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Acute acyclovir neurotoxicity in a hemodialyzed child
1Department of Pharmacy, British Columbia's Children's Hospital, University of British Columbia, Vancouver, Canada.
Acyclovir can cause severe neurotoxicity in children with end-stage renal failure, leading to coma. This toxicity is reversible upon drug discontinuation, even with dose adjustments for kidney impairment.
Area of Science:
- Pediatric Nephrology
- Virology
- Pharmacology
Background:
- Epstein-Barr virus-induced lymphoproliferative disease (EBV-LPD) is a serious complication post-kidney transplantation.
- Management of EBV-LPD often involves antiviral therapy, such as acyclovir.
- End-stage renal failure (ESRF) necessitates careful drug dosing due to impaired excretion.
Observation:
- A 5-year-old kidney transplant recipient with EBV-LPD developed severe neurological symptoms, including coma, after initiating acyclovir therapy.
- Despite a reduced acyclovir dose due to concurrent hemodialysis for acute rejection, high serum acyclovir concentrations were observed.
- Neurological status improved rapidly after acyclovir discontinuation.
Findings:
- Acyclovir accumulation in pediatric patients with ESRF can lead to significant neurotoxicity.
- High post-dose serum acyclovir levels (182.5 microM) correlated with the onset of severe neurological symptoms.
- The neurotoxicity observed was reversible, with improvement noted within 2 days of stopping the medication.
Implications:
- Clinicians must exercise extreme caution when prescribing acyclovir to pediatric patients with ESRF.
- Standard dose adjustments for renal impairment may be insufficient to prevent acyclovir neurotoxicity in this population.
- Monitoring serum acyclovir concentrations and neurological status is crucial in pediatric transplant patients with renal failure receiving this antiviral agent.
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