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rank
order of disease occurrence
count
number of persons who have a given disease
ratio
numerator not necessarily included in denominator
proportion
numerator is necessarily included in the denominator
point prevalence
proportion of a population that has a disease at a specific point in time
period prevalence
proportion of a population that had a disease at any time during a specified period, including pre-existing and new cases
person-time
time each person was observed
observational studies
individuals are followed in real-world settings
no intervention/exposure assignment by researcher
descriptive observational studies
describe occurrence of an outcome
case reports
detailed presentation of 1 case
case series
detailed presentation of 2 or more cases
cross-sectional study
surveys exposures and/or outcomes at a single point in time
descriptive cross-sectional study
examines patterns
measures prevalence not incidence
analytic cross-sectional study
measure association between exposure and disease
temporal sequence of exposure and outcome impossible to determine
odds
ratio of the number of ways the event can occur to the number of ways the event cannot occur
OR > 1
exposed group have higher odds of outcome compared to unexposed group
OR = 1
no association
OR < 1
exposed group have lower odds of outcome compared to unexposed group
cohort study
observational, analytic study
starting point is exposure
cohort
group of persons with common defining characteristic
RR > 1
association: exposed group have higher risk of outcome than unexposed group
RR = 1
no association
RR < 1
inverse association: exposed group have lower risk of outcome than unexposed group
population
who we want to learn about
sample
who we will study
case-control study
observational, analytic study
starting point is outcome (i.e. disease)
cases
individuals with outcome or disease
controls
individuals without the outcome or disease
experimental studies
evaluate specific intervention (exposure)
assign study groups
create a controlled environment such that the only thing that is different between study groups is exposure status
randomized
assignment to study groups is by chance
not under control of investigator
non-randomized
assignment to study groups is under control of investigator
randomized controlled trials
experimental study to assess the efficacy of an intervention in humans
efficacy
ability to achieve a desired effect under highly controlled conditions
effectiveness
do interventions work in circumstances that reflect real-world practice
concealment of allocation
procedure to protect the randomization before patients are entered into a trial
blinding
masking of the allocation after randomization of patients
single-blinded
patient does not know which study group they are allocated to
double-blinded
patient and researcher do not know which study group patients are allocated to
internal validity
how well was the study conducted?
external validity
how applicable are study findings?
confounding
confusion, or mixing, of effects; the effects of the exposure is mixed together with the effect of another variable, leading to distortion of the measure of association
confounder
some other factor that also associated with the outcome
stratified analysis
analysis according to strata (groups) of a factor/characteristic of participants