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Exercise testing in cystic fibrosis: Who and why?
Urquhart, D S; Saynor, Z L.
Afiliação
  • Urquhart DS; Department of Paediatric Respiratory and Sleep Medicine, Royal Hospital for Sick Children, Edinburgh, United Kingdom; Department of Child Life and Health, University of Edinburgh, United Kingdom. Electronic address: don.urquhart@nhslothian.scot.nhs.uk.
  • Saynor ZL; Department of Sport and Exercise Science, University of Portsmouth, United Kingdom; Paediatric and Adult Respiratory Outpatient Departments, University Hospital Southampton, Southampton, United Kingdom.
Paediatr Respir Rev ; 27: 28-32, 2018 Jun.
Article em En | MEDLINE | ID: mdl-30158079
ABSTRACT
Annual review exercise testing is recommended by the Cystic Fibrosis (CF) Trust. Testing to date has focused on evaluating aerobic fitness, a key prognostic indicator. Tests available range from simple field tests, to comprehensive evaluations of aerobic exercise (dys)function - cardiopulmonary exercise testing (CPET). 'Field tests', although easy to perform are limited in the information they provide,whereas CPET, the 'gold standard' measure of aerobic fitness, is recommended as the first-choice exercise test by the European CF Society Exercise Working Group. CPET offers a precise cardiovascular, respiratory and metabolic evaluation of exercise capacity, including assessment of mechanism(s) of exercise limitation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Seleção de Pacientes / Fibrose Cística / Teste de Esforço Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Paediatr Respir Rev Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Seleção de Pacientes / Fibrose Cística / Teste de Esforço Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Paediatr Respir Rev Ano de publicação: 2018 Tipo de documento: Article