Table 3.
Initial therapyc | No. (%) of patients in group |
||
---|---|---|---|
All patients (n = 232) | Therapy within 24 h that was deemed: |
||
Appropriate (n = 85; 37%) | Inappropriate (n = 147; 63%) | ||
Monotherapy | |||
Amoxicillin | 1 (0) | 0 (0) | 1 (1) |
BLBLIC | 24 (10) | 0 (0) | 24 (16) |
2GC | 14 (6) | 0 (0) | 14 (10) |
3GC | 29 (13) | 0 (0) | 29 (20) |
Aminoglycoside | 3 (1) | 1 (1) | 2 (1) |
Fluoroquinolone | 7 (3) | 2 (2)b | 5 (3) |
Cotrimoxazole | 2 (1) | 0 (0) | 2 (1) |
Carbapenem | 62 (27) | 57 (67) | 5 (3) |
Combination therapy | |||
Amoxicillin + aminoglycoside | 5 (2) | 2 (2) | 3 (2) |
Amoxicillin + fluoroquinolone | 4 (2) | 0 (0) | 4 (3) |
BLBLIC + aminoglycoside | 12 (5) | 4 (5) | 8 (5) |
BLBLIC + fluoroquinolone | 2 (1) | 1 (1)b | 1 (1) |
1GC + aminoglycoside | 1 (0) | 0 (0) | 1 (1) |
2GC + aminoglycoside | 16 (7) | 9 (11) | 7 (5) |
2GC + fluoroquinolone | 1 (0) | 1 (1)b | 0 (0) |
3GC + aminoglycoside | 6 (3) | 3 (4) | 3 (2) |
3GC + fluoroquinolone | 3 (1) | 0 (0) | 3 (2) |
β-Lactam + cotrimoxazole | 3 (1) | 0 (0) | 3 (2) |
Aminoglycoside + fluoroquinolone | 1 (0) | 0 (0) | 1 (1) |
Cotrimoxazole + aminoglycoside + fluoroquinolone | 1 (0) | 1 (1) | 0 (0) |
β-Lactam + aminoglycoside + fluoroquinolone | 7 (3) | 4 (5) | 3 (2) |
No antimicrobial therapy | 5 (2) | 0 (0) | 5 (3) |
Therapy started after 24 h | 23 (10) | 0 (0) | 23 (16) |
Appropriateness of therapy was judged according to in vitro susceptibility, duration of therapy, and, for oral fluoroquinolones or cotrimoxazole, severity of sepsis (see description in Materials and Methods).
In 3 instances, oral therapy with fluoroquinolones was deemed appropriate: once as monotherapy, once combined with an intravenous BLBLIC, and once combined with an intravenous second-generation cephalosporin.
1GC, first-generation cephalosporin; 2GC, second-generation cephalosporin; 3GC, third-generation cephalosporin; BLBLIC, β-lactam–β-lactamase inhibitor combination.