epidemiology intro Flashcards

1
Q

basics of epidemiology

A

study of distribution and determinants of health related states or events in specified populations and application of this study to control health problems

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2
Q

why observe and screen pop.

A

Risk estimates, relevance of interventions, accuracy of estimates, comparisons, increased screening increases incidence rate but can decrease mortality

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3
Q

epidemiology triad

A

time(day, year, ect), place(home, locality, environmental and socioeconomic), person(age, sex, eco status, behaviour ect)

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4
Q

exposure and outcome

A

exposure- exposure to supposed cause of outcome or possession of characteristic that is a determinant of outcome

outcome- possible results that can stem from exposure to a causal factor or from preventative interventions, identifiable changes in health status

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5
Q

random control trial when can’t you use it

A

opinions, rare or dangerous(ethics), experiences, mortality and other things you can’t blind test

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6
Q

RCT studies

A

observational, descriptive and analytical hypothesis generating
interventional studies are experimental usually RCT

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7
Q

Cross sectional studies basics and uses

A

get a sample and gather all exposure and outcome data at once
health service planning, resource allocation, can measure changes if conducting repeat cross sectional studies

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8
Q

cross sectional study advantages

A

QCE(quick cheap easy),
measure multiple exposures and outcomes
no loss follow up
generate and test hypotheses

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9
Q

cross sectional disadvantages

A

standardise measurements
bias responder and recall
associations difficult to interpret
not for rare diseases, short duration or emergent events

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10
Q

point prevelance

period prevelance

A

no. existing cases/total at risk pop.
at a given point
period prevalence includes new and existing cases not best to use

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11
Q

cohort studies basics

A

enrol at risk group and measure exposure status and follow over time

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12
Q

cohort study advantages

A

good for rare exposures, measures more than one outcome, clear temporal relationship(relationship involving time), prospective study minimises bias, ethical and legal

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13
Q

cohort study disadvantages

A

not good for rare outcomes, retrospective relies on good records, bias if follow exposed group more closely, prospective slow and expensive and loss of follow up

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14
Q

cumulative incidence

A

no. new outcomes/people at risk

over given time at risk

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15
Q

incidence rate

and benefits

A

no. new cases/person-at time risk

good for common diseased open population

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16
Q

case control study basics

A

compare exposure history between groups-retrospective

start with outcome and look for exposures

17
Q

case control study advantages

A

QEC, rare outcomes, multiple exposures can be measured, good for diseases with long latency period

18
Q

case control study disadvantages

A

select controls, recall bias, not good for rare exposures, can’t create incidence rates

19
Q

confounder

A

variable associated with outcome and exposure but doesn’t lie on the causal pathway

20
Q

chance, bias, confounding

A

representative sample, statistical inferences, valid measures