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.
Mario Tumbarello, Gabriele Giuliano, Marianna Criscuolo, Maria Ilaria Del Principe, Cristina Papayannidis, Nicola Stefano Fracchiolla, Michela Dargenio, Mariagiovanna Cefalo, Gianpaolo Nadali, Anna Candoni, Caterina Buquicchio, Francesco Marchesi, Marco Picardi, Federica Lessi, Monica Piedimonte, Lucia Prezioso, Matteo Piccini, Chiara Cattaneo, Alessandro Busca, Sara Brunetti, Elisa Buzzatti, Alessandra Dedola, Mariarita Sciumé, Nicola Di Renzo, Laura Cesini, Alessandra Vatteroni, Francesca Raffaelli, Livio Pagano
{"title":"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.","authors":"Mario Tumbarello, Gabriele Giuliano, Marianna Criscuolo, Maria Ilaria Del Principe, Cristina Papayannidis, Nicola Stefano Fracchiolla, Michela Dargenio, Mariagiovanna Cefalo, Gianpaolo Nadali, Anna Candoni, Caterina Buquicchio, Francesco Marchesi, Marco Picardi, Federica Lessi, Monica Piedimonte, Lucia Prezioso, Matteo Piccini, Chiara Cattaneo, Alessandro Busca, Sara Brunetti, Elisa Buzzatti, Alessandra Dedola, Mariarita Sciumé, Nicola Di Renzo, Laura Cesini, Alessandra Vatteroni, Francesca Raffaelli, Livio Pagano","doi":"10.1093/jac/dkae416","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>To evaluate clinical impact of ceftazidime/avibactam on treating infections due to MDR Gram-negative bacteria in patients with haematological malignancies (HMs).</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>Our study provides further evidence about the effectiveness of ceftazidime/avibactam in treating infections in patients with HMs.</p>","PeriodicalId":14969,"journal":{"name":"Journal of Antimicrobial Chemotherapy","volume":" ","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Antimicrobial Chemotherapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/jac/dkae416","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
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.
期刊介绍:
The Journal publishes articles that further knowledge and advance the science and application of antimicrobial chemotherapy with antibiotics and antifungal, antiviral and antiprotozoal agents. The Journal publishes primarily in human medicine, and articles in veterinary medicine likely to have an impact on global health.