VERSION: 1.0
CREATED: January 31, 2026
STATUS: Approved
DIAGNOSIS: Post-Stroke Management
ICD-10: I69.30 (Sequelae of cerebral infarction, unspecified), I69.398 (Other sequelae of cerebral infarction), I69.351 (Hemiplegia following cerebral infarction), I69.320 (Aphasia following cerebral infarction), I69.310 (Cognitive deficits following cerebral infarction), I69.10 (Sequelae of intracerebral hemorrhage, unspecified), Z86.73 (Personal history of transient ischemic attack and cerebral infarction without residual deficits)
SCOPE: Comprehensive post-stroke care from hospital discharge through long-term outpatient management. Covers secondary stroke prevention (antiplatelet, anticoagulation, statin, BP management), post-stroke rehabilitation, management of post-stroke complications (spasticity, depression, central pain, fatigue, cognitive decline, seizures, pseudobulbar affect), medication optimization, functional recovery monitoring, and return to activities. Excludes acute stroke management (see Acute Ischemic Stroke, ICH templates), acute rehabilitation admission protocols, and TIA workup (see TIA template).
PRIORITY KEY: STAT = Immediate | URGENT = Within hours | ROUTINE = Standard | EXT = Extended/atypical cases | - = Not applicable to this setting
Young stroke (<50) without clear etiology; recurrent stroke on appropriate therapy; protein C, protein S, antithrombin III, factor V Leiden, prothrombin G20210A, antiphospholipid antibodies
Normal; positive → hematology referral; may change anticoagulation strategy
Recurrent stroke; young patient; pregnancy loss history; livedo reticularis; lupus anticoagulant, anticardiolipin, anti-β2-glycoprotein I (confirm at 12 weeks)
Negative; positive (confirmed at 12 weeks) → anticoagulation per APS guidelines
JAK2 mutation (CPT 81270)
-
-
EXT
-
Polycythemia vera or essential thrombocythemia as stroke etiology in young patients with elevated Hgb/Hct or platelets
First-line antiplatelet for non-cardioembolic ischemic stroke; lifelong secondary prevention
81 mg daily :: PO :: daily :: 81 mg PO daily (preferred); 325 mg for first 3 weeks with minor stroke/TIA per CHANCE/POINT then reduce to 81 mg; lifelong
Active GI bleeding; aspirin allergy; thrombocytopenia <50K
GI symptoms; bleeding signs; annual CBC
STAT
STAT
ROUTINE
-
Clopidogrel
PO
Alternative to aspirin if aspirin-intolerant; DAPT with aspirin for 21 days after minor stroke/TIA (CHANCE/POINT protocol)
75 mg daily :: PO :: daily :: 75 mg PO daily; 300 mg loading dose for acute minor stroke; DAPT: aspirin 81 mg + clopidogrel 75 mg x 21 days then clopidogrel monotherapy
Bleeding signs; CYP2C19 genotyping if available; platelet function testing rarely needed
STAT
STAT
ROUTINE
-
Aspirin + Clopidogrel (DAPT — short-term)
PO
Dual antiplatelet x 21 days for minor ischemic stroke (NIHSS ≤3) or high-risk TIA (ABCD2 ≥4) per CHANCE/POINT trials
81 mg aspirin + 75 mg clopidogrel daily x 21 days :: PO :: daily :: Aspirin 81 mg + clopidogrel 75 mg (with 300 mg clopidogrel load) x 21 days from onset; then monotherapy (aspirin or clopidogrel); DO NOT continue DAPT beyond 21-90 days (increases bleeding without benefit)
Major bleeding; planned surgery; thrombocytopenia
Bleeding signs closely x 21 days; GI prophylaxis with PPI if high GI risk
STAT
STAT
ROUTINE
-
Ticagrelor + Aspirin (DAPT — alternative)
PO
Alternative DAPT for minor stroke/TIA per THALES trial; does NOT require CYP2C19 metabolism
90 mg BID ticagrelor + 81 mg aspirin daily x 30 days :: PO :: BID :: Ticagrelor 180 mg load then 90 mg BID + aspirin 81 mg x 30 days; then switch to monotherapy; alternative when clopidogrel resistance suspected
Active bleeding; history of ICH; severe hepatic impairment; concurrent strong CYP3A4 inhibitors
Bleeding; dyspnea (common, usually benign); bradycardia; liver function
STAT
STAT
ROUTINE
-
Apixaban
PO
Anticoagulation for stroke with AF; preferred DOAC for most patients; superior to warfarin (ARISTOTLE trial)
5 mg BID; 2.5 mg BID :: PO :: BID :: 5 mg BID standard; reduce to 2.5 mg BID if ≥2 of: age ≥80, weight ≤60 kg, creatinine ≥1.5; start 2-14 days after stroke depending on infarct size (1-3-6-12 day rule)
Active major bleeding; severe hepatic impairment; mechanical heart valve; pregnancy
Renal function q6 months; CBC annually; bleeding signs; Xa level if needed (not routine)
-
ROUTINE
ROUTINE
-
Rivaroxaban
PO
Anticoagulation for stroke with AF; once-daily dosing advantage; ROCKET-AF data
20 mg daily; 15 mg daily :: PO :: daily :: 20 mg PO daily with dinner (food enhances absorption); reduce to 15 mg daily if CrCl 15-50 mL/min; timing per infarct size
Active major bleeding; CrCl <15; severe hepatic impairment (Child-Pugh C); mechanical valve
Renal function q6 months; CBC annually; bleeding signs
-
ROUTINE
ROUTINE
-
Dabigatran
PO
Anticoagulation for stroke with AF; RE-LY trial; reversible with idarucizumab
150 mg BID; 110 mg BID :: PO :: BID :: 150 mg BID standard; 110 mg BID if age ≥80 or concurrent P-gp inhibitor; CrCl 30-50: 150 mg BID acceptable; avoid if CrCl <30
CrCl <30; mechanical valve; active bleeding
Renal function q6 months (renal elimination); thrombin time or ecarin clotting time if needed; idarucizumab for reversal
-
ROUTINE
ROUTINE
-
Warfarin
PO
Anticoagulation for mechanical heart valve; alternative when DOACs contraindicated; AF in severe renal failure
Individualized per INR :: PO :: daily :: Start 5 mg daily (2.5 mg if elderly, low weight, liver disease); adjust to INR 2-3 (2.5-3.5 for mechanical valve); check INR 2-3 days after start, then weekly until stable, then monthly
Active major bleeding; pregnancy (teratogenic); severe hepatic failure; non-adherence (requires monitoring)
INR q1-4 weeks (target 2-3); dietary vitamin K counseling; drug interactions; bridge plan for procedures
Pseudobulbar affect (PBA) — involuntary laughing/crying; occurs in 15-25% of stroke survivors; significantly impacts quality of life
20/10 mg capsule daily x 7 days; then BID :: PO :: BID :: 20 mg dextromethorphan/10 mg quinidine: 1 capsule daily x 7 days then 1 capsule BID; only FDA-approved treatment for PBA
Concurrent MAOIs; QT prolongation; concurrent quinidine; CYP2D6 substrates with narrow therapeutic index; AV block
QTc at baseline and after steady state; hepatic function; serotonin syndrome risk with concurrent serotonergic drugs
-
ROUTINE
ROUTINE
-
Modafinil
PO
Post-stroke fatigue (affects 30-70% of survivors); not responsive to treating depression alone; wakefulness-promoting agent
100 mg daily; 200 mg daily :: PO :: daily :: Start 100 mg each morning; may increase to 200 mg daily; take in morning to avoid insomnia; Schedule IV
Severe hepatic impairment; history of angioedema with modafinil; concurrent hormonal contraceptives (reduces efficacy)
BMP q3-6 months; HbA1c q3 months until <7% then q6 months; B12 annually (depletion)
-
ROUTINE
ROUTINE
-
Empagliflozin
PO
SGLT2 inhibitor for diabetes with cardiovascular benefit; reduces MACE and heart failure; renoprotective
10 mg daily; 25 mg daily :: PO :: daily :: Start 10 mg daily; may increase to 25 mg; take in morning; cardiovascular and renal benefit independent of HbA1c
Physical therapy for gait training, balance, strength, and fall prevention — begin inpatient and continue outpatient; most recovery occurs in first 3-6 months but improvement continues
-
STAT
ROUTINE
-
Occupational therapy for ADL retraining, upper extremity function, adaptive equipment, and energy conservation
-
STAT
ROUTINE
-
Speech-language pathology for aphasia, dysarthria, cognitive-communication deficits, and swallow evaluation (dysphagia screening before oral intake)
-
STAT
ROUTINE
-
Neuropsychological testing at 3-6 months post-stroke for cognitive assessment; vascular cognitive impairment screening; guide rehabilitation goals
-
-
ROUTINE
-
Cardiology referral for AF management, PFO closure evaluation (if age <60 + cryptogenic stroke + PFO), heart failure management, or complex antithrombotic decisions
-
URGENT
ROUTINE
-
Rehabilitation medicine (physiatry) for comprehensive rehabilitation program coordination; inpatient rehab evaluation if moderate-severe deficits
-
URGENT
ROUTINE
-
Psychiatry or psychology referral for post-stroke depression not responding to SSRI within 6-8 weeks; anxiety; PTSD; adjustment disorder
-
ROUTINE
ROUTINE
-
Social work for discharge planning, community resources, disability documentation, caregiver support, and financial assistance
-
ROUTINE
ROUTINE
-
Neurology follow-up in 1-2 weeks post-discharge for medication reconciliation, imaging review, and secondary prevention optimization; then q3-6 months
-
ROUTINE
ROUTINE
-
Driving evaluation by occupational therapist and neurology clearance when appropriate; varies by deficit and state law
-
-
ROUTINE
-
Vascular surgery or neurointerventional referral if symptomatic carotid stenosis ≥50% for CEA/CAS evaluation
Learn and recognize stroke warning signs (FAST: Face drooping, Arm weakness, Speech difficulty, Time to call 911); call 911 immediately if any symptom recurs — do not drive yourself
ROUTINE
ROUTINE
ROUTINE
Take all medications as prescribed; DO NOT stop antiplatelet, anticoagulant, or statin medications without consulting your neurologist — stopping these medications significantly increases recurrent stroke risk
ROUTINE
ROUTINE
ROUTINE
Monitor blood pressure at home twice daily (morning and evening) using validated automatic cuff; keep a log and bring to all appointments; target <130/80
-
ROUTINE
ROUTINE
Do not drive until cleared by your neurologist; stroke can affect vision, reaction time, and judgment; formal driving evaluation may be required
-
ROUTINE
ROUTINE
Participate actively in all prescribed rehabilitation therapies (PT, OT, speech); most recovery occurs in first 3-6 months but improvement can continue for years
-
ROUTINE
ROUTINE
Report new mood changes, persistent sadness, loss of interest, or involuntary crying/laughing to your neurologist — post-stroke depression and pseudobulbar affect are common and treatable
-
ROUTINE
ROUTINE
Maintain a medication list including all prescriptions, doses, and schedule; bring to every medical visit and keep a copy in your wallet
-
ROUTINE
ROUTINE
If on anticoagulation (apixaban, rivaroxaban, warfarin): report any unusual bleeding (gums, nosebleed, blood in urine/stool, easy bruising); carry anticoagulant alert card
Smoking cessation is the single most important lifestyle modification; reduces recurrent stroke risk by 50%; offer nicotine replacement, varenicline, or bupropion; referral to cessation program
-
ROUTINE
ROUTINE
Mediterranean-style or DASH diet: rich in fruits, vegetables, whole grains, fish, olive oil; limit sodium to <2300 mg/day (1500 mg if hypertensive); limit processed foods and red meat
-
ROUTINE
ROUTINE
Regular aerobic exercise: 30 minutes of moderate-intensity exercise (walking, swimming, cycling) 5 days/week; adapted to functional level; reduces stroke recurrence by 20-25%
-
ROUTINE
ROUTINE
Limit alcohol to ≤1 drink/day for women, ≤2 drinks/day for men; heavy alcohol increases hemorrhagic stroke risk; complete abstinence preferred if AF or liver disease
Stable neurologic exam; safe swallow; ambulates with appropriate assistance; medications optimized; follow-up arranged; caregiver available if needed; home PT/OT if not yet outpatient
Inpatient rehabilitation
Moderate-severe deficits requiring 3+ hours of therapy daily; medical stability; motivation and ability to participate; expected functional improvement
Skilled nursing facility
Medical complexity requiring nursing care; unable to tolerate 3h/day therapy; awaiting home modifications
APPENDIX B: Timing of Anticoagulation After Ischemic Stroke (for AF)¶
The "1-3-6-12 day rule" guides DOAC initiation based on infarct size:
Infarct Size
NIHSS
Start DOAC
Rationale
TIA (no infarct)
0
Day 1
No hemorrhagic transformation risk
Small infarct (<1.5 cm)
1-4
Day 3
Low HT risk
Moderate infarct (1.5-5 cm)
5-15
Day 6
Moderate HT risk; bridging not recommended
Large infarct (>5 cm or >1/3 MCA)
>15
Day 12
High HT risk; repeat imaging before starting
Notes:
- Repeat CT/MRI before starting DOAC for large infarcts to exclude hemorrhagic transformation
- These are guidelines, not absolute rules — individualize based on clinical judgment
- Bridging with heparin is generally NOT recommended (HAEST, RAF-NOAC data)
- If high recurrence risk and large infarct, consider aspirin bridge until DOAC timing