How to determine the best treatment: a mixed-treatment-comparisons meta- analysis (MTM) of trials of topical fluoride therapies for the prevention of dental.

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How to determine the best treatment: a mixed-treatment-comparisons meta- analysis (MTM) of trials of topical fluoride therapies for the prevention of dental caries Georgia Salanti, Julian Higgins, Valeria Marinho XIII Cochrane Colloquium Melbourne 2005

A series of seven Cochrane reviews examines the effect of fluoride in preventing caries Marinho, Higgins, Sheiham, Logan. CDSR Fluoride in Dentifrice Rinse Gel Varnish Outcome measure: SMD compares caries increment across the two groups (P  D > 0 favours D) Placebo, No treatment Background

Placebo Dentifrice Varnish Rinse Gel No treat The data

Placebo Dentifrice Varnish Rinse Gel P – D = M P – G = M The idea 3 D – G=M 2 – M 1 SD= 3 Extend the idea to analyse jointly the 130 studies by combining direct and indirect evidence in a RE model across the network

RE model, fitted in WinBUGS, taking into account correlation in multi-arm trials (I spare you the technical details) Joint analysis of all trials by taking advantage of indirect evidence: we gain precision! Should we be tempted do so? Check the validity of multiple treatments meta- analysis MT Meta-analysis

InterventionEffect size Probability it’s the best No treatment00% Placebo0.23(0.09,0.34)0% Dentifrice0.55(0.41,0.70)61% Gel0.45(0.32,0.58)3% Rinse0.51(0.37,0.65)12% Varnish0.51(0.34,0.67)24% Dentifrice appears as the best treatment Placebo seems to have an effect? DIC= – 82.12, Heterogeneity standard deviation = 0.20 (0.16,0.24) Results

Placebo Dentifrice Varnish Rinse Gel P – D = P – G = D – G = – 0.12 (SE 0.06) D – G = – 0.01 (SE 0.06) Incoherence = weighted difference between direct and indirect evidence The problem! Extended in all closed loops

How important is the apparent conflict between direct and indirect evidence? Can we identify sources of incoherence? What can we do to improve the agreement? Incoherence

Closed loops NGR NRV NGV PDR PDG PDV PGR PRV PGV DGR DRV DGV GRV NGRV PDGR PDRV PDGV PGRV DGRV PDGRV Estimates with 95% confidence intervals Indirect and direct evidence combined using the inverse variance method Incoherence in each loop Head to head comparison is overestimated when going through placebo Coherence seems better when we use another treatment as the intermediate step

Placebo Dentifrice Gel D – G = – 0.12 (0.06) D – G = – 0.01 (0.06) Incoherence Incoherence: Different placebo effects? P-Gel P-Dentifrice I cannot learn about D versus G through placebo Is this the case in my data?

Reference Placebo configuration DIC Placebo or NT (NT, P D,G,R,V ) – 70.5 NT P D,G,R,V – 82.1 NT P D, P G,R,V – 81.8 NT P D, P G,V, P R, – 81.0 NT P D, P G, P R, P V – 80.7 All placebos work the same Analyse separately NT and placebo controlled trials Compare different placebo effects

Placebo Dentifrice Gel Incoherence Incoherence: Confounding 1968 Comparison UnadjustedAdjusted (to 1969) PD 0.33 (SD 0.03) 0.30 (SD 0.05) PG 0.21 (SD 0.05) 0.25 (SD 0.06) DG indirect – 0.12 (SD 0.06)– 0.05 (SD 0.07) DG direct – 0.01 (SD 0.06) Example: year of randomisation 69 studies!

No. studiesDGRVPFupBaselineYearWater F (yes/no) NA NA NA No. studiesDGRVPFupBaselineYearWater F (yes/no) NA NA NA Differences in year reflect differences in baseline Possible confounders

Meta-analysis Meta-regression  0.04  0.08  0.01  InterventionEffect size Probability it’s the best Effect size Probability it’s the best Placebo 00%0 Dentifrice 0.31(0.27,0.36)62%0.30(0.25,0.35)31% Gel 0.23(0.13,0.34)6%0.24(0.13,0.35)5% Rinse 0.29(0.22,0.36)21%0.30(0.23,0.36)23% Varnish 0.24(0.09,0.38)11%0.30(0.14,0.45)41% 22 0.17(0.14,0.21) ) year ( β+ θ=SMD P-T i i MT Meta-regression i

No. studiesDGRVPFupBaselineYearWater F (yes/no) NA NA NA No. studiesDGRVPFupBaselineYearWater F (yes/no) NA NA NA

But don’t get too excited!!! –Need very careful examination of the underlying assumptions (especially absence of confounders) –We need user-friendly tools to assess incoherence –Expertise is needed (Bayesian models, multi-arms studies) Is this the future of meta-analysis in the Cochrane collaboration? Need ‘umbrella reviews’ to compare multiple interventions for the same condition Increased precision Comprehensive ranking