TABLE 2.
Details of antibiotic treatment a
Variable | CMZ (n = 81) | MEM (n = 46) | P value b |
---|---|---|---|
Total duration of study drug, median (IQR) | 8 (6–12) | 9 (5–12) | 0.920 |
Total duration of all antibiotics, median (IQR) | 11 (8–14) | 12 (10–16) | 0.087 |
Empiric therapy c | |||
None | 24 (29.6%) | 28 (60.9%) | 0.001 |
AMP | 1 (1.2%) | 0 | >0.999 |
SAM | 8 (9.9%) | 3 (6.5%) | 0.745 |
TZP | 9 (11.1%) | 4 (8.7%) | 0.768 |
CFZ | 1 (1.2%) | 0 | >0.999 |
CRO | 33 (40.7%) | 8 (17.4%) | 0.01 |
FEP | 1 (1.2%) | 1 (2.2%) | >0.999 |
MEM | 3 (3.7%) | NA | NA |
FQ d | 2 (2.5%) | 2 (4.3%) | 0.62 |
Oral cephalosporin e | 2 (2.5%) | 0 | 0.534 |
Treatment continuation after study therapy f | |||
Any | 16 (19.8%) | 24 (52.2%) | <0.001 |
SAM | 1 (1.2%) | 0 | >0.999 |
AMC | 0 | 1 (2.2%) | 0.362 |
TZP | 1 (1.2%) | 0 | >0.999 |
CMZ | NA | 16 (34.8%) | NA |
MEM | 2 (2.5%) | NA | NA |
FQ d | 4 (4.9%) | 1 (2.2%) | 0.653 |
SXT | 7 (8.6%) | 1 (2.2%) | 0.257 |
Other g | 1 (1.2%) | 2 (4.3%) | 0.297 |
Abbreviations. AMC, amoxicillin–clavulanic acid; AMP, ampicillin; CFZ, cefazolin; CRO, ceftriaxone; FEP, cefepime; FQ, fluoroquinolone (levofloxacin, ciprofloxacin, garenoxacin); NA, not available; SAM, ampicillin–sulbactam; SXT, trimethoprim–sulfamethoxazole; TZP, piperacillin–tazobactam.
Bold font indicates statistically significant results (P <0.05).
Empiric therapy was defined as antibiotics active against Gram-negative bacteria that have been used within 96 h prior to the start of the study drug (i.e., CMZ or MEM). Four patients (three in CMZ group and one in MEM group) received two antibiotics, and both antibiotics were counted separately.
FQ include two levofloxacin, one ciprofloxacin, and one garenoxacin in empiric treatment, and three levofloxacin and one ciprofloxacin in treatment continuation.
Oral cephalosporin includes one cefditoren pivoxil and one cefcapene pivoxil.
Two patients (one in CMZ group and one in MEM group) received two antibiotics, and both antibiotics were counted separately for each antibiotics category.
Includes one patient each treated with fosfomycin and minocycline (MEM group) and one patient who received CFZ (CMZ group).