[头孢唑仑对各种临床分离菌抗菌活性的上市后监测--II。革兰氏阴性菌]。

The Japanese journal of antibiotics Pub Date : 2002-02-01
Jun Igari, Toyoko Oguri, Nobuyoshi Hiramatsu, Kazumitsu Akiyama, Tsuneo Koyama
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引用次数: 0

摘要

作为一种上市后监测,我们每年都对头孢唑兰(CZOP)(一种头孢菌素制剂)对各种临床分离菌的体外抗菌活性进行评估,并与其他头孢菌素、氧头孢菌素、青霉素类、单内酰胺类和碳青霉烯类的体外抗菌活性进行比较。细菌对 CZOP 药物敏感性的变化也通过使用断点 MIC 计算出的细菌耐药性比率进行了评估。从 1996 年至 2000 年期间每年收集的临床材料中分离出 25 种(3 362 株)革兰氏阴性菌,包括卡氏莫拉菌(布兰哈姆氏菌)(n = 136)、流感嗜血杆菌(n = 289)、大肠埃希菌(n = 276)、肺炎克雷伯菌(n = 192)、土生克雷伯菌(n = 192)、嗜血杆菌(n = 289)、大肠埃希菌(n = 276)、肺炎克雷伯菌(n = 192)、嗜血杆菌(n = 276)、大肠埃希菌(n = 276)、肺炎克雷伯菌(n = 192)、肺炎克雷伯菌(n = 192)、氧乐菌(n = 157)、泄殖腔肠杆菌(n = 189)、产气肠杆菌(n = 93)、侯氏沙雷氏菌(n = 172)、液化沙雷氏菌(n = 24)、弗氏柠檬酸杆菌(n = 177)、科氏柠檬酸杆菌(n = 70)、奇异变形杆菌(n = 113)、普通变形杆菌(n = 89)、摩根氏摩根菌(n = 116)、普罗维登斯菌(n = 41)、假丝酵母菌(n = 42)。(n = 41)、铜绿假单胞菌 (n = 290)、荧光假单胞菌 (n = 56)、腐生假单胞菌 (n = 63)、鲍曼不动杆菌 (n = 146)、卢沃菲不动杆菌 (n = 34)、伯克霍尔德氏菌(101 人)、嗜麦芽气单胞菌(169 人)、脆弱拟杆菌(196 人)和普雷沃氏菌/卟啉单胞菌(173 人)。CZOP 对大肠杆菌、肺炎双球菌、氧乐菌和肉毒杆菌的抗菌活性很强,与新药申请批准前的研究结果一致或更优。CZOP 对白喉杆菌、科氏杆菌和铜绿假单胞菌的 MIC90 没有显著变化,与新药申请批准前的研究结果一致。CZOP 对泄殖酸大肠杆菌、产气大肠杆菌和奇异变形杆菌的 MIC90 逐年增加。然而,CZOP 对产气大肠杆菌和奇异变形杆菌的 MIC90 的增加并不被认为是药敏性的明显下降。在合同中,泄殖腔杆菌对 CZOP 的敏感性被怀疑在下降,因为该菌种对 CZOP 的耐药性为 20.6%。CZOP 对 C. freundii 的 MIC90 有不同程度的变化,或不是片面的,但高于新药申请批准前的数值。此外,CZOP 对流感嗜血杆菌的 MIC90 在 5 年中保持稳定,只是在 1999 年有所提高,总体上略高于新药申请批准前的数值。与其他头孢菌素一样,CZOP 对荧光假丝酵母菌、腐生酵母菌、头孢杆菌、嗜麦芽糖酵母菌、脆弱拟杆菌和普雷沃氏菌/卟啉单胞菌的抗菌活性较弱。在 5 年的研究期间,CZOP 对其他细菌的 MIC90 变化为 2 管或更多,但并不趋向于单边方向,这意味着敏感性下降。
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[Post-marketing surveillance of antibacterial activities of cefozopran against various clinical isolates--II. Gram-negative bacteria].

As a post-marketing surveillance, the in vitro antibacterial activities of cefozopran (CZOP), an agent of cephems, against various clinical isolates were yearly evaluated and compared with those of other cephems, oxacephems, penicillins, monobactams, and carbapenems. Changes in CZOP susceptibility for the bacteria were also evaluated with the bacterial resistance ratio calculated with the breakpoint MIC. Twenty-five species (3,362 strains) of Gram-negative bacteria were isolated from the clinical materials annually collected from 1996 to 2000, and consisted of Moraxella (Branhamella) catarrhalis (n = 136), Haemophilus influenzae (n = 289), Escherichia coli (n = 276), Klebsiella pneumoniae (n = 192), Klebsiella oxytoca (n = 157), Enterobacter cloacae (n = 189), Enterobacter aerogenes (n = 93), Serratia marcescens (n = 172), Serratia liquefaciens (n = 24), Citrobacter freundii (n = 177), Citrobacter koseri (n = 70), Proteus mirabilis (n = 113), Proteus vulgaris (n = 89), Morganella morganii (n = 116), Providencia spp. (n = 41), Pseudomonas aeruginosa (n = 290), Pseudomonas fluorescens (n = 56), Pseudomonas putida (n = 63), Acinetobacter baumannii (n = 146), Acinetobacter lwoffii (n = 34), Burkholderia cepacia (n = 101), Stenotrophomonas maltophilia (n = 169), Bacteroides fragilis group (n = 196), and Prevotella/Porphyromonas (n = 173). An antibacterial activity of CZOP against E. coli, K. pneumoniae, K. oxytoca, and S. marcescens was potent and consistent with or more preferable than the study results obtained until the new drug application approval. MIC90 of CZOP against M.(B.) catarrhalis, C. koseri, and P. aeruginosa was not considerably changed and consistent with the study results obtained until the new drug application approval. MIC90 of CZOP against E. cloacae, E. aerogenes, and P. mirabilis increased year by year. The increase in MIC90 of CZOP against E. aerogenes and P. mirabilis, however, was not considered to be an obvious decline in susceptibility. In contract, the susceptibility of E. cloacae to CZOP was suspected to be decreasing because this species showed 20.6% resistance to CZOP. MIC90 of CZOP against C. freundii was variably changed or not one-sidedly, but was higher than the values obtained until the new drug application approval. Additionally, MIC90 of CZOP against H. influenzae was stable during 5 years except being higher in 1999, and, as a whole, was a little higher than the values obtained until the new drug application approval. An antibacterial activity of CZOP against P. fluorescens, P. putida, B. cepacia, S. maltophilia, B. fragilis group, and Prevotella/Porphyromonas was weak like the other cephems. Changes in MIC90 of CZOP against the other bacteria were 2 tubes or more through 5-year study period, but did not tend towards a unilateral direction as meaning a decline in susceptibility.

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[Yearly changes in antibacterial activities of cefozopran against various clinical isolates between 1996 and 2000--I. Gram-positive bacteria]. [Yearly changes in antibacterial activities of cefozopran against various clinical isolates between 1996 and 2000--II. Gram-negative bacteria]. [Post-marketing surveillance of antibacterial activities of cefozopran against various clinical isolates--I. Gram-positive bacteria]. [Post-marketing surveillance of antibacterial activities of cefozopran against various clinical isolates--II. Gram-negative bacteria]. [Antimicrobial activities of carbapenems and fourth generation cephems against clinically isolated strains].
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