A comparison of respiratory and peripheral muscle strength, functional exercise capacity, activities of daily living and physical fitness in patients with cystic fibrosis and healthy subjects

Arıkan, Hülya; Yatar, İlker; Çalık-Kütükçü, Ebru; Arıbaş, Zeynep; Sağlam, Melda; Vardar-Yağlı, Naciye; Savcı, Sema; Inal-Ince, Deni̇z; Özçeli̇k, Uğur; Ki̇per, Nural

doi:10.1016/j.ridd.2015.07.020

Cited by 56 publications

(76 citation statements)

References 46 publications

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“…Recent studies have evaluated respiratory muscle strength and pulmonary function in CF patients relative to the different stages of disease severity (Dekerlegand et al, ; Dunnink et al, ; Pinet et al, ). Arikan et al () evaluated peripheral and respiratory muscle strength, functional capacity, ADL, and parameters of physical fitness in 19 patients with CF and mean ( SD ) FEV 1 of 86.56% (18.36%) compared with 20 healthy individuals. There was no statistically significant difference in respiratory muscle strength measurements between the two groups.…”

Section: Discussionmentioning

confidence: 99%

“…Peripheral muscle strength has been evaluated in patients with CF as an outcome of specific interventions of exercise training (Arikan et al, 2015;Rovedder et al, 2014). In the present study, were used the 1RM test that is considered the gold standard for assessing muscle strength in nonlaboratory situations (Levinger et al, 2009).…”

Section: Discussionmentioning

confidence: 99%

“…Recent studies (Arikan et al, ; Erickson, Seigler, McKie, McCully, & Harris, ) have assessed outcomes related to muscle strength in patients with CF, and they confirmed that these individuals have reduced peripheral muscle strength and skeletal muscle oxidative capacity compared with control subjects. Saglam et al () identified that inspiratory muscle strength, lung function, and nutritional status affect walk/run performance, whereas age and lung function influence walk performance in CF.…”

Section: Introduction and Statement Of Porposementioning

confidence: 89%

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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

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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.

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Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Section: Introduction and Statement Of Porposementioning

confidence: 89%

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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

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“…Respiratory muscle strength has previously been tested in patients with chronic obstructive pulmonary disease [34], cystic fibrosis [35], and ankylosing spondylitis [36] and found to have different levels of associations. In the latter study [36], they found correlations between thorax expansion and MIP and MEP, similar to our findings.…”

Section: Respiratory Muscle Strengthmentioning

confidence: 99%

Thoracic mobility and its relation to pulmonary function and rib-cage deformity in patients with early onset idiopathic scoliosis: a long-term follow-up

et al. 2020

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Study design A group of adult patients with idiopathic scoliosis, diagnosed before the age of ten, at a mean of 26.5 years after treatment with either brace or surgery during childhood and adolescence attended a clinical follow-up. Objectives To evaluate the relation between thoracic mobility, rib-cage deformity, and pulmonary function. Summary of background data Long-term studies of pulmonary function in relation to thoracic mobility after treatment in this patient group have not been published. Methods A total of 106 patients, 57 braced and 49 operated patients, attended the follow-up. We examined thoracic mobility (range of motion of the thoracic spine, thorax expansion, and breathing movements) and rib-cage deformity (curve size and trunk deformity) as well as pulmonary function, especially total lung capacity (TLC). Respiratory muscle strength was evaluated in a subgroup. Results Thoracic range of motion was significantly less among the surgically treated patients compared with both the bracetreated and comparison group. Thorax expansion and breathing movements during maximal breathing were significantly reduced in the scoliotic patients compared with the reference values, with no significant differences between the treatment groups. The brace-treated group had better pulmonary function than the operated group, as measured by the TLC, forced vital capacity (FVC), and forced expiratory volume in one second (FEV1) (percentage of predicted values). The respiratory muscle strength was significantly lower only in the surgically treated patients when compared with reference values. The results of a multivariate analysis revealed that the strongest factors explaining TLC percentage of predicted were gender, brace model, and smoking habits. Conclusions Thoracic mobility was significantly reduced at mean 26.5 years after completed treatment in both brace-treated and surgically treated patients with early onset scoliosis, compared with the reference values, which did not influence TLC as strongly as gender, brace model, and smoking habits. Levels of evidence Level III.

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“…In the study conducted with 20 healthy participants with 19 cystic fibrosis aged between 7 and 25 years, they used the MFT test to evaluate the motor performance of the participants. 13 The original effort scale (normal heart rate 60-200), defined by the Borg, consisting of a 6-20 scale, is used to measure all effort during physical activity. It was modified in 10 points scale.…”

Section: Field Testsmentioning

confidence: 99%

Exercise Testing in Children with Cystic Fibrosis

Hisarkaya¹,

Beyhan²,

Yavuz³

2019

Turkiye Klinikleri J Pediatr

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ystic fibrosis (CF) is a complex metabolic disease involving the mucous glands in the pancreas, sweat glands, respiratory tract, GIS and reproductive system. It is inherited in an autosomal recessive pattern. The probability of occurrence in Caucasian race is between 1/2000-2500 in live newborn infants. It is caused by a mutation of the cystic fibrosis transmembrane conductance regulator (CFTR) gene which is located on the

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A comparison of respiratory and peripheral muscle strength, functional exercise capacity, activities of daily living and physical fitness in patients with cystic fibrosis and healthy subjects

Cited by 56 publications

References 46 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

Thoracic mobility and its relation to pulmonary function and rib-cage deformity in patients with early onset idiopathic scoliosis: a long-term follow-up

Exercise Testing in Children with Cystic Fibrosis

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