Evidence based medicine Flashcards

1
Q

Define Evidence based medicine

A

The use of mathmatecal estimates of the risk of benefit and harm, derived from high quality research of population samples, to inform clinical descision-making in the diagnosis, investigation or managemnet of individual patients.

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2
Q

Describe the differences between observational and experimental studies

A

Observational studies are also called analytical studies, they can show and association between one variable and another and aim to identify causality.

Where as experimental studies (interventional studies are where a new treatment or intervention is trialed.

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3
Q

Name and describe the type of observational studies used

A

Cohort study- looks for causality
Case control stuyd- looks for causality
Cross-sectional/longitudinal studies- useful for looking at trends.

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4
Q

Define what bias is

A

Any trend in the collection, analysis, interpretation, publication or review of data that can lead to conclusions that are systemically different from the truth

This is a systematic deviation from the truth in one direction.

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5
Q

What is an error?

A

This is different from bias as errors occur randomly and bias is systematic

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6
Q

WHat is a confounding factor?

A

A factor that is associated with both the exposure of interets and the outcome of interest.

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7
Q

What is selection bias?

A

Sample does not represent population

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8
Q

What is detection bias?

A

Observations in treatment group pursued more than control group

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9
Q

What is observer bias?

A

Subjectivity of observer, variance in their decisions

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10
Q

What is recall bias?

A

Patients know which group they are in and may be more likely to report symptoms

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11
Q

What is response bias?

A

Patients enrolling themselves/self-selecting

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12
Q

What is publication bias?

A

Positive trials are more likely to be published.

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13
Q

Define incidence

A

The number of new cases of disease in a population, in a given time period, also known as the occurence rate. Usually reported as a percentage
Helps us to understand the risk of disease

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14
Q

Define prevelence

A

The total number of cases of a disease in a population, either in a time period or at a specific point in time.

Prevelence helps us to understand the burden of disease

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15
Q

What is a cohort study and when is it used?

A

A cohort of people are studied based on exposure and followed up to evaluate an outcome of interest.

The can be prospective or retrosepctive

Adv: incidence can be calculated in exposed and non-exposed individuals, multiple outcomes can be studied, bias less of an issue than in case-control studies

Disadv: requires large populations and take a long time (years) to do so are expensive

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16
Q

Explain what relative risk is

A

(outcome measure in cohort studies)

Risk in exposed group/ risk in unexposed group= RR

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17
Q

What is a case control study?

A

A comparision between individuals with a disease (outcome) of interest (cases) ad those without the disease of interest. The cases and controls are each assessed to determine if they have had exposure to the variable of interest.

Almost always retrospective

Adv: smaller sample sizes generally required, quicker reults, cheaper

Disadv: more prone to bias, can be difficult to prove causation, not possible to calcaulate incidence, selecting controls can be difficult, particulalry prone to recall bias

18
Q

Define what odds ratio is

A

The ratio of odds of exposure of those with the outcome to those without the outcome

If it is 1 this suggests there is no difference is odds of exposure between the 2 groups

19
Q

What is a cross-sectional study?

A

Looks at the outcome and exposure in a ppulation or an individual at a specific point in time- they look at a cross section of society.

If a cross sectional study is repeated multiple time in succession then this is a longitudinal study.

They both look at trends in a population. The CAN’T look for causality.

20
Q

Give examples of types of intervention trails

A

The randomised controlled trail (RCT)- this is the gold standard, these have little chance of bias but are time consuming and expensive

21
Q

What does single blind mean?

A

Patients don’t know which treatment they are taking (e.g. in an RCT)

22
Q

What does double blind mean?

A

Neither the patients or the clinical/scientists involved in alaysis know which treatments they are on.

23
Q

What is a systematic review?

A

A review of a clearly formulated question that used systematic methods to identify, select and critically appraise relevant research and to collect and analyse data from the studies that are included in the review.

24
Q

What is meta-analysis?

A

The data/statistical part of a systematic review. Pulls together data from individual studies and analyses this. The data is usually presented in a forest plot.

You can have a systematic review without a meta-analysis.

25
Q

What are the highest and lowest levels of evidence?

A

Highest: 1++ high quality meta-analyses, systematic review of RCTs or RCTs with very low risk of bias

Lowest: 4 expert opinion

26
Q

What does an A grade of recommendation mean?

A

At least one meta-anlysis, systematic review or RCT rated as 1 ++ and directly applicable to the guidelines target population or a body of evidence composed or studies rated as 1+ and with an overall consistency among them

27
Q

What does a B grade of recommendation mean?

A

A body of evidence composed of studies rated as 2++, directly applicable to the guideline’s target population and demonstrating overall conistiency among them or evidence extrapolated from studies rated as 1++ or 1+

28
Q

What does a grade C of recommendation mean?

A

A body of evidence composed of studies rated 2+ directly applicable to the guideline’s target population and demonstrating overall consistency among them, or evidence extrapolated from studies rated as 2++.

29
Q

What does grade D of recommendation mean?

A

Level of evidence 3 or 4 or evidence extrapolated from studies rated as 2+.

30
Q

What are the Bradford-Hill criteria for causation?

A

Strength of association- e.g. statistical significance
Consistency- mulitple different studies using different populations, locations and methods show the same association then causality is more likely.
Specificity- exposure causes only one disease
Temporality
Biological gradient
Plausibility
Coherence
Experiment
Analogy

31
Q

What does the criteris consistency mean?

A

Consistency- mulitple different studies using different populations, locations and methods show the same association then causality is more likely.

32
Q

What does the criteria strength of associated mean?

A

Strength- the larger the magnitude and if the study is statistically significant then causality is more likely.

33
Q

What does the criteria specificty mean?

A

Used to mean exposure causes only one disease but not is less relevant as we know rather than A causing B it tends to be a combination of A,C,D and E having a part in increasing the risk of B

34
Q

What does the criteria temporality mean?

A

Exposure must proced the onset of disease

35
Q

What does the criteria biological gradient mean?

A

Dose-response raltionship, this strongly suggests causality

36
Q

What does the criteria plausibilty mean?

A

Existsing modles explain how exposure causes disease.

37
Q

What does the criteria coherence mean?

A

similar to Plausibility

The association should make overall sense

38
Q

What does the criteria experment mean?

A

Manipulation of exposure should effect disease/outcome

39
Q

What does the criteria analogy mean?

A

When one causal agent is known, standards of eveidence are lowered for a second agent that is similar.

40
Q

What is the audit cycle?

A
  1. preparing for audit
  2. selecting criteria and standards
  3. measure what is happening now and report on
  4. make improvements
  5. sustain improvement and re-aduit

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