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口服及肠胃外给药制剂对青霉素敏感及耐药肺炎球菌的活性。

Activities of oral and parenteral agents against penicillin-susceptible and -resistant pneumococci.

作者信息

Pankuch G A, Visalli M A, Jacobs M R, Appelbaum P C

机构信息

Department of Pathology (Clinical Microbiology), Hershey Medical Center, Hershey, Pennsylvania 17033, USA.

出版信息

Antimicrob Agents Chemother. 1995 Jul;39(7):1499-504. doi: 10.1128/AAC.39.7.1499.

Abstract

This study examined bacteriostatic and bactericidal activities of oral and parenteral antibiotics for penicillin-susceptible and intermediately and fully penicillin-resistant pneumococci. beta-Lactamase inhibitors did not affect beta-lactam results. The activities of ampicillin, amoxicillin +/- clavulanate, WY-49605, cefuroxime, cefpodoxime, cefdinir, cefixime, and cefaclor against two penicillin-susceptible, two intermediately penicillin-resistant, and two fully penicillin-resistant pneumococcal strains were tested. For all three groups, bacteriostatic values of amoxicillin and WY-49605 were lower than were those of other beta-lactams tested. Of the cephalosporins, cefdinir, cefuroxime, and cefpodoxime yielded the lowest bacteriostatic values. All beta-lactams were bactericidal (reduced original counts by > or = 3 log10 CFU/ml) at 1 dilution above bacteriostatic values, except for cefpodoxime (bactericidal at 2 dilutions above bacteriostatic values for one susceptible strain and one intermediately resistant strain), cefuroxime (bactericidal at 2 dilutions above bacteriostatic values for one intermediately resistant strain), and ampicillin (bactericidal at 2 dilutions above bacteriostatic values for one intermediately resistant strain). The activities of piperacillin, piperacillin-tazobactam, ticarcillin, ticarcillin-clavulanate, ampicillin, ampicillin-sulbactam, ceftriaxone, ceftazidime, and ciprofloxacin against four penicillin-susceptible, two intermediately penicillin-resistant, and four fully penicillin-resistant pneumococcal strains were evaluated. Bacteriostatic values of piperacillin, ampicillin, and ceftriaxone for all groups were lower than were those of ticarcillin and ceftazidime. Bacteriostatic values of ciprofloxacin were unaffected by penicillin susceptibility. All beta-lactams were bactericidal at 1 dilution above the bacteriostatic value, except for piperacillin (bactericidal at 2 dilutions above the bacteriostatic value for one intermediately resistant strain), ticarcillin (bactericidal at 2 dilutions above the bacteriostatic value for one susceptible strain and one resistant strain), ampicillin (bactericidal at 2 dilutions above the bacteriostatic value for two resistant strains), ceftriaxone (bactericidal at 2 dilutions above the bacteriostatic value for one resistant strain), and ceftazidime (bactericidal at 2 dilutions above the bacteriostatic value for one susceptible strain).

摘要

本研究检测了口服和注射用抗生素对青霉素敏感、中度耐药和完全耐药肺炎链球菌的抑菌和杀菌活性。β-内酰胺酶抑制剂不影响β-内酰胺类药物的检测结果。测试了氨苄西林、阿莫西林±克拉维酸、WY-49605、头孢呋辛、头孢泊肟、头孢地尼、头孢克肟和头孢克洛对两株青霉素敏感、两株中度青霉素耐药和两株完全青霉素耐药肺炎链球菌菌株的活性。对于所有三组,阿莫西林和WY-49605的抑菌值低于所测试的其他β-内酰胺类药物。在头孢菌素类药物中,头孢地尼、头孢呋辛和头孢泊肟的抑菌值最低。除头孢泊肟(对一株敏感菌株和一株中度耐药菌株在高于抑菌值2倍稀释度时具有杀菌作用)、头孢呋辛(对一株中度耐药菌株在高于抑菌值2倍稀释度时具有杀菌作用)和氨苄西林(对一株中度耐药菌株在高于抑菌值2倍稀释度时具有杀菌作用)外,所有β-内酰胺类药物在高于抑菌值1倍稀释度时均具有杀菌作用(使原始菌数减少≥3 log10 CFU/ml)。评估了哌拉西林、哌拉西林-他唑巴坦、替卡西林、替卡西林-克拉维酸、氨苄西林、氨苄西林-舒巴坦、头孢曲松、头孢他啶和环丙沙星对四株青霉素敏感、两株中度青霉素耐药和四株完全青霉素耐药肺炎链球菌菌株的活性。所有组中哌拉西林、氨苄西林和头孢曲松的抑菌值低于替卡西林和头孢他啶。环丙沙星的抑菌值不受青霉素敏感性的影响。除哌拉西林(对一株中度耐药菌株在高于抑菌值2倍稀释度时具有杀菌作用)、替卡西林(对一株敏感菌株和一株耐药菌株在高于抑菌值2倍稀释度时具有杀菌作用)、氨苄西林(对两株耐药菌株在高于抑菌值2倍稀释度时具有杀菌作用)、头孢曲松(对一株耐药菌株在高于抑菌值2倍稀释度时具有杀菌作用)和头孢他啶(对一株敏感菌株在高于抑菌值2倍稀释度时具有杀菌作用)外,所有β-内酰胺类药物在高于抑菌值1倍稀释度时均具有杀菌作用。

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