Ventilation efficiency to exercise in patients with cystic fibrosis.

PEDIATRIC PULMONOLOGY(2019)

引用 10|浏览18
暂无评分
摘要
Introduction Exercise ventilation efficiency index in cardiopulmonary exercise testing (CPET) is elevated in patients with heart failure providing useful information on disease progression and prognosis. Few data, however, exist for ventilation efficiency index among cystic fibrosis (CF) patients. Aims To assess ventilation efficiency index (Delta VE/Delta VCO2 or V ' E/V ' CO2 slope) and intercept of ventilation (VE-intercept) in CF patients with mild, moderate, and severe cystic fibrosis (CF) lung disease. To assess possible correlations with ventilation inhomogeneity and structural damages as seen on high resolution computed tomography (HRCT). Methods CF patients with mild (FEV1 > 80%, n = 47), moderate (60% < FEV1 < 80%, n = 21), and severe (FEV1 < 60%, n = 9) lung disease, mean age 14.9 years participated. Peak oxygen uptake (VO(2)peak), pulmonary ventilation at peak exercise (VE), respiratory equivalent ratios for oxygen and carbon dioxide at peak exercise (VE/VO2, VE/VCO2), end-tidal CO2 (PetCO(2)), and Delta VE/Delta VCO2, Delta VE/Delta VO2 in a maximal CPET along with spirometry and multiple breath washout indices were examined. HRCT scans were performed and scored using Bhalla score. Results Mean Delta VE/Delta VCO2 showed no significant differences among the three groups (P = .503). Mean VEint discriminated significantly among the different groups (p(2)< 0.001). Ventilation efficiency index did not correlate either with LCI or Bhalla score. However, VE together with Delta VE/Delta VCO2 slope could predict Bhalla score (r(2) = 0.869, P = .006). Conclusion No significant differences were found regarding Delta VE/Delta VCO2 slope levels between the three groups. Ventilation intercept (VEint) was elevated significantly as disease progresses reflecting increased dead space ventilation. CF patients retain their ventilation efficiency to exercise even as lung function deteriorates by adopting a higher respiratory rate along with increased dead space ventilation.
更多
查看译文
关键词
cystic fibrosis,pulmonary function testing
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要