P-936. Impact of an Antimicrobial Susceptibility Reporting Change for Serratia marcescens

Abstract Background ­The use of labile, weak AmpC-inducing β-lactams (e.g., ceftriaxone (CRO), ceftazidime (CAZ), piperacillin-tazobactam (TZP)) for organisms with moderate risk of inducible AmpC production may lead to treatment failure due to AmpC overproduction. Recent guidance from the Infectious Disease Society of America and Clinical Laboratory Standards Institute state Serratia marcescens is at low risk of significant AmpC production and suggests it is reasonable to treat low-risk organisms with a labile, weak AmpC-inducing β-lactam. Prior to October 2023, S. marcescens isolates were reported as resistant to CRO, CAZ and TZP at our institution; these susceptibilities are now reported as tested.Figure 1.Inclusion-Exclusion FlowchartTable 1.Baseline Characteristics Methods This study evaluated safety, effectiveness, and antibiotic utilization before and after this change in susceptibility reporting. The primary outcome was AmpC stable β-lactam (cefepime or carbapenem) inpatient days of therapy (DOT). This pre-test (October 2022–September 2023), post-test (October 2023–September 2024) quasi-experiment included inpatients at Barnes-Jewish and St. Louis Children’s Hospitals with first-positive S. marcescens culture and at least 48 hours of antibiotic therapy. Exclusions included concomitant Gram-negative infections resistant to CRO, CAZ, or TZP, ocular cultures, and death prior to susceptibility results.Table 2.Days of Gram-Negative Antimicrobial TherapyTable 3.Clinical and Microbiological Outcomes Results A total of 268 patients were screened and 166 patients were included (Figure 1). Baseline characteristics including age, ICU status, immunocompromised status, and no or incomplete source control were well balanced between groups (Table 1). The most common infection source was pneumonia (30%). The median total DOT for AmpC stable β-lactams was 8 in the pre-group vs 5 in the post-group (P 0.001) (Table 2). In patients treated with ≥ 3 days of AmpC labile β-lactams who had repeat cultures, there was no emergence of resistance (0/26). No statistically significant differences in clinical outcomes were observed (Table 3). Conclusion In conclusion, a change in susceptibility reporting for S. marcescens was associated with a decrease in AmpC stable β-lactam use, with no significant changes in microbiological or clinical outcomes. Disclosures Christine R. Lockowitz, PharmD, BCIDP, AbbVie: Grant/Research Support|Premier Inc.: Honoraria Tamara Krekel, PharmD, BCPS, BCIDP, AbbVie: Advisor/Consultant|AbbVie: Honoraria|Shionogi: Advisor/Consultant|Shionogi: Honoraria David J. Ritchie, PharmD, BCPS (AQ-ID), Shionogi: Honoraria Rebekah Dumm, PhD D(ABMM), BD: Advisor/Consultant|BD: Grant/Research Support|Biomerieux: Advisor/Consultant|Biomerieux: Grant/Research Support|Diasorin: Grant/Research Support|Pattern Biosciences: Grant/Research Support|Qiagen: Grant/Research Support|Roche Diagnostics: Advisor/Consultant|Shionogi: Advisor/Consultant