Continuous Infusion Protocol for 3% Hypertonic Saline in Raised ICP
For continuous infusion of 3% hypertonic saline in raised intracranial pressure, target a serum sodium concentration of 145-155 mmol/L, with the infusion rate adjusted on a sliding scale to maintain this target range. 1, 2
Dosing Strategy
Continuous infusion of 3% hypertonic saline should be administered using a sliding scale protocol to achieve and maintain serum sodium levels between 145-155 mmol/L. 1, 2 This approach has been validated in multiple patient populations including traumatic brain injury, intracerebral hemorrhage, subarachnoid hemorrhage, and acute liver failure. 1
Key Dosing Parameters:
- Target serum sodium: 145-155 mmol/L 1, 2
- Target osmolality: 310-320 mOsm/kg (though should remain <296 mOsm/kg when possible during initial 7 days in stroke patients) 2, 3
- Mean treatment duration: Approximately 7.6 days (range 4-23 days) in pediatric studies, with similar durations in adult populations 4, 3
- Critical upper limit: Do not exceed serum sodium of 155-160 mmol/L to prevent complications including osmotic demyelination syndrome 1, 2
Monitoring Protocol
The American College of Surgeons and American Society of Anesthesiologists provide clear monitoring guidelines that are essential for safe administration:
- Measure serum sodium within 6 hours of initiating therapy to guide infusion rate adjustments 1, 2
- Monitor serum sodium every 2-4 hours initially during the acute phase 5
- Do not re-administer bolus doses until serum sodium is <155 mmol/L 1
- Track fluid, sodium, and chloride balances continuously to prevent complications 1
- Monitor for hypernatremia and hyperchloremia, particularly with prolonged infusions 1
Clinical Evidence Base
The continuous infusion strategy is supported by robust evidence across multiple neurological conditions:
Pediatric traumatic brain injury: A prospective study of 10 children demonstrated that continuous 3% saline infusion with target sodium levels of 157-187 mEq/L (mean highest 170.7 mEq/L) significantly decreased ICP spike frequency and increased cerebral perfusion pressure at 6,12,24,48, and 72 hours (p < 0.01) 4
Adult cerebrovascular disease: A retrospective analysis of 100 patients receiving continuous 3% saline (target sodium 145-155 mmol/L) within 72 hours of symptom onset showed fewer episodes of critically elevated ICP (92 vs 167, p = 0.027) and significantly decreased in-hospital mortality (17.0% vs 29.6%, p = 0.037) compared to historical controls 3
Acute liver failure: The infusion of hypertonic saline to maintain serum sodium between 145-155 mmol/L significantly decreased ICP in this population 6
Mechanism and Time Course
Understanding the pharmacodynamics helps optimize timing:
- Maximum ICP-lowering effect: Occurs 10-15 minutes after administration 1, 2
- Duration of effect: Lasts 2-4 hours 1, 2
- Mechanism: Creates an osmotic pressure gradient across the blood-brain barrier, displacing water from brain tissue to the hypertonic environment (Grade A evidence) 1
Safety Considerations and Pitfalls
Critical safety thresholds must be strictly observed:
- Avoid sodium levels >155-160 mmol/L to prevent osmotic demyelination syndrome, seizures, and hemorrhagic encephalopathy 1, 2, 5
- Avoid rapid correction: Do not exceed 10 mmol/L sodium correction per 24 hours 6, 5
- Renal monitoring: Two patients in the pediatric series developed acute renal failure requiring continuous veno-venous hemodialysis, though both recovered full renal function; this occurred concurrent with sepsis and multisystem organ dysfunction 4
- No evidence of osmotic demyelination syndrome has been reported with proper monitoring, even with sustained hypernatremia and bolus doses of 23.4% hypertonic saline 1
Comparison to Bolus Therapy
While bolus therapy (250 mL of 7.5% hypertonic saline over 15-20 minutes) is recommended for acute ICP crises, continuous infusion of 3% saline provides sustained control:
- Bolus therapy: Preferred for acute threatened herniation or sudden ICP elevation 1
- Continuous infusion: Preferred for sustained ICP control over days to weeks, particularly validated in pediatric traumatic brain injury and cerebrovascular disease 1, 4, 3
Important Limitations
Despite robust evidence for ICP reduction (Grade A), there is no evidence that hypertonic saline improves neurological outcomes (Grade B) or survival (Grade A) in randomized controlled trials. 1, 2 The therapy effectively manages the physiologic parameter of elevated ICP but has not demonstrated improvement in patient-centered outcomes. This distinction is critical for informed decision-making and family discussions.