Nicolle L E
Dept. of Medical Microbiology, University of Manitoba, Winnipeg, Canada.
Infection. 1992;20 Suppl 3:S203-5; discussion S206-10. doi: 10.1007/BF01704376.
Long-term, low-dose antimicrobial prophylaxis is effective for the prevention of acute uncomplicated urinary tract infection in women. Selected new antimicrobials should be assessed to determine their efficacy for this clinical use. Recommended guidelines for future studies of prophylactic therapy need to address several issues. The study population must be limited to women with recurrent symptomatic uncomplicated urinary tract infection. Antimicrobials studied should be excreted in the urine, with an in vitro spectrum that includes the common uropathogens. An extended half-life may be beneficial. Monitoring during the study should include monthly urine cultures and vaginal, periurethral and rectal colonization studies. The primary outcome measurement is symptomatic urinary tract infection. Secondary outcomes would include asymptomatic bacteriuria, adverse antimicrobial effects, colonization with potential uropathogens, and development of resistance. The comparative regimen should be one of the current standard regimens, trimethoprim/sulphamethoxazole, nitrofurantoin, or trimethoprim.
长期、低剂量抗菌药物预防对预防女性急性单纯性尿路感染有效。应评估选定的新型抗菌药物在该临床应用中的疗效。未来预防性治疗研究的推荐指南需要解决几个问题。研究人群必须限于有复发性症状性单纯性尿路感染的女性。所研究的抗菌药物应经尿液排泄,体外抗菌谱应包括常见的尿路病原体。延长的半衰期可能有益。研究期间的监测应包括每月进行尿液培养以及阴道、尿道周围和直肠定植研究。主要结局指标是有症状的尿路感染。次要结局包括无症状菌尿、抗菌药物不良反应、潜在尿路病原体定植以及耐药性的产生。对照方案应为当前标准方案之一,即甲氧苄啶/磺胺甲恶唑、呋喃妥因或甲氧苄啶。