Evidenced Based Dentistry 1 Flashcards

1
Q

what is the definition of risk

A

what are the chances

can be good or bad

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2
Q

what is the definition of outcome

A

something that might happen

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3
Q

what are statistics

A

numbers that summarize information

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4
Q

what are statistics based on

A

observations of large numbers of people

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5
Q

what are statistics useful for

A

predicting what is likely to happen in the future

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6
Q

what does the numerator represent

A

number of people who actually experience the outcome

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7
Q

what does the denominator represent

A

the number of people who could potentially experience the outcome

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8
Q

what are risks and odds

A

just ways of expressing chance in numbers

for binary events they just express the chance of being in one of the two states

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9
Q

how do you calculate risk

A

number of events of interest/total number of observations

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10
Q

how do you calculate odds

A

number of events of interest/number without the event

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11
Q

what are the questions to ask when interpreting risk

A

risk of what - what is the outcome?
how big is the risk - what are the chances of experiencing the outcome, what timeframe?
does the risk information reasonably apply to me or my patient?
how does this risk compare with others risks - should i do something about this risk

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12
Q

what are the questions to ask about risk reduction

A

reduced risk of what?
how big is the risk reduction?
does the risk reduction info reasonably apply to me?
any downsides?
is the benefit (risk reduction) worth the downsides?

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13
Q

what is the difference between the relative risk reduction and absolute risk reduction

A

relative risk reduction makes even small risk reductions sound big making us overestimate the benefits

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14
Q

what is the number needed to treat

A

the number of patients you would need to treat to prevent one patient from developing the disease/condition/outcome

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15
Q

what is a confidence interval

A

a confidence interval tells us the range of values that a true population treatment effect is likely t lie

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16
Q

describe what confidence intervals show

A

a CI that embraces/overlaps/contains/straddles the ‘value of no difference’ between treatments indicates that there is insufficient evidence for a difference between the treatment and control group in the population

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17
Q

what is the ratio value for confidence intervals

A

if the confidence interval embareces 1 then there is insufficient evidence
if this interval does not embrace 1 then there is sufficient evidence to suggest a difference

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18
Q

if two values are equal what is the value of no difference

A

0
there is sufficient evidence for a difference between two values in the population if the CI for the difference does not overlap 0

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19
Q

if two values are equal in a ratio what is the value of no difference

A

1

sufficient evidence for a difference between two values in the population if the CI for the ratio does not overlap 1

20
Q

what are the different study designs in human research

A

observational uncontrolled studies
controlled studies
randomized controlled trials

21
Q

what are observational uncontrolled studies

A

researchers watch what happens to a group of people

22
Q

what are controlled studies

A

cohort or case control

researchers observe what happens to people in different situations without intervening

23
Q

what are randomized controlled trials

A

patients randomly split into 2 groups - one gets intervention and the other placebo
any differenced at follow-up caused by intervention

24
Q

what is a case report/case series

A

a report on a single patient or series of patients with an outcome of interest - no control group is involved

25
Q

what is a case report/case study used for

A

identify the new disease outcome

hypothesis generation

26
Q

what are the disadvantages of a case study

A

cannot demonstrate the valid statistical associations

lack of control group

27
Q

what are cross sectional studies

A

the observation of a defined population at a single point in time - or time interval
exposure and outcome are determined at the same time

28
Q

what are cross sectional studies used for

A

estimating prevalence of a disease

investigate potential risk factors

29
Q

what are the disadvantages of cross sectional studies

A

causality
confounding
recall bias

30
Q

what is a case control study

A

the study of people with a disease and a suitable control group of people without the disease
looks back in time at exposure to a particular risk factor in both groups

31
Q

what is a case control study used for

A

looking at potential causes of disease

32
Q

what are the disadvantages of case control study

A
confounding 
recall/selection bias
selection of controls
time relationships (did exposure occur before disease)
33
Q

what is a cohort study

A

establish a group of individuals in population
measure exposures
follow up over a period of time
identify those that develop disease (outcome of interest)

34
Q

what is a cohort study used for

A

estimating incidence of disease
investigating causes of disease
determining prognosis
timing and direction of events

35
Q

what are disadvantages of cohort studies

A
controls difficult to identify 
confounding
blinding difficult
for rare diseases - need large samples
very expensive/time consuming
36
Q

what are randomized controlled trials

A

sometimes referred to as a clinical standard
considered the gold standard
for effectiveness and efficiency
particularly useful for clinical studies
provides strongest evidence on effectiveness of treatments

37
Q

what are the 4 design elements of RCT

A

specification of participants (inclusion/exclusion criteria)
control/comparison groups
randomisation
blinding/masking

38
Q

what are the inclusion/exclusion criteria

A

unambiguous

exact definitions

39
Q

what is the comparison groups

A

placebo

current standard treatment

40
Q

what is randomization

A

how participants/subjects/patients are allocated to treatments

41
Q

why is randomization done

A

eliminate bias

42
Q

how should randomization be done

A

by a computer

43
Q

what is blinding/masking

A

if the participant or researcher is unaware of which treatment is given it may influence the results

44
Q

what may change if participant/researcher is aware of which treatment is being given

A

participant
administrator of treatment
assessor of outcome
data analyst

45
Q

what are the advantages of RCTs

A

provide strongest and most direct epidemiological evidence for causality
but non blinded RCTs may overestimate effects

46
Q

what are disadvantages of RCTs

A

more difficult to design and conduct than observation studies due to ethical issues, feasibility, costs
still some risk of bias and generalizability often limited
not suitable for all research questions