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. 2020 Jan 21;368:l6802. doi: 10.1136/bmj.l6802

Table 2.

Adjusted analyses. Data are outcome measure (95% credible interval) unless stated otherwise

No of meta-analyses, trials Adjusted for patient blinding Adjusted for allocation concealment Adjusted for incomplete outcome data Adjusted for trial size
ROR Ф ĸ ROR Ф ĸ ROR Ф ĸ ROR Ф ĸ
(Ia) Effect of blinding patients in trials with patient reported outcomes
18, 132 NA 0.91 (0.61 to1.35) 0.20 (0.02 to 0.74) 0.21 (0.01 to 0.61) 0.91 (0.63 to 1.31) 0.17 (0.01 to 0.70) 0.18 (0.01 to 0.60) 0.89 (0.59 to 1.29)* 0.18 (0.02 to 0.74) 0.18 (0.01 to 0.60)
(Ib) Effect of blinding patients in trials with blinded observer reported outcomes
14, 95 NA 1.07 (0.74 to 1.56) 0.11 (0.01 to 0.57) 0.10 (0.01 to 0.57) 1.08 (0.72 to 1.58) 0.10 (0.01 to 0.52) 0.13 (0.01 to 0.72) 0.99 (0.69 to 1.39) 0.10 (0.01 to 0.54) 0.10 (0.01 to 0.57)
(IIa) Effect of blinding healthcare providers in trials with healthcare provider decision outcomes
29, 173 NA 1.03 (0.84 to 1.23) 0.07 (0.01 to 0.29) 0.06 (0.01 to 0.28) 0.98 (0.80 to 1.17) 0.06 (0.01 to 0.28) 0.07 (0.01 to 0.30) 1 (0.83 to 1.19) 0.06 (0.01 to 0.27) 0.06 (0.01 to 0.29)
(IIb) Effect of blinding healthcare providers in trials with blinded observers/patients assessing the outcome
13, 91 NA 1.03 (0.67 to 1.54) 0.13 (0.01 to 0.80) 0.10 (0.01 to 0.60) 1.07 (0.69 to 1.64) 0.12 (0.01 to 0.77) 0.09 (0.01 to 0.60) 0.98 (0.63 to 1.44) 0.13 (0.01 to 0.82) 0.09 (0.01 to 0.58)
(III) Effect of blinding outcome assessors (that is, observers) in trials with subjective outcomes
46, 397 1.03 (0.87 to 1.23) 0.10 (0.01 to 0.32) 0.06 (0.01 to 0.22) 1.04 (0.89 to 1.23) 0.10 (0.01 to 0.36) 0.05 (0.01 to 0.21) 1.02 (0.87 to 1.19) 0.08 (0.01 to 0.33) 0.05 (0.01 to 0.19) 1.03 (0.88 to 1.21) 0.10 (0.01 to 0.34) 0.06 (0.01 to 0.25)

NA=not applicable; ROR=ratio of odds ratios; ĸ=standard deviation increase in heterogeneity between trials; Ф=standard deviation in mean bias between meta-analyses.

*

One meta-analysis (three trials) was removed, which did not specify the size of the trial owing to the format given in the review.