Module 4 part 1 Flashcards

(36 cards)

1
Q

what is Descriptive Epidemiology

A

‘Person, place and time’
* Observational, it is What
* Who
* Where
* When

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is Analytic Epidemiology

A

Associations: exposures
and outcomes.
Causation
* Observational or
intervention studies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are the 5 study types

A

Cross-sectional, ecological studies, Cohort studies, Case-control studies, Randomised-controlled trials

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what studies are Descriptive
epidemiology

A

Cross-sectional and ecological studies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What studies are Analytic
epidemiology

A

All 5 but mainly Cohort studies, Case-control studies, Randomised-controlled trials

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is a cross-sectional study?

A

Measures exposures and/or outcomes at one point in time

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What do cross-sectional studies
measure?

A

Prevalence: the proportion of a defined population who have a disease at a point in time

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Equation for prevalence

A

Prevalence = number of people with disease at a given point in time / total number of people in the population at that point in time

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Cross-sectional studies can be used to d______, C_______ and G______ H______

A

DESCRIBE ( EgWhat is the prevalence of osteoarthritis in NZ?), COMPARE ( E.g. What is the prevalence of
osteoarthritis in NZ for people of different ages?) and GENERATE HYPOTHESIS (E.g. Which factors are associated with low back
pain among nurses?)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Components of “The GATE frame?” used for Epidemiological

A

Population (source), Exposure/Comparison (exposed group and unexposed group) and Outcome ( positive or negative for certain disease.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Do Epidemiological and cross sectional studies show causation. Why?

A

No, because exposure and outcome are Measured at the same Time

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Limitations of cross-sectional studies? (4)

A

Temporal sequencing, Measures prevalence not incidence, Not good for studying rare outcomes or exposures, Not good for assessing variable and transient exposures or
outcomes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is prevalence vs incidence

A

Incidence is a measure of the number of new cases of a characteristic that develop in a population in a specified time period; whereas prevalence is the proportion of a population who have a specific characteristic in a given time period, regardless of when they first developed the characteristic.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Incidence proportion?

A

measures the probability of developing a disease or health event over a specified time ((Number of new cases during a specific time period) / (Number of people at risk during that same time period).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

why do cross-sectional studies? (strengths)

A

Can assess multiple exposures and outcomes, Can be less expensive than some other study designs, Relatively quick, Hypothesis generating

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what are Ecological studies

A

Compare exposures and outcomes across GROUPS not individuals

17
Q

What are ecological studies used for?

A

To compare between populations, To assess population level factors, To consider hypotheses

18
Q

Weaknesses of ecological studies

A

ecological fallacy (a logical error where inferences about individuals are made from group-level data.), doesn’t show causation,

19
Q

why do ecological studies?

A

Population level exposures, Consideration of hypotheses, May be relatively easy to do, May be relatively inexpensive

20
Q

What is Temporal sequence

A

the order in which events or data points occur over time.

21
Q

what are two Measures of
association

A

Relative (Relative Risk), Absolute
(Risk Difference)

22
Q

Relative risk, what does this tell us and calculation

A

“Null Value”. Ratio of the incidences, How many times as likely is the exposed group to develop the outcome than the comparison group? IExposed / IComparison = Relative Risk

23
Q

what is Absolute
(Risk Difference) and what is alternative name

A

“Attributable Risk” How many extra/fewer cases of the outcome in the exposed group are attributable to the exposure?
IE − IC

24
Q

Explain what is means if incidence of exposed group is 50% and incidence of control group is 25% in terms of absolute risk

A

50-25 therefor There were 25 extra cases per 100 people over one year of (outcome eg disease) in (exposed group) compared to (control group) but Report differently for incidence proportion and
incidence rate

25
Relative risk vs risk difference
Relative risk= Clues to aetiology (causes), Strength of association Risk difference= Impact of exposure, Impact of removing exposure Both are important
26
What is a cohort study?
“…individuals are defined on the basis of presence or absence of exposure to a suspected risk factor” exposed vs not exposed over time.... do they develop a certain outcome
27
Cohort studies step by step
1. Identify a source population, 2. Recruit your sample population (Sample population must not already have the outcome of interest), 3. Assess exposure to identify which group participants belong in (exposed or not exposed i.e. comparison, 4. Follow up over time and Observe whether or not participants develop the outcome
28
Ways to gather data from cohort studies?
Calculate measures of occurrence and measures of association
29
Two types of Measures of occurrence
Incidence proportion= Number of people who develop the disease in a specific period / Number of people at risk of developing the disease at the start of the period Incidence rate= Number of people who develop the disease in a specific period / Number of person-years at risk of developing the disease
30
Two types of measures of association (two types for both)
Relative risk (2 types: rate and proportion) 1. Rate ratio= IRE / IRC 2. Risk ratio = IPE / IPC Risk difference: IRE – IRC and IPE - IPC
31
Limitations of cohort studies
Potential for misclassification of exposures/outcomes, Time consuming, Can be expensive
32
Strengths of cohort studies
Determine temporal sequence between exposure and outcome, Can examine multiple outcomes from an exposure, Can calculate incidence (and therefore relative risk and risk difference), Good for studying rare exposures
33
Two types of Cohort studies
1. Prospective cohort studies 2. Historical cohort studies (Sometimes called retrospective cohort studies)
34
Difference between Prospective cohort studies and Historical cohort studies (it long)
Prospective cohort studies follow a group forward in time to observe outcomes from baseline, providing detailed, real-time data but requiring long follow-ups and risking loss to follow-up. Historical (retrospective) cohort studies use existing past data to look backward in time, identifying exposures and outcomes that have already occurred, offering speed and cost-efficiency but with less control over data quality and a higher risk of bias
35
Important tip (look up until you get it)
Make sure you understand the difference between historical cohort studies, case-control studies and cross-sectional studies
36