dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:36:09Z
dc.date.accessioned2022-10-05T13:48:03Z
dc.date.available2014-05-20T13:36:09Z
dc.date.available2022-10-05T13:48:03Z
dc.date.created2014-05-20T13:36:09Z
dc.date.issued2010-06-01
dc.identifierEarly Human Development. Clare: Elsevier B.V., v. 86, n. 6, p. 385-389, 2010.
dc.identifier0378-3782
dc.identifierhttp://hdl.handle.net/11449/12452
dc.identifier10.1016/j.earlhumdev.2010.05.006
dc.identifierWOS:000280452000009
dc.identifier1346461670550428
dc.identifier2559637400719543
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3888295
dc.description.abstractAims: To determine the occurrence of isolated and recurrent episodes of conductive hearing loss (CHL) during the first two years of life in very low birth weight (VLBW) infants with and without bronchopulmonary dysplasia (BPD).Study design, subjects and outcome measures: In a longitudinal clinical study. 187 children were evaluated at 6, 9, 12,15 18 and 24 months of age by visual reinforcement audiometry, tympanometry and auditory brain response system.Results: of the children with BPD, 54.5% presented with episodes of CHL, as opposed to 34.7% of the children without BPD. This difference was found to be statistically significant. The recurrent or persistent episodes were more frequent among children with BPD (25.7%) than among those without BPD (8.3%). The independent variables that contributed to this finding were small for gestational age and a 5 min Apgar score.Conclusions: Recurrent CHL episodes are more frequent among VLBW infants with BPD than among VLBW infants without BPD. (C) 2010 Elsevier B.V. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationEarly Human Development
dc.relation2.025
dc.relation1,041
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectBronchopulmonary dysplasia
dc.subjectConductive hearing loss
dc.subjectVery low birth weight
dc.titleConductive hearing loss in children with bronchopulmonary dysplasia: A longitudinal follow-up study in children aged between 6 and 24 months
dc.typeArtigo


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