Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22014
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dc.contributor.authorPerret, Jennifer L-
dc.contributor.authorLodge, Caroline J-
dc.contributor.authorLowe, Adrian J-
dc.contributor.authorJohns, David P-
dc.contributor.authorThompson, Bruce R-
dc.contributor.authorBui, Dinh S-
dc.contributor.authorGurrin, Lyle C-
dc.contributor.authorMatheson, Melanie C-
dc.contributor.authorMcDonald, Christine F-
dc.contributor.authorWood-Baker, Richard-
dc.contributor.authorSvanes, Cecilie-
dc.contributor.authorThomas, Paul S-
dc.contributor.authorGiles, Graham G-
dc.contributor.authorChang, Anne B-
dc.contributor.authorAbramson, Michael J-
dc.contributor.authorWalters, E Haydn-
dc.contributor.authorDharmage, Shyamali C-
dc.date2019-10-30-
dc.date.accessioned2019-11-06T04:04:38Z-
dc.date.available2019-11-06T04:04:38Z-
dc.date.issued2019-10-30-
dc.identifier.citationThorax 2020; 75(1): 28-37en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22014-
dc.description.abstractAdult spirometry following community-acquired childhood pneumonia has variably been reported as showing obstructive or non-obstructive deficits. We analysed associations between doctor-diagnosed childhood pneumonia/pleurisy and more comprehensive lung function in a middle-aged general population cohort born in 1961. Data were from the prospective population-based Tasmanian Longitudinal Health Study cohort. Analysed lung function was from ages 7 years (prebronchodilator spirometry only, n=7097), 45 years (postbronchodilator spirometry, carbon monoxide transfer factor and static lung volumes, n=1220) and 53 years (postbronchodilator spirometry and transfer factor, n=2485). Parent-recalled histories of doctor-diagnosed childhood pneumonia and/or pleurisy were recorded at age 7. Multivariable linear and logistic regression were used. At age 7, compared with no episodes, childhood pneumonia/pleurisy-ever was associated with reduced FEV1:FVC for only those with current asthma (beta-coefficient or change in z-score=-0.20 SD, 95% CI -0.38 to -0.02, p=0.028, p interaction=0.036). At age 45, for all participants, childhood pneumonia/pleurisy-ever was associated with a restrictive pattern: OR 3.02 (1.5 to 6.0), p=0.002 for spirometric restriction (FVC less than the lower limit of normal plus FEV1:FVC greater than the lower limit of normal); total lung capacity z-score -0.26 SD (95% CI -0.38 to -0.13), p<0.001; functional residual capacity -0.16 SD (-0.34 to -0.08), p=0.001; and residual volume -0.18 SD (-0.31 to -0.05), p=0.008. Reduced lung volumes were accompanied by increased carbon monoxide transfer coefficient at both time points (z-score +0.29 SD (0.11 to 0.49), p=0.001 and +0.17 SD (0.04 to 0.29), p=0.008, respectively). For this community-based population, doctor-diagnosed childhood pneumonia and/or pleurisy were associated with obstructed lung function at age 7 for children who had current asthma symptoms, but with evidence of 'smaller lungs' when in middle age.en_US
dc.language.isoeng-
dc.subjectclinical epidemiologyen_US
dc.subjectrespiratory infectionen_US
dc.titleChildhood pneumonia, pleurisy and lung function: a cohort study from the first to sixth decade of life.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleThoraxen_US
dc.identifier.affiliationDepartment of Occupational Medicine, Haukeland University Hospital, Bergen, Norwayen_US
dc.identifier.affiliationDepartment of Medicine, Monash University, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationAllergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationCentre for International Health, University of Bergen, Bergen, Norwayen_US
dc.identifier.affiliationAllergy and Lung Health Unit, Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationNHMRC Centre of Research Excellence for Chronic Respiratory Disease‎, University of Tasmania, Hobart, Tasmania, Australiaen_US
dc.identifier.affiliationDepartment of Epidemiology and Preventive Medicine, Monash University, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationChild Health Division, Menzies School of Health Research, Darwin, Northern Territory, Australiaen_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Queensland Children's Hospital, Brisbane, Queensland, Australiaen_US
dc.identifier.affiliationQueensland University of Technology, Brisbane, Queensland, Australiaen_US
dc.identifier.affiliationCancer Epidemiology and Intelligence Division, Cancer Council Victoria, Melbourne, Victoria, Australiaen_US
dc.identifier.affiliationPrince of Wales' Hospital Clinical School and School of Medical Sciences, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australiaen_US
dc.identifier.affiliationRespiratory and Sleep Medicineen_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.affiliationDepartment of Respiratory Medicine, The Alfred Hospital, Melbourne, Victoria, Australiaen_US
dc.identifier.doi10.1136/thoraxjnl-2019-213389en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-7034-0615en_US
dc.identifier.orcid0000-0001-6481-3391en_US
dc.identifier.pubmedid31666389-
dc.type.austinJournal Article-
local.name.researcherMcDonald, Christine F
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
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