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
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
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
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
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
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
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)
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
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
10
Q
Discordant paid
A
- case is exposed, control is unexposed
- case is unexposed, control is exposed
- can learn something about exposure and disease
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)