Criteria for Neurointervention in Intracranial Hemorrhage
All salvageable patients with life-threatening brain lesions require urgent neurosurgical consultation and intervention after control of any life-threatening systemic hemorrhage. 1
Initial Assessment Algorithm
The decision for neurointervention follows a structured priority sequence:
Step 1: Control Life-Threatening Systemic Hemorrhage First
- Patients with exsanguinating hemorrhage require immediate intervention (surgery and/or interventional radiology) for bleeding control before addressing intracranial pathology. 1
- Maintain systolic blood pressure >100 mmHg or mean arterial pressure >80 mmHg during hemorrhage control interventions. 1
Step 2: Urgent Neurological Evaluation
Once systemic bleeding is controlled (or if no life-threatening systemic hemorrhage exists):
- Perform urgent neurological evaluation including pupillary assessment and Glasgow Coma Scale motor score (if feasible). 1
- Obtain immediate brain CT scan to determine severity of brain damage and identify life-threatening lesions. 1
Step 3: Determine Need for Neurosurgical Intervention
Life-threatening brain lesions requiring urgent neurosurgical consultation include: 1
Specific Indications for Surgical Intervention:
- Cerebellar hemorrhage with neurological deterioration, brainstem compression, and/or hydrocephalus from ventricular obstruction requires surgical evacuation. 2
- Patients with intracranial mass lesions causing significant mass effect or midline shift. 1
- Patients showing signs of impending herniation. 1
ICP Monitoring Criteria (Without Immediate Surgical Evacuation):
- Comatose patients with radiological signs of intracranial hypertension (without a life-threatening mass lesion or after emergency neurosurgery) require ICP monitoring regardless of need for emergency extra-cranial surgery. 1
- Maintain cerebral perfusion pressure ≥60 mmHg when ICP monitoring is available. 1
Perioperative Management Requirements
Hemodynamic Targets:
- Maintain SBP >100 mmHg or MAP >80 mmHg during emergency neurosurgery. 1
- Lower values may be tolerated only for the shortest possible time during difficult intraoperative bleeding control. 1
Coagulation Parameters:
- Maintain platelet count >50,000/mm³ for emergency neurosurgery (including ICP probe insertion); higher values are advisable. 1
- Maintain PT/aPTT <1.5 times normal control during emergency neurosurgery. 1
- Utilize point-of-care testing (TEG/ROTEM) if available to optimize coagulation function. 1
Antiplatelet Reversal for Surgery:
- Platelet transfusion is suggested for patients with aspirin- or ADP inhibitor-associated ICH who will undergo neurosurgical procedures. 1
- Perform platelet function testing prior to transfusion if possible; avoid transfusion if platelet function is within normal limits. 1
- Initial dose: one single donor apheresis unit of platelets. 1
Respiratory Parameters:
- Maintain PaO₂ between 60-100 mmHg during emergency neurosurgery. 1
- Maintain PaCO₂ between 35-40 mmHg during emergency neurosurgery. 1
Transfusion Thresholds:
- Transfuse RBCs for hemoglobin <7 g/dL during emergency neurosurgery. 1
- Higher thresholds may be used in elderly patients or those with limited cardiovascular reserve. 1
Emergency Temporizing Measures
For cerebral herniation awaiting or during emergency neurosurgery: 1
- Use osmotherapy (mannitol 0.25-2 g/kg IV over 30-60 minutes). 3
- Consider temporary hypocapnia (PaCO₂ temporarily reduced below 35 mmHg). 1
Critical Pitfalls to Avoid
- Do not delay neurosurgical consultation while attempting medical management alone in patients with life-threatening mass lesions. 1
- Do not allow hypotension (SBP <100 mmHg) or hypoxia (PaO₂ <60 mmHg), which worsen secondary brain injury. 2, 4
- Do not insert ICP monitors without correcting coagulopathy (platelets >50,000/mm³, PT/aPTT <1.5 times control). 1
- Mannitol may increase cerebral blood flow and risk of postoperative bleeding in neurosurgical patients; use judiciously. 3
- Mannitol may worsen intracranial hypertension in children with generalized cerebral hyperemia during the first 24-48 hours post-injury. 3