Exercise programme in patients with cystic fibrosis: A randomized controlled trial

Rovedder, Paula Maria Eidt; Flores, Josani Silva; Ziegler, Bruna; Casarotto, Fernanda Cano; Jaques, Patrícia Augustin; Barreto, Sérgio Saldanha Menna; Dalcin, Paulo de Tarso Roth

doi:10.1016/j.rmed.2014.04.022

Cited by 34 publications

(55 citation statements)

References 30 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…We calculated the sample size, using a correlation coefficient of r = 0.5 between the VEF 1 and the muscle strength in 1RM. An adequate sample size in the present study was found to be at least 38 subjects ∝ = 0.05 and 1 − β = 90% (Rovedder et al, ).…”

Section: Methodsmentioning

confidence: 89%

Peripheral muscle strength is associated with lung function and functional capacity in patients with cystic fibrosis

Rovedder

Borba

Anderle

et al. 2019

Physiotherapy Res Intl

Self Cite

View full text Add to dashboard Cite

Purpose Cystic fibrosis (CF) is an inherited disease that causes important multisystemic impairments. The present study aimed to evaluate the association of peripheral muscle strength with lung function and functional capacity in adolescents and adults with CF. Methods Cross‐sectional study with prospective data of patients enrolled in the Program for Adults with CF at Hospital de Clínicas de Porto Alegre. The testing procedures included peripheral muscle strength testing, pulmonary function tests, and the 6‐minute walk test. Results The sample consisted of 41 subjects (27 women) with a mean age of 24.6. Upper extremity muscle strength was associated with forced vital capacity and forced expiratory volume in the first second, and lower extremity muscle strength was associated with the distance covered in the 6‐minute walk test, oxygen saturation, forced expiratory volume in the first second, and forced vital capacity. Conclusions Muscle strength was positively associated with lung function variable and functional capacity in patients with CF.

show abstract

Section: Methodsmentioning

confidence: 89%

Peripheral muscle strength is associated with lung function and functional capacity in patients with cystic fibrosis

Rovedder

Borba

Anderle

et al. 2019

Physiotherapy Res Intl

Self Cite

View full text Add to dashboard Cite

show abstract

“…The high-quality evidence supporting the effectiveness of exercise interventions includes supervised programmes in an inpatient [56], outpatient [57] or community setting [58], and partially or unsupervised home-based programmes [59,60,61,62]. Specific activity guidelines do not exist in patients with CF, but most described programmes include moderate- to high-intensity aerobic training (generally ranging between 60 and 80% of peak capacity) and/or resistance training [56,58,59,62].…”

Section: Exercise Interventionsmentioning

confidence: 99%

“…Specific activity guidelines do not exist in patients with CF, but most described programmes include moderate- to high-intensity aerobic training (generally ranging between 60 and 80% of peak capacity) and/or resistance training [56,58,59,62]. Even though both modalities have the potential to improve physical fitness and pulmonary function (assessed by FVC and FEV 1 ; fig.…”

Section: Exercise Interventionsmentioning

confidence: 99%

Rehabilitation in Patients with Chronic Respiratory Disease Other than Chronic Obstructive Pulmonary Disease: Exercise and Physical Activity Interventions in Cystic Fibrosis and Non-Cystic Fibrosis Bronchiectasis

Burtin

Hebestreit

2015

Respiration

View full text Add to dashboard Cite

A relevant proportion of children and adults with cystic fibrosis (CF) have a marked decrease in exercise tolerance, which can be partly related to impaired muscle function and decreased physical activity levels in daily life, in addition to lung disease. Preliminary findings suggest that patients with non-CF bronchiectasis face the same problems. These patients might be excellent candidates for exercise and physical activity interventions. This review elaborates on the rationale for exercise training and activity behaviour changes and summarizes the existing evidence for these rehabilitation strategies in patients with bronchiectasis, both CF and non-CF bronchiectasis. Furthermore, practical considerations and safety aspects are discussed.

show abstract

“…O treinamento frequente de exercício físico pode aumentar a capacidade anaeróbica e aeróbica e contribuir para o aumento da ventilação, ajudando na expectoração das secreções nas vias aéreas (WILLIAMS et al, 2010;ROVEDDER et al, 2014;BUTTON et al, 2016).…”

Section: Fisioterapia Nas Alterações Musculoesqueléticasunclassified

Atuação Do Fisioterapeuta No Atendimento a Pacientes Com Fibrose Cística: Uma Revisão De Literatura

Silva¹,

Santos²,

Vinhal³

et al. 2017

Enci Bio

View full text Add to dashboard Cite

RESUMOA fibrose cística é uma doença autossômica recessiva, pleiotrópica e deletéria, que compromete o funcionamento dos sistemas digestivo, musculoesquelético e respiratório. Essa revisão de literatura abordou a atuação do fisioterapeuta no atendimento a pacientes com fibrose cística mediante dados bibliográficos disponíveis no PubMed, SciELO e PEDro entre os anos 2006 a 2016. Os resultados encontrados evidenciam que a fisioterapia tem um papel importante no tratamento do paciente com fibrose cística, promovendo principalmente a melhora da qualidade de vida e aumentado também a sobrevida. A atuação do fisioterapeuta no atendimento desses pacientes contempla: 1) fisioterapia respiratória, que auxilia na eliminação de secreções das vias aéreas em pacientes com fibrose cística utilizando técnicas clássicas e atuais como, drenagem postural, vibração e percussão, técnica de expiração forçada, técnica do ciclo ativo da respiração, pressão expiratória positiva oscilatória -flutter, pressão expiratória positiva e drenagem autógena; 2) fisioterapia nas alterações musculoesqueléticas, que inclui exercícios de cinesioterapia com resistência para a melhora da força muscular do paciente; 3) terapia manual visceral, que estimula e aumenta o peristaltismo, auxilia a secreção de fluidos glandulares, reduz o tempo de trânsito colônico e diminui a dor e o desconforto causados pelas disfunções digestivas; 4) o envolvimento e comprometimento da família, que aumenta a adesão do paciente ao tratamento e melhora efetivamente a avaliação prognóstica. Em conclusão, o tratamento fisioterapêutico da fibrose cística proporciona a melhora global do quadro fisiopatológico destes pacientes. PALAVRAS-CHAVE: CFTR, mucoviscosidade e técnicas fisioterapêuticas

show abstract

Exercise programme in patients with cystic fibrosis: A randomized controlled trial

Abstract: The study demonstrated that a home exercise programme had positive effects in adult patients with CF, including gain in muscle strength in UULL. No increase in tolerance to exercise was shown and improvement in the quality of life of the patients who received intervention.

Cited by 34 publications

References 30 publications

Peripheral muscle strength is associated with lung function and functional capacity in patients with cystic fibrosis

Peripheral muscle strength is associated with lung function and functional capacity in patients with cystic fibrosis

Rehabilitation in Patients with Chronic Respiratory Disease Other than Chronic Obstructive Pulmonary Disease: Exercise and Physical Activity Interventions in Cystic Fibrosis and Non-Cystic Fibrosis Bronchiectasis

Atuação Do Fisioterapeuta No Atendimento a Pacientes Com Fibrose Cística: Uma Revisão De Literatura

Contact Info

Product

Resources

About