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Ablation of right sided ventricular tachycardias
Ablation of right sided ventricular tachycardias

... majority (7/10) of which were found in the right ventricular apex -Female gender and left ventricular dysfunction were independently associated with increased risk for thrombosis in ARVC -During a median FU of 38 months (range 2-128), no thromboembolism event or sudden death was observed in OAC-grou ...
FAQs Example WWPF 2015- Gatesville ISD May 24
FAQs Example WWPF 2015- Gatesville ISD May 24

... Cardiac screening can detect a variety of potentially catastrophic genetic diseases. The simplest level of testing is an ECG, which looks at the electrical signals that the heart uses to contract and circulate blood through the body and lungs. An ECG involves placing electrodes on the chest around t ...
A 29-year-old male with chest pain and haemoptysis CASE FOR DIAGNOSIS
A 29-year-old male with chest pain and haemoptysis CASE FOR DIAGNOSIS

... angiosarcoma, accounting for 37% of cases [1]. Angiosarcomas are malignant neoplasms of endothelial cells varying from welldifferentiated anastomosing vascular channels to undifferentiated tumour arranged as solid sheets of anaplastic cells. Immunohistochemical stains for CD31, CD34 and factor VIIIr ...
Mitral Valve Regurgitation
Mitral Valve Regurgitation

... blood in the heart through the mitral valve. The mitral valve is 1 of 4 valves in the heart. It lies on the left side of the heart between the left upper chamber (atrium) and lower chamber (ventricle). The valve has 2 flaps called leaflets that normally close every time the ventricle squeezes to pum ...
Chronic recurrent ventricular tachycardia
Chronic recurrent ventricular tachycardia

... sign of heart disease. The symptoms depend on the ventricular rate and the underlying cardiac disorder, patients complaining of blackouts, angina, or palpitations, but they are often unaware of any change in heart rate. Repeated Holter ECG tape recording may help to detect the arrhythmia in patients ...
congestive heart failure in children: a survey of 114 patients
congestive heart failure in children: a survey of 114 patients

... CM in 17(30.3%) cases.' Tewenty-four patients (median age 2 years, mnge less than 1 monOI to 18 years) with idiopathic dilated CM were identified from Mayo Clinic records dating from 1973 to 1982. The most common presenting symptom was CHF (92%). Fifteen had died (96% one-year survival and 39% five- ...
Promote Accel™
Promote Accel™

... defibrillation for automated treatment of life-threatening ventricular arrhythmias. Cardiac Resynchronisation Therapy Defibrillators (CRT-Ds) are also intended to resynchronise the right and left ventricles in patients with congestive heart failure. Contraindications: Contraindications for use of the ...
Document
Document

... or excluding the presence of significant obstructive CHD in patients with life-threatening ventricular arrhythmias or in survivors of SCD, who have an intermediate or greater probability of having CHD by age, symptoms, and gender. (Class IIa level C) ...
The pathophysiology of heart failure
The pathophysiology of heart failure

... patients develop symptoms which include dyspnea from pulmonary congestion, and peripheral edema and ascites from impaired venous return. Constitutional symptoms such as nausea, lack of appetite, and fatigue are also common. There are several compensatory mechanisms that occur as the failing heart at ...
Rhythmical Excitation of the Heart
Rhythmical Excitation of the Heart

... The rhythmical electrical impulses in a normal heart allows: • The atria to contract about one sixth of a second ahead of ventricular contraction. • Allows ventricular filling before they pump the blood through the lungs and peripheral circulation. • Allows all portions of the ventricles to contrac ...
Atrial_Fibrillation
Atrial_Fibrillation

... The irregular ventricular contractions cause the systolic arterial pressure to vary from beat to beat as ventricular filling time changes. The pulse pressure also may vary from beat to beat because the diastolic runoff time varies from beat to beat. Atrial fibrillation often involves microreentry. A ...
Glycogen storage disease as a unifying mechanism of disease in
Glycogen storage disease as a unifying mechanism of disease in

... fourth decade of life, extremely slow heart rates may develop, suggesting a myopathic process affecting the accessory conducting fibres and the cells of the normal conduction axis of the heart, including the natural heart pacemaker, the sinus node. Many patients will require artificial pacemaker dev ...
In summary, the results suggest that environmental tempera- 3
In summary, the results suggest that environmental tempera- 3

... than in the healthy volunteers, but the difference was clinically insignificant. No significant difference was found between mitral E/E9 values in the four groups. ...
DOCX ENG
DOCX ENG

... identifies underlying myocardial pathology. We studied the relationship between LV function and myocardial pathology in ESRF patients with CMR. A total of 134 patients with ESRF underwent CMR. LV function was assessed with further images acquired after gadolinium-diethylentriaminepentaacetic acid (D ...
On Measuring the Absolute Ventricular Volumes for the Estimation of
On Measuring the Absolute Ventricular Volumes for the Estimation of

... To ignore V0 and report the elastance as p/V would be inadequate as there are marked differences in V0 in cases of infarction or dilated cardiomyopathy i.e. V0 is sensitive to the pathologic condition of the heart. In situations of high contractility V0 may have negative values. The similarity betwe ...
1 The Cardiac Cycle - Hamilton Grammar School Science Website
1 The Cardiac Cycle - Hamilton Grammar School Science Website

... Atrial systole transfers the remainder of the blood through the atrioventricular (AV) valves to the ventricles. Ventricular systole closes the AV valves and pumps the blood out through the semi lunar (SL) valves to the aorta and pulmonary artery. In diastole the higher pressure in the arteries close ...
ECG Leads
ECG Leads

... the endocardial surface of the posterior wall of the left ventricle. As these leads record from the opposite side of the heart instead of directly over the infarct, the changes of posterior infarction are reversed in these leads. The R waves increase in size, becoming broader and dominant, and are a ...
Moderated poster session 2
Moderated poster session 2

... Policlinico Universitario, Cardiology Dept., Messina, Italy Background: Aging exerts a number of significant changes in the cardiovascular system, particularly on the large arteries. Previous studies have suggested that stiffness index increase linearly with age. Objective: The aim of our study was ...
An unusual case of a bicuspid aortic valve and non compaction of
An unusual case of a bicuspid aortic valve and non compaction of

... Myocardial noncompaction (MNC) is a rare genetic disorder thought to result from an error in myocardial morphogenesis. During normal organogenesis, the meshwork of trabeculations on the luminal aspect of the heart compact to form the muscular walls. Myocardial noncompaction is thought to arise when ...
Myocardial biopsy in diagnosis of endomyo - Heart
Myocardial biopsy in diagnosis of endomyo - Heart

... consistent with 'congestive cardiomyopathy'. Thus, the study shows that the Q wave pattern on the electrocardiogram provides insufficient evidence for the diagnosis of myocardial infarction, and may be misleading in patients with cardiomyopathy. In such circumstances, endomyocardial biopsy from the ...
Transcripts/4_13 1-2 (McNicholas)
Transcripts/4_13 1-2 (McNicholas)

... ii. It is then pumped out through the aorta to circulate around the body. c. Four valves located in the heart chambers open and close like one-way gates to keep the blood moving in the right direction. i. Principle of a valve – if the pressure is greater on one side that the other, a valve with ope ...
Microvolt T-wave Alternans - the Sudden Cardiac Arrest Association
Microvolt T-wave Alternans - the Sudden Cardiac Arrest Association

... patients in whom coronary angiography  should not be delayed.  As such, MTWA  may be used to enhance the diagnostic  yield of traditional stress testing.  ...
cardiovascular evaluation of athletes
cardiovascular evaluation of athletes

... however, additional diagnostic tests are usually needed to determine the severity of the problem. The test to assess the severity of the defect is echocardiography, with electrocardiogram and chest X-ray providing additional measures of heart size. Other non-invasive tests must be used in specific si ...
Incremental Prognostic Value of Estimated LV€End
Incremental Prognostic Value of Estimated LV€End

... (Table 1). Using these measures, LVEDVI Estimated was calculated and compared with “true” CTCA-measured LVEDV. The correlation between measured LVEDVI and LVEDVIEstimated was very good (r ¼ 0.910, 95% confidence interval [95% CI]: 0.882 to 0.931; p < 0.0001). LVEDVI Estimated was significantly larger ...
Successful closure of ventricular septal defect in a patient with
Successful closure of ventricular septal defect in a patient with

... the complaint of heart failure. Noncompaction primarily affects the left ventricle, but the right ventricle may also be involved.[4,8,9] Asymptomatic cases have normal systolic function and increased left ventricular enddiastolic pressure, mimicking restrictive cardiomyopathy. Most patients are init ...
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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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