Aldridge K E, Henderberg A, Sanders C V
Department of Medicine, Louisiana State University Medical Center, New Orleans 70112.
J Antimicrob Chemother. 1990 Sep;26(3):353-9. doi: 10.1093/jac/26.3.353.
The in-vitro activity of various beta-lactam antibiotics, beta-lactam/beta-lactamase inhibitor combinations, clindamycin, and metronidazole was determined against Bacteroides fragilis group isolates that were resistant to both cefoxitin and cefotetan. Among the cephalosporins tested ceftizoxime was the most active with 80% of the strains susceptible, followed by cefotaxime (65% susceptible), and cefoperazone (47% susceptible). Piperacillin and clindamycin showed comparable activity to ceftizoxime with 80% and 81% susceptible, respectively. The addition of a beta-lactamase inhibitor (sulbactam, clavulanate, or tazobactam) enhanced the activity of the various beta-lactam agents from 4-fold to 16-fold overall. One strain of B. fragilis was found that was resistant to all beta-lactam agents either alone or in combination. All strains in this study were susceptible to less than or equal to 4 mg/l of metronidazole.
测定了多种β-内酰胺类抗生素、β-内酰胺/β-内酰胺酶抑制剂组合、克林霉素和甲硝唑对脆弱拟杆菌群分离株的体外活性,这些分离株对头孢西丁和头孢替坦均耐药。在所测试的头孢菌素中,头孢唑肟活性最强,80%的菌株敏感,其次是头孢噻肟(65%敏感)和头孢哌酮(47%敏感)。哌拉西林和克林霉素的活性与头孢唑肟相当,分别有80%和81%的菌株敏感。添加β-内酰胺酶抑制剂(舒巴坦、克拉维酸或他唑巴坦)总体上使各种β-内酰胺类药物的活性增强了4至16倍。发现有1株脆弱拟杆菌对所有单独或联合使用的β-内酰胺类药物均耐药。本研究中的所有菌株对甲硝唑浓度小于或等于4mg/l均敏感。