Document Type
Article
Publication Date
5-15-2026
Keywords
ceftazidime/avibactam, multidrug-resistant, gram-negative infections, early initiation, carbapenem-resistant Enterobacterales, Pseudomonas aeruginosa, antimicrobial resistance, real-world evidence, rapid diagnostics
Abstract
Ceftazidime-avibactam (CAZ-AVI) is a crucial treatment for multidrug-resistant (MDR) gram-negative infections; however, the impact of treatment timing and outcomes in real-world practice remains unclear. This study evaluated CAZ-AVI use across diverse U.S. centers, with emphasis on early initiation. We conducted a retrospective cohort study at 22 U.S. medical centers (2019–2025), including adults with MDR gram-negative infections who received CAZ-AVI ≥ 72 h. The primary outcome was composite clinical success, defined as 30-day survival, absence of microbiological recurrence, and resolution of fever and/or leukocytosis within 72 h of initiation. Early vs late initiation was assessed at 48 h. Classification and regression tree (CART) analysis was used to identify optimal thresholds. Among 613 patients (median age 60 years, 62.5% male, 57.1% admitted to the ICU within 24 h of index culture), the most common infection source was pneumonia (55.5%), and the most frequent pathogens were Pseudomonas aeruginosa (36.1%) and carbapenem-resistant Enterobacterales (34.7%). Composite clinical success occurred in 64.8%. CAZ-AVI initiation within 48 h was not significantly associated with improved outcomes (P = 0.064). Among patients who did not receive prior active antimicrobial therapy (n = 429), CART analysis identified a 42 h threshold. Initiation within 42 h was associated with higher clinical success (73.3% vs 63.4%, P = 0.046) and lower 30-day all-cause mortality (10.7% vs 19.1%, P = 0.030). In patients with pneumonia, the same threshold remained discriminatory, with improved clinical success and lower mortality. CAZ-AVI was effective for MDR gram-negative infections in real-world practice. Among patients without prior active therapy, initiation within 42 h was associated with improved outcomes, including in pneumonia.
Publisher Attribution
© 2026 Kunz Coyne et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.
Recommended Citation
Kunz Coyne, Ashlan J.; Judd, Chloe; Lucas, Kristen; Musawa, Mohammed Al; Van Helden, Sean; Holger, Dana; Althubyani, Ali; Yost, Christine; VanDorf, Sydney; Mynatt, Ryan; Kufel, Wesley D.; Hayes, Jillian; Deri, Connor R.; Wrenn, Rebekah H.; Slaton, Cara N.; Morrisette, Taylor; Davis, Melisa; Cabanilla, M. Gabriela; Shald, Elizabeth; White, Bryan P.; Sassine, Joseph; Truong, James; Rosenberg, Joshua; Andrade, Justin; Cerenzio, John; Medvedeva, Natalia; Ha, David; Eubank, Taryn A.; Garey, Kevin W.; Biagi, Mark; Todd, Michaela; Kang-Birken, S. Lena; Rux, Caleb; Molina, Kyle C.; Jankowski, Christopher A.; Claeys, Kimberly C.; Venugopalan, Veena; Veve, Michael P.; Orzol, Carolina; Eshaya, Mirna; Caniff, Kaylee E.; Bleick, Callan; and Rybak, Michael J., "Ceftazidime-avibactam for multidrug-resistant gram-negative infections: outcomes and timing of initiation across 22 US medical centers" (2026). Pharmacy Faculty Scholarship. 113.
https://orb.binghamton.edu/pharmacy_fac/113
Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.
Comments
10.1128/aac.00268-26