首页> 外文期刊>Annals of Clinical Microbiology and Antimicrobials >A multicentre clinical study on the injection of ceftriaxone/sulbactam compared with cefoperazone/sulbactam in the treatment of respiratory and urinary tract infections
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A multicentre clinical study on the injection of ceftriaxone/sulbactam compared with cefoperazone/sulbactam in the treatment of respiratory and urinary tract infections

机译:与头孢哌酮/舒巴坦相比,头孢曲松/舒巴坦注射液治疗呼吸道和泌尿道感染的多中心临床研究

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Objective This clinical study was designed to evaluate the efficacy and safety of this therapy in the treatment of respiratory and urinary infections caused by ceftriaxone-resistant bacteria in comparison with the effect of cefoperazone/sulbactam on cefoperazone-resistant bacteria. Methods A total of 285 patients aged from 18 to 65?years old, with a respiratory or urinary tract bacterial infection, were enrolled into this multicentre, open-label, controlled clinical study, and bacteria that were either ceftriaxone-resistant or cefoperazone-resistant were isolated from the patients, whose condition had not improved after three days of treatment with ceftriaxone or cefoperazone. To be selected for the study, bacterial cultures obtained from the patients had to be positive before enrolment, and all of the isolates were required to be β-lactamase-positive. Of these patients, 253 completed the trial, and 263 were enrolled into the intention-to-treat (ITT) analysis. All of the 285 patients were included in the safety analysis. Results The cure and effective rates were 39.55% and 85.07% in the ceftriaxone/sulbactam group and 36.43% and 79.84% in the cefoperazone/sulbactam group; the bacterial eradication rates were 83.58% and 83.72%; and the adverse-event rates were 7.48% and 7.80%, respectively. There were no significant differences between the two groups (p?>?0.05). Conclusion Ceftriaxone/sulbactam is as effective and well-tolerated as cefoperazone/sulbactam for the treatment of intermediate and severe bacterial infections caused by resistant strains.
机译:目的本临床研究旨在评估该疗法在治疗由头孢曲松耐药菌引起的呼吸道和泌尿道感染中的有效性和安全性,并与头孢哌酮/舒巴坦对头孢哌酮耐药菌的作用进行比较。方法总共285例年龄在18至65岁之间,患有呼吸道或泌尿道细菌感染的患者参加了这项多中心,开放标签,对照临床研究,且这些细菌对头孢曲松耐药或对头孢哌酮耐药从头孢曲松或头孢哌酮治疗三​​天后病情并未改善的患者中分离出。为了进行研究选择,从患者那里获得的细菌培养物在入组前必须是阳性的,并且所有分离株都必须是β-内酰胺酶阳性的。在这些患者中,有253位完成了试验,有263位参加了意向性治疗(ITT)分析。 285名患者全部纳入安全性分析。结果头孢曲松/舒巴坦组治愈率和有效率分别为39.55%和85.07%;头孢哌酮/舒巴坦组治愈率和有效率为36.43%和79.84%。细菌根除率为83.58%和83.72%;不良事件发生率分别为7.48%和7.80%。两组之间无显着差异(p≥0.05)。结论头孢曲松/舒巴坦与头孢哌酮/舒巴坦治疗中,重度由耐药菌株引起的细菌感染一样有效且耐受性良好。

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