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头孢他啶与其他抗生素联合使用的体外活性。

In vitro activity of ceftazidime in combination with other antibiotics.

作者信息

Simon C, Littschwager G

出版信息

Infection. 1985 Jul-Aug;13(4):184-9. doi: 10.1007/BF01642810.

Abstract

189 bacterial strains were investigated for their in vitro sensitivity against ceftazidime (alone and in combination with another antibiotic). Moreover, the possibility to prevent development of secondary bacterial resistance as observed in subcultures at subinhibitory antibiotic concentrations, was studied using specific antibiotic combinations. Of 115 staphylococcal strains (91 strains of Staphylococcus aureus, 24 strains of Staphylococcus epidermidis), 2% were sensitive, 82% were moderately sensitive and 16% were resistant to ceftazidime. On combining ceftazidime with vancomycin, synergism was found in 61% of the strains, and secondary resistance to ceftazidime could be prevented with this combination. The combination of ceftazidime and clindamycin showed synergism in 26% and an additive effect in 48% of the strains. Secondary resistance to ceftazidime did not develop with this combination in subcultures at subinhibitory concentrations in which loss of activity was only minimal with clindamycin alone. Rifampicin and fusidic acid were highly active against staphylococci. In combination with ceftazidime, only weak synergism or additive effects were seen in most strains; no antagonism could be observed. In subcultures at subinhibitory concentrations, secondary resistance to rifampicin and fusidic acid developed rapidly and could be partially prevented by adding ceftazidime. Of 60 Pseudomonas aeruginosa strains, 84% were sensitive, 13% were moderately sensitive and 2% were resistant to ceftazidime. Synergism was most frequently observed when ceftazidime was combined with tobramycin. Using this combination, secondary resistance of Pseudomonas strains to ceftazidime did not develop. When ceftazidime was combined with piperacillin, synergism was observed in most strains, but the development of secondary resistance in vitro was not prevented.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对189株细菌进行了体外实验,研究它们对头孢他啶(单独使用及与另一种抗生素联合使用时)的敏感性。此外,还使用特定的抗生素组合研究了在亚抑菌浓度的亚培养物中观察到的预防继发性细菌耐药性产生的可能性。在115株葡萄球菌菌株中(91株金黄色葡萄球菌,24株表皮葡萄球菌),2%对头孢他啶敏感,82%中度敏感,16%耐药。头孢他啶与万古霉素联合使用时,61%的菌株表现出协同作用,且该组合可预防对头孢他啶的继发性耐药。头孢他啶与克林霉素联合使用时,26%的菌株表现出协同作用,48%表现出相加作用。在亚抑菌浓度的亚培养物中,该组合未出现对头孢他啶的继发性耐药,单独使用克林霉素时活性损失极小。利福平与夫西地酸对葡萄球菌具有高活性。与头孢他啶联合使用时,大多数菌株仅表现出微弱的协同作用或相加作用;未观察到拮抗作用。在亚抑菌浓度的亚培养物中,对利福平和夫西地酸的继发性耐药迅速产生,添加头孢他啶可部分预防。在60株铜绿假单胞菌菌株中,84%对头孢他啶敏感,13%中度敏感,2%耐药。头孢他啶与妥布霉素联合使用时最常观察到协同作用。使用该组合时,铜绿假单胞菌菌株未出现对头孢他啶的继发性耐药。头孢他啶与哌拉西林联合使用时,大多数菌株观察到协同作用,但未预防体外继发性耐药的产生。(摘要截短于250字)

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