Suppr超能文献

磷霉素氨丁三醇与氧氟沙星/复方新诺明作为女性急性单纯性尿路感染单剂量疗法的多中心研究。

Fosfomycin trometamol versus ofloxacin/co-trimoxazole as single dose therapy of acute uncomplicated urinary tract infection in females: a multicentre study.

作者信息

Naber K G, Thyroff-Friesinger U

机构信息

Urologische Klinik, Elisabeth Krankenhaus, Straubing, Germany.

出版信息

Infection. 1990;18 Suppl 2:S70-6. doi: 10.1007/BF01643431.

Abstract

20 urologists took part in a single blind, randomized study. Female patients with acute uncomplicated UTI were recruited. The patients received either a single dose of 3 g fosfomycin trometamol versus 200 mg ofloxacin or 1.92 g co-trimoxazole. Follow-up examinations were carried out after one and four weeks. Of 562 patients 446 could be evaluated for efficacy and 496 for tolerance. Patients were analysed according to the amount of bacteriuria: "significant" (greater than or equal to 10(5)/ml), "low count" (10(2) - 10(4) ml) and "no bacteriuria" (less than or equal to 10(1)/ml), as well as according to the sensitivity of the infecting organisms: sensitive (resistant): fosfomycin trometamol less than or equal to 16 mg/l (greater than or equal to 128 mg/l), ofloxacin less than or equal to 1 mg/l (greater than or equal to 8 mg/l), co-trimoxazole less than or equal to 2/38 mg/l (greater than or equal to 16/304 mg/l). Up to one week the following results could be achieved: clinical improvement was attained in patients with "significant" bacteriuria (fosfomycin trometamol-150, ofloxacin-89, co-trimoxazole-69) in 94.7% for fosfomycin trometamol, in 95.4% for ofloxacin, and in 94% for co-trimoxazole; in patients with "low count" bacteriuria (fosfomycin trometamol-44, ofloxacin-18, co-trimoxazole-30) in 95.2% for fosfomycin trometamol, in 93.7% for ofloxacin, and in 96.4% for co-trimoxazole; and in patients with no bacteriuria (fosfomycin trometamol-11, ofloxacin-6, co-trimoxazole-4) in 81.8% for fosfomycin trometamol, in 100% for ofloxacin and in 100% for co-trimoxazole.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

20名泌尿科医生参与了一项单盲随机研究。招募患有急性非复杂性尿路感染的女性患者。患者分别接受单剂量3克磷霉素氨丁三醇、200毫克氧氟沙星或1.92克复方新诺明治疗。在1周和4周后进行随访检查。562名患者中,446名可评估疗效,496名可评估耐受性。根据菌尿数量(“大量”[大于或等于10⁵/ml]、“少量”[10² - 10⁴/ml]和“无菌尿”[小于或等于10¹/ml])以及感染菌的敏感性(敏感[耐药])对患者进行分析:磷霉素氨丁三醇小于或等于16毫克/升(大于或等于128毫克/升)、氧氟沙星小于或等于1毫克/升(大于或等于8毫克/升)、复方新诺明小于或等于2/38毫克/升(大于或等于16/304毫克/升)。截至1周可取得以下结果:“大量”菌尿患者(磷霉素氨丁三醇组150例、氧氟沙星组89例、复方新诺明组69例)中,磷霉素氨丁三醇的临床改善率为94.7%,氧氟沙星为95.4%,复方新诺明为94%;“少量”菌尿患者(磷霉素氨丁三醇组44例、氧氟沙星组18例、复方新诺明组30例)中,磷霉素氨丁三醇为95.2%,氧氟沙星为93.7%,复方新诺明为96.4%;无菌尿患者(磷霉素氨丁三醇组11例、氧氟沙星组6例、复方新诺明组4例)中,磷霉素氨丁三醇为81.8%,氧氟沙星为100%,复方新诺明为100%。(摘要截选至250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验