Observational Studies 2 (Sept 18) Flashcards

1
Q

How should a case be selected?

A
  • shoud select average cases that are representative of the average patient (not the sickest or healthiest)
  • specific criteria
  • prefer incident over prevalent cases (tend not to be long survivors with a disese- can recall exposure status better)
  • healthy survivor bias; people who can live longer with disease than typical people can
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2
Q

How should controls be selected?

A
  • must come from same source population as cases (if cases come from hospital, select controls from hospital)
  • do not have disease under investigation
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3
Q

Matching (in case control study)

A
  • want to make sure controls and cases are similar with respect to certain characteristics
  • individual matching: get a case then find a control the same day that shares characteristics
  • frequency (group) matching: group of controls is matched to a group of cases with respect to a particular characteristic
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4
Q

Stratified analyses

A
  • break up analysis into two groups and see if they are roughly the same
  • since we’ve selected certain number of men and women, we can compare odds ratios between men and women (example)
  • we make sure we have enough men in group and women in group to make sure this is possible
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5
Q

Potential problems if we don’t match in case control study

A
  • possible that we could end up with only cases of men and no male controls
  • can’t compare odds ratios between men and women
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6
Q

Disadvantages of matching in case control study

A
  • inefficient (discard potential controls if they do not meet the criteria to match)
  • hard to find controls if you match on many variables
  • over matching: match on something we think is important to control for but ends up being an important determinant of disease (eg. SES- if you choose people in the same neighbourhood and match on SES, you can no longer look at association between SES and disease)
  • don’t want to match on something you think in the beginning could influence the exposure and outcome relationship
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7
Q

Advantages of case control studies

A
  • useful for studying many risk factors (exposures)
  • good for studying rare diseases (diseases that we don’t see often or take a long time to develop- we have a concentrated population in one hospital so we can study them there)
  • pretty inexpensive (surveys, figure out exposure status, etc. and don’t have to follow through for many years)
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8
Q

Disadvantages of case control studies

A
  • can’t figure out incidence rates because if you match individually, by definition you have a set incidence rate (eg. in a population of 100 in the study, 50 have to be cases)
  • no prospective follow up (can’t estimate if people are likely to develop disease because you start out with them already having developed it)
  • can’t estimate exposure rates are in that population (defined sample that we’ve matched cases to controls) so we can’t figure out in general population what the frequency of exposure is
  • temporality: ask them to recall exposure but it is possible for them to forget or things change
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9
Q

Concordant pair

A
  • both the case and control are exposed or unexposed
  • doesn’t tell us about association between exposure and outcome
  • non informative pair
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10
Q

Discordant paid

A
  • case is exposed, control is unexposed
  • case is unexposed, control is exposed
  • can learn something about exposure and disease
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11
Q

Matched Pairs Odds Ratio

A
  • include only discordant pairs in calculation
  • set up 2x2 table with discordant and concordant pairs (cases exposed/unexposed as columns and controls exposed/not exposed as rows)
  • odds ratio= (# of pairs with case exposed/control not exposed)/(# of pairs with case not exposed/control exposed)
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