Pharmacology · Year 2 · from Pharmacology

Case 3: Gentamicin Therapeutic Drug Monitoring

Clinical Scenario

A 62-year-old male with infective endocarditis is being treated with gentamicin and requires dose adjustment based on therapeutic drug monitoring.

Patient Demographics

  • Age: 62 years
  • Sex: Male
  • Weight: 80 kg
  • Height: 175 cm

Chief Complaint

Follow-up for gentamicin level monitoring during treatment for endocarditis

History of Present Illness

The patient was admitted 5 days ago with Enterococcus faecalis endocarditis and started on ampicillin plus gentamicin for synergy. He has mild chronic kidney disease at baseline. Current regimen: Gentamicin 120 mg IV every 8 hours (started 3 days ago).

Physical Examination

  • Vital Signs: BP 130/75 mmHg, HR 82 bpm, RR 14, T 37.2C
  • General: Improving, less fatigued
  • Cardiovascular: Regular rhythm, grade II/VI systolic murmur
  • Neurological: No vestibular symptoms, hearing intact

Workup and Results

TestResultReference Range
Gentamicin peak (30 min post-dose)8.5 mcg/mL3-5 mcg/mL (synergy dosing)
Gentamicin trough (pre-dose)2.1 mcg/mL<1 mcg/mL
Creatinine1.6 mg/dL0.6-1.2 mg/dL
BUN28 mg/dL7-20 mg/dL
AudiometryNormal-

Diagnosis

Supratherapeutic gentamicin levels with elevated trough indicating accumulation and nephrotoxicity risk

Pharmacokinetic Principles Illustrated

  1. Therapeutic drug monitoring: Aminoglycosides require monitoring due to narrow therapeutic index and concentration-dependent toxicity.
  2. Peak levels: Correlate with bactericidal efficacy (concentration-dependent killing).
  3. Trough levels: Correlate with nephrotoxicity and ototoxicity risk; should be <1 mcg/mL for synergy dosing.
  4. Renal elimination: Gentamicin is eliminated almost entirely by glomerular filtration; dose adjustment required in renal impairment.
  5. Steady-state: Reached after 4-5 half-lives; levels drawn after reaching steady state.

Treatment

  1. Extend dosing interval to every 12 hours
  2. Reduce dose to 100 mg IV every 12 hours
  3. Repeat levels after 3 doses at new regimen
  4. Monitor serum creatinine daily
  5. Obtain weekly audiometry during prolonged therapy
  6. Target trough <1 mcg/mL for synergy dosing

Key Learning Points

  • Aminoglycoside dosing requires careful PK/PD optimization
  • Extended-interval (once-daily) dosing reduces nephrotoxicity while maintaining efficacy for standard indications
  • Synergy dosing uses lower doses with different target levels
  • Trough levels are better predictors of toxicity than peak levels

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