Session #4 Flashcards

1
Q

observe the outcomes without intervening to affect them

A

obervational studies

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2
Q

the researcher manipulates the exposure (usually the drug or treatment) to compare it to the standard of care

A

experimental studies

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3
Q

what are three examples of obervational studies?

A
  • cohort studies
  • case-control studies
  • cross sectional studies
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4
Q

how are ppl in cohort studies selected?

A

based on their exposure status

*cohort studies follow participants in time

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5
Q

what is a prospective cohort ?

A

compares disease prevalence in the exposed and unexposed

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6
Q

what is a retrospective cohort

A

begin with the exposure of interest and probe back for exposure information

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7
Q

what are the main advantages for cohort studies?

A
  • good for RARE EXPOSURES (not diseases)
  • good for calculating INCIDENCE among exposed and unexposed
  • -can study multiple diseases
  • -minimize error
  • -maintains temporal sequence
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8
Q

what is the main disadvantage to cohorts?

A

inefficient for RARE DISEASES (good for exposures)\

-long follow up

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9
Q

how are subjects selected for case-controlled studies?

A

-subjects are selected based on their disease status

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10
Q

in case-control studies, cases and controls should be different only in what regard?

A

past exposure

*theoretically, these should mimic cohort studies

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11
Q

what can case control studies demonstrate?

A

risk indicators and not risk factors due to retrospective nature of the study design

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12
Q

how are case-control studies set up?

A

the exposure has to be assessed RETROSPECTIVELY and the proportions of cases and controls who are exposed are unknown at the beginning of the study

*cases and controls must have had an EQUAL CHANCE OF BEING EXPOSED

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13
Q

what is the main advantage for case-control studies?

A
  • good for rare DISEASES
  • good for long latency periods
  • not expensive
  • can evaluate multiple exposures
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14
Q

what is the main disadvantage for case-control study?

A
  • not good for RARE EXPOSURES

- cannot DIRECTLY compute incidence of disease in exposed and non-exposed persons

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15
Q

how are cross-sectional studies set up?

A

-selection of subjects based on neither exposure or disease status

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16
Q

how are cross-sectional studies set up?

A
  • most basic study design
  • “point-in-time” or “snapshot” info
  • subject selected without regards to exposure or disease status
  • does not need explained etiologic objectives
17
Q

what are the advant of cross sectional

A
  • sampling and analytic methods provide for statstically valid inference to populations
  • exposure and disease are assessed at the individual level
18
Q

what is the purpose of randomization in RCTs?

A

to minimize confounding variables

  • to create groups that are not determined by another factor other than by chance
  • to minimize confounding (known and unknown)
19
Q

what is the purpose of blinding?

A

to remove bias or systematic error

20
Q

what is informed bias?

A

drawing different conclusions depending on their knowledge of which study arm particular participant is in

21
Q

selection bias

A

study recruiters can be eager to recruit “sick ppl” into experimental arm

22
Q

what is the difference btw systematic reviews and meta analysis?

A
systematic = complete summary
meta-analysis = combined analysis of data from different studies