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dc.contributor.author이진화*
dc.date.accessioned2016-08-28T10:08:17Z-
dc.date.available2016-08-28T10:08:17Z-
dc.date.issued2013*
dc.identifier.issn0341-2040*
dc.identifier.otherOAK-10300*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/223904-
dc.description.abstractBackground: The progression of lung hyperinflation in patients with chronic obstructive pulmonary disease (COPD) has not been studied in a long-term prospective cohort. We explored the longitudinal changes in lung volume compartments with the aim of identifying predictors of a rapid decline of the inspiratory capacity to total lung capacity ratio (IC/TLC). Methods: The study population comprised 324 patients with COPD who were recruited prospectively. Annual rates of changes in pulmonary function, including forced expiratory volume in 1 s (FEV1), forced vital capacity (FVC), total lung capacity (TLC), functional residual capacity (FRC), residual volume (RV), vital capacity (VC), IC, and IC/TLC, were estimated using the random coefficient models. Results: The mean annual rates of changes in pre- and post-bronchodilator FEV1 were -23.0 mL/year (p < 0.001) and -26.5 mL/year (p = 0.004). The mean annual rates of changes in VC, IC, TLC, and IC/TLC were -33.7 mL/year (p = 0.007), -53.9 mL/year (p < 0.001), -43.7 mL/year (p = 0.012), and -0.65 %/year (p = 0.001), respectively. RV, FRC, and RV/TLC did not change significantly during the study period. Multivariate logistic regression analysis showed that a high modified Medical Research Council (MMRC) dyspnea scale score, a high Charlson comorbidity index value, and low post-bronchodilator FEV1 were associated with rapid decline in IC/TLC. Conclusion: MMRC dyspnea scale, post-bronchodilator FEV1, and the Charlson comorbidity index at baseline were independent predictors of a rapid decline in IC/TLC. © 2013 Springer Science+Business Media New York.*
dc.languageEnglish*
dc.titleLongitudinal lung volume changes in patients with chronic obstructive pulmonary disease*
dc.typeArticle*
dc.relation.issue4*
dc.relation.volume191*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage405*
dc.relation.lastpage412*
dc.relation.journaltitleLung*
dc.identifier.doi10.1007/s00408-013-9478-0*
dc.identifier.wosidWOS:000321916800013*
dc.identifier.scopusid2-s2.0-84880828247*
dc.author.googleLee J.S.*
dc.author.googleKim S.O.*
dc.author.googleSeo J.B.*
dc.author.googleLee J.-H.*
dc.author.googleKim E.K.*
dc.author.googleKim T.-H.*
dc.author.googleKim W.J.*
dc.author.googleLee J.H.*
dc.author.googleLee S.-M.*
dc.author.googleLee S.*
dc.author.googleLim S.Y.*
dc.author.googleShin T.R.*
dc.author.googleYoon H.I.*
dc.author.googleLee S.W.*
dc.author.googleHuh J.W.*
dc.author.googleOh Y.-M.*
dc.author.googleLee S.-D.*
dc.contributor.scopusid이진화(56646645800;58376333800)*
dc.date.modifydate20240419140935*
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의과대학 > 의학과 > Journal papers
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