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Updated: Jun 7, 2026

Fetal Mouse Cardiovascular Imaging Using a High-frequency Ultrasound (30/45MHZ) System
Published on: May 5, 2018
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.
Abstract:
Objectives. Ninety-one fetuses with dilated or hypertrophic cardiomyopathy (DCM, HCM) and myocarditis were studied. Results. Group 1 "DCM" included 19 fetuses: 13 with hydrops (FH) and 5 with associated extracardiac anomalies (ECAs) (15.8%). Group 2 "Myocarditis" included twelve fetuses, having 11 with FH. Group 3 "HCM" included sixty fetuses: 26 had associated ECAs, 17 had maternal diabetes, and 17 were "idiopathic"; however, in one case, a metabolic disorder was found postnatally, and 4 had familiarity for HCM. Outcomes. Ten cases opted for termination of pregnancy. Two cases with DCM and 1 with HCM were lost at follow-up. Out of the cases that continued pregnancy, with known follow-up, mortality was 68.75% in Group 1, 63.6% in Group 2, and 31.3% in Group 3 (the majority with severe ECAs). Surviving cases with DCM and myocarditis improved, 2 with HCM worsened, 6 remained stable, and 26 improved or normalized. Conclusions. Our data show more severe prognosis in DCM and myocarditis and forms with severe associated ECAs.
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