# Impact of Antibiotic Therapy with Ceftazidime Avibactam vs. Best Available Therapy in Adult Patients with Bacteremia Caused by Carbapenem-Resistant Enterobacterales

**Authors:** Daniel Arboleda, Camilo Buitrago, Erika Paola Vergara, Laura Cristina Nocua-Báez, Carlos Humberto Saavedra, Jorge Alberto Cortés

PMC · DOI: 10.3390/antibiotics14030226 · Antibiotics · 2025-02-24

## TL;DR

This study compared ceftazidime avibactam to other treatments for a dangerous type of bacterial infection and found no significant difference in outcomes.

## Contribution

The study evaluates real-world treatment effectiveness of ceftazidime avibactam for CRE bacteremia in an endemic region.

## Key findings

- Ceftazidime avibactam showed no significant difference in mortality compared to best available therapy.
- Microbiological cure and clinical response rates were similar between the two treatment groups.
- No significant differences were observed in relapse or acute kidney injury rates between the treatments.

## Abstract

Background/Objectives: Carbapenem-resistant Enterobacterales (CRE) infection is associated with a higher mortality rate. The purpose of this study was to evaluate the effect of ceftazidime avibactam (CZA) for treating bacteremia caused by CRE compared to the best available therapy in an area where these microorganisms are endemic. Methods: A retrospective cohort study of patients with CRE bacteremia was conducted. We included adults with CRE bacteremia who were treated with CZA or the best available therapy (BAT) for more than 48 h, and the hospitalization time was recorded. The outcomes included death during hospitalization, relapse, and microbiological cure. Confounders were adjusted using propensity score-derived stabilized inverse probability of treatment weighting (IPTW). Results: A total of 169 patients with CRE bacteremia were included. About 72.6% of isolates had a class A serin carbapenamase, and 20.4% had metallo-β-lactamase co-production. A total of 107 patients were treated with CZA, 63% in monotherapy and 32% with aztreonam (ATM). Crude mortality during hospitalization was 36 (34.5%) in patients treated with CZA and 21 (33.2%) with BAT. No difference was observed between death rates (HR 0.86: IC 95% 0.40–1.83), microbiological cure (OR 1.31 IC 95% 0.46–3.67), clinical response (OR 1.39 IC 95% 0.35–5.43), acute kidney injury (OR 0.56 IC 95% 0.11–2.80) or relapse (OR 0.99 IC 95% 0.17–5.51) during the hospitalization after the adjustment. Conclusions: Among adult patients with CRE, no differences were observed between treatments with CZA and BAT after adjustment with IPTW.

## Linked entities

- **Chemicals:** ceftazidime avibactam (PubChem CID 90643431), aztreonam (PubChem CID 5742832)
- **Diseases:** bacteremia (MONDO:0005229)

## Full-text entities

- **Diseases:** CRE (MESH:D060467), infection (MESH:D007239), Bacteremia (MESH:D016470), acute kidney injury (MESH:D058186), death (MESH:D003643)
- **Chemicals:** CZA (MESH:C000595613), Carbapenem (MESH:D015780), ATM (MESH:D001398)
- **Species:** Homo sapiens (human, species) [taxon 9606], Enterobacterales (order) [taxon 91347]

## Full text

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## Figures

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC11939519/full.md

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Source: https://tomesphere.com/paper/PMC11939519