2022
DOI: 10.1007/s15010-022-01876-x
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Update of clinical application in ceftazidime–avibactam for multidrug-resistant Gram-negative bacteria infections

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Cited by 20 publications
(14 citation statements)
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“…When the bacteria are eliminated, the number of macrophages was reduced to avoid an overactive inflammatory response. [ 37–39 ] Cef and Euc did not increase macrophage aggregation in the bladder (Figure S1, Supporting Information). In comparison to the Con group, the expression of CD68 was significantly elevated in the Model group (Figure 5E,F), which was reversed in the treated groups.…”
Section: Resultsmentioning
confidence: 96%
“…When the bacteria are eliminated, the number of macrophages was reduced to avoid an overactive inflammatory response. [ 37–39 ] Cef and Euc did not increase macrophage aggregation in the bladder (Figure S1, Supporting Information). In comparison to the Con group, the expression of CD68 was significantly elevated in the Model group (Figure 5E,F), which was reversed in the treated groups.…”
Section: Resultsmentioning
confidence: 96%
“…Approved by the National Drug Administration (CFDA) on May 21, 2019, for the treatment of complex intraperitoneal infections (cIAI), hospital-acquired pneumonia (HAP)/ventilator-associated pneumonia (VAP), caused by Klebsiella pneumoniae (K. pneumoniae), Enterobacter cloacae, Escherichia coli (E. coli), Proteus mirabilis and Pseudomonas aeruginosa (P. aeruginosa) , aged ≥18 years. CAZ-AVI can combat infections caused by most MDR-E strains, including carbapenem-resistant Enterobacteriaceae (CRE) ( Zhen and Feng, 2021 ). CAZ-AVI) is composed of the third-generation cephalosporin ceftazidime with the novel non-β-lactamase β-lactamase inhibitor abvibatam (AVI), which inhibits class A, C, and some class D enzymes.…”
Section: Introductionmentioning
confidence: 99%
“…The presence and spread of MDR, XDR and even PDR Gram-negatives is dramatically limiting the treatment options for infections caused by these pathogens, whereas the pipeline of new antimicrobials is slow and novel compounds including tigecycline, eravacycline and cefiderocol do not always meet the expectations [5][6][7]. Current β-lactams combined with novel β-lactamase inhibitors provide some solutions especially against nonmetallo-β-lactamase producers [8], but they are not applicable in all cases, and resistance Antibiotics 2023, 12, 93 2 of 12 has already emerged [9,10]. Monotherapy with formerly abandoned antimicrobials such as fosfomycin and polymyxins is another option.…”
Section: Introductionmentioning
confidence: 99%