[factors Impacting The Growth And Nutritional Status Of Cystic Fibrosis Patients Younger Than 10 Years Of Age Who Did Not Undergo Neonatal Screening.]

dc.creatorHortencio, Taís Daiene Russo
dc.creatorNogueira, Roberto José Negrão
dc.creatorMarson, Fernando Augusto de Lima
dc.creatorHessel, Gabriel
dc.creatorRibeiro, José Dirceu
dc.creatorRibeiro, Antônio Fernando
dc.date2015-Feb
dc.date2015-11-27T13:46:09Z
dc.date2015-11-27T13:46:09Z
dc.date.accessioned2018-03-29T01:23:31Z
dc.date.available2018-03-29T01:23:31Z
dc.identifierRevista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo. , 2015-Feb.
dc.identifier1984-0462
dc.identifier10.1016/j.rpped.2014.11.004
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/25681074
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/202121
dc.identifier25681074
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1302354
dc.descriptionThe aim of this study was to evaluate by clinical and laboratory parameters how cystic fibrosis (CF) affects growth and nutritional status of children who were undergoing CF treatment but did not receive newborn screening. A historical cohort study of 52 CF patients younger than 10 years of age were followed in a reference center in Campinas, Southeast Brazil. Anthropometric measurements were abstracted from medical records until March/2010, when neonatal screening program was implemented. Between September/2009 and March/2010, parental height of the 52 CF patients were also measured. Regarding nutritional status, four patients had Z-scores ≤ -2 for height/age (H/A) and body mass index/age (BMI/A). The following variables were associated with improved H/A ratio: fewer hospitalizations, longer time from first appointment to diagnosis, longer time from birth to diagnosis and later onset of respiratory disease. Forced vital capacity [FVC(%)], forced expiratory flow between 25-75% of FVC [FEF25-75(%)], forced expiratory volume in the first second [FEV1(%)], gestational age, birth weight and early respiratory symptoms were associated with IMC/A. Greater number of hospitalizations, diagnosis delay and early onset of respiratory disease had a negative impact on growth. Lower spirometric values, lower gestational age, lower birth weight, and early onset of respiratory symptoms had negative impact on nutritional status. Malnutrition was observed in 7.7% of cases, but 23% of children had nutritional risk.
dc.description
dc.description
dc.languagepor
dc.relationRevista Paulista De Pediatria : Orgao Oficial Da Sociedade De Pediatria De Sao Paulo
dc.relationRev Paul Pediatr
dc.rightsaberto
dc.rightsCopyright © 2014 Associação de Pediatria de São Paulo. Publicado por Elsevier Editora Ltda. All rights reserved.
dc.sourcePubMed
dc.subjectAnthropometry
dc.subjectAntropometria
dc.subjectChild
dc.subjectCriança
dc.subjectCystic Fibrosis/complications
dc.subjectEstado Nutricional
dc.subjectFibrose Cística/complicações
dc.subjectNeonatal Screening
dc.subjectNutritional Status
dc.subjectTriagem Neonatal
dc.title[factors Impacting The Growth And Nutritional Status Of Cystic Fibrosis Patients Younger Than 10 Years Of Age Who Did Not Undergo Neonatal Screening.]
dc.typeArtículos de revistas


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