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EVIDENCE based MEDICINE

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Title: EVIDENCE based MEDICINE


1
EVIDENCE based MEDICINE
I N T R O D U C T I O N T O
  • BY
  • Dr. Mohamed Abdelhafez

2
History of EBM !
  • The ideas behind it are far from new - it is to
    be hoped that clinicians have to some extent
    always used the evidence (at least as they saw
    it!) to support their treatment of patients

3
History of EBM !
  • "Believe nothing
  • Merely because you have been told itOr because
    it is traditionalOr because you yourself have
    imagined it.Do not believe what your teacher
    tells youMerely out of respect for the
    teacher But whatever after due examination and
    analysisYou find conducive to the good, the
    benefitThe well-being of all thingsThat
    doctrine believe and cling toAnd take it as your
    guide." 

Buddha, 3rd Century BC 
4
History of EBM !
  • "Those who are enamoured of practice without
    science are like a pilot who goes into a ship
    without rudder or compass and never has any
    certainty where he is going. Practice should
    always be based upon a sound knowledge of
    theory."Leonardo da Vinci, Notebooks,
    1508-1518.

5
History of EBM !
  • The first recorded clinical trial dates back to
    more than 2000 years by Daniel of Judah compared
    the health effects of a vegetarian diet (the
    intervention) with those of the Royal Babylonian
    diet (control group) over a ten-day period.

6
History of EBM !
  • The Book of Daniel records (1.15-16) that
  • "At the end of the ten days their appearance was
    better and their bodies healthier than all the
    young men who had been eating the royal
    delicacies. So the warden removed their
    delicacies and the wine from their diet and gave
    them a diet of vegetables instead."

7
History of EBM !
  • Despite the dramatic findings of the study , the
    trial had obvious deficiencies by contemporary
    methodological standards (allocation bias) but
    the publication has remained influential over two
    millennia."

8
History of EBM !
  • Frederick II (1194-1250) who was interested in
    the effects of digestion.
  • He fed two knights identical meals then sent one
    to bed and the other out hunting .
  • The King had both knights killed so that he could
    examine their stomach contents and concluded the
    sleeping knight had evidence of better progress
    with digestion.

9
History of EBM !
  • The first reported controlled therapy trial took
    place in the United Kingdom in 1747.
  • Since the early 1600s, many people had felt that
    citrus fruits might reduce the incidence of
    scurvy during long ocean voyages.

James Lind studied sailors with scurvy and
evaluated six potential treatments one of which
involved using citrus fruits. The two sailors who
received the citrus treatment got better as Lind
reported.
10
Methods of Practicing Medicine
  • Knowledge (Study).
  • Clinical experience (Practice).
  • Reading (Non systematic way).
  • Expert and peer opinion.
  • Logic

11
Knowledge
  • The knowledge decreases with time after graduation

The Slippery Slope
Knowledge of best care
r0.54 plt0.001
Years since graduation
5 10 15 20
Shin et al CMAJ 1993
12
Experience
  • There always new developments in medicine.
  • Difficult to catch up.

New Techniques
New Drugs
13
Reading
  • Traditional Text Books are always outdated.

14
Reading
  • Quantity of journals and articles makes it
    impossible to keep updated.

20,000 biomedical journals 5,000 articles/day
15
Ask an Expert
  • There is always more than one expert opinion.

16
Logic
  • Logic doesnt always lead to the right
    conclusion.

sun
earth
17
Conclusion
  • The best way to practice medicine is to be based
    on the best available evidence together with our
    experience and patient preferences.

18
What is EBM ?
19
What is EBM ?
  • The development of evidence-based medicine has
    been rapid over the past 10 years, and has been
    led by Professor
  • David Sackett.

20
What is EBM ?
  • It is the integration of best research evidence
    with clinical experience and patient values .
  • Sackett,2000

21
Practicing Medicine Without Evidence
BACK TO SLEEP
  • In the 1980s studies found a dramatic drop in
    SIDS among children sleeping on their backs.

22
Practicing Evidence Based Medicine
  • Assess and examine your patient.
  • Construct a well built clinical question derived
    from the case.
  • Select the appropriate resource(s) and conduct a
    search.
  • Appraise that evidence for its validity and
    applicability.
  • Integrate that evidence with clinical expertise,
    patient preferences and apply it to practice.
  • Evaluate your performance with this patient.

23
Steps of Practicing EBM
Assess Your patient
Ask a clinical question
Acquire the best evidence
Apply the evidence to the patient care
Evaluate your performance
Appraise the evidence
24
Step I Assess Your Patient
  • History
  • Physical examination
  • Investigations
  • Determine the problem

After this we will start to construct a clinical
question built on the problem
25
Step II Ask Clinical Question
  • There are 2 types of clinical questions
  • Background question.
  • Foreground question.

26
Step II Ask Clinical Question
  • Background question
  • General knowledge about a disorder.
  • Components Question root what, how, where,
    etc verb disorder or intervention.
  • Examples What causes hypertension ?How do we
    tap ascites ?

27
Step II Ask Clinical Question
  • Foreground question
  • Specific knowledge about a disorder.
  • Components Patient or problem Intervention,
    prognostic factor, or exposure Comparison
    Outcome
  • Examples In patients with tense ascites is
    tapping superior to diuretic therapy in
    controlling ascites.

28
Types Of Clinical Question
Background
Foreground
Percentage of questions
Experience
29
Step II Ask Clinical Question
  • In practicing EBM we use Foreground questions.
  • We construct the question according to four
    components PICO
  • Patient or problem
  • Intervention, prognostic factor, or exposure
  • Comparison
  • Outcome

PICO
30
Step II Example for Clinical Question
  • Pauline is a new patient who recently moved to
    the area to be closer to her son and his family.
    She is 67 years old and has a history of
    congestive heart failure brought on by several
    myocardial infarctions.

PICO
31
Step II Example for Clinical Question
  • She has been hospitalized twice within the last 6
    months for worsening of heart failure. At the
    present time she remains in normal sinus rhythm.
    She is extremely diligent about taking her
    medications (enalapril, aspirin and simvastatin)
    and wants desperately to stay out of the
    hospital. She lives alone with several cats.

PICO
32
Step II Example for Clinical Question
  • You think she should also be taking digoxin but
    you are not certain if this will help keep her
    out of the hospital. You decide to research this
    question before her next visit.

PICO
33
Step II Example for Clinical Question
The structure of the question might look like
this
Patient / Problem
congestive heart failure, elderly
Intervention
digoxin
Comparison
none, placebo
PICO
Outcome
primary reduce need for hospitalization
secondary reduce mortality
In elderly patients with congestive heart
failure, is digoxin effective in reducing the
need for rehospitalization?
34
Step II Ask Clinical Question
  • Two additional elements of the well-built
    clinical question are the type of question and
    the type of study. This information can be
    helpful in focusing the question and determining
    the most appropriate type of evidence.

35
Step II Ask Clinical Question
  • The most common types of questions related to
    clinical tasks are

Diagnosis
how to select and interpret diagnostic tests .
Therapy
how to select treatments to offer patients that
do more good than harm and that are worth the
efforts and costs of using them
Prognosis
how to estimate the patient's likely clinical
course over time and anticipate likely
complications of disease
Harm/Etiology
how to identify causes for disease (including
iatrogenic forms)
36
Step II Ask Clinical Question
  • Type of Study

The Evidence Pyramid
37
The Hierarchy of Research
  • NOW, we will understand the study design

38
WAKE UP !!!
39
The Hierarchy of Research
40
The Hierarchy of Research
A
  • DESCRIPTIVE STUDIES

41
A Descriptive Studies
  • Case reports and series
  • Case series and case reports consist either of
    collections of reports on the treatment of
    individual patients, or of reports on a single
    patient.
  •  Case series and case reports, since they use no
    control group with which to compare outcomes,
    have no statistical validity .

42
A Descriptive Studies
  • Case reports and series

43
The Hierarchy of Research
  • COMPARATIVE STUDIES

44
The Hierarchy of Research
B
  • OBSERVATIONAL STUDIES

45
The Hierarchy of Research
B
  • OBSERVATIONAL STUDIES
  • I. Cohort Study

46
B Observational Studies
  • I. Cohort Study
  • A Cohort Study is a study in which patients who
    presently have a certain condition and/or receive
    a particular treatment (exposed) are followed
    over time and compared with another group who are
    not affected by the condition (controls).
  • Its a prospective study.

47
B Observational Studies
  • I. Cohort Study

48
B Observational Studies
  • I. Cohort Study
  • Advantages
  • Ethically safe.
  • Subjects can be matched.
  • Can establish timing and directionality of
    events.
  • Eligibility criteria and outcome assessments can
    be standardized.
  • Administratively easier and cheaper than RCT.

49
B Observational Studies
  • I. Cohort Study
  • Disadvantages
  • The controls may be difficult to identify.
  • Exposure may be linked to a hidden confounder.
  • Blinding is difficult.
  • Randomization not present.
  • For rare disease, large sample sizes or long
    follow-up necessary.

50
The Hierarchy of Research
B
  • OBSERVATIONAL STUDIES
  • II. Case Control Study

51
B Observational Studies
  • II. Case Control Study
  • Case control studies are studies in which
    patients who already have a certain condition are
    compared with people who do not.
  •  Its a retrospective study

52
B Observational Studies
  • II. Case Control Study

53
B Observational Studies
  • II. Case Control Study
  • Advantages
  • Quick and cheap.
  • Only feasible method for very rare disorders or
    those with long lag between exposure and outcome.
  • Fewer subjects needed than cross-sectional
    studies.

54
B Observational Studies
  • II. Case Control Study
  • Disadvantages
  • Reliance on recall or records to determine
    exposure status.
  • Confounders.
  • Selection of control groups is difficult.
  • Potential bias recall, selection.

55
B Observational Studies
  • Relative Risk
  • factor
  • RR

56
B Observational Studies RR
  • Relative risk is a measure of how much a
    particular risk factor (say cigarette smoking)
    influences the risk of a specified outcome (say,
    death by age 70)

57
B Observational Studies RR
  • For example, a relative risk of 2 associated with
    a risk factor means that persons with that risk
    factor have a 2 fold increased risk of having a
    specified outcome compared to persons without
    that risk factor.

58
B Observational Studies RR
  • A relative risk of 0.5 means that persons with
    that risk factor have half the risk of the
    specified outcome (a protective effect) compared
    to persons without the risk (protective) factor.

59
B Observational Studies RR
  • In Cohort study we can calculate the RR.
  • In Case-control study we calculate OR (odds
    ratio) instead.OR is about equal to the RR.
  • N.B. We cant calculate RR in case-control
    studies.

60
B Observational Studies RR
  • The Two by Two Table

Outcome
ve
- ve
ve
A
B
C
Factor
- ve
D
F
G
H
I
J
61
B Observational Studies RR
In Cohort study RR AR
Absolute Risk in exposure group
Absolute Risk in non-exposure group
No. of outcome
Total No.
62
B Observational Studies RR
In Case-control study OR Odds of exposure

Odds of exposure in the cases
Odds of exposures in the controls
No. of exposed
No. of unexposed
63
B Observational Studies RR
In Cohort study RR (A/C) / (D/G)
In Case-control study OR (A/D) / (B/F)
64
Examples for RR OR
  • EXAMPLE I

65
Examples I
  • In a study about the association of smoking and
    lung cancer, 6000 participants were enrolled.
  • 2000 were smokers and 4000 were non-smokers.
  • During 10 years of follow up, 100 of the smokers,
    and 100 of non-smokers developed lung cancer.

66
Examples I
67
Examples I
  • What is this study design ?
  • What is absolute risk and relative risk of
    developing lung cancer with smoking?

68
Examples I
Absolute risk of lung cancer among smokers 100
/ 2000 Absolute risk of lung cancer among
non-smokers 100 / 4000 Relative Risk 2 Lung
cancer increases by 2 fold with smoking.
69
Examples for RR OR
  • EXAMPLE II

70
Examples II
  • In a hypothetical study in which 200 cases of
    lung cancer were compared with 200 controls
    regarding their smoking habits. The history of
    smoking was inquired.
  • 127 of the lung cancer patients were smokers.
  • 79 of control group were smokers.

71
Examples II
72
Examples II
  • What is this study design ?
  • What is odds ratio ?
  • What association between smoking and lung cancer,
    you conclude from this study?

73
Examples II
  • Odds of exposure among cases 127 / 73
  • Odds of exposure among controls 79 / 121
  • Odds Ratio 2.66
  • Smoking increases the probability of having lung
    cancer by 2.66 fold.

74
The Hierarchy of Research
B
  • OBSERVATIONAL STUDIES
  • III. Cross Sectional Study

75
B Observational Studies
  • III. Cross Sectional Study
  • A study in which the exposure and outcome are
    determined simultaneously.
  • Thus the cause and effect relationship between
    the two cant be clearly established.
  • It is Snap Shot in Time study

76
B Observational Studies
  • III. Cross Sectional Study
  • Advantages
  • Cheap and simple.
  • Ethically safe.

77
B Observational Studies
  • III. Cross Sectional Study
  • Disadvantages
  • Establishes association at most, not causality
  • Recall bias susceptibility
  • Confounders may be unequally distributed
  • Neyman bias
  • Group sizes may be unequal.

78
The Hierarchy of Research
C
  • EXPERIMENTAL STUDIES
  • RCT

79
WAKE UP !!!
80
C The RCT
  • The Gold Standard Of Clinical Research

81
C The RCT
  • Randomized controlled trial is one in which
  • Patients are randomly assigned to two or more
    groups
  • One or more intervention groups and one control
    group
  • Followed up in time
  • The outcomes are compared.

82
C The RCT
  • Randomized controlled trial

83
C The RCT
  • Advantages
  • The least biased Design.
  • Blinding more likely
  • Randomization facilitates statistical analysis.

84
C The RCT
  • Disadvantages
  • Expensive time and money.
  • Volunteer bias.
  • Ethically problematic at times.

85
C The RCT
  • Evaluation of RCTs
  • For those who apply conclusions of RCTs in their
    clinical practice, its essential to know how to
    evaluate them properly.
  • A biased RCT can be hazardous to medical practice
    and patients.

86
C The RCT
  • Importance Of Randomization
  • Assigning patients at random reduces the risk of
    bias and increases the probability that
    differences (confounders) between the groups can
    be attributed to the treatment.
  • Confounder A variable, other than the one
    studied, that can cause or prevent the outcome of
    interest. A confounding variable may be due to
    chance or bias.

87
C The RCT
  • Importance Of Randomization
  • With proper randomization the basic
    characteristics of the participants are similar
    in all the groups.
  • These are called balanced groups.
  • The only variable will be the intervention.

88
C The RCT
  • The Double Blind Method
  • A double blind study is one in which neither the
    patient nor the physician knows whether the
    patient is receiving the treatment of interest or
    the control treatment.

89
C The RCT
  • The Double Blind Method

90
C The RCT
  • Importance Of Blinding
  • A double blind study is the most rigorous
    clinical research design because, in addition to
    the randomization of subjects which reduces the
    risk of bias, it can eliminate the placebo effect
    which is a further challenge to the validity of a
    study.

91
C The RCT
  • Double Blind

92
C The RCT
  • The placebo effect could be thought of in this
    way
  •  
  • Patients who believe they are receiving a new
    experimental treatment tend to be more optimistic
    about the outcome.
  • Doctors who believe that a patient is receiving a
    new experimental treatment tend to be more
    optimistic about that patient's chances, evaluate
    their state of health more favorably, and
    communicate positive expectations to the
    patients, who in turn try to get better so as to
    prove their doctor right!  

93
C The RCT
  • Importance Of Blinding
  • In a review of acupuncture for back pain
    including both non-blinded and blinded studies
  • Non-blinded studies showed a significant relative
    benefit of 1.8
  • Double blind studies showed that acupuncture has
    no benefit in pain relief.

94
C The RCT
  • Prospective, Blind Comparison To A Gold Standard
    Study
  • Studies that show the efficacy of a diagnostic
    test.
  • This is a controlled trial that looks at patients
    with varying degrees of an illness and
    administers both diagnostic tests, the test under
    investigation and the "gold standard" test to all
    of the patients in the study group.

95
C The RCT
  • Bias in RCTs
  • There are several bias that could affect the RCTs
    including
  • Sampling Bias
  • Selection Bias
  • Ascertainment Bias
  • Withdrawal or Drop Out Bias
  • Publication Bias

96
The Hierarchy of Research
D
  • Systematic Reviews
  • and
  • Meta-Analyses
  • TOP OF THE EVIDENCE PYRAMID

97
D Systematic Reviews and Meta-Analyses
  • A systematic review is a comprehensive survey of
    a topic in which all of the primary studies of
    the highest level of evidence  have been
    systematically identified, appraised and then
    summarized according to an explicit and
    reproducible methodology.

98
D Systematic Reviews and Meta-Analyses
  • A meta-analysis is a survey in which the results
    of all of the included studies are similar enough
    statistically that the results are combined and
    analyzed as if they were one study.  

99
D Systematic Reviews and Meta-Analyses
100
D Systematic Reviews and Meta-Analyses
  • In general
  • a good systematic review or meta-analysis will be
    a better guide to practice than an individual
    article.

101
D Systematic Reviews and Meta-Analyses
  • Three Main Pitfalls Specific
  • To Meta-analysis

102
D Systematic Reviews and Meta-Analyses
  • It's rare that the results of the different
    studies precisely agree, and often the number of
    patients in a single study is not large enough to
    come up with a decisive conclusion.  

103
D Systematic Reviews and Meta-Analyses
  • If the authors are interested in supporting a
    particular conclusion, they can include studies
    that support that conclusion and omit studies
    that do not.
  • Do the authors explain in their paper exactly on
    what basis they included studies , and do their
    reasons make sense?  

104
D Systematic Reviews and Meta-Analyses
  • Studies that show some kind of positive effect
    tend to be published more often than those that
    do not. This means that if the authors include
    only published studies, several weak positive
    studies may seem to add up to a strong positive
    result.
  • Do weak negative studies exist? This effect is
    known as Publication bias.

105
Next Session
  • RCT. (Design and Bias)
  • Searching the literature.
  • Appraising the evidence.
  • How to apply the evidence to my patient.

106
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