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Related Concept Videos

Cardiomyopathy VII: Pre and Post Operative Nursing Management01:28

Cardiomyopathy VII: Pre and Post Operative Nursing Management

Patients with hypertrophic cardiomyopathy (HCM) and left ventricular outflow tract (LVOT) obstruction who remain symptomatic despite optimal medical therapy may undergo a septal myectomy (Morrow procedure). This procedure involves excising a portion of the hypertrophied septum below the aortic valve using a heart-lung machine to improve blood flow through the LVOT. Effective preoperative and postoperative nursing management ensures successful patient outcomes, minimizes complications, and...
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...
Cardiomyopathy I: Introduction and Classification01:25

Cardiomyopathy I: Introduction and Classification

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...
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

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...
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 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,...

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Related Experiment Video

Updated: Jun 19, 2026

A Murine Closed-chest Model of Myocardial Ischemia and Reperfusion
13:42

A Murine Closed-chest Model of Myocardial Ischemia and Reperfusion

Published on: July 17, 2012

Intraoperative stress cardiomyopathy.

Edward Gologorsky1, Angela Gologorsky

  • 1Department of Anesthesiology, CVT Division, University of Miami Miller School of Medicine/Jackson Memorial Hospital, Miami, Florida 33136, USA. egologorsky@med.miami.edu

Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography
|October 16, 2009
PubMed
Summary

This case report highlights how transesophageal echocardiography aids in diagnosing intraoperative tako-tsubo cardiomyopathy, a form of stress cardiomyopathy, during surgery. Early diagnosis using this imaging technique is crucial for managing sudden hypotension and pulmonary edema.

Related Experiment Videos

Last Updated: Jun 19, 2026

A Murine Closed-chest Model of Myocardial Ischemia and Reperfusion
13:42

A Murine Closed-chest Model of Myocardial Ischemia and Reperfusion

Published on: July 17, 2012

Area of Science:

  • Cardiology
  • Anesthesiology
  • Medical Imaging

Background:

  • Intraoperative hypotension and pulmonary edema can mimic acute coronary syndromes.
  • Tako-tsubo cardiomyopathy (stress-induced cardiomyopathy) is a potential cause of these intraoperative complications.
  • Transesophageal echocardiography (TEE) is an advanced imaging modality used during surgery.

Observation:

  • A female patient under general anesthesia developed sudden hypotension and mild pulmonary edema during surgery.
  • Transesophageal echocardiography was immediately performed to investigate the cause.
  • The echocardiographic findings suggested stress-induced cardiomyopathy.

Findings:

  • The suspected diagnosis of intraoperative tako-tsubo cardiomyopathy was confirmed by computed tomographic angiography and cardiac catheterization.
  • Transesophageal echocardiography proved vital in the rapid differential diagnosis.
  • The patient experienced a full recovery.

Implications:

  • This case underscores the critical role of transesophageal echocardiography in diagnosing intraoperative cardiovascular emergencies.
  • TEE facilitates the differentiation between stress cardiomyopathy and acute coronary syndrome during surgery.
  • Prompt diagnosis and management improve patient outcomes in intraoperative hypotension scenarios.