Effectiveness of 7.5% hypertonic saline in children with severe traumatic brain injury

Dimitrios Rallis1, Panagiotis Poulos1, Maria Kazantzi1

  • 1Pediatric Intensive Care Unit, "Aghia Sophia" Children's Hospital, Athens, Greece.

Journal of Critical Care
|November 14, 2016
PubMed

Insights

This study found that 7.5% hypertonic saline (HTS) effectively reduced intracranial pressure (ICP) and improved cerebral perfusion pressure (CPP) in children with severe traumatic brain injury (TBI). HTS is a safe and beneficial second-tier osmotic therapy for pediatric TBI management.

Area of Science:

  • Pediatric Intensive Care
  • Neurocritical Care
  • Traumatology

Background:

  • Increased intracranial pressure (ICP) is a critical concern in severe traumatic brain injury (TBI).
  • Hyperosmolar therapies are essential for managing elevated ICP.
  • 7.5% hypertonic saline (HTS) is utilized as an osmotic agent in TBI management.

Purpose of the Study:

  • To evaluate the efficacy of 7.5% hypertonic saline (HTS) in controlling ICP.
  • To assess the impact of HTS on cerebral perfusion pressure (CPP) in pediatric severe TBI.
  • To determine the safety and neurological outcomes associated with HTS use.

Main Methods:

  • Retrospective review of medical records for pediatric patients (≤14 years) with severe TBI.
  • Analysis of ICP and CPP before and at 30, 60, and 120 minutes after HTS infusion.
  • Recording of adverse effects, neurological outcomes, and survival rates.

Main Results:

  • Twenty-nine pediatric patients received 136 HTS infusions.
  • A significant reduction in ICP and elevation in CPP were observed post-HTS infusion.
  • ICP and CPP levels remained within acceptable ranges, with no significant adverse events noted.

Conclusions:

  • 7.5% HTS is an effective second-tier osmotic therapy for reducing ICP and increasing CPP in children with severe TBI.
  • HTS administration was associated with survival in most patients, though one-third experienced severe neurological impairment.
  • Further research into long-term outcomes of HTS in pediatric TBI is warranted.
Abstract