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Meropenem/Vaborbactam Plus Aztreonam as a Possible Treatment Strategy for Bloodstream Infections Caused by Ceftazidime/Avibactam-Resistant Klebsiella pneumoniae: A Retrospective Case Series and Literature Review.
Belati, Alessandra; Bavaro, Davide Fiore; Diella, Lucia; De Gennaro, Nicolò; Di Gennaro, Francesco; Saracino, Annalisa.
Afiliação
  • Belati A; Clinic of Infectious Diseases, University Hospital Policlinico, University of Bari, Piazza Giulio Cesare n. 11, 70124 Bari, Italy.
  • Bavaro DF; Clinic of Infectious Diseases, University Hospital Policlinico, University of Bari, Piazza Giulio Cesare n. 11, 70124 Bari, Italy.
  • Diella L; Clinic of Infectious Diseases, University Hospital Policlinico, University of Bari, Piazza Giulio Cesare n. 11, 70124 Bari, Italy.
  • De Gennaro N; Clinic of Infectious Diseases, University Hospital Policlinico, University of Bari, Piazza Giulio Cesare n. 11, 70124 Bari, Italy.
  • Di Gennaro F; Clinic of Infectious Diseases, University Hospital Policlinico, University of Bari, Piazza Giulio Cesare n. 11, 70124 Bari, Italy.
  • Saracino A; Clinic of Infectious Diseases, University Hospital Policlinico, University of Bari, Piazza Giulio Cesare n. 11, 70124 Bari, Italy.
Antibiotics (Basel) ; 11(3)2022 Mar 10.
Article em En | MEDLINE | ID: mdl-35326836
OBJECTIVES: The aim of this study was to describe our experience of a combination treatment including meropenem/vaborbactam (M/V) plus aztreonam (ATM) for bloodstream infections (BSIs) due to ceftazidime/avibactam-resistant Klebsiella pneumoniae (CAZ/AVI-R-Kp), for which gene typing was not available at the time the blood culture (BC) results were obtained. METHODS: Between 20 July and 22 August 2021, in our hospital laboratory, the molecular test for carbapenemase gene typing was not available. All Gram-negative bloodstream infections were recorded, and characteristics of patients were analysed. Among them, three patients had positive BCs for CAZ/AVI-R-Kp, and the empirical therapy was switched to M/V plus ATM pending phenotypic testing of sensitivity to M/V. Therapy was subsequently targeted on the basis of the results of this test. RESULTS: KPC and NDM represent the most prevalent carbapenemases in our polyclinic. Three patients with CAZ/AVI-R-Kp sepsis were treated with M/V plus ATM not knowing the carbapenemase gene. Two had an NDM-Kp infection for which, upon obtaining the result of sensitivity to M/V, combination therapy was maintained. The third had KPC-Kp infection for which ATM was discontinued, after the acquisition of an antibiogram reporting full sensitivity to M/V (MIC = 0.25 mg/L). One patient with NDM-Kp infection died due to complications of the underlying disease for which he was hospitalised. CONCLUSIONS: Meropenem/vaborbactam plus ATM and subsequent de-escalation could represent a possible therapeutic strategy in severe CAZ/AVI-R-Kp infections when carbapenemase gene typing is not rapidly available.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Systematic_reviews Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Systematic_reviews Idioma: En Ano de publicação: 2022 Tipo de documento: Article