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To print: Select File and then Print from your browser's menu Title: Laboratory Monitoring Inadequate in Heart Failure Patients Treated with Spironolactone: Presented at AHA |
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"Laboratory Monitoring Inadequate in Heart Failure Patients Treated with Spironolactone: Presented at AHA" By Jill Stein DALLAS, TX -- November 14, 2005 -- Investigators are calling for more conscientious monitoring of potassium and creatinine concentrations in patients receiving spironolactone for heart failure. Keyur B. Shah, MD, Resident in Internal Medicine, University of Maryland, Baltimore, Maryland, United States, issued his group's recommendation based on a study that found that laboratory monitoring is insufficient in these patients despite the fact that hyperkalemia and renal dysfunction are common. "Systems need to be in place to assure that patients receiving spironolactone are carefully selected and closely monitored," Dr. Shah said here on November 13[th at the American Heart Association's Scientific Sessions 2005 (AHA). Dr. Shah and colleagues reviewed the charts of 840 heart failure patients who had been started on spironolactone therapy after the publication of the Randomized Aldactone Evaluation Study results. The RALES study demonstrated a 30% mortality benefit with spironolactone for severe heart failure. |
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