Table 2. Subgroup analyses based on various exclusion criteria for the TDI focal score.
Outcome | n [N] | WMD (95% CI) | P value | I2 (%) | Pheterogeneity |
---|---|---|---|---|---|
All included trials (9,10) | 4,767 [4] | 0.30 (0.14 to 0.46) | 0.0003 | 28 | 0.24 |
Duration: 52 wk (9) | 3,091 [2] | 0.30 (0.11 to 0.49) | 0.002 | 0 | 1.00 |
Duration: 24 wk (10) | 1,676 [2] | 0.30 (–0.09 to 0.69) | 0.13 | 76 | 0.04 |
Monotherapy (9) | 3,091 [2] | 0.30 (0.11 to 0.49) | 0.002 | 0 | 1.00 |
Combination therapy (10) | 1,676 [2] | 0.30 (–0.09 to 0.69) | 0.13 | 76 | 0.04 |
Roflumilast + salmeterol (10) (M2-127) | 933 [1] | 0.10 (–0.17 to 0.37) | 0.47 | — | — |
Roflumilast + tiotropium (10) (M2-128) | 743 [1] | 0.50 (0.23 to 0.77) | 0.0003 | — | — |
Moderate to severe (10) | 1,676 [2] | 0.30 (–0.09 to 0.69) | 0.13 | 76 | 0.04 |
Severe to very severe (9) | 3,091 [2] | 0.30 (0.11 to 0.49) | 0.002 | 0 | 1.00 |
TDI, the transition dyspnea index; n, number of patients; N, number of trials; WMD, weighted mean difference.