Fatal lactic acidosis during antiretroviral therapy

Corsino Rey1, Soledad Prieto, Alberto Medina

  • 1Pediatric Intensive Care Unit, Department of Pediatrics, Hospital Universitario Central de Asturias, University of Oviedo, Oviedo, Spain. crey@hcas.sespa.es

Insights

Fatal lactic acidosis, a rare complication of antiretroviral therapy, occurred in a pediatric patient with human immunodeficiency virus (HIV) infection. Early recognition of mitochondrial dysfunction is crucial for prevention.

Area of Science:

  • Pediatric critical care medicine
  • Infectious diseases
  • Pharmacology

Background:

  • Antiretroviral therapy (ART) is standard for managing human immunodeficiency virus (HIV) infection in children.
  • Mitochondrial dysfunction is a known, albeit rare, complication of certain nucleoside reverse transcriptase inhibitors used in ART.
  • Type B lactic acidosis is a metabolic derangement associated with mitochondrial toxicity.

Observation:

  • A 5-year-old girl with HIV infection on a regimen including ritonavir, stavudine, and didanosine presented with severe lactic acidosis.
  • The patient experienced worsening symptoms including nausea, vomiting, and rising serum lactate levels.
  • Despite intensive supportive care, including alkali administration and hemodiafiltration, the acidosis proved fatal.

Findings:

  • This case represents the first reported instance of fatal lactic acidosis in a pediatric patient receiving antiretroviral therapy.
  • The patient's clinical presentation and laboratory findings were consistent with severe mitochondrial dysfunction secondary to ART.
  • The specific combination of antiretroviral drugs may have contributed to the observed toxicity.

Implications:

  • Fatal lactic acidosis is a potential, previously unreported complication of ART in pediatric HIV patients.
  • Prompt identification of mitochondrial dysfunction is critical for timely intervention and potentially preventing fatal outcomes.
  • Further research into ART-associated mitochondrial toxicity in pediatric populations is warranted.
Abstract

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