Cargando…

Experience in neuromuscular diseases in children and adolescents and their comorbidities in a tertiary hospital

INTRODUCTION: Neuromuscular diseases include a large group of heterogeneous and rare pathologies that affect different components of the motor unit. It is essential to optimize resources to know the prevalence of comorbidities in the most frequent groups to establish an early multidisciplinary appro...

Descripción completa

Detalles Bibliográficos
Autores principales: Gascón-Navarro, J. A., De La Torre-Aguilar, M. J., Fernández-Ramos, J. A., Torres-Borrego, J., Pérez-Navero, J. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597309/
https://www.ncbi.nlm.nih.gov/pubmed/34784950
http://dx.doi.org/10.1186/s13052-021-01176-4
_version_ 1784600584111783936
author Gascón-Navarro, J. A.
De La Torre-Aguilar, M. J.
Fernández-Ramos, J. A.
Torres-Borrego, J.
Pérez-Navero, J. L.
author_facet Gascón-Navarro, J. A.
De La Torre-Aguilar, M. J.
Fernández-Ramos, J. A.
Torres-Borrego, J.
Pérez-Navero, J. L.
author_sort Gascón-Navarro, J. A.
collection PubMed
description INTRODUCTION: Neuromuscular diseases include a large group of heterogeneous and rare pathologies that affect different components of the motor unit. It is essential to optimize resources to know the prevalence of comorbidities in the most frequent groups to establish an early multidisciplinary approach in a specialized setting. PATIENTS AND METHODS: Retrospective descriptive study of pediatric and adolescent patients with neuromuscular diseases (NMDs). The Inclusion criteria were NMDs patients with motor neuron involvement divided into three groups, depending on the affected component of the motor unit. Group I: involvement of the motor neuron; Group II: peripheral neuropathies; Group III: myopathies. Demographic variables, association with comorbidities, need for respiratory support, and rehabilitative treatment were collected in each group. RESULTS: Ninety-six patients who met the inclusion criteria were studied. In group I, when compared to the other two groups, a higher incidence of scoliosis (68.3%, p = 0.011), deformity of the rib cage (31.3%, p = 0.0001), chronic respiratory insufficiency (62.5%, p = 0.001) and bronchial aspiration (12.5%, p = 0.03) was detected. In this group, 50%of the patients required non-invasive mechanical ventilation (p = 0.0001). The in-hospital requirement for respiratory physiotherapy was higher in group I (75%, p = 0.001). We observed a higher incidence of scoliosis in Group III compared to Group II. CONCLUSIONS: Neuromuscular diseases with motor neuron involvement present more comorbidities and require an early approach after diagnosis to improve prognosis.
format Online
Article
Text
id pubmed-8597309
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-85973092021-11-19 Experience in neuromuscular diseases in children and adolescents and their comorbidities in a tertiary hospital Gascón-Navarro, J. A. De La Torre-Aguilar, M. J. Fernández-Ramos, J. A. Torres-Borrego, J. Pérez-Navero, J. L. Ital J Pediatr Research INTRODUCTION: Neuromuscular diseases include a large group of heterogeneous and rare pathologies that affect different components of the motor unit. It is essential to optimize resources to know the prevalence of comorbidities in the most frequent groups to establish an early multidisciplinary approach in a specialized setting. PATIENTS AND METHODS: Retrospective descriptive study of pediatric and adolescent patients with neuromuscular diseases (NMDs). The Inclusion criteria were NMDs patients with motor neuron involvement divided into three groups, depending on the affected component of the motor unit. Group I: involvement of the motor neuron; Group II: peripheral neuropathies; Group III: myopathies. Demographic variables, association with comorbidities, need for respiratory support, and rehabilitative treatment were collected in each group. RESULTS: Ninety-six patients who met the inclusion criteria were studied. In group I, when compared to the other two groups, a higher incidence of scoliosis (68.3%, p = 0.011), deformity of the rib cage (31.3%, p = 0.0001), chronic respiratory insufficiency (62.5%, p = 0.001) and bronchial aspiration (12.5%, p = 0.03) was detected. In this group, 50%of the patients required non-invasive mechanical ventilation (p = 0.0001). The in-hospital requirement for respiratory physiotherapy was higher in group I (75%, p = 0.001). We observed a higher incidence of scoliosis in Group III compared to Group II. CONCLUSIONS: Neuromuscular diseases with motor neuron involvement present more comorbidities and require an early approach after diagnosis to improve prognosis. BioMed Central 2021-11-16 /pmc/articles/PMC8597309/ /pubmed/34784950 http://dx.doi.org/10.1186/s13052-021-01176-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Gascón-Navarro, J. A.
De La Torre-Aguilar, M. J.
Fernández-Ramos, J. A.
Torres-Borrego, J.
Pérez-Navero, J. L.
Experience in neuromuscular diseases in children and adolescents and their comorbidities in a tertiary hospital
title Experience in neuromuscular diseases in children and adolescents and their comorbidities in a tertiary hospital
title_full Experience in neuromuscular diseases in children and adolescents and their comorbidities in a tertiary hospital
title_fullStr Experience in neuromuscular diseases in children and adolescents and their comorbidities in a tertiary hospital
title_full_unstemmed Experience in neuromuscular diseases in children and adolescents and their comorbidities in a tertiary hospital
title_short Experience in neuromuscular diseases in children and adolescents and their comorbidities in a tertiary hospital
title_sort experience in neuromuscular diseases in children and adolescents and their comorbidities in a tertiary hospital
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597309/
https://www.ncbi.nlm.nih.gov/pubmed/34784950
http://dx.doi.org/10.1186/s13052-021-01176-4
work_keys_str_mv AT gasconnavarroja experienceinneuromusculardiseasesinchildrenandadolescentsandtheircomorbiditiesinatertiaryhospital
AT delatorreaguilarmj experienceinneuromusculardiseasesinchildrenandadolescentsandtheircomorbiditiesinatertiaryhospital
AT fernandezramosja experienceinneuromusculardiseasesinchildrenandadolescentsandtheircomorbiditiesinatertiaryhospital
AT torresborregoj experienceinneuromusculardiseasesinchildrenandadolescentsandtheircomorbiditiesinatertiaryhospital
AT pereznaverojl experienceinneuromusculardiseasesinchildrenandadolescentsandtheircomorbiditiesinatertiaryhospital