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 I: Introduction and Classification01:25

Cardiomyopathy I: Introduction and Classification

99
Cardiomyopathy, or CMP, is a group of diseases affecting the myocardial structure, impairing its ability to pump blood effectively. This condition can lead to arrhythmias, heart failure, or sudden cardiac death.Cardiomyopathies are classified into primary and secondary categories:Primary Cardiomyopathy refers to conditions involving only the heart muscle that are often idiopathic (of unknown cause) or genetic. They primarily affect the myocardium without the involvement of other systemic...
99
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

77
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...
77
Mechanism of Cardiac Arrhythmias01:28

Mechanism of Cardiac Arrhythmias

1.1K
Arrhythmias are irregular heart rhythms occurring when the heart's electrical impulses become abnormal. These disturbances can lead to various symptoms, depending on their severity and the underlying cause. Some common factors contributing to arrhythmias include hypoxia, ischemia, electrolyte imbalances, excessive catecholamine exposure, drug toxicity, and muscle overstretching. Arrhythmias can be classified into two main types based on the rate and site of origin of abnormal heart rhythms.
1.1K
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

78
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...
78
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

47
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,...
47
Disturbances in Heart Rhythm01:29

Disturbances in Heart Rhythm

1.4K
Arrhythmia or dysrhythmia refers to an abnormal heart rhythm caused by a defect in the heart's conduction system. It can cause the heart to beat irregularly, too quickly, or too slowly, leading to symptoms like chest pain, shortness of breath, and fainting. Factors such as stress, caffeine, alcohol, nicotine, cocaine, certain drugs, congenital defects, diseases, and electrolyte abnormalities can trigger arrhythmias.
Arrhythmias are categorized by their speed, rhythm, and origin. A slow heart...
1.4K

You might also read

Related Articles

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

Sort by
Same author

The march toward 750 hours: A call for thoughtful implementation.

Journal of the American Association of Nurse Practitioners·2025
Same author

Testing the reliability and validity of the nurse practitioner student competency assessment.

Journal of the American Association of Nurse Practitioners·2025
Same author

Implementation of an interprofessional staffing model: Utilizing nurse practitioners and the eICU.

Journal of the American Association of Nurse Practitioners·2025
Same author

History and evolution of nurse practitioners in Taiwan.

Journal of the American Association of Nurse Practitioners·2024
Same author

Navigating social media for professional development: Guidance for the NP.

The Nurse practitioner·2024
Same author

Role of Advanced Practice Providers in the Cardiac Intensive Care Unit Team.

Journal of the American College of Cardiology·2023

Related Experiment Video

Updated: Oct 1, 2025

Rat Model of Right-Sided Cardiac Remodeling and Arrhythmia Using Pulmonary Artery Banding
10:39

Rat Model of Right-Sided Cardiac Remodeling and Arrhythmia Using Pulmonary Artery Banding

Published on: August 30, 2024

838

Arrhythmogenic Right Ventricular Cardiomyopathy: Overview and Case Study.

Carolina D Tennyson1, Rebecca Yapejian2

  • 1Carolina D. Tennyson is a Nurse Practitioner specializing in the advanced heart failure population at the Duke Heart Center, Durham, North Carolina, and an Assistant Professor at Duke University School of Nursing, 307 Trent Drive, Office 3112, Durham, NC 27710 (carolina.tennyson@duke.edu).

AACN Advanced Critical Care
|March 8, 2022
PubMed
Summary

Arrhythmogenic right ventricular cardiomyopathy (ARVC) requires early diagnosis and management to prevent sudden cardiac death. This overview covers ARVC evaluation, diagnosis, and treatment, highlighting nursing considerations through a case study.

Keywords:
arrhythmogenic cardiomyopathyarrhythmogenic right ventricular cardiomyopathyelectrocardiographysudden cardiac death

More Related Videos

Dual-Dye Optical Mapping of Hearts from RyR2R2474S Knock-In Mice of Catecholaminergic Polymorphic Ventricular Tachycardia
09:36

Dual-Dye Optical Mapping of Hearts from RyR2R2474S Knock-In Mice of Catecholaminergic Polymorphic Ventricular Tachycardia

Published on: December 22, 2023

1.4K
Generation and Characterization of Right Ventricular Myocardial Infarction Induced by Permanent Ligation of the Right Coronary Artery in Mice
10:18

Generation and Characterization of Right Ventricular Myocardial Infarction Induced by Permanent Ligation of the Right Coronary Artery in Mice

Published on: February 1, 2022

3.2K

Related Experiment Videos

Last Updated: Oct 1, 2025

Rat Model of Right-Sided Cardiac Remodeling and Arrhythmia Using Pulmonary Artery Banding
10:39

Rat Model of Right-Sided Cardiac Remodeling and Arrhythmia Using Pulmonary Artery Banding

Published on: August 30, 2024

838
Dual-Dye Optical Mapping of Hearts from RyR2R2474S Knock-In Mice of Catecholaminergic Polymorphic Ventricular Tachycardia
09:36

Dual-Dye Optical Mapping of Hearts from RyR2R2474S Knock-In Mice of Catecholaminergic Polymorphic Ventricular Tachycardia

Published on: December 22, 2023

1.4K
Generation and Characterization of Right Ventricular Myocardial Infarction Induced by Permanent Ligation of the Right Coronary Artery in Mice
10:18

Generation and Characterization of Right Ventricular Myocardial Infarction Induced by Permanent Ligation of the Right Coronary Artery in Mice

Published on: February 1, 2022

3.2K

Area of Science:

  • Cardiology
  • Genetics
  • Electrophysiology

Background:

  • Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a primary inherited heart muscle disease.
  • It is characterized by fibrofatty replacement of the right ventricular myocardium.
  • Genetic factors play a significant role in ARVC pathogenesis.

Observation:

  • Clinical presentation varies, including arrhythmias, syncope, and sudden cardiac death.
  • Diagnostic criteria involve electrocardiographic, imaging, and genetic findings.
  • A case study illustrates nursing considerations and clinical management strategies.

Findings:

  • Comprehensive evaluation includes detailed patient history, physical examination, ECG, Holter monitoring, echocardiography, cardiac MRI, and genetic testing.
  • Treatment aims to manage arrhythmias, prevent sudden cardiac death, and address heart failure.
  • Nursing care is crucial for patient education, monitoring, and support.

Implications:

  • Early identification and intervention in ARVC patients can significantly reduce mortality.
  • Understanding ARVC pathophysiology guides therapeutic strategies and genetic counseling.
  • Multidisciplinary management involving cardiologists, electrophysiologists, geneticists, and nurses improves patient outcomes.