Skip to main navigation Skip to search Skip to main content

Clinical impact of ceftazidime/avibactam on the treatment of suspected or proven infections in a large cohort of patients with haematological malignancies: a multicentre observational real-world study

  • M. Tumbarello*
  • , G. Giuliano
  • , M. Criscuolo
  • , Principe M. I. Del
  • , C. Papayannidis
  • , N. S. Fracchiolla
  • , M. Dargenio
  • , M. Cefalo
  • , G. Nadali
  • , A. Candoni
  • , C. Buquicchio
  • , F. Marchesi
  • , M. Picardi
  • , F. Lessi
  • , M. Piedimonte
  • , L. Prezioso
  • , M. Piccini
  • , C. Cattaneo
  • , A. Busca
  • , S. Brunetti
  • E. Buzzatti, A. Dedola, M. Sciume, N. D. Renzo, L. Cesini, A. Vatteroni, F. Raffaelli, Livio Pagano
*Corresponding author
  • University of Siena
  • Azienda Ospedaliera Universitaria Senese
  • Alma Mater Studiorum University of Bologna
  • Ospedale Vito Fazzi
  • ASL Roma 2
  • Ospedale Policlinico
  • University of Modena and Reggio Emilia
  • Ospedale Dimiccoli Barletta
  • IRCCS Istituti fisioterapici ospitalieri - Istituto Regina Elena
  • Azienda Ospedaliera Universitaria Federico II
  • University of Padua
  • Sant'Andrea Hospital
  • Azienda Ospedaliero - Universitaria di Parma
  • University of Florence
  • University of Brescia
  • Azienda Ospedaliera - Universitaria Città della Salute e della Scienza di Torino
  • University of Rome Tor Vergata
  • University of Bologna

Research output: Contribution to journalArticle

Abstract

Objectives: To evaluate clinical impact of ceftazidime/avibactam on treating infections due to MDR Gram-negative bacteria in patients with haematological malignancies (HMs). Methods: We conducted a retrospective, observational study at 17 Italian haematological wards that included patients with HMs receiving ceftazidime/avibactam for the treatment of suspected or proven infections. The primary endpoint was all-cause mortality 30 days after infection onset. Secondary endpoints included the development of in vitro ceftazidime/avibactam resistance, adverse reactions and infection relapse. Results: Of 198 patients enrolled, 66 had fever of unknown origin and 132 had microbiologically proven infections (MPIs). Enterobacterales were responsible for 98 MPIs, with KPC producers accounting for 75% of these, and carbapenem-resistant Pseudomonas aeruginosa caused 25% of MPIs. The overall 30-day mortality rate was 17.7%. Infection relapse occurred in four patients with MPI. Patients who died within 30 days of infection onset tended to have pre-existing cerebrovascular diseases, a Charlson Comorbidity Index > 4 and septic shock at infection onset and had received inadequate initial antibiotic therapy. Thirty-day mortality was independently associated with septic shock at infection onset and inappropriate initial antibiotic therapy. Conclusions: Our study provides further evidence about the effectiveness of ceftazidime/avibactam in treating infections in patients with HMs.
Original languageEnglish
Pages (from-to)386-398
Number of pages13
JournalJournal of Antimicrobial Chemotherapy
Volume80
Issue number2
DOIs
Publication statusPublished - 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

All Science Journal Classification (ASJC) codes

  • Pharmacology
  • Microbiology (medical)
  • Pharmacology (medical)
  • Infectious Diseases

Keywords

  • hematological malignancy

Fingerprint

Dive into the research topics of 'Clinical impact of ceftazidime/avibactam on the treatment of suspected or proven infections in a large cohort of patients with haematological malignancies: a multicentre observational real-world study'. Together they form a unique fingerprint.

Cite this