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新型碳青霉烯类药物SM-7338的多中心体外评估

Multicenter in vitro evaluation of SM-7338, a new carbapenem.

作者信息

Jones R N, Aldridge K E, Allen S D, Barry A L, Fuchs P C, Gerlach E H, Pfaller M A

机构信息

Clinical Microbiology Institute, Tualatin, Oregon 97062.

出版信息

Antimicrob Agents Chemother. 1989 Apr;33(4):562-5. doi: 10.1128/AAC.33.4.562.

Abstract

A new carbapenem, SM-7338, was compared with imipenem, cefotaxime, and ceftazidime at five medical centers. Nearly 6,000 strains were tested by reference methods of the National Committee for Clinical Laboratory Standards, and SM-7338 inhibited the largest percentage of gram-negative bacilli. Its spectrum included all members of the family Enterobacteriaceae (99.7% were susceptible to less than or equal to 4 micrograms/ml), Pseudomonas spp. (but not Xanthomonas maltophilia), and Acinetobacter spp. The potency and spectrum of SM-7338 against the gram-positive organisms were less than those of imipenem and superior to those of ceftazidime. Only the enterococci and some oxacillin-resistant staphylococci were less susceptible to SM-7338 (MICs for 90% of isolates, greater than or equal to 8 micrograms/ml). Organisms resistant to ceftazidime were generally susceptible to SM-7338 and imipenem (76%). However, for one-third of the imipenem-resistant gram-negative bacilli (MICs, greater than 8 micrograms/ml), SM-7338 MICs were less than or equal to 4 micrograms/ml. Some endemic differences in patterns of SM-7338 activity against selected gram-negative species were found among some medical centers.

摘要

一种新型碳青霉烯类药物SM - 7338在五个医学中心与亚胺培南、头孢噻肟和头孢他啶进行了比较。采用美国国家临床实验室标准委员会的参考方法对近6000株菌株进行了检测,结果显示SM - 7338对革兰氏阴性杆菌的抑制率最高。其抗菌谱包括肠杆菌科所有成员(99.7%的菌株对小于或等于4微克/毫升的药物敏感)、假单胞菌属(但不包括嗜麦芽窄食单胞菌)和不动杆菌属。SM - 7338对革兰氏阳性菌的抗菌活性和抗菌谱低于亚胺培南,但优于头孢他啶。只有肠球菌和一些耐苯唑西林的葡萄球菌对SM - 7338的敏感性较低(90%的分离株的最低抑菌浓度大于或等于8微克/毫升)。对头孢他啶耐药的菌株通常对SM - 7338和亚胺培南敏感(76%)。然而,对于三分之一对亚胺培南耐药的革兰氏阴性杆菌(最低抑菌浓度大于8微克/毫升),SM - 7338的最低抑菌浓度小于或等于4微克/毫升。在一些医学中心发现了SM - 7338对某些革兰氏阴性菌的活性模式存在一些地区差异。

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