Anguita-Alonso Paloma, Rouse Mark S, Piper Kerryl E, Steckelberg James M, Patel Robin
Division of Infectious Diseases, Department of Medicine, Mayo Clinic College of Medicine, 200 First St. SW, Rochester, MN 55905, USA.
Antimicrob Agents Chemother. 2006 Apr;50(4):1263-7. doi: 10.1128/AAC.50.4.1263-1267.2006.
The activity of garenoxacin was compared to that of levofloxacin or penicillin in a rabbit model of Streptococcus mitis group (penicillin MIC, 0.125 microg/ml) and Streptococcus sanguinis group (penicillin MIC, 0.25 microg/ml) endocarditis. Garenoxacin and levofloxacin had MICs of 0.125 and 0.5 microg/ml, respectively, for both study isolates. Rabbits with catheter-induced aortic valve endocarditis were given no treatment, penicillin at 1.2x10(6) IU/8 h intramuscularly, garenoxacin at 20 mg/kg of body weight/12 h intravenously, or levofloxacin at 40 mg/kg/12 h intravenously. For both isolates tested, garenoxacin area under the curve (AUC)/MIC and maximum concentration of drug in serum (Cmax)/MIC ratios were 368 and 91, respectively. Rabbits were sacrificed after 3 days of treatment; cardiac valve vegetations were aseptically removed and quantitatively cultured. For S. mitis group experimental endocarditis, all studied antimicrobial agents were more active than no treatment (P<0.001), whereas for S. sanguinis group endocarditis, no studied antimicrobial agents were more active than no treatment. We conclude that AUC/MIC and Cmax/MIC ratios may not predict activity of some quinolones in experimental viridans group endocarditis and that garenoxacin and levofloxacin may not be ideal choices for serious infections caused by some quinolone-susceptible viridans group streptococci.
在兔模型中,比较了加替沙星与左氧氟沙星或青霉素对缓症链球菌组(青霉素MIC为0.125μg/ml)和血链球菌组(青霉素MIC为0.25μg/ml)心内膜炎的活性。对于两种研究分离株,加替沙星和左氧氟沙星的MIC分别为0.125和0.5μg/ml。对导管诱导的主动脉瓣心内膜炎兔不进行治疗,或肌肉注射青霉素1.2×10⁶IU/8小时,或静脉注射加替沙星20mg/kg体重/12小时,或静脉注射左氧氟沙星40mg/kg/12小时。对于两种测试的分离株,加替沙星的曲线下面积(AUC)/MIC和血清中药物最大浓度(Cmax)/MIC比值分别为368和91。治疗3天后处死兔子;无菌取出心脏瓣膜赘生物并进行定量培养。对于缓症链球菌组实验性心内膜炎,所有研究的抗菌药物均比不治疗更具活性(P< 0.001),而对于血链球菌组心内膜炎,没有研究的抗菌药物比不治疗更具活性。我们得出结论,AUC/MIC和Cmax/MIC比值可能无法预测某些喹诺酮类药物在实验性草绿色链球菌组心内膜炎中的活性,并且加替沙星和左氧氟沙星可能不是某些喹诺酮敏感的草绿色链球菌组链球菌引起的严重感染的理想选择。