Provide rescent stroke guideline
"ischemic stroke" AND "guidelines"
"acute ischemic stroke" AND "mechanical thrombectomy"
PMID: 39429201
"hemorrhagic stroke" AND "management"
"stroke" AND "secondary prevention" AND "AHA"
PMID: 38158224
| Time Window | Recommendation |
|---|---|
| 0–3 hours | IV alteplase 0.9 mg/kg (max 90 mg) over 60 min; initial 10% as bolus over 1 min. Recommended for all eligible patients ≥18 years regardless of age (≤80 or >80) |
| 3–4.5 hours | Recommended for patients ≤80 years, no history of both DM + prior stroke, NIHSS ≤25, not on oral anticoagulants, <1/3 MCA territory involvement |
| Mild disabling stroke | IV alteplase recommended even for mild but disabling deficits within 3 h |
| Severe stroke | Recommended despite increased hemorrhagic transformation risk — net benefit proven |
| Feature | Recommendation |
|---|---|
| Indication | Large vessel occlusion (LVO) of anterior circulation, proven on CTA/MRA |
| Time window (early) | 0–6 hours from last known well — regardless of IV alteplase eligibility |
| Time window (late) | 6–24 hours with imaging-guided patient selection (DAWN / DEFUSE-3 criteria): small core infarct + large penumbra via perfusion imaging |
| IV alteplase first? | Give IV alteplase before thrombectomy if eligible — do not delay thrombectomy for alteplase infusion |
| Device choice | Stent retrievers or large-bore aspiration catheters (equivalent outcomes); balloon guide catheters improve first-pass reperfusion |
| Posterior circulation | Basilar artery occlusion — EVT beneficial; evidence from ATTENTION and BAOCHE trials |
Time is brain: Every 1-hour delay to reperfusion worsens disability outcomes. Target door-to-puncture ≤90 min.
| Agent | Reversal |
|---|---|
| Warfarin | Prothrombin complex concentrate (PCC) + Vitamin K; avoid rFVIIa |
| Alteplase-related sICH | Cryoprecipitate 10 U IV (target fibrinogen ≥150 mg/dL) |
| Direct thrombin inhibitors | Idarucizumab (dabigatran) |
| Factor Xa inhibitors | Andexanet alfa |
| Risk Factor | Target |
|---|---|
| Blood pressure | <130/80 mmHg |
| LDL-C | <70 mg/dL (high-risk); consider <55 mg/dL for very high-risk |
| HbA1c | <7% for most diabetic patients |
| Smoking cessation | Immediate — doubles stroke risk |
| Guideline | Source | Year | PMID |
|---|---|---|---|
| Primary Prevention of Stroke | AHA/ASA (Stroke) | 2024 | 39429201 |
| PFO After Stroke | European Stroke Organisation | 2024 | 38752755 |
| Ischaemic Cerebrovascular Disease | Chinese Stroke Association | 2023 update | 38158224 |
| Reperfusion Therapy (AIS) | Chinese Stroke Association | 2024 | 39832918 |
| Tenecteplase vs. Alteplase Meta-Analysis | Neurology | 2024 | 39413337 |
| Cervical Artery Dissection Antithrombotic Rx | JAMA Neurol | 2024 | 38739383 |
| Global Stroke Guidelines Synthesis | World Stroke Organization (Int J Stroke) | 2023 | 36725717 |
Note: The AHA/ASA 2024 Acute Ischemic Stroke Treatment Guideline update (anticipated) had not been fully published as of the textbook editions available. The 2019 AHA/ASA criteria remain the current backbone for thrombolysis eligibility; tenecteplase has been increasingly incorporated as an equivalent alternative. Always verify local institutional protocols and the most current AHA/ASA full-text guidelines at AHA Professional Heart Daily.
Posterior circulation stroke management guideline
"posterior circulation stroke" AND "management"
"basilar artery occlusion" AND "thrombectomy"
PMID: 38752743
PMID: 39674187
PMID: 36239644
PMID: 36239645
PMID: 41655588
PMID: 39186280
"posterior circulation" AND "ischemic stroke" AND "thrombolysis"
PMID: 38395096
PMID: 41257736
| Territory | Classic Presentation |
|---|---|
| Basilar artery | Bilateral limb weakness, dysarthria, diplopia, oculomotor palsies, decreased consciousness; locked-in syndrome (bilateral ventral pontine lesion — paralysis except vertical gaze/blink) |
| Lateral medullary (Wallenberg/PICA) | Ipsilateral facial numbness + Horner's, contralateral body pain/temp loss, vertigo, dysphagia, ataxia |
| Cerebellar (PICA/AICA/SCA) | Vertigo, vomiting, gait ataxia, nystagmus, dysmetria; may mimic labyrinthitis |
| AICA | Vertigo, facial weakness, ipsilateral hearing loss, ataxia, Horner's |
| PCA | Contralateral homonymous hemianopia, amnesia, alexia without agraphia |
| Vertebrobasilar (proximal) | Dizziness, nausea, headache, dysphagia, hemiataxia, Horner's |
⚠️ Up to 25% of posterior fossa infarcts have a normal non-contrast CT — if posterior circulation stroke is suspected with normal CT, obtain urgent diffusion-weighted MRI. CTA/MRA is essential to identify vascular occlusion. — Tintinalli's Emergency Medicine
🔑 Key ESO/ESMINT 2024 expert consensus: IVT (including beyond 4.5 h) is suggested for BAO patients up to 24 hours unless contraindicated, given the very poor natural history of untreated BAO.
| Trial | Design | Time Window | Primary Outcome (mRS 0–3 at 90d) | Thrombectomy vs Control |
|---|---|---|---|---|
| ATTENTION (NEJM 2022, PMID 36239644) | RCT, 340 pts, China | 0–12 h | 46% vs 23% | aRR 2.06 (p<0.001); mortality 37% vs 55% |
| BAOCHE (NEJM 2022, PMID 36239645) | RCT, 217 pts, China | 6–24 h | 46% vs 24% | aRR 1.81 (p<0.001); trial stopped early for superiority |
| BASICS | RCT, Europe/Brazil | 0–6 h | Non-significant overall benefit | Benefit in moderate-severe NIHSS ≥10 |
| BEST | RCT, China | 0–8 h | Non-significant overall | High crossover rate |
| Clinical Situation | Recommendation |
|---|---|
| IVT vs no IVT | Expert Consensus: Suggest IVT up to 24 hours unless contraindicated |
| IVT + EVT vs direct EVT | Suggest IVT + EVT over direct EVT (bridging preferred) |
| EVT within 0–6 h (NIHSS ≥10) | Suggest EVT + BMT over BMT alone (very low certainty of evidence) |
| EVT within 6–24 h (NIHSS ≥10) | Suggest EVT + BMT over BMT alone (BAOCHE data) |
| NIHSS <10 (mild stroke) | No evidence to recommend EVT — BMT non-significantly better + safer |
| Extensive bilateral/brainstem ischaemic changes | Expert Consensus: against reperfusion therapy |
| Collateral scores | Reperfusion therapy regardless of collateral score (insufficient evidence to restrict) |
| Thrombectomy device | Suggest direct aspiration over stent retriever as first-line (limited evidence) |
| Failed EVT | Expert Consensus: rescue PTA/stenting considered |
| Antithrombotic during/after EVT | Suggest add-on antithrombotic if: no concurrent IVT AND EVT complicated (failed, imminent re-occlusion, or stenting required) |
| Intervention | Indication |
|---|---|
| Hypertonic saline (3% or 23.4%) or mannitol | Symptomatic ICP elevation as bridge to surgery; HTS slightly superior in meta-analysis |
| External ventricular drain (EVD) | Acute obstructive hydrocephalus |
| Suboccipital craniectomy (posterior fossa decompression) | Onset of brainstem compression or hydrocephalus — should be performed promptly, not delayed; "ventricular drainage alone is usually inadequate" — Adams & Victor's Neurology |
⚠️ Ventricular drainage alone is inadequate for cerebellar herniation — surgical decompression of swollen tissue is required as soon as edema becomes clinically apparent. A brief observation period is acceptable only if 4th ventricle and perimesencephalic cisterns remain open and patient is awake. — Adams & Victor's Principles of Neurology, 12th Ed.
| Etiology | Management |
|---|---|
| Cardioembolic (AF) | DOAC (apixaban preferred); initiate within 1–14 days based on infarct size |
| Large artery atherosclerosis (vertebral/basilar) | DAPT (aspirin + clopidogrel) for 21–90 days → single antiplatelet; high-intensity statin (LDL <70 mg/dL); aggressive BP control |
| Intracranial atherosclerosis | DAPT for ≥3 months; consider intracranial angioplasty/stenting only if refractory |
| Small vessel disease (lacunar) | Single antiplatelet; strict BP control (target <130/80 mmHg) |
| Vertebral artery dissection | Antiplatelet or anticoagulation — equivalent efficacy (CADISS trial); anticoagulation for 3–6 months then reassess |
| Subclavian steal | Surgical/endovascular revascularization if symptomatic |
| Factor | Target |
|---|---|
| Blood pressure (long-term) | Systolic <130 mmHg |
| LDL cholesterol | <70 mg/dL (atherosclerotic etiology); <55 mg/dL (very high risk) |
| HbA1c | <7% |
| Physical activity | 150 min moderate/week |
| Smoking | Cessation |
| Strategy | mRS 0–2 Ranking (SUCRA) | sICH Risk | Mortality |
|---|---|---|---|
| EVT + IVT | Best (0.83) | Highest | Intermediate |
| EVT alone | Intermediate (0.36) | Intermediate | Highest |
| IVT alone | Lowest (0.30) | Lowest | Lowest |
Combined EVT + IVT has the highest probability of best functional outcome for posterior circulation LVO. However, IVT alone is safest (lowest sICH, lowest mortality). Individualize based on patient profile.
| Guideline / Study | Source | Year | PMID |
|---|---|---|---|
| ESO/ESMINT BAO Acute Management | Eur Stroke J | 2024 | 38752743 |
| VERITAS Individual Patient Meta-Analysis | Lancet | 2025 | 39674187 |
| TRACE-5: Tenecteplase in BAO (24h window) | Lancet | 2026 | 41655588 |
| ATTENTION Trial (EVT 0–12h BAO) | NEJM | 2022 | 36239644 |
| BAOCHE Trial (EVT 6–24h BAO) | NEJM | 2022 | 36239645 |
| ATTENTION 1-year follow-up | JAMA Neurol | 2024 | 39186280 |
| IVT for Posterior Circulation Stroke | J Stroke Cerebrovasc Dis | 2024 | 38395096 |
| Revascularization Network Meta-analysis | BMC Neurol | 2025 | 41257736 |
Posterior circulation stroke management guideline
| Scenario | Recommendation |
|---|---|
| <4.5 h (standard) | Alteplase 0.9 mg/kg or tenecteplase 0.25 mg/kg — same criteria as anterior circulation |
| 4.5–24 h (BAO) | ESO/ESMINT 2024 Expert Consensus: Suggest IVT up to 24 h unless contraindicated |
| Tenecteplase in BAO within 24 h | TRACE-5 trial (Lancet 2026): mRS 0–1 rate 38% vs 29% (aRR 1.50, p=0.014) — superior to standard treatment |
| Time Window | Evidence | Recommendation |
|---|---|---|
| 0–12 h | ATTENTION trial: 46% vs 23% mRS 0–3 (p<0.001) | Recommend EVT + best medical treatment (NIHSS ≥10) |
| 6–24 h | BAOCHE trial: 46% vs 24% mRS 0–3 (p<0.001) | Recommend EVT + best medical treatment (NIHSS ≥10) |
| NIHSS <10 | VERITAS meta-analysis (Lancet 2025, n=988): no benefit | No EVT recommendation — BMT safer |
| Extensive bilateral/brainstem ischemia | ESO/ESMINT 2024 | Against reperfusion therapy |
| Etiology | Treatment |
|---|---|
| Atrial fibrillation | DOAC (apixaban preferred) |
| Vertebral/basilar atherosclerosis | DAPT × 21–90 days → single antiplatelet; statin (LDL <70); BP <130/80 |
| Vertebral artery dissection | Antiplatelet or anticoagulation × 3–6 months (equivalent — CADISS) |
| Small vessel disease | Single antiplatelet; BP control |
| Source | Year | PMID |
|---|---|---|
| ESO/ESMINT BAO Guideline | 2024 | 38752743 |
| VERITAS IPD Meta-analysis (Lancet) | 2025 | 39674187 |
| TRACE-5 Tenecteplase in BAO (Lancet) | 2026 | 41655588 |
| ATTENTION RCT — EVT 0–12h (NEJM) | 2022 | 36239644 |
| BAOCHE RCT — EVT 6–24h (NEJM) | 2022 | 36239645 |