Effect of Cyclosporine on Reperfusion Injury in Acute Myocardial Infarction
Experimental evidence suggests that cyclosporine may attenuate myocardial reperfusion injury. In a pilot trial, 58 patients with acute ST-elevation myocardial infarction were randomly assigned to receive an intravenous bolus of either cyclosporine or saline immediately before undergoing percutaneous...
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Published in: | The New England journal of medicine Vol. 359; no. 5; pp. 473 - 481 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Boston, MA
Massachusetts Medical Society
31-07-2008
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Subjects: | |
Online Access: | Get full text |
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Summary: | Experimental evidence suggests that cyclosporine may attenuate myocardial reperfusion injury. In a pilot trial, 58 patients with acute ST-elevation myocardial infarction were randomly assigned to receive an intravenous bolus of either cyclosporine or saline immediately before undergoing percutaneous coronary intervention. Creatine kinase release was significantly reduced in the patients who received cyclosporine. These results require confirmation in a larger trial.
Experimental evidence suggests that cyclosporine may attenuate myocardial reperfusion injury. In a pilot trial, creatine kinase release was significantly reduced in the patients who received cyclosporine.
Myocardial infarction is a disabling disease that is common in the United States, with more than 1.5 million new cases diagnosed each year.
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Infarct size is a major determinant of mortality in myocardial infarction.
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Limitation of infarct size has therefore been an important objective of strategies to improve outcomes. Currently, the most effective way to limit infarct size is to reperfuse the jeopardized myocardium as soon as possible with the use of coronary angioplasty or thrombolysis and to prevent reocclusion of the coronary artery with the use of antiplatelet therapy.
Although reperfusion is undoubtedly beneficial, it has detrimental . . . |
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ISSN: | 0028-4793 1533-4406 |
DOI: | 10.1056/NEJMoa071142 |