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Cardiac Resynchronisation Therapy in Patients with NYHA Class I-II
Cardiac Resynchronisation Therapy in Patients with NYHA Class I-II

... In studies including 3- to 6-months of follow-up, CRT, either alone or combined with an implantable cardioverter-defibrillator (ICD), has been shown to improve symptoms, exercise tolerance, and quality of life [14, 15, 20] and to reverse LV remodelling [16–18] in patients with moderate to severe HF ...
Syncope
Syncope

... Should they stay or should they go? ...
Fetal Echocardiography
Fetal Echocardiography

... The four chamber cardiac view can be obtained in 95% of fetuses between the late second and early third trimesters. Abnormal ventricular function.  Abnormal rhythm.  Effusion.  Some septal defects including AV canal.  Single ventricle defects.  Masses/tumors.  Situs/cardiac position abnormalit ...
Ventricular tachycardia (broad complex)
Ventricular tachycardia (broad complex)

... Normally the SAN stimulates impulses which spreads over atria in co-ordinated fashion to cause atrial contraction. Stimulation of the AVN results in conduction down the bundle of His to the bundle branches following a delay to ensure synchronous contraction. Subsequent conduction in the Purkinje sys ...
Sudden Cardiac Death With Apparently Normal Heart
Sudden Cardiac Death With Apparently Normal Heart

... abnormalities were nonspecific. Fourteen (5%) patients, of which 10 were women, had structurally normal hearts. In this subset, a possible substrate or trigger for SCD could be identified in 8 cases. Of the remaining 6 cases, none had identifiable conditions that may be associated with SCD. Seven pa ...
Circ editorial
Circ editorial

... community-based population. This study provides further evidence implicating aortic stiffness in adverse cardiac remodeling and impaired myocardial function. A previous longitudinal MESA study investigated 5960 participants using radial artery tonometry and found that the magnitude of wave reflectio ...
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6. Rheumatic heart disease in pregnancy

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Department of Medical Nursing, Faculty of Nursing, Chiang Mai
Department of Medical Nursing, Faculty of Nursing, Chiang Mai

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Properties of Cardiac Muscle - squ

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Feature Extraction from Heart sound signal for Anomaly Detection

... regularly spaced peaks. MFCCs are a way of representing the spectral information in a sound (heart) signals. Each coefficient has a value for each frame of the sound. The sequence of steps in obtaining MFCC is, (i) Partition the signals into frames (ii) Get the amplitude spectrum of each frame (iii) ...
Straight from the Heart F Francis LaBossière Profile WRHA Cardiac Sciences Program Newsletter
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Percutaneous Ventricular Restoration for Heart Failure After Anterior
Percutaneous Ventricular Restoration for Heart Failure After Anterior

... cohort A and B, U.S. feasibility, and Parachute III trials have been reported.7 Baseline LVEF was 27.9%. The device was successfully implanted in 96% of cases. Average length of hospital stay was 2.9 days. At 12 months, a highly significant 14% decline in LV volume was noted despite a modest 2% abso ...
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... without discomfort o Unstable is not relief with decreased activity, more severe, and the patient is unable to increase CO without increases in Sx ...
Aldosterone, ion channels, and sudden death: another - AJP
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... mineralocorticoid receptor (MR) because it was blocked with the MR antagonist spironolactone but not with the glucocorticoid receptor antagonist RU-38486. Confirming previous results from Bénitah and colleagues, this report also demonstrated that aldosterone, acting through the MR, increased Ca2⫹ c ...
Journal of Forensic Pathology
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Atrial Septal Defect
Atrial Septal Defect

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Maintenance of sinus rhythm and treatment of atrial fibrillation in

... more than systole as heart rate increases, the time available for flow across the mitral valve is reduced at higher heart rates. Therefore at any given stroke volume, tachycardia results in a higher instantaneous volume flow rate and a higher transmitral pressure gradient, which elevates left atrial ...
PDF file - Kardiologia Polska
PDF file - Kardiologia Polska

... Background: The development of malignant ventricular arrhythmias is a possible feature in Emery-Dreifuss muscular dystrophy (EDMD) patients with normal left ventricular systolic function. This event may be the cause of sudden cardiac death in EDMD patients. QTc dispersion (QTc-D), JTc dispersion (JT ...
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... 3. CALCULUS OF VALVE PROSTHESIS OPTIMAL DIAMETER Calculus of optimal diameter of valve prosthesis to be implanted is done in accord with valve type (aortic or mitral), patient hemodynamic characteristics and physical activity usually performed (repose or effort). For a correct choice of valve, it i ...
Slides - gserianne.com
Slides - gserianne.com

... • before atrial systole, blood flows passively into ventricles (~ 70%) • remaining 30% of blood pushed into ventricles during atrial systole • A-V valves open/semilunar valves close • ventricles are relaxed and are filling with blood • ventricular pressure begins to increase Ventricular Systole/Atri ...
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Alterations in Cardiovascular Function
Alterations in Cardiovascular Function

... degree of involvement of mitral/tricuspid valves variable • associated with Down’s syndrome • severity of sx depends on degree of mitral regurgitation. • sx in infants: CHF, tachypnea, tachycardia, FTT, incr URI, systolic murmur (LLSB) ...
Successful Treatment of Idiopathic Dilated
Successful Treatment of Idiopathic Dilated

... in a 27-year-old male chimpanzee. Treatment decisions—indicated by followup diagnostics including repeat electrocardiography, echocardiography, and clinical laboratory data—over the 22-month period during which he continues to be treated are described. In addition, electrocardiographic and echocardi ...
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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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