This document discusses different options for managing increased intracranial pressure (ICP), including mannitol, furosemide, and hypertonic saline. Mannitol works by increasing the gradient across the blood-brain barrier to rapidly reduce ICP over 6 hours, while hypertonic saline's primary mechanism is also increasing this gradient for immediate ICP reduction over 4 hours. Both have hemodynamic and potential adverse effects that require monitoring. The document concludes that while controversial, hypertonic saline 3% may be superior to mannitol 20% for treating elevated ICP.
This document discusses different options for managing increased intracranial pressure (ICP), including mannitol, furosemide, and hypertonic saline. Mannitol works by increasing the gradient across the blood-brain barrier to rapidly reduce ICP over 6 hours, while hypertonic saline's primary mechanism is also increasing this gradient for immediate ICP reduction over 4 hours. Both have hemodynamic and potential adverse effects that require monitoring. The document concludes that while controversial, hypertonic saline 3% may be superior to mannitol 20% for treating elevated ICP.
This document discusses different options for managing increased intracranial pressure (ICP), including mannitol, furosemide, and hypertonic saline. Mannitol works by increasing the gradient across the blood-brain barrier to rapidly reduce ICP over 6 hours, while hypertonic saline's primary mechanism is also increasing this gradient for immediate ICP reduction over 4 hours. Both have hemodynamic and potential adverse effects that require monitoring. The document concludes that while controversial, hypertonic saline 3% may be superior to mannitol 20% for treating elevated ICP.
of Increased Intracranial Pressure Splachnic Brain
Diah Mustika HW dr,SpN,KIC
JCCA, 20 Maret 2022 Intracranial Component AUTOREGULATION • Maintain the cerebral perfusion pressure (CPP) • Effective at MAP 60-150 mmHg • CBF = CPP (MAP-ICP) CVR 5 MANAGEMENT • Elevation of head 30o • Analgesia and sedation • Hyperventilation • Maintain : blood pressure, volume status, body temperature, CPP • Monitoring : haemoglobin, blood glucose, sodium • Hyperosmolar therapy OSMOLALITY
2(Na+K) + GD/18 + BUN/2,8
OR
2(Na+K) + GD/18 + Ur/6,4
Keep Osmolality between 310-320 mOsm/L
COMPARATION OF HYPEROSMOLAR THERAPY MANNITOL 20% • Dose : 0,25 – 1gr/kgBB every 3-6 hours over 15-30 minutes • Infuse via peripheral line, central line • Monitoring : – ICP (goal <20 mmHg) – Hypovolemia – Serum osmolality (<325 mOsm) • Contraindication : Renal failure, CHF HYPERTONIC SALINE 3% BOLUS
• Dose : 250 ml IV every 3-6 hours over
20-30 minutes • Infuse via central line • In a emergency, HTS 3% may administered via infuse via peripheral line • Monitoring : – ICP (goal <20 mmHg) – Serum sodium (<155 mEq/L) HYPERTONIC SALINE 3% INFUSION
• Dose : 50 - 150 ml/hours
• Infuse via central line • Monitoring : – ICP (goal <20 mmHg), – Serum sodium (<155 mEq/L) – Serum osmolality (<325 mOsm) HYPERTONIC SALINE 23,4%
• Dose: 30ml every 3-6 hours over 15 – 30
minutes • Infusion via central line • Monitoring : – ICP (goal <20 mmHg) – Serum sodium (goal <155 mE q/L) – Central pontine myelinolysis FUROSEMIDE
• Dose : 1mg/kgBB every 8 hours
• Better administration if combine with mannitol • Contraindication : Hypotension MANNITOL VS HTS 3% (1) Mannitol HTS 3%
Primary - Increases gradient across - Increases gradient across
hyperosmolar therapy such as Mannitol 20% or HTS 3% • Even it still controversial, administration of HTS 3% is superior than mannitol 20% • Furosemide can administered as concomitant therapy to reduce ICP 25