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研究性抗生素头孢吡肟/齐德巴坦作为治疗一名由广泛耐药铜绿假单胞菌引起的小儿难治性脓胸的治疗选择:病例报告

Investigational antibiotic cefepime/zidebactam as a therapeutic option for the treatment of an unyielding empyema in a paediatric patient caused by extensively drug-resistant Pseudomonas aeruginosa: a case report.

作者信息

Polati Vishnu Rao, Gattu Santosh, Maturu Venkata Nagarjuna, Prakasham P Swati, Maqsood Maryam

机构信息

Department of Infectious Diseases, Apollo Hospitals, Jubilee Hills, Hyderabad, Telangana, India.

Department of Pulmonology, Yashoda Hospitals, Hyderabad, Telangana, India.

出版信息

Eur J Clin Microbiol Infect Dis. 2025 Jun;44(6):1349-1355. doi: 10.1007/s10096-025-05106-8. Epub 2025 Mar 18.

DOI:10.1007/s10096-025-05106-8
PMID:40100511
Abstract

OBJECTIVE

Treatment option for the infections caused by MBL-producing P. aeruginosa is severely limited. Cefepime/zidebactam (WCK 5222) is a novel β-lactam/ β-lactam-enhancer combination, currently in global Phase 3 clinical development. It is reported to show a broad-spectrum in vitro activity and translational efficacy in non-clinical PK/PD models against carbapenem-resistant Gram-negative bacteria including MBL-producing P. aeruginosa. We present a case of a 13-year-old girl, suffering from tuberculosis with a refractory lung empyema caused by NDM-producing, XDR P. aeruginosa who did not respond to several rounds of colistin or aztreonam plus ceftazidime/avibactam therapies albeit effective source control, over 4 months period.

METHODS

The infecting organism was found to be susceptible to cefepime/zidebactam. After obtaining informed consent and necessary approvals, the patient was treated under compassionate ground.

RESULTS

The patient was treated with adult dose regimen of cefepime/zidebactam (due to higher body weight) for 21 days that led to clinical and microbiological cure.

CONCLUSION

This case highlights both severity of the antimicrobial resistance and hope offered by an under-trial novel antibiotic.

摘要

目的

由产金属β-内酰胺酶(MBL)的铜绿假单胞菌引起的感染,其治疗选择极为有限。头孢吡肟/齐他西克(WCK 5222)是一种新型的β-内酰胺/β-内酰胺增强剂组合,目前正处于全球3期临床开发阶段。据报道,它在体外对包括产MBL的铜绿假单胞菌在内的耐碳青霉烯革兰氏阴性菌具有广谱活性,并且在非临床药代动力学/药效学(PK/PD)模型中具有转化疗效。我们报告了一例13岁女孩的病例,她患有结核病,并伴有由产新德里金属β-内酰胺酶(NDM)的广泛耐药(XDR)铜绿假单胞菌引起的难治性肺脓肿,尽管进行了有效的源头控制,但在4个多月的时间里,对几轮黏菌素或氨曲南加头孢他啶/阿维巴坦治疗均无反应。

方法

发现感染菌对头孢吡肟/齐他西克敏感。在获得知情同意并得到必要批准后,患者在同情用药的情况下接受了治疗。

结果

患者接受了成人剂量方案的头孢吡肟/齐他西克治疗(由于体重较高),为期21天,实现了临床和微生物学治愈。

结论

该病例既凸显了抗菌药物耐药性的严重性,也展示了一种尚在试验中的新型抗生素带来的希望。

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Investigational antibiotic cefepime/zidebactam as a therapeutic option for the treatment of an unyielding empyema in a paediatric patient caused by extensively drug-resistant Pseudomonas aeruginosa: a case report.研究性抗生素头孢吡肟/齐德巴坦作为治疗一名由广泛耐药铜绿假单胞菌引起的小儿难治性脓胸的治疗选择:病例报告
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Transcending the challenge of evolving resistance mechanisms in through β-lactam-enhancer-mechanism-based cefepime/zidebactam.通过基于β-内酰胺增强机制的头孢吡肟/齐他培南克服不断进化的耐药机制的挑战。
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In vitro evolution of cefepime/zidebactam (WCK 5222) resistance in Pseudomonas aeruginosa: dynamics, mechanisms, fitness trade-off and impact on in vivo efficacy.铜绿假单胞菌中头孢吡肟/齐他培南(WCK 5222)耐药性的体外进化:动力学、机制、适应性权衡及对体内疗效的影响。
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Effective inhibition of PBPs by cefepime and zidebactam in the presence of VIM-1 drives potent bactericidal activity against MBL-expressing Pseudomonas aeruginosa.头孢吡肟和齐他培南侧链在 VIM-1 存在时对 PBPs 的有效抑制作用使产金属β-内酰胺酶的铜绿假单胞菌具有强大的杀菌活性。
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Efficacy of human-simulated bronchopulmonary exposures of cefepime, zidebactam and the combination (WCK 5222) against MDR Pseudomonas aeruginosa in a neutropenic murine pneumonia model.头孢吡肟、齐多夫定和联合制剂(WCK 5222)在中性粒细胞减少性肺炎小鼠模型中对耐多药铜绿假单胞菌的人模拟支气管肺部暴露的疗效。
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Carbapenemase-producing Gram-negative bacteria: current epidemics, antimicrobial susceptibility and treatment options.产碳青霉烯酶革兰阴性菌:当前的流行情况、抗菌药物敏感性及治疗选择
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Unexpected challenges in treating multidrug-resistant Gram-negative bacteria: resistance to ceftazidime-avibactam in archived isolates of Pseudomonas aeruginosa.治疗多重耐药革兰氏阴性菌时的意外挑战:铜绿假单胞菌存档菌株对头孢他啶-阿维巴坦的耐药性
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