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. 2006 Jul;44(7):2622–2625. doi: 10.1128/JCM.00576-06

TABLE 1.

Comparison of dalbavancin MIC results to those of vancomycin and teicoplanin tested against four gram-positive organism groupsa

Organism No. of strains tested
Dalbavancin MIC (μg/ml)e No. (%) of strains for which vancomycin MIC (μg/ml) wasf:
No. (%) of strains for which teicoplanin MIC (μg/ml) was:
Vancomycin Teicoplanin ≤1 2 4 ≤8 16 ≥32
S. aureusb 11,867 11,867 ≤0.5 11,472 (96.7) 394 (3.3) 1 (<0.1) 11,865 (>99.9) 2 (<0.1)

1
Coagulase-negative staphylococcic 3,450 3,450 ≤0.5 2,040 (59.1) 1,388 (40.2) 17 (0.5) 3,329 (96.4) 96 (2.8) 20 (0.6)
1 3 (<0.1) 2 (<0.1) 4 (0.1) 1 (<0.1)
β-Hemolytic streptococcid 1,051 1,050 ≤0.5 1,051 (100.0) 1,050 (100.0)

1
Viridans group streptococcid 381 380 ≤0.5 381 (100.0) 380 (100.0)
1
a

Susceptibility testing was by CLSI methods (4), and a total of 16,749 strains were tested.

b

For S. aureus, the CLSI susceptibility breakpoint for vancomycin is 2 μg/ml, and that for teicoplanin is ≤8 μg/ml (5).

c

For coagulase-negative staphylococci, the CLSI susceptibility breakpoint for vancomycin is 4 μg/ml, and that for teicoplanin is ≤8 μg/ml (5).

d

For β-hemolytic streptococci, the CLSI susceptibility breakpoint for vancomycin is ≤1 μg/ml (5), and intermediate and resistant categories have not been defined. No CLSI interpretive criteria for teicoplanin have been published for streptococcal isolates.

e

Two possible breakpoints (≤0.5 and ≤1 μg/ml) for dalbavancin were used. Higher concentrations (2 and ≥4 μg/ml) of dalbavancin were also tested, but the MIC of this drug was not higher than 1 μg/ml for any strain.

f

Higher concentrations (8, 16, and ≥32 μg/ml) of vancomycin were also tested, but the MIC of this drug was not higher than 4 μg/ml for any strain.