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The optimal treatment strategy for patients with ST-segment-elevation myocardial infarction (STEMI) who present to hospitals that lack percutaneous coronary intervention (PCI) capability is unclear. In this manufacturer-sponsored multicenter study, 1892 STEMI patients presenting within 3 hours of symptom onset who could not undergo primary PCI within 1 hour were randomized to transport for PCI as soon as feasible or to prompt tenecteplase administration followed by coronary angiography within 24 hours. The lysis group also received enoxaparin and dual antiplatelet therapy. The primary endpoint was the 30-day rate of death, shock, congestive heart failure, or reinfarction.
Eighty-one percent of randomizations occurred prehospital in an ambula…