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Ceftazidime-avibactam-based combination therapy for hospital-acquired central nervous system infections caused by carbapenem-resistant Klebsiella pneumoniae

头孢他啶/阿维巴坦 肺炎克雷伯菌 医学 头孢他啶 内科学 微生物学 碳青霉烯 回顾性队列研究 β-内酰胺酶抑制剂 共病 重症监护医学 铜绿假单胞菌 抗生素 生物 大肠杆菌 细菌 遗传学 基因 生物化学
作者
Xiaoyu Zhao,Shirong Li,Yixin Zhang,Jue Wang,Chuning Wang,Xiaohua Qin,Fupin Hu,Minggui Wang
出处
期刊:International Journal of Antimicrobial Agents [Elsevier BV]
卷期号:61 (5): 106777-106777 被引量:25
标识
DOI:10.1016/j.ijantimicag.2023.106777
摘要

Klebsiella pneumoniae (K. pneumoniae) is one of the most common bacteria in the hospital-acquired central nervous system (CNS) infections. Central nervous system infections caused by carbapenem-resistant K. pneumoniae (CRKP) are associated with significant mortality rates and high hospital costs due to limited antibiotic treatment options. This retrospective study aimed to evaluate the clinical efficacy of ceftazidime-avibactam (CZA) for the treatment of CNS infections caused by CRKP.Twenty-one patients with hospital-acquired CNS infections caused by CRKP who received treatment with CZA for ≥ 72 hours were enrolled. The primary outcome was to assess the clinical and microbiology efficacy of CZA for the treatment of CNS infections caused by CRKP.A high burden of comorbidity was discovered in 20 of 21 patients (95.2%). Most patients had a history of craniocerebral surgery and 17 (81.0%) of the patients were in the intensive care unit with a median APACHE II score of 16 (IQR 9-20) and SOFA score of 6 (IQR 3-7). Eighteen cases were treated by CZA-based combination therapies, while the remaining three cases were treated with CZA alone. At the end of the treatment, the overall clinical efficacy was 76.2% (16 of 21) with a bacterial clearance rate of 81.0% (17 of 21) and all-cause mortality of 23.8% (five of 21).This study showed that CZA-based combination therapy is an effective treatment option for CNS infections caused by CRKP.
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