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首页> 外文期刊>Canadian Journal of Infectious Diseases and Medical Microbiology: Journal Canadien des Maladies Infectieuses >Oral Fosfomycin for the Treatment of Acute and Chronic Bacterial Prostatitis Caused by Multidrug-Resistant Escherichia coli
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Oral Fosfomycin for the Treatment of Acute and Chronic Bacterial Prostatitis Caused by Multidrug-Resistant Escherichia coli

机译:口服磷霉素治疗多药耐药性大肠杆菌引起的急性和慢性细菌性前列腺炎

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Acute and chronic bacterial prostatitis in outpatients is commonly treated with oral fluoroquinolones; however, the worldwide dissemination of multidrug-resistant (MDR) Escherichia coli has resulted in therapeutic failures with fluoroquinolones. We reviewed the literature regarding the use of oral fosfomycin in the treatment of acute and chronic prostatitis caused by MDR E. coli. All English-language references on PubMed from 1986 to June 2017, inclusive, were reviewed from the search “fosfomycin prostatitis.” Fosfomycin demonstrates potent in vitro activity against a variety of antimicrobial-resistant E. coli genotypes/phenotypes including ciprofloxacin-resistant, trimethoprim-sulfamethoxazole-resistant, extended-spectrum β-lactamase- (ESBL-) producing, and MDR isolates. Fosfomycin attains therapeutic concentrations (≥4?μg/g) in uninflamed prostatic tissue and maintains a high prostate/plasma ratio up to 17 hours after oral administration. Oral fosfomycin’s clinical cure rates in the treatment of bacterial prostatitis caused by antimicrobial-resistant E. coli ranged from 50 to 77% with microbiological eradication rates of >50%. An oral regimen of fosfomycin tromethamine of 3?g·q 24?h for one week followed by 3?g·q 48?h for a total treatment duration of 6–12 weeks appeared to be effective. Oral fosfomycin may represent an efficacious and safe treatment for acute and chronic prostatitis caused by MDR E. coli.
机译:门诊患者的急性和慢性细菌性前列腺炎通常使用口服氟喹诺酮类药物治疗;然而,耐多药性大肠埃希菌在世界范围内的传播已导致氟喹诺酮类药物治疗失败。我们回顾了有关使用口服磷霉素治疗由MDR E. coli引起的急性和慢性前列腺炎的文献。 1986年至2017年6月期间(包括首尾两天)在PubMed上使用的所有英语参考文献均通过搜索“磷霉素前列腺炎”进行了审查。磷霉素显示出对多种抗菌抗性大肠杆菌基因型/表型的有效体外活性,包括环丙沙星抗性,甲氧苄啶-磺胺甲恶唑抗性,广谱β-内酰胺酶-(ESBL-)产生和MDR分离物。磷霉素在未发炎的前列腺组织中达到治疗浓度(≥4?μg/ g),并在口服后长达17小时内保持较高的前列腺/血浆比率。口服磷霉素的临床治愈率在50%至77%之间,在微生物根除率大于50%的情况下,可治愈细菌性前列腺炎。口服磷磷霉素三甲胺3?g·q 24?h一周,然后3?g·q 48?h口服,总疗程6-12周似乎是有效的。口服磷霉素可能代表由MDR大肠杆菌引起的急性和慢性前列腺炎的有效且安全的治疗方法。

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