What is the treatment for acute ischemic stroke?

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Last updated: September 30, 2025View editorial policy

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Treatment for Acute Ischemic Stroke

For acute ischemic stroke, intravenous recombinant tissue plasminogen activator (IV r-tPA) at 0.9 mg/kg (maximum 90 mg) should be administered within 4.5 hours of symptom onset, with treatment within 3 hours having the strongest evidence. 1

Initial Management

Intravenous Thrombolysis

  • IV r-tPA (alteplase) remains the mainstay of early treatment for acute ischemic stroke 2
  • Dosing: 0.9 mg/kg with maximum dose of 90 mg 2, 1
    • 10% given as bolus over 1 minute
    • Remaining 90% administered as continuous infusion over 60 minutes 2
  • Time window:
    • Most effective when given within 3 hours of symptom onset
    • Can be administered up to 4.5 hours after symptom onset 1
    • Earlier treatment associated with better outcomes 2

Blood Pressure Management

  • Before thrombolysis: BP must be <185/110 mmHg 1
  • During and after thrombolysis: Maintain BP <180/105 mmHg for 24 hours 1
  • BP management protocol 2:
    • For systolic >185 mmHg or diastolic >110 mmHg pre-treatment:
      • Labetalol 10-20 mg IV over 1-2 min (may repeat once) or
      • Nicardipine drip, 5 mg/h, titrate up by 2.5 mg/h at 5-15 min intervals (maximum 15 mg/h)
    • During and after treatment:
      • Monitor BP every 15 min for 2 hours, then every 30 min for 6 hours, then hourly for 16 hours

Contraindications for IV r-tPA

  • Symptom onset >4.5 hours or unknown onset time
  • Recent stroke or serious head injury (within 3 months)
  • Major surgery within 14 days
  • History of intracranial hemorrhage
  • GI or GU hemorrhage within 21 days 1

Endovascular Treatment

  • Indicated for patients with proximal large vessel occlusions 1
  • Can be performed within 6 hours of symptom onset for all eligible patients 1
  • Extended window up to 24 hours for selected patients based on imaging criteria 1
  • Mechanical thrombectomy is the preferred endovascular approach 1
  • Patients eligible for IV r-tPA should receive it before endovascular treatment 2

Antiplatelet Therapy

  • Aspirin 160-325 mg should be administered within 24-48 hours after stroke onset 1
  • Delay aspirin for 24 hours in patients who received IV r-tPA 1
  • Long-term antiplatelet options include:
    • Aspirin 75-100 mg daily
    • Clopidogrel 75 mg daily
    • Aspirin/extended-release dipyridamole 25/200 mg twice daily 1

Prevention of Complications

  • Neurological assessments: every 15 minutes during infusion and for 2 hours, then every 30 minutes for 6 hours, and hourly until 24 hours 1
  • VTE prophylaxis:
    • Start prophylactic-dose subcutaneous heparin (preferably LMWH) between days 2-4 for patients with restricted mobility 1
    • Intermittent pneumatic compression devices as an alternative 1
    • Avoid elastic compression stockings 1
  • Early mobilization and adequate hydration 1

Management of Complications

  • Symptomatic intracerebral hemorrhage is a serious complication of thrombolytic therapy 3, 4
  • Angioedema should be managed with antihistamines, glucocorticoids, and standard airway management 1
  • Bleeding complications require individualized management 1

Important Considerations

  • Time is critical - every effort should be made to minimize delays in treatment initiation 2
  • If patients are eligible for IV r-tPA, they should begin receiving it before being transported for additional imaging or endovascular treatment 2
  • The risk of symptomatic intracerebral hemorrhage increases with delayed administration of r-tPA beyond 3 hours 3
  • Recent evidence supports the efficacy of mechanical thrombectomy with stent retrievers, which were not widely used in earlier trials 5

While some studies have explored lower doses of r-tPA (0.6 mg/kg) 6, the standard dose of 0.9 mg/kg remains the recommended protocol in current guidelines 2, 1.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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