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Biventricular Pacemakers (Cardiac Resynchronization Therapy) for
Biventricular Pacemakers (Cardiac Resynchronization Therapy) for

... placement of a device that paces both ventricles and which coordinates ventricular pacing to maximize cardiac pumping function and left ventricular ejection fraction (LVEF). Summary of Evidence Evidence from clinical trials and systematic reviews supports the benefit of cardiac resynchronization the ...
Heart sound analysis for symptom detection and computer
Heart sound analysis for symptom detection and computer

... We will consider two types of abnormal heart sounds in this section: those resulting from coarctation of the aorta, and those exhibiting so-called ‘‘splits.’’ 5.1. Coarctation of the aorta As an example demonstrating the value of the S1 and S2 transfer functions for diagnosis, we will consider the c ...
Indications and Outcomes of Surgical Closure of Ventricular Septal
Indications and Outcomes of Surgical Closure of Ventricular Septal

... MARCH 2010:290 –7 ...
Gross Anatomy of the Heart
Gross Anatomy of the Heart

... and, consequently, is a more likely site for ventricular septal ...
PDF
PDF

... left ventricular end-diastolic diameter (LVEDD) >60 mm on echocardiography. Patients with valvular heart disease, congenital heart disease, infiltrative cardiomyopathy (i.e., sarcoidosis and amyloidosis), renal failure, acute myocardial infarction (AMI) within 1 month, poor compliance, or a history ...
Long-Term Outcome of Patients with Acromegaly and Congestive
Long-Term Outcome of Patients with Acromegaly and Congestive

... diagnosed 1 and 10 yr before, concomitantly, and 11 and 14 yr after diagnosis of acromegaly in two, five and two patients, respectively. At diagnosis of CHF, the NYHA classification was stages IV and III in seven and two patients, respectively. Basal echocardiographic findings in the nine patients a ...
Ventricular septal defect - Orphanet Journal of Rare Diseases
Ventricular septal defect - Orphanet Journal of Rare Diseases

... pulmonary vascular resistances. Symptoms include failure to thrive, along with the manifestations of the increase in flow of blood to the lungs. Diagnosis can be made by physical examination, but is confirmed by echocardiographic interrogation, which delineates the precise anatomy, and also provides ...
The diagnostic and prognostic value of right ventricular myocardial
The diagnostic and prognostic value of right ventricular myocardial

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The Hemodynamics of Calcific Aortic Valve Disease
The Hemodynamics of Calcific Aortic Valve Disease

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Introduction to fetal echo
Introduction to fetal echo

... The Eustachian valve (the junctional fold between the inferior vena cava and the right atrium) directs the inferior vena caval flow toward the foramen ovale that is very close to the inferior vena cava. The inferior caval flow itself is divided into two components: the oxygenated blood coming from ...
Nandrolone and resistance training induce heart remodeling: Role
Nandrolone and resistance training induce heart remodeling: Role

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The importance of long axis function
The importance of long axis function

... mitral valve disease. Hertz developed a camera that could display the motion mode (M-mode) of echo signals, and the first echocardiogram (or ultrasoundcardiogram as it was then known) was performed on 29 October 1953. Edler's work inspired new innovations in the field, and more than 25 million echoc ...
Superior Vena Cava Syndrome Caused by Right Atrial
Superior Vena Cava Syndrome Caused by Right Atrial

... history and physical examination may shed light on the diagnosis, imaging studies are usually required for establishing the diagnosis and pinpointing the causes. Herein, we report a case of facial edema resulting from obstruction of superior vena cava caused by right atrial carcinosarcoma with initi ...
Diastolic Heart Failure Demystified - CHEST Journal
Diastolic Heart Failure Demystified - CHEST Journal

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Sample Chapter 36 from Runge: Netter`s Cardiology, 2nd Edition
Sample Chapter 36 from Runge: Netter`s Cardiology, 2nd Edition

... inconsistent, and in many patients for whom surgical treatment is contemplated. Catheterization is performed to quantify the mitral valve area, to document key elements of hemodynamics such as cardiac output and systemic resistance, to define the degree of pulmonary hypertension, and to determine wh ...
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PDF Article

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DIasToLIC HEaRT FaILuRE – EmERgIng TREnDs
DIasToLIC HEaRT FaILuRE – EmERgIng TREnDs

... on finding on coronary angiogram, appropriate revascularization (PTCA or CABG) may be indicated. But high rates of recurrent DHF on patients with hypertension and CAD even after successful revascularization suggested that symptoms of DHF in these patients were not entirely due to ischamia13,27. ...
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... which was released by the American Heart Association in 2010. According to the Chain of survival concept,the following steps should be followed to save when someone collapses and has a cardiac arrest— 1.recognition of cardiac arrest and alerting the emergency medical response system. 2.to start CPR ...
Heart rate modulates the slow enhancement of contraction due to
Heart rate modulates the slow enhancement of contraction due to

... Total atrioventricular block was induced by injecting 10% formalin (0.6–2.0 ml) into the region of the atrioventricular node through a right atrial incision, and the atriostomy was closed by a purse-string suture. This procedure was performed during temporary occlusion of the coronary perfusion line ...
Diagnosis and treatment of catecholaminergic polymorphic
Diagnosis and treatment of catecholaminergic polymorphic

... et al11 showed that 10 (56%) of 18 patients resuscitated from an unexplained cardiac arrest (normal coronary arteries, normal ventricular function, and normal ECG) can be diagnosed as having catecholaminergic polymorphic VT. Overall, these data seem to support the idea that catecholaminergic polymor ...
Acute right ventricular failure–– from pathophysiology to new
Acute right ventricular failure–– from pathophysiology to new

... and flow enable the assessment of the impact of treatment on right ventricular function. This cautious interpretation accounts for the almost constant reflux due to the tricuspid insufficiency, which can be observed by central venous and right atrial pressure changes (see Fig. 3 and the illustrative ...
Cardiac risk assessment before the use of stimulant medications in
Cardiac risk assessment before the use of stimulant medications in

... methylphenidate, atomoxetine or amphetamines among children is 0.2 to 0.5 per 100,000 patient-years [32]. While it is recognized that adverse events are fre­ quently under-reported in general, the sudden death of a young individual on medication therapy is likely to be better reported. Thus, using t ...
Antepartum non-invasive evaluation of opening and closing timings
Antepartum non-invasive evaluation of opening and closing timings

... distress is associated with postmaturity (when the placenta malfunctions in a post-term pregnancy), or with complications of pregnancy, or labor that affects the mother and therefore also affect their fetus. The determination of CHD and fetal distress during fetal life, where the examiner must deal ...
2.4. Assessment of intrinsic contractility. Referring to figure 2.2
2.4. Assessment of intrinsic contractility. Referring to figure 2.2

... function, but according equation 2.23 an hyperbolic relation exists between EF and EDV, implicating a substantial sensitivity of EF on EDV at low EDV [118, 207, 214]. As a consequence the usefulness of EF as a measure of ventricular function is limited, but according to Robotham the ejection fractio ...
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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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