Departamentos de Medicina y Microbiología, Unidad Clínica de Enfermedades Infecciosas y Microbiología, Hospital Universitario Virgen Macarena; Instituto de Biomedicina de Sevilla (IBiS)/CSIC; Universidad de Sevilla, Seville, Spain.
CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III, Madrid, Spain.
J Antimicrob Chemother. 2023 Jul 5;78(7):1658-1666. doi: 10.1093/jac/dkad147.
Fosfomycin is a potentially attractive option as step-down therapy for bacteraemic urinary tract infections (BUTI), but available data are scarce. Our objective was to compare the effectiveness and safety of fosfomycin trometamol and other oral drugs as step-down therapy in patients with BUTI due to MDR Escherichia coli (MDR-Ec).
Participants in the FOREST trial (comparing IV fosfomycin with ceftriaxone or meropenem for BUTI caused by MDR-Ec in 22 Spanish hospitals from June 2014 to December 2018) who were stepped-down to oral fosfomycin (3 g q48h) or other drugs were included. The primary endpoint was clinical and microbiological cure (CMC) 5-7 days after finalization of treatment. A multivariate analysis was performed using logistic regression to estimate the association of oral step-down with fosfomycin with CMC adjusted for confounders.
Overall, 61 patients switched to oral fosfomycin trometamol and 47 to other drugs (cefuroxime axetil, 28; amoxicillin/clavulanic acid and trimethoprim/sulfamethoxazole, 7 each; ciprofloxacin, 5) were included. CMC was reached by 48/61 patients (78.7%) treated with fosfomycin trometamol and 38/47 (80.9%) with other drugs (difference, -2.2; 95% CI: -17.5 to 13.1; P = 0.38). Subgroup analyses provided similar results. Relapses occurred in 9/61 (15.0%) and 2/47 (4.3%) of patients, respectively (P = 0.03). The adjusted OR for CMC was 1.11 (95% CI: 0.42-3.29, P = 0.75). No relevant differences in adverse events were seen.
Fosfomycin trometamol might be a reasonable option as step-down therapy in patients with BUTI due to MDR-Ec but the higher rate of relapses would need further assessment.
磷霉素作为治疗菌血症性尿路感染(BUTI)的降阶梯治疗的潜在选择,但是可用数据很少。我们的目的是比较磷霉素氨丁三醇和其他口服药物作为 MDR 大肠杆菌(MDR-Ec)引起的 BUTI 降阶梯治疗的有效性和安全性。
参与 FOREST 试验(2014 年 6 月至 2018 年 12 月期间,在 22 家西班牙医院比较 IV 磷霉素与头孢曲松或美罗培南治疗 MDR-Ec 引起的 BUTI)的患者被降级为口服磷霉素(3g q48h)或其他药物。主要终点是治疗结束后 5-7 天的临床和微生物学治愈率(CMC)。采用多变量逻辑回归分析估计口服降阶梯与磷霉素与 CMC 的关联,调整混杂因素。
共有 61 名患者转为口服磷霉素氨丁三醇,47 名患者转为其他药物(头孢呋辛酯,28 名;阿莫西林/克拉维酸和复方磺胺甲噁唑,各 7 名;环丙沙星,5 名)。48/61 名(78.7%)接受磷霉素氨丁三醇治疗的患者和 38/47 名(80.9%)接受其他药物治疗的患者达到 CMC(差异,-2.2;95%CI:-17.5 至 13.1;P=0.38)。亚组分析提供了类似的结果。分别有 9/61(15.0%)和 2/47(4.3%)的患者出现复发(P=0.03)。CMC 的调整 OR 为 1.11(95%CI:0.42-3.29,P=0.75)。未观察到不良反应的相关差异。
磷霉素氨丁三醇可能是 MDR-Ec 引起的 BUTI 降阶梯治疗的合理选择,但复发率较高需要进一步评估。