Hypertrophic cardiomyopathy: Difference between revisions

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| [[Hypertrophic cardiomyopathy surgical treatment#Cardiac transplantation|Selection of Patients for Heart Transplantation]]
| [[Hypertrophic cardiomyopathy surgical treatment#Cardiac transplantation|Selection of Patients for Heart Transplantation]]


*'''Special Clinical Scenarios:''' [[Hypertrophic cardiomyopathy in special clinical scenarios#2011 ACCF/AHA Guideline Recommendations: Patients With LV Systolic Dysfunction (DO NOT EDIT)|Patients With LV Systolic Dysfunction]] | [[Hypertrophic cardiomyopathy risk factors for sudden death#2011 ACCF/AHA Guideline Recommendations: SCD Risk Stratification (DO NOT EDIT) |Sudden cardiac death Risk Stratification]] | [[Hypertrophic cardiomyopathy activities and circumstances to avoid#2011 AHA/ACC Guidelines Recommendations- Participation in Competitive or Recreational Sports and Physical Activity (DO NOT EDIT)|Participation in Competitive or Recreational Sports and Physical Activity]] | [[Hypertrophic cardiomyopathy medical treatment|Management of Atrial Fibrillation]] | [[Hypertrophic cardiomyopathy management during pregnancy|Pregnancy/Delivery]] | [[Hypertrophic cardiomyopathy with coronary artery disease|Concomitant Coronary Disease]]
*'''Special Clinical Scenarios:''' [[Hypertrophic cardiomyopathy in special clinical scenarios#2011 ACCF/AHA Guideline Recommendations: Patients With LV Systolic Dysfunction (DO NOT EDIT)|Patients With LV Systolic Dysfunction]] | [[Hypertrophic cardiomyopathy risk factors for sudden death#2011 ACCF/AHA Guideline Recommendations: SCD Risk Stratification (DO NOT EDIT) |Sudden cardiac death Risk Stratification]] | [[Hypertrophic cardiomyopathy activities and circumstances to avoid#2011 AHA/ACC Guidelines Recommendations- Participation in Competitive or Recreational Sports and Physical Activity (DO NOT EDIT)|Participation in Competitive or Recreational Sports and Physical Activity]] | [[Hypertrophic cardiomyopathy medical treatment#2011 AHA/ACC Guidelines Recommendations- Management of Atrial Fibrillation in HCM (DO NOT EDIT|Management of Atrial Fibrillation]] | [[Hypertrophic cardiomyopathy management during pregnancy|Pregnancy/Delivery]] | [[Hypertrophic cardiomyopathy with coronary artery disease|Concomitant Coronary Disease]]


==Resources==
==Resources==

Revision as of 20:36, 3 October 2012

For patient information click here

Hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy.
Image courtesy of Professor Peter Anderson DVM PhD and published with permission © PEIR, University of Alabama at Birmingham, Department of Pathology
ICD-10 I42.1-I42.2
ICD-9 425.4
DiseasesDB 6373
MeSH D002312

Hypertrophic Cardiomyopathy Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Hypertrophic Cardiomyopathy from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X Ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Interventions

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Hypertrophic cardiomyopathy On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Hypertrophic cardiomyopathy

CDC on Hypertrophic cardiomyopathy

Hypertrophic cardiomyopathy in the news

Blogs on Hypertrophic cardiomyopathy

Directions to Hospitals Treating Hypertrophic cardiomyopathy

Risk calculators and risk factors for Hypertrophic cardiomyopathy

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Hypertrophic cardiomyopathy or HCM, Asymmetric septal hypertrophy or ASH, Hypertrophic obstructive cardiomyopathy, HOCM, Idiopathic hypertrophic subaortic stenosis or IHSS, familial isolated hypertrophic obstructive cardiomyopathy, familial isolated hypertrophic subaortic stenosis, familial or idiopathic hypertrophic subaortic stenosis, familial or idiopathic hypertrophic obstructive cardiomyopathy, primitive hypertrophic obstructive cardiomyopathy, primitive hypertrophic subaortic stenosis, muscular subaortic stenosis, apical hypertrophic cardiomyopathy, which is also known as nonobstructive hypertrophic cardiomyopathy and Japanese variant hypertrophic cardiomyopathy or the Yamaguchi variant (since the first cases described were all in individuals of Japanese descent)

Overview

Classification

Pathophysiology

Genetics | Histopathologic Abnormalities | Anatomic Abnormalities | Outflow Obstruction | Ischemia | Arrhythmogenesis

Epidemiology and Demographcis

Screening

Differentiating Hypertrophic Cardiomyopathy from other Diseases

Natural History, Prognosis and Sudden Cardiac Death Risk

Diagnosis

History and Symptoms | Physical examination | Electrocardiogram | Echocardiography | Cardiac MRI | Cardiac CT | Positron Emission Tomography

Treatment

Special Patient Populations

Asymptomatic Patients | Management During Childhood | Hypotension/Cardiovascular collapse | Pregnancy

2011 ACCF/AHA Guideline Recommendations

Diagnostic testing:

Electrocardiogram | Echocardiography | Stress Testing | Cardiac Magnetic Resonance | Cardiac CT | Positron Emission Tomography

Management:

| Invasive Therapies | Alcohol septal ablation | Septal Myectomy | Pacing | Selection of Patients for ICDs | Selection of ICD-Device type | Selection of Patients for Heart Transplantation

Resources


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