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新型药物对囊性纤维化患者和其他慢性感染患者分离出的铜绿假单胞菌的体外活性比较。

Comparison between the in-vitro activity of new agents on Pseudomonas aeruginosa isolates from cystic fibrosis patients and other chronic infections.

作者信息

Gordts B, Vandenborre C, VanderAuwera P, Butzler J P

出版信息

J Antimicrob Chemother. 1984 Jul;14(1):25-9. doi: 10.1093/jac/14.1.25.

Abstract

The in-vitro activities of the newer antipseudomonal agents cefsulodin, ceftazidime, U-63196, aztreonam and piperacillin were compared, together with azlocillin, carbenicillin, ticarcillin and tobramycin against 98 strains of Pseudomonas aeruginosa. On all of the 43 isolates from cystic fibrosis patients and the 55 strains from other chronically infected patients, ceftazidime (MIC90: 5.0 and 2.8 mg/l respectively) and cefsulodin (MIC90: 8.2 and 3.1 mg/l) were the most active cephalosporins, and U-63196 the least active (MIC90: 40.1 and 46.1 mg/l). A high incidence of resistance (23 of 55 strains) to tobramycin was found only in the non-cystic fibrosis isolates. The activity of the other agents was comparable in the cystic fibrosis and non-cystic fibrosis isolates. MIC90 for aztreonam were 15.8 and 13.6 mg/l. Piperacillin was the most active penicillin in both populations (MIC90: 25.8 and 21.8 mg/l). Cross resistance was demonstrated in both populations for the penicillin compounds.

摘要

比较了新型抗假单胞菌药物头孢磺啶、头孢他啶、U - 63196、氨曲南和哌拉西林,以及阿洛西林、羧苄西林、替卡西林和妥布霉素对98株铜绿假单胞菌的体外活性。在从囊性纤维化患者分离出的所有43株菌株以及从其他慢性感染患者分离出的55株菌株中,头孢他啶(MIC90分别为5.0和2.8mg/L)和头孢磺啶(MIC90为8.2和3.1mg/L)是活性最高的头孢菌素,而U - 63196活性最低(MIC90为40.1和46.1mg/L)。仅在非囊性纤维化分离株中发现对妥布霉素的高耐药率(55株中有23株)。其他药物在囊性纤维化和非囊性纤维化分离株中的活性相当。氨曲南的MIC90分别为15.8和13.6mg/L。哌拉西林是这两组人群中活性最高的青霉素(MIC90分别为25.8和21.8mg/L)。在两组人群中均显示出青霉素类化合物存在交叉耐药性。

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