Grassi C, Mangiarotti P
Institute of Respiratory Diseases, University of Pavia, Italy.
Chemioterapia. 1987 Oct;6(5):364-73.
The clinical efficacy and tolerability of ceftriaxone in the treatment of pneumonia and other lower respiratory tract infections were evaluated in 827 patients (515 pneumonia, 312 other lower respiratory tract infections) reported in the international literature (daily dose: 1 of 2 g.i.v. or i.m. in most patients). Therapeutic success was achieved in 738 patients (89.2%). Microbiological results were evaluated in 295 patients. Eradication of the most common respiratory pathogens was achieved in 100% of cases and of Enterobacteriaceae in 85.7%-100%. Adverse effects occurred in 4.9% of patients. A large multicenter trial was carried out in Italy using a single daily dose of 1-2 g by i.v. or i.m. Six hundred ninety-six patients were admitted to the study (370 pneumonia, and 326 other lower respiratory tract infections). Therapeutic success was achieved in 668 cases (96%). Pathogens were eradicated in 88% of cases (184 pts evaluated). Side effects were observed in 4.6% of cases.
国际文献报道了827例患者(515例肺炎,312例其他下呼吸道感染)使用头孢曲松治疗肺炎及其他下呼吸道感染的临床疗效和耐受性(大多数患者每日剂量:静脉注射或肌肉注射2g,分1次给药)。738例患者(89.2%)治疗成功。对295例患者的微生物学结果进行了评估。100%的病例中最常见呼吸道病原体被清除,85.7%-100%的肠杆菌科细菌被清除。4.9%的患者出现不良反应。在意大利进行了一项大型多中心试验,采用每日1-2g静脉注射或肌肉注射的单一剂量。696例患者纳入研究(370例肺炎,326例其他下呼吸道感染)。668例(96%)治疗成功。88%的病例(184例接受评估)病原体被清除。4.6%的病例观察到副作用。