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Ventilatory abnormalities in patients with cystic fibrosis undergoing the submaximal treadmill exercise test

机译:接受次最大跑步机运动测试的囊性纤维化患者的通气异常

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摘要

BackgroundExercise has been studied as a prognostic marker for patients with cystic fibrosis (CF), as well as a tool for improving their quality of life and analyzing lung disease. In this context, the aim of the present study was to evaluate and compare variables of lung functioning. Our data included: (i) volumetric capnography (VCAP) parameters: expiratory minute volume (VE), volume of exhaled carbon dioxide (VCO2), VE/VCO2, ratio of dead space to tidal volume (VD/VT), and end-tidal carbon dioxide (PetCO2); (ii) spirometry parameters: forced vital capacity (FVC), percent forced expiratory volume in the first second of the FVC (FEV1%), and FEV1/FVC%; and (iii) cardiorespiratory parameters: heart rate (HR), respiratory rate, oxygen saturation (SpO2), and Borg scale rating at rest and during exercise. The subjects comprised children, adolescents, and young adults aged 6–25 years with CF (CF group [CFG]) and without CF (control group [CG]).
机译:背景研究运动已作为囊性纤维化(CF)患者的预后指标,也是改善其生活质量和分析肺部疾病的工具。在这种情况下,本研究的目的是评估和比较肺功能的变量。我们的数据包括:(i)体积二氧化碳图(VCAP)参数:呼气分钟量(VE),呼出二氧化碳量(VCO2),VE / VCO2,死区与潮气量之比(VD / VT)以及潮气二氧化碳(PetCO2); (ii)肺活量测定参数:强制肺活量(FVC),FVC第一秒的强制呼气量百分比(FEV1%)和FEV1 / FVC%; (iii)心肺参数:静止和运动时的心率(HR),呼吸率,血氧饱和度(SpO2)和Borg评分。受试者包括6至25岁的儿童,青少年和年轻成人,他们患有CF(CF组[CFG])而没有CF(对照组[CG])。

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