Effect of speech therapy on quality of life in patients with spinocerebelar ataxia type 3
Abstract Background Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of life (QOL). Objective To evaluate the impact of a speech therapy rehabilitation program on the QOL of patients with SCA3. Methods Al...
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| Published in: | Arquivos de neuro-psiquiatria Vol. 80; no. 10; pp. 1017 - 1025 |
|---|---|
| Main Authors: | , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
| Published: |
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil
Thieme Revinter Publicações Ltda
01-10-2022
Arquivos de Neuro-Psiquiatria Academia Brasileira de Neurologia - ABNEURO Academia Brasileira de Neurologia (ABNEURO) |
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| Abstract | Abstract
Background
Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of life (QOL).
Objective
To evaluate the impact of a speech therapy rehabilitation program on the QOL of patients with SCA3.
Methods
All participants were randomly assigned to two groups, an intervention group receiving speech therapy (STG) and a control group (CG). The International Cooperative Ataxia Rating Scale scores were 32.4 ± 20.2, and the Scale for the Assessment and Rating of Ataxia scores were 11.8 ± 8.0. The intervention consisted of a 12-session speech therapy rehabilitation program with oral, pharyngeal, and laryngeal strengthening exercises—the so-called ATAXIA–Myofunctional Orofacial and Vocal Therapy (A-MOVT). They all were submitted to pre- and postintervention evaluations using the World Health Organization's Quality of Life (WHOQOL-BREF) assessment, as well as the Living with Dysarthria (LwD), Quality of Life in Swallowing Disorders (SWAL-QOL), and Food Assessment Tool (EAT-10).
Results
The study sample consisted of 48 patients with SCA3 (STG = 25; CG = 23), mean age was 47.1 ± 11.4 years; mean age at symptom onset was 36.9 ± 11.3 years; disease duration was 11.9 ± 13.3 years. After the 3-month intervention, there were significant changes in the QOL in the STG compared with the CG, when assessed by the LwD (179.12 ± 62.55 vs. 129.88 ± 51.42,
p
< 0.001), SWAL-QOL (869.43 ± 153.63 vs. 911.60 ± 130.90,
p
= 0.010), and EAT-10 (5.16 ± 7.55 vs. 2.08 ± 3.85,
p
= 0.018).
Conclusions
Patients with SCA3 should receive continuous speech therapy as part of the A-MOVT program, because therapy helps to improve difficulty swallowing and dysarthria. |
|---|---|
| AbstractList | BACKGROUNDIndividuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of life (QOL). OBJECTIVETo evaluate the impact of a speech therapy rehabilitation program on the QOL of patients with SCA3. METHODSAll participants were randomly assigned to two groups, an intervention group receiving speech therapy (STG) and a control group (CG). The International Cooperative Ataxia Rating Scale scores were 32.4 ± 20.2, and the Scale for the Assessment and Rating of Ataxia scores were 11.8 ± 8.0. The intervention consisted of a 12-session speech therapy rehabilitation program with oral, pharyngeal, and laryngeal strengthening exercises-the so-called ATAXIA-Myofunctional Orofacial and Vocal Therapy (A-MOVT). They all were submitted to pre- and postintervention evaluations using the World Health Organization's Quality of Life (WHOQOL-BREF) assessment, as well as the Living with Dysarthria (LwD), Quality of Life in Swallowing Disorders (SWAL-QOL), and Food Assessment Tool (EAT-10). RESULTSThe study sample consisted of 48 patients with SCA3 (STG = 25; CG = 23), mean age was 47.1 ± 11.4 years; mean age at symptom onset was 36.9 ± 11.3 years; disease duration was 11.9 ± 13.3 years. After the 3-month intervention, there were significant changes in the QOL in the STG compared with the CG, when assessed by the LwD (179.12 ± 62.55 vs. 129.88 ± 51.42, p < 0.001), SWAL-QOL (869.43 ± 153.63 vs. 911.60 ± 130.90, p = 0.010), and EAT-10 (5.16 ± 7.55 vs. 2.08 ± 3.85, p = 0.018). CONCLUSIONSPatients with SCA3 should receive continuous speech therapy as part of the A-MOVT program, because therapy helps to improve difficulty swallowing and dysarthria. Background Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of life (QOL). Objective To evaluate the impact of a speech therapy rehabilitation program on the QOL of patients with SCA3. Methods All participants were randomly assigned to two groups, an intervention group receiving speech therapy (STG) and a control group (CG). The International Cooperative Ataxia Rating Scale scores were 32.4 20.2, and the Scale for the Assessment and Rating of Ataxia scores were 11.8 8.0. The intervention consisted of a 12-session speech therapy rehabilitation program with oral, pharyngeal, and laryngeal strengthening exercises-the so-called ATAXIA–Myofunctional Orofacial and Vocal Therapy (A-MOVT). They all were submitted to pre- and postintervention evaluations using the World Health Organization's Quality of Life (WHOQOL-BREF) assessment, as well as the Living with Dysarthria (LwD), Quality of Life in Swallowing Disorders (SWAL-QOL), and Food Assessment Tool (EAT-10). Results The study sample consisted of 48 patients with SCA3 (STG ¼ 25; CG ¼ 23), mean age was 47.1 11.4 years; mean age at symptom onset was 36.9 11.3 years; disease duration was 11.9 13.3 years. After the 3-month intervention, there were significant changes in the QOL in the STG compared with the CG, when assessed by the LwD (179.12 62.55 vs. 129.88 51.42, p < 0.001), SWAL-QOL (869.43 153.63 vs. 911.60 130.90, p ¼ 0.010), and EAT-10 (5.16 7.55 vs. 2.08 3.85, p ¼ 0.018). Conclusions Patients with SCA3 should receive continuous speech therapy as part of the A-MOVT program, because therapy helps to improve difficulty swallowing and dysarthria. Abstract Background Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of life (QOL). Objective To evaluate the impact of a speech therapy rehabilitation program on the QOL of patients with SCA3. Methods All participants were randomly assigned to two groups, an intervention group receiving speech therapy (STG) and a control group (CG). The International Cooperative Ataxia Rating Scale scores were 32.4 ± 20.2, and the Scale for the Assessment and Rating of Ataxia scores were 11.8 ± 8.0. The intervention consisted of a 12-session speech therapy rehabilitation program with oral, pharyngeal, and laryngeal strengthening exercises—the so-called ATAXIA–Myofunctional Orofacial and Vocal Therapy (A-MOVT). They all were submitted to pre- and postintervention evaluations using the World Health Organization's Quality of Life (WHOQOL-BREF) assessment, as well as the Living with Dysarthria (LwD), Quality of Life in Swallowing Disorders (SWAL-QOL), and Food Assessment Tool (EAT-10). Results The study sample consisted of 48 patients with SCA3 (STG = 25; CG = 23), mean age was 47.1 ± 11.4 years; mean age at symptom onset was 36.9 ± 11.3 years; disease duration was 11.9 ± 13.3 years. After the 3-month intervention, there were significant changes in the QOL in the STG compared with the CG, when assessed by the LwD (179.12 ± 62.55 vs. 129.88 ± 51.42, p < 0.001), SWAL-QOL (869.43 ± 153.63 vs. 911.60 ± 130.90, p = 0.010), and EAT-10 (5.16 ± 7.55 vs. 2.08 ± 3.85, p = 0.018). Conclusions Patients with SCA3 should receive continuous speech therapy as part of the A-MOVT program, because therapy helps to improve difficulty swallowing and dysarthria. Abstract Background Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of life (QOL). Objective To evaluate the impact of a speech therapy rehabilitation program on the QOL of patients with SCA3. Methods All participants were randomly assigned to two groups, an intervention group receiving speech therapy (STG) and a control group (CG). The International Cooperative Ataxia Rating Scale scores were 32.4 ± 20.2, and the Scale for the Assessment and Rating of Ataxia scores were 11.8 ± 8.0. The intervention consisted of a 12-session speech therapy rehabilitation program with oral, pharyngeal, and laryngeal strengthening exercises—the so-called ATAXIA–Myofunctional Orofacial and Vocal Therapy (A-MOVT). They all were submitted to pre- and postintervention evaluations using the World Health Organization's Quality of Life (WHOQOL-BREF) assessment, as well as the Living with Dysarthria (LwD), Quality of Life in Swallowing Disorders (SWAL-QOL), and Food Assessment Tool (EAT-10). Results The study sample consisted of 48 patients with SCA3 (STG = 25; CG = 23), mean age was 47.1 ± 11.4 years; mean age at symptom onset was 36.9 ± 11.3 years; disease duration was 11.9 ± 13.3 years. After the 3-month intervention, there were significant changes in the QOL in the STG compared with the CG, when assessed by the LwD (179.12 ± 62.55 vs. 129.88 ± 51.42, p < 0.001), SWAL-QOL (869.43 ± 153.63 vs. 911.60 ± 130.90, p = 0.010), and EAT-10 (5.16 ± 7.55 vs. 2.08 ± 3.85, p = 0.018). Conclusions Patients with SCA3 should receive continuous speech therapy as part of the A-MOVT program, because therapy helps to improve difficulty swallowing and dysarthria. Background Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of life (QOL). Objective To evaluate the impact of a speech therapy rehabilitation program on the QOL of patients with SCA3. Methods All participants were randomly assigned to two groups, an intervention group receiving speech therapy (STG) and a control group (CG). The International Cooperative Ataxia Rating Scale scores were 32.4 ± 20.2, and the Scale for the Assessment and Rating of Ataxia scores were 11.8 ± 8.0. The intervention consisted of a 12-session speech therapy rehabilitation program with oral, pharyngeal, and laryngeal strengthening exercises—the so-called ATAXIA–Myofunctional Orofacial and Vocal Therapy (A-MOVT). They all were submitted to pre- and postintervention evaluations using the World Health Organization's Quality of Life (WHOQOL-BREF) assessment, as well as the Living with Dysarthria (LwD), Quality of Life in Swallowing Disorders (SWAL-QOL), and Food Assessment Tool (EAT-10). Results The study sample consisted of 48 patients with SCA3 (STG = 25; CG = 23), mean age was 47.1 ± 11.4 years; mean age at symptom onset was 36.9 ± 11.3 years; disease duration was 11.9 ± 13.3 years. After the 3-month intervention, there were significant changes in the QOL in the STG compared with the CG, when assessed by the LwD (179.12 ± 62.55 vs. 129.88 ± 51.42, p < 0.001), SWAL-QOL (869.43 ± 153.63 vs. 911.60 ± 130.90, p = 0.010), and EAT-10 (5.16 ± 7.55 vs. 2.08 ± 3.85, p = 0.018). Conclusions Patients with SCA3 should receive continuous speech therapy as part of the A-MOVT program, because therapy helps to improve difficulty swallowing and dysarthria. Background Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of life (QOL). Objective To evaluate the impact of a speech therapy rehabilitation program on the QOL of patients with SCA3. Methods All participants were randomly assigned to two groups, an intervention group receiving speech therapy (STG) and a control group (CG). The International Cooperative Ataxia Rating Scale scores were 32.4 ± 20.2, and the Scale for the Assessment and Rating of Ataxia scores were 11.8 ± 8.0. The intervention consisted of a 12-session speech therapy rehabilitation program with oral, pharyngeal, and laryngeal strengthening exercises—the so-called ATAXIA–Myofunctional Orofacial and Vocal Therapy (A-MOVT). They all were submitted to pre- and postintervention evaluations using the World Health Organization's Quality of Life (WHOQOL-BREF) assessment, as well as the Living with Dysarthria (LwD), Quality of Life in Swallowing Disorders (SWAL-QOL), and Food Assessment Tool (EAT-10). Results The study sample consisted of 48 patients with SCA3 (STG = 25; CG = 23), mean age was 47.1 ± 11.4 years; mean age at symptom onset was 36.9 ± 11.3 years; disease duration was 11.9 ± 13.3 years. After the 3-month intervention, there were significant changes in the QOL in the STG compared with the CG, when assessed by the LwD (179.12 ± 62.55 vs. 129.88 ± 51.42, p < 0.001), SWAL-QOL (869.43 ± 153.63 vs. 911.60 ± 130.90, p = 0.010), and EAT-10 (5.16 ± 7.55 vs. 2.08 ± 3.85, p = 0.018). Conclusions Patients with SCA3 should receive continuous speech therapy as part of the A-MOVT program, because therapy helps to improve difficulty swallowing and dysarthria. Background Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of life (QOL). Objective To evaluate the impact of a speech therapy rehabilitation program on the QOL of patients with SCA3. Methods All participants were randomly assigned to two groups, an intervention group receiving speech therapy (STG) and a control group (CG). The International Cooperative Ataxia Rating Scale scores were 32.4 ± 20.2, and the Scale for the Assessment and Rating of Ataxia scores were 11.8 ± 8.0. The intervention consisted of a 12-session speech therapy rehabilitation program with oral, pharyngeal, and laryngeal strengthening exercises—the so-called ATAXIA–Myofunctional Orofacial and Vocal Therapy (A-MOVT). They all were submitted to pre- and postintervention evaluations using the World Health Organization's Quality of Life (WHOQOL-BREF) assessment, as well as the Living with Dysarthria (LwD), Quality of Life in Swallowing Disorders (SWAL-QOL), and Food Assessment Tool (EAT-10). Results The study sample consisted of 48 patients with SCA3 (STG = 25; CG = 23), mean age was 47.1 ± 11.4 years; mean age at symptom onset was 36.9 ± 11.3 years; disease duration was 11.9 ± 13.3 years. After the 3-month intervention, there were significant changes in the QOL in the STG compared with the CG, when assessed by the LwD (179.12 ± 62.55 vs. 129.88 ± 51.42, p < 0.001), SWAL-QOL (869.43 ± 153.63 vs. 911.60 ± 130.90, p = 0.010), and EAT-10 (5.16 ± 7.55 vs. 2.08 ± 3.85, p = 0.018). Conclusions Patients with SCA3 should receive continuous speech therapy as part of the A-MOVT program, because therapy helps to improve difficulty swallowing and dysarthria. Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of life (QOL). To evaluate the impact of a speech therapy rehabilitation program on the QOL of patients with SCA3. All participants were randomly assigned to two groups, an intervention group receiving speech therapy (STG) and a control group (CG). The International Cooperative Ataxia Rating Scale scores were 32.4 ± 20.2, and the Scale for the Assessment and Rating of Ataxia scores were 11.8 ± 8.0. The intervention consisted of a 12-session speech therapy rehabilitation program with oral, pharyngeal, and laryngeal strengthening exercises-the so-called ATAXIA-Myofunctional Orofacial and Vocal Therapy (A-MOVT). They all were submitted to pre- and postintervention evaluations using the World Health Organization's Quality of Life (WHOQOL-BREF) assessment, as well as the Living with Dysarthria (LwD), Quality of Life in Swallowing Disorders (SWAL-QOL), and Food Assessment Tool (EAT-10). The study sample consisted of 48 patients with SCA3 (STG = 25; CG = 23), mean age was 47.1 ± 11.4 years; mean age at symptom onset was 36.9 ± 11.3 years; disease duration was 11.9 ± 13.3 years. After the 3-month intervention, there were significant changes in the QOL in the STG compared with the CG, when assessed by the LwD (179.12 ± 62.55 vs. 129.88 ± 51.42, < 0.001), SWAL-QOL (869.43 ± 153.63 vs. 911.60 ± 130.90, = 0.010), and EAT-10 (5.16 ± 7.55 vs. 2.08 ± 3.85, = 0.018). Patients with SCA3 should receive continuous speech therapy as part of the A-MOVT program, because therapy helps to improve difficulty swallowing and dysarthria. |
| Abstract_FL | Resumo
Antecedentes
Indivíduos com ataxia espinocerebelar tipo 3 (AEC3) apresentam distúrbios da comunicação e deterioração da deglutição e, consequentemente, na qualidade de vida (QV).
Objetivo
Avaliar o impacto de um programa de reabilitação fonoaudiológica na QV em pacientes com AEC3.
Métodos
Todos os participantes foram alocados aleatoriamente em dois grupos, um grupo intervenção que recebeu terapia fonoaudiológica (GTF) e um grupo controle (GC). As pontuações das escalas: International Cooperative Ataxia Rating Scale (ICARS) foram 32,4 ± 20,2 e da Scale for the Assessment and Rating of Ataxia (SARA) foram 11,8 ± 8,0. A intervenção consistiu em um programa de reabilitação fonoaudiológica de 12 sessões composto por exercícios de fortalecimento oral, faríngeo e laríngeo - denominados ATAXIA - Terapia Miofuncional Orofacial e Vocal (A-TMOV). Todos foram submetidos a avaliações pré e pós-intervenção por meio dos protocolos World Health Organization's Quality of Life (WHOQOL-BREF), Vivendo com Disartria (VcD), Quality of Life in Swallowing Disorders (SWAL-QOL) e Food Assessment Tool (EAT-10).
Resultados
A amostra foi composta por 48 pacientes com AEC3 (25 no GTF e 23 no GC), média de idade 47,1 ± 11,4anos; média de idade de início dos sintomas 36,9 ± 11,3anos; duração da doença 11,9 ± 13,3anos. Após intervenção de três meses, houve mudanças significativas na QV no GTF em comparação com o GC quando avaliado pelo VcD (179,12 ± 62,55 versus129,88 ± 51,42,
p
< 0,001), SWAL-QOL (869,43 ± 153,63 versus 911,60 ± 130,90,
p
= 0,010), EAT-10 (5,16 ± 7,55 versus 2,08 ± 3,85,
p
= 0,018).
Conclusões
Pacientes com AEC3 devem receber terapia fonoaudiológica contínua como parte do programa A-TMOV, pois a terapia ajuda a melhorar a dificuldade de deglutição e a disartria. |
| Author | Padovani, Marina Haddad, Leonardo Barsottini, Orlando Chien, Hsin Fen Diaféria, Giovana Braga Neto, Pedro Haddad, Fernanda Bommarito, Silvana Voos, Mariana Callil Park, Sung Woo Pedroso, José Luiz |
| AuthorAffiliation | 1 Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Neurologia, São Paulo SP, Brazil 2 Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Fonoaudiologia, São Paulo SP, Brazil 7 Universidade de São Paulo, Faculdade de Medicina de São Paulo, Departamento de Ortopedia e Traumatologia, São Paulo SP, Brazil 3 Universidade Federal do Ceará, Serviço de Neurologia e Neurocirurgia, Fortaleza CE, Brazil 6 Universidade Pontífice Católica de São Paulo, Faculdade de Ciências Humanas e da Saúde, São Paulo SP, Brazil 5 Faculdade de Ciências Médicas da Santa Casa, Departamento de Fonoaudiologia, São Paulo SP, Brazil 4 Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço, São Paulo SP, Brazil |
| AuthorAffiliation_xml | – name: 1 Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Neurologia, São Paulo SP, Brazil – name: 5 Faculdade de Ciências Médicas da Santa Casa, Departamento de Fonoaudiologia, São Paulo SP, Brazil – name: 3 Universidade Federal do Ceará, Serviço de Neurologia e Neurocirurgia, Fortaleza CE, Brazil – name: 4 Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço, São Paulo SP, Brazil – name: 2 Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Fonoaudiologia, São Paulo SP, Brazil – name: 7 Universidade de São Paulo, Faculdade de Medicina de São Paulo, Departamento de Ortopedia e Traumatologia, São Paulo SP, Brazil – name: 6 Universidade Pontífice Católica de São Paulo, Faculdade de Ciências Humanas e da Saúde, São Paulo SP, Brazil – name: Universidade de São Paulo – name: Universidade Federal do Ceará – name: Universidade Federal de São Paulo – name: Faculdade de Ciências Médicas da Santa Casa de São Paulo – name: Universidade Pontífice Católica de São Paulo |
| Author_xml | – sequence: 1 givenname: Giovana orcidid: 0000-0001-9663-0477 surname: Diaféria fullname: Diaféria, Giovana organization: Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Neurologia, São Paulo SP, Brazil – sequence: 2 givenname: Silvana orcidid: 0000-0003-3708-7878 surname: Bommarito fullname: Bommarito, Silvana organization: Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Fonoaudiologia, São Paulo SP, Brazil – sequence: 3 givenname: Pedro orcidid: 0000-0001-9186-9243 surname: Braga Neto fullname: Braga Neto, Pedro organization: Universidade Federal do Ceará, Serviço de Neurologia e Neurocirurgia, Fortaleza CE, Brazil – sequence: 4 givenname: Sung Woo orcidid: 0000-0003-0157-2863 surname: Park fullname: Park, Sung Woo organization: Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço, São Paulo SP, Brazil – sequence: 5 givenname: Marina orcidid: 0000-0002-1795-317X surname: Padovani fullname: Padovani, Marina organization: Faculdade de Ciências Médicas da Santa Casa, Departamento de Fonoaudiologia, São Paulo SP, Brazil – sequence: 6 givenname: Fernanda orcidid: 0000-0002-5597-1176 surname: Haddad fullname: Haddad, Fernanda organization: Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço, São Paulo SP, Brazil – sequence: 7 givenname: Leonardo orcidid: 0000-0003-2988-0139 surname: Haddad fullname: Haddad, Leonardo organization: Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço, São Paulo SP, Brazil – sequence: 8 givenname: Mariana Callil orcidid: 0000-0001-6252-7287 surname: Voos fullname: Voos, Mariana Callil organization: Universidade Pontífice Católica de São Paulo, Faculdade de Ciências Humanas e da Saúde, São Paulo SP, Brazil – sequence: 9 givenname: Hsin Fen orcidid: 0000-0002-2490-6021 surname: Chien fullname: Chien, Hsin Fen organization: Universidade de São Paulo, Faculdade de Medicina de São Paulo, Departamento de Ortopedia e Traumatologia, São Paulo SP, Brazil – sequence: 10 givenname: José Luiz orcidid: 0000-0002-1672-8894 surname: Pedroso fullname: Pedroso, José Luiz email: jlpedroso.neuro@gmail.com organization: Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Neurologia, São Paulo SP, Brazil – sequence: 11 givenname: Orlando orcidid: 0000-0002-0107-0831 surname: Barsottini fullname: Barsottini, Orlando organization: Universidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Neurologia, São Paulo SP, Brazil |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36535286$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1007_s12311_023_01640_3 |
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| ContentType | Journal Article |
| Copyright | Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/). Copyright Arquivos de Neuro-Psiquiatria Oct 2022 Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. ( ) 2022 Academia Brasileira de Neurologia. This work is licensed under a Creative Commons Attribution 4.0 International License. |
| Copyright_xml | – notice: Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit – notice: Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/). – notice: Copyright Arquivos de Neuro-Psiquiatria Oct 2022 – notice: Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. ( ) 2022 Academia Brasileira de Neurologia. – notice: This work is licensed under a Creative Commons Attribution 4.0 International License. |
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| DOI | 10.1055/s-0042-1755203 |
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| DocumentTitleAlternate | Efeito da terapia fonoaudiológica na qualidade de vida de pacientes com ataxia espinocerebelar tipo 3 |
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| Keywords | Deglutition Disorders Fonoterapia Speech Therapy Qualidade de Vida Quality of Life Transtornos de Deglutição Machado-Joseph Disease Dysarthria Disartria Doença de Machado-Joseph |
| Language | English |
| License | CC BY 4.0 Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/). This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. This work is licensed under a Creative Commons Attribution 4.0 International License. http://creativecommons.org/licenses/by/4.0 |
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Hamdy, S; Woisard, V; Wuttge-Hannig, A; Ortega, P – volume: 28 start-page: 46 issue: 01 year: 2016 end-page: 52 article-title: Communicative aspects and coping strategies in patients with Parkinson's disease publication-title: CoDAS contributor: fullname: Costa, FP; Diaféria, G; Behlau, M – volume: 25 year: 2020 article-title: Effect of speech-language therapy in Machado-Joseph disease: case report publication-title: Audiol Commun Res contributor: fullname: Dos Santos Marques, T; Furia, CL; Lira, JO – volume: 29 start-page: 1 issue: 01 year: 2003 end-page: 13 article-title: Guidelines for the pathoanatomical examination of the lower brain stem in ingestive and swallowing disorders and its application to a dysphagic spinocerebellar ataxia type 3 patient publication-title: Neuropathol Appl Neurobiol contributor: fullname: Rüb, U; Brunt, ER; Del Turco, D – volume: 24 start-page: 763 issue: 04 year: 2015 end-page: 789 article-title: Nonspeech Oral Movements and Oral Motor Disorders: A Narrative Review publication-title: Am J Speech Lang Pathol contributor: fullname: Kent, RD – volume: 14 start-page: 136 issue: 01 year: 2009 end-page: 141 article-title: [The action of levodopa and its influence on voice and speech of patients with Parkinson disease] publication-title: Rev Soc Bras Fonoaudiol contributor: fullname: de Azevedo, LL; Cardoso, F – volume: 6 start-page: 35 year: 2011 end-page: 35 article-title: Machado-Joseph Disease: from first descriptions to new perspectives publication-title: Orphanet J Rare Dis contributor: fullname: Bettencourt, C; Lima, M – volume: 76 start-page: 674 issue: 10 year: 2018 end-page: 684 article-title: Cross-cultural adaptation and validation of the International Cooperative Ataxia Rating Scale (ICARS) to Brazilian Portuguese publication-title: Arq Neuropsiquiatr contributor: fullname: Maggi, FA; Braga Neto, P; Chien, HF – volume: 274 start-page: 1139 issue: 02 year: 2017 end-page: 1145 article-title: Phonoarticulation in spinocerebellar ataxia type 3 publication-title: Eur Arch Otorhinolaryngol contributor: fullname: Wolf, AE; Mourão, L; França Jr, MC; Machado Júnior, AJ; Crespo, AN – volume: 8 start-page: 187 issue: 05 year: 2005 end-page: 193 article-title: [The International Classification of Functioning, Disability and Health: Concepts, Uses and Perspectives] publication-title: Rev Bras Epidemiol contributor: fullname: Farias, N; Buchalla, CM – volume: 10 start-page: 291 issue: 02 year: 2011 end-page: 295 article-title: Sleep disorders in machado-joseph disease: frequency, discriminative thresholds, predictive values, and correlation with ataxia-related motor and non-motor features publication-title: Cerebellum contributor: fullname: Pedroso, JL; Braga Neto, P; Felício, AC – volume: 6 start-page: 266 issue: 03 year: 2004 end-page: 271 article-title: [The relation among sleep apnea, snore and mouth breathing] publication-title: Rev CEFAC contributor: fullname: Burger, RCP; Caixeta, EC; Di Ninno, CQMS – volume: 60 start-page: 11 issue: 01 year: 2008 end-page: 19 article-title: Living with dysarthria: evaluation of a self-report questionnaire publication-title: Folia Phoniatr Logop contributor: fullname: Hartelius, L; Elmberg, M; Holm, R; Lovberg, AS; Nikolaidis, S – volume: 13 start-page: 299 issue: 02 year: 2004 end-page: 310 article-title: The World Health Organization's WHOQOL-BREF quality of life assessment: psychometric properties and results of the international field trial. 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Background
Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in... Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of life (QOL). To... Background Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of... Background Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of... BACKGROUNDIndividuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of life... Background Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in quality of... Abstract Background Individuals with spinocerebellar ataxia type 3 (SCA3) present communication and swallowing disorders, and consequent deterioration in... |
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| SubjectTerms | Adult Ataxia Cerebellar Ataxia deglutition disorders Deglutition Disorders - etiology Dysarthria Humans Machado-Joseph Disease Middle Aged NEUROSCIENCES Original Original Article Pharynx PSYCHIATRY Quality of Life Rehabilitation Speech Speech Therapy Swallowing |
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| Title | Effect of speech therapy on quality of life in patients with spinocerebelar ataxia type 3 |
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