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. 2023 Sep 8;3(1):e148. doi: 10.1017/ash.2023.435

Table 1.

. Baseline characteristics

Characteristic Beta-lactam (n = 75) FQ or TMP/SMX (n = 119) p-value
Female sex, n (%) 49 (65.3) 76 (63.9) 0.835
Age, median (IQR) 71 (60–79) 72 (62–79) 0.730
BMI ≥35 kg/m 2 , n (%) 14 (18.9) 25 (21) 0.725
Allergy, n (%)
 • Penicillin 13 (17.3) 20 (16.8) 0.924
 • Cephalosporin 4 (5.3) 7 (5.9) 1.0
 • FQ 4 (5.3) 3 (2.5) 0.433
 • Sulfa 17 (22.7) 18 (15.1) 0.183
Charlson comorbidity index, median (IQR) 1 (0–2) 2 (1–3) 0.213
Renal stone, n (%) 16 (21.3) 35 (29.5) 0.213
Creatinine clearance at transition to PO antibiotic, n (%)
 • ≥50 mL/min 43 (57.3) 45 (38.1) 0.034
 • 30–49 mL/min 22 (29.3) 42 (35.6)
 • 10–29 mL/min 10 (13.3) 28 (23.7)
 • <10 mL/min or dialysis 0 (0) 3 (2.5)
Urologic procedure, n (%) 15 (20) 30 (25.2) 0.402
Foley catheter status, n (%)
 • Present on admission 6 (8) 13 (10.9) 0.505
 • Present during admission 20 (26.7) 53 (44.5) 0.012
 • Present on discharge 7 (9.3) 20 (16.8) 0.143
WBC, median (IQR)
 • Initiation of IV antibiotic 13.7 (9.2–18.4) 14.5 (9.7–20.8) 0.555
 • Initiation of PO antibiotic 8.1 (6.2–12.2) 9.1 (7.2–11.7) 0.511
Temperature ≥38 °C, n (%) 58 (77.3) 86 (72.3) 0.432
Day of defervescence, median days (IQR) 2 (2–3) 2 (2–3) 0.445
Infectious disease consult, n (%) 17 (22.7) 70 (58.8) <0.001
Blood cultures repeated, n (%) 82 (68.9) 26 (34.7) <0.001
 • Positive repeat cultures, n (%) 3 (2.5) 0 (0) 0.573
ICU admission, n (%) 4 (5.3) 19 (16) 0.038
Vasopressor required, n (%) 3 (4) 11 (9.2) 0.255
Empiric regimen, n (%)
 • Anti-pseudomonal beta-lactam 5 (6.7) 42 (35.3) <0.001
 • Aztreonam 2 (2.7) 3 (2.5)
 • Ceftriaxone 68 (90.7) 69 (58)
 • Ertapenem 0 (0) 3 (2.5)
 • Fluoroquinolone 0 (0) 2 (1.7)
Enterobacterales isolated, n (%)
 • Escherichia coli 58 (77.3) 92 (77.3) 0.995
 • Klebsiella species 13 (17.3) 21 (17.6)
 • Proteus mirabilis 4 (5.3) 6 (5)
Susceptibility, n (%)
 • Aminopenicillin 43 (57.3) 60 (50.4) 0.347
 • Cefazolin 75 (100) 41 (91.1)* 0.018
 • Ciprofloxacin 73 (97.3) 114 (95.8) 0.708
 • TMP/SMX 64 (85.3) 99 (83.2) 0.692
Treatment duration, n (%)
 • 7 days 1 (1.3) 12 (10.1) 0.802
 • 8–10 days 35 (46.7) 42 (35.3)
 • 11–13 days 19 (25.3) 33 (27.8)
 • 14 days 10 (13.3) 20 (16.8)
 • >14 days 10 (13.2) 12 (10)

*Standard therapy patients tested for cefazolin susceptibility (n = 45) due to change in Clinical Laboratory Standards Institute (CLSI) breakpoint change.