populations, applied to control of health problems.
Term
Epidemiologic Triangle
Example
Dengue: virus (agent) + mosquito vector + stagnant water (environment) + unimmunized person (host) = outbreak.
Definition
Three interacting elements causing disease: Agent (cause), Host (susceptibility), Environment (conditions). Breaking any point stops disease transmission.
Term
Chain of Infection
Example
COVID: virus (agent) → infected person (reservoir) → respiratory droplets (exit/transmission) → nasal mucosa (entry) → unvaccinated person (host).
Definition
Six sequential links: etiologic agent → reservoir → portal of exit → mode of transmission → portal of entry → susceptible host. Nursing breaks any link.
Term
Sporadic Disease
Example
A single case of plague in a province; not typical for that area.
Definition
Occasional, irregular occurrence of disease with no clear pattern.
Term
Endemic Disease
Example
Malaria endemic in Mindanao; dengue endemic in Metro Manila; filariasis in Visayas.
Definition
Constant, usual presence of a disease in a given geographic area or population.
Term
Epidemic / Outbreak
Example
Sudden spike in measles cases in a school when expected baseline is zero.
Definition
Occurrence of cases clearly in EXCESS of the expected number in a community or region.
Term
Pandemic
Example
COVID-19 pandemic (2020–present); 1918 Spanish flu pandemic.
Definition
Epidemic spreading across multiple countries or continents.
Term
Incidence Rate
Example
10 new TB cases per 100,000 population per year in a region.
Definition
Frequency of NEW cases of disease in a population at risk during a specific period. Measures RISK.
Term
Prevalence Rate
Example
50 total HTN cases (diagnosed + undiagnosed) per 1,000 adults at a single point in time.
Definition
Frequency of ALL EXISTING cases (new + old) at a point or period in a population. Measures BURDEN.
Term
Attack Rate
Example
In a food poisoning outbreak: 45 people ill out of 150 exposed = 30% attack rate.
Definition
Special incidence rate used in OUTBREAKS. Proportion of exposed population that becomes ill. Expressed as percentage (×100).
Term
Case Fatality Rate (CFR)
Example
COVID CFR in 2020: ~1–2% globally; measles CFR in unvaccinated: ~0.2%.
Definition
Proportion of diagnosed cases that result in DEATH. Measures disease SEVERITY/LETHALITY (expressed %).
Term
Vital Statistics
Example
Philippine Statistics Authority (PSA) compiles national vital statistics from civil registrars.
Definition
Data on vital events (births, deaths, marriages, fetal deaths) registered under civil registry law. Primary source: Birth and Death Certificates.
Term
Surveillance (Epidemiologic)
Example
PIDSR (Philippine Integrated Disease Surveillance and Response) monitors notifiable diseases; RHUs report weekly to municipal health offices.
Definition
Ongoing, systematic collection, analysis, interpretation, and dissemination of health data for PUBLIC HEALTH ACTION.
Term
PIDSR
Example
RHU nurse reports 5 measles cases to municipal health office within 24 hours; municipality reports to provincial ESU.
Definition
Philippine system for reporting notifiable diseases from health facilities upward to DOH Epidemiology Bureau. Nurses must report promptly (legal duty under RA 9173).
Diagrams To Know
- Epidemiologic Triangle (agent, host, environment; add vector as needed).
- Chain of Infection (6 links: agent → reservoir → exit → transmission → entry → host).
- Epidemic Curve (histogram: point-source = single sharp peak; propagated = successive waves).
- Natural History of Disease (prepathogenesis → subclinical pathogenesis → clinical disease → recovery/disability/death).
Formulas
Formula
Crude Birth Rate (CBR) = (Total live births in a year / Midyear population) × 1,000
Meaning
Total live births = registered births; Midyear population = (population Jan 1 + Dec 31) ÷ 2; Constant = 1,000 per person.
Watch Out
Student uses END-OF-YEAR population or uses constant 100,000 instead of 1,000. ALWAYS check the denominator in the question.
When To Use
Asked for birth rate of a region or country for a given year. Use midyear population as denominator.
Formula
Crude Death Rate (CDR) = (Total deaths in a year / Midyear population) × 1,000
Meaning
Total deaths = all deaths from all causes; Midyear population = average population; Constant = 1,000.
Watch Out
Confusing CDR with cause-specific death rate (which uses ×100,000). Read the question carefully.
When To Use
Asked for overall death rate. Use midyear population, same as CBR.
Formula
Infant Mortality Rate (IMR) = (Deaths under 1 year of age / Total live births) × 1,000
Meaning
Deaths under 1 year = neonatal + post-neonatal deaths; Total live births = denominator; Constant = 1,000 (NOT midyear population).
Watch Out
Using midyear population as denominator (WRONG). IMR, neonatal rate, and fetal rate all use LIVE BIRTHS as denominator, not population.
When To Use
Measuring child survival/health system quality. Denominator is LIVE BIRTHS, not population.
Formula
Neonatal Mortality Rate = (Deaths under 28 days / Total live births) × 1,000
Meaning
Deaths under 28 days (first 4 weeks of life); Total live births = denominator; Constant = 1,000.
Watch Out
Post-neonatal mortality (28 days to 1 year) is NOT included; IMR includes both neonatal and post-neonatal.
When To Use
Measuring newborn/maternal care quality. Early neonatal deaths are key quality indicator.
Formula
Maternal Mortality Rate/Ratio (MMR) = (Maternal deaths / Total live births) × 100,000
Meaning
Maternal deaths = deaths during pregnancy, childbirth, or 42 days postpartum; Total live births = denominator; Constant = 100,000 (may vary—read question).
Watch Out
Some questions use ×10,000 or ×1,000 instead of ×100,000. CHECK THE CONSTANT IN EVERY QUESTION. This is a high-frequency error.
When To Use
Measuring maternal health/obstetric care quality. A key MDG/SDG indicator.
Formula
Fetal Death Rate = (Fetal deaths / [Total live births + Fetal deaths]) × 1,000
Meaning
Fetal deaths = stillbirths (>20 weeks or ≥350g); Denominator includes BOTH live births AND fetal deaths; Constant = 1,000.
Watch Out
Denominator is NOT midyear population; it is (live births + fetal deaths). Easy to miss the addition of fetal deaths to denominator.
When To Use
Measuring intrauterine loss. Denominator is different from IMR (includes fetal deaths in denominator).
Formula
Cause-of-Death (Specific Death) Rate = (Deaths from specific cause / Midyear population) × 100,000
Meaning
Deaths from specific cause = e.g., TB deaths, cancer deaths, pneumonia deaths; Midyear population = population at risk; Constant = 100,000.
Watch Out
Using 1,000 instead of 100,000 (WRONG). This rate uses 100,000, not 1,000. The large constant reflects that cause-specific rates are typically smaller.
When To Use
Measuring the burden of a specific disease as a cause of death in a population.
Formula
Proportionate Mortality Rate = (Deaths from specific cause / Total deaths) × 100
Meaning
Deaths from specific cause = e.g., TB deaths; Total deaths = all-cause deaths in the period; Constant = 100 (expressed as percentage).
Watch Out
This is a PROPORTION, not a true rate (no time-at-risk denominator). Denominator is total deaths, not population. Do NOT confuse with cause-specific death rate.
When To Use
Showing what proportion of all deaths are due to a specific cause. Does NOT include population; compares within deaths only.
Section Title
Vital Statistics Formulas (EXAM CRITICAL)
Important Facts
- CRITICAL DENOMINATOR RULE: CBR and CDR use MIDYEAR POPULATION. IMR, neonatal, fetal, and maternal rates use LIVE BIRTHS (or live births + fetal deaths).
- CONSTANT MULTIPLIERS: CBR, CDR, IMR, neonatal, fetal, attack rate = ×1,000. Maternal mortality = ×100,000. Cause-specific death = ×100,000. Proportionate mortality = ×100 (%).
- Incidence Rate = (new cases / population at risk) × constant. Prevalence Rate = (all existing cases / total population) × constant.
- Attack Rate = (number ill / number exposed) × 100. Used in OUTBREAKS. Often expressed as a percentage.
Diagrams To Know
- Formula hierarchy: Crude rates (use midyear population) vs. infant/maternal/fetal rates (use live births) vs. cause-specific rates (use population × 100,000).
Formulas
Formula
Incidence Rate = (NEW cases of disease during a period / Population at risk) × constant
Meaning
NEW cases = cases appearing for the first time in the specified period; Population at risk = those who can contract the disease; Constant = 1,000, 10,000, or 100,000 depending on frequency.
Watch Out
Including old/prevalent cases in the numerator (WRONG—incidence counts NEW cases only). Confusing with prevalence. Check that denominator is population at risk (not just patients already diagnosed).
When To Use
Measuring the RISK or probability of developing disease over time. Compare two populations or time periods for disease risk.
Formula
Prevalence Rate = (ALL EXISTING cases at a point or period in time / Total population) × constant
Meaning
ALL existing cases = new + old; Point/period = snapshot at one time (point prevalence) or during a period (period prevalence); Constant = typically 1,000 or 100,000.
Watch Out
Including only new cases (WRONG—prevalence includes all cases). Confusing with incidence. If disease is chronic (long duration), prevalence is much higher than incidence.
When To Use
Measuring the BURDEN or overall load of disease in a population. Planning services (how many patients to treat?). Affected by BOTH incidence and duration of disease.
Formula
Attack Rate = (Number of cases [among exposed] / Number of people exposed) × 100
Meaning
Number of cases = people who became ill (in outbreak); Number exposed = people at risk in the outbreak; Constant = 100 (expressed as percentage).
Watch Out
Using as a true rate (with time denominators); it is a PROPORTION. Only used in outbreak contexts. Do NOT confuse with incidence rate (which has a time-period denominator).
When To Use
OUTBREAK investigation ONLY. Describes what proportion of exposed people became ill. Always expressed as a percentage.
Formula
Case Fatality Rate (CFR) = (Deaths from a specific disease / Number of cases of that disease) × 100
Meaning
Deaths from specific disease = persons who died; Number of cases = all diagnosed cases; Constant = 100 (expressed as percentage). Describes LETHALITY.
Watch Out
Using population as denominator (WRONG—denominator is cases, not population). Confusing with cause-specific death rate (which uses population as denominator). CFR measures case severity; cause-specific rate measures disease burden in population.
When To Use
Measuring disease SEVERITY. High CFR = severe disease (e.g., rabies ~100%, measles ~0.2% unvaccinated). Indicates case management quality.
Section Title
Morbidity & Disease-Frequency Formulas
Important Facts
- INCIDENCE vs. PREVALENCE (EXAM CLASSIC): Incidence = NEW cases (risk over time). Prevalence = ALL cases (burden at one point). Incidence answers 'risk of developing'; prevalence answers 'how many already have it?'
- Prevalence is affected by THREE factors: incidence (new cases), duration of disease, and recovery/death rate. A chronic disease with low incidence but long duration can have high prevalence.
- ATTACK RATE is a special incidence rate used ONLY in outbreak investigations. Always expressed as percentage (×100). Describes proportion of exposed people who became ill.
- CASE FATALITY RATE measures case-level SEVERITY (% of diagnosed cases that die). High CFR ≠ high mortality in population (depends on incidence too).
- CAUSE-SPECIFIC DEATH RATE uses population as denominator (×100,000); CFR uses cases as denominator (×100). Know the difference.
Diagrams To Know
- Incidence vs. Prevalence diagram: Show how prevalence is influenced by incidence, duration, and recovery rate.
Formulas
Formula
Sensitivity = (True Positives / [True Positives + False Negatives]) × 100
Meaning
True Positives (TP) = test positive AND disease present; False Negatives (FN) = test negative BUT disease present; Sensitivity = ability to DETECT disease (rule OUT when negative).
Watch Out
High sensitivity = few false negatives (few missed cases). BUT high sensitivity may include false positives (false alarms). Do NOT confuse with specificity.
When To Use
Choosing a screening test when you want to IDENTIFY ALL DISEASED people (minimize missed cases). For serious diseases (e.g., cancer, TB), use high-sensitivity test.
Formula
Specificity = (True Negatives / [True Negatives + False Positives]) × 100
Meaning
True Negatives (TN) = test negative AND no disease; False Positives (FP) = test positive BUT no disease; Specificity = ability to EXCLUDE disease (rule IN when positive).
Watch Out
High specificity = few false positives (few false alarms). BUT may miss some true cases. Do NOT confuse with sensitivity. Sensitivity & specificity are inversely related (usually).
When To Use
Choosing a diagnostic (confirmatory) test when you want to CONFIRM disease (minimize false alarms). For high-anxiety diseases (e.g., HIV), use high-specificity confirmatory test.
Formula
Positive Predictive Value (PPV) = (True Positives / [True Positives + False Positives]) × 100
Meaning
TP = test positive AND disease; FP = test positive BUT no disease; PPV = probability that a POSITIVE TEST truly indicates disease. DEPENDS ON DISEASE PREVALENCE.
Watch Out
PPV is NOT intrinsic to the test (like sensitivity/specificity); it CHANGES with disease prevalence in the population. A test with high sensitivity/specificity may have LOW PPV in a low-prevalence population (many false positives).
When To Use
Interpreting a positive test result in a specific population. High prevalence = higher PPV (more true positives relative to false positives).
Section Title
Screening, Test Validity & Study Designs
Important Facts
- Good screening program criteria: Disease is IMPORTANT, DETECTABLE early, TREATABLE, and test is SAFE, ACCEPTABLE, and COST-EFFECTIVE.
- Sensitivity & specificity are TEST properties (intrinsic). PPV depends on DISEASE PREVALENCE (extrinsic—changes with population).
- For screening: prioritize HIGH SENSITIVITY (don't miss cases). For confirmatory diagnosis: prioritize HIGH SPECIFICITY (confirm with certainty).
- Descriptive studies (case reports, cross-sectional surveys) describe patterns by person, place, time. Analytic studies (cohort, case-control, RCT) test associations.
- Cohort study = follow exposed & unexposed forward (INCIDENCE); yields Relative Risk. Case-control = compare diseased & non-diseased for past exposure; yields Odds Ratio. RCT = investigator assigns intervention; strongest evidence.
Key Definitions
Term
Screening
Example
Mammography screening for breast cancer in asymptomatic women; Pap smear for cervical cancer screening.
Definition
Application of a test to apparently HEALTHY people to detect disease early (secondary prevention). Different from diagnostic testing (which confirms suspected disease).
Term
Sensitivity
Example
A TB test with 95% sensitivity correctly identifies 95 of 100 TB patients (5 missed).
Definition
Ability of a test to correctly identify those WHO HAVE the disease (true positives). High sensitivity = few false negatives = RULE OUT disease when negative.
Term
Specificity
Example
A TB confirmatory test with 98% specificity correctly identifies 98 of 100 non-TB people as negative (2 false alarms).
Definition
Ability of a test to correctly identify those WHO DO NOT HAVE the disease (true negatives). High specificity = few false positives = RULE IN disease when positive.
Term
Positive Predictive Value (PPV)
Example
HIV test with 99% sensitivity and specificity: In high-prevalence group, PPV is 99%; in low-prevalence group, PPV is 50%.
Definition
Probability that a POSITIVE test result actually indicates DISEASE presence. DEPENDS ON DISEASE PREVALENCE in the population tested.
Diagrams To Know
- 2×2 table: TP, FP, FN, TN (for sensitivity, specificity, PPV calculations).
- Study design flowchart: Descriptive vs. Analytic; Cohort vs. Case-Control vs. RCT.
Section Title
Outbreak Investigation & Epidemic Curve
Important Facts
- Steps of outbreak investigation (MEMORISE IN ORDER): (1) Establish/verify diagnosis. (2) Define and identify cases. (3) Describe by person, place, time (epi curve). (4) Formulate & test hypothesis. (5) Implement control. (6) Communicate findings.
- Epidemic curve shape = KEY clue to outbreak type. Point-source = single sharp peak (all exposed at same time). Propagated = successive waves (generation-to-generation spread).
- Incubation period = time from exposure to symptom onset. Determines shape/timing of epi curve for point-source outbreaks.
- Generation time (serial interval) = time between cases in successive generations. Longer generation time = wider spacing between peaks in propagated outbreaks.
- Control measures target the chain of infection: isolation (break transmission), vaccination (protect host), quarantine (remove susceptible), sanitation (reduce exposure).
Key Definitions
Term
Outbreak Investigation
Example
2023 measles outbreak in a school: verify diagnosis, count cases, plot epidemic curve, interview cases for exposure (assembly? lunch hall?), implement vaccination, report to DOH.
Definition
Systematic multi-step process to identify source and mode of transmission during an epidemic. Key steps: verify diagnosis, define cases, describe by person/place/time, formulate hypothesis, test hypothesis, implement control measures, communicate findings.
Term
Epidemic Curve (Epi Curve)
Example
Food poisoning from one catered event = point-source (all ill within 1–2 days, single peak). Measles in unvaccinated school = propagated (successive generations of cases, multiple peaks).
Definition
Histogram of case counts over TIME. SHAPE distinguishes outbreak type: POINT-SOURCE (single sharp peak) vs. PROPAGATED (successive waves/person-to-person).
Term
Point-Source Outbreak
Example
Hotel food poisoning event on Jan 15 → cases appear Jan 16–17 (incubation 1–2 days) → curve peaks Jan 17 → no new cases after Jan 18.
Definition
Cases result from SINGLE, SHORT exposure to a source (e.g., contaminated food, one event). Epi curve shows SINGLE SHARP PEAK. Incubation period determines peak duration.
Term
Propagated (Person-to-Person) Outbreak
Example
Measles in school: Gen 1 (5 cases) → Gen 2 (20 cases 2 weeks later) → Gen 3 (60 cases 4 weeks later). Multiple peaks on epi curve.
Definition
Cases result from PERSON-TO-PERSON transmission over SUCCESSIVE GENERATIONS. Epi curve shows SUCCESSIVE WAVES (multiple peaks). Duration depends on generation time and control measures.
Term
Case Definition
Example
Measles case definition: fever ≥38°C × 3 days + cough/coryza/conjunctivitis + rash, OR lab confirmation. Used to count suspected & confirmed cases consistently.
Definition
Standardized criteria (symptoms, timeline, lab findings, exposure) used to IDENTIFY and COUNT cases uniformly during outbreak investigation.
Diagrams To Know
- Epidemic curve shapes: point-source (single sharp peak) vs. propagated (successive waves).
- Outbreak investigation flowchart: 6-step process from diagnosis verification to communication.
Section Title
Philippine Surveillance & Health Data Sources
Important Facts
- In the Philippines, epidemiologic surveillance is coordinated by the DOH EPIDEMIOLOGY BUREAU, supported by PIDSR (passive + active) and ESUs (regional, provincial, municipal, city).
- NOTIFIABLE DISEASES must be reported under PIDSR: measles, polio, diphtheria, tetanus, pertussis, TB, leprosy, rabies, malaria, dengue, cholera, typhoid, filariasis, leptospirosis, plague, etc.
- Timely reporting of notifiable diseases is a LEGAL DUTY of nurses under RA 9173 (Nursing Practice Law). Failure to report is reportable to PRC/BN.
- Civil registration (Birth and Death Certificates) is the PRIMARY SOURCE of vital statistics. Nurse's role: encourage birth/death registration for accurate demographic data.
- Accurate documentation in nursing records feeds into PIDSR, FHSIS, and vital statistics. Small nursing errors multiply in population-level data.
Key Definitions
Term
PIDSR (Philippine Integrated Disease Surveillance and Response)
Example
RHU identifies TB case → completes TB notification form → reports to municipal health office within 24 hrs → municipality to provincial ESU → province to DOH Epi Bureau.
Definition
National system for reporting NOTIFIABLE diseases from health facilities upward to DOH Epidemiology Bureau. Passive & active surveillance. Nurses must report promptly (RA 9173 duty).
Term
ESU (Epidemiology and Surveillance Unit)
Example
Municipal ESU coordinates PIDSR reporting from all health facilities in the municipality; receives reports from RHUs, processes, forwards to provincial ESU.
Definition
Surveillance units established at regional, provincial, city/municipal levels to coordinate disease reporting, outbreak response, and health surveillance.
Term
Passive Surveillance
Example
RHU nurse reports measles cases weekly to municipal health office as part of standard PIDSR reporting.
Definition
Health facilities ROUTINELY REPORT cases of notifiable diseases to higher levels (RHU → Municipal → Provincial → DOH). Passive = facilities self-report.
Term
Active Surveillance
Example
During cholera outbreak, public health nurse visits homes in affected area, screens residents, identifies suspected cases.
Definition
Health workers ACTIVELY SEEK and identify cases (not waiting for facility reports). Used during outbreaks or for targeted diseases.
Term
Vital Statistics
Example
Philippine Statistics Authority (PSA) compiles national vital statistics from municipal civil registrars; used to calculate CBR, CDR, IMR, MMR.
Definition
Data on vital events: births, deaths, marriages, fetal deaths, divorces. Registered under civil registry law. PRIMARY SOURCE: Birth and Death Certificates from civil registrars.
Term
FHSIS (Field Health Service Information System)
Example
RHU submits FHSIS report monthly to municipal health office showing number of ANC visits, immunizations given, TB cases treated.
Definition
Routine service data system collecting data from RHUs and health centers on outpatient visits, immunizations, deliveries, consultations. Used for monitoring service load and coverage.
Term
Census
Example
Philippine Census conducted every 5 years (2010, 2015, 2020); used as basis for population projections and rate denominators.
Definition
PERIODIC COMPLETE COUNT of population. Conducted by Philippine Statistics Authority (PSA). Source of denominator for rates; identifies demographic trends.
Diagrams To Know
- PIDSR reporting flow: RHU → Municipal ESU → Provincial ESU → DOH Epidemiology Bureau.
- Data sources pyramid: Civil registration (vital statistics) at base; FHSIS (service data) and PIDSR (disease surveillance) in middle; surveys/special studies at top.
Section Title
Levels of Prevention & Natural History of Disease
Important Facts
- Three levels of prevention correspond to stages of disease: Primary = prepathogenesis (before disease). Secondary = early pathogenesis (subclinical/early symptoms). Tertiary = late pathogenesis (clinical).
- PRIMARY PREVENTION (most important, lowest cost): health promotion (general health ed, good nutrition, exercise) + specific protection (immunization, sanitation, safe food/water, occupational safety).
- SECONDARY PREVENTION = EARLY DETECTION + PROMPT TREATMENT. Screening (Pap smear, mammography, BP check, TB sputum exam, glucose screening) identifies early disease.
- TERTIARY PREVENTION = disability limitation (surgery, medication, PT) + rehabilitation (return to function/work). For CHRONIC diseases (diabetes, post-stroke, post-TB).
- SCREENING is secondary prevention. A good screening program has important, detectable, treatable disease + safe, acceptable, cost-effective test.
Key Definitions
Term
Primary Prevention
Example
Health education on nutrition (promotion); immunization against measles (specific protection); sanitation improvement (specific protection).
Definition
Interventions BEFORE disease occurs. Includes HEALTH PROMOTION (general wellness) and SPECIFIC PROTECTION (disease-specific prevention). Target: susceptible population.
Term
Secondary Prevention
Example
Screening for TB (chest X-ray, sputum exam); case-finding for hypertension (BP screening); early treatment of diagnosed TB.
Definition
Interventions during EARLY STAGE of disease (subclinical pathogenesis). Early DETECTION and PROMPT TREATMENT to limit progression. Target: early-stage diseased individuals.
Term
Tertiary Prevention
Example
Physical therapy for stroke survivors (limit disability); vocational rehabilitation for TB patients (promote function).
Definition
Interventions AFTER disease is clinically established. Goal: LIMIT DISABILITY and PROMOTE REHABILITATION. Target: symptomatic diseased individuals.
Term
Prepathogenesis
Example
Unvaccinated child before measles infection; person without HTN before blood pressure elevation.
Definition
Stage BEFORE disease occurs. Person is susceptible but no disease present. Intervention: primary prevention (health ed, immunization, sanitation).
Term
Pathogenesis
Example
TB: subclinical = infection present but no cough/symptoms; clinical = cough, fever, weight loss.
Definition
Stage of disease development. Includes SUBCLINICAL PHASE (no symptoms; disease processes underway) and CLINICAL PHASE (symptoms present). Interventions: secondary (early) and tertiary (late).
Diagrams To Know
- Natural history diagram: Prepathogenesis → Subclinical pathogenesis → Clinical pathogenesis → Recovery/Disability/Death.
- Three levels of prevention mapped to natural history: Primary (prepathogenesis), Secondary (subclinical/early clinical), Tertiary (clinical/outcome).
Must Remember
- VITAL RATES DENOMINATORS (Critical, high-frequency error): CBR & CDR = use MIDYEAR POPULATION ×1,000. IMR, neonatal, fetal, maternal = use LIVE BIRTHS (maternal = ×100,000, others = ×1,000). Cause-specific death = POPULATION ×100,000. DO NOT MIX UP DENOMINATORS.
- INCIDENCE = NEW cases (RISK over time); PREVALENCE = ALL existing cases (BURDEN at one point in time). Incidence is the RISK of contracting; prevalence is the LOAD of disease. Prevalence is influenced by incidence, disease duration, recovery rate, and death rate.
- ATTACK RATE (special incidence rate) = (number ill / number exposed) ×100. Used ONLY in OUTBREAKS. Expressed as PERCENTAGE. Do NOT confuse with incidence rate (which has time-period denominator).
- CASE FATALITY RATE (CFR) = (deaths from disease / cases of disease) ×100. Measures disease SEVERITY/LETHALITY. Do NOT confuse with cause-specific death rate (which uses population as denominator, not cases).
- EPIDEMIOLOGIC TRIANGLE = AGENT + HOST + ENVIRONMENT. Breaking ANY ONE POINT interrupts disease transmission. Add VECTOR as needed (mosquito, snail, tick carries agent to host). CHAIN OF INFECTION = 6 links: agent → reservoir → exit → transmission → entry → host.
- THREE LEVELS OF PREVENTION: PRIMARY = health promotion & specific protection BEFORE disease (immunization, sanitation, health ed). SECONDARY = early detection & prompt treatment DURING subclinical/early stage (screening, case-finding). TERTIARY = disability limitation & rehabilitation AFTER disease is established (PT, rehabilitation, chronic disease management).
- ENDEMIC = constant, usual presence in area (expected baseline); EPIDEMIC/OUTBREAK = cases clearly IN EXCESS of expected; PANDEMIC = epidemic across countries. Do NOT confuse endemic with epidemic (endemic is expected; epidemic is excess).
- SENSITIVITY & SPECIFICITY are INTRINSIC test properties. Sensitivity = ability to DETECT disease (rule OUT when negative—high sensitivity for screening). Specificity = ability to EXCLUDE disease (rule IN when positive—high specificity for diagnosis). PPV depends on disease PREVALENCE and changes with population.
- PHILIPPINE SURVEILLANCE: DOH Epidemiology Bureau coordinates PIDSR (Philippine Integrated Disease Surveillance and Response) through ESUs (regional, provincial, municipal, city). Notifiable disease reporting through PIDSR is a LEGAL DUTY (RA 9173). Passive surveillance = facilities self-report; Active = health workers actively seek cases.
- EPIDEMIC CURVE SHAPE distinguishes outbreak type: POINT-SOURCE = single sharp peak (all exposed at same time, within incubation period). PROPAGATED = successive waves (person-to-person transmission across generations). Know how to interpret epi curves to identify source and transmission mode.
Last Minute Tips
- FORMULA DENOMINATORS ARE KILLERS ON THE NLE: Before calculating ANY rate, IDENTIFY the denominator. Is it midyear population? Live births? Total deaths? Total cases? Write it down. Cause-specific death uses POPULATION ×100,000 (not cases). Maternal/infant/fetal rates use LIVE BIRTHS. CBR/CDR use MIDYEAR POPULATION. A correct formula with wrong denominator = wrong answer.
- INCIDENCE vs. PREVALENCE questions are SUPER COMMON. If the question says 'New cases during the year' = incidence. If it says 'All cases present at one time' or 'How many people have the disease right now?' = prevalence. Prevalence includes old cases; incidence includes only new cases. When in doubt, check: does the time span include disease duration? Prevalence does; incidence does not.
- DON'T OVERTHINK SENSITIVITY/SPECIFICITY: Sensitivity = Detect (Sick) = TP/(TP+FN). Specificity = Exclude (Not sick) = TN/(TN+FP). Memorize: High sensitivity = HIGH RECALL, low miss rate (use for screening so you don't miss cases). High specificity = HIGH PRECISION, low false-alarm rate (use for diagnosis/confirmation so you're sure). If the question emphasizes 'don't miss any cases' = high sensitivity. If it emphasizes 'be certain before treating' = high specificity.
- EPIDEMIC CURVE TIMING IS THE CLUE: If all cases appear within a FEW DAYS (within one incubation period) and share a common exposure = POINT-SOURCE (e.g., food poisoning). If cases appear in WAVES weeks apart and cases are linked to other cases = PROPAGATED person-to-person. The epi curve shape tells the story: sharp peak = point-source; multiple humps = propagated.
- PRIMARY PREVENTION = DO NOT GET SICK. SECONDARY = FIND IT EARLY. TERTIARY = MINIMIZE DAMAGE. Simple mnemonics: Primary = healthy people get healthier (immunization, health ed). Secondary = sick people detected early (screening, case-finding). Tertiary = sick people recover function (PT, rehab). If the intervention is health education to prevent disease = primary. If it's a screening test = secondary. If it's physical therapy for a stroke survivor = tertiary.
Comparison Tables
Rows
Values
- NEW cases only (appearing during the period)
- ALL existing cases (new + old) at a point/period
Property
What does it count?
Values
- RISK of developing disease
- BURDEN of disease in population
Property
What does it measure?
Values
- New cases during the period
- All cases present at point/period in time
Property
Numerator
Values
- Population at risk (disease-free at start)
- Total population (includes diseased + non-diseased)
Property
Denominator
Values
- Expressed per unit TIME (rate)
- Point or period in time (snapshot)
Property
Time element
Values
- Incidence only (new cases)
- Incidence + duration + recovery/death rate
Property
Affected by
Values
- Comparing RISK between populations/time periods; identifying causes
- Planning services (how many patients to treat?); understanding disease burden
Property
Useful for
Values
- 10 NEW TB cases per 100,000 population per YEAR
- 50 total TB cases (old + new) per 100,000 population AT A POINT IN TIME
Property
Example
Columns
- Feature
- Incidence
- Prevalence
Table Title
Incidence vs. Prevalence (EXAM CLASSIC)
Rows
Values
- Ability to correctly ID those WITH disease (true positives)
- Ability to correctly ID those WITHOUT disease (true negatives)
- Probability that a POSITIVE test truly indicates disease
Property
Definition
Values
- TP / (TP + FN) × 100
- TN / (TN + FP) × 100
- TP / (TP + FP) × 100
Property
Formula
Values
- INTRINSIC to test (fixed property)
- INTRINSIC to test (fixed property)
- Test properties + disease PREVALENCE in population
Property
What it depends on
Values
- High sensitivity for screening (catch all diseased people; minimize missed cases)
- High specificity for diagnosis (confirm disease; minimize false alarms)
- Interpret positive result; depends on how common disease is in tested population
Property
Goal in practice
Values
- Usually inversely related to specificity
- Usually inversely related to sensitivity
- Increases with disease prevalence
Property
Inverse relationship
Values
- High sensitivity = few FN (rarely miss cases); can have many FP
- High specificity = few FP (rarely false-alarm); can have many FN
- High PPV = positive test is trustworthy. Low PPV = positive test unreliable (need confirmation)
Property
Interpretation
Values
- TB screening: 95% sensitivity misses 5 TB cases per 100
- TB diagnosis (GeneXpert): 98% specificity; only 2 false-positive per 100 non-TB people
- HIV rapid test in low-prevalence area: high sensitivity/specificity but LOW PPV (need confirmatory test)
Property
Example
Columns
- Concept
- Sensitivity
- Specificity
- Positive Predictive Value (PPV)
Table Title
Sensitivity vs. Specificity vs. PPV (TEST VALIDITY)
Rows
Values
- Constant, usual presence of disease in a given area
- Cases CLEARLY IN EXCESS of expected number in a community/region
- Epidemic spreading across MULTIPLE COUNTRIES or CONTINENTS
Property
Definition
Values
- Cases are EXPECTED; normal for that area
- Cases are UNEXPECTED (exceed baseline)
- Crosses international/global boundaries
Property
Expected baseline
Values
- Limited to specific area/region
- Single community, city, or region
- Multiple countries or continents
Property
Geographic scope
Values
- Ongoing, year-round or seasonal pattern
- Temporary surge; usually controlled within weeks/months
- May persist months to years across globe
Property
Duration
Values
- Routine prevention (immunization, sanitation); accepted as normal
- Active outbreak investigation and control measures
- International coordination, global health response
Property
Response needed
Values
- Malaria endemic in Mindanao; dengue endemic in Metro Manila
- Measles outbreak in school (2023); cholera outbreak in a barangay
- COVID-19 pandemic (2020–present); 1918 Spanish flu pandemic
Property
Philippine example
Columns
- Feature
- Endemic
- Epidemic/Outbreak
- Pandemic
Table Title
Endemic vs. Epidemic vs. Pandemic
Rows
Values
- SINGLE source; all exposed at same time (or very close time window)
- PERSON-TO-PERSON transmission across successive GENERATIONS
Property
Source of cases
Values
- SHORT exposure period (hours to 1–2 days)
- Exposure spans MULTIPLE WEEKS/MONTHS (ongoing transmission)
Property
Duration of exposure
Values
- SINGLE SHARP PEAK; all cases appear within one incubation period
- SUCCESSIVE WAVES or multiple peaks; each peak = new generation of cases
Property
Epidemic curve shape
Values
- All cases appear within incubation period of source exposure (e.g., 1–2 days for food poisoning, 10–14 days for measles)
- Cases spread over multiple generation times (e.g., 1–2 weeks apart for measles, 2–3 days for flu)
Property
Timeline
Values
- Remove/control source (discard contaminated food, close restaurant); quarantine is less critical
- Isolation + quarantine CRITICAL; vaccine/immunization important
Property
Control measures
Values
- Common exposure (place, event, food) among all cases
- Cases LINKED in a chain; secondary cases have epidemiologic link to primary case
Property
Investigation clue
Values
- Food poisoning from hotel catered event on Jan 15 → all become ill Jan 16–17 (incubation 1–2 days) → epi curve peaks Jan 17 with single sharp peak
- Measles in school: Gen 1 (5 students) → Gen 2 (20 students, 2 weeks later) → Gen 3 (60+ students, 4 weeks later) → multiple waves on epi curve
Property
Example
Columns
- Feature
- Point-Source Outbreak
- Propagated (Person-to-Person) Outbreak
Table Title
Point-Source vs. Propagated Outbreak (EPIDEMIC CURVE)
Rows
Values
- BEFORE disease occurs (prepathogenesis)
- Health promotion + specific protection
- Health education, immunization, sanitation, safe food/water, nutrition, exercise, occupational safety, smoking cessation
- Susceptible (disease-free) population
Property
PRIMARY
Values
- EARLY stage of disease (subclinical pathogenesis)
- EARLY DETECTION + PROMPT TREATMENT
- Screening (Pap smear, mammography, BP check, TB sputum), case-finding, early diagnosis, prompt treatment to limit progression
- Asymptomatic or early-stage diseased individuals
Property
SECONDARY
Values
- AFTER disease is clinically established (clinical pathogenesis + outcomes)
- Disability LIMITATION + REHABILITATION
- Surgery, medications, physiotherapy, occupational therapy, vocational training, disability support, chronic disease management
- Symptomatic diseased individuals (chronic conditions)
Property
TERTIARY
Columns
- Prevention Level
- Timing (Natural History)
- Focus
- Interventions
- Target Population
Table Title
Three Levels of Prevention (COMMON CONFUSION)
Rows
Values
- EPIDEMIOLOGIC TRIANGLE: Agent + Host + Environment (chain of infection)
- WEB OF CAUSATION: Multiple interacting risk factors; NO single cause
Property
Causation model
Values
- SPECIFIC infectious agent (bacteria, virus, parasite, fungus)
- MULTIPLE risk factors interact (genetic, lifestyle, environmental, behavioral)
Property
Cause
Values
- TB (Mycobacterium tuberculosis), measles (virus), malaria (Plasmodium parasite), dengue (virus transmitted by mosquito)
- Hypertension (diet + genetics + stress + obesity + age), diabetes (genetics + obesity + physical inactivity), cancer (smoking + genetics + exposure + age)
Property
Examples
Values
- 6-link chain: agent → reservoir → portal of exit → transmission → portal of entry → host
- NOT applicable; multiple risk factors converge over time
Property
Chain of infection
Values
- Break the chain at any link: isolate (break transmission), vaccinate (protect host), sanitation (reduce exposure), treat early
- Address multiple risk factors: lifestyle modification, screening, early detection, chronic disease management
Property
Prevention approach
Columns
- Feature
- Communicable Disease
- Non-Communicable Disease
Table Title
Communicable vs. Non-Communicable Disease Causation
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