Cox C E
Department of Urology, University of Tennessee Center, Memphis.
Am J Med. 1989 Nov 30;87(5A):252S-254S. doi: 10.1016/0002-9343(89)90073-9.
Intravenous ciprofloxacin has been investigated in the treatment of serious infections, including those of the urinary tract. In this double-blind, randomized study, its effectiveness as a prophylactic agent in men undergoing transurethral surgical procedures was compared with that of another intravenous agent, cefotaxime. One hundred six men with genitourinary tract obstruction were enrolled in the study. The 102 men evaluable for determination of efficacy (53 in the ciprofloxacin group and 49 in the cefotaxime group) received a single intravenous infusion of either 300 mg ciprofloxacin or 1,000 mg of cefotaxime prior to resection of the prostate for benign prostatic hypertrophy and prostatic carcinoma or internal urethrotomy for urethral stricture. A mean of 32.1 and 40.3 minutes for the ciprofloxacin and cefotaxime groups, respectively, elapsed between the end of the intravenous infusion and the onset of surgery; all but one patient in the ciprofloxacin group underwent catheterization after surgery, of which the mean duration was 3.7 days for both groups. At the time of hospital discharge, patients were evaluated clinically; 50 patients in the ciprofloxacin group (94 percent) and 45 in the cefotaxime group (92 percent) had no bacteriologic evidence of genitourinary tract infection. At follow-up two to six weeks after surgery for the patients with no bacteriologic evidence of genitourinary tract infection, fewer patients in the ciprofloxacin group (8 percent) than in the cefotaxime group (16 percent) remained without evidence of infection. Both drugs were well tolerated. This study demonstrated that a single intravenous dose of ciprofloxacin was as effective as a single dose of cefotaxime in reducing the incidence of infection following transurethral surgical procedures.
静脉注射环丙沙星已被用于治疗严重感染,包括尿路感染。在这项双盲随机研究中,将其作为预防性药物用于接受经尿道外科手术男性患者的有效性与另一种静脉注射药物头孢噻肟进行了比较。106例患有泌尿生殖道梗阻的男性患者参与了该研究。102例可评估疗效的男性患者(环丙沙星组53例,头孢噻肟组49例)在因良性前列腺增生、前列腺癌行前列腺切除术或因尿道狭窄行尿道内切开术前,分别接受了单次静脉输注300mg环丙沙星或1000mg头孢噻肟。环丙沙星组和头孢噻肟组静脉输注结束至手术开始的平均时间分别为32.1分钟和40.3分钟;环丙沙星组除1例患者外,所有患者术后均接受了导尿,两组的平均导尿持续时间均为3.7天。出院时,对患者进行临床评估;环丙沙星组50例患者(94%)和头孢噻肟组45例患者(92%)没有泌尿生殖道感染的细菌学证据。对没有泌尿生殖道感染细菌学证据的患者在术后2至6周进行随访时,环丙沙星组仍无感染证据的患者(8%)少于头孢噻肟组(16%)。两种药物耐受性均良好。这项研究表明,单次静脉注射环丙沙星在降低经尿道外科手术后感染发生率方面与单次注射头孢噻肟同样有效。