A carregar...
Publicação
Reabilitação respiratória à pessoa adulta com fibrose quística: protocolo de revisão scoping
| Nome: | Descrição: | Tamanho: | Formato: | |
|---|---|---|---|---|
| 464.39 KB | Adobe PDF |
Orientador(es)
Resumo(s)
A Fibrose Quística é uma doença genética e autossómica recessiva. Caracteriza-se por um aumento da viscosidade das secreções, sendo a sua principal manifestação a nível respiratório, nomeadamente a dispneia, a tosse e a broncorreia excessiva. O tratamento e gestão da doença, incluem a Reabilitação Respiratória, realizada por equipas multidisciplinares, tendo como efeitos a melhoria da função respiratória, condição física, tolerância ao esforço e qualidade de vida. A metodologia seguirá as orientações da JBI Manual for Evidence Synthesis. Tendo por base o acrónimo PCC, serão considerados na revisão scoping estudos que façam referência a intervenções de Reabilitação Respiratória (Conceito) dirigidas à pessoa adulta com Fibrose Quística (População) independentemente do contexto. A pesquisa será realizada em três etapas nas bases de dados MEDLINE Complete, CINAHL Complete, Scopus, RCAAP e ProQuest Dissertations & Thesis (acesso através da plataforma Web of Science). A revisão será levada a cabo por dois revisores de forma independente e a extração dos dados será realizada através de um instrumento criado pelos mesmos. Os resultados serão apresentados numa tabela síntese. Esta revisão permitirá mapear a evidência disponível sobre as intervenções de Reabilitação Respiratória dirigidas à pessoa adulta com Fibrose Quística, de forma a contribuir para a tomada de decisão no planeamento de cuidados individualizados e efetivos, promovendo a melhoria da sua qualidade de vida.
Cystic fibrosis is a genetic and autosomal recessive disorder. It is characterized by increased secretion viscosity, with its main clinical manifestations occurring at the respiratory level, namely dyspnea, persistent cough, and excessive bronchorrhea. The treatment and management of the disease include respiratory rehabilitation, carried out by multidisciplinary teams, which aims to improve respiratory function, physical condition, exercise tolerance, and quality of life. This scoping review will follow the methodology outlined in the JBI Manual for Evidence Synthesis. Based on the PCC mnemonic, studies referring to respiratory rehabilitation interventions (Concept) targeted at adults with cystic fibrosis (Population), regardless of context, will be considered. The search will be conducted in three stages using the following databases: MEDLINE Complete, CINAHL Complete, Scopus, RCAAP and ProQuest Dissertations & Theses (accessed via the Web of Science platform). Study selection and data extraction will be conducted independently by two reviewers, using a data extraction tool developed by the review team. The results will be presented in a summary table. This review will allow mapping of the available evidence regarding respiratory rehabilitation interventions for adults with cystic fibrosis, supporting decision-making in the planning of individualized and effective care that contributes to improved quality of life.
Cystic fibrosis is a genetic and autosomal recessive disorder. It is characterized by increased secretion viscosity, with its main clinical manifestations occurring at the respiratory level, namely dyspnea, persistent cough, and excessive bronchorrhea. The treatment and management of the disease include respiratory rehabilitation, carried out by multidisciplinary teams, which aims to improve respiratory function, physical condition, exercise tolerance, and quality of life. This scoping review will follow the methodology outlined in the JBI Manual for Evidence Synthesis. Based on the PCC mnemonic, studies referring to respiratory rehabilitation interventions (Concept) targeted at adults with cystic fibrosis (Population), regardless of context, will be considered. The search will be conducted in three stages using the following databases: MEDLINE Complete, CINAHL Complete, Scopus, RCAAP and ProQuest Dissertations & Theses (accessed via the Web of Science platform). Study selection and data extraction will be conducted independently by two reviewers, using a data extraction tool developed by the review team. The results will be presented in a summary table. This review will allow mapping of the available evidence regarding respiratory rehabilitation interventions for adults with cystic fibrosis, supporting decision-making in the planning of individualized and effective care that contributes to improved quality of life.
Descrição
Palavras-chave
Adulto Fibrose quística Reabilitação pulmonar Doença respiratória crónica Adult Cystic fibrosis Pulmonary rehabilitation Chronic respiratory diseas
Contexto Educativo
Citação
Editora
Licença CC
Sem licença CC