Does the effect of comprehensive respiratory physiotherapy home-program differ in children with cystic fibrosis and non-cystic fibrosis bronchiectasis?

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dc.authoridGurses, H. Nilgun/0000-0002-5846-6781
dc.authoridzeren, Melih/0000-0002-9749-315X
dc.authoridDENİZOĞLU KÜLLİ, Hilal/0000-0002-8003-4440
dc.authoridUcgun, Hikmet/0000-0002-7211-1805
dc.authorwosidGurses, H. Nilgun/AAD-3070-2020
dc.authorwosidzeren, Melih/HNR-7817-2023
dc.authorwosidDENİZOĞLU KÜLLİ, Hilal/AAD-4119-2020
dc.contributor.authorGürses, Hülya Nilgün
dc.contributor.authorÜçgün, Hikmet
dc.contributor.authorZeren, Melih
dc.contributor.authorDenizoğlu Külli, Hilal
dc.contributor.authorÇakır, Erkan
dc.date.accessioned2023-03-22T19:47:25Z
dc.date.available2023-03-22T19:47:25Z
dc.date.issued2022
dc.departmentBelirleneceken_US
dc.description.abstractBronchiectasis is a form of airway damage as a consequence of endobronchial infection and inflammation and may be present in different diseases. The underlying aetiologies include both cystic fibrosis (CF) and a group of non-cystic fibrosis diseases (NCFB) such as immunodeficiency, primary ciliary dyskinesia, or severe pulmonary infection. Although children with CF and non-cystic fibrosis bronchiectasis (NCFB) have many similar clinical features, their responses to exercise may be different. The aim of this study was to compare the efficacy of a comprehensive respiratory physiotherapy (CRP) home-program in children with CF and NCFB. Thirty children with CF and thirty children with NCFB were included in the study. Both groups performed the CRP home-program twice daily for 8 weeks. Pulmonary function, exercise capacity, and respiratory and peripheral muscle strength were assessed at baseline and after 8 weeks of training. Both groups experienced significant improvements in pulmonary function, exercise capacity, and respiratory and peripheral muscle strength (p < 0.001). Maximum expiratory pressure, exercise capacity, and peripheral muscle strength were further improved in NCFB group compared to CF (p < 0.05); however, there was a great variability in the improvements for each variable. Conclusion: CRP is beneficial both for children with CF and NCFB and adherence to the program was high in both groups.en_US
dc.identifier.doi10.1007/s00431-022-04509-5
dc.identifier.endpage2970en_US
dc.identifier.issn0340-6199
dc.identifier.issn1432-1076
dc.identifier.issue8en_US
dc.identifier.pmid35595860en_US
dc.identifier.scopus2-s2.0-85130211151en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage2961en_US
dc.identifier.urihttps://doi.org/10.1007/s00431-022-04509-5
dc.identifier.urihttps://hdl.handle.net/20.500.14034/693
dc.identifier.volume181en_US
dc.identifier.wosWOS:000799515400001en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.journalEuropean Journal Of Pediatricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCystic fibrosisen_US
dc.subjectNon-cystic fibrosis bronchiectasisen_US
dc.subjectRespiratory physiotherapyen_US
dc.subjectPulmonary functionen_US
dc.subjectExercise capacityen_US
dc.subjectRespiratory and peripheral muscle strengthen_US
dc.subject6-Minute Walk Testen_US
dc.subjectPhysical-Activityen_US
dc.subjectPulmonary Rehabilitationen_US
dc.subjectFunctional-Capacityen_US
dc.subjectChest Physiotherapyen_US
dc.subjectExerciseen_US
dc.subjectGuidelinesen_US
dc.subjectStatementen_US
dc.subjectSocietyen_US
dc.subjectAirwayen_US
dc.titleDoes the effect of comprehensive respiratory physiotherapy home-program differ in children with cystic fibrosis and non-cystic fibrosis bronchiectasis?en_US
dc.typeArticleen_US

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