Demin A A, Drobysheva V P
Therapeutic Department, Novosibirsk Medical Institute.
Antibiot Khimioter. 1998;43(6):12-5.
Efficacy and safety of ceftriaxone (Oframax, Ranbaxy, India) in the treatment of 25 patients with Staphylococcus endocarditis (SE) were studied. The drug was administered intravenously in a dose of 2-4 g a day for 4 weeks and simultaneously gentamicin was used intramuscularly in a dose of 2-3 mg/kg body weight a day every 8 hours for 2 weeks. The treatment was followed by observation of the patients for up to 2 years under the hospital or dyspensary conditions. The disease was due to S. epidermidis (17 patients) or S.aureus (8 patients). The efficacy was controlled in the dynamics. The criteria of the therapy efficacy were disappearance of the disease clinical signs, normalization of the blood count and urinalysis and the pathogen eradication by the results of the control bacteriological blood analysis. The cure without any surgical correction was observed in 68 per cent of the patients and that with the valve replacement was stated in 24 per cent of the patients. The lethal outcome due to bacteriotoxic shock was recorded in 8 per cent of the patients. The SE relapsing was stated in 28 per cent of the patients 3 or more months after the ceftriaxone therapy completion. 10 patients (40 per cent) with evident clinicolaboratory improvement were discharged from the hospital 2 (4 patients) and 3 (6 patients) weeks after the therapy start for the treatment with ceftriaxone as outpatients. In 2 patients nausea as the adverse reaction was observed. Therefore, the complex clinicolaboratory investigation showed that the combined use of ceftriaxone and gentamicin was efficient and safe in the treatment of SE. Ceftriaxone may be considered as a basic drug for the therapy of SE. In some patients with SE the treatment with ceftriaxone may be completed under outpatient conditions.
研究了头孢曲松(印度兰伯西公司的奥复星)治疗25例葡萄球菌性心内膜炎(SE)患者的疗效和安全性。药物静脉给药,剂量为每日2 - 4克,持续4周,同时庆大霉素每8小时肌肉注射一次,剂量为每日2 - 3毫克/千克体重,持续2周。治疗后在医院或门诊条件下对患者进行长达2年的观察。该疾病由表皮葡萄球菌(17例患者)或金黄色葡萄球菌(8例患者)引起。疗效通过动态监测。治疗效果的标准为疾病临床症状消失、血常规和尿液分析正常化以及对照细菌学血液分析结果显示病原体根除。68%的患者未经任何手术矫正治愈,24%的患者进行了瓣膜置换。8%的患者因细菌毒性休克导致死亡。28%的患者在头孢曲松治疗结束后3个月或更长时间出现SE复发。10例(40%)临床实验室指标明显改善的患者在治疗开始后2周(4例患者)和3周(6例患者)出院,以门诊患者身份接受头孢曲松治疗。2例患者出现恶心不良反应。因此,综合临床实验室研究表明,联合使用头孢曲松和庆大霉素治疗SE有效且安全。头孢曲松可被视为治疗SE的基本药物。在一些SE患者中,头孢曲松治疗可在门诊条件下完成。