5 Therapeutic Monitoring of Anti-Infective Medications

Learn how to interpret anti-infective drug concentrations, select relevant safety tests, and reassess dosing in light of renal function and clinical context.

Interpreting drug concentrations

is useful when it is established for a medication; not every laboratory test is a drug concentration. Interpret a level with the patient’s current clinical status and the institution’s drug-monitoring protocol.

Before responding to an unexpected level, confirm the dose and sample timing. Review the dose history, adherence, administration, interacting medicines, and relevant clinical changes. Use drug-specific guidance and clinical response; do not adjust a dose from a level in isolation.

Gentamicin monitoring

A gentamicin is collected immediately before the next dose. Interpret the result alongside and the exact dose and sample times. Impaired or changing renal clearance can cause aminoglycoside accumulation.

Before adjusting therapy, review the level, , and dose history, and follow the applicable protocol.

Vancomycin exposure targets

For serious MRSA infections, the recommended exposure target is an of 400–600400\text{–}600, assuming an MIC of 1 mg/L1\ \mathrm{mg/L}. This target is intended to balance efficacy and safety.

-only targeting of 15–20 mg/L15\text{–}20\ \mathrm{mg/L} is no longer recommended for this indication. Monitoring and dose decisions should not be based on the white blood cell count alone.

Fluconazole and renal dosing

Fluconazole is primarily eliminated by the kidneys. For multiple-dose therapy, the general approach is to give the usual and then adjust the for .

A single-dose vaginal candidiasis regimen is an exception to this multiple-dose approach. The specific regimen depends on the indication and the patient. For example, with a creatinine clearance of 40 mL/min40\ \mathrm{mL/min}, consider reducing the according to and the clinical indication.

Amphotericin B safety monitoring

During amphotericin B therapy, monitor , potassium, magnesium, liver function, and blood counts. The medication can affect and cause electrolyte abnormalities, including low potassium and low magnesium.

Responding to a low voriconazole level

When a voriconazole is unexpectedly low, first confirm sample timing and review adherence, administration, interacting medicines, and relevant clinical changes. Assess the result using the drug-specific protocol before changing the dose.

Voriconazole also warrants liver-function monitoring.

Acyclovir and renal safety

Acyclovir is substantially eliminated unchanged by the kidneys. During high-dose intravenous therapy, monitor and promptly reassess the dose and interval using current when kidney function worsens.

Adequate hydration is important to help reduce renal risk.