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Dyspnea perception in cystic fibrosis patients

机译:囊性纤维化患者的呼吸困难知觉

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We evaluated dyspnea perception in cystic fibrosis patients compared with normal subjects, during an inspiratory resistive loading test and 6-min walk test. We also evaluated the correlation between dyspnea scores induced by resistive loads and by the 6-min walk test. In this prospective, cross-sectional study, 31 patients with cystic fibrosis (≥15 years of age) and 31 age-, gender-, and ethnicity-matched healthy volunteers (20 females and 11 males per group) underwent inspiratory resistive loading, spirometry, and the 6-min walk test. As the magnitude of the inspiratory loads increased, dyspnea scores increased (P
机译:在吸气性阻力负荷测试和6分钟步行测试期间,我们评估了与正常受试者相比囊性纤维化患者的呼吸困难知觉。我们还评估了阻力负荷和6分钟步行测试引起的呼吸困难评分之间的相关性。在这项前瞻性,横断面研究中,对31例囊性纤维化患者(≥15岁)和31例年龄,性别和种族相匹配的健康志愿者(每组20名女性和11名男性)进行了吸气阻力负荷,肺活量测定,以及6分钟的步行测试。随着吸气量的增加,呼吸困难评分增加(P

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