P-1481. Short-Treatment with Ceftazidime-Avibactam for Carbapenemase-Producing Enterobacterales Bacteremia

Abstract Background Ceftazidime-avibactam (CA) and CA plus aztreonam (ATM) are the preferred treatment options for KPC and metallo-beta-lactamase (MBL) carbapenemase-producing Enterobacterales bacteremia (CPEB). However, data regarding short therapy are scarce. Methods Prospective observational cohort study performed in a university hospital in Argentina between August 2018 and February 2024. All adult patients with CPEB who received adequate empirical treatment with CA or CA+ATM, with a median duration of 7 days (IQR: 7-8), with clinical response and source control of infection were included. They were followed for 30 days to evaluate mortality. Results Twenty-two patients were included. They had a median age of 61 years (IQR: 49-70.5). The median APACHE II and Pitt scores were 18 (IQR: 13.25-24) and 2 (IQR: 1-4). Sixty-eight percent of the patients were immunocompromised, being hematological malignancies (45.45%), high-dose corticosteroids (40.9%) biological agents/anti-lymphocyte therapies (36.36%), and neutropenia (31.81%) the most frequent causes. Eighty-six percent had a clinical source of bacteremia; abdominal, central venous catheter, and urinary tract being the most common. Klebsiella spp. (72.72%) was the main etiological isolated microorganism, and the resistance mechanisms involved were KPC production (77.2%), MBL production (13.6%), and KPC+MBL production (9%). Recent colonization with KPC-CPE and MBL-CPE was detected in 68.1% and 9% of the patients. Septic shock at onset and intensive care unit requirement were 40.9% and 45.4% respectively. Empirical and definitive antibiotic therapy were combined in 66.6% and 9% of the patients. Thirty-day overall and infection-related mortality were 22.7% and 9%. Conclusion This data showed that short-course antibiotic treatment with CA or CA+ATM for patients with CPEB who had clinical response with source control of infection might be adequate. Disclosures Diego Torres, Medical Doctor, Gador: Honoraria|GSK: Advisor/Consultant|Khight Therapeutics: Honoraria|MSD: Honoraria

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Journal
Open Forum Infectious Diseases
Published
2025-01-29
DOI
https://doi.org/10.1093/ofid/ofae631.1651
Primary Topic
Antibiotic Resistance in Bacteria
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article
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article

P-1481. Short-Treatment with Ceftazidime-Avibactam for Carbapenemase-Producing Enterobacterales Bacteremia

Pablo Bonvehí, Marcia Querci, Silvia Relloso, Jimena Carlos et al.
Open Forum Infectious Diseases
Antibiotic Resistance in Bacteria
article

P-1481. Short-Treatment with Ceftazidime-Avibactam for Carbapenemase-Producing Enterobacterales Bacteremia

Pablo Bonvehí, Marcia Querci, Silvia Relloso, Jimena Carlos, Jorgelina Smayevsky, Elena Temporiti, Diego Torres, Fabián Herrera, Federico Nicola, Rocío Sáenz-Díez Rojas, Florencia Bues, M Leone
article en

Abstract

Abstract Background Ceftazidime-avibactam (CA) and CA plus aztreonam (ATM) are the preferred treatment options for KPC and metallo-beta-lactamase (MBL) carbapenemase-producing Enterobacterales bacteremia (CPEB). However, data regarding short therapy are scarce. Methods Prospective observational cohort study performed in a university hospital in Argentina between August 2018 and February 2024. All adult patients with CPEB who received adequate empirical treatment with CA or CA+ATM, with a median duration of 7 days (IQR: 7-8), with clinical response and source control of infection were included. They were followed for 30 days to evaluate mortality. Results Twenty-two patients were included. They had a median age of 61 years (IQR: 49-70.5). The median APACHE II and Pitt scores were 18 (IQR: 13.25-24) and 2 (IQR: 1-4). Sixty-eight percent of the patients were immunocompromised, being hematological malignancies (45.45%), high-dose corticosteroids (40.9%) biological agents/anti-lymphocyte therapies (36.36%), and neutropenia (31.81%) the most frequent causes. Eighty-six percent had a clinical source of bacteremia; abdominal, central venous catheter, and urinary tract being the most common. Klebsiella spp. (72.72%) was the main etiological isolated microorganism, and the resistance mechanisms involved were KPC production (77.2%), MBL production (13.6%), and KPC+MBL production (9%). Recent colonization with KPC-CPE and MBL-CPE was detected in 68.1% and 9% of the patients. Septic shock at onset and intensive care unit requirement were 40.9% and 45.4% respectively. Empirical and definitive antibiotic therapy were combined in 66.6% and 9% of the patients. Thirty-day overall and infection-related mortality were 22.7% and 9%. Conclusion This data showed that short-course antibiotic treatment with CA or CA+ATM for patients with CPEB who had clinical response with source control of infection might be adequate. Disclosures Diego Torres, Medical Doctor, Gador: Honoraria|GSK: Advisor/Consultant|Khight Therapeutics: Honoraria|MSD: Honoraria

Open Forum Infectious DiseasesVol. 12(Supplement_1)
Centro de Educación Médica e Investigaciones Clínicas Norberto Quirno (AR)
Openalex Percentile: Top 99%
Antibiotic Resistance in Bacteria
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