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

790
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,...
790
Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

753
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...
753
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

805
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...
805
Heart Failure VI: Adjunct Therapies01:22

Heart Failure VI: Adjunct Therapies

632
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.
632
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

952
Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
952
Dysrhythmias VI: Management of Dysrhythmias01:25

Dysrhythmias VI: Management of Dysrhythmias

597
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...
597

You might also read

Related Articles

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

Sort by
Same author

Generalized Coronary Spasm after Pulsed Field Ablation: Not a device complication alone, but a possible interaction between technology and host biology.

Heart rhythm·2026
Same author

Influence of High-Frequency Low-Tidal Volume Versus Jet Ventilation on Acute and Long-Term Outcomes Following Pulmonary Vein Isolation.

Journal of cardiovascular electrophysiology·2026
Same author

Sex differences in atrial fibrillation treatment with catheter ablation in Southern Brazil: Real-world insights from a Latin American registry-SBR-AF.

Heart rhythm O2·2026
Same author

Catheter Ablation in the Brazilian Unified Health System (SUS): Between Consolidated Evidence and Limited Access.

Arquivos brasileiros de cardiologia·2026
Same author

Transesophageal echocardiography versus fluoroscopy-guided left bundle branch area pacing: a comparative study.

Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing·2026
Same author

Post Pacing Interval Following Failed Anti-Tachycardia Pacing Predicts Epicardial Ventricular Tachycardia Circuits in Patients With Non-Ischemic Cardiomyopathy.

Journal of cardiovascular electrophysiology·2026

Related Experiment Video

Updated: May 1, 2026

Benefits of Cardiac Resynchronization Therapy in an Asynchronous Heart Failure Model Induced by Left Bundle Branch Ablation and Rapid Pacing
12:45

Benefits of Cardiac Resynchronization Therapy in an Asynchronous Heart Failure Model Induced by Left Bundle Branch Ablation and Rapid Pacing

Published on: December 11, 2017

10.2K

Cardiac resynchronization therapy: who benefits?

Jason S Chinitz1, Andre d'Avila1, Martin Goldman1

  • 1Mount Sinai School of Medicine, New York, NY.

Annals of Global Health
|April 23, 2014
PubMed
Summary

Cardiac resynchronization therapy (CRT) improves heart failure outcomes in many patients. This review explores factors beyond standard criteria to identify individuals most likely to benefit from CRT, optimizing patient selection for this therapy.

Keywords:
biventricular pacingcardiac resynchronization therapycardiomyopathydyssynchronyheart failureimplantable cardioverter defibrillator

More Related Videos

Real-Time Cardiac Mapping with a Noninvasive Imageless Electrocardiographic Imaging System
10:17

Real-Time Cardiac Mapping with a Noninvasive Imageless Electrocardiographic Imaging System

Published on: April 11, 2025

2.4K
A Novel Digital Platform for a Monitored Home-based Cardiac Rehabilitation Program
04:24

A Novel Digital Platform for a Monitored Home-based Cardiac Rehabilitation Program

Published on: April 19, 2019

14.2K

Related Experiment Videos

Last Updated: May 1, 2026

Benefits of Cardiac Resynchronization Therapy in an Asynchronous Heart Failure Model Induced by Left Bundle Branch Ablation and Rapid Pacing
12:45

Benefits of Cardiac Resynchronization Therapy in an Asynchronous Heart Failure Model Induced by Left Bundle Branch Ablation and Rapid Pacing

Published on: December 11, 2017

10.2K
Real-Time Cardiac Mapping with a Noninvasive Imageless Electrocardiographic Imaging System
10:17

Real-Time Cardiac Mapping with a Noninvasive Imageless Electrocardiographic Imaging System

Published on: April 11, 2025

2.4K
A Novel Digital Platform for a Monitored Home-based Cardiac Rehabilitation Program
04:24

A Novel Digital Platform for a Monitored Home-based Cardiac Rehabilitation Program

Published on: April 19, 2019

14.2K

Area of Science:

  • Cardiology
  • Medical Devices
  • Heart Failure Management

Background:

  • Cardiac resynchronization therapy (CRT) is proven to improve heart failure symptoms, hospitalizations, remodeling, and mortality in selected patients.
  • Current guidelines identify patients likely to benefit, yet approximately 30% do not respond favorably.
  • Existing guidelines may exclude patients who could potentially benefit from CRT.

Purpose of the Study:

  • To evaluate factors predicting patient response to CRT.
  • To identify patient subgroups most likely to benefit from CRT.
  • To refine patient selection criteria for CRT.

Main Methods:

  • Review of evidence on factors influencing CRT response.
  • Analysis of QRS morphology, QRS duration, cardiomyopathy etiology, and rhythm.
  • Consideration of antibradycardia pacing needs and baseline New York Heart Association (NYHA) class.

Main Results:

  • Patient selection for CRT requires assessment of factors beyond standard criteria, including QRS morphology (especially left bundle-branch block), QRS duration, and cardiomyopathy etiology.
  • Baseline NYHA class influences the type of benefit expected; early-stage patients may see structural improvements, while severe cases might gain functional capacity.
  • Factors like rhythm and need for pacing also impact CRT outcomes.

Conclusions:

  • Optimizing CRT benefits involves considering a broader range of patient-specific factors.
  • Accurate patient selection is crucial for maximizing positive responses and minimizing detrimental effects of CRT.
  • This review aids in better determining which patients will gain the most from this evolving therapy.