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Glucose-Insulin-Potassium for Acute Myocardial Infarction
Author(s) -
Robert A. Kloner,
Richard W. Nesto
Publication year - 2008
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.107.697979
Subject(s) - medicine , myocardial infarction , cardiology , insulin , potassium , chemistry , organic chemistry
The “holy grail” in the field of cardioprotection is to develop pharmacological agents that can be administered as adjunctive treatment to reperfusion that will reduce myocardial infarct size and improve clinical outcomes. Numerous pharmacological agents and strategies have been studied over the years with variable results in both animal models and humans. Of drugs that have been studied, only a few have shown benefit in clinical trials. Aside from agents or devices than can restore and maintain reperfusion (thrombolytics, balloons, stents, aspirin, clopidogrel, IIb/IIIa inhibitors, low–molecular-weight heparin, and others), the only commonly used adjunctive agents shown to have cardioprotective effects when administered early after coronary occlusion and in addition to reperfusion are β-blockers. Angiotensin-converting enzyme inhibitors and angiotensin receptor blockers are also used, but these can be given after infarction (as late as 1 week) and must be continued long-term to reduce left ventricular remodeling. Recently, adenosine and induced hypothermia have also shown promise as early adjunctive agents. For example, when intravenous adenosine was coupled with early reperfusion therapy, myocardial infarct size by single-photon emission computed tomography analysis and the composite end point of death and heart failure were reduced at 6 months.1 Hypothermia, induced by use of a heat-exchange cooling catheter, benefited a subgroup of patients who were successfully cooled to ≤35°C before reperfusion.2 Superoxide dismutase, magnesium, inhibitors of neutrophil adhesion, complement inhibitors, fluosol, RheothRx, the KATP channel/nitrate nicorandil, and others failed to show a benefit as adjuncts to reperfusion.3 Clinical research evaluating many of these agents in acute myocardial infarction has halted.One of the most controversial of these adjunctive agents still under investigation is GIK (glucose-insulin-potassium),4,5 a “cocktail” delivered at the time of infarction that has demonstrated variable results in both the prereperfusion and postreperfusion eras. GIK was one of the first …

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