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      Evaluation of ceftazidime/avibactam for treatment of carbapenemase-producing carbapenem-resistant Enterobacterales with OXA-48 and/or NDM genes with or without combination therapy

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          Abstract

          Background

          Carbapenem-resistant Enterobacterales (CRE) is an urgent public health threat of significant global concern. Few observational studies have evaluated the clinical outcomes for treatment of CRE harbouring OXA-48 or NDM genes with ceftazidime/avibactam. Previous findings showed lower 30 day mortality with ceftazidime/avibactam ranges between 8.3% and 22%.

          Method

          This single-centre retrospective cohort study included adult patients aged ≥18 years admitted to King Abdulaziz Medical City (KAMC) who had received ceftazidime/avibactam for at least 72 h for infections caused by CRE with genes encoding for carbapenemase production (CP-CRE).

          Results

          A total of 211 patients, mostly male (57%), having CP-CRE infections treated with ceftazidime/avibactam were included, with an average age of 62 years. More than 50% of patients were critically ill, for which 46% received invasive ventilation and 36% were on inotropes. The most frequent infectious disease was hospital/ventilator-acquired pneumonia with Klebsiella pneumoniae being the most frequent causative pathogen. The majority of isolates harboured OXA-48 (81%), followed by NDM ± OXA-48 (19%). The overall clinical cure and 30 day mortality was 78% and 21% respectively (stratified per gene: 79% and 21.6% for OXA-48 and 75% and 17.5% for NDM ± OXA-48).

          Conclusions

          This was the largest study that evaluated clinical outcomes associate with CP-CRE harbouring OXA-48 gene infections treated with ceftazidime/avibactam. Clinical cure and 30 day mortality were consistent with those of previous studies. Findings suggested that combination therapy with ceftazidime/avibactam had no direct impact on clinical outcomes for CP-CRE with OXA-48.

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          Most cited references14

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          The global epidemiology of carbapenemase-producing Enterobacteriaceae.

          Carbapenemase-producing Enterobacteriaceae (CPE) are an important and increasing threat to global health. Both clonal spread and plasmid-mediated transmission contribute to the ongoing rise in incidence of these bacteria. Among the 4 classes of β-lactamases defined by the Ambler classification system, the carbapenemases that confer carbapenem resistance in Enterobacteriaceae belong to 3 of them: Class A (K. pneumoniae carbapenemases, KPC), Class B (metallo-β-lactamases, MBL including New Delhi metallo-β-lactamases, NDM) and Class D (OXA-48-like carbapenemases). KPC-producing CPE are the most commonly occurring CPE in the United States. MBL-producing CPE have been most commonly associated with the Indian Subcontinent as well as with specific countries in Europe, including Romania, Denmark, Spain, and Hungary. The epicenter of OXA-48-like-producing is in Turkey and surrounding countries. Detailed knowledge of the epidemiology and molecular characteristics of CPE is essential to stem the spread of these pathogens.
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            Efficacy of ceftazidime-avibactam plus aztreonam in patients with bloodstream infections caused by MBL- producing Enterobacterales

            In vitro data support the use of combination of aztreonam (ATM) with ceftazidime-avibactam (CAZ-AVI), but clinical studies are lacking. The aim of our study was to compare the outcome of patients with bloodstream infections (BSIs) due to MBLs-producing Enterobacterales treated either with CAZ-AVI plus ATM or other active antibiotics (OAAs). Prospective observational study including patients admitted to three hospitals in Italy and Greece. The primary outcome measure was the 30-day all-cause mortality. Secondary outcomes were clinical failure at day 14 and length of stay (LOS) after BSI diagnosis. Cox regression analysis including a propensity score (PS) for receiving CAZ-AVI plus ATM was performed to evaluate primary and secondary outcomes. A PS-based matched analysis was also performed. We enrolled 102 pts with BSI, 82 had infections caused by NDM-producing (79 K.pneumoniae and 3 E.coli) and 20 by VIM-producing (14 K.pneumoniae, 5 Enterobacter spp, 1 M.morganii) strains. The 30-day mortality rate was 19.2% in CAZ-AVI/ATM group vs 44% in OAAs group (p=0.007). The PS-adjusted analysis showed that the use of CAZ-AVI/ATM was associated with lower 30-day mortality (HR 0.37, 95% CI 0.13-0.74, p=0.01), lower clinical failure at day 14 (HR 0.30, 95% CI 0.14-0.65, p=0.002) and shorter LOS (sHR 0.49, 95% CI 0.30-0.82, p=0.007). The PS-matched analysis confirmed these findings. CAZ-AVI/ATM combination offers therapeutic advantage compared to OAAs for patients with BSI due to MBL-producing Enterobacterales. Further studies are warranted.
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              Effectiveness of ceftazidime/avibactam as salvage therapy for treatment of infections due to OXA-48 carbapenemase-producing Enterobacteriaceae

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                Author and article information

                Contributors
                Journal
                JAC Antimicrob Resist
                JAC Antimicrob Resist
                jacamr
                JAC-Antimicrobial Resistance
                Oxford University Press (US )
                2632-1823
                October 2022
                11 October 2022
                11 October 2022
                : 4
                : 5
                : dlac104
                Affiliations
                Department of Pharmaceutical Care, Ministry of National Guard Health Affairs , Riyadh, Saudi Arabia
                Department of Pharmacy Practice, College of Pharmacy, Princess Nourah bint Abdulrahman University , Riyadh, Saudi Arabia
                Department of Pharmaceutical Care, King Abdullah bin Abdulaziz University Hospital , Riyadh, Saudi Arabia
                College of Pharmacy, Princess Nourah bint Abdulrahman University , Riyadh, Saudi Arabia
                College of Pharmacy, Princess Nourah bint Abdulrahman University , Riyadh, Saudi Arabia
                College of Pharmacy, Princess Nourah bint Abdulrahman University , Riyadh, Saudi Arabia
                College of Pharmacy, Princess Nourah bint Abdulrahman University , Riyadh, Saudi Arabia
                Department of Infection Prevention and Control, Ministry of National Guard, Health Affairs , Riyadh, Saudi Arabia
                Department of Infection Prevention and Control, Ministry of National Guard, Health Affairs , Riyadh, Saudi Arabia
                College of Public Health and Health Informatics, King Saud bin Abdulaziz University for Health Sciences , Riyadh, Saudi Arabia
                Department of Medicine, Ministry of National Guard Health Affairs , Riyadh, Saudi Arabia
                College of Medicine, King Saud bin Abdulaziz University for Health Sciences , Riyadh, Saudi Arabia
                Department of Medicine, Ministry of National Guard Health Affairs , Riyadh, Saudi Arabia
                College of Medicine, King Saud bin Abdulaziz University for Health Sciences , Riyadh, Saudi Arabia
                Department of Clinical Trial Services, King Abdullah International Medical Research Center , Riyadh, Saudi Arabia
                Department of Medicine, Ministry of National Guard Health Affairs , Riyadh, Saudi Arabia
                Author notes
                Article
                dlac104
                10.1093/jacamr/dlac104
                9552550
                36237571
                d877a34f-ff74-4343-946c-3e7bf400229a
                © The Author(s) 2022. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 23 May 2022
                : 08 September 2022
                Page count
                Pages: 9
                Categories
                Original Article
                AcademicSubjects/MED00740
                AcademicSubjects/SCI01150

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