Study Designs Flashcards

1
Q

Define epidemiology

A

Study of how often disease occurs in diff grps of ppl + y

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2
Q

What’s another way to say:
-disease occurrence
-risk factors
-disease prognosis

A

-Disease prevalence
-protective factors
-disease outcomes

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3
Q

Observational studies ?
What investigators do/don’t ?

A

-question , observe, measure diff factors, record results
-no change or intervention w participants’ lives

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4
Q

Intervention studies?
Investigators do/don’t?
Another name?

A

-intervention in pre-planned way (e.g. new treatment) - result recorded
Aka experimental studies

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5
Q

3 types of observational studies ?

A

Cross-sectional
Case-control
Cohort

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6
Q

2 types of intervention ?

A

-non-randomised
-randomised controlled trial (RCT)

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7
Q

2 things that strength of evidence depend on?

A

Study design + quality

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8
Q

Define exposure

A

Risk / protective factor

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9
Q

Cross-sectional study ?
2 types of samples?
2 uses?

A

Sample from defines pop is surveyed - ‘snapshot’ - all factors (exposure/outcome) measures at one point in time.

-representative or random ?

-asses association between exposure and outcome / asses prevalence of disease

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10
Q

Pros(2) and cons(2) of cross-sectional study ?

A

-cause and effect relationship hard to determine so not strong evidence
-evidence distorted by confounding factors
-quick
-inexpensive

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11
Q

Cohort study is what? Used to do what?

A

-group selected - exposure status measures - follow up to see who develops disease outcome

-occurrence in exposed vs unexposed

  • assess to association between exposure vs outcome
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12
Q

Cohort studies are 1) longitudinal and 2) prospective … this means what?

A

1) tracking people over time
2) Following people forward into the future

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13
Q

What are confounding factors?

A

factors that affect both disease exposure and outcome, and can distort results.

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14
Q

Pros (1) and cons(4) of cohort studies.

A
  • we know exposure comes before disease , so stronger evidence for cause/effect relationship vs cross-sectional
    -large numbers needed
    -not feasible for very rare diseases
    -time consuming + expensive due to large no.s + follow up
    -association distorted by confounding factors (same w all observational studies)
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15
Q

What’s a case-control study ? Why is it used ?
How is it carried out?

Which group is ‘case’ or ‘control’

A
  • select group of ppl w/ or w/out outcome disease , then previous exposure status found - compared between 2 groups

-used to find association between exposure and outcome

Case = w disease outcome
Control = w/out disease outcome

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16
Q

Pros(2) and cons (4) of case control study?

A

-can’t measure risk or prevalence of disease , and we decide no. In each group
- have to use ‘odds’ ration to assess association
-ideal for rare disease
-less expensive and quicker than cohort - smaller no.s and no follow ups
-potential recall error or bias
-association may be distorted w confounding factors

17
Q

Pros(2) and cons (4) of case control study?

A

-can’t measure risk or prevalence of disease , and we decide no. In each group
- have to use ‘odds’ ration to assess association
-ideal for rare disease
-less expensive and quicker than cohort - smaller no.s and no follow ups
-potential recall error or bias
-association may be distorted w confounding factors

18
Q

Does systematic review of observational studies eliminate the issue w confounders?

A

No

19
Q

When and how can we deal w confounders

A

At analysis stage
-use adjusted analysis
-statistical model ( tells us to what extent confounding factors affected results)

20
Q

What’s an RCT? Used for what ?

A

-used to find impact of intervention on outcome
-participants recruited - fit criteria - give informed consent
-participants randomised to either intervention or control
-follow up - RCT longitudinal and prospective
-incidence compared in both groups

21
Q

Disadvantage of RCT ethically

A

Everyone wants/ needs intervention .
Ensure that everyone eventually get intervention , but control get it after study so it doesn’t affect outcome.

22
Q

What’s good about randomisation

A

Ensures similar baseline characteristics of men in both groups

23
Q

RCT’s have high or low confounders? Why?

A

Low- due to randomisation

24
Q

1 pro of RCT and 3 cons

A
  • Strongest evidence for cause and effect relationship
  • large number sneezed- time and money consuming
    -can’t be used to study exposures that can’t be changed
25
Q

What’s a systematic review of RCTs

A

All RCTs in topic identified - evaluated and results summarised - like meta analysis

26
Q

Is it better than systematic review for observational studies ? Why?

A

Yes - confounders minimised w randomisation.