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Longitudinal measures of lung function in infants with bronchopulmonary dysplasia

dc.contributor.authorFilbrun, Amy G.en_US
dc.contributor.authorPopova, Antonia P.en_US
dc.contributor.authorLinn, Marisa J.en_US
dc.contributor.authorMcIntosh, Nancy A.en_US
dc.contributor.authorHershenson, Marc B.en_US
dc.date.accessioned2011-04-07T18:52:13Z
dc.date.accessioned2011-04-07T18:52:13Z
dc.date.available2012-05-14T20:40:08Zen_US
dc.date.issued2011-04en_US
dc.identifier.citationFilbrun, Amy G.; Popova, Antonia P.; Linn, Marisa J.; McIntosh, Nancy A.; Hershenson, Marc B. (2011). "Longitudinal measures of lung function in infants with bronchopulmonary dysplasia." Pediatric Pulmonology 46(4): 369-375. <http://hdl.handle.net/2027.42/83461>en_US
dc.identifier.issn8755-6863en_US
dc.identifier.issn1099-0496en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/83461
dc.description.abstractWe previously demonstrated that infants with a history of bronchopulmonary dysplasia (BPD) exhibit airflow obstruction and air trapping. The purpose of this study was to assess longitudinal changes in pulmonary function in infants with a history of BPD over the first 3 years of life, and the relationship to somatic growth. Spirometry was measured using the raised volume rapid thoracoabdominal compression technique, and lung volumes measured by plethysmography. Eighteen infants (mean gestational age ± SD 27.3 ± 2.2 weeks, birthweight 971 ± 259 g) underwent two lung function studies. Average age at first test was 58.8 weeks. Spirometry demonstrated significant reductions in forced expiratory volume in 0.5 sec (FEV 0.5 , 76.0 ± 15.9% predicted, Z-score −2.13 ± 1.69), forced expiratory flow at 75% of expired forced vital capacity (FEF 75 , 54.8 ± 31.1%, −3.58 ± 2.73), and FEF 25–75 (67.8 ± 33.3%, −1.79 ± 1.76). Group mean total lung capacity (TLC) was in the low normal range (82.9 ± 13.5% predicted) and residual volume (RV)/TLC was mildly elevated (122.4 ± 38.2% predicted). Repeat testing was performed an average of 32.7 weeks after initial testing. At re-evaluation, group mean lung volumes and flows tracked at or near their previous values; thus, in general, there was a lack of catch-up growth. However, compared to infants with below average or average somatic growth (as represented by g/day), infants with above average growth showed significantly greater improvements in percent predicted FVC, FEV 0.5 , TLC, and RV/TLC (all P  < 0.05, ANOVA). We conclude that longitudinal measures of pulmonary function in infants and young children with BPD demonstrate significant airflow obstruction and modest restriction, which tends to persist with time. On the other hand, infants with above average somatic growth showed greater lung growth than their peers. Additional studies examining the effects of various nutritional regimens on lung function are warranted. Pediatr Pulmonol. 2011; 46:369–375. © 2010 Wiley-Liss, Inc.en_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherMiscellaneous Medicalen_US
dc.titleLongitudinal measures of lung function in infants with bronchopulmonary dysplasiaen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPediatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan ; Department of Pediatrics and Communicable Diseases, University of Michigan, 1500 East Medical Center Drive, L2221 Women's Hospital, Box 0212, Ann Arbor 48109-0212, MI.en_US
dc.contributor.affiliationumDepartment of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michiganen_US
dc.identifier.pmid21438170en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/83461/1/21378_ftp.pdf
dc.identifier.doi10.1002/ppul.21378en_US
dc.identifier.sourcePediatric Pulmonologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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