Dilated vs restrictive cardiomyopathy

• [DOC File]ITE Review: Cardiovascular

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  -dilated (most common), restrictive or hypertrophic. Idiopathic Dilated Cardiomyopathy-dilatation of all four chambers, systolic pump failure-get sings of left and right sided failure-afib most common dysrhythmia-treat with diuretic, vasodilators, (digitalis) Restrictive Cardiomyopathy

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• [DOC File]Referencias 14 al - ResearchGate

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  Left ventricular filling dynamics by Doppler echocardiography in dilated cardiomyopathy: one-year follow-up in patients treated with captopril compared to placebo. Cardiology. 1992;81(4-5):196-206.

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• [DOCX File]Title

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  If no cause may be found, idiopathic dilated cardiomyopathy is considered (greičiausiai tai virusinė etiologija). Most common cause of . ... Restrictive cardiomyopathy. Pericardial disease. The most important differential question - whether symptoms are due to . heart failure. or missed .

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• [DOC File]b

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  Cardiomyopathy - diseases of the myocardium associated with cardiac dysfunction; five types of cardiomyopathy: dilated, hypertrophic, restrictive, arrhythmogenic right ventricular, and unclassified (Cleveland Clinic: Current Clinical Medicine, 2nd ed., William D. Carey, 2010)

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• [DOCX File]MRCP Notes Compilation - Nigel Fong - Notes Site - Home

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  causes include myeloma, chronic disease (e.g. RA), hereditary (familial mediterranean fever etc). Can lead to nephropathy, restrictive cardiomyopathy, peripheral neuropathy, macroglossia, hepatomegaly, fatigue and weight loss. This is quite commonly asked so watch out for it. Waldenstom macrogloblunaemia . is a condition with ...

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• [DOC File]EKG and Interpretation - Josh Corwin

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  -Secondary Mitral Regurgitation – papillary musc dysfunction or dilation of the mitral annulus in pts c dilated cardiomyopathy of any origin. Surgery won’t help unless good EF >30%. Aortic Stenosis- usually elderly, becomes ↑ingly sclerotic + stenotic; MC smokers + HTN

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• [DOCX File]WordPress.com

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  ENDOCRINE. CONDITION. Who is at risk? Signs/Symptoms. Lab/Diagnostics. Nursing Management. Hyperthyroid. Primary vs secondary. Graves, goiter, amiodarone-induced ...

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• [DOCX File]Microsoft

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  Familial restrictive cardiomyopathy (RCM), a rare form of cardiomyopathy, is characterized by diastolic dysfunction with restrictive physiology due to fibrosis and stiffness of the myocardium. Familial RCM has high incidence of sudden cardiac death, particularly in children with 2-year survival of 50% which drops up to 25% in 5-year survival ...

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• [DOC File]Lecture-based Exam Review Questions

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  Dilated Cardiomyopathy – .S3 gallop and ST changes. Restrictive Cardiomyopathy – Uncommon condition. Hypertrophic Cardiomyopathy – May have a genetic component. 21. A 53y/o black male is in your office for a work physical from his computer software design company. He reports his health to be “very good,” and there is no history of ...

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• [DOCX File]WordPress.com

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  Dilated cardiomyopathy (DCM) Info. ... Restrictive Cardiomyopathy . Arrhythmogenic RV Cardiomyopathy . Unclassified Cardiomyopathies. Heart Failure (HF) Info. Previously referred to as Congestive Heart Failure (CHF) HF is a clinical syndrome with s/s of fluid overload or inadequate tissue perfusion.

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• [DOCX File]PART 1 – APPLICANT DETAILS - Department of Health

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  A total of 314 new cases of cardiomyopathy were reported during the 10-year study period: 184 cases of DCM (58.6%), 80 cases of HCM (25.5%), 42 cases of unclassified cardiomyopathy (13.4%), and 8 cases of restrictive cardiomyopathy (2.5%).

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• [DOCX File]Paraneoplastic phenomena - divineinterventionpodcasts

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  Vs. HHNS (not acidotic) Pathophys: insulin prevents release of glucagon --> decreased lipolysis, production of ketone bodies . Skin hyperpigmentation, Hgb 15, blood glucose 300: hereditary hemochromatosis. Pathophys: C282Y mutation --> increased reabsorption of iron from gut

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• [DOCX File]Home | Universitiamo

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  Dilated cardiomyopathy, hypertrophic and restrictive Congenital heart disease Cardiotoxicity of drugs and involvement in cardiovascular diseases oncohaematological treated with chemotherapy and bone marrow transplant

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• [DOC File]Microsoft

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  Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a genetic disease characterized by myocyte loss and fibro-fatty tissue replacement. Diagnosis of ARVC remains a clinical challenge mainly at its early stages and in patients with minimal echocardiographic right ventricular (RV) abnormalities. ARVC shares some common features with other ...

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• [DOCX File]1. Respiratory Medicine - Nigel Fong

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  causes include myeloma, chronic disease (e.g. RA), hereditary (familial mediterranean fever etc). Can lead to nephropathy, restrictive cardiomyopathy, peripheral neuropathy, macroglossia, hepatomegaly, fatigue and weight loss. Biopsy shows apple green on congo red stain. Chronic lymphocytic leukaemia (CLL)

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