PMID- 23621986 OWN - NLM STAT- MEDLINE DCOM- 20140130 LR - 20240505 IS - 1471-2466 (Electronic) IS - 1471-2466 (Linking) VI - 13 DP - 2013 Apr 27 TI - Dyspnea affective response: comparing COPD patients with healthy volunteers and laboratory model with activities of daily living. PG - 27 LID - 10.1186/1471-2466-13-27 [doi] AB - BACKGROUND: 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. FAU - O'Donnell, Carl R AU - O'Donnell CR AD - Division of Pulmonary, Critical Care, and Sleep Medicine, Beth Israel Deaconess Medical Center, Boston, MA, 02215, USA. codonne1@bidmc.harvard.edu FAU - Schwartzstein, Richard M AU - Schwartzstein RM FAU - Lansing, Robert W AU - Lansing RW FAU - Guilfoyle, Tegan AU - Guilfoyle T FAU - Elkin, Daniel AU - Elkin D FAU - Banzett, Robert B AU - Banzett RB LA - eng GR - R01 NR010006/NR/NINR NIH HHS/United States GR - NR10006/NR/NINR NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural DEP - 20130427 PL - England TA - BMC Pulm Med JT - BMC pulmonary medicine JID - 100968563 RN - 142M471B3J (Carbon Dioxide) SB - IM MH - Activities of Daily Living/*psychology MH - Aged MH - Aged, 80 and over MH - Anxiety/epidemiology MH - Carbon Dioxide/adverse effects MH - Case-Control Studies MH - Dyspnea/chemically induced/*psychology MH - *Emotions MH - Female MH - Humans MH - Incidence MH - Male MH - Middle Aged MH - Pilot Projects MH - Pulmonary Disease, Chronic Obstructive/*psychology MH - Tidal Volume PMC - PMC3663820 EDAT- 2013/04/30 06:00 MHDA- 2014/01/31 06:00 PMCR- 2013/04/27 CRDT- 2013/04/30 06:00 PHST- 2012/11/09 00:00 [received] PHST- 2013/04/17 00:00 [accepted] PHST- 2013/04/30 06:00 [entrez] PHST- 2013/04/30 06:00 [pubmed] PHST- 2014/01/31 06:00 [medline] PHST- 2013/04/27 00:00 [pmc-release] AID - 1471-2466-13-27 [pii] AID - 10.1186/1471-2466-13-27 [doi] PST - epublish SO - BMC Pulm Med. 2013 Apr 27;13:27. doi: 10.1186/1471-2466-13-27.