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1.
Adv Emerg Nurs J ; 41(3): 271-278, 2019.
Article in English | MEDLINE | ID: mdl-31356253

ABSTRACT

Alteplase is a tissue plasminogen activator approved for treating acute ischemic stroke (AIS), acute myocardial infarction (AMI), and acute massive pulmonary embolism. Two additional tissue plasminogen activators, tenecteplase and reteplase, are also approved for AMI treatment. However, neither tenecteplase nor reteplase is approved for AIS treatment. The U.S. Food and Drug Administration has received reports of accidental administration of tenecteplase or reteplase instead of alteplase in patients with AIS, which can lead to potential overdose. Primary factors contributing to medication errors include use of the abbreviations "TPA," "tPA," or "TNK" in written or verbal orders and use of these agents in similar settings. Steps to reduce the likelihood of accidental substitution include use of full brand or generic names and inclusion of the indication in written and verbal orders, addition of alerts in automated dispensing machines and ordering systems, and use of stroke boxes containing alteplase and materials for administration.


Subject(s)
Brain Ischemia/drug therapy , Decision Making , Emergency Service, Hospital , Stroke/drug therapy , Tenecteplase/therapeutic use , Tissue Plasminogen Activator/therapeutic use , Humans , Medication Errors/prevention & control , Recombinant Proteins/therapeutic use , United States , United States Food and Drug Administration
2.
Expert Opin Drug Saf ; 18(2): 87-96, 2019 02.
Article in English | MEDLINE | ID: mdl-30712409

ABSTRACT

INTRODUCTION: Alteplase, reteplase, and tenecteplase are tissue plasminogen activators (TPA) approved for the management of acute myocardial infarction. Only alteplase is also approved for the treatment of acute ischemic stroke (AIS). The US Food and Drug Administration has received reports of accidental administration of tenecteplase or reteplase instead of alteplase in patients with AIS, which can result in failure to treat patients with the intended agent and lead to potential overdose. AREAS COVERED: This review compares the molecular and clinical features of alteplase, reteplase, and tenecteplase (TNK), identifies factors contributing to medication errors among these agents, and provides steps to reduce medication errors. EXPERT OPINION: Primary factors contributing to medication errors among tissue plasminogen activators include the use of the abbreviations 'TPA,' 'tPA,' or 'TNK' in written or verbal orders and use of these agents in similar settings (e.g. emergency departments and critical care areas). Steps to reduce the likelihood of accidental substitution of tenecteplase or reteplase for alteplase in patients with AIS include the use of full brand or generic names and inclusion of the indication in written and verbal orders, the addition of alerts in automated dispensing machines and ordering systems and use of stroke boxes containing alteplase and materials for administration.


Subject(s)
Brain Ischemia/drug therapy , Fibrinolytic Agents/administration & dosage , Stroke/drug therapy , Drug Approval , Drug Overdose/prevention & control , Fibrinolytic Agents/adverse effects , Humans , Medication Errors/prevention & control , Myocardial Infarction/drug therapy , Recombinant Proteins/administration & dosage , Recombinant Proteins/adverse effects , Tenecteplase/administration & dosage , Tenecteplase/adverse effects , Tissue Plasminogen Activator/administration & dosage , Tissue Plasminogen Activator/adverse effects
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