Fetal Echocardiography is Useful for Screening Fetuses with a Family History of Cardiomyopathy
Autor: | John J. Parent, Nicholas B. Zaban, Robert K. Darragh |
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Rok vydání: | 2020 |
Předmět: |
Inotrope
Fetus medicine.medical_specialty medicine.diagnostic_test business.industry Cardiomyopathy Dilated cardiomyopathy 030204 cardiovascular system & hematology Vascular surgery medicine.disease Cardiac surgery 03 medical and health sciences 0302 clinical medicine 030228 respiratory system Internal medicine Pediatrics Perinatology and Child Health medicine Cardiology Family history Cardiology and Cardiovascular Medicine business Fetal echocardiography |
Zdroj: | Pediatric Cardiology. 41:1766-1772 |
ISSN: | 1432-1971 0172-0643 |
DOI: | 10.1007/s00246-020-02439-3 |
Popis: | We screened all fetal echocardiograms performed at our institution for the past 5 years for the indication of family history of cardiomyopathy. Twenty-six patients were identified who had fetal echocardiograms performed due to a family history of cardiomyopathy. Three out of 26 patients (11.5%) had findings of decreased ventricular function and dilation consistent with cardiomyopathy. All who had cardiomyopathy on fetal echocardiography had parents with genetic mutations (2 maternal, 1 paternal), including one mother who had a cardiac transplant at age 8 for dilated cardiomyopathy. All 3 affected infants had prenatal planning for high level care and were transferred to our facility immediately after birth for cardiology evaluation and management. 2 patients required inotropic support in the newborn period. One patient was transplanted at age 2 months. One patient required ECMO support for one week and initially recovered, but subsequently required mechanical support and listing for heart transplant. We recommend patients with a strong family history of cardiomyopathy in either parent, especially those with known genetic mutations associated with cardiomyopathy, have fetal echocardiograms performed. |
Databáze: | OpenAIRE |
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