Grassi C, Albera C, Pozzi E
Institute of Respiratory Diseases, University of Pavia, Italy.
Am J Med. 1992 Apr 6;92(4A):103S-107S. doi: 10.1016/0002-9343(92)90319-7.
Nine centers in Italy participated in a worldwide, multicenter study comparing the effectiveness and safety of lomefloxacin and amoxicillin in patients with acute exacerbations of chronic bronchitis caused mainly by gram-negative pathogens. The 157 enrolled patients received either 400 mg lomefloxacin once daily (n = 78) or 500 mg amoxicillin every 8 hours (n = 79) for 7-10 days. A total of 131 patients were evaluable for bacteriologic efficacy and 154 for clinical efficacy. At 2-4 days after the conclusion of treatment, the bacterial eradication rate was 84.8% for lomefloxacin-treated patients and 64.6% for amoxicillin-treated patients (p = 0.0065); the clinical success rate (cure plus improvement) for lomefloxacin was 94.7% and for amoxicillin was 83.3% (p = 0.0212). The reinfection rate was lower in the lomefloxacin group than in the amoxicillin group (3.0% vs 13.8%, p = 0.0382). Both drug regimens were well tolerated. Once-a-day treatment with 400 mg lomefloxacin was more effective than 500 mg amoxicillin three times daily for the treatment of acute exacerbations of chronic bronchitis caused by gram-negative pathogens.
意大利的九个中心参与了一项全球多中心研究,比较洛美沙星和阿莫西林在主要由革兰氏阴性病原体引起的慢性支气管炎急性加重患者中的有效性和安全性。157名入组患者接受了为期7 - 10天的治疗,其中78名患者每日一次服用400mg洛美沙星,79名患者每8小时服用500mg阿莫西林。共有131名患者可评估细菌学疗效,154名患者可评估临床疗效。治疗结束后2 - 4天,洛美沙星治疗组的细菌根除率为84.8%,阿莫西林治疗组为64.6%(p = 0.0065);洛美沙星的临床成功率(治愈加改善)为94.7%,阿莫西林为83.3%(p = 0.0212)。洛美沙星组的再感染率低于阿莫西林组(3.0%对13.8%,p = 0.0382)。两种药物治疗方案耐受性均良好。对于由革兰氏阴性病原体引起的慢性支气管炎急性加重,每日一次服用400mg洛美沙星比每日三次服用500mg阿莫西林更有效。