Epidemiology Module 2 Flashcards

(32 cards)

1
Q

How to define population?

A

a group of individuals, population experience (individuals thru time) or population cross-section (individuals at a point in time)

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2
Q

What are odds?

A

Pevent/Pnonevent

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3
Q

2 measures of frequency:

A

prevalence (cases in a pop. at a given time) and incidence (new occurring cases/pop during specified time frame)

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4
Q

Prevalence definition

A

new and existing outcomes of interest. can be measured on different time scales. 2 types: point (# cases/total specified pop. at time of outcome ascertainment) and period (# cases/total specified pop at mid-point of time period)

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5
Q

What is prevalence affected by?

A

number of new cases, duration, rate of recover/death

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6
Q

Incidence definition

A

new events. excludes prevalent cases. 2 measures: CI (incidence proportion) and incidence density (incidence rate)

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7
Q

What is cumulative incidence and its assumptions?

A

fixed population experiencing a new event during a specified time period. Assumes follow up for entire period and static population.

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8
Q

Cumulative Incidence (Risk) proportion

A

occurred in a specified time period/number of total people in population. Can be enumerated like 30-day mortality, monthly risk, or annual incidence (proportion). dimensionless.

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9
Q

What are the difficulties with CI?

A

competing risks, multiple events, dynamic populations, loss to follow-up

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10
Q

What is attack rate?

A

incidence proportion of becoming afflicted during an epidemic (usually infectious)

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11
Q

What is case fatality rate?

A

proportion of people who then proceed to die (often no time period, infectious diseases, i.e. rabies)

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12
Q

What is incidence density (IR)?

A

new events/accumulated person-time of observation. accounts for variable time to event and loss to follow-up, but not potential bias due to loss. i.e. deaths/person-days of patients at risk. count number of injuries instead of number of people. if repeated events, don’t consider independent and subsequent aren’t counted? provides ave. prognosis

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13
Q

What are the technical difficulties with ID?

A

difficult to explain, waiting time. if steady-state conditions, the waiting time is the reciprocal of ID (i.e. 3.57 cases/person-year. 3.57^-1=.28 years, so you would wait about three months to see one case of the outcome

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14
Q

CI interpretation vs ID interpretation

A

time mortality vs mortality; time risk vs outcome per person-time; time incidence (proportion) vs incidence (density). CI goes from 0-1 while ID is 0-infinity.

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15
Q

Choosing CI vs ID

A

cumulative over duration of follow-up vs does not assume a particular time frame; difficulty with differing length of follow-up vs variable length of follow-up ok; difficulty with loss to follow-up vs handles loss to follow-up; difficulty with repeated events vs handles multiple occurrences; assumes fixed cohort vs handles dynamic population

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16
Q

Issues with Prevalence and Incidence

A

Numerator: definition of a case and multiple episodes of a disease? Denominator: who is at risk? competing risks? treat previously occurring disease in the same individual? P = understand burden of disease; I = etiologic associations

17
Q

What is crude rate?

A

events in a stated time period/population at risk

18
Q

What are problems with crude comparisons?

A

age associations and issues. other factors may alter death and disease as well

19
Q

What is a specific rate (stratum-specific)?

A

events among members in a stated time period/total members of category

20
Q

What is an adjusted/standardized rate?

A

hypothetical event rate that would have occurred if the observed rates happened in a population that is distributed like the standard population. can mask important differences

21
Q

What is age standardization?

A

removes effect of age. fictional. direct and indirect methods.

22
Q

What is a direct adjustment?

A

identify study and standard population. e.g. summary age-adjusted rate (disease/death rate in study pop. if study pop. had same age distribution as standard pop.).

23
Q

What is an indirect adjustment?

A

used b/c limited info on study pop or its small so age-specific rates are unstable. Final measure is a ratio: standardized mortality ratio or standardized morbidity ratio. cannot be compared. only between study and standard.

24
Q

What is SMR?

A

observed deaths/#expected deaths

25
How do you interpret SMR?
SMR = 1.0 --> no difference; SMR>1.0 --> higher than expected; SMR<1.0 --> lower than expected
26
How to read a prevalence or incidence graph
P: Orange line = health related event; arrows = outcome that was present at beginning or end of the specified time period; circles = incidence of new outcome or resolution; I: circles represent event; arrows are people that have not experienced event at end of follow-up
27
What is a catchment population?
People who use medical facility's services
28
What is a steady state?
I=E in a pop
29
What is a rate?
time is an integral part of denominator
30
CI vs IR vs P
new cases/pop at risk; new cases/person-time at risk; existing cases/total pop
31
What is the formulaic relationship between CI and IR?
CI=sum(IRiXti) --> don't need sum if constant IR and small CI
32
What is the relationship between prevalence and incidence?
P/(1-p)=IRXD (d = duration) for a stable state and incidence and duration do not change. if the frequency of the disease is rare (<10%) the euation becomes P=IRxD