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Ventricular interdependence analysis in patients with congenital
Ventricular interdependence analysis in patients with congenital

... which affect the right ventricle (RV). Objective: To determine and compare the different types of VI in patients with congenital heart disease (CHD) involving RV with systolic and diastolic dysfunction. Methods: A cross-sectional, comparative study was performed in patients with CHD with volume over ...
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Pediatric Chest Pain, Palpitations and Syncope

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an update Arrhythmogenic right ventricular cardiomyopathy:
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... This condition may lead to sudden cardiac death from left ventricular hypertrophy. In hypertension, the heart may increase to 600 g or more and the muscle mass thus outgrows it coronary supply, even if the coronary arteries are healthy. Atheroma is often associated with hypertension, so that the enl ...
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Valve and Vessel Anatomy and Views

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Section 5: Management of Asymptomatic Patients with Reduced Left
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... exists for the use of beta blocker therapy in the management of patients with ALVD from ischemic heart disease, based on the benefits seen in patients with cardiac dysfunction and no overt HF after acute MI. The Carvedilol PostInfarct Survival Control in Left Ventricular Dysfunction (CAPRICORN) stud ...
Click here for handout
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... • Hypoplastic Left Heart Syndrome(HLHS) accounts for ~9% of congenital heart defects • responsible for as many as 25% of cardiac deaths in the newborn period • 95% fatal by 1 month of life before the era of effective surgical palliation • Mean survival 4-23 days • Very rare case reports of survival ...
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... Lab tests indicative of inflammation : ESR (erythrocyte sedimentation rate), CRP (C-Reactive protein), leukocytosis. – ECG changes. ...
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... First and foremost, Olsen et al. (11) studied only a small number of patients—35 in the serial follow-up group and 29 in the surgical group— which not only limited the ability to perform multivariate or subset analyses (as noted), but also required the use of composite end points, which comprised bo ...
The Cardiac Cycle - Dr. Salah A. Martin
The Cardiac Cycle - Dr. Salah A. Martin

... • Meanwhile, the atria have been filling with blood. When atrial pressure exceeds ventricular pressure, AV valves open and ventricular filling, phase 1 begins again. Page 11. Ventricular and Atrial Contraction • Although we have been highlighting the flow of blood on the right side of the heart, rem ...
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hgbl indy

... A. Branzi. Cardiovascular Department, University of Bologna, Bologna, Italy. Purpose: Non-functional recovery of the graft (primary graft failure, PGF) is still the major cause of early adverse outcome after heart transplantation (HT). While several donor- and recipient-related factors have been tak ...
ASD AND PS - Mike Poullis
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MULTIPLE VALVE DISEASES
MULTIPLE VALVE DISEASES

... dysfunction and without severe pulmonary hypertension (systolic pulmonary artery pressure . 60 mmHg) IIaC Severe isolated TR with mild or no symptoms and progessive dilation or deterioration of right ventricular function ...
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Hypertrophic cardiomyopathy



Hypertrophic cardiomyopathy (HCM) is a primary disease of the myocardium (the muscle of the heart) in which a portion of the myocardium is hypertrophied (thickened) without any obvious cause, creating functional impairment of the cardiac muscle. It is a leading cause of sudden cardiac death in young athletes.The occurrence of hypertrophic cardiomyopathy is a significant cause of sudden unexpected cardiac death in any age group and as a cause of disabling cardiac symptoms. Younger people are likely to have a more severe form of hypertrophic cardiomyopathy.HCM is frequently asymptomatic until sudden cardiac death, and for this reason some suggest routinely screening certain populations for this disease.A cardiomyopathy is a disease that affects the muscle of the heart. With HCM, the myocytes (cardiac contractile cells) in the heart increase in size, which results in the thickening of the heart muscle. In addition, the normal alignment of muscle cells is disrupted, a phenomenon known as myocardial disarray. HCM also causes disruptions of the electrical functions of the heart. HCM is most commonly due to a mutation in one of nine sarcomeric genes that results in a mutated protein in the sarcomere, the primary component of the myocyte (the muscle cell of the heart). These are predominantly single-point missense mutations in the genes for beta-myosin heavy chain (MHC), myosin-binding protein C, cardiac troponinT, or tropomyosin. These mutations cause myofibril and myocyte structural abnormalities and possible deficiencies in force generation. Not to be confused with dilated cardiomyopathy or any other cardiomyopathy.While most literature so far focuses on European, American, and Japanese populations, HCM appears in all ethnic groups. The prevalence of HCM is about 0.2% to 0.5% of the general population.
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