Features and outcomes in utero and after birth of fetuses with myocardial disease

Vlasta Fesslova1, Maurizio Mongiovì, Salvatore Pipitone

  • 1Center of Fetal Cardiology, Policlinico San Donato IRCCS, Via Morandi 30, San Donato Milanese, 20097 Milan, Italy.

Insights

Fetal cardiomyopathy (dilated cardiomyopathy, hypertrophic cardiomyopathy) and myocarditis present a severe prognosis, particularly when associated with hydrops fetalis or extracardiac anomalies. Early diagnosis and management are crucial for improved outcomes.

Area of Science:

  • Cardiology
  • Fetal Medicine
  • Pediatric Cardiology

Background:

  • Cardiomyopathies and myocarditis are significant causes of fetal cardiac dysfunction.
  • Understanding their impact on fetal outcomes is critical for prenatal counseling and management.

Purpose of the Study:

  • To investigate the prognosis and outcomes of fetuses diagnosed with dilated cardiomyopathy (DCM), hypertrophic cardiomyopathy (HCM), and myocarditis.
  • To identify factors influencing survival and disease progression in these fetal cardiac conditions.

Main Methods:

  • Retrospective study of 91 fetuses diagnosed with DCM, HCM, or myocarditis.
  • Analysis of associated conditions such as hydrops fetalis (FH) and extracardiac anomalies (ECAs).
  • Review of pregnancy outcomes, including termination, mortality, and postnatal follow-up.

Main Results:

  • Dilated cardiomyopathy (DCM) and myocarditis groups showed high mortality rates (68.75% and 63.6%, respectively).
  • Hypertrophic cardiomyopathy (HCM) had a lower mortality rate (31.3%), especially in cases without severe ECAs.
  • Survivors with DCM and myocarditis generally improved, while some HCM cases worsened or stabilized.

Conclusions:

  • Fetal DCM and myocarditis carry a more severe prognosis compared to HCM.
  • The presence of severe extracardiac anomalies significantly worsens the outlook for fetuses with cardiomyopathy and myocarditis.
  • Outcomes vary, with some fetuses improving while others experience worsening or stable conditions postnatally.

Related Concept Videos

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...
Myocarditis I: Introduction01:21

Myocarditis I: Introduction

Myocarditis is inflammation of the myocardium, which is the muscular layer of the heart.EtiologyMyocarditis has a diverse etiology, including a wide range of infectious and non-infectious causes:Infectious CausesViral: Common viruses include Coxsackie A and B, adenovirus, parvovirus B19, enteroviruses, and influenza A.Bacterial: Examples include infections caused by Streptococcus, Staphylococcus, and Mycoplasma species.Rickettsial: Infections like Rocky Mountain spotted fever can result in...
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 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,...
Myocarditis II: Clinical Features and Diagnostic Tests01:27

Myocarditis II: Clinical Features and Diagnostic Tests

Myocarditis is an inflammation of the heart muscle. The symptoms vary widely, encompassing asymptomatic presentations to severe, acute manifestations.Clinical PresentationAsymptomatic cases: In some instances, myocarditis may be asymptomatic, with the infection resolving without intervention. These cases often go undetected unless discovered incidentally through diagnostic imaging or tests conducted for other reasons.General Early Symptoms: Early symptoms of myocarditis are non-specific and can...
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...