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Levels of evidence

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Title: Levels of evidence


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Levels of evidence
  • Ia Meta-analysis or systematic review of RCTs
  • Ib Randomised trial
  • IIa Controlled non-randomised study
  • IIb Cohort study
  • III Case-control study
  • IV Descriptive study
  • Non-systematic review
  • Consensus report
  • Leading article

3
Survey of 85 physicians (36 from internal
medicine)Very important in influencing my
prescribing
  • Own training and experience 88
  • Scientific papers 62
  • Advice from colleagues 48
  • Detail men 20
  • Drug adds 4
  • Patient preference 2

(Avorn J. Am J Med 1982734-8)
4
Is impaired cerebral blood flow a major cause of
senile dementia?
  • Yes 71
  • No 14
  • No opinion 15
  • 32 found cerebral vasodilators useful in
    managing confused geriatric patients

5
Survey of 85 physicians (36 from internal
medicine)Very important in influencing my
prescribing
  • Own training and experience 88
  • Scientific papers 62
  • Advice from colleagues 48
  • Detail men 20
  • Drug adds 4
  • Patient preference 2

(Avorn J. Am J Med 1982734-8)
6
Drug adds
  • 287 advertisements for anti-hypertensive or
    lipid-lowering drugs
  • - 125 promotional claims with references
  • - 23 refs. unretrievable (data on file,
    monographs)
  • - 45 of 102 claims not supported by reference
  • (Lancet 200336127)

7
Randomised trials
  • Unclear randomisation method
  • - effect exaggerated by 30, on average
  • No blinding
  • - effect exaggerated by 14, on average

(BMJ 200132342-6)
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Outcome reporting bias
  • 102 RCTs approved by the Copenhagen
    Frederiksberg Ethics Review Committee 1994-95
  • and subsequently published
  • Incompletely reported outcomes for meta-analysis
  • 50 for efficacy, 65 for safety

9
Outcome reporting bias
  • Unreported outcomes
  • 86 of trialists denied unreported outcomes
    despite evidence in publications protocols
  • Only half of the trialists responded to the
    question

10
Outcome reporting bias
  • Full outcome reporting is associated with plt0.05
  • Odds ratio 2.4 (1.4 - 4.0) for efficacy
  • Odds ratio 4.7 (1.8 - 12) for safety

11
Are primary outcomes consistent between
protocols and publications?
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Conclusions
  • Trial outcomes are often inadequately reported
    for inclusion in meta-analyses
  • Reporting of outcomes is biased to favour plt0.05
  • Primary outcomes are omitted, changed, or
    newly-introduced in over 60 of trials

Protocols should be publicly available
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Positive studies are more likely to be
published than negative studies
  • Hazard ratio for 130 clinical trials
  • positive (Plt0.05) vs negative (Pgt0.10)
  • 3.13 (1.76 to 5.58), P0.0001
  • Median time to publication 4.7 vs 8 years

15
Cochrane Reviews
  • Freely available from
  • www.cochrane.dk

16
Based on Cochrane Reviews when possible
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NSAIDs
  • Systematic reviews of RCTs have found no
    important differences in effect between different
    NSAIDs or doses but have found differences in
    toxicity related to increased doses and possibly
    to the nature of the NSAID itself.
  • The only meta-analysis that found one drug to be
    more effective than another was funded by the
    manufacturer
  • Clinical Evidence 19992

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Clinical Evidence(NSAIDs)
  • We have favoured systematic reviews that have not
    been sponsored or authored by industry ...
  • it is easy to seemingly follow the rules for
    systematic reviews and yet adopt inclusion and
    exclusion criteria that omit inconvenient
    studies. In fact, it is hard to find a systematic
    review sponsored by, or co-authored by, industry
    that concludes that the companys product is not
    better than those of its competitors.

19
Celecoxib
  • Conclusion, industry supported meta-analysis
  • Celecoxib ... has significantly improved
    gastrointestinal safety and tolerability (BMJ
    Sept 2002)
  • Conclusion, Cochrane Review
  • For an individual with RA the potential benefits
    of celecoxib need to be balanced against the
    uncertainty that the short-term reduced incidence
    of upper GI complications are maintained in the
    long-term and its increased cost in comparison to
    traditional NSAIDs.

20
Industrisponsorerede forsøg med lægemidler
  • Ofte problemer med
  • Design
  • Data-analyse
  • Afrapportering
  • Konklusion

21
Forsøg med psykofarmaka
  • Gamle præparater
  • - Alt for høj dosis, alt for hurtig dosisøgning.
  • Nye præparater tilsyneladende lige sÃ¥ gode,
  • med langt færre bivirkninger.
  • Men udbredt manipulation med dosis, data-analyse
    og afrapportering.
  • (J Nerv Ment Dis 2002190583)
  • (BMJ 20033261171)

22
Behandling for skizofreni
  • Olanzapin 17.000 kr/Ã¥r
  • Haloperidol 2.400 kr/Ã¥r
  • Forbrug i primærsektoren
  • Olanzapin 216 mio kr i 2002
  • Haloperidol 4 mio kr i 2002
  • the new drugs have no unequivocal advantages for
    first line use (BMJ 20003211371)

23
Industrisponsoreret forskning versus offentligt
sponsoreret forskning
  • Chancen for et positivt udfald 4 gange sÃ¥ stor
    for forsøg eller systematiske oversigter over
    flere forsøg.
  • (BMJ 20033261167)
  • Chancen for en positiv konklusion 5 gange sÃ¥ stor
    for forsøg, trods samme effekt.
  • (JAMA 2003290921)

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Cochrane Reviews
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Hvilken forskning mangler vi?
  • - Sammenligninger med gamle, billige præparater,
    og på en fair måde (offentlig finansiering)
  • - Sammenligninger med andet end lægemidler
  • Forebyggelse af ikke-insulinkrævende sukkersyge
  • - metformin 31 effekt
  • - motion og vægttab 56 effekt
  • (N Engl J Med 2002346393)
  • - Forskning i skadevirkninger

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