Cardiovascular Compromise in Children with Neuromuscular Disease with Respiratory Disturbance: An Audit for Better Follow-Up
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://doi.org/10.25754/pjp.2020.15784 |
Resumo: | Abstract Introduction: Neuromuscular diseases can be followed by cardiomyopathy and/or arrhythmias that have prognostic consequences. Although respiratory failure is the most frequent cause of death in this group of patients, heart disease is independent of ventilatory compromise and should be investigated. We aimed to investigate the cardiovascular follow-up and diagnosis of a population of patients with neuromuscular disease with respiratory compromise. Methods: Digital files of patients with neuromuscular diseases with respiratory compromise, in active follow-up at a pediatric pulmonology unit of a Portuguese tertiary hospital, were reviewed. Data on demographic, neuromuscular diseases and cardiovascular follow-up characteristics were analyzed. Results: All 49 patients with neuromuscular diseases were analyzed. The median age was 14.3 (1.1-25.1) years and 28 (57%) were males. All of the patients had some type of respiratory compromise. Cardiac evaluation was performed in 35 (71%) patients, with at least six to 12 months of interval, and the following diagnoses were ascertained: dilated cardiomyopathy in three patients with Duchenne muscular dystrophy; right ventricular hypertrophy, mild ascending aortic dilatation and left ventricular diastolic dysfunction in three patients with congenital muscular dystrophy; frequent ventricular ectopic beats and left ventricular diastolic dysfunction in two patients with myotonic dystrophy. Only three patients with neuromuscular diseases with predictable cardiovascular involvement had not been evaluated at our center. Discussion: Most of the patients with neuromuscular diseases with a predictable cardiovascular involvement had been evaluated in a cardiology consultation. The cardiovascular changes present in the group of patients evaluated agree with those described in the literature and the patients are followed-up on according to the recommendations. The diagnosis and monitoring of these cardiovascular changes are mandatory in order to control their progression and impact. |
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Cardiovascular Compromise in Children with Neuromuscular Disease with Respiratory Disturbance: An Audit for Better Follow-UpOriginal articlesAbstract Introduction: Neuromuscular diseases can be followed by cardiomyopathy and/or arrhythmias that have prognostic consequences. Although respiratory failure is the most frequent cause of death in this group of patients, heart disease is independent of ventilatory compromise and should be investigated. We aimed to investigate the cardiovascular follow-up and diagnosis of a population of patients with neuromuscular disease with respiratory compromise. Methods: Digital files of patients with neuromuscular diseases with respiratory compromise, in active follow-up at a pediatric pulmonology unit of a Portuguese tertiary hospital, were reviewed. Data on demographic, neuromuscular diseases and cardiovascular follow-up characteristics were analyzed. Results: All 49 patients with neuromuscular diseases were analyzed. The median age was 14.3 (1.1-25.1) years and 28 (57%) were males. All of the patients had some type of respiratory compromise. Cardiac evaluation was performed in 35 (71%) patients, with at least six to 12 months of interval, and the following diagnoses were ascertained: dilated cardiomyopathy in three patients with Duchenne muscular dystrophy; right ventricular hypertrophy, mild ascending aortic dilatation and left ventricular diastolic dysfunction in three patients with congenital muscular dystrophy; frequent ventricular ectopic beats and left ventricular diastolic dysfunction in two patients with myotonic dystrophy. Only three patients with neuromuscular diseases with predictable cardiovascular involvement had not been evaluated at our center. Discussion: Most of the patients with neuromuscular diseases with a predictable cardiovascular involvement had been evaluated in a cardiology consultation. The cardiovascular changes present in the group of patients evaluated agree with those described in the literature and the patients are followed-up on according to the recommendations. The diagnosis and monitoring of these cardiovascular changes are mandatory in order to control their progression and impact.Sociedade Portuguesa de Pediatria2020-01-27info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.25754/pjp.2020.15784eng2184-44532184-3333Rato, JoãoRebelo, MónicaAnjos, RuiMoreno, TeresaBandeira, TeresaSaianda, AnaFerreira, Rosárioinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-08-03T02:57:56Zoai:ojs.revistas.rcaap.pt:article/15784Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:25:30.497316Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Cardiovascular Compromise in Children with Neuromuscular Disease with Respiratory Disturbance: An Audit for Better Follow-Up |
title |
Cardiovascular Compromise in Children with Neuromuscular Disease with Respiratory Disturbance: An Audit for Better Follow-Up |
spellingShingle |
Cardiovascular Compromise in Children with Neuromuscular Disease with Respiratory Disturbance: An Audit for Better Follow-Up Rato, João Original articles |
title_short |
Cardiovascular Compromise in Children with Neuromuscular Disease with Respiratory Disturbance: An Audit for Better Follow-Up |
title_full |
Cardiovascular Compromise in Children with Neuromuscular Disease with Respiratory Disturbance: An Audit for Better Follow-Up |
title_fullStr |
Cardiovascular Compromise in Children with Neuromuscular Disease with Respiratory Disturbance: An Audit for Better Follow-Up |
title_full_unstemmed |
Cardiovascular Compromise in Children with Neuromuscular Disease with Respiratory Disturbance: An Audit for Better Follow-Up |
title_sort |
Cardiovascular Compromise in Children with Neuromuscular Disease with Respiratory Disturbance: An Audit for Better Follow-Up |
author |
Rato, João |
author_facet |
Rato, João Rebelo, Mónica Anjos, Rui Moreno, Teresa Bandeira, Teresa Saianda, Ana Ferreira, Rosário |
author_role |
author |
author2 |
Rebelo, Mónica Anjos, Rui Moreno, Teresa Bandeira, Teresa Saianda, Ana Ferreira, Rosário |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Rato, João Rebelo, Mónica Anjos, Rui Moreno, Teresa Bandeira, Teresa Saianda, Ana Ferreira, Rosário |
dc.subject.por.fl_str_mv |
Original articles |
topic |
Original articles |
description |
Abstract Introduction: Neuromuscular diseases can be followed by cardiomyopathy and/or arrhythmias that have prognostic consequences. Although respiratory failure is the most frequent cause of death in this group of patients, heart disease is independent of ventilatory compromise and should be investigated. We aimed to investigate the cardiovascular follow-up and diagnosis of a population of patients with neuromuscular disease with respiratory compromise. Methods: Digital files of patients with neuromuscular diseases with respiratory compromise, in active follow-up at a pediatric pulmonology unit of a Portuguese tertiary hospital, were reviewed. Data on demographic, neuromuscular diseases and cardiovascular follow-up characteristics were analyzed. Results: All 49 patients with neuromuscular diseases were analyzed. The median age was 14.3 (1.1-25.1) years and 28 (57%) were males. All of the patients had some type of respiratory compromise. Cardiac evaluation was performed in 35 (71%) patients, with at least six to 12 months of interval, and the following diagnoses were ascertained: dilated cardiomyopathy in three patients with Duchenne muscular dystrophy; right ventricular hypertrophy, mild ascending aortic dilatation and left ventricular diastolic dysfunction in three patients with congenital muscular dystrophy; frequent ventricular ectopic beats and left ventricular diastolic dysfunction in two patients with myotonic dystrophy. Only three patients with neuromuscular diseases with predictable cardiovascular involvement had not been evaluated at our center. Discussion: Most of the patients with neuromuscular diseases with a predictable cardiovascular involvement had been evaluated in a cardiology consultation. The cardiovascular changes present in the group of patients evaluated agree with those described in the literature and the patients are followed-up on according to the recommendations. The diagnosis and monitoring of these cardiovascular changes are mandatory in order to control their progression and impact. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-01-27 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://doi.org/10.25754/pjp.2020.15784 |
url |
https://doi.org/10.25754/pjp.2020.15784 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
2184-4453 2184-3333 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Sociedade Portuguesa de Pediatria |
publisher.none.fl_str_mv |
Sociedade Portuguesa de Pediatria |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
|
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1799133524303806465 |