ICH Flashcards
ICH
Spontaneous rupture of blood vessels
in the cerebral parenchyma
Leading to focal haematoma formation and
Subsequent mass effect
types of brain hemorrhage
epidural hematoma, subdural hematoma, subarachnoid hemorrhage, ICH
Primary ICH causes
Primary (80%)
hypertensive arteriopathy (70%)
Amyloid angiopathy
Eclampsia
Secondary ICH causes
Secondary-
Bleeding from pre-existing lesion
Coagulopathies (including drug-induced disorders)
malformations
localisation of ICH
Supratentorial haemorrhages (85%)
-cortical, lobar (30-35%)
- deep haematomas – basal ganglia, internal capsule, thalamus (35%)
2) Infratentorial haemorrhages (15%)
-cerebellar (5-10%)
-brainstem (5%)
3) Intraventricular haemorrhages
causes
Hypertension
Vascular malformations: aneurysm, AVM, cavernoma, venous sinus thrombosis
Trauma
Bleeding in pre-exsiting lesions – tumours/haemorrhagic transformation
Infection –mycotic aneurysms
Angiopathies
Coagulopathies
Drugs
hypertension causing ICH
Most common cause of ICH
2 mechanisms causing bleeding:
1) rupture of artery affected by chronic HTN
2) acute/subacute severe hypertension –rupture of previously unaffected artery (malignant HTN)
Basal ganglia, thalamus, pons, cerebellum
HTN leads to lipohyalinosis of small arteries
Coagulopathies causing ICH
Anticoagulants- risk of ICH with long term anticoagulants 2%
Antiplatelets – 1% (increased if on two different antiplatelets)
Fibrinolytics -4-6%
Other coagulopathies – leukemia, liver disease (alcohol), thrombocytopenia
Angiopathies (abnormal vessels) causing ICH
Cerebral amyloid angiopathies
50-60 yo
Beta-amyloid deposits in small/medium cerebral arteries
Lobar haematomas/repeated microhaemorrhages
Vasculitis – e.g. Polyarteritis nodosa/SLE/syphilis
vascular abnormality causing ICH symptoms
Aneurysm: sudden onset headache, photophobia, neck stiffness
AVM: seizure
Cavernoma: seizure
venous sinus thrombosis : headache, visual disturbance
(Hypertensive) : hypertension
Haemorrhagic stroke: stroke presentation
management
Correct clotting – Vit K antagonist (combination of Prothrombin complex and IV vitamin K). Patients on DOAC should also be considered for reversal.
Control BP – SBP 150-220 –treat immediately within 6 hours of symptom onset to achieve 130-139mmHg within 1 hour and sustained for 7 days