4.7 Article

Therapeutic drug monitoring and clinical outcomes in severely ill patients receiving amoxicillin: a single-centre prospective cohort study

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ELSEVIER
DOI: 10.1016/j.ijantimicag.2022.106601

Keywords

Therapeutic drug monitoring; Amoxicillin; Toxicity; Efficacy; Clinical outcomes

Funding

  1. [HUG PRD 8-2017-2]

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Therapeutic drug monitoring (TDM) of amoxicillin is important for overcoming antimicrobial resistance. This study aimed to define target amoxicillin plasma concentrations and assess their association with clinical outcomes. Results showed significant variations in amoxicillin concentrations, but low trough levels did not correlate with clinical failure. Although no toxicity threshold was established, patients with the highest trough concentrations did not experience increased adverse events, suggesting that trough levels up to 40 mg/L may be safe.
Therapeutic drug monitoring (TDM) of ,B-lactam antibiotics is increasingly used to overcome rising antimicrobial resistance and improve antibiotic exposure. However, there is little guidance on target amoxicillin plasma concentrations. We aimed to define these by evaluating associations between amoxicillin concentrations and clinical outcomes. This single-centre prospective cohort study enrolled severely ill and/or immunosuppressed adult patients receiving amoxicillin for suspected or confirmed bacterial infection. TDM with >1 intermediate and >1 trough level was performed 24 h after therapy initiation. Primary and secondary outcomes were incidence of adverse events (AEs) and clinical failure through Day 30, respectively. A total of 156 patients were included. Important variations were observed both for intermediate (mean 13 mg/L, S.D. 13) and trough (mean 7 mg/L, S.D. 9) amoxicillin levels. Of 111 patients, 33 (30%) had trough levels below the non-species-related breakpoint (2 mg/L). AEs occurred in 27/156 patients (17%); no intermediate- or trough-level threshold predicting toxicity could be established. Patients with the highest-quartile trough levels (9.07-51.5 mg/L) did not experience significantly increased AEs [6/28 (21%) vs. 13/83 (16%); P = 0.6]. Nearly one-third (48/156; 31%) experienced clinical failure; low trough levels did not correlate with failure. There were few amoxicillin AEs yet a relatively high incidence of clinical failure. While no toxicity threshold could be established, the absence of increased AEs among patients with the highest trough concentrations suggests that trough levels up to 40 mg/L may be safe, at least for limited durations. Larger trials must further define optimal amoxicillin concentrations. [ClinicalTrials.gov ID: NCT03790631]. (c) 2022 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved.

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