Enfrentando a escuridão: Seguimento por seis meses da Distrofia Neuroaxonal Infantil
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Data de Publicação: | 2024 |
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Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/45039 |
Resumo: | Objectives: The objectives of this study were to report a case of Infantile Neuroaxonal Dystrophy, document the progression of neurological impairments over a period of 6 months, and apply a specific assessment scale. Methodology: This study is an experimental case report with a descriptive approach, conducted through teleconsultation and remote monitoring, with the active participation of a physiotherapist who regularly attends to a 4-year-old female patient diagnosed with INAD. The study was submitted to the Ethics Committee of the State University of Paraiba (UEPB) and obtained approval with the number CAAE 74421623.3.0000.5187. The patient was assessed using the Pediatric Evaluation Form from the School Clinic of Physiotherapy (CEF) at UEPB and the Infantile Neuroaxonal Dystrophy Rating Scale (INAD-RS). Results: After the 6-month period, consisting of 30 physiotherapy sessions, twice a week, including stretching exercises and postures from the Neuroevolutionary Concept of Bobath, there was a regression in the child's functional performance, as evidenced by a decrease of 9 points in the INAD-RS score, indicating disease progression. Consequently, guidance was provided to the family environment and health-related advice was given to parents and caregivers. Conclusions: This case report highlights the importance of prior knowledge about INAD, as well as the need for the use of specific assessment scales for its evaluation. It is believed that this study will contribute to furthering the scientific knowledge of professionals in the field. Therefore, the continuation of this research is necessary due to its clinical relevance. |
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Enfrentando a escuridão: Seguimento por seis meses da Distrofia Neuroaxonal Infantil Facing the darkness: A six-month follow-up of Infantile Neuroaxonal DystrophyEnfrentando la oscuridad: Seguimiento de seis meses de la Distrofia Neuroaxonal InfantilNeurodegeneraciónDistrofia neuroaxonial infantilRetraso motor.NeurodegenerationInfantile Neuroaxonal dystrophyMotor delay.NeurodegeneraçãoDistrofia neuroaxonal infantilAtraso motor.Objectives: The objectives of this study were to report a case of Infantile Neuroaxonal Dystrophy, document the progression of neurological impairments over a period of 6 months, and apply a specific assessment scale. Methodology: This study is an experimental case report with a descriptive approach, conducted through teleconsultation and remote monitoring, with the active participation of a physiotherapist who regularly attends to a 4-year-old female patient diagnosed with INAD. The study was submitted to the Ethics Committee of the State University of Paraiba (UEPB) and obtained approval with the number CAAE 74421623.3.0000.5187. The patient was assessed using the Pediatric Evaluation Form from the School Clinic of Physiotherapy (CEF) at UEPB and the Infantile Neuroaxonal Dystrophy Rating Scale (INAD-RS). Results: After the 6-month period, consisting of 30 physiotherapy sessions, twice a week, including stretching exercises and postures from the Neuroevolutionary Concept of Bobath, there was a regression in the child's functional performance, as evidenced by a decrease of 9 points in the INAD-RS score, indicating disease progression. Consequently, guidance was provided to the family environment and health-related advice was given to parents and caregivers. Conclusions: This case report highlights the importance of prior knowledge about INAD, as well as the need for the use of specific assessment scales for its evaluation. It is believed that this study will contribute to furthering the scientific knowledge of professionals in the field. Therefore, the continuation of this research is necessary due to its clinical relevance.Objetivos: Os objetivos do presente estudo foram relatar um caso de Distrofia Neuroaxonal Infantil, a evolução dos comprometimentos neurológicos por um período de 6 meses e aplicar uma escala específica de avaliação. Metodologia: Trata-se de um estudo experimental do tipo relato de caso com abordagem descritiva, realizado na modalidade de teleconsulta e acompanhamento a distância, com a participação ativa de uma fisioterapeuta que acompanha regularmente uma paciente do sexo feminino de 4 anos de idade com diagnóstico de INAD. O estudo foi submetido ao Comitê de Ética da Universidade Estadual da Paraíba (UEPB) e obteve aprovação com o número CAAE 74421623.3.0000.5187. A paciente foi avaliada utilizando a Ficha de Avaliação Pediátrica da Clínica Escola de Fisioterapia (CEF) da UEPB e a escala Infantile Neuroaxonal Dystrophy Rating Scale (INAD-RS). Resultados: Após o período de 6 meses, 30 sessões de fisioterapia, 2 vezes por semana com manobras de alongamento e posturas do conceito neuroevolutivo Bobath, houve regressão no desempenho funcional da criança, uma vez que ela reduziu 9 pontos na INAD-RS, evidenciando progressão da doença. Assim, foram propostas orientações para o ambiente familiar e orientações em saúde aos pais e cuidadores. Considerações Finais: Este relato de caso reforça a importância do conhecimento prévio da INAD, bem como a necessidade da utilização de escalas específicas para a sua avaliação. Acredita-se que este estudo contribuirá para aprofundar o conhecimento científico dos profissionais da área. Portanto, a continuidade desta pesquisa é necessária devido à sua relevância clínica.Objetivos: Los objetivos de este estudio fueron informar un caso de Distrofia Neuroaxonial Infantil, documentar la progresión de los trastornos neurológicos durante un período de 6 meses y aplicar una escala de evaluación específica. Metodología: Este estudio es un informe de caso experimental con un enfoque descriptivo, realizado a través de teleconsulta y monitoreo remoto, con la participación activa de un fisioterapeuta que atiende regularmente a una paciente de 4 años diagnosticada con INAD. El estudio fue sometido al Comité de Ética de la Universidad Estatal de Paraíba (UEPB) y obtuvo la aprobación con el número CAAE 74421623.3.0000.5187. Se evaluó a la paciente utilizando el Formulario de Evaluación Pediátrica de la Clínica Escolar de Fisioterapia (CEF) de la UEPB y la Escala de Evaluación de Distrofia Neuroaxonial Infantil (INAD-RS). Resultados: Después del período de 6 meses, que consistió en 30 sesiones de fisioterapia, dos veces por semana, que incluyeron ejercicios de estiramiento y posturas del Concepto Neuroevolutivo de Bobath, hubo una regresión en el desempeño funcional del niño, como lo demuestra una disminución de 9 puntos en la puntuación de INAD-RS, lo que indica una progresión de la enfermedad. En consecuencia, se brindó orientación al entorno familiar y se dieron consejos relacionados con la salud a los padres y cuidadores. Conclusiones: Este informe de caso destaca la importancia del conocimiento previo sobre INAD, así como la necesidad de utilizar escalas de evaluación específicas para su evaluación. Se cree que este estudio contribuirá a ampliar el conocimiento científico de los profesionales en el campo. Por lo tanto, es necesaria la continuación de esta investigación debido a su relevancia clínica.Research, Society and Development2024-02-13info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/4503910.33448/rsd-v13i2.45039Research, Society and Development; Vol. 13 No. 2; e4813245039Research, Society and Development; Vol. 13 Núm. 2; e4813245039Research, Society and Development; v. 13 n. 2; e48132450392525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/45039/35929Copyright (c) 2024 Ana Beatriz Aragão Monteiro Santos ; Kelly Soares Fariashttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessSantos , Ana Beatriz Aragão Monteiro Farias, Kelly Soares 2024-03-04T09:47:20Zoai:ojs.pkp.sfu.ca:article/45039Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-03-04T09:47:20Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
Enfrentando a escuridão: Seguimento por seis meses da Distrofia Neuroaxonal Infantil Facing the darkness: A six-month follow-up of Infantile Neuroaxonal Dystrophy Enfrentando la oscuridad: Seguimiento de seis meses de la Distrofia Neuroaxonal Infantil |
title |
Enfrentando a escuridão: Seguimento por seis meses da Distrofia Neuroaxonal Infantil |
spellingShingle |
Enfrentando a escuridão: Seguimento por seis meses da Distrofia Neuroaxonal Infantil Santos , Ana Beatriz Aragão Monteiro Neurodegeneración Distrofia neuroaxonial infantil Retraso motor. Neurodegeneration Infantile Neuroaxonal dystrophy Motor delay. Neurodegeneração Distrofia neuroaxonal infantil Atraso motor. |
title_short |
Enfrentando a escuridão: Seguimento por seis meses da Distrofia Neuroaxonal Infantil |
title_full |
Enfrentando a escuridão: Seguimento por seis meses da Distrofia Neuroaxonal Infantil |
title_fullStr |
Enfrentando a escuridão: Seguimento por seis meses da Distrofia Neuroaxonal Infantil |
title_full_unstemmed |
Enfrentando a escuridão: Seguimento por seis meses da Distrofia Neuroaxonal Infantil |
title_sort |
Enfrentando a escuridão: Seguimento por seis meses da Distrofia Neuroaxonal Infantil |
author |
Santos , Ana Beatriz Aragão Monteiro |
author_facet |
Santos , Ana Beatriz Aragão Monteiro Farias, Kelly Soares |
author_role |
author |
author2 |
Farias, Kelly Soares |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Santos , Ana Beatriz Aragão Monteiro Farias, Kelly Soares |
dc.subject.por.fl_str_mv |
Neurodegeneración Distrofia neuroaxonial infantil Retraso motor. Neurodegeneration Infantile Neuroaxonal dystrophy Motor delay. Neurodegeneração Distrofia neuroaxonal infantil Atraso motor. |
topic |
Neurodegeneración Distrofia neuroaxonial infantil Retraso motor. Neurodegeneration Infantile Neuroaxonal dystrophy Motor delay. Neurodegeneração Distrofia neuroaxonal infantil Atraso motor. |
description |
Objectives: The objectives of this study were to report a case of Infantile Neuroaxonal Dystrophy, document the progression of neurological impairments over a period of 6 months, and apply a specific assessment scale. Methodology: This study is an experimental case report with a descriptive approach, conducted through teleconsultation and remote monitoring, with the active participation of a physiotherapist who regularly attends to a 4-year-old female patient diagnosed with INAD. The study was submitted to the Ethics Committee of the State University of Paraiba (UEPB) and obtained approval with the number CAAE 74421623.3.0000.5187. The patient was assessed using the Pediatric Evaluation Form from the School Clinic of Physiotherapy (CEF) at UEPB and the Infantile Neuroaxonal Dystrophy Rating Scale (INAD-RS). Results: After the 6-month period, consisting of 30 physiotherapy sessions, twice a week, including stretching exercises and postures from the Neuroevolutionary Concept of Bobath, there was a regression in the child's functional performance, as evidenced by a decrease of 9 points in the INAD-RS score, indicating disease progression. Consequently, guidance was provided to the family environment and health-related advice was given to parents and caregivers. Conclusions: This case report highlights the importance of prior knowledge about INAD, as well as the need for the use of specific assessment scales for its evaluation. It is believed that this study will contribute to furthering the scientific knowledge of professionals in the field. Therefore, the continuation of this research is necessary due to its clinical relevance. |
publishDate |
2024 |
dc.date.none.fl_str_mv |
2024-02-13 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/45039 10.33448/rsd-v13i2.45039 |
url |
https://rsdjournal.org/index.php/rsd/article/view/45039 |
identifier_str_mv |
10.33448/rsd-v13i2.45039 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/45039/35929 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2024 Ana Beatriz Aragão Monteiro Santos ; Kelly Soares Farias https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2024 Ana Beatriz Aragão Monteiro Santos ; Kelly Soares Farias https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Research, Society and Development |
publisher.none.fl_str_mv |
Research, Society and Development |
dc.source.none.fl_str_mv |
Research, Society and Development; Vol. 13 No. 2; e4813245039 Research, Society and Development; Vol. 13 Núm. 2; e4813245039 Research, Society and Development; v. 13 n. 2; e4813245039 2525-3409 reponame:Research, Society and Development instname:Universidade Federal de Itajubá (UNIFEI) instacron:UNIFEI |
instname_str |
Universidade Federal de Itajubá (UNIFEI) |
instacron_str |
UNIFEI |
institution |
UNIFEI |
reponame_str |
Research, Society and Development |
collection |
Research, Society and Development |
repository.name.fl_str_mv |
Research, Society and Development - Universidade Federal de Itajubá (UNIFEI) |
repository.mail.fl_str_mv |
rsd.articles@gmail.com |
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1797052638177525760 |