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. Author manuscript; available in PMC: 2018 Feb 18.
Published in final edited form as: Clin Microbiol Infect. 2017 Feb 1;23(8):544–549. doi: 10.1016/j.cmi.2017.01.017

Table 3.

Summary of main findings from studies assessing the relationship between vancomycin MIC and prognosis in MSSA bacteraemia and left-sided IE

Study Design SAB/IE (n) Overall mortality Genetic factors Main outcomes analysis

Low VAN MIC (<1.5 μg/mL) High VAN MIC (≥1.5 μg/mL)
Kalil, 2014 [11] Systematic review and metaanalysis SAB (8291, both MRSA and MSSA) 25.8% (1430/5551) 26.8% (734/2740) NA RD 1.6% (95% CI −2.3 to 5.6); p 0.43 (for absolute risk of mortality, combining 30-day mortality and in- hospital mortality)
Holmes, 2011 [1] Prospective multicentre cohort study SAB (532; 266 of which MSSA treated with β-lactams only) 12.2% (24/193) 26.8% (18/68) NA p 0.011 (for 30-day mortality)
Holmes, 2014 [12] Analysis of a subset of strains from [1] SAB (252 MSSA isolates) NA NA Associated to HVM: CC8, agr dysfunction, agr genotype II, blaZ, sea, clfA, splA and ACME locus Associated to LVM: CC22, CC88 and CC188 Associated to HVM: CC8 p <0.001), agr dysfunction (p 0.014), agr genotype II (p 0.043), blaZ (p 0.002), sea (p <0.001), clfA (p <0.001), splA (p <0.001) and ACME locus (p 0.02). Associated to LVM: CC22 (p <0.001), CC88 (p <0.001) and CC188 (p 0.002)
Aguado, 2011 [2] Retrospective, single-centre cohort Catheter- related SAB (99, all MSSA) 10.5% (8/76) 26.1% (6/23) NA p 0.13 (for 30-day mortality) OR = 22.9, (95% CI 6.7 to 78.1) for complicated SAB
López-Cortés, 2015 [4] Prospective, single-centre cohort SAB (135, all MSSA) 23.6% (25/106) 10.3% (3/29) No differences in agr distribution or absence of δ-haemolysin between isolates with HVM and those with LVM. HVM was not more frequent in specific clones RR = 0.44 (95% CI 0.14 to 1.35) for 14-day mortality
Viedma, 2014 [3] Retrospective, single-centre cohort SAB (84, all MSSA) 24.1%, (7/29) 45.5% (25/55) HVM: agr II polymorphism: 17.2% ; average levels of RNAIII gene expression: ΔCt 1.5 ± 2.11
LVM: agr II polymorphism: 41.8% ; average levels of RNAIII gene expression: ΔCt 4.05 ± 3.29
In-hospital mortality: p 0.057 agr dysfunction: p 0.023. RNAIII expression: p <0.01
Cervera, 2014 [5] Prospective, single-centre cohort MSSA IE (93) 31% (16/53) 53% (21/40) NA In-hospital mortality: p 0.035; Patients with HVM presented significantly more severe embolic events
Current study Prospective, multicentre cohort MSSA IE (62) 32% (9/28) 27% (9/34) HVM: agrII polymorphism: 19%
LVM: agrII polymorphism: 38%
In-hospital mortality: p 0.780. agrII polymorphism: p 0.157

CI, confidence interval; HVM, high vancomycin MIC; IE, infective endocarditis; LVM, low vancomycin MIC; MIC, minimum inhibitory concentration; MRSA, methicillin-resistant Staphylococcus aureus; MSSA, methicillin-susceptible S. aureus; NA, not addressed; OR, odds ratio; RD, relative difference; RR, relative risk; SAB, S. aureus bacteraemia; VAN, vancomycin.