Targeted antimicrobial regimens for Gram-negative prosthetic joint infections: a prospective multicenter study

医学 四分位间距 抗菌剂 抗生素 内科学 前瞻性队列研究 外科 临床终点 随机对照试验 微生物学 生物 化学 有机化学
作者
Jaap L. J. Hanssen,Robert J. P. van der Wal,Rachid Mahdad,Stefan B. Keizer,Nathalie M. Delfos,J. C. T. van der Lugt,Karin Ellen Veldkamp,Peter A. Nolte,Masja Leendertse,L. B. S. Gelinck,Femke Mollema,Emile F. Schippers,Hanke G. Wattel-Louis,Rob G. H. H. Nelissen,Henk Scheper,Mark de Boer
出处
期刊:Antimicrobial Agents and Chemotherapy [American Society for Microbiology]
标识
DOI:10.1128/aac.01232-24
摘要

ABSTRACT Fluoroquinolones (FQs) are considered the most effective antimicrobial treatment for Gram-negative prosthetic joint infection (GN-PJI). Alternatives are needed due to increasing FQ resistance and side effects. We aimed to compare different targeted antimicrobial strategies for GN-PJI managed by debridement, antibiotics, and implant retention (DAIR) or one-stage revision surgery (1SR) and to review the literature of oral treatment options for GN-PJI. In this prospective, multicenter, registry-based study, all consecutive patients with a PJI caused by a Gram-negative microorganism (including mixed infections with Gram-positive microorganisms), managed with DAIR or 1SR from 2015 to 2020, were included. Minimum follow-up was 1 year. Patients underwent targeted therapy with oral FQ, oral cotrimoxazole, or intravenous or oral β-lactams. Survival analysis was performed with use of Kaplan-Meier and Cox proportional hazards models to identify factors potentially associated with treatment failure. Seventy-four patients who received either FQ ( n = 47, 64%), cotrimoxazole ( n = 13, 18%), or β-lactams ( n = 14, 18%) were included. Surgical strategy consisted of DAIR ( n = 72) or 1SR ( n = 2). Median follow-up was 449 days (interquartile range 89–738 days). Failure free survival did not differ between the FQ (72%) and cotrimoxazole (92%) groups (log rank, P = 0.13). This outcome did not change when excluding all pseudomonal PJI in the FQ group. Cotrimoxazole is a potential effective targeted antimicrobial therapy for patients with GN-PJI. A randomized controlled trial is needed to confirm the findings of this study.

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