Management of hypertrophic cardiomyopathy

• [DOCX File]WordPress.com

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  Medical Management for MI. Goal: minimize myocardial damage, preserve myocardial function, and prevent complications. ... Hypertrophic Cardiomyopathy (HCM) Restrictive Cardiomyopathy . Arrhythmogenic RV Cardiomyopathy . Unclassified Cardiomyopathies. Heart Failure (HF) Info.

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• [DOC File]CARDIOMYOPATHY

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  Rosenweig A, Watkins H, Hwang D-S, et al. Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes. N Engl J Med 1991; 325:1753–1760. Spirito P, Seidman CE, McKenna WJ, Maron BJ. The management of hypertrophic cardiomyopathy. N Engl J Med 1997; 336:775–785. Topol EJ, Traill TA, Fortuin NJ.

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• [DOC File]Learning Objectives, Chapter 19, Common Cardiovascular ...

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  3. Discuss key differences in the clinical management of dilated and hypertrophic cardiomyopathy. 4. Describe key differences in clinical presentation between arterial and venous peripheral vascular disease. 5. Compare and contrast the clinical findings of chronic aortic aneurysm with those of acute aortic dissection. 6.

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• [DOC File]NEEDS STATEMENT - American Medical Seminars

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  Assess prognosis in patients with hypertrophic cardiomyopathy. Apply appropriate treatment strategies in patients with hypertrophic cardiomyopathy. Differential Diagnosis of Chest Pain. Upon completion of this session, the participant should be able to: EBM, GL, COMP. Assess for and identify causes of chest pain.

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• [DOC File]developinganaesthesia - Home

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  Risk Factors for Sudden Death in Patients with Hypertrophic Cardiomyopathy 1. The overall mortality among patients with hypertrophic cardiomyopathy is less than 1 percent per year. However, a subgroup of patients is at high risk for sudden death, primarily as a result of ventricular arrhythmias. Risk factors can be stratified into major and minor.

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• [DOC File]Stress Induced Cardiomyopathy - developinganaesthesia

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  Hypertrophic cardiomyopathy. Management. Management consists of: 1. Immediate attention to any ABC issues. Oxygenation is the first priority. Some patients may develop acute pulmonary edema, and require CPAP . 2. Pain control: Titrate IV opioid analgesia as required. 3. Maintain continuous ECG monitoring. 4. Hypotension:

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• [DOCX File]www.annalsthoracicsurgery.org

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  Supplemental Material. 1. Patients and . M. e. thods. 1.1. Study population. Between February 2009 and December 2018, a total of 117 consecutive children with hypertrophic obstructive cardiomyopathy (HOCM), aged from 0.6 to 17.5 years and undergoing surgical treatment at our institution, were included in the present study.

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• [DOCX File]GeneDx

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  The Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC) recommends genetic testing in patients fulfilling diagnostic criteria for HCM, including to enable genetic testing of at-risk relatives, by a certified diagnostic laboratory with expertise in the interpretation of cardiomyopathy-related variants.7

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• [DOCX File]GeneDx

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  Management for hypertrophic cardiomyopathy is summarized in specific consensus documents from the American College of Cardiology Foundation / American Heart Association (ACCF/AHA), and the European Society of Cardiology (ESC).4,5 Treatment for cardiomyopathy and surveillance for progression is critical and is strongly influenced by knowledge of the underlying genetic cause.1,2,3 Patients with HCM can be

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• [DOC File]Myocarditis and Cardiomyopathies

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  Hypertrophic cardiomyopathies: mostly left ventricle; abnormal diastolic function. Restrictive cardiomyopathies have elements of both. Dilated Cardiomyopathy. Dilated Cardiomyopathy: ventricular chamber enlargement and dilation (may also effect atria), accompanied by an alteration in systolic pump function that results in clinical syndrome of CHF

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• [DOCX File]Johns Hopkins Anesthesiology & Critical Care Medicine

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  Perioperative Management of Patients With Hypertrophic Cardiomyopathy Patients for Non-cardiac Procedures - What Do I Really Need to Know? Oct 231:10-4:10 PM W176a

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• [DOCX File]Imperial College London

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  The Sarcomeric Human Cardiomyopathy Registry (SHaRe) originates from international centers deeply invested in clinical investigation and state of the art management of HCM. The registry was established by aggregating patient data from longitudinal institutional datasets, curated by experienced providers, to support robust statistical analyses.

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• [DOC File]Lippincott Williams & Wilkins

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  Discuss key differences in the clinical management of dilated and hypertrophic cardiomyopathy. Explain that cardiomyopathies are diseases of the heart muscle that cause cardiac dysfunction resulting in heart failure, dysrhythmias, or sudden death. PowerPoint slide 19. discusses dilated cardiomyopathy. PowerPoint slide 20

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• [DOC File]STANFORD UNIVERSITY MEDICAL CENTER

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  Understand the appearance of pathology on cardiac MRI, including, but not limited to, myocardial infarction, hypertrophic obstructive cardiomyopathy (HOCM), and arrhythmogenic right ventricular dysplasia (ARVD). Understand vascular anatomy of the upper and lower extremities.

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