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Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

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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...
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Cardiomyopathy V: Interprofessional Care01:29

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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...
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Pulmonary Hypertension: Classification and Pathogenesis01:30

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Pulmonary hypertension (PH) is a severe health condition in which the mean pulmonary arterial pressure increases to 25 mmHg or more, even when the body is at rest. This high pressure in the blood vessels that transport blood from the heart to the lungs can cause various symptoms, including shortness of breath, can lead to right heart failure, and significantly affect the overall quality of life.
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Cardiomyopathy II: Dilated Cardiomyopathy01:30

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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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Heart Failure II: Pathophysiology01:29

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Systolic Heart Failure and Compensatory MechanismsSystolic heart failure (also termed HFrEF, Heart Failure with Reduced Ejection Fraction) is the most prevalent type of heart filure. It results in a decreased volume of blood being pumped from the ventricle. The aortic arch and carotid sinuses have baroreceptors that detect reduced blood pressure, triggering the sympathetic nervous system (SNS) to release epinephrine and norepinephrine. Initially, this response aims to boost heart rate and...
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Pathophysiology of Heart Failure01:17

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Heart failure (HF) is a progressive syndrome involving ventricles that leads to inadequate cardiac output. It can be classified based on location and output or ejection fraction. Ejection fraction (EF) is an essential measurement in the diagnosis and surveillance of HF. Reduced EF corresponds to systolic heart failure (HFrEF). However, HF with preserved ejection fraction (HFpEF) is becoming increasingly prevalent. Also known as diastolic HF, this form of HF is related to aging. The...
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Related Experiment Video

Updated: Mar 14, 2026

Author Spotlight: Effect of Left Atrial Ligation on Avian Embryonic Hearts and HLHS Implications
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Hypoplastic left heart syndrome: current perspectives.

Christopher E Greenleaf1, J Miguel Urencio1, Jorge D Salazar1

  • 1University of Mississippi Medical Center, 2500 North State Street, Jackson MS 39216, USA.

Translational Pediatrics
|October 7, 2016
PubMed
Summary
This summary is machine-generated.

Hypoplastic left heart syndrome (HLHS) treatment has advanced significantly, transforming a fatal diagnosis into a manageable condition. This review explores current HLHS management options, including surgical palliation, transplant, and hybrid approaches.

Keywords:
Hypoplastic left heart syndrome (HLHS)congenital cardiac anomaliessingle ventricle

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Area of Science:

  • Cardiology
  • Pediatric Surgery
  • Congenital Heart Disease

Background:

  • Hypoplastic left heart syndrome (HLHS) was historically a fatal diagnosis.
  • Significant advancements in pre-, intra-, and postoperative care have improved outcomes.
  • The Norwood procedure in 1983 marked a turning point in HLHS intervention.

Approach:

  • This paper reviews current trends and perspectives in HLHS treatment.
  • It details five distinct management strategies.
  • The focus is on contemporary approaches to pediatric heart conditions.

Key Points:

  • Norwood stage I as the start of 3-stage palliation.
  • Heart transplantation as a viable option.
  • True hybrid and hybrid-bridge-to-Norwood procedures.
  • Compassionate care for unreconstructible cases.

Conclusions:

  • HLHS management has evolved dramatically, offering multiple therapeutic pathways.
  • Current options provide tailored solutions from palliative care to complex surgical interventions.
  • The outlook for HLHS patients has improved substantially due to medical progress.