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V.A. Kurien

Bio: V.A. Kurien is an academic researcher. The author has contributed to research in topics: Cardiogenic shock & Myocardial infarction. The author has an hindex of 1, co-authored 1 publications receiving 495 citations.

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Journal ArticleDOI
TL;DR: Serum-F.F.A.A.) levels measured in 200 patients during the first forty-eight hours after an acute myocardial infarction have been related to the prevalence of arrhythmias detected by continuous monitoring of the electrocardiogram, to the clinical state of the patients, and to serum-enzyme and blood-glucose levels.

496 citations


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Journal ArticleDOI
TL;DR: Insulin-glucose infusion followed by a multidose insulin regimen improved long-term prognosis in diabetic patients with acute myocardial infarction.

1,529 citations

Journal ArticleDOI
Shamir R. Mehta1, Salim Yusuf1, Rafael Diaz, Jun Zhu2  +478 moreInstitutions (5)
26 Jan 2005-JAMA
TL;DR: In this large, international randomized trial, high-dose GIK infusion had a neutral effect on mortality, cardiac arrest, and cardiogenic shock in patients with acute STEMI.
Abstract: Context Glucose-insulin-potassium (GIK) infusion is a widely applicable, low-cost therapy that has been postulated to improve mortality in patients with acute ST-segment elevation myocardial infarction (STEMI). Given the potential global importance of GIK infusion, a large, adequately powered randomized trial is required to determine the effect of GIK on mortality in patients with STEMI. Objective To determine the effect of high-dose GIK infusion on mortality in patients with STEMI. Design, setting, and participants Randomized controlled trial conducted in 470 centers worldwide among 20,201 patients with STEMI who presented within 12 hours of symptom onset. The mean age of patients was 58.6 years, and evidence-based therapies were commonly used. Intervention Patients were randomly assigned to receive GIK intravenous infusion for 24 hours plus usual care (n = 10,091) or to receive usual care alone (controls; n = 10,110). Main outcome measures Mortality, cardiac arrest, cardiogenic shock, and reinfarction at 30 days after randomization. Results At 30 days, 976 control patients (9.7%) and 1004 GIK infusion patients (10.0%) died (hazard ratio [HR], 1.03; 95% confidence interval [CI], 0.95-1.13; P = .45). There were no significant differences in the rates of cardiac arrest (1.5% [151/10 107] in control and 1.4% [139/10,088] in GIK infusion; HR, 0.93; 95% CI, 0.74-1.17; P = .51), cardiogenic shock (6.3% [640/10 107] vs 6.6% [667/10 088]; HR, 1.05; 95% CI, 0.94-1.17; P = .38), or reinfarction (2.4% [246/10,107] vs 2.3% [236/10,088]; HR, 0.98; 95% CI, 0.82-1.17; P = .81). The rates of heart failure at 7 days after randomization were also similar between the groups (16.9% [1711/10,107] vs 17.1% [1721/10,088]; HR, 1.01; 95% CI, 0.95-1.08; P = .72). The lack of benefit of GIK infusion on mortality was consistent in prespecified subgroups, including in those with and without diabetes, in those presenting with and without heart failure, in those presenting early and later after symptom onset, and in those receiving and not receiving reperfusion therapy (thrombolysis or primary percutaneous coronary intervention). Conclusion In this large, international randomized trial, high-dose GIK infusion had a neutral effect on mortality, cardiac arrest, and cardiogenic shock in patients with acute STEMI.

624 citations

Journal ArticleDOI
TL;DR: Accumulation of 5′-AMP during ischemia results in an activation of AMP-activated protein kinase, which phosphorylates and inactivates ACC during reperfusion, and the subsequent decrease in malonyl-CoA levels will result in accelerated fatty acid oxidation rates during reperFusion of ischemic hearts.

606 citations

Journal ArticleDOI
TL;DR: Endogenous triacylglycerol as a source of fatty acids and Carnitine palmitoyltransferase 1 activity and Acetyl-CoA carboxylase regulation of fatty acid oxidation.

550 citations

Journal ArticleDOI
TL;DR: In chronic angina patients, ranolazine monotherapy was well tolerated and increased exercise performance throughout its dosing interval at all doses studied without clinically meaningful hemodynamic effects.

526 citations