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哌拉西林/他唑巴坦对重症监护病房分离的615株铜绿假单胞菌的体外活性

In vitro activity of piperacillin/tazobactam against 615 Pseudomonas aeruginosa strains isolated in intensive care units.

作者信息

Bonfiglio G, Laksai Y, Franceschini N, Perilli M, Segatore B, Bianchi C, Stefani S, Amicosante G, Nicoletti G

机构信息

Istituto di Microbiologia, Università di Catania, Italia.

出版信息

Chemotherapy. 1998 Sep-Oct;44(5):305-12. doi: 10.1159/000007127.

Abstract

From May 1996 to September 1997, 615 Pseudomonas aeruginosa strains isolated from patients in intensive care units collected from different Italian laboratories were studied. The susceptibility of piperacillin/tazobactam, in comparison with other antipseudomonal antibiotics, to their NCCLS breakpoints was evaluated: amikacin 79. 6%, carbenicillin 67.0%, ceftazidime 73.4%, ciprofloxacin 55.8%, imipenem 64.1%, piperacillin 88.1%, piperacillin/tazobactam 92.4% and ticarcillin/clavulanic acid 69.0%. Seventy-three strains were selected because of their resistance to piperacillin and the mechanisms underlying such a resistance were investigated. Isoelectric focusing and hydrolysis assays revealed the presence of 15 plasmid-mediated beta-lactamases. Chromosomal beta-lactamase derepression was demonstrated in 34 isolates. The remaining 24 piperacillin-resistant strains did not produce beta-lactamases and an 'intrinsic mechanism' of resistance was inferred. The piperacillin/tazobactam combination restored resistance in 25 piperacillin strains. Nine of these were derepressed for chromosomal beta-lactamase, 8 showed impermeability and 8 showed plasmid enzymes.

摘要

1996年5月至1997年9月,对从意大利不同实验室收集的重症监护病房患者中分离出的615株铜绿假单胞菌菌株进行了研究。评估了哌拉西林/他唑巴坦与其他抗假单胞菌抗生素相比对其NCCLS断点的敏感性:阿米卡星为79.6%,羧苄西林为67.0%,头孢他啶为73.4%,环丙沙星为55.8%,亚胺培南为64.1%,哌拉西林为88.1%,哌拉西林/他唑巴坦为92.4%,替卡西林/克拉维酸为69.0%。由于73株菌株对哌拉西林耐药,因此对其耐药机制进行了研究。等电聚焦和水解试验显示存在15种质粒介导的β-内酰胺酶。34株分离株显示出染色体β-内酰胺酶去阻遏。其余24株对哌拉西林耐药的菌株不产生β-内酰胺酶,推测存在“内在耐药机制”。哌拉西林/他唑巴坦组合恢复了25株哌拉西林菌株的耐药性。其中9株染色体β-内酰胺酶去阻遏,8株显示通透性降低,8株显示质粒酶。

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