What to give a stroke patient?

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Last updated: December 23, 2025View editorial policy

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Acute Stroke Management

For acute ischemic stroke patients presenting within 3 hours of symptom onset, administer intravenous alteplase (tPA) 0.9 mg/kg (maximum 90 mg) with 10% as a bolus over 1 minute and 90% infused over 60 minutes—this is the standard of care with the strongest evidence for improved functional outcomes. 1

Immediate Actions Upon Presentation

Time-Critical Assessment

  • Establish the exact time of symptom onset or last known normal time immediately—this single determination dictates all treatment eligibility. 2
  • Obtain urgent non-contrast CT or MRI to exclude hemorrhage and assess for contraindications to thrombolysis. 1, 2
  • Calculate the NIHSS score to quantify stroke severity and guide treatment decisions. 2
  • Target door-to-tPA time of ≤60 minutes for eligible patients. 2

Blood Pressure Management Before tPA

  • If systolic BP >185 mmHg or diastolic >110 mmHg, administer labetalol 10-20 mg IV over 1-2 minutes (may repeat once) or nicardipine drip starting at 5 mg/h, titrating by 2.5 mg/h every 5-15 minutes (maximum 15 mg/h). 1
  • Do not administer tPA if BP cannot be reduced and maintained below 185/110 mmHg. 1

Thrombolytic Therapy Protocol

Within 0-3 Hours of Symptom Onset

  • Administer IV alteplase 0.9 mg/kg (maximum 90 mg): 10% as bolus over 1 minute, remaining 90% infused over 60 minutes. 1, 2
  • This produces a number needed to treat of 8 for achieving minimal or no disability (mRS 0-1). 1, 2
  • Favorable outcomes occur in 31-50% of tPA-treated patients versus 20-38% with placebo. 2

Within 3-4.5 Hours of Symptom Onset

  • Administer the same tPA dosing regimen (0.9 mg/kg, maximum 90 mg) using identical administration protocol. 1
  • Number needed to treat is 14 in this time window. 1
  • The benefit decreases with time: odds ratio for favorable outcome is 2.81 within 90 minutes, declining to 1.40 at 3-4.5 hours. 2, 3

Critical Contraindications to Verify

  • Do not give tPA to patients on direct oral anticoagulants (DOACs) until commercially available validated assessment tools for DOAC levels exist. 1
  • **Verify INR <1.7 for patients on warfarin**, aPTT within normal limits, and platelet count >100,000. 1
  • Exclude intracranial hemorrhage on imaging before any tPA administration. 1

Post-tPA Monitoring Protocol

Neurological and Vital Sign Monitoring

  • Check BP and perform neurological assessments every 15 minutes during and for 2 hours after tPA infusion, then every 30 minutes for 6 hours, then hourly until 24 hours. 1, 2
  • Maintain systolic BP ≤180 mmHg and diastolic ≤105 mmHg after tPA administration. 1
  • If systolic BP 180-230 mmHg or diastolic 105-120 mmHg post-tPA: give labetalol 10 mg IV over 1-2 minutes, may repeat every 10-20 minutes (maximum 300 mg). 1

Management of Symptomatic Intracranial Hemorrhage

  • If severe headache, acute hypertension, nausea, vomiting, or neurological worsening occurs: stop tPA infusion immediately, obtain emergency head CT, and administer cryoprecipitate 10 units over 10-30 minutes plus tranexamic acid 1000 mg IV over 10 minutes. 1

Delayed Antiplatelet Therapy

  • Do not administer aspirin, heparin, or other antithrombotics within 24 hours of tPA. 1, 2, 3
  • Obtain follow-up CT or MRI at 24 hours to exclude hemorrhage before starting any antiplatelet or anticoagulant therapy. 1
  • After 24-hour scan excludes hemorrhage, start aspirin 81-325 mg daily indefinitely. 1

For Patients NOT Receiving tPA

Immediate Aspirin Administration

  • Give aspirin 160-325 mg immediately after CT excludes hemorrhage and dysphagia screening is passed. 1, 2, 3
  • Aspirin must be given within 48 hours of symptom onset to reduce risk of early recurrent ischemic stroke. 1
  • In dysphagic patients, administer aspirin 80 mg via enteral tube or 325 mg rectal suppository. 1

Anticoagulation NOT Recommended

  • Do not routinely use anticoagulation (unfractionated heparin, LMWH) in unselected acute ischemic stroke patients—this increases hemorrhage risk without proven benefit. 1, 2, 4

Mechanical Thrombectomy Consideration

Endovascular Therapy Criteria

  • Consider mechanical thrombectomy with stent retrievers for patients with: age ≥18 years, pre-stroke mRS 0-1, internal carotid artery or proximal MCA (M1) occlusion, NIHSS ≥6, and ASPECTS ≥6 on CT. 2
  • Thrombectomy produces 43.7% good outcomes (mRS 0-2) versus 28.2% with medical therapy alone (adjusted OR 2.1). 2
  • Endovascular therapy may be considered for patients on DOACs who cannot receive tPA. 1

Blood Pressure Management for Non-tPA Candidates

Conservative Approach

  • If systolic BP <220 mmHg or diastolic <120 mmHg: observe without antihypertensive treatment unless other end-organ damage exists (aortic dissection, acute MI, pulmonary edema). 1
  • If systolic BP >220 mmHg or diastolic 121-140 mmHg: give labetalol 10-20 mg IV over 1-2 minutes (may repeat every 10 minutes, maximum 300 mg) or nicardipine 5 mg/h IV, titrating by 2.5 mg/h every 5 minutes (maximum 15 mg/h). 1
  • Target a 10-15% reduction in BP, not normalization. 1

Critical Pitfalls to Avoid

  • Never delay tPA administration for insertion of Foley catheters or other lines—insert these rapidly before tPA or defer until after infusion. 1
  • Never use unproven neuroprotective agents like Cerebrolysin—no neuroprotective medication has demonstrated benefit in acute ischemic stroke. 3
  • Never extend tPA treatment beyond 4.5 hours—the ATLANTIS trial showed no benefit and increased symptomatic ICH (7.0% vs 1.1%) and fatal ICH (3.0% vs 0.3%) when tPA was given 3-5 hours after onset. 5
  • Never give prophylactic anticonvulsants in acute stroke—these are not indicated. 2

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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