• J. Am. Coll. Cardiol. · Sep 2003

    Randomized Controlled Trial Clinical Trial

    Glucose-insulin-potassium infusion inpatients treated with primary angioplasty for acute myocardial infarction: the glucose-insulin-potassium study: a randomized trial.

    • Iwan C C van der Horst, Felix Zijlstra, Arnoud W J van 't Hof, Carine J M Doggen, Menko-Jan de Boer, Harry Suryapranata, Jan C A Hoorntje, Jan-Henk E Dambrink, Rijk O B Gans, Henk J G Bilo, and Zwolle Infarct Study Group.
    • Department of Cardiology, Isala Klinieken, Hospital de Weezenlanden, Zwolle, The Netherlands.
    • J. Am. Coll. Cardiol. 2003 Sep 3;42(5):784-91.

    ObjectivesIn this study we considered the question of whether adjunction of glucose-insulin-potassium (GIK) infusion to primary coronary transluminal angioplasty (PTCA) is effective in patients with an acute myocardial infarction (MI).BackgroundA combined treatment of early and sustained reperfusion of the infarct-related coronary artery and the metabolic modulation with GIK infusion has been proposed to protect the ischemic myocardium.MethodsFrom April 1998 to September 2001, 940 patients with an acute MI and eligible for PTCA were randomly assigned, by open-label, to either a continuous GIK infusion for 8 to 12 h or no infusion.ResultsThe 30-day mortality was 23 of 476 patients (4.8%) receiving GIK compared with 27 of 464 patients (5.8%) in the control group (relative risk [RR] 0.82, 95% confidence interval [CI] 0.46 to 1.46). In 856 patients (91.1%) without signs of heart failure (HF) (Killip class 1), 30-day mortality was 5 of 426 patients (1.2%) in the GIK group versus 18 of 430 patients (4.2%) in the control group (RR 0.28, 95% CI 0.1 to 0.75). In 84 patients (8.9%) with signs of HF (Killip class > or =2), 30-day mortality was 18 of 50 patients (36%) in the GIK group versus 9 of 34 patients (26.5%) in the control group (RR 1.44, 95% CI 0.65 to 3.22).ConclusionsGlucose-insulin-potassium infusion as adjunctive therapy to PTCA in acute MI did not result in a significant mortality reduction in all patients. In the subgroup of 856 patients without signs of HF, a significant reduction was seen. The effect of GIK infusion in patients with signs of HF (Killip class > or =2) at admission is uncertain.

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