TY - JOUR
T1 - Targeted antimicrobial regimens for Gram-negative prosthetic joint infections
T2 - a prospective multicenter study
AU - Hanssen, Jaap L.J.
AU - van der Wal, Robert J.P.
AU - Mahdad, Rachid
AU - Keizer, Stefan
AU - Delfos, Nathalie M.
AU - van der Lugt, Joris C.T.
AU - Veldkamp, Karin Ellen
AU - Nolte, Peter A.
AU - Leendertse, Masja
AU - Gelinck, Luc B.S.
AU - Mollema, Femke P.N.
AU - Schippers, Emile F.
AU - Wattel-Louis, Hanke G.
AU - Nelissen, Rob G.H.H.
AU - Scheper, Henk
AU - de Boer, Mark G.J.
N1 - Publisher Copyright:
Copyright © 2024 American Society for Microbiology. All Rights Reserved.
PY - 2024/12
Y1 - 2024/12
N2 - 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.
AB - 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.
KW - antimicrobial treatment
KW - Gram-negative PJI
KW - prosthetic joint infections
KW - total hip
KW - total knee
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UR - http://www.scopus.com/inward/citedby.url?scp=85211827690&partnerID=8YFLogxK
U2 - 10.1128/aac.01232-24
DO - 10.1128/aac.01232-24
M3 - Article
C2 - 39535202
AN - SCOPUS:85211827690
SN - 0066-4804
VL - 68
SP - 1
EP - 12
JO - Antimicrobial agents and chemotherapy
JF - Antimicrobial agents and chemotherapy
IS - 12
ER -