Symptoms of High Vancomycin Levels
The most common symptoms of elevated vancomycin levels include nephrotoxicity (kidney damage), infusion-related reactions ("red man syndrome"), and ototoxicity (hearing and balance disturbances). 1
Nephrotoxicity
- Acute kidney injury (AKI) is the most common serious adverse effect of high vancomycin levels, characterized by increases in serum creatinine of ≥0.5 mg/dL or 150% increase from baseline 2, 3
- Risk of nephrotoxicity significantly increases with sustained trough concentrations >20 μg/mL 4, 3
- Nephrotoxicity occurs in approximately 10-20% of patients receiving conventional doses and 30-40% of patients receiving high-dose therapy 3
- The mechanism involves increased production of reactive oxygen species and oxidative stress 3
Infusion-Related Reactions
- "Red man syndrome" - flushing of the upper body, particularly the neck and face 1
- Hypotension, which can be severe enough to cause shock in rare cases 1
- Wheezing and dyspnea (difficulty breathing) 1
- Urticaria (hives) and pruritus (itching) 1
- Chest and back pain with muscle spasm 1
- These reactions typically resolve within 20 minutes but may persist for several hours 1
- More common with rapid infusion; less frequent when vancomycin is administered over ≥60 minutes 1
Ototoxicity
- Hearing loss, which may be transient or permanent 1, 5
- Tinnitus (ringing in the ears) 1, 5
- Vertigo and dizziness 1, 6
- Sensation of "fullness" in the ears 4
- "Buzzing" or whistling sounds in the ears 6
- Risk increases with high serum concentrations, especially when combined with other ototoxic medications 1, 5
- Ototoxicity is relatively rare with modern vancomycin formulations, with a prevalence of only 8% in patients receiving long-term therapy 7
Hematologic Effects
- Reversible neutropenia, typically starting 1 week or more after beginning therapy or after a total dose of >25g 1
- Thrombocytopenia (rare) 1
- Reversible agranulocytosis (very rare) 1
Dermatologic Reactions
- Severe dermatologic reactions can occur, including:
- Rashes, including exfoliative dermatitis 1
Gastrointestinal Effects
Risk Factors for Toxicity
- Trough serum concentrations >20 μg/mL 4, 2
- High daily doses (>4 g/day) 3
- Prolonged therapy (>7 days) 3
- Concomitant administration of other nephrotoxic or ototoxic agents 1, 3
- Pre-existing renal impairment 1, 3
- Pre-existing hearing loss 1, 7
- Admission to intensive care unit 3
Monitoring Recommendations
- Regular monitoring of trough serum vancomycin concentrations is essential for patients receiving prolonged courses of therapy 4, 2
- Monitor renal function with serum creatinine measurements 4, 2
- For patients with symptoms of ototoxicity, consider audiometric evaluation 4, 7
- For patients receiving high-dose therapy or with risk factors, more frequent monitoring is warranted 4, 2
Management of Elevated Levels
- Hold the next scheduled dose of vancomycin and recheck the trough level before administering subsequent doses 2
- Once the trough level decreases to the target range (15-20 mg/L for serious infections), resume vancomycin at a reduced dose or with an extended dosing interval 2
- For patients with normal renal function, consider reducing the dose by approximately 15-20% or extending the dosing interval 2
- In cases of severe toxicity, especially with significant renal impairment, consider alternative antibiotics 2, 4