Journal of Global Antimicrobial Resistance (Mar 2024)

Evaluation of clinical and microbiological factors related to mortality in patients with Gram-negative bacterial infections treated with ceftazidime–avibactam: A prospective multicentric cohort study

  • Beatriz Arns,
  • Guilherme Geraldo Lovato Sorio,
  • Tarsila Vieceli,
  • Dariane Pereira,
  • Ândrea Celestino de Souza,
  • Priscila Lamb Wink,
  • Julia Hoefel Paes,
  • Leonardo David,
  • Fernanda Barboza,
  • Stella Hickmann,
  • Gustavo Alves,
  • Antônio Cândido Santos,
  • Anelise da Rosa,
  • Marcelle Duarte Alves,
  • Cibele Massotti Magagnin,
  • Eduardo Gomes,
  • Alexandre Prehn Zavascki,
  • Maria Helena Rigatto

Journal volume & issue
Vol. 36
pp. 393 – 398

Abstract

Read online

Objectives: This study aimed to evaluate the clinical and microbiological risk factors associated with mortality in patients treated with ceftazidime–avibactam for carbapenem-resistant Gram-negative bacterial infections. Methods: This multicentric prospective cohort study included hospitalized adult patients with a microbiologically confirmed infection treated with ceftazidime–avibactam for ≥48 hours. The clinical and microbiological risk factors for 30-day mortality were evaluated using a Cox regression model. Results: Of the 193 patients evaluated from the five tertiary hospitals, 127 were included in the study. Thirty-five patients (27.6%) died within 30 days. Infections with AmpC beta-lactamase-carrying bacteria were independently related to 30-day mortality (adjusted hazard ratio [aHR] 2.49, 95% confidence interval [CI] 1.28–4.84, P < 0.01) after adjusting for time from infection to antimicrobial prescription (P = 0.04). Further, these bacterial infections were also related to higher in-hospital mortality (aHR 2.17, 95% CI 1.24–3.78, P < 0.01). Only one patient developed resistance to ceftazidime–avibactam during treatment. Conclusions: Treatment with ceftazidime–avibactam had worse clinical outcomes in patients with infections with bacteria with chromosomally encoded AmpC beta-lactamase. However, these findings should be confirmed in future studies.

Keywords