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Related Concept Videos

Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

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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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Antifungal Agents01:15

Antifungal Agents

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Amphotericin B is a broad-spectrum antifungal agent that exploits structural differences between fungal and mammalian cell membranes. Its amphipathic structure—featuring a hydrophobic polyene-lactone ring and a hydrophilic region containing mycosamine and carboxylic acid groups—enables selective binding to ergosterol, a sterol predominantly found in fungal plasma membranes. This selective interaction underlies the drug’s antifungal activity, although weak binding to...
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Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

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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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Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

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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...
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Cardiomyopathy I: Introduction and Classification01:25

Cardiomyopathy I: Introduction and Classification

887
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...
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Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

812
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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A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo
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Reversible dilated cardiomyopathy associated with amphotericin B therapy.

J R Soares1, M C P Nunes, A F Leite

  • 1Hospital das Clinicas of the Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.

Journal of Clinical Pharmacy and Therapeutics
|December 10, 2014
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Summary

Amphotericin B can cause reversible dilated cardiomyopathy, a rare side effect. This case highlights potential cardiotoxicity in patients without predisposing factors, warranting further investigation.

Keywords:
amphotericin Bcardiomyopathycardiotoxicity

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Area of Science:

  • Cardiology
  • Infectious Diseases
  • Pharmacology

Background:

  • Amphotericin B (AmB) is a critical antifungal and antileishmanial agent.
  • Its clinical utility is often limited by significant adverse effects.
  • Reversible dilated cardiomyopathy is a rare but documented complication of AmB therapy.

Observation:

  • A case of acute dilated cardiomyopathy developed in a previously healthy 45-year-old man during AmB treatment for visceral leishmaniasis.
  • The patient had no predisposing factors for heart failure, differentiating this case from previous reports.
  • Cardiac function normalized post-treatment, consistent with reversible cardiotoxicity.

Findings:

  • This report presents the first instance of AmB-induced dilated cardiomyopathy in a patient lacking known cardiac risk factors.
  • The findings suggest AmB may possess direct cardiotoxic potential.
  • The cardiotoxicity appears to be reversible upon discontinuation of the drug.

Implications:

  • Clinicians should consider AmB-induced cardiotoxicity in patients presenting with unexplained heart failure, even without risk factors.
  • Further research is necessary to elucidate the mechanisms of AmB-induced cardiotoxicity.
  • This case underscores the importance of vigilant cardiac monitoring during AmB therapy.