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Referral and warning signs
When to refer
ALL suspected acute strokes require IMMEDIATE emergency assessment at a facility capable of performing urgent CT head scan (H/RR). Referral to stroke unit/neurologist/neurosurgery as appropriate based on stroke type, severity, and potential interventions (thrombolysis, mechanical thrombectomy, neurosurgery). Referral for rehabilitation services (physio, OT, speech therapy).
Red flags
- Sudden onset of focal neurological deficit (FAST symptoms)
- Decreased level of consciousness
- Severe headache (especially sudden 'thunderclap' onset)
- Signs of brainstem involvement (diplopia, vertigo, ataxia, bilateral weakness)
- Seizures at onset
Signs and symptoms
- Sudden onset of focal neurological deficits:
- - Unilateral weakness or numbness (hemiparesis/hemianaesthesia) - commonly face, arm, and/or leg.
- - Aphasia/Dysphasia (difficulty speaking or understanding speech).
- - Dysarthria (slurred speech).
- - Visual disturbances (hemianopia - loss of half of visual field, diplopia - double vision, sudden vision loss).
- - Dizziness, vertigo, loss of balance, ataxia (impaired coordination).
- - Severe headache (more common in haemorrhagic stroke, especially subarachnoid).
- - Altered level of consciousness (confusion, drowsiness, coma).
- - Seizures (may occur at onset or later).
Risk factors
- Hypertension (most important modifiable risk factor)
- Atrial Fibrillation (major risk for embolic stroke)
- Diabetes Mellitus
- Dyslipidemia
- Smoking
- Ischaemic Heart Disease / Previous MI
- Carotid artery stenosis
- Previous Stroke or Transient Ischaemic Attack (TIA)
- Age
- Family history of stroke
- Obesity, physical inactivity
- Sickle Cell Disease
- Certain blood clotting disorders
- Excessive alcohol consumption
- Illicit drug use (cocaine, amphetamines)
Diagnosis
Clinical assessment
Diagnosis based on rapid onset of characteristic focal neurological deficits. Use FAST acronym (Face drooping, Arm weakness, Speech difficulty, Time to call emergency) for public/rapid recognition. Differentiate stroke subtypes clinically if possible (see UCG table: Intracerebral Haemorrhage - gradual onset, reduced alertness; Subarachnoid - abrupt severe headache; Ischaemic (thrombotic) - gradual/stuttering onset; Ischaemic (embolic) - sudden maximal deficit). Important to rule out stroke mimics (seizure with post-ictal paralysis, migraine with aura, hypoglycaemia, tumour, infection, functional disorders).
Investigations
- Non-Contrast CT Scan (Head): Essential initial imaging. Rapidly differentiates ischaemic from haemorrhagic stroke (blood appears bright). Crucial before giving antiplatelet/anticoagulant/thrombolytic therapy. May be normal in early ischaemic stroke.
- MRI Scan (Head): More sensitive for detecting early ischaemia (DWI sequence), small infarcts, posterior fossa strokes, and helps identify cause (e.g., MRA for vessel occlusion/stenosis). Less readily available acutely.
- Blood Glucose: Rule out hypoglycaemia.
- ECG: Look for atrial fibrillation, signs of MI.
- Blood tests: FBC, U&Es, Coagulation screen (INR/PTT), Lipids.
- Echocardiogram: Assess for cardiac source of emboli (AF, valve disease, LV thrombus).
- Carotid Doppler Ultrasound: Assess for significant carotid stenosis.
- Lumbar Puncture: If subarachnoid haemorrhage suspected and CT negative (look for xanthochromia).
Diagnostic criteria
Clinical presentation of acute focal neurological deficit, with stroke subtype (ischaemic vs haemorrhagic) confirmed primarily by non-contrast CT head scan.
Management
Non-pharmacological management
- Acute Phase (Hyperacute care often in Stroke Unit where available):
- - ABCs: Ensure patent airway, adequate breathing/oxygenation (target SpO2 >94%), maintain circulation.
- - Blood Pressure Management: Controversial in acute ischaemic stroke. Generally, permit 'permissive hypertension' (e.g., up to 220/120 mmHg) unless patient eligible for thrombolysis (target <185/110) or has other compelling indication (e.g., APO, MI, aortic dissection). Lower BP cautiously if extremely high. In haemorrhagic stroke, more aggressive BP lowering often indicated (e.g., target SBP <140-160 mmHg).
- - Blood Glucose Control: Treat hypoglycaemia. Treat significant hyperglycaemia (e.g., insulin if >10-12 mmol/L).
- - Temperature Control: Treat fever aggressively (antipyretics).
- - Swallow Assessment: NPO until swallow screen performed to prevent aspiration. NG tube for feeding/meds if dysphagic.
- - Mobilisation: Early mobilisation and physiotherapy/occupational therapy/speech therapy as soon as stable.
- - DVT Prophylaxis: Intermittent pneumatic compression devices +/- prophylactic heparin (usually delayed 24-48h after ischaemic stroke, contraindicated initially in haemorrhagic).
Pharmacological treatment
- Acute Ischaemic Stroke:
- - Thrombolysis (IV Alteplase/tPA): If patient presents within treatment window (typically <4.5 hours from symptom onset), meets eligibility criteria (confirmed ischaemic stroke on CT, no contraindications like recent bleed/surgery, high BP), and facility has capability. (Highly specialized).
- - Antiplatelet Therapy: Aspirin 150-300mg started within 24-48 hours (after excluding haemorrhage on CT, and ideally 24h after thrombolysis if given).
- - Statin Therapy: High-intensity statin (e.g., Atorvastatin 40-80mg) should be started.
- Acute Haemorrhagic Stroke:
- - Reverse anticoagulation if applicable (e.g., Vitamin K/PCC for warfarin).
- - BP control (e.g., IV Labetalol, Nicardipine).
- - Neurosurgical consultation for potential evacuation of haematoma (esp. cerebellar) or management of hydrocephalus/raised ICP.
- Subarachnoid Haemorrhage:
- - Neurosurgical/Neurointerventional management of aneurysm (clipping/coiling).
- - Nimodipine to prevent vasospasm.
- - BP control, ICP management.
- Secondary Prevention (Chronic management after ischaemic stroke/TIA):
- - Antiplatelet therapy: Aspirin 75-100mg daily OR Clopidogrel 75mg daily (or combination for short period in specific cases).
- - Statin therapy (high intensity).
- - Antihypertensive therapy (target usually <140/90 or <130/80 depending on guidelines/risk).
- - Anticoagulation (Warfarin or DOAC): If stroke due to atrial fibrillation.
- - Risk factor management (diabetes, smoking cessation, lifestyle).
Monitoring
- Neurological status (e.g., using NIH Stroke Scale).
- Vital signs (BP, HR, SpO2, Temp).
- Blood glucose.
- Swallow function.
- Monitor for complications (cerebral oedema, haemorrhagic transformation, aspiration pneumonia, DVT/PE, UTI, pressure sores).
Complications
- Cerebral oedema / Increased intracranial pressure
- Haemorrhagic transformation of ischaemic stroke
- Seizures
- Aspiration pneumonia
- Deep Vein Thrombosis (DVT) / Pulmonary Embolism (PE)
- Urinary Tract Infection (UTI)
- Pressure sores
- Depression, anxiety, cognitive impairment
- Spasticity, contractures
- Shoulder pain (subluxation)
- Residual neurological deficit / Disability
- Recurrent stroke
Prevention
- Control of hypertension, diabetes, dyslipidemia.
- Smoking cessation.
- Management of atrial fibrillation (anticoagulation).
- Healthy diet, regular exercise, weight management.
- Carotid endarterectomy/stenting for significant symptomatic stenosis.
- Antiplatelet therapy for secondary prevention.
Patient education
- Explanation of stroke type, cause, and extent of damage.
- Risk factors and importance of secondary prevention (medications, lifestyle).
- Medication adherence (antiplatelets, statins, antihypertensives, anticoagulants).
- Recognizing signs of recurrent stroke (FAST) and seeking immediate help.
- Rehabilitation process and potential long-term deficits.
- Driving restrictions.
- Support groups and resources.
Uganda-specific notes
Stroke burden is increasing due to rise in NCDs. Access to urgent CT/MRI, thrombolysis, and specialized stroke care/rehabilitation is extremely limited, primarily available at national referral level. Management often focuses on clinical diagnosis, supportive care, BP control (often less aggressive targets due to limited monitoring), Aspirin for ischaemic stroke, and secondary prevention.
References
- Uganda Clinical Guidelines (UCG) 2023
Chapter 4, Section 4.1.11