Abstract
Background
Fosfomycin is an appealing cystitis treatment; however, guidelines recommend against fosfomycin for non-E. coli gram negatives due to reduced in vitro activity associated with FosA, an enzyme that hydrolyzes fosfomycin but does not always result in full resistance. These concerns have yet to be corroborated in efficacy studies. The purpose of this study was to determine if fosfomycin is an acceptable treatment for cystitis caused by non-E. coli gram negatives with high rates of FosA.
Methods
This was a single-center, retrospective, cohort study evaluating the efficacy of fosfomycin for cystitis caused by E. coli versus non-E. coli gram negatives with high rates of FosA, including K. pneumoniae, P. aeruginosa, K. aerogenes, K. oxytoca, M. morganii, and E. cloacae. Patients with an inpatient or outpatient fosfomycin order to treat cystitis caused by these bacteria were included. Patients were excluded if there was a lack of cystitis symptoms, evidence of pyelonephritis, polymicrobial culture, or ≥ 48 hours of antimicrobial therapy prior to fosfomycin. The primary outcome was 30-day treatment failure defined as persistence or recurrence of cystitis symptoms with either a positive culture (same bacteria) or antibiotic re-treatment.
Results
104 cases of cystitis were included in the study, 53 in the E. coli group and 51 in the non-E. coli group. Patient characteristics are presented in Table 1. The E. coli group had a higher median BMI; 26 (49%) vs 13 (25%) were obese (p=0.013). With 32 (63%) cases, K. pneumoniae was the most common non-E.coli and all but 10 cases were Enterobacterales. Treatment failure occurred in 17 (32%) of the E. coli group and 18 (35%) of the non-E. coli group (p=0.73) (Table 2). Among the failures, about half had a repeat positive culture, all failures received re-treatment, and median time to failure was 10 days for E. coli vs 7 days for non-E. coli. Figure 1 shows time to failure within groups, and Figure 2 shows failures by species.
Conclusion
These data suggest failure rates for fosfomycin are relatively high in all cases of gram negative cystitis, regardless of FosA. Presence of FosA may not be as clinically relevant as guidelines suggest when deciding to use fosfomycin for cystitis. Additional studies are needed to validate these findings.
Disclosures
John C. Williamson, PharmD, Armata Pharmaceuticals: Grant/Research Support|Blue Collar Vaccines and Therapeutics: Board Member|Blue Collar Vaccines and Therapeutics: Ownership Interest|Paratek Pharmaceuticals: Grant/Research Support|ST Pharm Co, Ltd: Grant/Research Support