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在甲氧苄啶-磺胺甲恶唑(TMP-SMX)耐药尿路病原体高发的地理区域,经验性使用TMP-SMX治疗无并发症的尿路感染女性。

Empiric use of trimethoprim-sulfamethoxazole (TMP-SMX) in the treatment of women with uncomplicated urinary tract infections, in a geographical area with a high prevalence of TMP-SMX-resistant uropathogens.

作者信息

Raz R, Chazan B, Kennes Y, Colodner R, Rottensterich E, Dan M, Lavi I, Stamm W

机构信息

Infectious Diseases Unit, Haemek Medical Center, Afula; and Technion, Institute of Technology, Haifa, Israel.

出版信息

Clin Infect Dis. 2002 May 1;34(9):1165-9. doi: 10.1086/339812. Epub 2002 Apr 4.

Abstract

This study evaluated whether trimethoprim-sulfamethoxazole (TMP-SMX) is effective for treatment of uncomplicated urinary tract infections (UTIs) due to TMP-SMX-resistant (TMP-SMX-R) pathogens. Healthy nonpregnant premenopausal women with symptomatic lower UTI were assessed for the presence of pyuria and bacteriuria; if either was present, a urine sample was cultured and TMP-SMX was prescribed. Clinical and microbiologic cure was assessed at days 5-9 and 28-42 after cessation of therapy. For 71%, of patients, cultures grew TMP-SMX-susceptible (TMP-SMX-S) microorganisms, and for 29%, cultures grew TMP-SMX-R organisms. Escherichia coli remained the predominant bacteria in both groups of cultures. At visit 2, microbiological cure had been achieved in 86% of the patients in the TMP-SMX-S group and 42% of those in the TMP-SMX-R group. Similar differences were found at visit 3 by clinical evaluation. Treatment with TMP-SMX of uncomplicated UTI caused by TMP-SMX-R microorganisms results in microbiologic and clinical failure. In high-resistance areas, TMP-SMX should not be the empiric drug of choice for uncomplicated UTI.

摘要

本研究评估了甲氧苄啶-磺胺甲恶唑(TMP-SMX)对治疗由耐TMP-SMX病原体引起的非复杂性尿路感染(UTI)是否有效。对有症状的下尿路感染的健康非孕绝经前女性评估是否存在脓尿和菌尿;如果存在其中任何一项,则对尿样进行培养并开具TMP-SMX处方。在治疗停止后的第5 - 9天和第28 - 42天评估临床和微生物学治愈情况。71%的患者培养出对TMP-SMX敏感(TMP-SMX-S)的微生物,29%的患者培养出耐TMP-SMX(TMP-SMX-R)的微生物。大肠杆菌在两组培养物中均为主要细菌。在第2次随访时,TMP-SMX-S组86%的患者和TMP-SMX-R组42%的患者实现了微生物学治愈。通过临床评估在第3次随访时发现了类似差异。用TMP-SMX治疗由耐TMP-SMX微生物引起的非复杂性UTI会导致微生物学和临床治疗失败。在高耐药地区,TMP-SMX不应作为非复杂性UTI的经验性首选药物。

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