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©The Author(s) 2025.
World J Crit Care Med. Sep 9, 2025; 14(3): 105645
Published online Sep 9, 2025. doi: 10.5492/wjccm.v14.i3.105645
Published online Sep 9, 2025. doi: 10.5492/wjccm.v14.i3.105645
Table 7 Tiers of therapy for intracranial hypertension
Tier 0: Basic neurocritical care management for ventilated patients at risk of intracranial hypertension |
ICU admission with proper monitoring, including: (1) Invasive arterial pressure monitoring; (2) End-tidal CO2 monitoring; and (3) Core temperature measurement |
Venous return optimization with: (1) Head-of-bed elevation to 30-45 ℃; (2) Midline head positioning; and (3) Avoidance of tight cervical collars when possible |
Avoidance of ICP spikes with: (1) Analgesia and (2) Mild sedation (not ICP directed) to prevent pain, agitation and ventilator asynchrony |
Avoidance of secondary insults, including: |
(1) Hypoxemia: Target SpO2 94%-98% |
(2) Hypotension: Avoid hypotension by targeting a minimal systolic arterial pressure of 100-110 mmHg or to CPP 60-70 mmHg |
(3) Hypocapnia: Target PaCO2 to normal levels (35-40 mmHg) |
(4) Hyponatremia: Target serum Na+ to 140-145 mmol/L |
(5) Hyperthermia: Target core temperature to below 38 ℃ |
(6) Hypoglycemia: Target glucose levels to 110-180 mg/dL |
Avoid anemia (i.e., Hb < 7.0 g/dL) |
Consider anti-seizure prophylaxis for up to 1 week |
Tier 1: Deep sedation, CPP optimization, EVD drainage and hyperosmolar therapy |
Revise Tier 0 treatment: |
(1) Target CPP of 60-70 mmHg or MAP 80-90 mmHg in absence of invasive ICP monitoring |
(2) Maintain PaCO2 at lower end of normal (35-38 mmHg) |
Intermittent bolus hyperosmolar treatment: (1) Hypertonic saline; and (2) Mannitol |
Increase sedation beyond mild sedation to lower ICP (if measured) or to a target RASS of -4/-5 (if ICP not measured), but not to target burst-suppression |
Cerebrospinal fluid drainage if external ventricular drain in situ or consider the placement of an EVD |
Consider EEG monitoring (if available) |
Tier 2: Additional measures with controversial effect |
Mild hypocapnia in a lower range (32-35 mmHg) |
Trial of neuromuscular paralysis (among ICP monitored patients) |
If ICP decreases with a bolus, consider a continuous infusion |
Trial of hemodynamic augmentation beyond usual CPP targets: |
Perform MAP challenge to assess cerebral autoregulation: If ICP decreases with increased MAP, consider sustaining higher MAP, but no more than a CPP greater than 90 mmHg |
Avoid any other adjustments during MAP challenges |
In patients without ICP monitors, this trial may be considered with TCCD/TCD measurements |
Tier 3: Highly efficacious therapies to reduce ICP, but with demonstrated increased risk of complications (i.e., should not be routinely used except under specific circumstances) |
Barbiturate coma with pentobarbital or thiopentone to ICP control (if efficacious) or to pupil abnormality correction (when ICP is not measured) |
Secondary decompressive craniectomy |
Mild hypothermia (35-36 ℃) with active cooling measures |
- Citation: Bianchini L, Matos PMPG, Roepke RML, Besen BAMP. Management of intracranial hypertension with and without invasive intracranial pressure monitoring. World J Crit Care Med 2025; 14(3): 105645
- URL: https://www.wjgnet.com/2220-3141/full/v14/i3/105645.htm
- DOI: https://dx.doi.org/10.5492/wjccm.v14.i3.105645