Analytical Studies Flashcards

1
Q

Case control design

A
  • retrospective
  • group of cases and controls (diseased and non-diseased)
  • then retrospective data on exposure to putative risk factors is collected
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2
Q

Causality

A

-Case control study is often the first step in suspected associations of causality

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3
Q

Advantages of case control

A
  • easy
  • less time consuming
  • less expensive
  • suitable for investigating rare diseases
  • subjects are not exposed to any new risks
  • several etiological factors for a single disease can be studied
  • no attritition problems
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4
Q

Disadvantages of case control studies

A
  • highly prone to selection and recall bias
  • control group selective may be difficult
  • incidence cannot be measured-so odds ratio only-no relative risk- can be measured
  • cannot prove causality
  • temporality is difficult to determine
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5
Q

Eligibility criteria

A

-key in case control studies

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6
Q

Power of case control

A
  • up to a ratio of 4:1 when the number of controls is increased, the power of a study increases
  • but not after exceeding the ratio
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7
Q

Odds ratio

A
  • estimates the risk of exposure
  • incidence rates aren’t available so relative risk cant be used
  • if the condition is very rare then odds ratio approximates the relative risk
  • can have values between 0 and infinity but no negative values
  • log transformations are needed to calculate confidence intervals
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8
Q

Cohort study

A
  • a cohort is a group of persons sharing a common aspect

- examples are birth cohort or exposure cohort

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9
Q

Inception cohort

A

-a group of patients who are assembled at a single point of time based on a common factor

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10
Q

How does a cohort study work?

A
  • exposure cohorts are followed up in parallel with a non-exposed group to detect the development of a disease
  • the disease is yet to occur when the study starts
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11
Q

Cohort study basic requirements

A
  • easily obtainable, cooperative and stable cohort that can be followed up as needed
  • non-exposed control cohort must be comparable to the study cohort in all aspects except the exposure
  • they must not have the disease at the time of inception into the study
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12
Q

Controls in a cohort study

A
  • Can be internal control or external control
  • internal controls are a subgroup of the exposure cohort
  • retrospective cohort is allowed
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13
Q

Relative risk in cohort studies

A
  • can be calculated as the ratio of the disease (outcome) in the exposed to the disease in non-exposed
  • odds ratio can also be calculated
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14
Q

Disadvantages of cohort study

A
  • time consuming and difficult
  • not suitable for rare diseases
  • only one etiological factor can be studied at a time
  • attrition/drop out is a major issue
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15
Q

Advantages of cohort study

A
  • less prone to selective and recall bias
  • incidence can be measured so relative risk can be measured
  • causal association can be strongly supported compared to case-control
  • temporality is established easily
  • multiple effects o a single exposure could be observed
  • dose response relationships could be calculated
  • natural course of exposure to disease pathway be studied in addition
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16
Q

Nested case-control study

A
  • a study in which both the cases and controls are drawn from within a cohort rather than including the entire cohort population in the study
  • much cheaper but with the same findings
  • case control studies can also be nested within study designs such as cross-sectional studies