Table 6. Results for the efficacy and safety-related endpoints from the network meta-analysis.
Endpoint | Patient subgroup | Model (RE/FE) | Pairwise comparison | OR (CrI) |
---|---|---|---|---|
Clinical Treatment Success | Adult | RE | DAL vs VAN | 0.99 (0.68; 1.51) |
DAL vs LZD | 0.69 (0.41; 1.00) | |||
DAL vs DAP | 1.05 (0.61; 2.10) | |||
DAL vs TIG | 1.18 (0.71; 2.10) | |||
Mixed Population | RE | DAL vs VAN | 0.96 (0.69; 1.35) | |
DAL vs LZD | 0.73 (0.50; 1.02) | |||
DAL vs DAP | 1.00 (0.63; 1.76) | |||
DAL vs TIG | 1.14 (0.72; 1.83) | |||
DAL vs TEI | 1.67 (0.44; 7.37) | |||
Microbiological success | Adult | RE | DAL vs VAN | 1.31 (0.40; 4.93) |
DAL vs LZD | 0.53 (0.11; 1.85) | |||
DAL vs DAP | 1.85 (0.32; 12.72) | |||
DAL vs TIG | 2.29 (0.44; 14.36) | |||
Mixed Population | RE | DAL vs VAN | 1.21 (0.41; 4.01) | |
DAL vs LZD | 0.61 (0.16; 1.87) | |||
DAL vs DAP | 1.71 (0.33; 10.11) | |||
DAL vs TIG | 2.10 (0.47; 11.32) | |||
Discontinuation due to AEs/SAEs | Adult | FE | DAL vs VAN | 1.08 (0.59; 1.98) |
DAL vs LZD | 1.24 (0.68; 2.30) | |||
DAL vs DAP | 1.28 (0.53; 3.09) | |||
DAL vs TIG | 1.43 (0.65; 3.23) | |||
Patients experiencing AEs | Adult | FE | DAL vs VAN | 0.85 (0.70; 1.03) |
DAL vs LZD | 0.78 (0.62; 0.98) | |||
DAL vs DAP | 1.05 (0.76; 1.46) | |||
DAL vs TIG | 0.78 (0.59; 1.02) | |||
Patients experiencing SAEs | Adult | FE | DAL vs VAN | 0.54 (0.30; 0.96) |
DAL vs LZD | 0.99 (0.61; 1.66) | |||
DAL vs DAP | 0.48 (0.24; 0.95) | |||
DAL vs TIG | 0.58 (0.25; 1.35) | |||
All-cause mortality | Adult | FE | DAL vs VAN | 0.26 (0.05; 0.93) |
DAL vs LZD | 0.20 (0.04; 0.77) | |||
DAL vs DAP | 0.34 (0.05; 1.71) | |||
DAL vs TIG | 0.06 (0.00; 0.44) |
Abbreviations: AE: adverse event; CrI: credible interval; DAL: dalbavancin; DAP: daptomycin; FE: Fixed Effect; LZD: linezolid; RE: random effect; SAE: serious adverse event; TEI: teicoplanin; TIG: tigecycline; VAN: vancomycin.
In bold, statistically significant.