Initial Management of Suspected Intracranial Hemorrhage
Immediately stabilize the patient with airway, breathing, and circulation (ABCs), obtain urgent non-contrast head CT to confirm the diagnosis, and simultaneously initiate reversal of any anticoagulation while maintaining strict blood pressure control with systolic BP <140 mmHg. 1, 2
Immediate Diagnostic Evaluation
- Obtain non-contrast head CT scan urgently as the gold standard diagnostic tool to confirm intracranial hemorrhage and determine location, size, and presence of mass effect 3, 4, 5
- Perform urgent neurological assessment including pupillary examination and Glasgow Coma Scale motor score (if feasible) to determine severity of brain injury 1
- Consider CT angiography (CTA) plus venography in specific scenarios: lobar hemorrhage in patients <70 years, deep/posterior fossa hemorrhage in patients <45 years, or deep/posterior fossa hemorrhage in patients 45-70 years without hypertension history to exclude macrovascular causes 1
Critical Initial Interventions
Blood Pressure Management
- Target systolic blood pressure <140 mmHg (strictly avoiding SBP <110 mmHg) within the first 6 hours of symptom onset to reduce hematoma expansion risk 1, 2
- Maintain mean arterial pressure >80 mmHg during any emergency interventions 1
- Intensive BP reduction directly reduces hematoma expansion and improves outcomes 2
Immediate Anticoagulation Reversal
For Vitamin K Antagonists (Warfarin):
- Discontinue warfarin immediately when intracranial hemorrhage is confirmed or suspected 1
- If INR ≥1.4: Administer 4-factor prothrombin complex concentrate (PCC) IV (weight-based dosing according to INR and PCC type) PLUS vitamin K 10 mg IV 1
- 4-factor PCC is strongly preferred over fresh frozen plasma (FFP) due to faster onset of action 1
- If PCC unavailable, use FFP 10-15 mL/kg IV with vitamin K 10 mg IV 1
- Repeat INR testing 15-60 minutes after PCC administration, then serially every 6-8 hours for 24-48 hours 1
- If repeat INR remains ≥1.4 within 24-48 hours, redose with vitamin K 10 mg IV 1
For Direct Oral Anticoagulants (DOACs):
- Discontinue DOACs immediately when hemorrhage is confirmed or suspected 1, 2
- For dabigatran: Administer idarucizumab 5 g IV in two divided doses if drug was given within 3-5 half-lives or if renal insufficiency is present 1
- For factor Xa inhibitors (rivaroxaban, apixaban, edoxaban): Administer 4-factor PCC 50 U/kg IV or activated PCC (FEIBA) 50 U/kg IV 1, 2
- Administer activated charcoal 50 g to intubated patients with enteral access who present within 2 hours of oral DOAC ingestion 1
- Reversal decisions should be guided primarily by bleeding severity and dosing history, NOT laboratory testing 1, 6
For Heparin:
- Administer protamine sulfate 1 mg per 100 units of heparin given in the previous 2-3 hours (maximum 50 mg single dose) 1, 2
For Low Molecular Weight Heparin (Enoxaparin):
- For therapeutic-dose enoxaparin given within 8 hours: Administer protamine 1 mg per 1 mg of enoxaparin (maximum 50 mg single dose) 6, 2
- For prophylactic-dose enoxaparin, routine reversal is NOT recommended unless aPTT is significantly prolonged 6
- If life-threatening bleeding persists, consider redosing protamine at 0.5 mg per 100 anti-Xa units 6
For Antiplatelet Agents:
- Stop aspirin, clopidogrel, and dipyridamole/ASA immediately 1
- Do NOT routinely administer platelet transfusions unless neurosurgical intervention is planned 1
Triage and Consultation Decisions
Neurosurgical Consultation
- Obtain urgent neurosurgical consultation for all salvageable patients with life-threatening brain lesions after control of any systemic hemorrhage 1
- Immediate neurosurgical referral for cerebellar hemorrhage with altered consciousness or new brainstem symptoms 1
- Urgent consultation for acute hydrocephalus requiring external ventricular drainage (EVD) 1
- Supratentorial hemorrhage: Surgical evacuation has not proven superior to conservative management in most patients, but consider early intervention in select patients with GCS 9-12 1
Admission Location
- Admit medically stable patients to a stroke unit or neuro-intensive care unit 1, 3
- Critically ill patients require intensive care unit admission 1
Monitoring and Supportive Care
- Institute intracranial pressure (ICP) monitoring for comatose patients with radiological signs of intracranial hypertension, regardless of need for emergency extra-cranial surgery 1
- Cardiac monitoring for at least 24 hours to screen for atrial fibrillation and serious arrhythmias 1
- Maintain cerebral perfusion pressure 50-70 mmHg 2
- Monitor body temperature and treat fever >38°C 1
- Antiseizure medications are indicated ONLY for documented seizures, not prophylactically 1
Critical Pitfalls to Avoid
- Never delay anticoagulation reversal while waiting for laboratory results—base decisions on bleeding severity and medication history 1, 6
- Do not use recombinant Factor VIIa (rFVIIa) for warfarin reversal—it increases arterial thromboembolic events without clinical benefit 1
- Avoid deferring goals of care discussions or DNR decisions for at least 24-48 hours after stroke onset to allow time for response to therapy, unless patient has preexisting wishes 1
- Do not restart anticoagulation before repeat imaging confirms hemorrhage stability—premature resumption dramatically increases mortality and rebleeding risk 6, 2
- Never give therapeutic anticoagulation during active intracranial bleeding 6