10.2: Observational Studies ✅ Flashcards

1
Q

Cross-sectional studies: characteristics

A

1) Descriptive

2) Analytic

-Random sample taken from the source population
-All assessments happen at a specific time point
-Exposure and outcome are assessed simultaneously
-Mostly deal with the present
-Many countries have annual cross-sectional studies to assess health of the population (called surveys)

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2
Q

Descriptive

A

Assessment of only 1 variable at a time

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3
Q

Analytic

A

Assessment of association between 2 variables

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4
Q

Descriptive measures for Cross-sectional studies

A

Proportions (categorical)

Prevalence (binary categorical)

Mean/median (numeric)

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5
Q

Measures of association for Cross-sectional

A

Odds ratio (binary categorical)

Mean difference (categorical exposure vs numeric outcome)

Regression/correlation coefficient (numeric exposure vs numeric outcome)

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6
Q

Pros of Cross-sectional studies

A

Easy

Cheap

Gives the opportunity to readily assess the prevalence of disease in a population

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7
Q

Cons of cross-sectional studies

A

Observational design often leads to information bias
-as mostly self reporting

Prone to confounding
-as can’t assess all potential confounders

Impossible to assess risk of a disease (incidence)

Impossible to establish temporality in an association
-as exposure and outcome are assessed simultaneously

Not appropriate for inferring causality between an exposure and an outcome (high likelihood of reverse causation)

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8
Q

Case group

A

A group of patients with a specific disease

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9
Q

Control group

A

Random sample of individuals not suffering from the specific disease

-has to be recruited from the source population

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10
Q

Case-control studies: characteristics

A

Case group usually matched for key characteristics to eliminate confounding

Overmatching should be avoided and restricted to 2-3 factors
-rest should be adjusted at the analysis stage.

Final step involves assessment of a series of exposures in cases and controls which occurred in the past

Retrospective

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11
Q

Retrospective

A

Start with the disease and then look back in time for identification of exposures

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12
Q

Measure of association for Case-control

A

Odds ratio (categorical)

Mean difference (numeric)

*note: outcome is ALWAYS binary

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13
Q

Descriptive measures for Case-control

A

Never calculated

->only analytical

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14
Q

Pros of Case-control

A

Can investigate determinants of rare diseases

Easy to perform

Cheap

Possible to assess several exposures and potential confounders for a single outcome

Possible to investigate exposures that happened in the long past

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15
Q

Cons of case-control

A

Observational design, prone to information bias (measurements are based on self-reports)

Prone to recall bias
(assessments of exposures are based on self reports of events that happened many years back)

Very prone to confounding

If the control group is not a representative sample, can lead to selection bias

Impossible to assess the risk of disease

Difficult to prove the causality due to confounding and bias

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16
Q

Cohort studies characteristics

A

Random sample is selected from the source population

Before study, all participants suffering from the disease of interest are excluded

At the study baseline, all exposures of interest and potential confounders are assessed

Following this, participants continue to live normally and researchers record new cases of disease during follow-up

Ascertainment of disease cases occur from clinical examination, hospital or national registries or self reports in specific time intervals

In a follow up, reassessment of exposures to see if they have changed

Main aim is to investigate whether the risk of different diseases differs based on different exposures

Prospective due to time-lapse between exposure and outcome

17
Q

Descriptive measures of Cohort studies

A

Incidence (binary)

Mean/median (numeric)

*note: descriptive measures are rarely calculated in cohort studies

18
Q

Measures of association for Cohort studies

A

Risk ratio (binary categorical)

Rate ratio (binary categorical when person-years can be calculated)

Mean difference (categorical vs numeric exposure)

*note: Odds ratio could be calculated when the binary outcome is very rare

19
Q

Pros of Cohort studies

A

Can assess risk of disease
–> calculate relative risk

Can assess temporal associations

Can assess several exposures and outcomes so results are more valid

Can investigate risk factors for chronic diseases

Study samples are usually large, increases internal validity

20
Q

Cons of cohort studies

A

Observational design, so is prone to informational bias
(as measurements based on self reports)

Selection drop out can lead to risk of selection bias

Observational design = prone to confounding

Hard to assess risk of rare disease outcomes
(as a large sample would be required)

Difficult to prove causality due to possible bias and confounding, but easier than compared to other observational study designs