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Survival outcomes 1 year after reperfusion therapy with either alteplase or reteplase for acute myocardial infarction: results from the Global Utilization of Streptokinase and t-PA for Occluded Coronary Arteries (GUSTO) III Trial.
Topol, E J; Ohman, E M; Armstrong, P W; Wilcox, R; Skene, A M; Aylward, P; Simes, J; Dalby, A; Betriu, A; Bode, C; White, H D; Hochman, J S; Emanuelson, H; Vahanian, A; Sapp, S; Stebbins, A; Moliterno, D J; Califf, R M.
Affiliation
  • Topol EJ; Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA. topole@ccf.org
Circulation ; 102(15): 1761-5, 2000 Oct 10.
Article in En | MEDLINE | ID: mdl-11023929
ABSTRACT

BACKGROUND:

New recombinant plasminogen activators have been developed to simulate the fibrinolytic action of the physiological serine protease tissue plasminogen activator (alteplase, t-PA), and have prolonged half-life features permitting bolus administration. One such activator, reteplase (r-PA), was compared with t-PA in the Global Utilization of Streptokinase and t-PA for Occluded Coronary Arteries (GUSTO)-III Trial. METHODS AND

RESULTS:

At 1-year follow-up, survival status was ascertained in 97.4% of the 15 059 patients enrolled in the GUSTO-III trial. At 1 year, the mortality rate for the t-PA-assigned group was 11.06%, and for r-PA it was 11.20% (P=0. 77). The absolute mortality difference of 0.14% has 95% CIs of -1. 21% to 0.93%. There were no significant differences in outcome by intention-to-treat for the 2 different plasminogen activators in the prespecified groups (age, infarct location, time-to-treatment). The absolute difference in mortality rates between t-PA and r-PA progressively narrowed over the predetermined observation times after random assignment; it was 0.31% at 24 hours, 0.26% at 7 days, 0.23% at 30 days, and 0.14% at 1 year. Of note, mortality rate in the trial between 30 days and 1 year in 13 883 patients was 4.02% and did not differ between the treatment groups. However, this mortality rate was substantially greater than in GUSTO-I, in which mortality rate for t-PA versus streptokinase between 30 days and 1-year was 2.97% (heart rate 1.36, 95% CI 1.23, 1.50, P<0.001).

CONCLUSIONS:

The r-PA and t-PA strategies yielded similar survival outcomes after 30 days in this trial. The increase in mortality rate during extended follow-up compared with previous trials may reflect higher-risk patients and highlights the need for improved secondary prevention strategies.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Streptokinase / Recombinant Proteins / Tissue Plasminogen Activator / Fibrinolytic Agents / Myocardial Infarction Type of study: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Circulation Year: 2000 Document type: Article Affiliation country:
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Collection: 01-internacional Database: MEDLINE Main subject: Streptokinase / Recombinant Proteins / Tissue Plasminogen Activator / Fibrinolytic Agents / Myocardial Infarction Type of study: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Circulation Year: 2000 Document type: Article Affiliation country: