Lecture 7, part 2 Flashcards

1
Q

What are sources of exposure info?

A

Pre-existing records
Self-report
Physical/biological observations

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2
Q

Examples of pre-existing records

A

Medical records
Insurance records
Employment records
Vital stats
Tax or property records

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3
Q

Advantages of pre-existing records

A

Inexpensive
Relatively easy to work with
Usually unbiased since data were collected for non-study purposes

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4
Q

Disadvantages of pre-existing records

A

Exposure info may not be precise enough to address the research question
Records frequently do not contain data on potentially confounding factors

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5
Q

Examples of self-report

A

Interviews
Surveys
Diaries

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6
Q

Advantages of self-report

A

Opportunity to question subjects on as many factors as necessary
Good for collecting info on exposures not routinely recorded

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7
Q

Disadvantages of self-report

A

Rely on participants’ ability to know and recall info
Potential response bias due to stigma, response expectations, observation, etc.
Participants may not be sufficiently aware of their exposure status

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8
Q

Examples of physical/biological observations

A

Physical exams
Lab tests of biological specimens
Environmental monitoring

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9
Q

Advantages of physical/biological observations

A

Biomarkers of exposure often more objective
Allow ascertainment of internal dose/exposure
Higher quality data

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10
Q

Disadvantages of physical/biological observation

A

Can be invasive and expensive to collect
Appropriate lab tests may not be available
May be subject to bias if interpretation or clinical observation is influenced by exposure

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11
Q

______of the exposure is crucially important

A

Timing

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12
Q

Relevant etiologic period defintion

A

Time during which an exposure will affect dz occurrence

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13
Q

How should study design be grounded?

A

In knowledge of natural hx of dz as well as hypothesized biological mechanism

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14
Q

What should be considered in terms of f/u?

A

Length required to observe the outcome of interest

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15
Q

Induction period definition

A

Interval between causal action and dz initiation

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16
Q

Latent period definition

A

Interval between dz onset and detection

17
Q

What should be considered to determine the length of f/u?

A

Minimum latency
Maximum latency

18
Q

Minimum latency considerations

A

How soon can dz result after exposure has first occurred

19
Q

Maximum latency considerations

A

Once exposure has ceased, when does the alteration in risk disappear (if at all?)

20
Q

Characteristics of good measurement of outcome

A

Should be as precise and objective as possible

21
Q

What types of measurements of outcome are possible?

A

Categorical
Continuous
Dichotomous

22
Q

What should be be done in measuring outcome when the measures are weaker/more subjective?

A

Use triangulation, or supplement

23
Q

Sources of outcome data

A

Self-report
Employee records
Medical/pharmacy/insurance records
Physical exams/blood testing
Death or dz registries
Multiple sources

24
Q

Definition of information bias

A

Systematic error in the measurement of the exposure and/or outcome

25
Q

Key characteristics of information bias

A

Occurs after participants have entered study
Pertains to how data are collected
Can bias results away or toward the null
Can occur in any type of study design

26
Q

What is the most common type of information bias?

A

Misclassification bias