Qualidade de vida em portadores de doença falciforme

Detalhes bibliográficos
Autor(a) principal: Menezes, Adeline Soraya de Oliveira da Paz [UNIFESP]
Data de Publicação: 2013
Outros Autores: Len, Claudio Arnaldo [UNIFESP], Hilário, Maria Odete Esteves [UNIFESP], Terreri, Maria Teresa Ramos Ascensão [UNIFESP], Braga, Josefina Aparecida Pellegrini [UNIFESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1590/S0103-05822013000100005
http://repositorio.unifesp.br/handle/11600/7664
Resumo: OBJECTIVE: To evaluate the quality of life in children and adolescents with sickle cell disease attending a blood reference center, and to assess the quality of life of their relatives. METHODS: Cross-sectional study that included 100 patients with sickle cell disease, which were divided into three subgroups according to age: 5 to 7 (n=18), 8 to 12 (n=32), and 13 to 18 years-old (n=50), and their parents. The Control Group included 50 healthy children and adolescents from a public local school, also divided into the same three age subgroups and their caregivers. The Pediatric Quality of life Inventory (PedsQL), version 4.0, was applied in both groups. The generic questionnaire Medical Outcomes Study 36 - Item Short-Form Health Survey (SF-36) was applied to the relatives. The answers were linearly transformed into a score and compared by non-parametric tests. RESULTS: The PedsQL scores of patients were significantly lower than those obtained in the Control Group (p<0.0001) in all studied areas (physical, emotional, social skills, and school activities). Similarly, SF-36 scores applied to the patients' parents were lower than those obtained in the Control Group in all studied aspects (p<0.0001). CONCLUSIONS: Sickle cell disease affects the quality of life of children, adolescents, and their families. Patients sense restrictions in the emotional, social, family and physical aspects, among others.
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spelling Qualidade de vida em portadores de doença falciformeQuality of life in patients with sickle cell diseaseCalidad de vida en portadores de enfermedad falciformequality of lifeanemia, sickle cellChildrenadolescentsqualidade de vidaanemia falciformeCriançasadolescentesOBJECTIVE: To evaluate the quality of life in children and adolescents with sickle cell disease attending a blood reference center, and to assess the quality of life of their relatives. METHODS: Cross-sectional study that included 100 patients with sickle cell disease, which were divided into three subgroups according to age: 5 to 7 (n=18), 8 to 12 (n=32), and 13 to 18 years-old (n=50), and their parents. The Control Group included 50 healthy children and adolescents from a public local school, also divided into the same three age subgroups and their caregivers. The Pediatric Quality of life Inventory (PedsQL), version 4.0, was applied in both groups. The generic questionnaire Medical Outcomes Study 36 - Item Short-Form Health Survey (SF-36) was applied to the relatives. The answers were linearly transformed into a score and compared by non-parametric tests. RESULTS: The PedsQL scores of patients were significantly lower than those obtained in the Control Group (p<0.0001) in all studied areas (physical, emotional, social skills, and school activities). Similarly, SF-36 scores applied to the patients' parents were lower than those obtained in the Control Group in all studied aspects (p<0.0001). CONCLUSIONS: Sickle cell disease affects the quality of life of children, adolescents, and their families. Patients sense restrictions in the emotional, social, family and physical aspects, among others.OBJETIVO: Evaluar la calidad de vida relacionada a la salud en niños y adolescentes con enfermedad falciforme asistidas en un servicio de hemoterapia de referencia y medir la calidad de vida relacionada a la salud de los respectivos familiares. MÉTODOS: Estudio transversal y seccional en 100 pacientes portadores de enfermedad falciforme, divididos en tres subgrupos conforme a la franja de edad: de 5 a 7 (n=18), de 8 a 12 (n=32) y de 13 a 18 (n=50) años con sus respectivos padres. El Grupo Control fue compuesto por 50 niños y adolescentes sanos de una escuela pública local, también divididos en los mismos tres subgrupos de edad y sus respectivos cuidadores. Se aplicó el cuestionario genérico «Pediatric Quality of Life Inventory» (PedsQL), versión 4.0, a ambos grupos. A los familiares se aplicó el cuestionario genérico Medical Outcomes Study 36 - Item Short-Form Health Survey (SF-36). Las respuestas obtenidas fueron linealmente transformadas en un escore y comparadas con la ayuda de pruebas no paramétricas. RESULTADOS: Los escores de los pacientes en el PedsQL fueron inferiores a aquellos del Grupo Control (p<0,0001) en los aspectos estudiados (capacidades física, emocional, social y actividad escolar). Del mismo modo, los escores del SF-36 aplicados a los padres de los pacientes fueron más bajos que los de padres del Grupo Control en todos los aspectos estudiados (p<0,0001). CONCLUSIONES: La enfermedad falciforme compromete la calidad de vida de los niños, de los adolescentes y de sus respectivas familias. Los pacientes perciben restricciones en los aspectos emocional, social, familiar y físico, entre otros.OBJETIVO: Avaliar a qualidade de vida relacionada à saúde de crianças e adolescentes com doença falciforme assistidas em um hemocentro de referência e mensurar a qualidade de vida relacionada à saúde dos respectivos familiares. MÉTODOS: Estudo transversal e seccional com 100 pacientes portadores de doença falciforme, divididos em três subgrupos conforme a faixa etária: de 5 a 7 (n=18), de 8 a 12 (n=32) e de 13 a 18 anos (n=50) e com seus respectivos pais. O Grupo Controle foi composto por 50 crianças e adolescentes saudáveis de uma escola pública local, também divididos nos três subgrupos de idade e seus respectivos cuidadores. Foi aplicado o questionário genérico Pediatric Quality of Life Inventory (PedsQL), versão 4.0, em ambos os grupos. Aos familiares foi aplicado o questionário genérico Medical Outcomes Study 36 - Item Short-Form Health Survey (SF-36). As respostas obtidas foram linearmente transformadas em um escore e comparadas com o auxílio de testes não paramétricos. RESULTADOS: Os escores dos pacientes no PedsQL foram inferiores àqueles do Grupo Controle (p<0,0001) nos aspectos estudados (capacidades física, emocional, social e atividade escolar). Da mesma forma, os escores do SF-36 aplicados aos pais dos pacientes foram mais baixos que os de pais do Grupo Controle em todos os aspectos estudados (p<0,0001). CONCLUSÕES: A doença falciforme compromete a qualidade de vida das crianças, dos adolescentes e de suas respectivas famílias. Os pacientes percebem restrições nos aspectos emocional, social, familiar e físico, dentre outros.UNIFESPUNIFESP-EPM Departamento de PediatriaUNIFESP, EPM Depto. de PediatriaSciELOSociedade de Pediatria de São PauloUniversidade Federal de São Paulo (UNIFESP)Menezes, Adeline Soraya de Oliveira da Paz [UNIFESP]Len, Claudio Arnaldo [UNIFESP]Hilário, Maria Odete Esteves [UNIFESP]Terreri, Maria Teresa Ramos Ascensão [UNIFESP]Braga, Josefina Aparecida Pellegrini [UNIFESP]2015-06-14T13:45:20Z2015-06-14T13:45:20Z2013-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion24-29application/pdfhttp://dx.doi.org/10.1590/S0103-05822013000100005Revista Paulista de Pediatria. Sociedade de Pediatria de São Paulo, v. 31, n. 1, p. 24-29, 2013.10.1590/S0103-05822013000100005S0103-05822013000100005.pdf0103-0582S0103-05822013000100005http://repositorio.unifesp.br/handle/11600/7664porRevista Paulista de Pediatriainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-06T02:16:07Zoai:repositorio.unifesp.br/:11600/7664Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-06T02:16:07Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Qualidade de vida em portadores de doença falciforme
Quality of life in patients with sickle cell disease
Calidad de vida en portadores de enfermedad falciforme
title Qualidade de vida em portadores de doença falciforme
spellingShingle Qualidade de vida em portadores de doença falciforme
Menezes, Adeline Soraya de Oliveira da Paz [UNIFESP]
quality of life
anemia, sickle cell
Children
adolescents
qualidade de vida
anemia falciforme
Crianças
adolescentes
title_short Qualidade de vida em portadores de doença falciforme
title_full Qualidade de vida em portadores de doença falciforme
title_fullStr Qualidade de vida em portadores de doença falciforme
title_full_unstemmed Qualidade de vida em portadores de doença falciforme
title_sort Qualidade de vida em portadores de doença falciforme
author Menezes, Adeline Soraya de Oliveira da Paz [UNIFESP]
author_facet Menezes, Adeline Soraya de Oliveira da Paz [UNIFESP]
Len, Claudio Arnaldo [UNIFESP]
Hilário, Maria Odete Esteves [UNIFESP]
Terreri, Maria Teresa Ramos Ascensão [UNIFESP]
Braga, Josefina Aparecida Pellegrini [UNIFESP]
author_role author
author2 Len, Claudio Arnaldo [UNIFESP]
Hilário, Maria Odete Esteves [UNIFESP]
Terreri, Maria Teresa Ramos Ascensão [UNIFESP]
Braga, Josefina Aparecida Pellegrini [UNIFESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Menezes, Adeline Soraya de Oliveira da Paz [UNIFESP]
Len, Claudio Arnaldo [UNIFESP]
Hilário, Maria Odete Esteves [UNIFESP]
Terreri, Maria Teresa Ramos Ascensão [UNIFESP]
Braga, Josefina Aparecida Pellegrini [UNIFESP]
dc.subject.por.fl_str_mv quality of life
anemia, sickle cell
Children
adolescents
qualidade de vida
anemia falciforme
Crianças
adolescentes
topic quality of life
anemia, sickle cell
Children
adolescents
qualidade de vida
anemia falciforme
Crianças
adolescentes
description OBJECTIVE: To evaluate the quality of life in children and adolescents with sickle cell disease attending a blood reference center, and to assess the quality of life of their relatives. METHODS: Cross-sectional study that included 100 patients with sickle cell disease, which were divided into three subgroups according to age: 5 to 7 (n=18), 8 to 12 (n=32), and 13 to 18 years-old (n=50), and their parents. The Control Group included 50 healthy children and adolescents from a public local school, also divided into the same three age subgroups and their caregivers. The Pediatric Quality of life Inventory (PedsQL), version 4.0, was applied in both groups. The generic questionnaire Medical Outcomes Study 36 - Item Short-Form Health Survey (SF-36) was applied to the relatives. The answers were linearly transformed into a score and compared by non-parametric tests. RESULTS: The PedsQL scores of patients were significantly lower than those obtained in the Control Group (p<0.0001) in all studied areas (physical, emotional, social skills, and school activities). Similarly, SF-36 scores applied to the patients' parents were lower than those obtained in the Control Group in all studied aspects (p<0.0001). CONCLUSIONS: Sickle cell disease affects the quality of life of children, adolescents, and their families. Patients sense restrictions in the emotional, social, family and physical aspects, among others.
publishDate 2013
dc.date.none.fl_str_mv 2013-03-01
2015-06-14T13:45:20Z
2015-06-14T13:45:20Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0103-05822013000100005
Revista Paulista de Pediatria. Sociedade de Pediatria de São Paulo, v. 31, n. 1, p. 24-29, 2013.
10.1590/S0103-05822013000100005
S0103-05822013000100005.pdf
0103-0582
S0103-05822013000100005
http://repositorio.unifesp.br/handle/11600/7664
url http://dx.doi.org/10.1590/S0103-05822013000100005
http://repositorio.unifesp.br/handle/11600/7664
identifier_str_mv Revista Paulista de Pediatria. Sociedade de Pediatria de São Paulo, v. 31, n. 1, p. 24-29, 2013.
10.1590/S0103-05822013000100005
S0103-05822013000100005.pdf
0103-0582
S0103-05822013000100005
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Revista Paulista de Pediatria
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 24-29
application/pdf
dc.publisher.none.fl_str_mv Sociedade de Pediatria de São Paulo
publisher.none.fl_str_mv Sociedade de Pediatria de São Paulo
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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