Evidenced-based Dentistry Flashcards

1
Q

What are the advantages of a sytematic review compared to a single study

A
  • Saves readers time
  • Provides reliable evidence
  • Resolves inconsistencies – single studies brings all these conflicting studies together
  • Identifies gaps
  • Identifies where questions have been fully answered and it is unethical to conduct anymore studies
  • Explores differences between studies – identifying factors that influence the effect of an intervention
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the importance of systematic reviews

A
  • Reduce large quantities of info into manageable portions, makes it easy for professionals to access research
  • Formulate policy and develop guidelines - guidelines are based on these
  • Efficient use of recourses – studies have already been done
  • Increased power and precision - small studies alone don’t mean much but pulled together, it gives greater power in estimates
  • Limit bias and improve accuracy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is a process of systematic review

A
  • Authors – two or more authors, one is a topic expert and the other methodological
  • Study protocol – in advance set out what they plan to do methodologically
  • Create a specific question using PICO
  • Search strategy
    o Using multiple electronic databases
    o Include published and unpublished literature
    o Ensure search is both comprehensive and repeatable
  • Inclusion/exclusion
    o Specific
    o Agreed in advance
  • Critical appraisal
    o Thorough
    o Assess for risk of bias
  • Synthesis
    o Can be qualitative (narrative) or quantitative (meta-analysis)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are the key characteristics of a systematic review

A

o well formulated question
o comprehensive data search
o unbiased selection and abstraction process
o assessment of papers
o synthesis of data

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

How do we produce a well formulated question

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

PICO

What is meant by participants

A

who is the review looking at

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

What is meant by interventions

PICO

A

What is the px being exposed to

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

What is the comparison

PICO

A
  • control group
  • what will the intervention be compared to
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is outcome

PICO

A

which outcome will tell you which intervention is most effective

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

What do we define the inclusion/exclusion criteria based on

A

the question
PICO

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

What should we consider using when doing the comprehensive data search

A

o Electronic Databases
o Reference lists
o Hand searching
o English language/non-english language
speak to librarians for help

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

What are the different reporting bias

A

positive results are more likely to be
o Published – publication bias
o Published rapidly – time lag bias
o Published in English – language bias
o Cited by others – citation bias

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

How do we conduct an unbiased selection and abstraction process

A
  • Select relevant papers
  • Data extraction to a predefined data extraction form
  • Process should be conducted independently by at least 2 reviewers
  • Clear description of reasons for exclusion
  • Adequate description of included studies
  • Details of studies funding source
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

How do we assess the papers

A
  • How well the studies have been designed and conducted – methodology
  • Process should be conducted independently by at least 2 reviewers
  • Results of the assessment should be reflected in the analysis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What can the assessment of papers be used as

A

o as a threshold for inclusion of studies
o as a possible explanation for differences in results between trials
o in sensitivity analyses
o as weights in statistical analysis of results

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

What are the 2 main quality assessment tools in the assesment of papers

A

composite scales
component approach

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is composite scales

A

assign numerical value to individual items to provide overall estimate of quality

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is a component approach

A

assess relevant methodological aspects individually e.g randomisation, blinding, dropouts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Why is the component approach preferred to the composite scale

A

more specific in the downfalls of the studies
don’t know the specifics of what made the study unreliable in the composite scale

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What does the risk of bias assessment consist of

done as part of the assessment of papers

A

o determines extent to which results of study can be believed
o direction of bias: causes overestimation or underestimation of effect
o magnitude of bias

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What aspects of methodology does a risk of bias assessment for RCT consist of

A

Random sequence generation (selection bias)
Allocation concealment (selection bias)
Blinding (outcome assessors)
Incomplete outcome data (attrition bias)
Selective outcome reporting (reporting bias)
Other bias

22
Q

What is a variation in risk of bias be an explanation for

A

heterogeity between results of different studies
significant risk of bias in included studies should give rise to cautious conclusions in a systematic review

23
Q

What are the two types of data synthesis

A

qualitative - narrative
quantitative - metanylsis

24
Q

When is meta-analysis inappropriate

A

when not enough data or heterogeneity exists

25
Q

What is meta-analysis

A
  • This is the process of using statistical methods to combine the results of different studies
26
Q

What are the aims of meta-analysis

A
  • Aim is to integrate findings, pool the data and identify overall trends in results
    o Calculates a treatment effect based on pooled data from a group of studies
    o Estimates a common tx effect across studies
    o Improves precision of a point estimate by using all available data
27
Q

What are the advantages of meta-analysis

A

o increase in power
o improvement in precision
o ability to answer questions not posed by individual studies

28
Q

What are the disadvantages of meta-analysis

A

potential to mislead, need to be careful when it is undertaken

29
Q

When should meta-analysis be undertaken

A

o minimal differences in characteristics across studies
o same outcome measure
o data in each study is available

30
Q

What are the 2 different types of data

A

dichotomous
continous

31
Q

What is dichotomous data

A

1 out of 2 forms
e.g death or no death

32
Q

What are the choices of summary statistics for dichomotous data

A
  • odds ratio
  • risk ratio
  • percent risk reduction or relative risk reduction
  • risk difference or absolute risk reduction
  • number needed to treat
33
Q

What are the summary statistic choices for continous

A
  • weighted mean difference
  • standardised mean difference
34
Q

When is more weight given to a study

A

o more participants
o more events
o lower variance

35
Q

How can results be displayed graphically

A

forest plot

36
Q

Describe the different features of a forest plot

A
  • Horizontal line at bottom is the scale measuring tx effect
  • Vertical line in the middle si where tx and control have same effect and there is no different between the two
  • For each study there is an ID, data is then divided into the experimental and control group, a weight is given
  • There is then a label above the graph to tell you what ratio has been used and the data is shown using a line and also numerically
  • Each study has a blob which is placed where the data measure the effect
  • The horizontal line running through the blob is called a confidence interval and is a measure of how we think this result may vary with chance
  • The wider the line is, the less confident and if it overlaps the vertical no effect line, then insufficient evidence to support a difference in the two interventions
37
Q

What are the 3 types of heterogeneity

A
  • clinical
  • methodological
  • statistical
38
Q

What is clinical heterogenity

A

the way study has been conducted
variation in participants, interventions, outcomes, study design
e.g age, baseline disease severity, dosage etc

39
Q

What is methodological heterogeneity

A

Variation in methods used
* Variations in study design and risk of bias
* e.g use of allocation concealment

40
Q

What is statistical heterogeneity

A

Excessive variation in results of studies

Variation in the intervention effects being evaluated in the different studies and is a consequence of clinical or methodological diversity

Manifests itself in the observed intervention effects being more different from each other than one would expect due to chance alone

41
Q

How do we identify heterogeneity

A

o if studies are estimating the same thing, we would expect confidence intervals to overlap to a large extent
o statistical heterogeneity may appear in a forst plot as poor overlap of confidence intervals
o Chi squared test
o P<0.1 demonstrates statically significant heterogeneity and then it may be inappropriate to pool data
o I2 statistic is the percentage variation due to heterogeneity rather than chance and <50% is acceptable

42
Q

What is subgroup analysis

A
  • Studies divided into sub groups
  • Should be decided in advance, not after seeing data
  • Done where it is suspected in advance that certain features may alter the effect of an intervention
43
Q

What is the main aim of subgroup analysis

A
  • The main aim of a subgroup analysis is to identify either consistency of or large differences in the magnitude of treatment effect among different categories of patients.
44
Q

What are examples of subgroups that could be utilised in subgroup analysis

A

o gender
o age groups
o specific disease subtypes

45
Q

What is sensitivity analysis

A

Repeating metaanalysis
.g if some studies eligibility is dubious due to a lack of full details: run the metaanalysis the first time using the dubious studies and the second time using the non-dubious studies
* Need for sensitivity analysis usually decided in review process but can be predecided in the protocol

46
Q

What info can the sensitivity analysis give us

A
  • When sensitivity analyses shows that the overall result and conclusions are not affected by the ‘dubiosness’ then the results can be regarded wit a higher degree of sensitivity
  • On the other hand, it may show that the missing information from these dubious studies has a large impact on results and so the search for the missing info can be undergone e.g contacting trial authors
47
Q

What is the fixed effect

A

o Assumes studies are so similar that they are effectively different parts of one large study
o Assumes that the true answer for each study is the same
o If I2 <50% (heterogeneous) then can use this model of meta-analysis

48
Q

What is the random effect

A

o Assumes studies are slightly different
o Assumes that the true answer for each study will be slightly different
o More conservative/wider CI
o If I2 >50% then can use this model of meta-analysis

49
Q

What is GRADE

A
  • Used to estimate certainty of evidence
    o high
    o moderate
    o low
    o very low
50
Q

What are the 5 factors that can lower the quality grade

A

o high or unclear risk of bias – due to design issues or poor conduct of studies
o inconsistency between studies – heterogeneity
o indirectness – pico
o imprecision – numbers and CI
o publication bias – likely that negative/null results not published