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磷霉素与β-内酰胺类抗生素对葡萄球菌和需氧革兰氏阴性杆菌的协同作用。

Synergy of fosfomycin with beta-lactam antibiotics against staphylococci and aerobic gram-negative bacilli.

作者信息

Chin N X, Neu N M, Neu H C

出版信息

Drugs Exp Clin Res. 1986;12(12):943-7.

PMID:3569007
Abstract

Fosfomycin inhibits bacterial cell wall synthesis at the initial stage. It can act synergistically with beta-lactams. The effect of the combination of fosfomycin and selected penicillins and cephalosporins against staphylococci, Pseudomonas aeruginosa, Pseudomonas cepacia and selected Gram-negative bacteria was determined. Synergy was determined by agar dilution and checkerboard titration methods; synergy was defined as an FIC index less than or equal to 0.5 and partial synergy greater than 0.5 to 0.75. Concentrations of drugs used were those that would be reached in man by intravenous and oral routes. Fosfomycin combined with nafcillin and with cefotaxime against staphylococci showed synergy for most isolates. For methicillin-resistant Staphylococcus aureus, synergy or partial synergy was found for 90% of isolates. Synergy was less frequently found with Staphylococcus epidermidis. The MICs for S. aureus were reduced from greater than or equal to 32 micrograms/ml to less than or equal to 1 microgram/ml. Fosfomycin was synergistic with ticarcillin, piperacillin, azlocillin, ceftazidime, aztreonam and imipenem against 31 to 61% of P. aeruginosa. MICs were reduced from greater than or equal to 128 micrograms/ml to 8-32 micrograms/ml, depending upon the agent. Although fosfomycin acted synergistically with azlocillin, piperacillin and ceftazidime against some P. cepacia, most often there was an indifferent interaction and MICs were in the resistant range, greater than or equal to 128 micrograms/ml. The interaction of fosfomycin and ampicillin was synergistic against a number of strains of Enterobacteriaceae, Proteus vulgaris and Providencia rettgeri, yielding MICs in an achievable range. The combination of fosfomycin with beta-lactams may be clinically useful in selected situations, particularly for methicillin-resistant staphylococci and beta-lactam-resistant P. aeruginosa.

摘要

磷霉素在初始阶段抑制细菌细胞壁合成。它可与β-内酰胺类药物发挥协同作用。测定了磷霉素与选定的青霉素类和头孢菌素类联合使用对葡萄球菌、铜绿假单胞菌、洋葱伯克霍尔德菌及选定革兰氏阴性菌的效果。协同作用通过琼脂稀释法和棋盘滴定法测定;协同作用定义为FIC指数小于或等于0.5,部分协同作用大于0.5至0.75。所用药物浓度为通过静脉和口服途径在人体中可达到的浓度。磷霉素与萘夫西林及头孢噻肟联合用于葡萄球菌时,对大多数分离株显示协同作用。对于耐甲氧西林金黄色葡萄球菌,90%的分离株呈现协同作用或部分协同作用。表皮葡萄球菌较少出现协同作用。金黄色葡萄球菌的最低抑菌浓度从大于或等于32微克/毫升降至小于或等于1微克/毫升。磷霉素与替卡西林、哌拉西林、阿洛西林、头孢他啶、氨曲南和亚胺培南联合使用时,对31%至61%的铜绿假单胞菌具有协同作用。最低抑菌浓度根据药物不同从大于或等于128微克/毫升降至8至32微克/毫升。尽管磷霉素与阿洛西林、哌拉西林和头孢他啶联合使用对某些洋葱伯克霍尔德菌有协同作用,但大多数情况下相互作用不明显,最低抑菌浓度处于耐药范围,大于或等于128微克/毫升。磷霉素与氨苄西林联合使用对多种肠杆菌科菌株、普通变形杆菌和雷氏普罗威登斯菌具有协同作用,最低抑菌浓度处于可达到的范围内。磷霉素与β-内酰胺类药物联合使用在特定情况下可能具有临床应用价值,特别是对于耐甲氧西林葡萄球菌和对β-内酰胺类耐药的铜绿假单胞菌。

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