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Activase® is a standard of care for treating eligible patients with acute ischemic stroke (AIS) within 3 hours of symptom onset2

The American Heart Association/American Stroke Association (AHA/ASA) practice guidelines recommend Activase for treatment of AIS2:

Intravenous Activase (0.9 mg/kg, maximum dose 90 mg) is recommended for selected patients who can be treated within 3 hours of ischemic stroke symptom (Class 1; Level of Evidence A, 2019 AHA/ASA Guidelines)

Indication for Use6:

  • Activase is indicated for the treatment of AIS. Exclude intracranial hemorrhage prior to initiation of treatment. Administration should occur as soon as possible but within 3 hours after symptom onset.

If mechanical thrombectomy is considered, AHA/ASA guidelines recommend that Activase is administered first2:

Patients eligible for IV alteplase should receive alteplase even if mechanical thrombectomy (MT) is being considered (Class 1; Level of Evidence A, 2019 AHA/ASA Guideline)

In addition, according to the Society of Vascular and Interventional Neurology (SVIN), pre-MT intravenous thrombolysis in emergent large vessel occlusion ischemic stroke patients combined with MT is recommended for eligible patients and should not be skipped in favor of MT alone (Level of Evidence-A, Class of Recommendation-1)9

Example MT device indication for patients who first received IV alteplase

  • The MT device is indicated for use to restore blood flow in the neurovasculature by removing thrombus for the treatment of AIS to reduce disability in patients with a persistent, proximal anterior circulation, LVO, and smaller infarcts who have first received IV alteplase. Endovascular therapy with the device should start within 6 hours of symptom onset*10,11

Evaluate Activase treatment procedures and protocols to ensure all changes and guidelines are incorporated

Various resources are used in making treatment decisions. Clinical judgment and the hospital protocol review process should guide clinical decisions. 

Prescribing Information Revisions

  • February 2015 – the Activase Prescribing Information (PI) was revised to reflect the Physician Labeling Rule (PLR).6 The PLR reinforces clear section definitions for the appropriate categorization of prescribing information. Therefore, information in the Activase PI has changed
  • January 2017/March 2018 – the Activase PI was revised with updated Important Safety Information6
  • September 2022 – the Activase PI was revised with updates to the dosage and administration section6

FDA Recommendation

  • September 2015 – the Food and Drug Administration (FDA) issued a recommendation informing healthcare professionals that the FDA had been notified of medication errors involving Activase and TNKase due to the use of the abbreviations "tPA" and "TNK." The letter provided the following recommendations:
    • Do not use the abbreviation “tPA” to prescribe the drug product Activase. Use either the brand name of the drug product Activase or the generic name alteplase on written prescriptions and verbal orders
    • Do not use the abbreviation “TNK” to prescribe TNKase. Use either the full brand name of the drug product TNKase or the generic name tenecteplase on written prescriptions and verbal orders
    • Remove the abbreviation "tPA” from all standardized order sets and treatment protocols to avoid confusion
    • Do not use the abbreviation “tPA” when publishing medical literature or clinical guidelines

AHA/ASA Recommendations

  • October 2019 – the AHA/ASA released new AIS treatment guidelines including updated recommendations for Activase use2

*Please refer to the instructions for use for the Trevo® XP ProVue Retriever and the Solitaire™ Platinum Revascularization Device for more information.

DID YOU KNOW?

  • ACTIVASE is increasingly being administered to eligible patients with AIS. Over 616,000 patients have been treated since approval.3
  • The FDA stated that “tPA” is the abbreviation for the drug class that encompasses all tissue plasminogen activators. To avoid confusion and medication errors, it has directed healthcare professionals to use either the brand name, Activase, or the generic name, alteplase, in written prescriptions and verbal orders.12
HCP team

Find information about stroke protocols.

IMPORTANT SAFETY INFORMATION & INDICATIONS

Indications

Activase® (alteplase) is indicated for the treatment of acute ischemic stroke. Exclude intracranial hemorrhage as the primary cause of stroke signs and symptoms prior to initiation of treatment. Initiate treatment as soon as possible but within 3 hours after symptom onset.

Activase is indicated for use in acute myocardial infarction (AMI) for the reduction of mortality and reduction of the incidence of heart failure.

Limitation of Use: The risk of stroke may outweigh the benefit produced by thrombolytic therapy in patients whose AMI puts them at low risk for death or heart failure.

Activase is indicated for the lysis of acute massive pulmonary embolism (PE), defined as:

  • Acute pulmonary emboli obstructing blood flow to a lobe or multiple lung segments.
  • Acute pulmonary emboli accompanied by unstable hemodynamics, e.g., failure to maintain blood pressure without supportive measures.

Important Safety Information

Contraindications

Do not administer Activase to treat acute ischemic stroke in the following situations in which the risk of bleeding is greater than the potential benefit: current intracranial hemorrhage (ICH); subarachnoid hemorrhage; active internal bleeding; recent (within 3 months) intracranial or intraspinal surgery or serious head trauma; presence of intracranial conditions that may increase the risk of bleeding (e.g., some neoplasms, arteriovenous malformations, or aneurysms); bleeding diathesis; and current severe uncontrolled hypertension.

Do not administer Activase to treat acute myocardial infarction or pulmonary embolism in the following situations in which the risk of bleeding is greater than the potential benefit: active internal bleeding; history of recent stroke; recent (within 3 months) intracranial or intraspinal surgery or serious head trauma; presence of intracranial conditions that may increase the risk of bleeding; bleeding diathesis; and current severe uncontrolled hypertension.

Warnings and Precautions

Bleeding

Activase can cause significant, sometimes fatal internal or external bleeding, especially at arterial and venous puncture sites. Avoid intramuscular injections and trauma to the patient. Perform venipunctures carefully and only as required. Fatal cases of hemorrhage associated with traumatic intubation in patients administered Activase have been reported. Aspirin and heparin have been administered concomitantly with and following infusion with Activase in the management of acute myocardial infarction and pulmonary embolism. The concomitant administration of heparin and aspirin with and following infusions of Activase for the treatment of acute ischemic stroke during the first 24 hours after symptom onset has not been investigated. Because heparin, aspirin, or Activase may cause bleeding complications, carefully monitor for bleeding, especially at arterial puncture sites. Hemorrhage can occur 1 or more days after administration of Activase, while patients are still receiving anticoagulant therapy. If serious bleeding occurs, terminate the Activase infusion, and treat appropriately.

In the following conditions, the risks of bleeding with Activase are increased and should be weighed against the anticipated benefits: recent major surgery or procedure; cerebrovascular disease; recent intracranial hemorrhage; recent gastrointestinal or genitourinary bleeding; recent trauma; hypertension; acute pericarditis; subacute bacterial endocarditis; hemostatic defects including those secondary to severe hepatic or renal disease; significant hepatic dysfunction; pregnancy; diabetic hemorrhagic retinopathy or other hemorrhagic ophthalmic conditions; septic thrombophlebitis or occluded AV cannula at seriously infected site; advanced age; and patients currently receiving oral anticoagulants, or any other condition in which bleeding constitutes a significant hazard or would be particularly difficult to manage because of its location.

Hypersensitivity

Hypersensitivity, including urticarial / anaphylactic reactions, have been reported after administration of Activase. Rare fatal outcome for hypersensitivity was reported. Angioedema has been observed during and up to 2 hours after Activase infusion in patients treated for acute ischemic stroke and acute myocardial infarction. In many cases, patients received concomitant angiotensin-converting enzyme inhibitors. Monitor patients treated with Activase during and for several hours after infusion for hypersensitivity. If signs of hypersensitivity occur, e.g. anaphylactoid reaction or angioedema develops, discontinue the Activase infusion and promptly institute appropriate therapy (e.g., antihistamines, intravenous corticosteroids, epinephrine).

Thromboembolism

The use of thrombolytics can increase the risk of thrombo-embolic events in patients with high likelihood of left heart thrombus, such as patients with mitral stenosis or atrial fibrillation. Activase has not been shown to treat adequately underlying deep vein thrombosis in patients with PE. Consider the possible risk of re-embolization due to the lysis of underlying deep venous thrombi in this setting.

Cholesterol Embolization

Cholesterol embolism, sometimes fatal, has been reported rarely in patients treated with thrombolytic agents; the true incidence is unknown. It is associated with invasive vascular procedures (e.g., cardiac catheterization, angiography, vascular surgery) and/or anticoagulant therapy.

Coagulation Tests May be Unreliable during Activase Therapy

Coagulation tests and/or measures of fibrinolytic activity may be unreliable during Activase therapy unless specific precautions are taken to prevent in vitro artifacts. When present in blood at pharmacologic concentrations, Activase remains active under in vitro conditions, which can result in degradation of fibrinogen in blood samples removed for analysis.

Adverse Reactions

The most frequent adverse reaction associated with Activase therapy is bleeding.

Please see the full Prescribing Information for additional Important Safety Information and Instructions for Use.

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