Mario Tumbarello1, Enrico Maria Trecarichi1, Alberto Corona2, Francesco Giuseppe De Rosa3, Matteo Bassetti4, Cristina Mussini5, Francesco Menichetti6, Claudio Viscoli7, Caterina Campoli8, Mario Venditti9, Andrea De Gasperi10, Alessandra Mularoni11, Carlo Tascini12, Giustino Parruti13, Carlo Pallotto14, Simona Sica15, Ercole Concia16, Rosario Cultrera17, Gennaro De Pascale18, Alessandro Capone19, Spinello Antinori20, Silvia Corcione3, Elda Righi4, Angela Raffaella Losito1, Margherita Digaetano5, Francesco Amadori6, Daniele Roberto Giacobbe7, Giancarlo Ceccarelli9, Ernestina Mazza10, Francesca Raffaelli1, Teresa Spanu21, Roberto Cauda1, Pierluigi Viale8. 1. Institute of Infectious Diseases, Fondazione Policlinico Universitario A. Gemelli - Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS)-Università Cattolica del Sacro Cuore, Rome. 2. Intensive Care Unit Department of Emergency, Luigi Sacco Hospital-Azienda Socio Sanitaria Territoriale (ASST)-Fatebenefratelli Sacco, University of Milan. 3. Department of Medical Sciences, University of Turin. 4. Infectious Disease Division, Santa Maria Misericordia University Hospital, Udine. 5. Clinica delle Malattie Infettive, Università di Modena e Reggio Emilia. 6. Infectious Diseases Department, Cisanello Hospital, Pisa. 7. Infectious Diseases Division, Università di Genova e Ospedale Policlinico San Martino IRCCS per l'oncologia e le neuroscienze, Genoa. 8. Infectious Diseases Unit, Department of Medical and Clinical Sciences, S. Orsola-Malpighi Hospital, Alma Mater Studiorum University of Bologna. 9. Dipartimento di Salute Pubblica e Malattie Infettive, Policlinico Umberto I Università 'Sapienza', Rome. 10. Anestesia Rianimazione 2-ASST ospedale Niguarda Ca Granda, Milan. 11. Infectious Diseases Istituto mediterraneo per i trapianti e terapie ad alta specializzazione-IRCCS Palermo. 12. Prima divisione di Malattie Infettive, Ospedale Cotugno, Azienda Ospedaliera dei Colli, Napoli. 13. Unità Operativa Complessa Malattie Infettive, Azienda Unità Sanitaria Locale Pescara. 14. Infectious Diseases Section, Department of Medicine, University of Perugia. 15. Institute of Hematology, Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario Agostino Gemelli, Rome. 16. Malattie Infettive, Ospedale Universitario di Verona. 17. Malattie Infettive, Dipartimento di Scienze Mediche, Università degli Studi di Ferrara. 18. Department of Intensive Care and Anaesthesiology, Fondazione Policlinico Universitario A. Gemelli IRCCS - Università Cattolica del Sacro Cuore, Rome. 19. Istituto Nazionale per le Malattie Infettive Lazzaro Spallanzani IRCCS Rome. 20. Department of Clinical and Biomedical Sciences "L. Sacco," University of Milan. 21. Institute of Microbiology, Fondazione Policlinico Universitario A. Gemelli IRCCS-Università Cattolica del Sacro Cuore, Rome, Italy.
Abstract
Background: Ceftazidime-avibactam (CAZ-AVI) has been approved in Europe for the treatment of complicated intra-abdominal and urinary tract infections, as well as hospital-acquired pneumonia, and for gram-negative infections with limited treatment options. CAZ-AVI displays in vitro activity against Klebsiella pneumoniae carbapenemase (KPC) enzyme producers, but clinical trial data on its efficacy in this setting are lacking. Methods: We retrospectively reviewed 138 cases of infections caused by KPC-producing K. pneumoniae (KPC-Kp) in adults who received CAZ-AVI in compassionate-use programs in Italy. Case features and outcomes were analyzed, and survival was then specifically explored in the large subcohort whose infections were bacteremic. Results: The 138 patients started CAZ-AVI salvage therapy after a first-line treatment (median, 7 days) with other antimicrobials. CAZ-AVI was administered with at least 1 other active antibiotic in 109 (78.9%) cases. Thirty days after infection onset, 47 (34.1%) of the 138 patients had died. Thirty-day mortality among the 104 patients with bacteremic KPC-Kp infections was significantly lower than that of a matched cohort whose KPC-Kp bacteremia had been treated with drugs other than CAZ-AVI (36.5% vs 55.8%, P = .005). Multivariate analysis of the 208 cases of KPC-Kp bacteremia identified septic shock, neutropenia, Charlson comorbidity index ≥3, and recent mechanical ventilation as independent predictors of mortality, whereas receipt of CAZ-AVI was the sole independent predictor of survival. Conclusions: CAZ-AVI appears to be a promising drug for treatment of severe KPC-Kp infections, especially those involving bacteremia.
Background: Ceftazidime-avibactam (CAZ-AVI) has been approved in Europe for the treatment of complicated intra-abdominal and urinary tract infections, as well as hospital-acquired pneumonia, and for gram-negative infections with limited treatment options. CAZ-AVI displays in vitro activity against Klebsiella pneumoniae carbapenemase (KPC) enzyme producers, but clinical trial data on its efficacy in this setting are lacking. Methods: We retrospectively reviewed 138 cases of infections caused by KPC-producing K. pneumoniae (KPC-Kp) in adults who received CAZ-AVI in compassionate-use programs in Italy. Case features and outcomes were analyzed, and survival was then specifically explored in the large subcohort whose infections were bacteremic. Results: The 138 patients started CAZ-AVI salvage therapy after a first-line treatment (median, 7 days) with other antimicrobials. CAZ-AVI was administered with at least 1 other active antibiotic in 109 (78.9%) cases. Thirty days after infection onset, 47 (34.1%) of the 138 patients had died. Thirty-day mortality among the 104 patients with bacteremic KPC-Kp infections was significantly lower than that of a matched cohort whose KPC-Kp bacteremia had been treated with drugs other than CAZ-AVI (36.5% vs 55.8%, P = .005). Multivariate analysis of the 208 cases of KPC-Kp bacteremia identified septic shock, neutropenia, Charlson comorbidity index ≥3, and recent mechanical ventilation as independent predictors of mortality, whereas receipt of CAZ-AVI was the sole independent predictor of survival. Conclusions: CAZ-AVI appears to be a promising drug for treatment of severe KPC-Kp infections, especially those involving bacteremia.
Authors: Ruta Petraitiene; Vidmantas Petraitis; Povilas Kavaliauskas; Bo Bo W Maung; Farehin Khan; Ethan Naing; Thein Aung; Vilma Zigmantaite; Ramune Grigaleviciute; Audrius Kucinskas; Rimantas Stakauskas; Benjamin N Georgiades; Chase A Mazur; Joshua A Hayden; Michael J Satlin; Thomas J Walsh Journal: Antimicrob Agents Chemother Date: 2020-03-24 Impact factor: 5.191
Authors: Jason M Pogue; Ronald N Jones; John S Bradley; David R Andes; Sujata M Bhavnani; George L Drusano; Michael N Dudley; Robert K Flamm; Keith A Rodvold; Paul G Ambrose Journal: Antimicrob Agents Chemother Date: 2020-01-27 Impact factor: 5.191