Acute Ischaemic Stroke
Encounter flow
12/12 authoredCanonical 12-phase frame with authored status for this dossier.
Frame
Acute focal deficit suggesting ischaemia — exclude hemorrhage, mimic, post-ictal (AHA/ASA 2019)
stroke alert activated
Patient inputs (14)
Age affects EVT eligibility and bleeding risk (AHA/ASA 2019; DESTINY II, Jüttler NEJM 2014 — age <60 for hemicraniectomy)
Hypoglycaemia mimics stroke; hyperglycaemia worsens outcome (AHA/ASA 2019 Class I)
eGFR for contrast (CTA/CTP) and DOAC dose adjustment (AHA/ASA 2019)
Rule out hemorrhage before thrombolysis; ASPECTS scoring (AHA/ASA 2019 Class I)
LVO identification for EVT triage (AHA/ASA 2019 Class I)
NIHSS gates thrombolysis and EVT eligibility (≥6 for EVT; AHA/ASA 2019 Class I)
LKW determines tPA/TNK window ≤4.5 h (ECASS III, Hacke NEJM 2008) and EVT window ≤6 h or 6–24 h with mismatch (DAWN, Nogueira NEJM 2018; DEFUSE 3, Albers NEJM 2018)
SBP <185/110 pre-tPA; <180/105 × 24 h post-tPA (AHA/ASA 2019 Class I); <220/120 if no thrombolysis
INR >1.7 contraindicates thrombolysis per AHA/ASA 2019 exclusion criteria
Platelets <100k contraindicates thrombolysis per AHA/ASA 2019 exclusion criteria
DOAC last dose; need anti-Xa or DTI levels; affects tPA eligibility (AHA/ASA 2019)
Major surgery <14 d / GI/GU bleed <21 d are tPA contraindications (AHA/ASA 2019)
Mismatch selection for 6–24 h window (DAWN, Nogueira NEJM 2018; DEFUSE 3, Albers NEJM 2018)
AF as cardioembolic source → anticoagulation timing decision (2024 ESC AF guidelines)
* = hard-required. Engine cannot meaningfully run until these are filled.
Severity triggers (13)
- informationallife_threateningbasilar_occlusionBasilar artery occlusion — any NIHSS (ATTENTION 2022; BAOCHE 2022)Trigger could not be auto-evaluated — needs clinician judgement.
- informationallife_threateninghemorrhagic_transformation_post_tpaNew severe headache, HTN, N/V, or NIHSS decline ≥4 within 24 h post-tPA (AHA/ASA 2019)Trigger could not be auto-evaluated — needs clinician judgement.
- informationallife_threateningmalignant_mca_patternNIHSS ≥15, infarct >50% MCA territory on imaging, age <60, decline within 48 h (DESTINY II, Jüttler NEJM 2014)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalseverelvo_within_24hLVO on CTA + within 24 h LKW + ASPECTS ≥6 OR imaging mismatch (AHA/ASA 2019 Class I)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalseverenihss_deterioration_ge_4NIHSS increase ≥4 points within 24 h regardless of pre-existing therapy (AHA/ASA 2019 Class I)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalseveretoast_laa_phenotypeTOAST class: large-artery atherosclerosis — carotid stenosis ≥50% ipsilateral on CTA/MRA/duplex OR intracranial atherosclerosis on vessel wall MRITrigger could not be auto-evaluated — needs clinician judgement.
- informationalseveretoast_ce_phenotypeTOAST class: cardioembolic — AF on telemetry/ECG; LV thrombus on TTE; mechanical valve; large embolic-pattern infarct (cortical or multi-territory)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalseveretoast_ode_phenotypeTOAST class: other-determined etiology — vessel-wall MRI dissection sign; antiphospholipid antibodies positive; hypercoag panel positive (protein C/S, antithrombin, factor V Leiden); CNS vasculitis on DSATrigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatepre_tpa_bp_above_ceilingSBP >185 OR DBP >110 with otherwise tPA-eligible patient (AHA/ASA 2019 Class I)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatepost_tpa_bp_above_ceilingSBP >180 OR DBP >105 within 24 h post-tPA (AHA/ASA 2019 Class I)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatedysphagia_aspiration_riskFailed bedside swallow screen (3-oz water test, GUSS, or formal SLP evaluation) prior to any PO including oral medications (AHA/ASA 2019 Class I)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatetoast_svo_phenotypeTOAST class: small-vessel occlusion (lacunar) — infarct <1.5 cm on DWI in perforator territory; classic lacunar syndrome (pure motor, pure sensory, ataxic-hemiparesis, sensorimotor, dysarthria-clumsy-hand)Trigger could not be auto-evaluated — needs clinician judgement.
- informationalmoderatetoast_ude_phenotypeTOAST class: undetermined etiology (cryptogenic / ESUS) — all large-artery + cardioembolic + small-vessel workup negativeTrigger could not be auto-evaluated — needs clinician judgement.
Workflow calculators
Run this disease's risk and dosing calculators inline.
Recommended regimen
Acute reperfusion (IV thrombolysis ± EVT) + BP control + early antiplatelet (AHA/ASA 2019)- alteplasefirst linetissue_plasminogen_activator0.9 mg/kg IV (max 90 mg); 10% as bolus over 1 min, remaining 90% as infusion over 60 min • IV • single course (max: 90 mg total)triggers: LKW_<=4.5h, no_hemorrhage, no_contraindicationNINDS / ECASS-III — thrombolysis ≤4.5h reduces disabilityrxcui 8410
- tenecteplasefirst linetissue_plasminogen_activator0.25 mg/kg IV single bolus over 5 sec (max 25 mg) • IV • single bolus (max: 25 mg total)triggers: LKW_<=4.5h, AcT_eligibleAcT (Lancet 2022) — TNK 0.25 mg/kg non-inferior to alteplase; preferred per 2026 AHA/ASArxcui 259280
outpatient playbook — drug actions (5)
- 1. atorvastatin80 mg PO daily • PO • once dailytrigger: Atherosclerotic stroke; LDL ≥552026 ACC/AHA Lipid — high-intensity statin LDL <55 mg/dL post-stroke (AHA/ASA 2021 Class I)
- 2. apixaban OR rivaroxabanApixaban 5 mg PO BID (2.5 mg if 2 of: age ≥80 / weight ≤60 kg / Cr ≥1.5); rivaroxaban 20 mg PO daily with food (15 mg if CrCl 15–50) • PO • BID / dailytrigger: AF detected; sustained per ESC AF2024 ESC AF — DOAC preferred; ARISTOTLE / ROCKET-AF anchor
- 3. aspirin81 mg PO daily • PO • once dailytrigger: Non-cardioembolic stroke; no DAPT indicationAHA/ASA 2021 — chronic antiplatelet for non-cardioembolic ischemic stroke
- 4. ACEI/ARB + thiazideLisinopril 10–40 mg PO daily; chlorthalidone 12.5–25 mg PO daily; titrate to BP <130/80 • PO • dailytrigger: BP ≥130/802025 AHA/ACC HTN; PROGRESS trial perindopril-indapamide reduced recurrent stroke
- 5. varenicline OR nicotine replacement OR bupropionVarenicline 0.5 mg PO daily × 3 d → 0.5 BID × 4 d → 1 mg BID × 11 wk • PO / patch / lozenge • per agenttrigger: Active tobacco useAHA/ASA 2021 Class I — smoking cessation pharmacotherapy for stroke survivors
Auto-drafted A&P note
outpatientSubjective
- Possible entry pathways: Sudden focal neurological deficit (FAST/BEFAST; AHA/ASA 2019); Aphasia / dysarthria of sudden onset (AHA/ASA 2019); Hemiparesis / facial droop (AHA/ASA 2019).
Objective
- No vitals, labs, or imaging entered for this encounter.
Assessment
**Acute Ischaemic Stroke** (neuro.ischaemic-stroke.v1). Phenotype framing: TOAST classification (Adams Stroke 1993): large-artery atherothrombotic / cardioembolic / lacunar / cryptogenic / other Scope: Acute focal deficit suggesting ischaemia — exclude hemorrhage, mimic, post-ictal (AHA/ASA 2019) No severity triggers fired against current inputs.
Plan
Regimen axis: **Acute reperfusion (IV thrombolysis ± EVT) + BP control + early antiplatelet (AHA/ASA 2019)** — step "Step 1 — IV thrombolysis ≤4.5 h (NINDS 1995; ECASS III, Hacke NEJM 2008)". 1. alteplase 0.9 mg/kg IV (max 90 mg); 10% as bolus over 1 min, remaining 90% as infusion over 60 min IV single course (tissue_plasminogen_activator, first line) — NINDS / ECASS-III — thrombolysis ≤4.5h reduces disability 2. tenecteplase 0.25 mg/kg IV single bolus over 5 sec (max 25 mg) IV single bolus (tissue_plasminogen_activator, first line) — AcT (Lancet 2022) — TNK 0.25 mg/kg non-inferior to alteplase; preferred per 2026 AHA/ASA Setting playbook (outpatient) — Stroke-clinic follow-up at 90 d + 12 mo: TOAST-driven secondary prevention reconciliation, BP <130/80, LDL <55, DOAC adherence, mRS outcome capture, post-stroke depression / cognitive screen, OSA + driving + vocational evaluation (AHA/ASA 2021) 3. atorvastatin 80 mg PO daily PO once daily — Atherosclerotic stroke; LDL ≥55 (2026 ACC/AHA Lipid — high-intensity statin LDL <55 mg/dL post-stroke (AHA/ASA 2021 Class I)) 4. apixaban OR rivaroxaban Apixaban 5 mg PO BID (2.5 mg if 2 of: age ≥80 / weight ≤60 kg / Cr ≥1.5); rivaroxaban 20 mg PO daily with food (15 mg if CrCl 15–50) PO BID / daily — AF detected; sustained per ESC AF (2024 ESC AF — DOAC preferred; ARISTOTLE / ROCKET-AF anchor) 5. aspirin 81 mg PO daily PO once daily — Non-cardioembolic stroke; no DAPT indication (AHA/ASA 2021 — chronic antiplatelet for non-cardioembolic ischemic stroke) 6. ACEI/ARB + thiazide Lisinopril 10–40 mg PO daily; chlorthalidone 12.5–25 mg PO daily; titrate to BP <130/80 PO daily — BP ≥130/80 (2025 AHA/ACC HTN; PROGRESS trial perindopril-indapamide reduced recurrent stroke) 7. varenicline OR nicotine replacement OR bupropion Varenicline 0.5 mg PO daily × 3 d → 0.5 BID × 4 d → 1 mg BID × 11 wk PO / patch / lozenge per agent — Active tobacco use (AHA/ASA 2021 Class I — smoking cessation pharmacotherapy for stroke survivors) Non-pharmacologic actions: - AHA "Get With The Guidelines" outcome measure documentation — mRS, smoking cessation, statin compliance, BP at target, antithrombotic on board, AF screen completed (AHA/ASA 2021) - Recurrent-stroke counselling — symptom recognition, when to call 911, do NOT delay even if symptoms transient - Advance directives + power-of-attorney discussion (AHA/ASA 2021) - Pulmonary rehab referral if comorbid COPD (GOLD 2026) - Diabetes self-management education if applicable (ADA 2026) - Sleep study (PSG or home test) if STOP-BANG ≥3 (AHA/ASA 2021) - Polysomnography-directed CPAP titration if OSA confirmed (AHA/ASA 2021) - Mediterranean diet counselling (PREDIMED trial) - Aerobic exercise prescription 150 min/wk moderate intensity (AHA/ASA 2021 Class I) AVOID / contraindication checks: - TPA_contraindications_INR_platelets_recent_surgery (AHA/ASA 2019) - TPA_BP_<185/110_required_pre_thrombolysis (AHA/ASA 2019 Class I) - DAPT_only_minor_stroke_or_high_risk_TIA (POINT 2018; CHANCE 2013) - Antiplatelet_after_tPA_wait_24h_with_repeat_CT (AHA/ASA 2019 Class I) - Glucose_correction_before_code_stroke (AHA/ASA 2019)
Monitoring
Regimen monitoring: - NIHSS q15 min during tPA infusion (AHA/ASA 2019) - NIHSS q1 h × 24 h post-tPA (AHA/ASA 2019) - BP q15 min × 2 h then q30 min × 6 h then q1 h (AHA/ASA 2019) - Repeat CT at 24 h post-tPA before antiplatelet (AHA/ASA 2019 Class I) - Continuous telemetry for AF detection (AHA/ASA 2019) - Glucose q4 h target 140–180 mg/dL (AHA/ASA 2019) Setting (outpatient) monitoring: - Clinic visit at 7–14 d post-discharge for medication reconciliation (AHA/ASA 2021) - Stroke clinic at 90 d (mRS, secondary prevention bundle audit) and 12 mo (long-term outcome) - BP home log + clinic check q3 mo until at goal then q6 mo (2025 AHA/ACC HTN) - Lipid panel at 4–6 wk after statin start; then q6–12 mo (2026 ACC/AHA Lipid) - HbA1c q3 mo if diabetic until controlled, then q6 mo (ADA 2026) - Renal function q6 mo on DOAC; q3 mo if CrCl 30–50 (2024 ESC AF) - INR weekly until stable then q4 wk if on warfarin (ACCP 2018) - PHQ-9 + MoCA at 90 d, 6 mo, 12 mo (AHA/ASA 2021) Follow-up plan: Secondary prevention: high-intensity statin LDL <55 (2026 ACC/AHA Lipid), BP <130/80 (2025 AHA/ACC HTN), DAPT/anticoag per source, dysphagia/SLP, rehab, AF screen - Close-out criterion: secondary-prevention bundle prescribed + outpatient stroke clinic scheduled Monitoring phase: Neuro checks q15 min × 2 h → q30 min × 6 h → q1 h × 16 h; BP per AHA/ASA 2019 protocol; continuous telemetry for AF
Disposition
Current setting: outpatient — Stroke-clinic follow-up at 90 d + 12 mo: TOAST-driven secondary prevention reconciliation, BP <130/80, LDL <55, DOAC adherence, mRS outcome capture, post-stroke depression / cognitive screen, OSA + driving + vocational evaluation (AHA/ASA 2021) Disposition criteria: - Continue indefinite secondary-prevention regimen — no de-escalation of antiplatelet/anticoagulant unless explicit risk-benefit shift (AHA/ASA 2021) - Transition from rehab to community-based exercise programs at 6–12 mo per functional status (AHA/ASA 2021) Escalation triggers (move to higher acuity): - Any new TIA-spectrum or stroke-like event → ED (AHA/ASA 2021) - BP persistently >140/90 despite 3-drug regimen → resistant HTN workup (cardio.htn.resistant.v1; 2025 AHA/ACC HTN) - PHQ-9 ≥15 OR suicidal ideation → urgent psych referral (AHA/ASA 2021) - MoCA <26 OR cognitive decline noted by family → neurocognitive workup; consider donepezil per AHA/ASA 2021 - Statin intolerance → ezetimibe + PCSK9i if LDL >55 (2026 ACC/AHA Lipid) - DOAC bleeding event → temporary hold, reversal if life-threatening (idarucizumab / andexanet), reassess net benefit
Earlier-Return Triggers
Return-precaution thresholds (watch for): - [LIFE_THREATENING] Basilar artery occlusion — any NIHSS (ATTENTION 2022; BAOCHE 2022) - [LIFE_THREATENING] New severe headache, HTN, N/V, or NIHSS decline ≥4 within 24 h post-tPA (AHA/ASA 2019) - [LIFE_THREATENING] NIHSS ≥15, infarct >50% MCA territory on imaging, age <60, decline within 48 h (DESTINY II, Jüttler NEJM 2014)
Citations
- 2026 AHA/ASA Guideline for the Early Management of Patients With Acute Ischemic Stroke (Stroke 2026; DOI 10.1161/STR.0000000000000513) + 2024 AHA/ASA Primary Prevention + 2024 ESC AF + 2025 AHA/ACC HTN + 2026 ACC/AHA Dyslipidemia [PMID:7477192](https://pubmed.ncbi.nlm.nih.gov/7477192/) - Cited evidence (PMID 18815396) [PMID:18815396](https://pubmed.ncbi.nlm.nih.gov/18815396/) - Cited evidence (PMID 35779553) [PMID:35779553](https://pubmed.ncbi.nlm.nih.gov/35779553/) - Cited evidence (PMID 25517348) [PMID:25517348](https://pubmed.ncbi.nlm.nih.gov/25517348/) - Cited evidence (PMID 25671798) [PMID:25671798](https://pubmed.ncbi.nlm.nih.gov/25671798/) Last reconciled with current guidelines: 2026-05-18.
- 2026 AHA/ASA Guideline for the Early Management of Patients With Acute Ischemic Stroke (Stroke 2026; DOI 10.1161/STR.0000000000000513) + 2024 AHA/ASA Primary Prevention + 2024 ESC AF + 2025 AHA/ACC HTN + 2026 ACC/AHA Dyslipidemia — PMID:7477192
- Cited evidence (PMID 18815396) — PMID:18815396
- Cited evidence (PMID 35779553) — PMID:35779553
- Cited evidence (PMID 25517348) — PMID:25517348
- Cited evidence (PMID 25671798) — PMID:25671798