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哌拉西林/他唑巴坦:一种新型β-内酰胺类/β-内酰胺酶抑制剂组合

Piperacillin/tazobactam: a new beta-lactam/beta-lactamase inhibitor combination.

作者信息

Schoonover L L, Occhipinti D J, Rodvold K A, Danziger L H

机构信息

College of Pharmacy, Washington State University, Spokane, USA.

出版信息

Ann Pharmacother. 1995 May;29(5):501-14. doi: 10.1177/106002809502900510.

Abstract

OBJECTIVE

To discuss the antimicrobial activity, pharmacokinetics, clinical efficacy, and adverse effect profile of piperacillin/tazobactam, a new beta-lactan/beta-lactamase inhibitor combination.

DATA SOURCES

Literature was identified by MEDLINE search of the medical literature, review of selected references, and data provided by the manufacturer.

STUDY SELECTION

In vitro susceptibility data were surveyed from studies following the methods of the National Committee for Clinical Laboratory Standards. Data evaluating clinical efficacy were selected from all published trials and abstracts. Additional information concerning safety, chemistry, and pharmacokinetics was reviewed.

DATA SYNTHESIS

The antimicrobial activity of piperacillin is enhanced by addition of tazobactam against gram-positive, gram-negative, and anaerobic bacteria. Tazobactam is active against a broad spectrum of plasmid and chromosomally mediated enzymes and has minimal ability to induce class I chromosomally mediated beta-lactamase enzymes. Piperacillin/tazobactam's expanded activity appears encouraging in the treatment of mixed aerobic and anaerobic infections. Direct comparisons of ticarcillin/clavulanate and piperacillin/tazobactam for the treatment of lower respiratory tract infections showed piperacillin/tazobactam to be clinically superior, and in the treatment of skin and soft tissue infections the 2 agents were comparable. For the treatment of intraabdominal infections, piperacillin/tazobactam was at least as effective as imipenem/cilastatin and clindamycin plus gentamicin.

CONCLUSIONS

The combination of tazobactam with piperacillin results in an antimicrobial agent with enhanced activity against most beta-lactamase-producing organisms. Preliminary data indicate that piperacillin/tazobactam has proven clinical efficacy in the treatment of a variety of infections, especially polymicrobic infections.

摘要

目的

探讨新型β-内酰胺类/β-内酰胺酶抑制剂组合哌拉西林/他唑巴坦的抗菌活性、药代动力学、临床疗效及不良反应。

资料来源

通过检索MEDLINE医学文献、查阅选定参考文献以及制造商提供的数据来获取文献。

研究选择

按照美国国家临床实验室标准委员会的方法,从各项研究中收集体外药敏数据。从所有已发表的试验和摘要中选取评估临床疗效的数据。同时查阅了有关安全性、化学性质和药代动力学的其他信息。

资料综合

添加他唑巴坦后,哌拉西林对革兰氏阳性菌、革兰氏阴性菌和厌氧菌的抗菌活性增强。他唑巴坦对多种质粒介导和染色体介导的酶具有活性,且诱导I类染色体介导的β-内酰胺酶的能力极小。哌拉西林/他唑巴坦在治疗需氧菌与厌氧菌混合感染方面展现出令人鼓舞的广泛活性。在治疗下呼吸道感染时,替卡西林/克拉维酸与哌拉西林/他唑巴坦的直接比较显示,哌拉西林/他唑巴坦在临床上更具优势;而在治疗皮肤及软组织感染时,这两种药物疗效相当。在治疗腹腔内感染方面,哌拉西林/他唑巴坦至少与亚胺培南/西司他丁以及克林霉素加庆大霉素的疗效相当。

结论

他唑巴坦与哌拉西林联合使用可产生一种对大多数产β-内酰胺酶的微生物具有增强活性的抗菌药物。初步数据表明,哌拉西林/他唑巴坦在治疗多种感染,尤其是多种微生物感染方面已证实具有临床疗效。

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