Extras Flashcards

1
Q

What are the (4) concerns with drawing conclusions from cross-sectional studies?

A

Reverse Causality

Confounding

Recall Bias

Can only study prevalence (not incidence!!)

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2
Q

What are the (5) strengths of prospective cohort studies?

A
  • Exposure collected before outcome known (no reverse causality)
  • Repeatd measurements of exposure
  • Can test hypothesies for >1 exposure
  • Selection bias unlikely (if selected from single group)
  • exposure unlikely to be biased as measured before outcome
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3
Q

What are the (6) weaknesses of prospective cohort studies?

A
  • Not possible ot assciate incidence/ris of outcome (when not collected at baseline)
  • exposure self reported (not objective)
  • long periods of time for rare outcomes (costly)
  • loss to follow up bias (i.e. smokers may be more likely to drop out over time than non smokers)
  • very low response rate = may not represent population of interest
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4
Q

Why is it useful to have both the adjusted and non adjuste results (confounders)?

A

COMPARE
See how strongly associations were confounded by the variable included in the adjustment

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5
Q

When describing a confidence interval what must you say?

A

State exposure

Increase/decreas in risk

State outcome

When compared to baseline (state)

CI not overlapping 1 = associated with increase/decrease but overlapping 1 = no association

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6
Q

How can authors check whether subjects included in their analysis were representative of the population of interest?

A

Compare prevalence of outcome & exposure with national data

OR
Compare with subjects recruited at baseline & subjects included in the analysis

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7
Q

What is the main requirement when selecting a sample from a population?

A

Should be selected at RANDOM to ensure they are representative of the target population

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8
Q

What is Meta-analysis?

A

A statistical technique for combining the estimates of exposure-outcome association for >1 study weighting accoridng to the size of the study

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9
Q

What type of bias may distort meta analysis?

And in what way are the results usually affected by this type of bias?

A

Publication bias

usually = over-estimatinbg size of association between exposure and outcome

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10
Q

What is the most appropriate way to summarise location and variablility of non-normally distributed data?

A

Median

IQR

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11
Q

Explain what is meant by intention to treat analysis:

A

Subjects are analysed in the groups to which they were randomised regardoless of whether they adhered to their allocated treatment or not & any lost to follow up

Why?? To remove confounding & bias

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12
Q

Why is the intention to treat analysis preferred for randomised controlled trials?

A

Treatment and control groups are only truely comparable at the point of randomisation (otherwise introduce confounding & bias)

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13
Q

What is ecological fallacy?

A

The asumption that average characteristics for populations apply to individuals

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14
Q

How may ecological fallacy affect the interpretation of study findings?

A

Incorrect conclusions may be drawn

Strength of association may be over or under estimated

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15
Q

What is ordinal?

A
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16
Q

What is nominal?

A
17
Q

If diff %’s in loss to follow up in treatment and control groups what is the implication?

A

Loss to follow up bias may affect results

18
Q

What is assumed about patients lost to follow up?

A

They still smoke/ do not adhere to treatment

19
Q

What does the power calculation show?

A

Work out how many patients would be required in each group to demonstrate differences between them

20
Q

What is the null risk ratio?

What does a risk ratio of 5, 3 & 11 mean?

A

Null = 1

5 = 5 X higher risk

3 = 3 x higher risk

11 = 11 x higher risk

n.b. always round decimals up or down

21
Q

When describing which study design is ideal what should you say?

A
  • RCT is top of the heirachy
  • BUT not suitable if exposure cannot be randomly assigned/is unethical
  • Cohort is next in heirachy
  • BUT if outcome is rare = too long & expensive
  • Case-controls are next in the heirachy