Intracardiac thrombus in children with dilated cardiomyopathy

Ahmet Irdem1, Osman Başpınar2, Mehmet Kervancıoğlu2

  • 1Department of Pediatric Cardiology, Gaziantep University Faculty of Medicine, Gaziantep, Turkey. ahmetirdem81@hotmail.com.

Insights

Patients with dilated cardiomyopathy and cardiac thrombus face high thromboembolism risk. Antiplatelet therapy may be beneficial, even for those with left ventricular ejection fraction (LVEF) over 30%.

Area of Science:

  • Cardiology
  • Internal Medicine

Background:

  • Patients with dilated cardiomyopathy (DCM) and cardiac thrombus have a significant risk of fatal thromboembolic events.
  • Left ventricular systolic ejection fraction (LVEF) is a key indicator of cardiac function in DCM.

Purpose of the Study:

  • To evaluate the efficacy of antiplatelet therapy in patients with DCM and cardiac thrombus, particularly those with reduced LVEF.
  • To investigate thrombus formation in relation to LVEF in DCM patients.

Main Methods:

  • Retrospective review of 83 DCM patients (June 2004 - December 2011).
  • Analysis of intracardiac thrombus incidence and correlation with LVEF.
  • Assessment of antiplatelet therapy (acetylsalicylic acid) use in patients with LVEF ≤30%.

Main Results:

  • Intracardiac thrombus was detected in 6% of DCM patients.
  • No statistically significant difference in mean LVEF was found between patients with and without thrombus (35.2±2.7% vs. 34.7±11.0%, p=0.910).
  • Patients with LVEF ≤30% were routinely treated with acetylsalicylic acid.

Conclusions:

  • Thrombus development occurred in DCM patients with LVEF >30% even without antiplatelet therapy.
  • Prophylactic antithrombotic/antiplatelet therapy is recommended at diagnosis for DCM patients, including those with LVEF >30%.
Abstract

Related Concept Videos

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,...
790
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...
805
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...
826
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...
952
Mitral Stenosis II: Clinical features and Diagnostic Tests01:23

Mitral Stenosis II: Clinical features and Diagnostic Tests

Mitral stenosis is a heart condition in which the mitral valve, which allows blood to flow from the left atrium to the left ventricle, becomes narrowed or stenotic. This narrowing hinders blood flow and leads to clinical symptoms requiring specific medical evaluations and management strategies. The following overview outlines the clinical symptoms, assessments, diagnostic findings, prevention methods, and treatments for mitral stenosis.Clinical ManifestationsDyspnea (shortness of breath): This...
557
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...
753