Psychosocial and Quality-of-Life Impacts of Cancer Treatment in Children and Adolescents

Detalhes bibliográficos
Autor(a) principal: Pereira, Clara Ignácio Pessoa
Data de Publicação: 2023
Outros Autores: Nascimento, Isadora Bolela, Cruz, Aristides Schier da, Volc, Sahlua Miguel, Tormen, Tiago Hessel
Tipo de documento: Artigo
Idioma: por
eng
spa
Título da fonte: Revista Brasileira de Cancerologia (Online)
Texto Completo: https://rbc.inca.gov.br/index.php/revista/article/view/3888
Resumo: Introduction: As important as the diagnosis and treatment of pediatric cancer are the care related to psychosocial, educational, and emotional impact. Objective: To evaluate in children and adolescents diagnosed with cancer the psychosocial and quality-of-life impacts and the presence of a companion during the procedures. Method: Cross-sectional descriptive study of patients aged 8 to 18 years of age diagnosed with malignant neoplasms. Patients responded the questionnaires PedsQL 4.0 Quality of Life (8 to 12 years), PedsQL 3.0 Cancer Module (8 to 12 years), PedsQL 4.0 Quality of Life (13 to 18 years), PedsQL 3.0 Cancer Module (13 to 18 years) and another about companions created by the authors. Results: There were 25 pediatric oncology patients were included who felt happier in the presence of a companion, and less anxious during the procedures. A great impact on quality of life was perceived. In the Quality-of-Life questionnaire, no significant difference (p=0.627) between the groups of patients aged 8 to 12 years and 13 to 18 years were found, but the group aged 8 to 12 years had a significantly higher impact on the Cancer Module questionnaire (p=0.0094). Conclusion: The impact on quality of life and psychosocial is fairly large in pediatric oncology patients. The youngest appear to suffer great psychosocial impact. Patients claim they are happier in the presence of a companion, and more anxious in its absence.
id INCA-1_7dd4058ea28c5fa321c10fa37b7c34e3
oai_identifier_str oai:rbc.inca.gov.br:article/3888
network_acronym_str INCA-1
network_name_str Revista Brasileira de Cancerologia (Online)
repository_id_str
spelling Psychosocial and Quality-of-Life Impacts of Cancer Treatment in Children and AdolescentsImpactos Psicosociales y en la Calidad de Vida del Tratamiento del Cáncer en Niños y AdolescentesImpactos Psicossociais e na Qualidade de Vida do Tratamento Oncológico em Crianças e Adolescentesneoplasias/terapiasaúde da criançaimpacto psicossocialqualidade de vidaneoplasms/therapychild healthpsychosocial impactquality of lifeneoplasias/terapiasalud infantilimpacto psicosocialcalidad de vidaIntroduction: As important as the diagnosis and treatment of pediatric cancer are the care related to psychosocial, educational, and emotional impact. Objective: To evaluate in children and adolescents diagnosed with cancer the psychosocial and quality-of-life impacts and the presence of a companion during the procedures. Method: Cross-sectional descriptive study of patients aged 8 to 18 years of age diagnosed with malignant neoplasms. Patients responded the questionnaires PedsQL 4.0 Quality of Life (8 to 12 years), PedsQL 3.0 Cancer Module (8 to 12 years), PedsQL 4.0 Quality of Life (13 to 18 years), PedsQL 3.0 Cancer Module (13 to 18 years) and another about companions created by the authors. Results: There were 25 pediatric oncology patients were included who felt happier in the presence of a companion, and less anxious during the procedures. A great impact on quality of life was perceived. In the Quality-of-Life questionnaire, no significant difference (p=0.627) between the groups of patients aged 8 to 12 years and 13 to 18 years were found, but the group aged 8 to 12 years had a significantly higher impact on the Cancer Module questionnaire (p=0.0094). Conclusion: The impact on quality of life and psychosocial is fairly large in pediatric oncology patients. The youngest appear to suffer great psychosocial impact. Patients claim they are happier in the presence of a companion, and more anxious in its absence.Introducción: Tan importante como el diagnóstico y tratamiento del cáncer pediátrico, son los cuidados sobre el impacto psicosocial, educativo y emocional. Objetivo: Evaluar en niños y adolescentes diagnosticados de cáncer el impacto psicosocial y en la calidad de vida y la presencia de un acompañante durante los procedimientos. Método: Estudio transversal descriptivo de pacientes de 8 a 18 años con diagnóstico de neoplasia maligna. Los pacientes respondieron a los cuestionarios: PedsQL 4.0 Calidad de Vida (8 a 12 años), PedsQL 3.0 Módulo de Cáncer (8 a 12 años), PedsQL 4.0 Calidad de Vida (13 a 18 años), PedsQL 3.0 Módulo de Cáncer (13 a 18 años) y otro sobre cuidadores elaborado por los autores. Resultados: Se incluyeron 25 pacientes de oncología pediátrica que se sentían más felices con la presencia de un acompañante y menos ansiosos al realizar procedimientos. Se percibió un gran impacto en la calidad de vida. En el cuestionario de Calidad de Vida, no hubo diferencia significativa (p=0,627) entre los grupos de pacientes de 8 a 12 años y de 13 a 18 años, pero el grupo de 8 a 12 años tuvo un impacto significativamente mayor en el cuestionario del Módulo de Cáncer (p=0,0094). Conclusión: El impacto en la calidad de vida y psicosocial es razonablemente grande en los pacientes oncológicos pediátricos. Los de menor edad parecen sufrir un mayor impacto psicosocial. Los pacientes dicen sentirse más felices con la presencia de un acompañante, y más ansiosos en su ausencia.Introdução: Tão importante quanto o diagnóstico e o tratamento do câncer pediátrico são os cuidados relacionados ao impacto psicossocial, educacional e emocional. Objetivo: Avaliar em crianças e adolescentes com diagnóstico de câncer os impactos psicossociais, de qualidade de vida e da presença de acompanhante durante os procedimentos. Método: Estudo transversal, descritivo, com pacientes de 8 a 18 anos e diagnóstico de neoplasia maligna. Os pacientes responderam aos questionários: PedsQL 4.0 Qualidade de Vida (8 a 12 anos), PedsQL 3.0 Módulo de Câncer (8 a 12 anos), PedsQL 4.0 Qualidade de Vida (13 a 18 anos), PedsQL 3.0 Módulo de Câncer (13 a 18 anos) e outro sobre acompanhantes elaborado pelos autores. Resultados: Foram incluídos 25 pacientes pediátricos oncológicos que se sentiam mais felizes na presença de um acompanhante e menos ansiosos durante os procedimentos. Foi percebido grande impacto na qualidade de vida. No questionário Qualidade de Vida, não houve diferença significativa (p=0,627) entre os grupos de pacientes com 8 a 12 anos e 13 a 18 anos, porém o grupo com 8 a 12 anos teve impacto significativamente maior no questionário Módulo de Câncer (p=0,0094). Conclusão: O impacto psicossocial e na qualidade de vida é razoavelmente grande em pacientes pediátricos oncológicos. Além disso, os mais jovens parecem sofrer um impacto psicossocial maior. Os pacientes se dizem mais felizes com a presença de acompanhante, e mais ansiosos na sua ausência.INCA2023-08-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArtigos, Avaliado pelos paresapplication/pdfapplication/pdfapplication/pdftext/htmlhttps://rbc.inca.gov.br/index.php/revista/article/view/388810.32635/2176-9745.RBC.2023v69n3.3888Revista Brasileira de Cancerologia; Vol. 69 No. 3 (2023): July/Aug./Sept.; e-123888Revista Brasileira de Cancerologia; Vol. 69 Núm. 3 (2023): jul./ago./sept.; e-123888Revista Brasileira de Cancerologia; v. 69 n. 3 (2023): jul./ago./set.; e-1238882176-9745reponame:Revista Brasileira de Cancerologia (Online)instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)instacron:INCAporengspahttps://rbc.inca.gov.br/index.php/revista/article/view/3888/3096https://rbc.inca.gov.br/index.php/revista/article/view/3888/3323https://rbc.inca.gov.br/index.php/revista/article/view/3888/3236https://rbc.inca.gov.br/index.php/revista/article/view/3888/3131Copyright (c) 2023 Revista Brasileira de Cancerologiahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessPereira, Clara Ignácio PessoaNascimento, Isadora BolelaCruz, Aristides Schier daVolc, Sahlua MiguelTormen, Tiago Hessel2024-01-10T15:07:59Zoai:rbc.inca.gov.br:article/3888Revistahttps://rbc.inca.gov.br/index.php/revistaPUBhttps://rbc.inca.gov.br/index.php/revista/oairbc@inca.gov.br0034-71162176-9745opendoar:2024-01-10T15:07:59Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)false
dc.title.none.fl_str_mv Psychosocial and Quality-of-Life Impacts of Cancer Treatment in Children and Adolescents
Impactos Psicosociales y en la Calidad de Vida del Tratamiento del Cáncer en Niños y Adolescentes
Impactos Psicossociais e na Qualidade de Vida do Tratamento Oncológico em Crianças e Adolescentes
title Psychosocial and Quality-of-Life Impacts of Cancer Treatment in Children and Adolescents
spellingShingle Psychosocial and Quality-of-Life Impacts of Cancer Treatment in Children and Adolescents
Pereira, Clara Ignácio Pessoa
neoplasias/terapia
saúde da criança
impacto psicossocial
qualidade de vida
neoplasms/therapy
child health
psychosocial impact
quality of life
neoplasias/terapia
salud infantil
impacto psicosocial
calidad de vida
title_short Psychosocial and Quality-of-Life Impacts of Cancer Treatment in Children and Adolescents
title_full Psychosocial and Quality-of-Life Impacts of Cancer Treatment in Children and Adolescents
title_fullStr Psychosocial and Quality-of-Life Impacts of Cancer Treatment in Children and Adolescents
title_full_unstemmed Psychosocial and Quality-of-Life Impacts of Cancer Treatment in Children and Adolescents
title_sort Psychosocial and Quality-of-Life Impacts of Cancer Treatment in Children and Adolescents
author Pereira, Clara Ignácio Pessoa
author_facet Pereira, Clara Ignácio Pessoa
Nascimento, Isadora Bolela
Cruz, Aristides Schier da
Volc, Sahlua Miguel
Tormen, Tiago Hessel
author_role author
author2 Nascimento, Isadora Bolela
Cruz, Aristides Schier da
Volc, Sahlua Miguel
Tormen, Tiago Hessel
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Pereira, Clara Ignácio Pessoa
Nascimento, Isadora Bolela
Cruz, Aristides Schier da
Volc, Sahlua Miguel
Tormen, Tiago Hessel
dc.subject.por.fl_str_mv neoplasias/terapia
saúde da criança
impacto psicossocial
qualidade de vida
neoplasms/therapy
child health
psychosocial impact
quality of life
neoplasias/terapia
salud infantil
impacto psicosocial
calidad de vida
topic neoplasias/terapia
saúde da criança
impacto psicossocial
qualidade de vida
neoplasms/therapy
child health
psychosocial impact
quality of life
neoplasias/terapia
salud infantil
impacto psicosocial
calidad de vida
description Introduction: As important as the diagnosis and treatment of pediatric cancer are the care related to psychosocial, educational, and emotional impact. Objective: To evaluate in children and adolescents diagnosed with cancer the psychosocial and quality-of-life impacts and the presence of a companion during the procedures. Method: Cross-sectional descriptive study of patients aged 8 to 18 years of age diagnosed with malignant neoplasms. Patients responded the questionnaires PedsQL 4.0 Quality of Life (8 to 12 years), PedsQL 3.0 Cancer Module (8 to 12 years), PedsQL 4.0 Quality of Life (13 to 18 years), PedsQL 3.0 Cancer Module (13 to 18 years) and another about companions created by the authors. Results: There were 25 pediatric oncology patients were included who felt happier in the presence of a companion, and less anxious during the procedures. A great impact on quality of life was perceived. In the Quality-of-Life questionnaire, no significant difference (p=0.627) between the groups of patients aged 8 to 12 years and 13 to 18 years were found, but the group aged 8 to 12 years had a significantly higher impact on the Cancer Module questionnaire (p=0.0094). Conclusion: The impact on quality of life and psychosocial is fairly large in pediatric oncology patients. The youngest appear to suffer great psychosocial impact. Patients claim they are happier in the presence of a companion, and more anxious in its absence.
publishDate 2023
dc.date.none.fl_str_mv 2023-08-10
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Artigos, Avaliado pelos pares
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://rbc.inca.gov.br/index.php/revista/article/view/3888
10.32635/2176-9745.RBC.2023v69n3.3888
url https://rbc.inca.gov.br/index.php/revista/article/view/3888
identifier_str_mv 10.32635/2176-9745.RBC.2023v69n3.3888
dc.language.iso.fl_str_mv por
eng
spa
language por
eng
spa
dc.relation.none.fl_str_mv https://rbc.inca.gov.br/index.php/revista/article/view/3888/3096
https://rbc.inca.gov.br/index.php/revista/article/view/3888/3323
https://rbc.inca.gov.br/index.php/revista/article/view/3888/3236
https://rbc.inca.gov.br/index.php/revista/article/view/3888/3131
dc.rights.driver.fl_str_mv Copyright (c) 2023 Revista Brasileira de Cancerologia
https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2023 Revista Brasileira de Cancerologia
https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
text/html
dc.publisher.none.fl_str_mv INCA
publisher.none.fl_str_mv INCA
dc.source.none.fl_str_mv Revista Brasileira de Cancerologia; Vol. 69 No. 3 (2023): July/Aug./Sept.; e-123888
Revista Brasileira de Cancerologia; Vol. 69 Núm. 3 (2023): jul./ago./sept.; e-123888
Revista Brasileira de Cancerologia; v. 69 n. 3 (2023): jul./ago./set.; e-123888
2176-9745
reponame:Revista Brasileira de Cancerologia (Online)
instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
instacron:INCA
instname_str Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
instacron_str INCA
institution INCA
reponame_str Revista Brasileira de Cancerologia (Online)
collection Revista Brasileira de Cancerologia (Online)
repository.name.fl_str_mv Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
repository.mail.fl_str_mv rbc@inca.gov.br
_version_ 1797042238884151296