Rifampicin reduces plasma concentration of linezolid in patients with infective endocarditis

Bock, M.; Hasselt J.G.C. van; Schwartz, F.; Wang, H.; Høiby, N.; Fuursted, K.; ... ; Moser, C. (2023)

Article / Letter to editor

BACKGROUND\nOBJECTIVES\nPATIENTS AND METHODS\nRESULTS\nCONCLUSIONS\nLinezolid in combination with rifampicin has been used in treatment of infective endocarditis especially for patients infected with staphylococci.\nBecause rifampicin has been reported to reduce the plasma concentration of linezolid, the present study aimed to characterize the population pharmacokinetics of linezolid for the purpose of quantifying an effect of rifampicin cotreatment. In addition, the possibility of compensation by dosage adjustments was evaluated.\nPharmacokinetic measurements were performed in 62 patients treated with linezolid for left-sided infective endocarditis in the Partial Oral Endocarditis Treatment (POET) trial. Fifteen patients were cotreated with rifampicin. A total of 437 linezolid plasma concentrations were obtained. The pharmacokinetic data were adequately described by a one-compartment model with first-order absorption and first-order elimination.\nWe demonstrated a substantial increase of linezolid clearance by 150% (95% CI: 78%-251%), when combined with rifampicin. The final model was evaluated by goodness-of-fit plots showing an acceptable fit, and a visual predictive check validated the model. Model-based dosing simulations showed that rifampicin cotreatment decreased the PTA of linezolid from 94.3% to 34.9% and from 52.7% to 3.5% for MICs of 2 mg/L and 4 mg/L, respectively.\nA substantial interaction between linezolid and rifampicin was detected in patients with infective endocarditis, and the interaction was stronger than previously reported. Model-based simulations showed that increasing the linezolid dose might compensate without increasing the risk of adverse effects to the same degree.

• All authors: Bock, M.; Hasselt J.G.C. van; Schwartz, F.; Wang, H.; Høiby, N.; Fuursted, K.; Ihlemann, N.; Gill, S.; Christiansen, U.; Bruun, N.E.; Elming, H.; Povlsen, J.A.; Køber, L.; Høfsten, D.E.; Fosbøl, E.L.; Pries-Heje, M.M.; Christensen, J.J.; Rosenvinge, F.S.; Torp-Pedersen, C.; Helweg-Larsen, J.; Tønder, N.; Iversen, K.; Bundgaard, H.; Moser, C.
• Date: 2023-10-12
• Journal: Journal of Antimicrobial Chemotherapy
• Volume: 78
• Issue: 12
• Pages: 2840–2848
• DOI: doi:10.1093/jac/dkad316