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. 2017 Nov 14;12(11):e0187792. doi: 10.1371/journal.pone.0187792

Table 2. Summary information of all RCTs included in the network meta-analysis.

Trial acronym Source Design Population Treatment (sample size) Primary Endpoint
Aikawa 2013 [49] R/MC/Ph3/OL Confirmed MRSA-cSSTI DAP (n = 88)
VAN (n = 22)
Clinical and microbiological response at TOC
DAP-SST-98-01 and
DAP-SST-99-01
[45] R/MC/Ph3/SB cSSSI DAP (n = 534)
PRP (cloxacillin, nafcillin, OXA, or flucloxacillin), or VAN (n = 558)
Clinical response at TOC
DISCOVER 1 [32] R/MC/Ph3/DB ABSSSI DAL (n = 288)
VAN, with an option to switch to oral LZD (n = 285)
Early clinical response (after 48 to 72 hours of therapy)
DISCOVER 2 [32] R/MC/Ph3/DB ABSSSI DAL (n = 371)
VAN, with an option to switch to oral LZD (n = 368)
Early clinical response (after 48 to 72 hours of therapy)
Breedt 2005 [44] R/MC/Ph3/DB cSSSI TIG (n = 275)
VAN + AZA (n = 271)
Clinical response at TOC
Florescu 2008 [53] R/MC/Ph3/DB Confirmed MRSA-cSSSI, cIAI or pneumonia TIG (n = 118; patients with cSSSI: 83)
VAN or LZD (n = 39; patients with cSSSI: 27)
Clinical response at TOC
Itani 2010 [50] R/MC/Ph4/OL Confirmed MRSA-cSSTI LZD (n = 537)
VAN (n = 515)
Clinical cure at EOT
VER001-9 [33] R/MC/Ph3/DB cSSSI DAL (n = 571)
LZD (n = 283)
Clinical success at TOC
Katz 2008 [46] R/MC/SB cSSSI DAP (n = 48)
VAN (n = 48)
Clinical response at 7–14 days post-therapy
Kohno 2007 [12] R/MC/OL Confirmed MRSA-cSSTI, pneumonia or sepsis LZD (n = 100; patients with cSSTI: 31)
VAN (n = 51; patients with cSSTI:17)
Clinical and microbiological outcome EOT
Konychev 2013 [54] R/MC/Ph3/OL cSSTI with or without bacteraemia DAP (n = 81)
SSP or VAN (n = 39)
Clinical success at TOC
Lin 2008 [51] R/MC/Ph3/DB cSSTI or pneumonia LZD (n = 71; patients with cSSTI: 33)
VAN (n = 71; patients with cSSTI: 29)
Effective treatment rate at EOT and FU
Sacchidanand 2005 [47] R/MC/Ph3/DB cSSSI TIG (n = 295)
VAN + AZA (n = 298)
Clinical cure rate at TOC
Sharpe 2005 [13] R/OL Confirmed MRSA-cSSTI LZD (n = 30)
VAN (n = 30)
Clinical and microbiological outcomes
Stevens 2002 [14] R/MC/OL Presumed or confirmed MRSA-cSSTI, pneumonia or urinary tract infection LZD (n = 240; patients with cSSTI: 102)
VAN (n = 220; patients with cSSTI: 108)
Clinical and microbiological outcomes at TOC
Teras 2008 [48] R/MC/Ph3/DB cSSSI TIG (n = 196)
VAN + AZA (n = 191)
Clinical response at TOC
Weigelt 2005 [15] R/MC/OL Presumed or confirmed MRSA-cSSTI LZD (n = 476)
VAN (n = 454)
Clinical response at TOC
Wilcox 2004 [52] R/MC/Ph3/OL cSSTI, pneumonia, right-sided endocarditis, or bacteraemia LZD (n = 215; patients with cSSTI: 123)
TEI (n = 215; patients with cSSTI: 117)
Clinical outcome at the EOT and TOC visits
Wilcox 2009 [55] R/MC/OL Presumed or confirmed MRSA-cSSSI or CRBSI LZD (n = 363; patients with cSSSI: 164)
VAN (n = 363; patients with cSSSI: 151)
Microbiologic outcome at TOC

Abbreviations: ABSSSI: acute bacterial skin and skin structure infection; AZA: aztreonam; CRBI: catheter-related bloodstream infection; cSSSI: complicated skin and skin structure infection; cSSTI: complicated skin and soft tissue infection; DAL: dalbavancin; DAP: daptomycin; DB: double blinded; EOT: end of treatment; ITT: intent to treat; LZD: linezolid; MC: multicentre; MRSA: methicillin-resistant Staphylococcus aureus; OL: open label; OMA: omadacycline; OXA: oxacillin; Ph: phase; R: randomised; SB: single blinded; SSP: semi-synthetic penicillin; TEI: teicoplanin; TIG: tigecycline; TOC: test of cure; tx: treatment; TZD: tedizolid phosphate; VAN: vancomycin.