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1996年至2000年巴西圣保罗肺炎链球菌和流感嗜血杆菌的耐药性

Antimicrobial resistance of Streptococcus pneumoniae and Haemophilus influenzae in Sao Paulo, Brazil from 1996 to 2000.

作者信息

Koeth L M, Felmingham D, Jacobs M R, Rossi F

机构信息

Laboratory Specialists, Inc., 1651 A. Crossings Parkway, Westlake, OH 44145, USA.

出版信息

Int J Antimicrob Agents. 2004 Apr;23(4):356-61. doi: 10.1016/j.ijantimicag.2003.09.022.

Abstract

This study was undertaken to assess the in vitro activity of several antimicrobial agents against Brazilian isolates of Streptococcus pneumoniae and Haemophilus influenzae from 1996 to 2000. The antibiotics used were penicillin, amoxicillin/clavulanic acid (A/C), ampicillin, amoxicillin, cefaclor, cefdinir, cefixime, cefprozil, ceftriaxone, cefuroxime, azithromycin, clarithromycin, erythromycin, ciprofloxacin, levofloxacin, ofloxacin, chloramphenicol, clindamycin, doxycycline and trimethoprim/sulphamethoxazole (T/S). MICs were determined by the National Committee for Clinical Laboratory Standards (NCCLS) method and interpreted using NCCLS and PK/PD breakpoints. For S. pneumoniae 80.0% were penicillin susceptible, 18.3% intermediate, 1.7% resistant; most active agents were amoxicillin, A/C, ceftriaxone and levofloxacin; T/S was the least active agent. Beta-lactamase was produced by 13.7% of H. influenzae. All were susceptible to A/C, cefdinir, cefixime, ceftriaxone and quinolones. The least active agents were T/S and macrolides.

摘要

本研究旨在评估1996年至2000年期间几种抗菌药物对巴西分离的肺炎链球菌和流感嗜血杆菌的体外活性。所用抗生素包括青霉素、阿莫西林/克拉维酸(A/C)、氨苄西林、阿莫西林、头孢克洛、头孢地尼、头孢克肟、头孢丙烯、头孢曲松、头孢呋辛、阿奇霉素、克拉霉素、红霉素、环丙沙星、左氧氟沙星、氧氟沙星、氯霉素、克林霉素、多西环素和甲氧苄啶/磺胺甲恶唑(T/S)。最低抑菌浓度(MIC)采用美国国家临床实验室标准委员会(NCCLS)方法测定,并根据NCCLS和药代动力学/药效学(PK/PD)界值进行解释。对于肺炎链球菌,80.0%对青霉素敏感,18.3%为中介,1.7%耐药;活性最强的药物为阿莫西林、A/C、头孢曲松和左氧氟沙星;T/S活性最低。13.7%的流感嗜血杆菌产生β-内酰胺酶。所有菌株对A/C、头孢地尼、头孢克肟、头孢曲松和喹诺酮类均敏感。活性最低的药物为T/S和大环内酯类。

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