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dc.contributor.authorRodrigues Leite, Luanna
dc.contributor.authorVasconcelos Queiroz, Karen Caroline
dc.contributor.authorCenachi Coelho, Cristiane
dc.contributor.authorAndrade Vergara, Alberto
dc.contributor.authorFagundes Donadio, Márcio Vinícius
dc.contributor.authorDa Silva Aquino, Evanirso
dc.date.accessioned2022-03-07T18:26:06Z
dc.date.available2022-03-07T18:26:06Z
dc.date.issued2021
dc.identifier.citationRodrigues Leite, Luanna; Vasconcelos Queiroz, Karen Caroline; Cenachi Coelho, Cristiane [et al.]. Functional performance in the modified shuttle test in children and adolescents with cystic fibrosis. Revista Paulista de Pediatria, 2021, 39, e2019322. Disponible en: <https://www.scielo.br/j/rpp/a/mS6bzwKXCwNbM9QQ7zJpVnB/?lang=en>. Fecha de acceso: 7 mar. 2022. DOI: 10.1590/1984-0462/2021/39/2019322.en
dc.identifier.issn0103-0582ca
dc.identifier.urihttp://hdl.handle.net/20.500.12328/3164
dc.description.abstractObjective: To evaluate factors associated with the performance of children and adolescents with cystic fibrosis (CF) in the Modified Shuttle Test (MST) and compare it with healthy children and adolescents. Methods: This is a cross-sectional study, with children and adolescents divided into two groups: cystic fibrosis (CFG) and control (CG). Variables evaluated in the MST: walking distance, test level, heart rate variation (∆Hr), post-test mean arterial pressure (MAP Pt) and peripheral oxygen saturation variation (∆SPO2). Statistical analysis included Mann Whitney and Spearman coefficient tests, being significant p<0.05. Results: Sixty individuals aged 6-16 years old were evaluated. Anthropometric data was similar between groups. Differences between groups were shown for: baseline heart rate (BHr), peak heart rate (PHr), ∆Hr, recovery heart rate (RHr), post-test respiratory rate (PtBr), saturation variables, peripheral oxygen level (SpO2B) and level test. The ∆Hr and MAP Pt had a moderate positive correlation with distance and level test for both groups (respectively: r=0.6 / p<0.001; r=0.6 / p<0.001). In CFG, the level test had a significant association (r=0.4 - p=0.02) with %FEV1. Conclusions: Children with cystic fibrosis presented functional limitation in the Modified Shuttle Test, which was influenced by lung function.en
dc.format.extent8ca
dc.language.isoengca
dc.publisherSociedade De Pediatria De Sao Pauloca
dc.relation.ispartofRevista Paulista de Pediatriaca
dc.relation.ispartofseries39;
dc.rightsThis is an open-access article distributed under the terms of the Creative Commons Attribution License.en
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.otherProva d'exercicica
dc.subject.otherFibrosi quísticaca
dc.subject.otherAptitud cardiorespiratòriaca
dc.subject.otherFenòmens fisiològics respiratorisca
dc.subject.otherPrueba de ejercicioes
dc.subject.otherFibrosis quísticaes
dc.subject.otherAptitud cardiorrespiratoriaes
dc.subject.otherFenómenos fisiológicos respiratorioses
dc.subject.otherExercise testen
dc.subject.otherCystic fibrosisen
dc.subject.otherCardiorespiratory fitnessen
dc.subject.otherRespiratory physiological phenomenaen
dc.titleFunctional performance in the modified shuttle test in children and adolescents with cystic fibrosisen
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.subject.udc61ca
dc.identifier.doihttps://dx.doi.org/10.1590/1984-0462/2021/39/2019322ca


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This is an open-access article distributed under the terms of the Creative Commons Attribution License.
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