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本文引用的文献

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Ceftazidime-avibactam for the treatment of febrile neutropenia in HSCT recipients and acute leukemia patients post induction chemotherapy.头孢他啶-阿维巴坦用于治疗异基因造血干细胞移植受者和急性白血病患者诱导化疗后的发热性中性粒细胞减少症。
Sci Rep. 2024 Dec 28;14(1):31322. doi: 10.1038/s41598-024-82795-9.
2
Challenges and Opportunities with Antibiotic Discovery and Exploratory Research.抗生素发现与探索性研究的挑战与机遇。
ACS Infect Dis. 2024 Aug 9;10(8):2445-2447. doi: 10.1021/acsinfecdis.4c00530. Epub 2024 Jul 22.
3
Use of Ceftazidime-Avibactam in Children Admitted to Pediatric Intensive Care Units.头孢他啶-阿维巴坦在儿科重症监护病房住院儿童中的应用。
Children (Basel). 2024 May 29;11(6):664. doi: 10.3390/children11060664.
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Patient outcomes by baseline pathogen resistance phenotype and genotype in CERTAIN-1, a Phase 3 study of cefepime-taniborbactam versus meropenem in adults with complicated urinary tract infection.CERTAIN-1 研究中基线病原体耐药表型和基因型对患者结局的影响,该研究为一项比较头孢吡肟-他唑巴坦与美罗培南治疗成人复杂性尿路感染的 3 期研究。
Antimicrob Agents Chemother. 2024 Jul 9;68(7):e0023624. doi: 10.1128/aac.00236-24. Epub 2024 May 23.
5
Cefepime/Enmetazobactam: First Approval.头孢吡肟/恩他唑巴坦:首次批准。
Drugs. 2024 Jun;84(6):737-744. doi: 10.1007/s40265-024-02035-2. Epub 2024 May 18.
6
Brave New World of Artificial Intelligence: Its Use in Antimicrobial Stewardship-A Systematic Review.人工智能的全新世界:其在抗菌药物管理中的应用——一项系统综述
Antibiotics (Basel). 2024 Mar 28;13(4):307. doi: 10.3390/antibiotics13040307.
7
activity of cefepime/taniborbactam and comparator agents against Gram-negative bacterial bloodstream pathogens recovered from patients with cancer.头孢吡肟/他尼硼巴坦及对照药物对从癌症患者中分离出的革兰氏阴性菌血流病原体的活性。
JAC Antimicrob Resist. 2024 Apr 10;6(2):dlae060. doi: 10.1093/jacamr/dlae060. eCollection 2024 Apr.
8
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针对革兰氏阴性杆菌的新型抗生素。

New antibiotics targeting Gram-negative bacilli.

作者信息

Al-Tawfiq Jaffar A, Sah Ranjit, Mehta Rachana, Apostolopoulos Vasso, Temsah Mohamad-Hani, Eljaaly Khalid

机构信息

Infectious Disease Unit, Specialty Internal Medicine, Johns Hopkins Aramco Healthcare, Dhahran, Saudi Arabia.

Division of Infectious Diseases, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.

出版信息

Infez Med. 2025 Mar 1;33(1):4-14. doi: 10.53854/liim-3301-2. eCollection 2025.

DOI:10.53854/liim-3301-2
PMID:40071252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11892437/
Abstract

Antimicrobial resistance (AMR) is an emerging global threat. It increases mortality and morbidity rates and places a heavy burden on healthcare systems. Healthcare professionals can address the increasing issue of AMR by advocating responsible antibiotic use and supporting the development of new medications. Despite the economic, logistic, and scientific challenges, it is reassuring that new agents continue to be developed. This review addresses new antibiotics in the pipeline. A review of the literature was conducted including Medline, and Clinicaltrials.org, for approved and in pipeline antibiotics in phase 3 or new drug applications (NDA). We found several new antibiotics and reviewed their current development status, mode of action, spectra of activity, and indications for which they have been approved. The included studies from phase 3 clinical trials were mainly utilized for the treatment of acute bacterial skin and skin structure infections, community-acquired bacterial pneumonia, and pneumonia acquired in healthcare settings. The availability of these agents is limited for high-priority organisms. The identified antibiotics were primarily based on previously known molecules or pre-existing antimicrobial agents. There is a limited number of antibiotics against high priority organisms. New antimicrobial agents targeting the top-priority organisms identified by the World Health Organization are urgently needed. However, some antibiotics target ESBL-producing Enterobacterales, carbapenem-resistant Enterobacterales, .

摘要

抗菌药物耐药性(AMR)是一个新出现的全球威胁。它会增加死亡率和发病率,并给医疗系统带来沉重负担。医疗专业人员可以通过倡导合理使用抗生素和支持新药物研发来应对日益严重的AMR问题。尽管存在经济、后勤和科学方面的挑战,但令人欣慰的是仍在不断研发新的药物。本综述探讨了正在研发中的新型抗生素。我们检索了包括Medline和Clinicaltrials.org在内的文献,以查找已批准的以及处于3期临床试验或新药申请(NDA)阶段的在研抗生素。我们发现了几种新型抗生素,并综述了它们目前的研发状况、作用方式、活性谱以及已获批的适应证。纳入的3期临床试验研究主要用于治疗急性细菌性皮肤及皮肤结构感染、社区获得性细菌性肺炎以及医院获得性肺炎。这些药物对于高优先级病原体的可及性有限。已鉴定出的抗生素主要基于先前已知的分子或现有的抗菌药物。针对高优先级病原体的抗生素数量有限。迫切需要针对世界卫生组织确定的高优先级病原体的新型抗菌药物。然而,一些抗生素针对产超广谱β-内酰胺酶(ESBL)的肠杆菌科细菌、耐碳青霉烯类肠杆菌科细菌……