dc.contributorCtr Univ Tridngulo
dc.contributorFac Med Ribeirao Preto
dc.contributorUniversidade Federal de São Paulo (UNIFESP)
dc.creatorAfonso, Juliana Lima
dc.creatorTambascio, Joana
dc.creatorSouza, Hugo Celso Dutra de
dc.creatorJardim, José Roberto [UNIFESP]
dc.creatorMartinez, José Antônio Baddini
dc.creatorGastaldi, Ada Clarice [UNIFESP]
dc.date.accessioned2016-01-24T14:34:18Z
dc.date.accessioned2022-10-07T20:53:25Z
dc.date.available2016-01-24T14:34:18Z
dc.date.available2022-10-07T20:53:25Z
dc.date.created2016-01-24T14:34:18Z
dc.date.issued2013-09-01
dc.identifierRevista Portuguesa de Pneumologia. Barcelona: Elsevier Doyma Sl, v. 19, n. 5, p. 211-216, 2013.
dc.identifier0873-2159
dc.identifierhttp://repositorio.unifesp.br/handle/11600/36665
dc.identifierWOS000325382700006.pdf
dc.identifier10.1016/j.rppneu.2013.03.002
dc.identifierWOS:000325382700006
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/4024338
dc.description.abstractObjective: To characterise and compare the in vitro transport properties of respiratory mucoid secretion in individuals with no lung disease and in stable patients with chronic obstructive pulmonary disease (COPD) and bronchiectasis.Methodology: Samples of mucus were collected, from 21 volunteers presenting no lung disease who had undergone surgery, from 10 patients presenting chronic COPD, and from 16 patients with bronchiectasis. Mucociliary transport (MCT), transport by cough (SCM), and contact angle (CAM) were evaluated.Results: MCT was found to be greater in healthy individuals (1.0 +/- 0.19) than in COPD (0.91 +/- 0.17) and bronchiectasis (0.76 +/- 0.23) patients (p < 0.05), whereas SCM was greater in COPD patients (16.31 +/- 7.35 cm) than in patients with bronchiectasis (12.16 +/- 6.64 cm) and healthy individuals (10.50 +/- 25.8 cm) (p < 0.05). No significant differences were observed between the groups regarding CAM.Conclusion: Mucus from healthy individuals allows better mucociliary transport compared to that from patients with lung diseases. However, the mucus from COPD patients allows a better transport by coughing, demonstrating that these individuals have adapted to a defence mechanism compared to patients with bronchiectasis, who have impairment in their ciliary and cough transport mechanisms. (c) 2012 Sociedade Portuguesa de Pneumologia. Published by Elsevier Espana, S.L. All rights reserved.
dc.languagepor
dc.publisherElsevier B.V.
dc.relationRevista Portuguesa de Pneumologia
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.rightsAcesso aberto
dc.subjectCOPD
dc.subjectBronchiectasis
dc.subjectRespiratory mucus
dc.subjectMucociliary clearance
dc.titleTransport of mucoid mucus in healthy individuals and patients with chronic obstructive pulmonary disease and bronchiectasis
dc.typeArtigo


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