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Current concepts
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Emerging Risk Factors
• Helicobacter pylori
• HIV/AIDs
• CMV/EBV/HSV
• Increased CRP
• Hyperhomocysteinaemia
• RAS
CVD and major risk actorsCVD and major risk actors
• Tobacco
• Diet
• Alcohol
• Physical Activity
Behavioural
Risk Factors
Non-modifiable
Risk Factors
•Age
•Sex
•Race
•Genes
• SCD
• CADASIL
• MELAS
• Migraine with aura
Genetic factors:
MODIFIABLE RISK FACTORS
•Hypertension
•DM
•dyslipidaemia
•Obesity / Overweight
•OCP
•Migraine
•polycythemia
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Blood supply to the brain
CLASSIFICATION OF STROKE
Stroke
Primary Hemorrhagic
(20% of Strokes)
Primary Ischemic
(80% of Strokes)
Thrombotic
50%
Embolic
30%
Intracerebral
Hemorrhage 15%
Subarachnoid
Hemorrhage 5%
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Normal
ml/100g/mi
n
50 – 55 25 20 15
8
Ischemia
Edema Loss of Na/K+
electrical pump
↑lactate activity failure; ↓
ATP
Penumbra
Infarction
Cell
Death
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Penumbra
Infarction
Stroke Warning Signs
CLINICAL FEATURES OF
STROKE
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Brain swelling
Ventricular compression
Focal cortical effacement
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Ischemic stroke Hemorrhage stroke
Craniocerebral / cervical trauma
Meningitis/encephalitis
Intracranial mass
•Tumor
•Subdural hematoma
Seizure with persistent neurological signs
Migraine with persistent neurological signs
Metabolic
•Hyperglycemia (nonketotic hyperosmolar coma)
•Hypoglycemia
•Post-cardiac arrest ischemia
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Brain tissue
ischemia
Cerebral arterial
stenosis/occlusion
LAA/CE/SVD/others
Decreased CBF
Cerebral autoregulation
(endothelial function etc)
First stroke
blood
pressure
glucose
smoking
lipids
mass popl.
strategy
hypertension
TIA
Atrial fibrillation
other vascular disease
high risk strategy
stroke
mortality
acute treatment
Secondary
prevention
recurrent
stroke
Stroke related
disability
Rehabilitation
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THANK YOU
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Stroke

Notas del editor

  1. Once the brain cells die from a lack of oxygen, the part of the body that part of the brain controls is affected through paralysis, language, motor skills, or vision. These symptoms usually persists for stroke survivors making routine daily functions extremely difficult.
  2. Noninvasive vascular tests include magnetic-resonance angiography, computed tomography angiography, and carotid ultrasound. Invasive vascular tests include conventional cerebral angiography and measurement of lesions. However, invasive measures can be risky; they should be undertaken only when the risk of stroke or death is less than 1%.
  3. Cranial computerised tomography (CT) is widely available and not only reliably distinguishes between haemorrhage and ischemic stroke or subarachnoid haemorrhage but can also rule out many other brain diseases. Signs of early ischemia can sometimes be detected as early as two hours after stroke onset, but this may be difficult even for the trained examiner, in particular in very early studies. Early infarct signs include sulcus effacement, swelling of the basal ganglia and the hyper-intense middle cerebral artery sign. Early signs of extensive infarction with intracranial midline shifts indicate a very serious event and a high risk, both for secondary haemorrhage and large malignant oedema formation and may justify repeated imaging after a short interval. Parenchymal haemorrhage can be identified almost immediately either in deep structures in patients with hypertension or in atypical areas in patients without hypertension or under adequate treatment, usually due to cerebral amyloid angiopathy. Infratentorial haemorrhage or cerebellar infarcts can be identified similar to supratentorial lesions, but smaller haemorrhages/ischemic infarcts in particular in the brain stem may easily be missed. In addition, CT may detect subarachnoid blood in the majority of cases with subarachnoid hemorrhage. Sometimes haemorrhages may even be interpreted as primary, but indeed are secondary to ischemic events. involvement of clearly defined vascular territories are indicative of such conditions, which are easier to identify in MRI studies. Brain haemorrhages tend to grow in the first 6-12 hours after stroke in about 40%-50% of all patients even without clinical deterioratio, which makes a second early CT study necessary. CT angiography (CTA) is a reliable tool to obtain information on extra- and intracranial arterial patency, and its use in clinical practice often adds value to the diagnostic work-up (Schellinger et al. 2003).