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Changes in Cardiac Geometry Due to Hypertrophy
Changes in Cardiac Geometry Due to Hypertrophy

... realize they have the symptoms of athlete’s heart unless they undergo certain medical tests because athlete's heart is a normal, physiological adaptation of the body to the stresses of physical conditioning and aerobic exercise. This can make it difficult to determine if the cause of cardiac enlarg ...
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Causes of stopped circulation

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normally prevents backflow of blood into the left
normally prevents backflow of blood into the left

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Silicone Casting of the Chambers of the Heart and the Great Vessels
Silicone Casting of the Chambers of the Heart and the Great Vessels

... Orientation of the overlapping chambers of the heart is difficult for first year veterinary medical students to conceptualize and confounding when attempting to determine ventricular volume using imaging techniques. To better visualize and understand the spatial relationship between the ventricles, ...
Non Invasive Haemodynamic Monitoring
Non Invasive Haemodynamic Monitoring

... Gujjar et al (2008) J Clin Monit Comput 22:175-180. • Furthermore, this technique is sensitive to the placement of the electrodes on the body, variations in patient body size, and other physical factors that impact on electric conductivity between the electrodes and the skin (eg, temperature and ...
Subcutaneous implantable cardioverter-defibrillator
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Cardiac Blood Tests in Cats

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Arrhythmogenic right ventricular cardiomyopathy secondary to

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Chest X-ray Interpretation

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Aortic and Mitral Valve Surgery on the Beating Heart is Lowering
Aortic and Mitral Valve Surgery on the Beating Heart is Lowering

... draining the heart while simultaneously the aorta is clamped and retrograde CS perfusion is started around 300 ml/min, giving retrograde mean pressure of 50 – 60 mm Hg [Eke 1997]. The incision parallel to the interatrial septum is made in the LA, exposing the LA where the good visualization of the i ...
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Unbalanced Atrioventricular Septal Defect

... clinical records, echocardiograms, and procedural records. Data will be de-identified and securely stored at the CHSS Data Center at The Hospital for Sick Children, Toronto, Canada. The data will be abstracted by the Data Center staff. In addition to data submission from the participating center, an ...
Scholars Journal of Medical Case Reports Acute Dilated
Scholars Journal of Medical Case Reports Acute Dilated

... emboli (PE) as a complication of severe right heart failure. This is rarely documented as a complication associated with acute DCM. One patient improved with aggressive heart failure treatment, and one patient died despite diuresis, neurohormonal blockade and inotropic support. Our case highlights t ...
Heart failure with Preserved Ejection Fraction
Heart failure with Preserved Ejection Fraction

... administration highlighting the fundamental differences in cardiac physiology between these two types of heart failure. The consequences of increased ventricular stiffening are most evident during physical exertion or exercise. Stroke volume reserve is diminished as a result of inefficient ventricul ...
Chronic degenerative atrioventricular valvular disease
Chronic degenerative atrioventricular valvular disease

... these may be treated successfully with aggressive techniques. Common treatment regimens include a lower sodium diet, which may become increasingly restrictive as the disease progresses. Exercise is restricted until symptoms of heart failure are controlled, and then only mild to moderately intense ac ...
The Heart - USD Biology
The Heart - USD Biology

... equilibrates through the foramen of Panizza. This keeps the left aortic pressure high enough to keep the left aortic valve closed. During ventricular contraction, a cusp on the aortic valve of the right aorta closes the foramen of Pinazza. The pressure generated by the right ventricle (low pressure ...
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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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