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Cardiovascular toxicity Cardiac Structure The cardiovascular system
Cardiovascular toxicity Cardiac Structure The cardiovascular system

... Doxorubicin and daunorubicin are antineoplastic agents whose clinical usefulness is limited because of cardiotoxicity. The acute effects mimic anaphylactic-type responses such as tachycardia and various arrhythmias. These effects are usually manageable and most likely are due to the potent release o ...
NOTES Mod #6 Inflammatory
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... Hear a typical friction rub-caused by the beating of the heart against inflamed pericardium or lung pleura; various etiologies. Sound usually continuous, heard diffusely over chest. Typically has three components, one systolic and two diastolic. Systolic occurs with ventricular contraction, diastol ...
Antidysrhythmic and Antihypertensive Agents
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SIGNAL AVERAGED ECG
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... detailed type of ECG. During this procedure, multiple ECG tracings are obtained over a period of approximately 20 minutes in order to capture abnormal heartbeats which may occur only intermittently. A computer captures all the electrical signals from the heart and averages them to provide the physic ...
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... consistent with acute fulminant myocarditis (AFM). Anti-inlammatory and immunosuppressive treatment with prednisolone (3*16 mg for 1 month), anticoagulation with intravenous unfractioned heparin followed by oral warfarin (for 3 months) and cardiac supportive treatment with ramipril (2.5 mg/day) and ...
Muscular Subaortic Stenosis: The Temporal
Muscular Subaortic Stenosis: The Temporal

... should last as long as papillary muscle contraction, i.e., to end-systole.- If the Venturi effect is the cause of SAM and SAM-septal contact, then one would expect SAM-septal contact to cease before end-systole because of a reduced ejection velocity, or because of a decrease in left ventricular pres ...
Adults with congenital heart disease: Patched but not cured
Adults with congenital heart disease: Patched but not cured

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dysrhythmia cheat sheet
dysrhythmia cheat sheet

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Adult Rheumatic Focus on Cardiac & Other Social Issues

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Pediatric Cardiology - Case Report

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kuiu - CecchiniCuore.org

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Cardiovascular Surgery

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heart and circulation sdg

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Sinus of Valsalva Aneurysm with Right Ventricular Outflow Tract

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History of fall
History of fall

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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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