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幽门螺杆菌临床分离株对21种抗菌药物的敏感性

Susceptibility of clinical isolates of Campylobacter pylori to twenty-one antimicrobial agents.

作者信息

McNulty C A, Dent J C

机构信息

Public Health Laboratory, Gloucestershire Royal Hospital, UK.

出版信息

Eur J Clin Microbiol Infect Dis. 1988 Aug;7(4):566-9. doi: 10.1007/BF01962617.

Abstract

The MICs of 21 antimicrobial agents were determined for 97 clinical isolates of Campylobacter pylori. The beta-lactams (penicillin, ampicillin, cefoxitin and cephalexin), macrolides (erythromycin and azithromycin), quinolones (ciprofloxacin and ofloxacin), nitrofurans, gentamicin and tetracycline all had MIC90 values of less than or equal to 0.5 mg/l. Aztreonam, flucloxacillin, amifloxacin and rifampicin had moderate activity. All isolates were resistant to vancomycin, cefsulodin and amphotericin B. Five percent of the strains were inhibited by 8 mg/l of polymyxin. Of the oral agents tested, the nitrofurans and ampicillin are probably the most appropriate antimicrobial agents. Azithromycin and the oral form of cefuroxime are promising alternatives. Cefsulodin, vancomycin and amphotericin B would be suitable constituents of selective media for isolation of Campylobacter pylori.

摘要

对97株幽门螺杆菌临床分离株测定了21种抗菌药物的最低抑菌浓度(MIC)。β-内酰胺类(青霉素、氨苄西林、头孢西丁和头孢氨苄)、大环内酯类(红霉素和阿奇霉素)、喹诺酮类(环丙沙星和氧氟沙星)、硝基呋喃类、庆大霉素和四环素的MIC90值均小于或等于0.5mg/L。氨曲南、氟氯西林、阿米氟沙星和利福平具有中等活性。所有分离株对万古霉素、头孢磺啶和两性霉素B均耐药。5%的菌株被8mg/L的多粘菌素抑制。在所测试的口服药物中,硝基呋喃类和氨苄西林可能是最合适的抗菌药物。阿奇霉素和口服头孢呋辛是有前景的替代药物。头孢磺啶、万古霉素和两性霉素B将是用于分离幽门螺杆菌的选择性培养基的合适成分。

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