Epidemiology Flashcards

1
Q

Study (scientific, schematic, data-driven) of the distribution (frequency and pattern) and determinants (causes, risk factors) of health-related stages or events in specified populations and the application to the control of health problems

A

Epidemiology

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2
Q

Epidemiology is concerned with two key factors of health events:

A

Frequency

Pattern

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3
Q

Number of health events (such as number of cases of meningitis or diabetes) but also to the relationship of that number to the size of the population

The rate allows epidemiologists to compare disease occurence across different populations

A

Frequency

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4
Q

Occurence of health related events by time, place and person

May be annual, seasonal, weekly, daily, hourly, weekday vs any other breakdown of time that may influence disease or injury occurence (time pattern)

Geographical variation, urban/rural differences, location of work site or schools (place pattern)

A

Pattern

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5
Q

Characterizing health events by time, place and person

A

Descriptive epidemiology

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6
Q

Any factor, whether event, characteristic or other definable entity, that brings about a change in health condition or other defined characteristic

Causes and other factors that influence the occurence of disease and other health-related events

A

Determinant

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7
Q

Anything that affects the well-being of a population

A

Health-related states or events

ex. disease

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8
Q

Concerned about collective health of the people in a community or population

A

Epidemiologist

Focuses on identifying the exposure or source that caused illness, number of persons similarly exposed; the potential for further spread in the community and interventions to prevent additional cases or recurrence

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9
Q

Explained disease from rarional rather than supernatural point of view

“On airs, waters and places”

Environmental and host factors such as behavior might influence development of disease

A

Hippocrates

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10
Q

Haberdasher and councilman who published a landmark analysis of mortality data in 1662

First to quantify patterns of birth, death and disease occurence noting disparities between males and females, high infant mortality, urban/rural differences and seasonal variations

A

John Graunt 1662

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11
Q

Father of modern vital statistics and surveillance

A

William Farr 1800

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12
Q

Anesthesiologist

Father of field epidemiology

Studied cholera outbreaks discovering cause and prevention of disease

Descriptive epi -> hypothesis generation -> hypothesis testing (analytic) -> application

A

John Snow

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13
Q

John Snow developed this tool showing the geographic distribution of cases

A

Spot map

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14
Q

Rotavirus vaccine SE

A

intusucception

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15
Q

Set of standard criterua for classifying whether a person has a particularly disease, syndrome or other health condition

A

Case definition

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16
Q

Graphing annual cases or rate of a disease over period of years

Long term

A

Secular trend

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17
Q

Disease occurence can be graphed by week or month over the course of a year or more to show its seasonal pattern

A

Seasonality

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18
Q

Suggests hypothesis about the time and source of exposure, the mode of transmission and causative agent

Uses histogram

A

Epidemic period

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19
Q

Single most important “person” attribute

A

Age

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20
Q

Key feature of analytic epidemiology

A

Comparison group

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21
Q

Quantifies the association between exposures and outcomes and to test hypotheses about casual relationships

A

Analytic epidemiology

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22
Q

Two kinds of analytic epidemiology

A

Experimental

Observational

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23
Q

Investigator determines through a controlled process the exposure for each indivdual (clinical trial) or community (community trial) and then tracks the individuals or communities over time to detect the effects of the exposure

A

Experimental studies

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24
Q

Epidemiologist simply observes the exposure and disease status of each participant

A

Observational studies

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25
Observational study types:
Cohort Case-control Cross-sectional
26
Epidemiologist records whether each study participant is exposed or not and tracks to see if they develop disease Investigator observes rather than determines participant’s exposure status (not randomly assigned) After a period of time, the investigator compares the disease rate in rhe exposed group with the disease rate in unexposed If the disease rare is substantively different in the exposed group compared to the unexposed group, the exposure is said to be associated with illness
Cohort study
27
Well known cohort study that established the rates and risk factors of heart disease
Framingham study
28
Participants enrolled as the study begins and are then followed prospectively over time to identify occurence of the outcomes of interest
Follow-up/Prospective Cohort
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Both the exposure and the outcome have already occured The investigator calculates and compares rates of disease in the exposed and unexposed groups Used in investigations of disease in groups if easily identified people such as workers at a participar factor or attendees at a wedding
Retrospective cohort study
30
Investigators start by enrolling a group of people with disease and a comparison group (without disease) Investigators compare previous exposures between the two groups The control group provides an estimate of the baseline or expected amount of exposure in the population. If the amount of exposure among the case group is substantially higher than the amount you would expect based on the control, then illness is said to be ASSOCIATED with that exposure
Case-Control
31
Sample of persons from a population is enrolled and their exposures and health outcomes are measured simultaneously Assess the PREVALENCE of health outcome at that point of time without regard to duration Weaker than either because it cannot disentangle risk factors for occurence of disease (incidence) from risk factors for survival with the disease Synonymous to
Cross-sectional study Survey Prevalance rather than incidence
32
Subjects are enrolled or grouped on the basis of their exposure, then are followed to document occurence of disease Difference in disease RATES between the exposed and unexposed groups lead investigators to conlcude that exposure is associated with disease
Cohort study
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Subjects are enrolled according to whether they have the disease or not, then are questioned or tested to determine prior exposure Difference in EXPOSURE prevalence between the case and control allows investigators to conclude that the exposure is associated with the disease
Case-control study
34
Measure exposure and disease status at the same time and are better suited to descriptive epidemiology than causation
Cross-sectional study
35
Simplest model for causation Traditional model for infectious disease
Epidemiologic Triad
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Epidemiologic triad
External agent Susceptible host Environment
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Chemical contaminant responsible for eosinophilia-myalgia
L-tryptophan
38
Attempt to account for the multifactorial nature of causation An individual factor that contributes to cause disease is shown as a piece of pie After all the pieces of a pie fall into place, the pie is complete and disease occurs
Causal pie
39
The individual factors in causal pies
Component causes
40
The complete pie which might be considered a casual pathway is called
Sufficient cause
41
A component that appears in every pie or pathway is called without it, disease does not occur
Necessary cause
42
Hypertension/Stroke Cause
Component Cause
43
Treponema pallidum/Syphilis Cause?
Necessary cause
44
Type A personality/Heart disease Cause?
Component cause
45
Skin contact with a strong acid/Burn Cause?
Sufficient cause
46
3 forms of route of anthrax infection
Cutaneous (95%) Inhalation - fatal; mail related Intestinal
47
Progression of a disease process in an individual over time in the absence of treatment
Natural history of disease
48
Stages of Natural History of Disease
Stage of susceptibility Stage of subclinical disease Stage of clinical disease Stage of recovery: disability or death
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Stage of subclinical disease extending from the time of exposure to onset of disease symptoms Asymptomatic or inapparent Some pathologic change detectable with laboratory, radiographic, or other screening methods
Incubation period - infectious disease | Latency period - chronic disease
50
Paralytic shellfish poisoning (tingling, numbness around lips and fingertips, giddiness, incoherent speech, respiratory paralysis, sometimes death) Incubation period:
Saxitoxin and similar toxins from shellfish Few minutes to 30 minutes
51
Incubation period of radium (watch dial painters) to developing bone cancer
8-40 years
52
Most screening programs attempt to identify the disease process during this phase of its natural history since intervention at this early stage is likely to be more effective than treatment given after the disease has progressed and become symptomatic
Incubation period
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The onset of symptom marks the transition from subclinical to clinical disease Most diagnoses are made during this stage
Stage of clinical disease
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Illness that ranges from mild to severe or fatal
Spectrum of disease
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End of disease process
Recovery Disability Death
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Proportion of exposed persons who become infected
Infectivity
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Proportion of infected individuals who develop clinically apparent disease
Pathogenecity
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Proportion of clinically apparent cases that are severe or fatal
Virulence
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Agent leaves its reservoir or host through a portal of exit, conveyed by some mode of transmission and enters through an appropriate portal of entry to infect a susceptible host
Chain of infections
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Habitat in which the agent normally lives, grows and multiplies May or may not be the source from which agent is transferred to a host
Reservoir
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Those who can transmit the agent during the incubation period before clinical illness begins
Incubatory carrier
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Those who have recovered from their illness but remain capable of transmitting to others
Convalescent carriers
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Continue to harbor a pathogen such as Hepatits B virus or Salmonella typhi for months or years after their initial infection
Chronic carrier
64
Infectious disease that is transmissible under natural conditions from vertebrate animals to humans
Zoonosis
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Types of direct transmissio
Direct contact | Droplet spread
66
Types of Indirect transmission
Airborne Vehicleborne Vectorborne (mechanical or biologic)
67
Final link in the chain of infection
Susceptible host
68
If a high enough proportion of individuals in a population are resistant to an agent, then those few who are susceptible will be protected by the resistant majority
Herd immunity
69
Increase, often sudden, in the number of cases of a disease above what is normally expected in that population i that area
Epidemic
70
Epidemic in a more limited geographic area
Outbreak
71
Aggregation of cases grouped in place and time that are suspected to be greater than the number expected even though the expected number may not be known
Cluster
72
Epidemic that had spread over several countries or continents usually affecting a large number of people
Pandemic
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Persistent, high levels of disease occurence
Hyperendemic
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Epidemic and their manner of spread through a population
Common-source Propagated Mixed Other
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Group of person are all exposed to an infectious agent or a toxin from the same source
Common-source outbreak
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If the group is exposed over a relatively bried period so that everyone who becomes ill does so within one incubation period
Point source (common source) outbreak
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Point-source outbreak plot
Steep upslope more gradual downslope | Log-normal distribution
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Pattern reflecting the intermittent nature of exposure
Intermittent common source outbreak
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Transmission from one person to another by direct person-to-person contact, vehicleborne, vectorborne
Propagated outbreaks
80
Common source outbreak followed by secondary person-to-person spread
Mixed epidmeic
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Neither common-source nor propagated from person to person
Epidemic not caused by point, intermittent or propagated source