Section of Microbiology, Department of Laboratory Diagnostics, Military Institute of Medicine-National Research Institute, Warsaw, Poland.
Department of Anesthesiology and Intensive Therapy, Military Institute of Medicine-National Research Institute, Warsaw, Poland.
Eur J Clin Microbiol Infect Dis. 2024 Aug;43(8):1579-1587. doi: 10.1007/s10096-024-04859-y. Epub 2024 May 29.
Amongst all etiologic hospital-acquired infection factors, K. pneumoniae strains producing New Delhi metallo-β-lactamase (KP-NDM) belong to pathogens with the most effective antibiotic resistance mechanisms. Clinical guidelines recommend using ceftazidime/avibactam with aztreonam (CZA + AT) as the preferred option for NDM-producing Enterobacterales. However, the number of observations on such treatment regimen is limited. This retrospective study reports the clinical and microbiological outcomes of 23 patients with KP-NDM hospital-acquired infection treated with CZA + AT at a single center in Poland.
The isolates were derived from the urine, lungs, blood, peritoneal cavity, wounds, and peritonsillar abscess. In microbiological analysis, mass spectrometry for pathogen identification, polymerase chain reaction, or an immunochromatographic assay for detection of carbapenemase, as well as VITEK-2 system, broth microdilution, and microdilution in agar method for antimicrobial susceptibility tests were used, depending of the pathogens' nature. CZA was administered intravenously (IV) at 2.5 g every eight hours in patients with normal kidney function, and aztreonam was administered at 2 g every eight hours IV. Such dosage was modified when renal function was reduced.
KP-NDM was eradicated in all cases. Four patients (17.4%) died: three of them had a neoplastic disease, and one - a COVID-19 infection.
The combination of CZA + AT is a safe and effective therapy for infections caused by KP-NDM, both at the clinical and microbiological levels. The synergistic action of all compounds resulted in a good agreement between the clinical efficacy of CZA + AT and the results of in vitro susceptibility testing.
在所有病因医院获得性感染因素中,产新德里金属β-内酰胺酶(KP-NDM)的肺炎克雷伯菌菌株属于具有最有效抗生素耐药机制的病原体。临床指南建议使用头孢他啶/阿维巴坦联合氨曲南(CZA+AT)作为治疗产 NDM 的肠杆菌科的首选方案。然而,这种治疗方案的观察数量有限。本回顾性研究报告了在波兰的一家单中心对 23 例产 KP-NDM 医院获得性感染患者使用 CZA+AT 的临床和微生物学结果。
分离株来自尿液、肺部、血液、腹腔、伤口和扁桃体周围脓肿。在微生物学分析中,根据病原体的性质,使用质谱法进行病原体鉴定、聚合酶链反应或免疫层析法检测碳青霉烯酶,以及 VITEK-2 系统、肉汤微量稀释法和琼脂微量稀释法进行抗菌药物敏感性试验。在肾功能正常的患者中,静脉注射头孢他啶(IV)2.5 g,每 8 小时一次,静脉注射氨曲南 2 g,每 8 小时一次。当肾功能降低时,会对剂量进行调整。
所有病例均消除了 KP-NDM。4 例患者(17.4%)死亡:其中 3 例患有肿瘤疾病,1 例患有 COVID-19 感染。
CZA+AT 的联合应用是治疗 KP-NDM 感染的一种安全有效的方法,无论是在临床还是微生物学方面。所有化合物的协同作用导致 CZA+AT 的临床疗效与体外药敏试验结果之间具有良好的一致性。