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Endoscopic Aortic Valve Replacement
Endoscopic Aortic Valve Replacement

... and AXT in comparison to CAVR. In addition, the variety of skin incisions and bone cutting at least at some stage presented even more trauma to the patient than the old sternotomy. Also it is interesting to note how easily the golden truths—good cardiac protection during cardioplegia (such as retrog ...
Ruptured Congenital Sinus of Valsalva Aneurysm
Ruptured Congenital Sinus of Valsalva Aneurysm

... receiving chamber. Also, tricuspid valve fluttering and diastolic pulmonic valve opening may be noted.29 As increased blood flow enters the pulmonary artery, left atrium (LA), and LV, LV volume overload will be seen with significantly sized shunts. In addition to LV volume overload, rupture into the ...
Anger, ventricular arrhythmias and sudden death
Anger, ventricular arrhythmias and sudden death

... prospective epidemiological and clinical studies, supported by experimental studies, that suggest a link between psychosocial factors such as anger, anxiety, depression, hostility/type A behavior, social supports and work characteristics and ventricular arrhythmias, sudden death and cardiac autonomi ...
Primary Prophylaxis of Sudden Death in Hypertrophic
Primary Prophylaxis of Sudden Death in Hypertrophic

... class 1 individuals.6 It is probable that dilated cardiomyopathy with EF less than 30 in NYHA class 2 and 3 patients will become a class 1 or at least class 2A indication for prophylactic ICD with emerging guidelines both in the United States and elsewhere. Hypertrophic Cardiomyopathy Most individua ...
Evaluation of Diastolic Dysfunction Using Cardiac MRI
Evaluation of Diastolic Dysfunction Using Cardiac MRI

... •  These change the magnetization of the protons in the tagged plane compared with the neighboring non-tagged regions, resulting in a difference in signal intensity. •  When placed at end diastole and then imaged throughout the cardiac cycle, tags reveal the deformation and displacement of the myoca ...
Aortic valve replacement – Continuous vs Interrupted suturing
Aortic valve replacement – Continuous vs Interrupted suturing

... Surgical perspectives on Congenital Heart Disease Critical Care Update May 2010 ...
Atrial Fibrillation, Atrioventricular Nodal Ablation and Biventricular
Atrial Fibrillation, Atrioventricular Nodal Ablation and Biventricular

... and morbidity, significant improvement was seen. The annual total mortality and incidence of sudden death were 6.3% and 2.0%, respectively, values that are low and comparable with those for drug treatment. These deaths were attributed directly to the AV node ablation and pacing. Thus, apart from the ...
Determination of reference values for tricuspid annular plane
Determination of reference values for tricuspid annular plane

... capacity, mean right atrial pressure, and survival in children with pulmonary hypertension (27). Reference TAPSE values are required in order to predict prognosis in children with congenital heart defects before and after surgery and in patients with pulmonary hypertension and left heart disorders. ...
Untitled - Journal of Postgraduate Medical Institute
Untitled - Journal of Postgraduate Medical Institute

... Doppler, without evident structural alterations in this chamber. With the progression of DD, this compensatory mechanism fails and the total atrial filling capacity is compromised, leading to atrial remodeling. Left atrial pressure increases to maintain adequate left ventricular filling, leading to ...
Ventricular Assist Devices and Total Artificial Hearts
Ventricular Assist Devices and Total Artificial Hearts

... It is critical that the list of information below is submitted for review to determine if the policy criteria are met. If any of these items are not submitted, it could impact our review and decision outcome: ...
Article - International Journal of Biomedicine (IJBM)
Article - International Journal of Biomedicine (IJBM)

... blood inflow from SVC/IVC and pulmonary veins into the “atrial unit” during systolic/membrane blood suction and during the retraction of the tricuspid and mitral valves in the ventricular cavity during the blood expulsion from them. Thus, a united systole of “three-chamber unit” of ventricles is the ...
Arrhythmogenic right ventricular dysplasia/cardiomyopathy versus
Arrhythmogenic right ventricular dysplasia/cardiomyopathy versus

... ARVD-C has been reported as a rare disease involving primarily the right ventricular wall with variable degrees of involvement of the left ventricle [1, 2, 4]. It is considered a variant of dilated cardiomyopathy with genetic components and variable penetrance [13]. It is commonly associated with su ...
One and a half ventricular repair as an alternative
One and a half ventricular repair as an alternative

... One and a half ventricular repair is a surgical option for congenital cardiac anomalies characterized by a hypoplastic but potentially or partially usable right ventricle. In the hemodynamic physiology of this circulation, the SVC is in series with the pulmonary artery, the lungs are also important ...
Surgical Treatment for Congestive Heart Failure
Surgical Treatment for Congestive Heart Failure

... damage or symptoms pertaining to the disease. • Stage B: patients have some sort of structural damage to the heart, usually detected with an echocardiogram test, but are yet to experience any symptoms • Stage C: patients are those patients who have structural damage and also have prior or current sy ...
Peds 819 TF - Heart Volunteer
Peds 819 TF - Heart Volunteer

... anesthesia is relatively low (1.7%). (Lynch, 2011, 951). For the critical outcome of survival with good neurological outcome, we have identified very low quality limited clinicial evidence from an observational study of 12 children with dilated cardiomyopathy or myocarditis, and documented ventricul ...
Echocardiographic Evaluation of Left Ventricular Systolic and
Echocardiographic Evaluation of Left Ventricular Systolic and

... of systemic hypertension, given that it is the most common cause of left ventricular (LV) hypertrophy and congestive heart failure in adults.2 These guidelines are further supported by the 2013 European Society of Hypertension (ESH)/European Society of Cardiology (ESC) guidelines for systemic hypert ...
geometric changes - The International Heart Institute of Montana
geometric changes - The International Heart Institute of Montana

... need for reporting further findings that should contribute to a better understanding of the dynamics of the tricuspid valve. Methods: Thirteen sonomicrometry transducers were placed in the hearts of each of seven sheep. Six transducers were placed in the tricuspid annulus (TA), at the base of each l ...
Pediatric Interventional Catheterization Fact Sheet
Pediatric Interventional Catheterization Fact Sheet

... As in any procedure, there are always some risks, such as infection. The interventional cardiologist will discuss the risks with patients and parents prior to the procedure. ...
Scintigraphic perfusion defects due to right ventricular
Scintigraphic perfusion defects due to right ventricular

... speckle-tracking strain imaging [10]. In addition, significantly reduced LV ejection fraction was observed as well as an impaired LV longitudinal shortening and reduced LV twist. Whether this acutely induced LV dyssynchrony is responsible for the further development of heart failure after long-term ...
A Guide to the Etiology, Pathophysiology, Diagnosis, and
A Guide to the Etiology, Pathophysiology, Diagnosis, and

... Like the carrot placed in front of the donkey ...
Cardiac tumors
Cardiac tumors

... cardiovascular symptoms, particularly if this occurs in conjunction with cardiomegaly, a new or changing heart murmur, electrocardiographic conduction delay, or arrhythmia.  Emboli thought to originate in the heart should also raise the possibility of cardiac involvement with tumor.  Cardiac metas ...
Myxomatous valve degeneration: A look at the latest developments
Myxomatous valve degeneration: A look at the latest developments

... complications can occur that lead to the death of the patient. For this reason the exact diagnosis and monitoring of the progression in a timely manner is of critical clinical interest in order to be able to predict the risk of decompensation, determine a prognosis and adopt an appropriate medical p ...
Anesthesia for cardiac transplantation
Anesthesia for cardiac transplantation

... although cAMP levels are affected by different mechanisms [3]. As l-tyroxine also increases cAMP levels, this drug (0.8 µg/kg) should be considered especially during prolonged CPB courses which have been shown to be associated with decreased triiodthyronine levels [1;4;5]. Due to the reduced muscula ...
Ventricular Tachycardia
Ventricular Tachycardia

... Your heart rate is controlled by electrical signals transmitted across the heart muscle. When something goes wrong and signals are sent too rapidly, tachycardia can occur. Most often, ventricular tachycardia is caused by other heart problems such as coronary artery disease, high blood pressure, an e ...
Document
Document

... blocked at the AV junction, therefore, the atria and the ventricles beat independently from each other. This arrhythmia is dangerous because it significantly decreases cardiac output, and could lead to asystole. Possible causes: acute inferior and anterior myocardic infraction, coronary heart diseas ...
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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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