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新型口服头孢菌素头孢丙烯的体外活性、药代动力学特性、安全性及临床疗效综述

Review of in vitro activity, pharmacokinetic characteristics, safety, and clinical efficacy of cefprozil, a new oral cephalosporin.

作者信息

Barriere S L

机构信息

Department of Pharmaceutical Services, University of California, Los Angeles for the Health Sciences.

出版信息

Ann Pharmacother. 1993 Sep;27(9):1082-9. doi: 10.1177/106002809302700914.

Abstract

OBJECTIVE

To review the pharmacokinetics, microbiology, clinical efficacy, safety, and tolerance of cefprozil, a new, broad-spectrum oral cephalosporin.

DATA SOURCES

Published clinical trials and microbiologic, pharmacokinetic, and safety data were identified by MEDLINE; additional references were derived from bibliographies of these articles; microbiologic data on file were provided by Bristol-Myers Squibb.

STUDY SELECTION

Only published comparative clinical trial reports are included in the review of clinical efficacy. Noncomparative clinical data pertaining to uses of cefprozil not approved by the Food and Drug Administration are not included.

DATA SYNTHESIS

Data are presented on the in vitro microbiologic activity of cefprozil against 10,152 bacterial isolates, including most of the clinically important streptococci (e.g., Streptococcus pyogenes, Streptococcus pneumoniae), beta-lactamase-positive and -negative Staphylococcus aureus and Haemophilus influenzae, Moraxella catarrhalis, Escherichia coli, Proteus mirabilis, Clostridium difficile, and numerous other gram-negative aerobes and anaerobes. In clinical trials, cefprozil appears to be at least as effective as commonly used comparison agents such as cefaclor, cefixime, and amoxicillin/clavulanic acid. Additionally, cefprozil is better tolerated than the latter two agents, especially with regard to gastrointestinal adverse effects.

CONCLUSIONS

Cefprozil is a broad-spectrum cephalosporin that provides coverage against both gram-negative and -positive bacteria that may cause otitis media, pharyngitis/tonsillitis, skin and skin-structure infections, secondary bacterial infection of acute bronchitis, and acute bacterial exacerbations of chronic bronchitis. The beta-lactamase stability of cefprozil appears to exceed that of other oral cephalosporins for some important pathogens. Cefprozil is used primarily for second-line treatment as less-expensive, first-line generic alternatives generally are available. Cefprozil demonstrates clinical advantages over many other orally administered beta-lactam antibiotics in terms of antimicrobial spectrum, a once- or twice-daily dosing regimen, and/or reduced incidence of adverse effects.

摘要

目的

综述新型广谱口服头孢菌素头孢丙烯的药代动力学、微生物学特性、临床疗效、安全性及耐受性。

资料来源

通过MEDLINE检索已发表的临床试验以及微生物学、药代动力学和安全性数据;其他参考文献来自这些文章的参考文献目录;百时美施贵宝公司提供了存档的微生物学数据。

研究选择

临床疗效综述仅纳入已发表的比较性临床试验报告。未纳入与食品药品监督管理局未批准的头孢丙烯用途相关的非比较性临床数据。

资料综合

列出了头孢丙烯对10152株细菌分离株的体外微生物活性数据,这些细菌包括大多数临床上重要的链球菌(如化脓性链球菌、肺炎链球菌)、β-内酰胺酶阳性和阴性金黄色葡萄球菌、流感嗜血杆菌、卡他莫拉菌、大肠杆菌、奇异变形杆菌、艰难梭菌以及许多其他革兰阴性需氧菌和厌氧菌。在临床试验中,头孢丙烯似乎至少与常用对照药物如头孢克洛、头孢克肟和阿莫西林/克拉维酸一样有效。此外,头孢丙烯的耐受性优于后两种药物,尤其是在胃肠道不良反应方面。

结论

头孢丙烯是一种广谱头孢菌素,可覆盖可能导致中耳炎、咽炎/扁桃体炎、皮肤及皮肤结构感染、急性支气管炎继发细菌感染以及慢性支气管炎急性细菌加重的革兰阴性和阳性细菌。对于某些重要病原体,头孢丙烯的β-内酰胺酶稳定性似乎超过其他口服头孢菌素。由于通常有价格较低的一线通用替代药物,头孢丙烯主要用于二线治疗。在抗菌谱、一日一次或两次给药方案和/或降低不良反应发生率方面,头孢丙烯比许多其他口服β-内酰胺抗生素具有临床优势。

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