Abrupt onset of neurological deficit that is attributable to a focal vascular cause Signs and symptoms last more than 24 hours
RISK FACTORS NON-MODIFIABLE:- Age Gender – Equal for men & women Heredity – family history, prior transient ischemic attack, or prior stroke increases risk
MODIFIABLE RISK FACTORS High blood pressure Diabetes Cigarette smoking TIA (Aspirin) High blood cholesterol Obesity Heart Disease Atrial fibrillation Oral contraceptive use Physical inactivity Sickle cell disease Hypercoagulability
Based on symptoms Cortical lesion Focal seizures Aphasia Never produce hemiplegia Differential limb involvement Cortical senory loss
Corona radiata One limb more involved than other Cortical sensory loss No cortical signs Internal capsule Dense hemiplegia Homonymous hemianopia Hemia n esthesia
Thalamus Contralateral hemisensory loss associated with agonising or burning pain - Dejerine roussy syndrome Brain stem Midbrain Weber syn . - Ipsilateral 3rd nerve palsy + contralateral hemiplegia Claud's syn - 3 rd + Cintrolateral ataxia
Pons ( 4 p's ) Pinpoint pupil Pyrexia Paralysis Gaze palsy Loss of dolls eye reflex
Stem occlusion contralateral hemiplegia contralateral hemianeasthesia homonymous hemianopia conjugate gaze palsy dysarthria due to facial weakness Dominant – global aphasia Nondominant - constructional apraxia
Distal branch- weakness of hand weakness of hand and arm facial weakness with Bro ca’s aphasia If superior division – motor sensory and broca’s aphasia(FRONTAL & SUPERIOR PARIETAL CORTEX) If inferior division- wernicke’s aphasia(INFERIOR PARIETAL AND TEMPORAL CORTEX)
ANTERIOR CEREBRAL ARTERY A1 OCCLUSION – No loss due to collateral through anterior communicating artery A2 OCCLUSION – paralysis of contralateral leg less degree paresis of contralateral arm cortical sensory loss of lower limb urinary incontinence
STROKE WITHIN POSTERI O R CIRCULATION POSTERIOR CEREBRAL ARTERY VERTEBRAL AND POSTERIOR INFERIOR CEREBELLAR ARTERY BASILAR ARTERY
POSTERIOR CEREBRAL ARTERY P1 SYNDROME - C/L Hemiplegia + 3 rd nerve palsy(WEBER’S SYNDROME) C/L ataxia + 3 rd nerve palsy (CLAUDE’S SYNDROME) C/L Hemisensory loss followed by agonizing pain in the affected area (THALAMIC DEJERINE ROUSSY SYNDROME) P2 SYNDROME -C/L homonymous hemianopia with macula sparing
VERTEBRAL AND PICA
LATERAL MEDULLARY SYNDROME(occlusion of vertebral, posterior inferior cerebellar , superior, middle or inferior lateral medullary artery) Vertigo, Numbness of ipsilateral face and c/l limb,diplopia , dysphagia , dysarthria , hoarseness,ipsilateral horner’s syndrome
Medial medullary syndrome(occlusion of vertebral artery or branch of vertebral or lower basilar artery) ipsilateral atrophy of half the tongue contralateral paralysis of arm and leg sparing face
BASILAR ARTERY Supply base of pons and superior cerebellum Fall into three groups PARAMEDIAN(wedge of pons on either side of midline) SHORT CIRCUMFERENTIAL(Lateral 2/3 rd of pons,middle & superior cerebellar peduncles) SUPERIOR CEREBELLAR & ANTERIOR INFERIOR CEREBELLAR( Cerebellar hemispheres)
BASILAR ARTERY SYNDROME Complete Occlusion b/l long tract signs(sensory and motor) Signs of cranial nerve & cerebellar dysfunction Occlusion of a branch u/l motor and sensory signs and cranial nerves
FEATURE THROMBOTIC EMBOLIC HAEMORRHAGIC Age Middle or old Young Middle or old Onset and progression Less rapid, stepwise In seconds Catastrophic, rapidly prog. Time of onset In sleep, soon after waking Any time During activity Vomiting Ab, occasional Absent Recurrent Headache Mild or absent Mild or ab Prominent Early resolution Variable Possible Unusual Meningeal irritation Absent Absent May be present BP High Normal Usually high
FEATURE THROMBOTIC EMBOLIC HEMORRHAGIC Carotid bruit Highly supportive Possible Not seen CT Scan Pale infarct Pale infarct Haemorrhage CSF Usually normal Normal Blood stained, increased presurre