Fosfomycin Susceptibility Among Multidrug-Resistant Extended-Spectrum β-Lactamase and Metallo-β-Lactamase–Producing Uropathogens in a Tertiary Care Hospital

Aditi Kothari, Parul Chaturvedi, Upasana Bhumbla
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Abstract

Urinary tract infections (UTIs) affect an estimated 150 million people each year worldwide involving women more than men. Because of unrestricted use of antimicrobials and accelerating antimicrobial resistance, therapeutic options for treatment of UTIs are becoming limited. Fosfomycin, a broad-spectrum, rapidly absorbable, antimicrobial agent with good bioavailability and substantial activity against multidrug-resistant (MDR) isolates has antimicrobial activity against a substantial percentage of these MDR isolates. A cross-sectional study over a period of 20 months on urine samples of all patients of all age groups clinically suspected of UTI was conducted in a tertiary care center of southern Rajasthan. Samples were processed immediately as per standard microbiological techniques, followed by culture by a semiquantitative method and antimicrobial susceptibility testing using the Kirby-Bauer disk diffusion method. All gram-negative pathogens were screened for extended-spectrum β-lactamase and further metallo-β-lactamase production using standard disk diffusion tests. Of the 1858 positive samples isolated, the most common uropathogen was Escherichia coli (59.96%), with 8.97% confirmed extended-spectrum β-lactamase–producing isolates. Fosfomycin had susceptibility of 96.69%, with its sensitivity and specificity being 98.15% and 6.98% more than nitrofurantoin, respectively. Among the metallo-β-lactamase producers, fosfomycin had susceptibility of 78.58%, with sensitivity and specificity being 91.67% and 25% more than nitrofurantoin, respectively. With an increasing threat due to MDR uropathogens in both hospitals and in the community, fosfomycin, with its unique mechanism of action, appears to be a better oral, effective, and safe therapeutic option and a viable potential alternative over other drugs for treatment of UTIs.
一家三级医院中产多药耐药性广谱β-内酰胺酶和金属β-内酰胺酶的泌尿道病原体对磷霉素的敏感性
据估计,全世界每年有 1.5 亿人受到尿路感染(UTI)的影响,其中女性患者多于男性患者。由于抗菌药的使用不受限制以及抗菌药耐药性的加速,治疗尿路感染的方法越来越有限。磷霉素是一种广谱、可快速吸收的抗菌药,具有良好的生物利用度,对耐多药(MDR)分离株有很强的抗菌活性。 拉贾斯坦邦南部的一家三级医疗中心对所有年龄组临床疑似尿毒症患者的尿样进行了为期 20 个月的横断面研究。样本按照标准微生物学技术立即进行处理,然后采用半定量法进行培养,并使用柯比-鲍尔盘扩散法进行抗菌药敏感性测试。所有革兰氏阴性病原体都经过了扩展谱β-内酰胺酶筛查,并使用标准盘扩散试验进一步检测了金属-β-内酰胺酶的产生。 在分离出的 1858 份阳性样本中,最常见的尿路病原体是大肠埃希菌(59.96%),其中 8.97% 证实分离出产扩展谱β-内酰胺酶的菌株。磷霉素的敏感性为 96.69%,其敏感性和特异性分别比硝基呋喃妥因高出 98.15%和 6.98%。在金属-β-内酰胺酶产生者中,磷霉素的敏感性为 78.58%,其敏感性和特异性分别比硝基呋喃妥因高出 91.67% 和 25%。 随着医院和社区中 MDR 尿路病原体的威胁日益增加,具有独特作用机制的磷霉素似乎是一种更好的口服、有效和安全的治疗选择,是治疗 UTIs 的其他药物的可行替代品。
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