TNK–Tissue Plasminogen Activator Compared With Front-Loaded Alteplase in Acute Myocardial Infarction

Author:

Cannon Christopher P.1,Gibson C. Michael1,McCabe Carolyn H.1,Adgey A. A. Jennifer1,Schweiger Marc J.1,Sequeira Rafael F.1,Grollier Gilles1,Giugliano Robert P.1,Frey Martin1,Mueller Hiltrud S.1,Steingart Richard M.1,Weaver W. Douglas1,Van de Werf Frans1,Braunwald Eugene1

Affiliation:

1. From the Cardiovascular Division, Department of Medicine, Brigham and Women’s Hospital and Harvard Medical School, Boston, Mass (C.P.C., C.H.M., R.P.G., E.B.); West Roxbury (Mass) Veterans Administration Medical Center (C.M.G.); Royal Victoria Hospital, Belfast, Northern Ireland, UK (A.A.J.A.); Baystate Medical Center, Springfield, Mass (M.J.S.); University of Miami/Jackson Memorial Hospital, Miami, Fla (R.F.S.); CHU Côte de Nacre, Caen, France (G.G.); Sarasota Memorial Hospital, Sarasota, Fla (M.F...

Abstract

Background —Bolus thrombolytic therapy is a simplified means of administering thrombolysis that facilitates rapid time to treatment. TNK-tissue plasminogen activator (TNK-tPA) is a highly fibrin-specific single-bolus thrombolytic agent. Methods and Results —In TIMI 10B, 886 patients with acute ST-elevation myocardial infarction presenting within 12 hours were randomized to receive either a single bolus of 30 or 50 mg TNK-tPA or front-loaded tPA and underwent immediate coronary angiography. The 50-mg dose was discontinued early because of increased intracranial hemorrhage and was replaced by a 40-mg dose, and heparin doses were decreased. TNK-tPA 40 mg and tPA produced similar rates of TIMI grade 3 flow at 90 minutes (62.8% versus 62.7%, respectively, P =NS); the rate for the 30-mg dose was significantly lower (54.3%, P =0.035) and was 65.8% for the 50-mg dose ( P =NS). A prespecified analysis of weight-based TNK-tPA dosing using median TIMI frame count demonstrated a dose response ( P =0.001). Similar dose responses were observed for serious bleeding and intracranial hemorrhage, but significantly lower rates were observed for both TNK-tPA and tPA after the heparin doses were lowered and titration of the heparin was started at 6 hours. Conclusions —TNK-tPA, given as a single 40-mg bolus, achieved rates of TIMI grade 3 flow similar to those of the 90-minute bolus and infusion of tPA. Weight-adjusting TNK-tPA appears to be important in achieving optimal reperfusion; reduced heparin dosing appears to improve safety for both agents. Together with the safety results from the parallel Assessment of the Safety of a New Thrombolytic: TNK-tPA (ASSENT I) trial, an appropriate dose of this single-bolus thrombolytic agent has been identified for phase III testing.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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