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Therapeutic drug monitoring of polymyxin B cerebrospinal fluid concentrations in patients with carbapenem-resistant Gram-negative bacteria-induced central nervous system infection.
- Source :
-
The Journal of antimicrobial chemotherapy [J Antimicrob Chemother] 2024 Aug 01; Vol. 79 (8), pp. 1969-1973. - Publication Year :
- 2024
-
Abstract
- Objectives: Central nervous system (CNS) infections caused by carbapenem-resistant Gram-negative bacteria (CR-GNB) present a major health and economic burden worldwide. This multicentre prospective study aimed to assess the feasibility and usefulness of CSF therapeutic drug monitoring (TDM) after intrathecal/intraventricular administration of polymyxin B in patients with CNS infections.<br />Methods: Forty-two patients treated with intrathecal/intraventricular administration of polymyxin B against CR-GNB-induced CNS infections were enrolled. CSF trough level (Cmin) was collected beginning on Day 2 post-polymyxin B initiation and thereafter. The primary outcomes were clinical cure and 28-day all-cause mortality.<br />Results: All patients started with intrathecal/intraventricular administration of polymyxin B at a dose of 5 g/day, corresponding to a median CSF Cmin of 2.93 mg/L (range, 0.21-25.74 mg/L). Clinical cure was 71.4%, and the median CSF Cmin of this group was higher than that of clinical failure group [3.31 (IQR, 1.73-5.62) mg/L versus 2.25 (IQR, 1.09-4.12) mg/L; P = 0.011]. In addition, with MICs ≤ 0.5 mg/L, maintaining polymyxin B CSF Cmin above 2.0 mg/L showed a higher clinical cure rate (P = 0.041). The 28-day all-cause mortality rate was 31.0% and had no association with CSF Cmin.<br />Conclusions: After intrathecal/intraventricular administration of polymyxin B, CSF concentrations fluctuated considerably inter- and intra-individual. Polymyxin B CSF Cmin above 2.0 mg/L was associated with clinical cure when MICs were ≤ 0.5 mg/L, and the feasibility of TDM warrants additional clinical studies.<br /> (© The Author(s) 2024. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)
- Subjects :
- Humans
Male
Female
Middle Aged
Prospective Studies
Aged
Adult
Central Nervous System Infections drug therapy
Central Nervous System Infections cerebrospinal fluid
Central Nervous System Infections microbiology
Central Nervous System Infections mortality
Injections, Spinal
Treatment Outcome
Microbial Sensitivity Tests
Cerebrospinal Fluid microbiology
Drug Monitoring
Polymyxin B therapeutic use
Polymyxin B administration & dosage
Polymyxin B pharmacokinetics
Anti-Bacterial Agents cerebrospinal fluid
Anti-Bacterial Agents therapeutic use
Anti-Bacterial Agents pharmacokinetics
Anti-Bacterial Agents administration & dosage
Gram-Negative Bacterial Infections drug therapy
Gram-Negative Bacterial Infections cerebrospinal fluid
Gram-Negative Bacterial Infections mortality
Gram-Negative Bacterial Infections microbiology
Carbapenems therapeutic use
Carbapenems pharmacokinetics
Carbapenems pharmacology
Gram-Negative Bacteria drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1460-2091
- Volume :
- 79
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- The Journal of antimicrobial chemotherapy
- Publication Type :
- Academic Journal
- Accession number :
- 38870067
- Full Text :
- https://doi.org/10.1093/jac/dkae193