Tedeschi Sara, Giannitsioti Efthymia, Mayer Christian
Department of Medical and Surgical Sciences, Alma Mater Studiorum, University of Bologna, 40138 Bologna, Italy.
Infectious Diseases Unit, Department of Integrated Infectious Risk Management, IRCCS, Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.
Microorganisms. 2025 Apr 23;13(5):963. doi: 10.3390/microorganisms13050963.
Due to the involvement of biofilms in the pathogenesis of bone and joint infections (BJI), the treatment of these infections is often challenging, especially when multidrug- or extensively drug-resistant (MDR/XDR) pathogens are involved. Intravenous fosfomycin (FOS) is a phosphoenolpyruvate analogue with a unique mode of action and broad-spectrum activity against both Gram-positive (GP) and Gram-negative (GN) pathogens. It is used in various severe and deep-seated infections, including BJIs. This review article focuses on preclinical and clinical data surrounding the use of FOS for biofilm-related BJIs. Data from several in vitro and animal models of infection demonstrated that FOS, especially in combination with other antibiotics, is effective against biofilms of (methicillin-resistant) spp., (vancomycin-resistant) spp., carbapenem-resistant and extended-spectrum beta-lactamase-producing Enterobacterales, and MDR . Data from clinical studies, mostly retrospective observational studies and case reports/case series, revealed that FOS was typically used in combination with other antibiotics for the treatment of various BJI, including acute and chronic osteomyelitis, prosthetic joint infections, and fracture-related infections, in adult and pediatric patients. Success rates often exceeded 80%. FOS exhibits good and fast penetration into bone tissue and is generally well tolerated, with only a few adverse drug reactions, such as gastrointestinal disorders and electrolyte imbalances. Collectively, the data indicate that FOS is a valuable option as part of combination regimens for the treatment of BJIs caused by both GP and GN bacteria.
由于生物膜参与骨与关节感染(BJI)的发病机制,这些感染的治疗往往具有挑战性,尤其是当涉及多重耐药或广泛耐药(MDR/XDR)病原体时。静脉注射磷霉素(FOS)是一种磷酸烯醇丙酮酸类似物,具有独特的作用方式,对革兰氏阳性(GP)和革兰氏阴性(GN)病原体均有广谱活性。它用于包括BJI在内的各种严重和深部感染。这篇综述文章重点关注围绕FOS用于生物膜相关BJI的临床前和临床数据。来自多个体外和动物感染模型的数据表明,FOS,尤其是与其他抗生素联合使用时,对(耐甲氧西林)葡萄球菌属、(耐万古霉素)肠球菌属、耐碳青霉烯类和产超广谱β-内酰胺酶的肠杆菌科细菌以及MDR的生物膜有效。临床研究数据,大多是回顾性观察研究和病例报告/病例系列,显示FOS通常与其他抗生素联合用于治疗成人和儿童患者的各种BJI,包括急性和慢性骨髓炎、人工关节感染以及骨折相关感染。成功率通常超过80%。FOS在骨组织中具有良好且快速的渗透性,一般耐受性良好,只有少数药物不良反应,如胃肠道紊乱和电解质失衡。总体而言,数据表明FOS作为联合治疗方案的一部分,是治疗由GP和GN细菌引起的BJI的一个有价值的选择。