Hypertonic saline (HS)

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  • May reduce ICP in patients refractory to mannitol
  • Potentially deleterious effect on stroke penumbra in animal studies.
  • Benefit
    • Osmotic action → reduce ICP
    • Vasoregulatory
    • Immunological
    • Neurochemical actions;
    • Expands intravascular volume → augmenting CPP.
  • Mechanism of action
    • Osmotic effect by drying out endothelial cells → water to move from CSF to cerebral vessels
  • Does not have a strong diuretic effect because it can be reabsorbed by in the kidney
  • Contra indication
    • Congestive heart failure or renal insufficiency due to their already increased fluid and sodium loads
  • Side effects
    • Hyperchloremic metabolic acidosis due to the addition of NaCl.
    • Route specific
      • Thrombophlebitis
      • Extravasation
  • Studies are not adequate to make recommendations regarding use.
  • ℞:
    • Continuous infusion: 3% saline at 25–50 ml/hr may be given through a peripheral IV.
    • Bolus: 10–20ml of 7.5–23.4% saline must be given through a central line.
    • 3mL/kg over 20min, raising serum sodium by around 2-3mmol/L
  • Stop
    • HS should be discontinued after ≈ 72 hours to avoid rebound edema.
    • Hold if serum osmolarity > 320 mOsm/L.
  • Vs Mannitol
    • Mangat, 2014:
      • HTS was more effective in lowering ICP burden but did not have a significant effect on mortality.
      • Hypertonic saline better than mannitol in reducing ICP while maintaining CCP (in the form of total number/% of days in High ICP and low CPP states)
    • Diringer 2013:
      • HS may have a more profound and long- lasting effect on ICP compared with mannitol, but outcome benefits over mannitol have not been demonstrated.
    • Mannitol has haemodynamic, osmotic and diuretic effects
    • HS has osmotic and diuretic effects