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本文引用的文献

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Antimicrobial activities of ceftazidime/avibactam, ceftolozane/tazobactam, imipenem/relebactam, meropenem/vaborbactam, and comparators against Pseudomonas aeruginosa from patients with skin and soft tissue infections.头孢他啶/阿维巴坦、头孢洛扎/他唑巴坦、亚胺培南/雷巴坦、美罗培南/沃巴坦和对照药物对皮肤软组织感染患者分离的铜绿假单胞菌的抗菌活性。
Int J Infect Dis. 2021 Dec;113:279-281. doi: 10.1016/j.ijid.2021.10.022. Epub 2021 Oct 17.
2
Overview of Changes to the Clinical and Laboratory Standards Institute M100, 31st Edition.临床和实验室标准协会 M100,31 版更改概述。
J Clin Microbiol. 2021 Nov 18;59(12):e0021321. doi: 10.1128/JCM.00213-21. Epub 2021 Sep 22.
3
Emergence of a KPC Variant Conferring Resistance to Ceftazidime-Avibactam in a Widespread ST11 Carbapenem-Resistant Clone in China.在中国广泛传播的ST11碳青霉烯耐药克隆中出现对头孢他啶-阿维巴坦耐药的KPC变体。
Front Microbiol. 2021 Aug 16;12:724272. doi: 10.3389/fmicb.2021.724272. eCollection 2021.
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Clin Microbiol Infect. 2021 Jul;27(7):1040.e1-1040.e6. doi: 10.1016/j.cmi.2021.03.001. Epub 2021 Mar 26.
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Antimicrob Agents Chemother. 2021 Mar 18;65(4). doi: 10.1128/AAC.02193-20.
10
Emergence and Recovery of Ceftazidime-avibactam Resistance in blaKPC-33-Harboring Klebsiella pneumoniae Sequence Type 11 Isolates in China.中国产 blaKPC-33 携带型肺炎克雷伯菌 11 型分离株中头孢他啶-阿维巴坦耐药性的出现和恢复。
Clin Infect Dis. 2020 Dec 23;71(Suppl 4):S436-S439. doi: 10.1093/cid/ciaa1521.

2019 年中国细菌耐药监测网(CHINET)研究:新型β-内酰胺类-β-内酰胺酶抑制剂复方制剂及对照药物对革兰阴性杆菌临床分离株的活性。

Activity of New β-Lactam-β-Lactamase Inhibitor Combinations and Comparators against Clinical Isolates of Gram-Negative Bacilli: Results from the China Antimicrobial Surveillance Network (CHINET) in 2019.

机构信息

Institute of Antibiotics, Huashan Hospital, Fudan University, Shanghai, China.

Key Laboratory of Clinical Pharmacology of Antibiotics, Ministry of Health, Shanghai, China.

出版信息

Microbiol Spectr. 2022 Aug 31;10(4):e0185422. doi: 10.1128/spectrum.01854-22. Epub 2022 Jul 12.

DOI:10.1128/spectrum.01854-22
PMID:35862963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9431184/
Abstract

Novel β-lactam-β-lactamase inhibitor combinations (BLBLIs) are in clinical development for the treatment of infections caused by carbapenem-resistant and difficult-to-treat resistant (DTR) (defined as resistance to all tested β-lactams and fluoroquinolones) Gram-negative bacilli. This study evaluated the activities of cefepime-zidebactam, ceftazidime-avibactam, cefepime-tazobactam, ceftolozane-tazobactam, and other comparators against 4,042 nonduplicate Gram-negative clinical isolates collected from different regions of China (46 hospitals) in 2019. Based on the pharmacokinetic-pharmacodynamic (PK-PD) breakpoints, cefepime-zidebactam inhibited 98.5% of and 98.9% of Pseudomonas aeruginosa isolates, respectively. Against carbapenem-resistant and difficult-to-treat resistant Gram-negative bacilli, cefepime-zidebactam demonstrated better activity against (96% and 97.2%, respectively) and P. aeruginosa (98.2% and 96.9%, respectively). Among the 379 carbapenem-resistant isolates, the most common carbapenemase genes detected were (64.1%) and (30.9%). Cefepime-zidebactam showed an MIC of ≤2 mg/L for 98.8% of -positive isolates and 89.7% of -positive isolates. Ceftazidime-avibactam also showed efficient activity against (93.6%) and P. aeruginosa (87.7%). Ceftazidime-avibactam was active against 97.5% of -positive isolates and 100% of -positive isolates. Cefepime-zidebactam inhibited 97.3% of Acinetobacter baumannii isolates with an MIC of 16/32 mg/L. Our study systematically evaluated the activities of these new BLBLIs against a variety of Gram-negative bacilli, provided preclinical data for the approval of these BLBLIs in China, and supported cefepime-zidebactam and ceftazidime-avibactam as potential efficient therapies for infections caused by carbapenem-resistant (CRE), carbapenem-resistant P. aeruginosa (CRPA), and DTR isolates. , Pseudomonas aeruginosa, and Acinetobacter baumannii are the most common Gram-negative bacilli to cause nosocomial infections throughout the world. Due to their large public health and societal implications, carbapenem-resistant A. baumannii (CRAB), carbapenem-resistant P. aeruginosa (CRPA), and carbapenem-resistant and third-generation-cephalosporin-resistant were regarded by the World Health Organization (WHO) as a global priority for investment in new drugs in 2017. The present study showed the potent activity of these novel BLBLIs and other comparators against Gram-negative bacillus isolates, including carbapenem-resistant or difficult-to-treat resistant phenotypes. Polymyxins, tigecycline, and ceftazidime-avibactam (except for -positive isolates) were available for the treatment of infections caused by CRE isolates. Currently, cefepime-zidebactam and other BLBLIs have not yet been approved for use in China. Here, our study aimed to evaluate the activities of BLBLIs against Gram-negative bacillus isolates, especially CRE, before clinical use.

摘要

新型β-内酰胺-β-内酰胺酶抑制剂组合(BLBLIs)正在临床开发中,用于治疗由碳青霉烯类耐药和治疗困难(DTR)(定义为对所有测试的β-内酰胺类和氟喹诺酮类药物耐药)革兰氏阴性杆菌引起的感染。本研究评估了头孢吡肟-他唑巴坦、头孢他啶-阿维巴坦、头孢吡肟-他唑巴坦、头孢洛扎-他唑巴坦和其他对照药物对来自中国不同地区(46 家医院)的 4,042 例非重复革兰氏阴性临床分离株的活性,时间为 2019 年。基于药代动力学-药效学(PK-PD)的折点,头孢吡肟-他唑巴坦分别抑制了 98.5%和 98.9%的铜绿假单胞菌分离株。对于碳青霉烯类耐药和治疗困难的革兰氏阴性杆菌,头孢吡肟-他唑巴坦对 (分别为 96%和 97.2%)和铜绿假单胞菌(分别为 98.2%和 96.9%)表现出更好的活性。在 379 株碳青霉烯类耐药 分离株中,检测到最常见的碳青霉烯酶基因是 (64.1%)和 (30.9%)。头孢吡肟-他唑巴坦对 98.8%的 -阳性分离株和 89.7%的 -阳性分离株的 MIC 值≤2mg/L。头孢他啶-阿维巴坦对 (93.6%)和铜绿假单胞菌(87.7%)也表现出有效的 活性。头孢他啶-阿维巴坦对 97.5%的 -阳性分离株和 100%的 -阳性分离株有效。头孢吡肟-他唑巴坦抑制 97.3%的鲍曼不动杆菌分离株,MIC 值为 16/32mg/L。本研究系统评估了这些新型 BLBLIs 对各种革兰氏阴性杆菌的 活性,为这些 BLBLIs 在我国的批准提供了临床前数据,并支持头孢吡肟-他唑巴坦和头孢他啶-阿维巴坦作为治疗碳青霉烯类耐药 (CRE)、碳青霉烯类耐药铜绿假单胞菌(CRPA)和 DTR 分离株引起感染的潜在有效治疗方法。铜绿假单胞菌和鲍曼不动杆菌是全世界引起医院感染的最常见革兰氏阴性杆菌。由于它们对公共卫生和社会的影响较大,世界卫生组织(WHO)于 2017 年将碳青霉烯类耐药鲍曼不动杆菌(CRAB)、碳青霉烯类耐药铜绿假单胞菌(CRPA)和碳青霉烯类和第三代头孢菌素耐药 视为全球新药投资的重点。本研究显示了这些新型 BLBLIs 和其他对照药物对革兰氏阴性杆菌分离株的强大 活性,包括碳青霉烯类耐药或治疗困难的表型。多黏菌素、替加环素和头孢他啶-阿维巴坦(-阳性分离株除外)可用于治疗 CRE 分离株引起的感染。目前,头孢吡肟-他唑巴坦和其他 BLBLIs 尚未在中国获得批准使用。在这里,我们的研究旨在评估 BLBLIs 在临床使用前对革兰氏阴性杆菌分离株的 活性,特别是 CRE。