MACOCHA Score
Critical Clarification
The MACOCHA score is NOT a stroke recurrence risk prediction tool—it is a score used to predict difficult intubation in critically ill patients in the intensive care unit. 1 The question appears to confuse MACOCHA with stroke risk stratification scores like ABCD2 or ABCD3-I, which are used to predict stroke recurrence after TIA or minor stroke.
If You Meant Stroke Risk Stratification (ABCD2/High-Risk TIA or Stroke)
For patients presenting with high-risk features for stroke recurrence (motor weakness, speech disturbance, or symptoms within 48 hours):
Immediate Actions (Within 24 Hours)
Patients with motor weakness, speech disturbance, or presentation within 48 hours of symptom onset require immediate emergency department evaluation with stroke team activation, as the 7-day stroke recurrence risk can reach 36% in high-risk patients without urgent intervention. 2
- Send immediately to ED with advanced stroke care capabilities (on-site brain imaging and acute stroke treatment access) 2, 1
- Complete urgent brain imaging (CT or MRI) within 24 hours—MRI with diffusion-weighted imaging shows 77% sensitivity within 3 hours versus only 16% for CT 1
- Perform non-invasive vascular imaging (CTA or MRA from aortic arch to vertex) without delay to identify large vessel occlusions requiring mechanical thrombectomy and carotid stenosis requiring urgent revascularization 2, 1
- Obtain ECG immediately and initiate cardiac rhythm monitoring to detect atrial fibrillation 2, 1
Risk Stratification by Timing
Very High Risk (within 48 hours): 2
- Transient, fluctuating, or persistent unilateral weakness (face, arm, leg)
- Transient, fluctuating, or persistent language/speech disturbance
- Recurrence risk: 1.5% at 2 days, 2.1% at 7 days with optimal rapid intervention 2
High Risk (48 hours to 2 weeks): 2
- Same symptoms as above but presenting later
- Requires comprehensive evaluation by stroke specialist within 24 hours of healthcare contact
Antiplatelet Management
For nondisabling stroke or high-risk TIA (ABCD2 score ≥4) without severe carotid stenosis or atrial fibrillation, initiate dual antiplatelet therapy with aspirin plus clopidogrel within 24 hours of presentation. 3
- Continue dual antiplatelet therapy for 21 days, then transition to single antiplatelet agent 3
- This reduces 90-day stroke risk from 7.8% to 5.2% (hazard ratio 0.66) 3
- Do NOT use dual antiplatelet therapy beyond 30 days—adverse events including major bleeding and mortality occur more frequently with no reduction in ischemic events 4
Carotid Stenosis Management
If carotid stenosis ≥70% is identified, urgent carotid revascularization (endarterectomy or stenting) should be performed, as absolute benefit is highest within the first 2 weeks after the event. 1, 5
- Symptomatic carotid stenosis ≥70% is an independent predictor of in-hospital stroke recurrence 5
- These patients should receive single antiplatelet therapy, not dual therapy 3
Atrial Fibrillation Management
For patients with atrial fibrillation, initiate oral anticoagulation with a direct oral anticoagulant (DOAC) preferred over warfarin. 2
- For TIA without cerebral infarction: Initiate anticoagulation early due to low hemorrhagic transformation risk 2
- For minor stroke (NIHSS ≤5): Can initiate within days 2
- For large stroke (NIHSS >15 or complete arterial territory involvement): Delay anticoagulation for 14 days to allow blood-brain barrier healing 2
- DOACs reduce stroke/systemic embolism by 19% and hemorrhagic stroke by 51% versus warfarin 2
Additional Secondary Prevention
- Continue statin therapy if already taking at time of stroke onset 1
- Control hypertension with antihypertensive agents 2
- Address modifiable risk factors: smoking cessation, weight loss, regular exercise, diabetes management 2, 4
Common Pitfalls
- Do NOT use anticoagulation acutely in non-cardioembolic stroke—it increases bleeding risk more than aspirin without proven benefit 1
- Do NOT delay carotid revascularization beyond 2 weeks in symptomatic severe stenosis—benefit decreases significantly with time 1
- Do NOT continue dual antiplatelet therapy beyond 21-30 days in most patients—bleeding risk outweighs benefit 3, 4