Paper 1 Flashcards

1
Q

Describe evidence based dentistry

A

Use of best current available scientific evidence to make clinical decisions about the care of individual patients

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2
Q

6 uses of evidence based dentistry

A

Determining causes of dental disease
Diagnosis
Treatment
Prevention
Examine quality of care reported by patients
Economic tool

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3
Q

5 steps in the practice of evidence based dentistry

A
  1. Formulate clinical question
  2. Search for evidence
  3. Evaluate evidence through critical appraisal
  4. Apply results to clinical practice
  5. Implement and monitor the process
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4
Q

Give 5 sources of evidence

A

Colleagues
Textbooks
Dental journals
Internet
Conferences/courses

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5
Q

3 advantages of using a colleague as a source of evidence

A

Information is based on clinical experience
Easily accessible
Often more directly relevant

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6
Q

3 disadvantages of using a colleague as a source of evidence

A

May not be up to date
Conflicting opinions
May have limited or no experience

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7
Q

2 advantages of using a textbook as a source of evidence

A

Easily accessible
Written by experts in a field

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8
Q

2 disadvantages of using a textbook as a source of evidence

A

May not be up to date
Often not peer reviewed before publishing so rigour of evidence not assessed

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9
Q

4 advantages of using a dental journal as a source of evidence

A

Written by experts in a field
Most are peer reviewed
Up to date
Open access

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10
Q

3 disadvantages of using a dental journal as a source of evidence

A

Usually specialty based
Often niche topics
Expensive

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11
Q

2 advantages of using the internet as a source of evidence

A

Access to large datasbases
Free access to journals

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12
Q

3 disadvantages of using the internet as a source of evidence

A

Volume of material
Lack of quality control if not from peer-reviewed journals
Conflicting opinions

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13
Q

2 advantages of using conferences as a source of evidence

A

Evidence from experts
Up to date review of the current literature

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14
Q

2 disadvantages of using conferences as a source of evidence

A

Time consuming
Expensive to attend

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15
Q

4 important features of an information source

A

Valid
Relevant
Comprehensive
User friendly

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16
Q

What is strongest in the hierarchy of evidence

A

Meta-analysis and systematic reviews

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17
Q

What is weakest in the hierarchy of evidence

A

Case reports, opinion papers and letters

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18
Q

Why is research undertaken

A

To find out new knowledge

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19
Q

6 advantages of applying evidence based dentistry to clinical practice

A

Increase in confidence in diagnosis and treatment
Chance to offer more treatment options
Ensures effective and efficient treatment processes
Increases treatment acceptance
Improves satisfaction for patients
Increases referrals

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20
Q

5 disadvantages of applying evidence based dentistry to clinical practice

A

Information can overwhelm a clinician
Systematic reviews produce insufficient evidence
Clinician may not be trained in an appropriate procedure
Patients may not find intervention acceptable
Lack of resources can restrict choices available

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21
Q

3 examples of the use of EBD in contemporary clinical practice

A

NICE: National institute of health care and excellence
SIGN: Scottish intercollegiate guidelines network
Cochrane reviews

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22
Q

Define an observational study

A

Study that does not intervene in any way

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23
Q

Define an experimental study

A

Study in which the investigator deliberately intervenes to observe the effect of the intervention

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24
Q

Give 2 examples of observational studies

A

Cross sectional studies
Longitudinal studies

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25
Q

Define cross sectional studies

A

A descriptive observational study that provides a snapshot picture of a community at a point in time

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26
Q

4 advantages of cross sectional studies

A

Relatively simple
Data collected at around the same time
Little demanded of subjects
Does not have problems with prolonged follow-up

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27
Q

3 disadvantages of cross sectional studies

A

Lack time dimension therefore show association not causation
Subject to over-interpretation
Need a reasonable prevalence so not efficient for very rare conditions

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28
Q

Define longitudinal studies

A

An analytic observational study conducted over a length of time

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29
Q

2 examples of longitudinal studies

A

Case-control studies
Cohort studies

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30
Q

Define case-control studies

A

A retrospective longitudinal study where information is obtained from past records or interviews

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31
Q

2 advantages of case-controlled studies

A

Highly efficient, saves time
Lower costs

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32
Q

2 disadvantages of case-controlled studies

A

Medical records may be missing, incomplete or inaccurate
Interviews rely on accurate recall of information from many years ago

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33
Q

Define cohort studies

A

A prospective longitudinal study where data is collected forward from a given starting point

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34
Q

4 advantages of cohort studies

A

Multiple end-points can be assessed
Cause to effect time sequence clear
All measures of risk can be assessed
Exposure prior to outcome avoiding bias

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35
Q

3 disadvantages of cohort studies

A

Time consuming if the outcome does not occur for a long time after exposure may be costly, participants lost to follow-up
Large number subjects required to observe events if outcome not frequent
Subject to confounding

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36
Q

Define bias

A

Inaccuracy that is different in its size or direction in one of groups under study which can lead to systemic error in results

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37
Q

6 sources of bias

A

Selection
Allocation
Measurement
Recall
Observer
Publication

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38
Q

Define confounding

A

Confounding is distortion of the exposure - outcome association due to the association of another factor with both outcome and exposure

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39
Q

Give 4 examples of experimental studies

A

Randomised controlled trials
Quasi experiments
Parallel group studies
Matched design or cross-over studies

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40
Q

Define randomised controlled trials

A

Trials that randomly assigns participants to experimental or control group

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41
Q

Define Quasi experiments

A

Non-randomised trials

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42
Q

Define parallel group studies

A

Compare treatment between subjects

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43
Q

Define matched design or cross-over studies

A

Compare treatment within subjects

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44
Q

3 types of randomised controlled trials

A

Double blind RCT
Single blind RCT
Non blind RCT

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45
Q

Describe randomisation

A

Each participant equal chance of being placed in intervention or non-intervention group which can’t be predicted

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46
Q

What does randomisation achieve

A

Minimises some types of bias

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47
Q

Define fixed randomisation

A

Methods of allocation and randomisation are determined at the outset of the trial

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48
Q

4 methods of fixed randomisation

A

Random numbers
Simple randomisation
Block randomisation
Stratified randomisation

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49
Q

4 methods of random number randomisation

A

Computer generated
Dice
Random number table
Shuffled cards or envelopes

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50
Q

Describe simple randomisation

A

Each subject randomly allocated intervention or non-intervention as they enter the study

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51
Q

Describe block randomisation

A

Subjects are put in to blocks and are split equally and randomly between the treatment and the control group

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52
Q

Describe stratified randomisation

A

Subgroups created and confounders are equally distributed in the treatment and control groups and within each subgroup block randomisation takes place

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53
Q

Define adaptive randomisation

A

Used to balance characteristics and maintain similarity as a trial progresses

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54
Q

2 advantages of randomised controlled trials

A

Randomisation controls for confounding
Blinding controls for bias

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55
Q

5 disadvantages of randomised controlled trials

A

Complex with high requirements for organisation, time, cost and resources
Raises ethical questions
Large numbers needed to assess of small improvements
Long term follow up may be needed
Treatment may be obsolete by the time results available

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56
Q

Define single blinding

A

Only the investigator or the patient, knows whether they are in the intervention or non-intervention group

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57
Q

Define double blinding

A

Neither investigator or patients knows whether they are in the intervention or non-intervention group

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58
Q

Describe the aim of clinical trial CONSORT guidelines

A

Ensure that trials are correctly carried out and reported without bias

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59
Q

Describe a review of the literature

A

A systematic way of collecting and synthesising previous research

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60
Q

Define a standard review

A

An overview of selected published works written by a subject expert

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61
Q

2 disadvantages of a standard review

A

Can lack thoroughness
Risk of bias

62
Q

Define a systematic review

A

A research method for identifying and critically appraising all relevant research and collecting and analysing the data

63
Q

6 steps in conducting a systematic review

A

Defining the review question and eligibility criteria
Searching for studies
Selecting the studies
Data extraction
Data synthesis
Interpretation

64
Q

3 advantages of systematic reviews

A

Thorough review of evidence base
Provide reliable and manageable summary data
Minimise bias

65
Q

4 disadvantages of systematic reviews

A

Labour intensive
Need to be updated
Answer only a very focused question
Risk misinterpretation of evidence

66
Q

3 features of a good systematic review

A

Quality
Thorough
Minimisation of bias

67
Q

Define meta-analysis

A

Statistical combination of results from 2 or more homogenous studies to give a pooled effect estimate, presented on a forest plot

68
Q

Why is meta-analysis carried out

A

Improves precision of results presented

69
Q

Define a narrative review

A

Provides a brief synopsis of the appraised evidence in a literature review

70
Q

Why is a narrative review carried out

A

Gives readers an understanding of how the included studies vary when there is a lack of homogeneity of available data for a full meta-analysis

71
Q

Define GRADE

A

Overall judgement of all of the evidence and the quality of all the studies

72
Q

6 features a GRADE outcome is based on

A

Risk of bias
Inconsistency across studies
Imprecision across studies
Indirectness across studies
Publication bias
Type of study

73
Q

1 way of assessing risk of bias in randomised studies

A

Cochrane risk of bias tool

74
Q

7 domains of Cochrane risk of bias tool for randomised trials

A

Random sequence generation
Allocation concealment
Blinding of participants and personnel
Blinding of outcome assessment
Incomplete outcome data
Selective reporting
Other bias

75
Q

2 ways of assessing risk of bias in non-randomised studies

A

Newcastle-Ottawa scale * 0-9 scale
Down’s & Black

76
Q

Describe Cochrane collaboration

A

Charitable organisation which produces high quality, relevant systematic reviews

77
Q

3 goals of the Cochrane collaboration

A

Produce trusted evidence
Advocate for evidence
Inform health and care decisions

78
Q

Define a population

A

The entire group of individuals

79
Q

Define a sample

A

Selected group of individuals to represent the population in a research study

80
Q

Define a variable

A

A characteristic or condition that can change or take on different values

81
Q

Define independent variable

A

Characteristic/condition that is manipulated by the study

82
Q

Define dependent variable

A

Characteristic/condition that is affected by the change in the value of the independent variable

83
Q

Define 2 types of qualitative data

A

Nominal
Ordinal

84
Q

Define nominal data

A

Data with no particular order. e.g, hair/eye colour

85
Q

Define ordinal data

A

Data that can be catergorised with some order e.g. pain threshold (mild/moderate/severe)

86
Q

Define 2 types of numerical (quantitative) data

A

Discrete
Continuous

87
Q

Define discrete data

A

Data that consist of indivisible categories or fixed numbers. e.g., number of teeth, number of children in a family

88
Q

Define continuous data

A

Data that is infinitely divisible into whatever units a researcher may choose e.g. weight in tonne, kilogram, gram, milligram

89
Q

Describe a nominal scale

A

An unordered set of categories identified only by name, only determines whether two individuals are the same or different

90
Q

Describe an ordinal scale

A

An ordered set of categories, can tell you the direction of difference between two individuals

91
Q

Describe an interval scale

A

An ordered series of equal-sized categories which can identify the direction and magnitude of a difference, the 0 point is arbitrary

92
Q

Describe a ratio scale

A

An ordered series of equal-sized categories which can identify the direction and magnitude of a difference, a value of 0 indicates none of the variable

93
Q

Describe 3 measures of central tendency

A

Mean
Median
Mode

94
Q

Define mean

A

Average or arithmetic mean of the data

95
Q

Define median

A

Middle value when the scores are ranked in order

96
Q

Define mode

A

Most frequently occurring value

97
Q

Describe 3 measures of dispersion

A

Range
Interquartile range
Standard deviation

98
Q

Define range

A

Highest to lowest values

99
Q

Define interquartile range

A

Values that capture the middle 50% of the distribution, the upper and lower quartiles

100
Q

Define standard deviation

A

Measure of spread of how individuals within the sample differ either side of the mean

101
Q

Define standard error

A

Measure of how far the mean of the sample is likely to be from the actual target population mean

102
Q

Define confidence interval

A

The probability that the mean for a population lies within a range of values, usually 95%

103
Q

What does the width of a confidence interval suggest

A

The precision of the estimate and the wider the interval range, the less precise are the results

104
Q

Describe normal distribution

A

Symmetrical, bell curve where mean = median = mode

105
Q

In a normal distribution, what proportion of the sample will have a value within ± 1 standard deviation of the mean

106
Q

In a normal distribution, what proportion of the sample will have a value within ± 2 standard deviations of the mean

107
Q

In a normal distribution, what proportion of the sample will have a value within ± 3 standard deviations of the mean

108
Q

Describe what a low standard deviation indicates

A

Most values are close to the average

109
Q

2 ways of identifying if data is non-normally distributed

A

Mean is very different from the median
Two standard deviations below the mean gives an impossible answer

110
Q

3 examples of normally distributed data

A

Height, weight, haemoglobin

111
Q

3 examples of skewed data

A

Salaries, number of marriages, GCSE’s passed

112
Q

Define internal validity

A

The degree to which the results of the study are likely to be true, believable and free from bias

113
Q

Define external validity

A

The degree that the results obtained can be generalised to the wider population

114
Q

Define intention to treat analysis

A

All the study participant are included in the analyses as part of the groups to which they are randomised regardless of whether they completed the study or not

115
Q

4 methods of controlling confounding factors

A

Restriction
Matching
Randomisation using stratified sampling
Statistic methods using regression analysis

116
Q

What information does hypothesis testing provide

A

The possibility that chance alone might be responsible for any observed differences

117
Q

Describe non-statistical hypothesis testing

A

Hypothesis test where a decision is made whether the hypothesis is true purely on the basis of evidence presented

118
Q

Describe statistical hypothesis testing

A

Hypothesis test where statistical decisions about populations or processes is based on empirical data

119
Q

Define the null hypothesis

A

That the difference in observations between two groups is purely due to chance

120
Q

Describe the p-value

A

The probability that an observed difference could have occurred by chance

121
Q

Describe what a value p<0.05 indicates

A

There is enough evidence to reject the null hypothesis in favour of the alternative hypothesis

122
Q

Describe what a value p≥0.05 indicates

A

There is not enough evidence to reject null hypothesis

123
Q

Describe clinical significance

A

The practical importance of a treatment effect and whether it has a real genuine, palpable, noticeable effect on daily life

124
Q

Describe critical appraisal

A

Assessing the validity of the research and the statistical techniques employed in studies and generating clinically useful information from them

125
Q

6 steps in critically appraising research

A

Are aims, clinical question and hypothesis clearly defined?
Is the study design appropriate to answer the clinical question?
Is the sample size determined?
Is the statistical analysis appropriate?
Are the conclusions based on the results?
Can I apply the results of this study to my patients?

126
Q

Describe Type I error

A

False-positive, an investigator rejects a null hypothesis that is actually true

127
Q

Describe Type II error

A

False-negative, investigator fails to reject a null hypothesis that is actually false

128
Q

Define selection bias and how it can be avoided

A

Differences between baseline characteristics of the groups being compared
Avoided through randomisation

129
Q

Define performance bias and how it can be avoided

A

Difference between groups in the care provided
Avoided through blinding

130
Q

Define detection bias and how it can be avoided

A

Differences between groups in how outcomes are determined
Avoided through blinding

131
Q

Define attrition bias and how it can be avoided

A

Differences between groups in withdrawals from the study
Avoided through intention-to-treat analysis

132
Q

Describe parametric tests

A

Statistical tests that allow us to inferences about normally distributed data

133
Q

Describe non-parametric tests

A

Tests that make fewer assumptions about the data and can be used to assess a more diverse range of data

134
Q

Describe a one-tailed test

A

Test used when the alternative hypothesis specifies a direction

135
Q

Describe a two-tailed test

A

Test used when there isn’t a direction of difference between groups for the alternative hypothesis

136
Q

Describe independent samples

A

Two groups with different members

137
Q

Describe paired samples

A

Same population at different times/locations (natural coupling) or two individuals with the same characteristics (matched coupling)

138
Q

2 descriptive ways of presenting categorical data

A

Mode
Frequency

139
Q

2 descriptive ways of presenting continuous non-normally distributed data

A

Median
Range

140
Q

2 descriptive ways of presenting continuous normally distributed data

A

Mean
Standard deviation

141
Q

Which 2 statistical tests are most appropriate when 2 groups are being studied and the data is categorical

A

Chi-square test
Fisher’s Exact test

142
Q

Which statistical test is most appropriate when more than 2 groups are being studied and the data is categorical

A

McNemars test

143
Q

Which statistical test is most appropriate when 2 groups are being studied and the data is continuous and normally distributed

A

Student t-test

144
Q

Which statistical test is most appropriate when more than 2 groups are being studied and the data is continuous and normally distributed

A

ANOVA Test

145
Q

Which statistical test is most appropriate when 2 groups are being studied and the data is continuous and non-normally distributed

A

Mann-Whiteny U Test

146
Q

Which statistical test is most appropriate when more than 2 groups are being studied and the data is continuous and non-normally distributed

A

Kruskal Wallis Test

147
Q

4 considerations when determining if research findings are applicable to your patients

A

Is the study population similar to mine
Are the settings similar
Are all the outcomes accounted for
Are my patients values and beliefs similar

148
Q

Describe the relationship between power and research study sample size

A

The power of research study increases the larger the sample size, a large power (minimum 80%)

149
Q

Describe how to formulate the research question for experimental and observational studies

A

PI/ECO: population, intervention or exposure, comparator, outcome

150
Q

Describe minimisation in adaptive randomisation and when it is used

A

Investigators decide which factors/traits they wish to be equally distributed between the arms of a study
Useful in small studies and where the distribution of multiple factors is important