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Acute illnesses, such as myocarditis, may provide both Zyvox (Linezolid)- Multum initial and sustained risk of SCD due to inflammation and fibrosis of the myocardium. Less commonly, SCD happens in patients who Zyvox (Linezolid)- Multum not have apparent structural heart disease. These conditions are usually inherited arrhythmia syndromes.

Identifying the patients at risk for SCD remains vitalsource bookshelf challenge.

A multinational group developed and Zyvox (Linezolid)- Multum models to predict sudden cardiac death (SCD) and pump failure death in patients with heart failure and preserved ejection fraction (HFpEF) by using data from 4116 patients in the Irbesartan in Heart Failure with Preserved Ejection Fraction trial (I-Preserve) and validating them in the Candesartan in Heart failure: Assessment of Reduction in Mortality and morbidity (CHARM)-Preserved and Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist (TOPCAT) trials.

A chronic infarct scar can serve Zyvox (Linezolid)- Multum the focus for reentrant ventricular tachyarrhythmias. This can occur shortly after the infarct or years later. Interestingly, post-MI remodeling and ischemic cardiomyopathy may be associated with increased interstitial fibrosis even in noninfarcted areas of the heart. Fibroblasts and myocytes shown to be coupled through gap junctions and fibroblasts can reduce repolarization reserve of myocytes.

In addition to post-MI remodeling, many other structural heart Zyvox (Linezolid)- Multum associated with sudden cardiac death (SCD) (eg, dilated cardiomyopathy, hypertrophic cardiomyopathy, and aortic stenosis) are also associated with increased myocardial fibrosis.

Patients resuscitated from out-of-hospital cardiac arrest represent a group of patients with increased recurrence of cardiac arrest and have been shown to express an increased incidence of silent ST-segment depression.

Experiments inducing myocardial ischemia in animal models have a strong relationship with the development of ventricular fibrillation (VF). However, in patients with prior myocardial infarction and scarring, ventricular arrhythmias, especially ventricular tachycardia (VT), do not require an acute ischemic trigger. In postmortem studies of people who have died from SCD, extensive atherosclerosis is a common pathologic finding. No single coronary artery lesion is associated with an increased risk for SCD.

Many of these hearts also reveal evidence of plaque fissuring, hemorrhage, and thrombosis. The Zyvox (Linezolid)- Multum Surgery Study (CASS) showed that improving or restoring blood flow to an ischemic myocardium decreased the risk of SCD, especially in patients with 3-vessel disease and heart failure, when compared with medical treatment over Zyvox (Linezolid)- Multum 5-year period. The efficacy of beta-blocking agents, such as propranolol, in decreasing sudden death mortality, especially when administered to patients who had MI with VF, VT, and high-frequency PVCs, may be due in part to the ability of beta-blockers to decrease ischemia, but they are also effective in patients with nonischemic cardiomyopathy for Zyvox (Linezolid)- Multum of SCD.

Beta-blockers also increase the VF threshold in ischemic animals and decrease the rate of ventricular ectopy in patients who had MI. Reperfusion of ischemic myocardium with thrombolysis or direct percutaneous coronary intervention can induce transient electrical instability by several different mechanisms.

Coronary artery spasm is a condition that exposes the myocardium to both ischemia and reperfusion insults. It is occasionally associated with VT, VF, and SCD. Since some of the episodes Zyvox (Linezolid)- Multum coronary vasospasm may be silent, this disease should be considered in a patient with unexplained SCA.

Nonatherosclerotic coronary artery abnormalities, including congenital lesions, coronary artery embolism, coronary arteritis, and mechanical abnormalities of the coronary artery, have been associated with an increased incidence of sudden death. Patients with nonischemic cardiomyopathies represent the second largest group of patients who experience SCD in the United States. Nonischemic myopathies, for Zyvox (Linezolid)- Multum purpose of this article, can be divided into the categories dilated and hypertrophic.

Dilated cardiomyopathyDilated cardiomyopathy can result from prior ischemia and myocardial infarction or from nonischemic causes. Nonischemic dilated cardiomyopathy (DCM) is becoming increasingly more common, with an incidence of approximately 7. Extensive fibrosis of the subendocardium, leading to dilated ventricles and subsequent generation of reentrant tachyarrhythmias, is a proposed factor in mechanism of sudden death. Multiple factors have been shown to contribute to increased risk for SCD in this population.

The most important hemodynamic predictor is an increase in end-diastolic pressure and subsequent wall tension. Other important factors are increased sympathetic tone, neurohumoral activation, and Zyvox (Linezolid)- Multum abnormalities. Many drugs used in the treatment of heart failure, such as antiarrhythmics, inotropic agents, and diuretics, have direct or indirect (eg, through electrolyte abnormalities) proarrhythmic properties, which may provoke arrhythmias in some cases.



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