Key concepts and framing

  • The topic centers on diseases moving across populations and how we measure them quantitatively; some math is unavoidable.
  • Morbidity vs mortality (terminology in the transcript):
    • Morbidity is typically disease occurrence; mortality is death. The transcript notes morbidity as death, which is nonstandard, but we’ll reflect the wording there while also noting the conventional definitions.
  • Mortality and morbidity provide the foundation for epidemiologic studies; standard methods of measurement are needed to compare across populations.
  • Why compare populations?
    • For programming and resource allocation decisions, we need to compare disease burden across populations.
    • Populations differ in size and structure (age, sex, etc.), so raw counts are not enough; rates and standardization help.
  • Key progression in analysis:
    • Start with crude rates (unadjusted).
    • Move to age/sex standardization and adjusted rates for better cross-population comparability.

Rates, counts, and what they mean

  • A rate contains three key elements:
    • Event frequency (numerator): number of events of interest (e.g., deaths, new cases).
    • Population at risk (denominator): the population among which the events occur.
    • Time period over which the events are counted (time component).
  • Rate base multiplier (e.g., per 1000, per 100,000):
    • Multipliers make rates interpretable and comparable. Some conventions depend on the type of event.
    • Common bases include 1,000 and 100,000.
    • Examples: infant mortality and some birth-related rates use different bases; you’ll learn these conventions as you dive into each rate type.
  • Counts vs rates (conceptual):
    • Counts tell you how many events occurred in a population, but they’re sensitive to population size.
    • Rates adjust for population size and time to allow comparison across populations and over time.
  • Percent (as discussed in class):
    • Percent within a country may reflect the proportion of all disease that a specific disease represents (denominator is all cases in the country, numerator is cases of the disease of interest).
    • This is different from rates, which incorporate a population-at-risk denominator and a time period.

Crude rates: definition, example, and intuition

  • Definition:
    • Crude rate = number of events in a population during a specified time period divided by the population size (often at the midpoint of the year), multiplied by a base (commonly 1,000 or 100,000).
    • Not adjusted for age, sex, or other factors.
  • Common example: crude mortality rate (death rate) or crude death rate.
  • US crude death rate example (2017):
    • Deaths ≈ 2,800,0002{,}800{,}000 in the year.
    • Midpoint population (denominator) is used; the result is often presented as deaths per 100,000 population.
    • Reported example: about 8.64imes1028.64 imes 10^{2} deaths per 100,000100{,}000 population, i.e., roughly 864864 deaths per 100,000 people.
    • General form: extCDR=DP<em>extmidimes10kext{CDR} = \frac{D}{P<em>{ ext{mid}}} imes 10^k where DD = deaths, P</em>extmidP</em>{ ext{mid}} = population at midpoint, and the base multiplier 10k10^k reflects the chosen base (e.g., 10310^3 for per 1,000, per 1,000,000, or 10510^5 for per 100,000).
  • A sample of crude death rates across countries may be presented per 1,000 population (or per 1,000 people) instead of per 100,000; this affects the numeric value but not the underlying concept.
  • Strengths of crude rates:
    • Simple to calculate and interpret.
    • Reflect the overall burden of a population.
  • Limitations of crude rates:
    • Do not adjust for population structure (age, sex, etc.).
    • Differences between populations may reflect demographic structures rather than true differences in underlying risk.
  • Discussion prompt (from transcript): factors that can increase crude death rate in a country:
    • Age structure (older populations tend to have higher death rates).
    • Safety/violence-related factors.
    • Economic and health context (wealthier vs poorer countries; older populations vs higher disease burden).
  • Takeaway:
    • Crude rates are useful as a starting point, but be cautious when comparing across populations with different age and sex structures.
    • Next class will cover specific (age- and sex-specific) and adjusted rates to address these issues.
  • Pros and cons recap:
    • Pros: simple to calculate, easy to interpret, reflects burden.
    • Cons: not adjusted for key demographic differences; can be misleading for cross-population comparisons.

Natality measures and perinatal periods (birth-related metrics)

  • Natality refers to measures around birth; several key rates and time windows are used.
  • Important time periods around birth:
    • Fetal period: begins around gestational week 20; survival outside the womb becomes plausible around ~20 weeks.
    • Late fetal period: from ~week 28 gestation to birth.
    • Neonatal period: from birth (0 days) to 28 days old.
    • Neonatal vs perinatal distinction is nuanced; focus here is on neonatal (0–28 days) and post-neonatal (28 days to 1 year).
    • Infant period: from birth to 12 months (1 year).
  • Crude birth rate (CBR):
    • Definition: number of live births in a year divided by the population at the midpoint of the year, multiplied by a base (commonly 1,000).
    • Rate base multiplier: typically 1,000 for births.
    • Denominator: population size at midpoint of the year; numerator: live births in the year.
  • Live birth definition (infant milestone for birth measures):
    • A live birth is a birth in which the baby shows signs of life after birth (breathing, heartbeat, umbilical cord pulsation, etc.).
  • Fertility rate (fertility in demography):
    • Definition: number of live births divided by the number of women of childbearing age, typically 15–44 years, multiplied by 1,000.
    • Formula: extFR=extlivebirthsN1544imes1000.ext{FR} = \frac{ ext{live births}}{N_{15-44}} imes 1000.
    • Practical note: used to track reproductive performance and potential future population growth.
  • The United States fertility rate over time (illustrative):
    • The rate has fallen substantially over the 20th and early 21st centuries, with a notable rise in the postwar era and declines in more recent decades.
    • The economy is a major correlate: economic upswings often coincide with higher fertility, downturns with lower fertility.
  • Infant mortality rate (IMR):
    • Definition: number of infant deaths (death before age 1) during a year divided by the number of live births in the same year, multiplied by a base (commonly 1,000).
    • Formula: extIMR=D<em>extinfantBimes1000,ext{IMR} = \frac{D<em>{ ext{infant}}}{B} imes 1000, where D</em>extinfantD</em>{ ext{infant}} = infant deaths, BB = live births.
    • In the United States, IMR has declined markedly from the mid-20th century (e.g., from around 60 per 1,000 live births in 1935 to about 7–8 per 1,000 in more recent years).
  • Neonatal and post-neonatal mortality rates:
    • Neonatal mortality rate (NMR): deaths within the first 28 days of life per 1,000 live births.
    • extNMR=DextneonatalBimes1000.ext{NMR} = \frac{D_{ ext{neonatal}}}{B} imes 1000.
    • Post-neonatal mortality rate (PNMR): deaths from 28 days to 1 year per 1,000 live births.
    • extPNMR=DextpostneonatalBimes1000.ext{PNMR} = \frac{D_{ ext{post-neonatal}}}{B} imes 1000.
    • Relationship: extIMR=extNMR+extPNMR.ext{IMR} = ext{NMR} + ext{PNMR}.
  • Fetal death rate (FDR):
    • Definition: deaths after 20 weeks gestation, typically per 1,000 live births (or per 1,000 pregnancies, depending on convention).
    • In the transcript: fetal deaths after 20 weeks or more gestation, used in calculations adding to live births in the denominator and multiplied by 1,000.
  • Maternal mortality rate (MMR):
    • Definition: maternal deaths assigned to causes related to pregnancy, per 100,000 live births.
    • Formula: extMMR=DextpregnancyrelatedBimes100,000.ext{MMR} = \frac{D_{ ext{pregnancy-related}}}{B} imes 100{,}000.
    • Important nuance: a death must be related to the pregnancy; deaths from unrelated causes during pregnancy do not count.
  • Summary of perinatal conceptual map:
    • Fetal period (before birth) → fetal deaths counted in FDR alongside live births via denominators.
    • Neonatal period (0–28 days) and post-neonatal period (28 days–1 year) together compose IMR via NMR and PNMR.
    • Infant mortality rate (IMR) covers deaths in the first year of life; equals the sum of neonatal and post-neonatal mortality rates.
    • Birth-related measures rely on live births in the denominator and period-specific death counts (or births) in the numerator.

Population structure, interpretation, and adjustments

  • Age structure matters:
    • Countries with older populations can have higher crude death rates simply due to age, not necessarily higher risk of death overall.
    • Conversely, younger populations may show lower crude death rates even if absolute disease burden is substantial.
  • This is why crude rates must be used with caution when comparing across populations with different age or sex structures.
  • Next steps (not covered in this class but foreshadowed): specific rates (age- and sex-specific) and adjusted rates (standardized rates) to control for population structure.

Practical takeaways and exam expectations

  • Crude rates are a starting point for comparing disease frequencies but can be misleading if population structure differs.
  • Be prepared to calculate and interpret the following on exams and homework:
    • Crude death rate: extCDR=DPextmidimes1000ext(orimes100,000ext).ext{CDR} = \frac{D}{P_{ ext{mid}}} imes 1000 ext{ (or } imes 100{,}000 ext{)}.
    • Infant mortality rate: extIMR=DextinfantBimes1000.ext{IMR} = \frac{D_{ ext{infant}}}{B} imes 1000.
    • Neonatal mortality rate: extNMR=DextneonatalBimes1000.ext{NMR} = \frac{D_{ ext{neonatal}}}{B} imes 1000.
    • Post-neonatal mortality rate: extPNMR=DextpostneonatalBimes1000.ext{PNMR} = \frac{D_{ ext{post-neonatal}}}{B} imes 1000.
    • Relationship: extIMR=extNMR+extPNMR.ext{IMR} = ext{NMR} + ext{PNMR}.
    • Fetal death rate: extFDR=DextfetalBimes1000.ext{FDR} = \frac{D_{ ext{fetal}}}{B} imes 1000.
    • Maternal mortality rate: extMMR=DextpregnancyrelatedBimes100,000.ext{MMR} = \frac{D_{ ext{pregnancy-related}}}{B} imes 100{,}000.
    • Fertility rate: extFR=extlivebirthsN1544imes1000.ext{FR} = \frac{ ext{live births}}{N_{15-44}} imes 1000.
    • Live births and live-birth-based rates rely on population at midpoint and the appropriate multiplier.
  • Ethical and practical considerations:
    • Differences in healthcare access, public health infrastructure, vaccinations, sanitation, and socioeconomic status can drive observed differences in infant and maternal mortality.
    • Crude rates do not reflect disparities within populations (e.g., by race/ethnicity); important for equity-focused work.
  • Exam strategy hinted in the transcript:
    • Expect questions that require calculating the range of natality measures (fertility rate, infant mortality, neonatal and post-neonatal mortality, fetal death rate, maternal mortality) using the provided definitions and base multipliers.
    • Expect to discuss why crude rates should be used cautiously in cross-country comparisons and how standardization helps.

Quick reference: essential formulas (LaTeX)

  • Crude death rate (per 1,000 or 100,000):
    • extCDR=DPextmidimes103extorimes105.ext{CDR} = \frac{D}{P_{ ext{mid}}} imes 10^3 ext{ or } imes 10^5.
  • Infant mortality rate (per 1,000 live births):
    • extIMR=DextinfantBimes1000.ext{IMR} = \frac{D_{ ext{infant}}}{B} imes 1000.
  • Neonatal mortality rate (per 1,000 live births):
    • extNMR=DextneonatalBimes1000.ext{NMR} = \frac{D_{ ext{neonatal}}}{B} imes 1000.
  • Post-neonatal mortality rate (per 1,000 live births):
    • extPNMR=DextpostneonatalBimes1000.ext{PNMR} = \frac{D_{ ext{post-neonatal}}}{B} imes 1000.
  • Infant mortality relationship:
    • extIMR=extNMR+extPNMR.ext{IMR} = ext{NMR} + ext{PNMR}.
  • Fetal death rate (per 1,000 births):
    • extFDR=DextfetalBimes1000.ext{FDR} = \frac{D_{ ext{fetal}}}{B} imes 1000.
  • Maternal mortality rate (per 100,000 live births):
    • extMMR=DextpregnancyrelatedBimes100,000.ext{MMR} = \frac{D_{ ext{pregnancy-related}}}{B} imes 100{,}000.
  • Fertility rate (per 1,000 women aged 15–44):
    • extFR=extlivebirthsN1544imes1000.ext{FR} = \frac{ ext{live births}}{N_{15-44}} imes 1000.