Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Dysrhythmias VI: Management of Dysrhythmias01:25

Dysrhythmias VI: Management of Dysrhythmias

Dysrhythmia management involves a multifaceted approach, incorporating pharmacological treatments, medical procedures, surgical interventions, lifestyle modifications, and patient education.Pharmacological ManagementAntiarrhythmic Drugs:Class I (Sodium Channel Blockers): This class includes quinidine and procainamide, which reduce the speed of impulse conduction in the heart, stabilize the cardiac membrane, and control arrhythmias. Quinidine and procainamide are Class IA agents that prolong the...
Heart Failure Drugs: Inotropic Agents01:26

Heart Failure Drugs: Inotropic Agents

Positive inotropic agents are commonly used as the first line of treatment for heart failure. One such agent is digoxin, derived from the genus Digitalis, which has been known for centuries but effectively utilized since 1785. However, these cardiac glycosides can have potentially toxic effects due to their mechanism of action, which involves inhibiting Na+/K+-ATPase and increasing contractility. Digoxin is absorbed orally and distributed in various tissues, including the CNS. It has a long...
Heart Failure VI: Adjunct Therapies01:22

Heart Failure VI: Adjunct Therapies

Additional therapies for treating patients with heart failure (HF) may include procedural interventions, supplemental oxygen, the management of sleep disorders, and nutritional therapy.Procedural InterventionsImplantable Cardioverter-Defibrillator: For patients at risk of life-threatening arrhythmias due to severe left ventricular dysfunction, an Implantable Cardioverter-Defibrillator (ICD) can detect and terminate these arrhythmias, preventing sudden cardiac death and improving survival rates.

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

[Canalopathies, arrhythmogenic right ventricular cardiomyopathy and artefacts].

Herzschrittmachertherapie & Elektrophysiologie·2019
Same author

[Recognizing rare cardiac diseases by electrocardiogram].

Der Internist·2018
Same author

[Chronic hypoxia and cardiovascular risk : Clinical significance of different forms of hypoxia].

Herz·2017
Same author

[Erratum to: Multiple inappropriate defibrillator shocks due to insulation failure of a Biotronik Linox defibrillator lead with externalized conductor].

Herzschrittmachertherapie & Elektrophysiologie·2016
Same author

[Cheyne-Stokes respiration in patients with chronic heart failure: only a diagnostic marker or also a cardiovascular risk factor?].

Deutsche medizinische Wochenschrift (1946)·2014
Same author

[Autonomic dysfunction and cardiac arrhythmia in patients with obstructive and central sleep apnea].

Deutsche medizinische Wochenschrift (1946)·2011

Related Experiment Video

Updated: May 17, 2026

A New Single Chamber Implantable Defibrillator with Atrial Sensing: A Practical Demonstration of Sensing and Ease of Implantation
16:40

A New Single Chamber Implantable Defibrillator with Atrial Sensing: A Practical Demonstration of Sensing and Ease of Implantation

Published on: February 28, 2012

Prophylactic implantable defibrillators in dilated cardiomyopathy.

W Grimm1

  • 1Department of Internal Medicine and Cardiology, Philipps-University Marburg and UKGM GmbH, Baldingerstr., 35033, Marburg, Germany. grimmw@med.uni-marburg.de

Herz
|October 12, 2012
PubMed
Summary

Risk stratification for implantable cardioverter-defibrillator (ICD) therapy in dilated cardiomyopathy (DCM) remains challenging. Left ventricular ejection fraction is a key predictor, but timing and complications affect prophylactic ICD use.

More Related Videos

Percutaneous Contrast Echocardiography-guided Intramyocardial Injection and Cell Delivery in a Large Preclinical Model
14:24

Percutaneous Contrast Echocardiography-guided Intramyocardial Injection and Cell Delivery in a Large Preclinical Model

Published on: January 21, 2018

Related Experiment Videos

Last Updated: May 17, 2026

A New Single Chamber Implantable Defibrillator with Atrial Sensing: A Practical Demonstration of Sensing and Ease of Implantation
16:40

A New Single Chamber Implantable Defibrillator with Atrial Sensing: A Practical Demonstration of Sensing and Ease of Implantation

Published on: February 28, 2012

Percutaneous Contrast Echocardiography-guided Intramyocardial Injection and Cell Delivery in a Large Preclinical Model
14:24

Percutaneous Contrast Echocardiography-guided Intramyocardial Injection and Cell Delivery in a Large Preclinical Model

Published on: January 21, 2018

Area of Science:

  • Cardiology
  • Electrophysiology
  • Heart Failure Management

Background:

  • Prophylactic implantable cardioverter-defibrillator (ICD) therapy is indicated for dilated cardiomyopathy (DCM) patients with low ejection fraction.
  • Current guidelines recommend ICDs for DCM patients with NYHA class II-III heart failure and LVEF ≤ 35%.
  • Cardiac resynchronization therapy combined with ICDs is standard for DCM with LBBB and ICD indication.

Purpose of the Study:

  • To investigate arrhythmia risk stratification for prophylactic ICD therapy in DCM.
  • To evaluate the effectiveness and challenges of current ICD indications in DCM.
  • To identify unresolved issues in prophylactic ICD therapy for DCM patients.

Main Methods:

  • Analysis of arrhythmia risk predictors in a large DCM patient cohort (Marburg Cardiomyopathy Study).
  • Review of current clinical guidelines and trial data (e.g., SCD-HeFT) for ICD indications.
  • Assessment of challenges including risk stratification, optimal timing, and complication rates.

Main Results:

  • Left ventricular ejection fraction (LVEF) was the sole significant independent predictor of arrhythmia risk in DCM.
  • Despite guidelines, precise arrhythmia risk stratification remains difficult, necessitating a high number to treat.
  • A significant number of DCM patients experience improved LVEF, potentially avoiding prophylactic ICDs.
  • Prophylactic ICD therapy carries a considerable complication rate, including inappropriate shocks and lead issues.

Conclusions:

  • LVEF is a critical but insufficient predictor for prophylactic ICD implantation in DCM.
  • Optimal timing and patient selection for ICD therapy in DCM require further refinement.
  • Managing complications and the number needed to treat are significant considerations for prophylactic ICDs in DCM.