Impact of the Inclusion of an Aminoglycoside to the Initial Empirical Antibiotic Therapy for Gram-Negative Bloodstream Infections in Hematological Neutropenic Patients: a Propensity-Matched Cohort Study (AMINOLACTAM Study)

To test the hypothesis that the addition of an aminoglycoside to a β-lactam antibiotic could provide better outcomes than β-lactam monotherapy for the initial empirical treatment of hematological neutropenic patients with subsequently documented Gram-negative bacillus (GNB) bloodstream infection (BS...

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Veröffentlicht in:Antimicrobial agents and chemotherapy 2021-07, Vol.65 (8), p.e0004521
Hauptverfasser: Albasanz-Puig, A, Gudiol, C, Puerta-Alcalde, P, Ayaz, C M, Machado, M, Herrera, F, Martín-Dávila, P, Laporte-Amargós, J, Cardozo, C, Akova, M, Álvarez-Uría, A, Torres, D, Fortún, J, García-Vidal, C, Muñoz, P, Bergas, A, Pomares, H, Mercadal, S, Durà-Miralles, X, García-Lerma, E, Pallarès, N, Carratalà, J
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Sprache:eng
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Zusammenfassung:To test the hypothesis that the addition of an aminoglycoside to a β-lactam antibiotic could provide better outcomes than β-lactam monotherapy for the initial empirical treatment of hematological neutropenic patients with subsequently documented Gram-negative bacillus (GNB) bloodstream infection (BSI), a multinational, retrospective, cohort study of GNB BSI episodes in hematological neutropenic patients in six centers (2010 to 2017) was conducted. Combination therapy (β-lactam plus aminoglycoside) was compared to β-lactam monotherapy. The primary endpoint was the case fatality rate, assessed at 7 and 30 days from BSI onset. Secondary endpoints were nephrotoxicity and persistent BSI. Propensity score (PS) matching was performed. Among 542 GNB BSI episodes, 304 (56%) were initially treated with combination therapy, with cefepime plus amikacin being most common (158/304 [52%]). Overall, Escherichia coli (273/304 [50.4%]) was the main etiological agent, followed by Pseudomonas aeruginosa, which predominated in the combination group (76/304 [25%] versus 28/238 [11.8%];  
ISSN:0066-4804
1098-6596
1098-6596
DOI:10.1128/AAC.00045-21