Phillips H L, Nolen T M, Hutchison J
Ala Med. 1989 Apr;58(10):28-32.
The efficacy and safety of ciprofloxacin (500 mg administered every 12 hours) were evaluated in 62 patients enrolled in a prospective, open study. Fifty-three courses in the treatment of 56 infection sites suitable for evaluation were assessed. The infection sites involved were skin and skin structure (28), respiratory tract (21), urinary tract (5), and gastrointestinal tract (2). Bacterial isolates included 16 Pseudomonas aeruginosa, 13 Staphylococcus aureus, and 8 Escherichia coli. Signs and symptoms of infection completely resolved in 46 (82%) of the infection sites. Nine (16%) improved, and one (2%) failed to respond. Ciprofloxacin was well tolerated.
在一项前瞻性开放性研究中,对62例患者使用环丙沙星(每12小时给药500毫克)的疗效和安全性进行了评估。对适合评估的56个感染部位的53个疗程进行了评估。涉及的感染部位包括皮肤及皮肤结构(28个)、呼吸道(21个)、泌尿道(5个)和胃肠道(2个)。分离出的细菌包括16株铜绿假单胞菌、13株金黄色葡萄球菌和8株大肠杆菌。46个(82%)感染部位的感染体征和症状完全消失。9个(16%)有所改善,1个(2%)无反应。环丙沙星耐受性良好。