2 Epidemiology Study Designs Flashcards

1
Q

A hypothesis usually takes the form

A

Exposure X is associated with an increase/decrease risk of outcome Y.

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2
Q

2 types of error

A

systematic error (referring to bias)

random error (referring to imprecision).

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3
Q

what is bias

A

systematic error or derivation from the truth of results

due to incorrect measurements or non-representative sample.

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4
Q

Selection bias

A

allocation of subjects not representative of whole population. Controlled by randomisation with concealment.

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5
Q

Performance bias

A

performing intervention different for different patients, results are not controlled. Controlled by double blinding, use of placebo.

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6
Q

Detection bias

A

Evaluation of outcomes is different between groups. Controlled by blinded outcome assessment that doesn’t pinpoint only one group.

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7
Q

Measurement/observation/information bias

A

systematic error of poor measurement of outcomes. Controlled by review of measurement tools.

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8
Q

Recall/responder bias

A

inaccurate responses/recalled. Controlled by a good study design.

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9
Q

Attrition bias

A

different flow up between groups, + drop outs. Controlled by analysis of subjects as randomised.

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10
Q

What is confounding

A

non-causal association observed due to third variable.

describes an association that is true but potentially misleading.

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11
Q

How can confounding be controlled

A

design phase:
randomising
restricting
matching parts of the population.

analysis stage:
stratification of results
adjusting by statistical modelling.

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12
Q

Explain reliability

A

Reliability tools measure accurately and consistently. = PRECISION

Test-retest reliability: results consistent by measuring twice.

Inter-rater reliability: assesses the degree of agreement between judges.

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13
Q

Explain validity

A

refers to the legitimacy of the research = ACCURACY

Internal validity: correct results for group studied

External validity: generalisable results

Construct validity: test measure what it claims to be measuring

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14
Q

Case study

A

Reports observations of single individual, case series is an aggregate.

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15
Q

Ecological study

A

looks at groups of people rather than individuals.

Compares disease frequencies between different populations at 1 time or 1 population at different times.

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16
Q

Cross-sectional study

A

Also called a prevalence study

measures prevalence and presence/absence of exposure.

only 1 point in time no past/future

17
Q

Case-control study

A

1 group has disease other does not, look back and determine how many from each group had the risk factor.

Retrospective

Uses O.R

18
Q

Cohort study

A

Comparison of groups of people who share common characteristics within a define time period

Prospective = see who develops

Retrospective = exposure and outcome already occurred

Uses R.R

19
Q

RCT

A

Patients randomly allocated to treatment and control group, compare outcomes due to intervention

Randomisation controls for confounding by distributing confounders evenly

20
Q

Cross over trial

A

normal RCT, washout period, then swap intervention and controls groups.

21
Q

n of 1 trial

A

cross over trial with only one patient

22
Q

Cluster of RCT

A

Unit of measure is not an individual but a group. Often used in communities where there is a risk of contamination

23
Q

What is a systematic review

A

answers a defined research question by summarising evidence of eligibility criteria.

24
Q

What is a meta analysis

A

statistical methods to summarise results of studies

25
Q

Narrative review

A

broad
author can use literature to support view point
limited critical appraisal

26
Q

characteristics of systematic review

A

minimise bias
answers question
summary of data
regularly updated.

27
Q

Steps of a meta analysis

A
  1. Formulate structured clinical question
  2. Conduct extensive search documenting search strategy
  3. Select studies for inclusion, justify exclusion
  4. Assessment of methodological quality of including studies
  5. Abstraction of relevant data
  6. Data synthesis (meta-analysis)
28
Q

Describe blinding

A

people are unaware of which trial group the participants are in.

minimise performance and detection bias such as the care that is provided to the comparison groups.