Neonatal cardiomyopathy: a 20-year overview of a reference centre

Background: Cardiomyopathies (CMs) are rare multifactorial diseases of the heart muscle. Neonatal forms present as a myocardial injury in the absence of primary valvular, great vessels or septal anomalies. Despite being uncommon diseases, CMs may lead to potentially severe sequelae and considerable...

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Main Authors: Inês Noites, Paulo Soares, Joana O. Miranda, Hercília Guimarães
Format: Article
Language:English
Published: Hygeia Press di Corridori Marinella 2020-03-01
Series:Journal of Pediatric and Neonatal Individualized Medicine
Subjects:
Online Access:https://www.jpnim.com/index.php/jpnim/article/view/759
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spelling doaj-36ba7a88fdf9400a887306ae97f4f3472020-11-25T03:32:24ZengHygeia Press di Corridori MarinellaJournal of Pediatric and Neonatal Individualized Medicine2281-06922020-03-0191e090129e09012910.7363/090129638Neonatal cardiomyopathy: a 20-year overview of a reference centreInês Noites0Paulo Soares1Joana O. Miranda2Hercília Guimarães3Faculty of Medicine, University of Porto, Porto, PortugalNeonatal Intensive Care Unit, Centro Materno Pediátrico, Centro Hospitalar Universitário de S. João, Porto, PortugalFaculty of Medicine, University of Porto, Porto, Portugal; Pediatric Cardiology Division, Centro Materno Pediátrico, Centro Hospitalar Universitário de S. João, Porto, PortugalFaculty of Medicine, University of Porto, Porto, Portugal; Neonatal Intensive Care Unit, Centro Materno Pediátrico, Centro Hospitalar Universitário de S. João, Porto, Portugal; Cardiovascular R&D Unit, Faculty of Medicine, University of Porto, Porto, PortugalBackground: Cardiomyopathies (CMs) are rare multifactorial diseases of the heart muscle. Neonatal forms present as a myocardial injury in the absence of primary valvular, great vessels or septal anomalies. Despite being uncommon diseases, CMs may lead to potentially severe sequelae and considerable risk of neonatal death. This study aimed to provide an overview of neonatal CM (NCM) and describe its aetiology, initial clinical findings, morbidity and mortality. Methods: Retrospective observational study of all newborns diagnosed with CM admitted to the Neonatal Intensive Care Unit (NICU) of Centro Hospitalar Universitário de S. João, in Porto, Portugal, between 1997 and 2017. Data collected included demographic and perinatal information, clinical presentation, CM type and aetiology, treatments, complications and outcome. Results: Twenty-eight newborns with CM diagnosis were selected: 26 neonates were considered to have primary CM forms and 2 secondary CMs. Of those 26 diagnosed with primary CMs, 16 had hypertrophic CM, 8 had dilated CM, and 2 had tachycardia-induced CM. Secondary CMs comprehended 1 case of infiltrative CM and another of CM due to corticosteroids toxicity. Cardiac murmur (57.1%) was the most common finding, followed by heart failure (HF, 28.6%), cyanosis (21.4%), arrhythmia and sepsis (17.9%, each), and hypertension (10.7%). Two newborns were placed on a heart transplant waiting list. Three neonates developed congestive HF and 1 had a sudden cardiac death event. A total of 4 (14.3%) newborns have deceased during the NICU stay. More than 90% of the neonates were prescribed more than one medicine at discharge. Conclusion: NCMs require critical intensive care management. Unspecific symptoms characterise clinical findings. The majority of newborns have idiopathic primary CMs, but rare heterogeneous aetiologies may be the underlying cause in some cases. Thus, a multidisciplinary approach is mandatory.https://www.jpnim.com/index.php/jpnim/article/view/759cardiomyopathiesnewbornneonatal intensive care unitaetiologyclinical presentationoutcome
collection DOAJ
language English
format Article
sources DOAJ
author Inês Noites
Paulo Soares
Joana O. Miranda
Hercília Guimarães
spellingShingle Inês Noites
Paulo Soares
Joana O. Miranda
Hercília Guimarães
Neonatal cardiomyopathy: a 20-year overview of a reference centre
Journal of Pediatric and Neonatal Individualized Medicine
cardiomyopathies
newborn
neonatal intensive care unit
aetiology
clinical presentation
outcome
author_facet Inês Noites
Paulo Soares
Joana O. Miranda
Hercília Guimarães
author_sort Inês Noites
title Neonatal cardiomyopathy: a 20-year overview of a reference centre
title_short Neonatal cardiomyopathy: a 20-year overview of a reference centre
title_full Neonatal cardiomyopathy: a 20-year overview of a reference centre
title_fullStr Neonatal cardiomyopathy: a 20-year overview of a reference centre
title_full_unstemmed Neonatal cardiomyopathy: a 20-year overview of a reference centre
title_sort neonatal cardiomyopathy: a 20-year overview of a reference centre
publisher Hygeia Press di Corridori Marinella
series Journal of Pediatric and Neonatal Individualized Medicine
issn 2281-0692
publishDate 2020-03-01
description Background: Cardiomyopathies (CMs) are rare multifactorial diseases of the heart muscle. Neonatal forms present as a myocardial injury in the absence of primary valvular, great vessels or septal anomalies. Despite being uncommon diseases, CMs may lead to potentially severe sequelae and considerable risk of neonatal death. This study aimed to provide an overview of neonatal CM (NCM) and describe its aetiology, initial clinical findings, morbidity and mortality. Methods: Retrospective observational study of all newborns diagnosed with CM admitted to the Neonatal Intensive Care Unit (NICU) of Centro Hospitalar Universitário de S. João, in Porto, Portugal, between 1997 and 2017. Data collected included demographic and perinatal information, clinical presentation, CM type and aetiology, treatments, complications and outcome. Results: Twenty-eight newborns with CM diagnosis were selected: 26 neonates were considered to have primary CM forms and 2 secondary CMs. Of those 26 diagnosed with primary CMs, 16 had hypertrophic CM, 8 had dilated CM, and 2 had tachycardia-induced CM. Secondary CMs comprehended 1 case of infiltrative CM and another of CM due to corticosteroids toxicity. Cardiac murmur (57.1%) was the most common finding, followed by heart failure (HF, 28.6%), cyanosis (21.4%), arrhythmia and sepsis (17.9%, each), and hypertension (10.7%). Two newborns were placed on a heart transplant waiting list. Three neonates developed congestive HF and 1 had a sudden cardiac death event. A total of 4 (14.3%) newborns have deceased during the NICU stay. More than 90% of the neonates were prescribed more than one medicine at discharge. Conclusion: NCMs require critical intensive care management. Unspecific symptoms characterise clinical findings. The majority of newborns have idiopathic primary CMs, but rare heterogeneous aetiologies may be the underlying cause in some cases. Thus, a multidisciplinary approach is mandatory.
topic cardiomyopathies
newborn
neonatal intensive care unit
aetiology
clinical presentation
outcome
url https://www.jpnim.com/index.php/jpnim/article/view/759
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AT paulosoares neonatalcardiomyopathya20yearoverviewofareferencecentre
AT joanaomiranda neonatalcardiomyopathya20yearoverviewofareferencecentre
AT herciliaguimaraes neonatalcardiomyopathya20yearoverviewofareferencecentre
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