Case Control studies Flashcards

1
Q

what is a case control study

A

observational study of people with disease of interest and suitable control group of people without disease
= to identify risk factors for an outcome

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2
Q

what is the relationship between a potential risk factor and disease examined by comparing the two groups on?

A

whether the risk factor is present
how frequent the risk factor is
the amount of the risk factor (e.g dose)

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3
Q

what is a retrospective study

A

starts by knowing who has the disease and work back to find who was exposed
so starts after onset of disease and looks back at risk factors

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4
Q

what is a prospective retrospective study

A

cases and controls in case-control study can be accumulated prospectively
as each new case is diagnosed, it is entered into the study BUT still looks back retrospectively from disease to exposure

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5
Q

what is the approach of case controls studies

A

figure out if diseased cases differ from non-diseases controls in terms of prior exposure
compare frequency of exposure

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6
Q

why cant disease incidence rate be calculated for case-control study

A

because it doesnt follow a disease-free population over time

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7
Q

what does an odds ratio of 1 indicate

A

no association between exposure and disease

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8
Q

what does an odds ratio of <1 suggest

A

potential protective effect

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9
Q

what does an odds ratio of >1 indicate

A

positive association between exposure and disease, meaning exposure may be a risk factor

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10
Q

what are the essential features of a case-control study

A

directionality (outcome to exposure)
timing (retrospective for exposure)
rare or new disease - always the design choice if disease is rare

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11
Q

how do you choose cases in case control study

A

define outcome - standard diagnostic criteria and severity/duration of disease
age range for inclusion
temporal boundaries
geographical boundaries of study

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12
Q

how do you source cases for case-control study

A

population-based - identify and recruit all incident cases from population using disease registry, vital records, or defined area
hospital based - identify cases where you can find them BUT may not be representative

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13
Q

what should the control group represent

A

the population of individuals who would have been identified and included as cases had they developed the disease
all exclusions or restrictions must apply to cases and controls

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14
Q

outline population-based controls

A

usually first choice
drawn from specific geographical area and time
randomly select controls from same area and same time period
use government lists, NHS, electoral role or telephone survey

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15
Q

what are advantages of population controls

A

exclusion criteria is easy to apply
cases and controls are from the same study base
representative of whole study base

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16
Q

what are disadvantages of using population controls

A

low participation rates could cause possible bias
inconvenience of finding controls
recall bias - could have been modifications since diagnosis or changes in past habits
may not be motivated to take part

17
Q

what are neighbourhood controls

A

selected from residences in same geographical area as cases
attempts to reduce variability of socioeconomic status

18
Q

what are advantages of neighbourhood controls

A

selection doesnt need roster of people - avoids problem of using telephone lists
possible risk factors which vary georgraphically may be more balanced between cases and controls

19
Q

what are disadvanatges of neighbourhood controls

A

costly
possibly not representative of study base
increased chance of selection of people living alone
difficult to document non-response
possible over-matching if exposure is related to residence

20
Q

outline hospitalised or disease registry controls

A

control diseases should be subject to same surveillance and detection procedures as cases
controls come from same source as cases e.g hospital admissions, and disease registries

21
Q

what is an example of a hospitalised control

A

study of smoking and MI among women
cases from admission to coronary care units at 152 hospitals
controls drawn from admissions to other wards in same hospital

22
Q

what are advantages of hospitalised controls

A

easy to identify controls, readily available in sufficient numbers
more likely to be aware of previous exposures than healthy individuals
more likely to cooperate than healthy individuals - reducing bias due to non-response

23
Q

what are disadvantages of hospitalised controls

A

they are ill
disease may have common aetiology or be on the causal pathway
more likely to smoke, more likely to be from lower SES, more likely to be heavy drinkers
-bias
if taken from specialist hospitals there could be differences in SES

24
Q

what are other categories of controls?

A

friends - cheap, convenient, but could over-match when related to exposure
relatives - useful if genetic factors are involved, but there is risk of over-matching

25
Q

how many control groups should there be

A

one but can have 2
second is a replication group
but both groups should be independant - no overlap

26
Q

what can be matched for in order to control for confounding factors?

A

sex
date of birth
georgraphical area
SES
maternal age

27
Q

what are disadvantages of matching

A

increased effort to find suitable controls
exclusion of cases if no match is found
longer study duration (control selection delayed until case identified)
OVERMATCHING

28
Q

what is overmatching

A

when a matching variable is involved in or is closely related to the mechanism whereby the exposure influences disease risk
- could be on causal pathway
could be a surrogate
could be strongly associated with BOTH disease and exposure
overmatching will bias the relative risk toward 1

29
Q

what is an example of overmatching

A

study of smoking and lung cancer - matched on carrying a cigarette lighter or not

30
Q

what are the rules of matching

A

only match on risk factors whose confounding effects need to be controlled for but are not of scientific interest in the study
a matched study is best to have a matched statistical analysis

31
Q

how many controls should there be per case when matching

A

1:1 is good
increasing number of controls per case increases statistical power but 1:4 is as far as it should go
inefficient beyond this point

32
Q

what is a nested case-control study

A

cases and controls drawn from cohort study
useful when wanting more detailed measurements on subset of cohort
also for matching on confounders
otherwise the same as a normal case-control study

33
Q

what is an example of a case control study

A

serum vitamin D status in group of migraine patients compared with health controls
70 migrainers 70 healthy
matched on age and sex
result: signficant negative association between migraine headache and serum vitamin D
significant trend with decreasing odds with increasing serum vitamin D

34
Q

what care needs to be taken in case-control studies

A

care in study design, especially with issues such as control selection and matching

35
Q

what are advantages of case-control study

A

several aetiological factors for single disease
optimal for the study of rare disease
well suited for disease with long latency period
relatively quick
small number of subjects so allows more detail assessment
inexpensive
yields relative risk estimate

36
Q

what are disadvantages of case control study

A

potential for selection bias - in controls and matching
retrospective collection of information - recall is not always reliable
can only look at ONE disease
yields relative risk not absolute risk