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Aminoglycoside ototoxicity in pediatric patients receiving long-term peritoneal dialysis

B A Warady1, L Reed, G Murphy

  • 1Division of Nephrology, Children's Mercy Hospital, Kansas City, Missouri 64108.

Insights

Children on peritoneal dialysis face ototoxicity risks from aminoglycoside (AG) therapy. Intravenous AG poses a higher risk than intraperitoneal AG, necessitating careful monitoring of hearing function.

Area of Science:

  • Pediatric Nephrology
  • Ototoxicology
  • Auditory Neuroscience

Background:

  • Aminoglycoside (AG) antibiotics are crucial for treating infections in children undergoing long-term peritoneal dialysis (PD).
  • Otototoxicity is a known side effect of AG therapy, but its specific impact on children with PD requires further investigation.

Purpose of the Study:

  • To evaluate the risk of ototoxicity in children on long-term peritoneal dialysis receiving aminoglycoside therapy.
  • To compare the ototoxic effects of intravenous versus intraperitoneal AG administration in this patient population.

Main Methods:

  • Pure-tone audiometry (PTA) and auditory brainstem response (ABR) were used for baseline and follow-up auditory evaluations in 14 children and 7 controls.
  • Vestibular testing was conducted in a subset of patients.
  • Auditory function was assessed before and after intraperitoneal AG therapy.

Main Results:

  • Children on PD had poorer baseline auditory function at high frequencies (6.0 and 8.0 kHz) compared to controls.
  • Four patients (28%) developed hearing loss, primarily those with a history of intravenous AG therapy.
  • No hearing loss was observed in patients receiving only intraperitoneal AG or with no prior AG exposure (P < 0.005).
  • PTA was more sensitive than ABR in detecting hearing abnormalities.

Conclusions:

  • Children on peritoneal dialysis are at risk for aminoglycoside-induced ototoxicity.
  • Intraperitoneal AG administration may be associated with lower ototoxicity risk than intravenous administration, warranting further research.
  • Close monitoring of AG levels and auditory function is essential for all children on PD receiving AG therapy, regardless of administration route.

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