Dyspnea during 6MWT in stable patients with chronic obstructive pulmonary disease
M. Satake, T. Shioya, H. Takahashi, K. Sugawara, C. Kasai, N. Kiyokawa, T. Watanabe, S. Fujii, T. Shiki, M. Honma (Akita, Japan)
Source: Annual Congress 2008 - Physiological response to exercise performance
Session: Physiological response to exercise performance
Session type: E-Communication Session
Number: 3293
Disease area: Airway diseases
Abstract Aim: The purpose of this study was to examine the dyspnea during the six-minute walk test (6MWT) in patients with chronic obstructive pulmonary disease. Subjects and Methods: Fourteen subjects (14 male, age 75.6 ± 7.2 years old, with FEV1 66.4 ± 19.3 % of predicted) took part in the study. Throughout the 6MWT, oxygen uptake, carbon dioxide production, minute ventilation, and heart rate were measured using a portable cardiopulmonary exercise system (MetaMax 3B, Cortex, Germany). Dyspnea and oxygen saturation were recorded at the end of each minute during the 6MWT. Dyspnea was measured using the Borg 0-10 dyspnea scale. Inspiratory capacity (IC) was measured at every two minute during the 6MWT. Results: This study showed that the distance walked in the 6MWT was 521.0 ± 98.6 m, the Borg dyspnea scale at the end of the 6MWT was 3.6 ± 1.8, and peak oxygen uptake was 13.41 ± 2.54 ml/min/kg. The value of oxygen saturation showed 89.8 ± 5.6 after 6MWT. The value of IC was 1.34 ± 0.36 L before 6MWT, and 1.21 ± 0.29 L after 6MWT. The value of IC was significantly lower at the end of 6MWT compared to that before 6MWT (p<0.05). The degree of dyspnea significantly increased with time, and the value of oxygen uptake showed a tendency to become higher during 6MWT. Conclusions: This study suggested that the dyspnea during 6MWT was caused by not only the dynamic hyperinflation but also the sense of respiratory effort.
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M. Satake, T. Shioya, H. Takahashi, K. Sugawara, C. Kasai, N. Kiyokawa, T. Watanabe, S. Fujii, T. Shiki, M. Honma (Akita, Japan). Dyspnea during 6MWT in stable patients with chronic obstructive pulmonary disease. Eur Respir J 2008; 32: Suppl. 52, 3293
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