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dc.contributor.authorO’Donnell, Carl R
dc.contributor.authorSchwartzstein, Richard Martin
dc.contributor.authorLansing, Robert
dc.contributor.authorGuilfoyle, Tegan
dc.contributor.authorElkin, Daniel
dc.contributor.authorBanzett, Robert B.
dc.date.accessioned2013-10-17T20:17:51Z
dc.date.issued2013
dc.identifier.citationO’Donnell, Carl R, Richard M Schwartzstein, Robert W Lansing, Tegan Guilfoyle, Daniel Elkin, and Robert B Banzett. 2013. Dyspnea affective response: comparing COPD patients with healthy volunteers and laboratory model with activities of daily living. BMC Pulmonary Medicine 13: 27.en_US
dc.identifier.issn1471-2466en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:11181051
dc.description.abstractBackground: Laboratory-induced dyspnea (breathing discomfort) in healthy subjects is widely used to study perceptual mechanisms, yet the relationship between laboratory-induced dyspnea in healthy volunteers and spontaneous dyspnea in patients with chronic lung disease is not well established. We compared affective responses to dyspnea 1) in COPD patients vs. healthy volunteers (HV) undergoing the same laboratory stimulus; 2) in COPD during laboratory dyspnea vs. during activities of daily living (ADL). Methods: We induced moderate and high dyspnea levels in 13 COPD patients and 12 HV by increasing end-tidal CO2 (PETCO2) during restricted ventilation, evoking air hunger. We used the multidimensional dyspnea profile (MDP) to measure intensity of sensory qualities (e.g., air hunger (AH) and work/effort (W/E)) as well as immediate discomfort (A1) and secondary emotions (A2). Ten of the COPD subjects also completed the MDP outside the laboratory following dyspnea evoked by ADL. Results: COPD patients and HV reported similar levels of immediate discomfort relative to sensory intensity. COPD patients and HV reported anxiety and frustration during laboratory-induced dyspnea; variation among individuals far outweighed the small differences between subject groups. COPD patients reported similar intensities of sensory qualities, discomfort, and emotions during ADL vs. during moderate laboratory dyspnea. Patients with COPD described limiting ADL to avoid greater dyspnea. Conclusions: In this pilot study, we found no evidence that a history of COPD alters the affective response to laboratory-induced dyspnea, and no difference in affective response between dyspnea evoked by this laboratory model and dyspnea evoked by ADL.en_US
dc.language.isoen_USen_US
dc.publisherBioMed Centralen_US
dc.relation.isversionofdoi:10.1186/1471-2466-13-27en_US
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3663820/pdf/en_US
dash.licenseLAA
dc.subjectDyspneaen_US
dc.subjectSymptom assessmenten_US
dc.subjectCOPDen_US
dc.titleDyspnea affective response: comparing COPD patients with healthy volunteers and laboratory model with activities of daily livingen_US
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden_US
dc.relation.journalBMC Pulmonary Medicineen_US
dash.depositing.authorBanzett, Robert B.
dc.date.available2013-10-17T20:17:51Z
dc.identifier.doi10.1186/1471-2466-13-27*
dash.contributor.affiliatedLansing, Robert
dash.contributor.affiliatedBanzett, Robert
dash.contributor.affiliatedSchwartzstein, Richard


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