Detalhes bibliográficos
Ano de defesa: |
2023 |
Autor(a) principal: |
KÜSTER, NATACH WYSOCKI
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Orientador(a): |
Leite, Ana Paula Dassie
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Banca de defesa: |
Não Informado pela instituição |
Tipo de documento: |
Dissertação
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Tipo de acesso: |
Acesso aberto |
Idioma: |
por |
Instituição de defesa: |
Universidade Estadual do Centro-Oeste
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Programa de Pós-Graduação: |
Programa de Pós-Graduação em Desenvolvimento Comunitário (Mestrado Interdisciplinar)
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Departamento: |
Unicentro::Departamento de Saúde de Irati
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País: |
Brasil
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Palavras-chave em Português: |
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Palavras-chave em Inglês: |
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Área do conhecimento CNPq: |
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Link de acesso: |
http://tede.unicentro.br:8080/jspui/handle/jspui/2209
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Resumo: |
Objective: Objective: Obtain data regarding vocal self-assessment and quality of life of people diagnosed with Multiple Sclerosis. Method: This is an observational, analytical and cross-sectional study. Participants were people diagnosed with MS, of both sexes, who responded to questionnaires to characterize the sample, Brazil Criteria Questionnaire for socioeconomic description; vocal self-assessment instruments (Vocal Disadvantage Index - IDV-10 - and the Living with Dysarthria - VcD protocol), quality of life self-assessment instruments in patients diagnosed with MS (Functional Determination of Quality of Life in Multiple Sclerosis test DEFU and test Multiple Sclerosis Impact Scale - MSIS-29) and clinical assessment using the Expanded Disability Status Scale (EDSS). The data were statistically analyzed in a descriptive and inferential way. Results: Of the 31 people diagnosed with MS evaluated, the majority were adult women with a median age of 32 years. Regarding clinical evaluation, the EDSS indicated that the majority of participants had little involvement in MS and the predominant clinical form is relapsing-remitting. A positive relationship was noted between self-perceived vocal handicap and dysarthria with quality of life scores in people with MS. Conclusion: The self-perception of quality of life of assessed MS patients is linked to the clinical form of the disease and functional disability, measured using the EDSS. Regarding vocal self-perception, it is observed that there is a relationship between the impact of dysphonia and dysarthria with quality of life data, and the greater the impairment of the disease, the greater the vocal handicap and the perception regarding dysarthria and worse quality of life. There were no relationships between voice, quality of life and clinical data and the other socioeconomic variables analyzed. |