Intro Lecture Flashcards

(25 cards)

1
Q

Define endemic

A

constant presence of disease or infectious agent within a given geographic area or population group

may also refer to usual prevalence of a disease within an area or group

ex- tuberculosis is endemic to the US

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2
Q

Define Epidemic

A

occurrence in a community or region of cases with frequency clearly in excess of normal expectancy

time is a consideration
could mean just 1 case of disease or 100s

Example- FMD

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3
Q

Define Pandemic

A

epidemic occurring over a very wide area, crossing international boundaries and affecting a large number of people- may cross continents

Ex- HIV, SPnaish Flu, Plague

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4
Q

Define Epidemiology

A

study of disease in populations

study of distribution and determinants of heath-realted states or events in specified populations and the application of this study to control health problems

scientific inquiry

data driven
systematic and unbiased approach
collection, analysis, interpretation

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5
Q

What are examples of health related states and events

A

states- preggers, obesity, diabetes, lameness

events- parturition, visit to the dog park
abnormal blood sugar test, stepping on a nail

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6
Q

What is a CASE DEFINITION

A

set of standard criteria
clinical description
laboratory criteria
case classification

National Stnadards that ensure comparability
ie listeria cases in orego women in 200 compared to 2015, iowa compared to Minnisota

surveillance and putbreak definitions often differ

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7
Q

What are the three parts to an epidemiologic approach?

A

count- cases/events by person/place/thing

divide- by the appropriate denominator to calculate rates

compare rates over time for groups

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8
Q

What are the 2 types of epi studies?

A

Descriptive/analytic

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9
Q

What is a descriptive study?

A

who, where, and when- person place time

characterizing patterns

hypothesis generating

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10
Q

What is an analytic epi study?

A

determinants

identifying causes

hypothesis testing

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11
Q

What are the strengths/limitations of descriptive studies?

A

strengths- inexpensive, quick, overall descriptive pattern, generate hypothesis

weakness- cannot control for confounding factors, difficult to est cause and effect, cannot test hypotheses

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12
Q

What are the 5 W’s of dscriptive epi?

A
What- case definition
who- person/animal
where- place
when- time
why/how- causes, risk factors, modes of transmission
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13
Q

What are the properties we look at for person/animal?

A

inherent characteristics- age, sex, species, ethnicity/race/breed

biological characteristics- immune status

acquired characteristics- marital status

activities- occupation, leisure, use of meds/drugs

socioeconomic status

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14
Q

What are the properties we look at for place?

A

where is the disease?, most common? most rare?

does it vary by region? tropical/temperature?

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15
Q

What are the properties we look at for time?

A

seasonal? inlfuenze, WNV, salmonellosis

day of week/time of day?

difference after intervention?

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16
Q

What are the 2 types of descriptive studies?

A

case reports and case series

cross sectional analysis

17
Q

What is a cross-sectional studies?

A

exposure and disease assessed simultaneously

one point in time

specific population

18
Q

What are the strengths/limitations of cross sectional studies?

A

strength- fast, based on general population, lots of data

weak- difficult to separate cause and effect, temporal relationship cant be defined, dz with remissions could be missclassified

19
Q

What is the major difference between descriptive.analytic epidemiology?

A

descriptive- distribution of disease

analytical- determinants of disease

20
Q

What are the key features of analytical epidemiology?

A

KEY- comparison group

experimental studies- clinical trial

observational studies- cohort/case-control

21
Q

What is a cohort study?

A

based on EXPOSURE status

persons are enrolled as dz free, w/ or w/o exposure of interest

followed over time

22
Q

What are the strengths/limitations of of cohort studies?

A

strengths- risk ratio, info on incidence, temporal relationship, rare exposures

weakness- time concuming, large sample size, expensive, lots of follow-up/bias, not efficient for rare data

23
Q

What is a case-control study?

A

based on DISEASE status

persons w/ disease (cases) and w/o disease (controls)

faster/cheaper

can investigate multiple exposures for one dz- useful for when dz is rare

not good for when dz exposure is rare

odds ratio

24
Q

Advantages to case-control matching?

A

confounding variables-

better than adjustment, littermates/genetic/environmental influence, avoids wasting power on known factors

ie non-hospitalized control group

25
Disadvantages to case-control matching?
cannot evaluate the matched variable expensive matching something that is a confounder leads to loss of data