1.Thrombolytic Agents
Alteplase (tPA): 0.9 mg/kg (max 90 mg). Bolus 10% IV push over 1 min; remaining 90% over 60 min.[+]
Tenecteplase (TNK): 0.25 mg/kg (max 25 mg) single IV bolus. Equivalent first-line alternative to alteplase (AHA/ASA 2026, Class I); single-bolus delivery simplifies transfer for thrombectomy.[+]
2.Blood Pressure Management
Pre-treatment: BP must be <185/110 mmHg. Labetalol 10–20 mg IV push (may repeat) or Nicardipine infusion 5–15 mg/hr.[+]
If BP remains refractory despite aggressive treatment, do not give tPA. Treating above 185/110 increases sICH risk.
Post-treatment (24h): Maintain <180/105 mmHg. Monitor q15min × 2h, then q30min × 6h, then q1h × 16h.[+]
3.Inclusion Criteria
Clinical diagnosis of ischemic stroke with disabling deficit; LKW <4.5 h; age ≥18.
4.Key Exclusions (Do Not Give)
Hemorrhage: Any ICH or SAH on CT.[+]
Coagulopathy: Platelets <100,000, INR >1.7, PTT >40 s.[+]
Anticoagulants: Therapeutic LMWH within 24h. DOAC within 48h unless normal thrombin time/anti-Xa confirmed.[+]
Head history: Severe head trauma or stroke within 3 months. Major intracranial/intraspinal surgery within 3 months.[+]
Bleeding risk: GI malignancy or bleed within 21 days; aortic arch dissection; active internal bleeding. CT hypodensity >1/3 MCA territory.[+]
5.Relative Exclusions
Minor or rapidly improving symptoms — treat if disabling. Major surgery or trauma <14 days. Seizure at onset — treat if imaging confirms stroke. Pregnancy. Recent MI (<3 months).[+]
6.Wake-Up / Unknown Onset
Eligible if: MRI DWI+ and FLAIR− suggests onset <4.5 h; or CTP favorable penumbral profile per WAKE-UP / EXTEND.[+]
7.Tenecteplase vs Alteplase — When to Choose
Per 2026 AHA/ASA guidelines, tenecteplase and alteplase are equivalent first-line choices (COR 1, LOE A). Select based on clinical context.[+]
Choose Tenecteplase (TNK) when:
Transferring for thrombectomy (drip-and-ship): single bolus means no IV pump during transport. Also preferred when rapid administration is needed or nursing resources are limited.[+]
Supported by the ORIGINAL trial (JAMA 2024), which confirmed noninferiority across 1,465 patients — mRS 0–1 at 90 days 72.7% vs 70.3%, identical sICH rates (1.2% each). Simpler single-bolus administration eliminates the 60-minute infusion pump.[+]
Choose Alteplase when:
Extended window (>4.5 h) perfusion-selected patients: alteplase has more trial data (EXTEND, WAKE-UP). Also use alteplase when institutional protocol or formulary requires it.[+]
Do not use TNK at doses >0.25 mg/kg — higher doses (0.4 mg/kg) showed increased hemorrhage in early trials. The approved stroke dose is 0.25 mg/kg IV bolus only.