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. 2025 Feb 12;5(1):e44. doi: 10.1017/ash.2025.4

Table 2.

Comparison of aggregate primary and secondary outcomes between cohorts

Outcome Pre-intervention
n = 147
Post-intervention
n = 169
P
Total days of therapy, median (IQR) 10 (7.5 – 14) 7 (7 – 10) < 0.01
Received seven days of therapy, n (%) 19 (12.9) 98 (58) < 0.01
Initial use of intravenous therapy, n (%) 146 (99.3) 164 (97) 0.14
Use of oral switch therapy, n (%) Any oral agent 85 (57.8) 122 (72.2) <0.05
Beta-lactam 42 (28.6) 45 (26.6) 0.70
Fluoroquinolone 33 (22.4) 63 (37.3) < 0.05
Cefdinir 21 (14.3) 7 (4.1) <0.01
TMP-SMX 10 (6.8) 13 (7.7) 0.76
Amoxicillin 8 (5.4) 2 (1.2) < 0.05
Cephalexin 6 (4.1) 26 (15.4) < 0.01
Amoxicillin-clavulanate 7 (4.8) 10 (5.9) 0.65
Other oral agent a 0 (0) 1 (0.6) N/A
Days to oral switch, mean (SD) 4.8 (2.4) 4.5 (3.7) < 0.05
Use of repeat blood cultures, n (%) Repeat blood cultures collected 74 (50.3) 51 (30.2) < 0.01
Positive repeat blood cultures for same gram-negative pathogen 3 (2) 4 (2.4) 0.84
Cases with repeat blood cultures positive for a contaminant organism 7 (4.8) 3 (1.8) 0.13
Length of hospitalization, median (IQR) 5 (3–10) 4 (3–8) 0.15
90-day incidence of C. difficile infection, n (%) 7 (4.8) 1 (0.6) < 0.05
90-day rehospitalization, n (%) 49 (33.3) 56 (33.1) 0.97
90-day recurrence of GN-BSI, n (%) 2 (1.4) 3 (1.8) 0.57
90-day mortality, n (%) 21 (14.3) 13 (7.7) 0.06

n, number of members; %, percentage of sample size; IQR, interquartile ratio; SD, standard deviation; GN-BSI, gram-negative bloodstream infection.

a

Fosfomycin (n = 1).