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Amoxicillin Blood Concentration in High-Dose Intravenous Discontinuous Amoxicillin: Look Beyond Numbers. Max-Amox
Mélissa Clément1, Florence Anglade2, Lucie Gibold3
1Department of Internal Medicine, CH Henri Mondor, Aurillac, France; Department of Internal Medicine, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Monitoring amoxicillin trough plasma concentrations (ATPC) showed high variability and is not sufficient alone for dose adjustment. High ATPC, low urinary pH, and amoxicillin crystalluria (AC) indicate potential toxicity.
Area of Science:
- Pharmacology
- Nephrology
- Infectious Diseases
Background:
- High-dose amoxicillin is crucial for severe infections like endocarditis.
- Amoxicillin can cause dose-dependent toxicities, notably crystal nephropathy.
- Monitoring amoxicillin trough plasma concentrations (ATPC) may prevent toxicity, but its routine use is understudied.
Purpose of the Study:
- To evaluate the distribution and variability of ATPC in patients receiving high-dose amoxicillin.
- To assess the clinical relevance of ATPC monitoring in routine practice.
Main Methods:
- Prospective clinical trial in adults receiving high-dose intravenous amoxicillin.
- Primary outcome: distribution of ATPCs over three days during the first week of treatment.
- Secondary outcomes: urine tests for amoxicillin crystalluria (AC), pH, and density.
Main Results:
- Seventy patients were included; high inter-individual variability in ATPC was observed.
- Amoxicillin crystalluria (AC) occurred in 47.8% of patients, increasing with urinary pH ≤ 6.
- Higher ATPCs were associated with AC and/or acute kidney injury.
Conclusions:
- High variability in ATPC suggests it's insufficient as a sole monitoring tool for amoxicillin dosage.
- Elevated ATPC, low urinary pH, and AC presence are indicators of potential iatrogenic effects.
- These findings may guide interventions like hydration, urine alkalinization, and dosage reduction.
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