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Electrocardiogram (EKG, ECG) - Dr. Ray Winstead`s Front Page
Electrocardiogram (EKG, ECG) - Dr. Ray Winstead`s Front Page

... “What your EKG indicates during your stress test is a classic case of coronary ischemia in the left ventricle.” [Ischemia is a restriction in blood supply to tissues, causing a shortage of oxygen and glucose needed for cellular metabolism.] “This coronary ischemia did not show up on the EKG when you ...
Shone`s complex – a rare case report
Shone`s complex – a rare case report

... membrane, parachute mitral valve, subaortic stenosis, coarctation of aorta. We report a 2 year old female child who was initially diagnosed as having aortic stenosis but continued having breathlessness despite being treated with diuretics and beta blockers. She was brought to us in CCF and we diagno ...
Congestive Heart Failure
Congestive Heart Failure

... heart failure who have angina or significant ischemia Reasonable in patients who have chest pain that may or may not be cardiac in origin, in whom cardiac anatomy is not known, and in patients with known or suspected coronary artery disease who do not have angina. Measure cardiac output, degree of l ...
Hypertrophic Cardiomyopathy in Cats
Hypertrophic Cardiomyopathy in Cats

... • More effective than diltiazem in controlling blockage of blood flow as the left ventricle pumps blood into the aorta, the main artery of the body (condition known as “dynamic outflow tract obstruction”) • Role in pets without clinical signs is unresolved, but authors generally use if dynamic outfl ...
Tobacco Smoke
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... the lines of closure of the valve leaflets. Infective endocarditis (IE) is characterized by large, irregular masses on the valve cusps that can extend onto the chordae . Nonbacterial thrombotic endocarditis (NBTE) typically exhibits small, bland vegetations, usually attached at the line of closure. ...
Pediatric Left Atrial Myxoma: Surgical Excision and Mitral Valve Plasty
Pediatric Left Atrial Myxoma: Surgical Excision and Mitral Valve Plasty

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chapter 1: cardiology - Physician Assistant Boards
chapter 1: cardiology - Physician Assistant Boards

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What is Sudden Death in Athletes
What is Sudden Death in Athletes

... sometimes biochemical tests establish a post-mortem diagnosis of HCM. To see a representational sample of a gross heart specimen and histological studies, click here. In congenital anomalies, each variation of normal anatomy may have its specific mechanism of induction of hemodynamic compromise and ...
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TREATMENT OF DILATED CARDIOMYOPATHY in patient with

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Dear Colleagues - Centre for Rare Cardiovascular Diseases
Dear Colleagues - Centre for Rare Cardiovascular Diseases

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Print this article - Nepal Journals Online
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... assess the validity of using separate cardiac reference data for this ethnic group. In Nepal, clinicians are using reference range for echocardiographic values from western literature and books. In clinical practice, it has been long felt that reference range from western data cannot be fully applie ...
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THE HEART

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Valvular Heart Disease

... the sinuses: the left and right. Thus the aortic leaflets are named after the coronary arteries: the left coronary leaflet, the right coronary leaflet, and the noncoronary leaflet. The commissure between the left and noncoronary leaflets sits over the anterior leaflet of the mitral valve, while the ...
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Feline Cardiomyopathies
Feline Cardiomyopathies

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S 132 Abstracts lion. Eur J Echocardiography Abstracts Supplement
S 132 Abstracts lion. Eur J Echocardiography Abstracts Supplement

... Cardiology Dept., Szczecin, Poland Purpose: Similar grade el the lell ventricular (LV) syslolic injury can coexisl wilh diflerenl grade of diastolic dysfunction. Patients wilh reslriclive inflow pallern have more severe dysfunction than those wilh impaired relaxalion. Myocardial pedormance index (MP ...
ppt
ppt

... disease characterized by reduced blood supply to the heart muscle major cause: coronary artery disease risk factors: age, smoking, hypercholesterolemia, diabetes, hypertension, male, family history ...
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Angie`s Info Off Scholar

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Artificial Heart Left Ventricular Assist Devices (LVADs) : A Bridge

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Echotech Reporting Guidelines
Echotech Reporting Guidelines

... • Ensure CW Doppler tracings recorded from 5 and 3 chamber views and right parasternal view with stand alone probe • Aortic valve area is mandatory in patients with moderate and severe aortic stenosis • Aortic valve area should always be calculated when aortic flow rate is affected by conditions suc ...
Summer 2013
Summer 2013

... Binu Philips, MD, Srinivasa Madhavan, MD, MSPH, Cynthia James, ScM, PhD, Crystal Tichnell, MGC, Brittney Murray, MS, Saman Nazarian, MD, PhD, Hugh Calkins, MD, Harikrishna Tandri, MD, and Alan Cheng, MD This poster described clinical features that may aid in the differentiation of ARVD/C and cardiac ...
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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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