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Why Grade the Evidence?

Why Grade the Evidence?. target audience for Cochrane reviews clinicians interested in the question policy makers, consumers many in audience will have limitations time methodological sophistication. Implications of Limitations. limited time/sophistication

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Why Grade the Evidence?

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  1. Why Grade the Evidence? • target audience for Cochrane reviews • clinicians interested in the question • policy makers, consumers • many in audience will have limitations • time • methodological sophistication

  2. Implications of Limitations • limited time/sophistication • is evidence strong, inferences secure? • is evidence weak, inferences insecure? • shorthand summary • enhance usefulness of reviews • Gray Elrodt in the Berkshires • post-MI smoking cessation, aspirin, beta blocker, ACE inhibitor, statin

  3. Grade for Specific Question • too vague: alendronate in osteoporosis • patients – post-menopausal women • intervention • daily alendronate, dose 10 to 20 mg. • outcome – non-vertebral fractures

  4. What Influences Grade? • study design • basic • detailed design and execution • consistency • directness • reporting bias

  5. Summary Methodological Quality • study design • randomization • observational study • detailed design and execution • concealment • balance in known prognostic factors • intention to treat principle observed • blinding • completeness of follow-up

  6. Summary Methodologic Quality • consistency of results • if inconsistency, look for explanation • patients, intervention, outcome, methods • no clear threshold • size of effect, confidence intervals, statistical significance

  7. Risk Difference of Conversion to Sinus Rhythm Amiodarone vs Placebo or Digoxin or CCB Favours Control Favours Amiodarone AF Duration > 48 hrs ' Bianconi 2000 0.02 (-0.06 to 0.11) ' Galperin 2000 0.33 (0.19 to 0.47) ' Hohnloser 2000 0.16 (0.06 to 0.26) ' Natale 2000 0.67 (0.51 to 0.83) ' Villani 2000 0.20 (0.06 to 0.33) AF Duration </= 48 hrs ' Cowan 1986 0.08 (-0.19 to 0.36) ' Noc 1990 0.77 (0.52 to 1.00) ' Capucci 1992 -0.11 (-0.41 to 0.20) ' Cochrane 1994 0.13 (-0.06 to 0.33) ' Donovan 1995 0.03 (-0.21to 0.27) ' Hou 1995 0.21 (-0.01 to 0.43) ' Kondili 1995 0.14 (-0.16 to 0.44) ' Galve 1996 0.08 (-0.11 to 0.27) ' Kontoyannis 1998 0.31 (0.11 to 0.50) ' Bellandi 1999 0.27 (0.13 to 0.41) ' Cotter 1999 0.28 (0.13 to 0.43) ' Kochiadakis 1999 0.28 (0.15 to 0.41) ' Joseph 2000 0.19 (-0.02 to 0.39) ' Peukurinen 2000 0.52 (0.31 to 0.72) ' Vardas 2000 0.41 (0.28 to 0.53) ' Cybulski 2001 0.39 (0.24 to 0.54) ' Pooled Risk Difference 0.26 (0.18 to 0.34) -0.6 -0.4 -0.2 0 0.2 0.4 0.6 0.8 1 1.2

  8. Relative Risk of Hospital Mortality: Adult Patients Favours Favours Private Private For-Profit Not-For-Profit Number of Number of Study % Weight Hospitals Patients ! Shortell 653 144,159 1.43 ! Keeler 220 4,937 0.04 ! Hartz 2,368 3,107,616 11.38 ! Manheim MH 1,252 1,537,660 9.78 ! Manheim FS 1,617 2,228,593 2.59 ! Kuhn 2,580 3,353,676 12.34 ! Pitterle 3,482 4,529,206 14.11 ! Mukamel 1,653 5,298,812 17.21 ! Bond 3,224 4,210,468 12.66 ! Yuan Medical 3,316 7,386,000 11.90 ! Yuan Surgical -- 4,396,000 5.05 ! Lanska 799 16,983 0.00 ! McClellan 2,875 181,369 1.48 ! Sloan 2,360 7,079 0.03 Totals 26,399 36,402,558 100.00 ! Random Effects Pooled Estimate 0.7 0.8 0.9 1 1.1 1.2 1.3 Relative Risk and 95% CI

  9. Directness of Evidence • indirect treatment comparisons • interested in A versus B • have A versus C and B versus C • alendronate vs risedronate • both versus placebo, no head-to-head

  10. Four Levels of “Directness” • patients meet trials’ eligibility criteria • not included, but no reason to question • slight age difference, comorbidity, race • some question, bottom line applicable • valvular atrial fibrillation • serious question about biology • heart failure trials applicability to aortic stenosis

  11. Levels of Directness • interventions • same drugs and doses • similar drugs and doses • same class and biology • questionable class and biology • outcomes • same outcomes • similar (duration, quality of life) • less breathlessness for role function • laboratory exercise capacity for q of life

  12. Magnitude, Precision, Reporting Bias • magnitude not generally part of quality • but very large magnitude can upgrade • precision not generally part of quality • but sparse data can lower quality • reporting bias • high likelihood can lower quality

  13. Grading System • high quality well done RCT • intermediate quasi-RCT • low well done observational • insufficient anything else

  14. Moving Down • study execution • serious flaws can lower by one level • fatal flaws can lower by two levels • consistency • important inconsistency can lower by one level • directness of evidence • some uncertainty re relevance lower by one level • major uncertainty re relevance lower by two levels • selection bias • strong evidence lower by 1 level

  15. Moving Up • very strong association, up 2 levels • insulin in diabetic ketoacidosis • strong, consistent association with no plausible confounders, up 2 levels • fluoride for preventing cavities • strong association can move up 1 level • ? HRT ?

  16. Conclusion • challenges in grading • balancing simplicity and complexity • judgement always required • consistent grading system required • must consider study design, execution, consistency, directness • magnitude, precision, publication bias only when extreme

  17. Questions for Discussion • should Cochrane reviews provide: • grades of evidence across studies for all important outcomes? • overall grade of evidence across outcomes? • same grading system across reviews? • bonus; while Cochrane reviews shouldn’t provide recommendations should they include structured discussion including • trade-offs • translation of evidence in to practice

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