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. 2021 Jul 19;60(10):4450–4462. doi: 10.1093/rheumatology/keab429

Table 2.

Rates and rate ratios for serious adverse events, serious infections and non-serious adverse events from network meta-analysis and pairwise meta-analysis

Number of patients Rate
Rate ratio (PMA)
I2 Rate ratio (NMA)
SUCRA
Estimate 95% LL 95% UL Estimate 95% LL 95% UL Estimate 95% LL 95% UL
Serious adverse events
MTX + placebo 3425 71 62.9 80.5 1 1 0.6
MTX + bDMARD 3082 115.2 104.2 126.3 1.07 0.91 1.27 0.0% 1.11 0.94 1.3 0.4
bDMARD 785 139.5 118.9 160.2 1.4 1.05 1.87 0.0% 1.39 1.12 1.73 0.2
tsDMARD 1246 55.6 44.3 66.9 0.93 0.65 1.33 0.0% 0.88 0.59 1.31 0.7
MTX + tsDMARD 215 87.3 56.8 117.8 0.72 0.33 1.57 NA 0.88 0.54 1.44 0.6
SSZ 34 88.2 −11.6 188.1 3.6 0.19 69.75 NA 7.89 0.39 158.73 0.1
MTX + SSZ 36 13.9 −24.6 52.4 0.49 0.01 24.5 NA 0.97 0.02 50.36 0.5
MTX + Steroid 174 11.2 −0.5 22.9 0.41 0.08 2.1 NA 0.43 0.2 0.93 0.9
Overall 8997 69.8 64.9 74.8
Serious infections
MTX + placebo 3390 18.7 14.2 23.6 1 1 0.5
MTX + bDMARD 3082 26.7 21.4 32.0 0.99 0.70 1.39 0.0% 1.05 0.72 1.51 0.4
bDMARD 785 14.6 7.9 21.3 1.34 0.59 3.06 9.3% 1.22 0.67 2.21 0.3
tsDMARD 1246 13.1 7.7 18.6 1.00 0.51 1.96 0.0% 1.01 0.44 2.28 0.5
MTX + tsDMARD 215 26.8 9.9 43.6 0.53 0.14 1.97 NA 0.74 0.29 1.86 0.7
SSZ
MTX + SSZ
MTX + Steroid 57 12.6 −12.1 37.4 0.53 0.04 6.60 0.7
Overall 8775 18.9 16.2 21.6
Non-serious adverse events
MTX + placebo 3061 937.9 903.3 972.4 1 1 0.5
MTX + bDMARD 2638 1126.8 1088.6 1165.1 0.96 0.92 1.01 2.7% 0.97 0.90 1.05 0.6
bDMARD 511 1142.2 1069.3 1215.2 0.93 0.85 1.01 0.0% 0.96 0.85 1.08 0.7
tsDMARD 1246 1504.4 1445.8 1562.9 1.06 0.98 1.15 0.0% 1.07 0.93 1.21 0.3
MTX + tsDMARD 215 947.1 846.7 1047.5 0.94 0.71 1.23 NA 0.98 0.81 1.20 0.6
SSZ 102 957.4 767.6 1147.3 1.04 0.74 1.47 0.0% 1.04 0.70 1.54 0.4
MTX + SSZ 104 958.5 770.4 1146.7 1.04 0.74 1.47 0.0% 1.05 0.71 1.54 0.4
MTX + Steroid 174 479.1 402.4 555.8 0.93 0.69 1.25 NA 0.97 0.76 1.24 0.6
Overall 8051 1048.2 1027.5 1068.9

Pooled incidence rate per 1000 patient- years and rate ratios for serious adverse events, serious infections and non-serious adverse events across treatment strategies based on studies with direct comparisons. For strategies with zero events reported in one or both arms, a continuity correction of a fixed value (0.5) was added to each cell to create an event rate to allow odds ratio comparisons of the event rates between studies. Higher SUCRA values indicate a greater likelihood of a given treatment causing the least number of events, such that when the SUCRA value is 1, the treatment is the best, and when it is 0, it is the worst. I2 test reflects the the percentage of the variability in effect estimates that is due to heterogeneity. bDMARD: biologic DMARD; I2: I square statistics; NA: not applicable as only one study was available for that strategy; NMA: network meta-analysis; PMA: pairwise meta-analysis; SUCRA: Surface Under the Cumulative RAnking curve; tsDMARD: targeted synthetic DMARD.