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. 2022 Sep 7;76(1):66–77. doi: 10.1093/cid/ciac738

Table 4.

Distribution of Pathogens by Extended-Spectrum β-Lactamase, Ciprofloxacin, Trimethoprim–Sulfamethoxazole, and Nitrofurantoin Susceptibility—Microbiologic Modified Intent-to-Treat Population

Susceptibility Category Sulopenem
(N = 517)
n (%)
Ciprofloxacin
(N = 554)
n (%)
Total
(N = 1071)
n (%)
Ciprofloxacin-nonsusceptible 150 (29.0) 143 (25.8) 293 (27.4)
β-lactam–nonsusceptible 330 (63.8) 345 (62.3) 675 (63.0)
ȃExtended-spectrum β-lactamase–positive 73 (14.1) 72 (13.0) 145 (13.5)
ȃOnly amoxicillin/ampicillin–nonsusceptible 88 (17.0) 95 (17.1) 183 (17.1)
Trimethoprim–sulfamethoxazole-nonsusceptible 171 (33.1) 167 (30.1) 338 (31.6)
Nitrofurantoin-nonsusceptible 97 (18.8) 95 (17.1) 192 (17.9)
Nonsusceptible to 3 classes 65 (12.6) 51 (9.2) 116 (10.8)
Nonsusceptible to 4 classes 25 (4.8) 28 (5.1) 53 (4.9)

Patients were considered extended-spectrum β-lactamase–positive if they had a baseline urine specimen positive for at least 1 Enterobacterales with a ceftriaxone minimum inhibitory concentration >1 µg/mL. A pathogen is β-lactam–resistant if it is resistant to at least 1 of the following drugs: sulopenem, cefazolin, ertapenem, meropenem, ampicillin, ceftazidime, ceftriaxone, amoxicillin, imipenem, piperacillin-tazobactam. Nonsusceptible to 3 classes = nonsusceptible to ciprofloxacin, trimethoprim–sulfamethoxazole, and at least 1 β-lactam. Nonsusceptible to 4 classes = nonsusceptible to ciprofloxacin, trimethoprim–sulfamethoxazole, at least 1 β-lactam, and nitrofurantoin.